“although the operative non- dentistry may be perfect but
TRANSCRIPT
1
Non-
Pharmacological
Behaviour
Management
DR MITAKSHARA NIRWAN
ldquoAlthough the operative
dentistry may be perfect but
appointment is a failure if the
child departs in tearsrdquo
- Mc Elory (1895)
Behavior Behaviour is an Observable act which can be described in similar ways by more than one person It is defined as any change observed in the functioning of an organism
Behavior management The means by which the dental health team effectively amp efficiently performs dental treatment amp simultaneously instills a positive dental attitude in the child (Wright1975)
Behavior modification Defined as the attempt to alter human behavior amp emotion in beneficial way amp in accordance with laws of learning
Behavior shaping Is the procedure which slowly develops behavior by reinforcing a successive approximation of the desired behavior until the desired behavior comes in to being
BEHAVIORAL PATTERNS IN
CHILDREN
According to age
bull Pre-cooperative stage ndash less than 2 years bull Cooperative stage- above 2 years
Clinical classification of behaviour patterns
2
bull Cooperative bull Lacking cooperative ability bull Potentially cooperative
Lampshirersquos Classification
Pinkhamrsquos Classification
2
I Co-operative behavior (+ve)
1) Cooperative behaviour
2) Lacking co-operative
ability
3) Potentially cooperative
behavior
Wright Classification
II Uncooperative behaviour (-ve)
1Uncontrolled
behaviorhystericalincorrigible
2Defiant behaviorobstinate
3Timid behavior
4Tense cooperative
5Whining behavior
6Stoic behavior
Wilson classification
Normalbold
Tasteful timid
Hysterical rebellious
Nervous fearful
Factors affecting behavior of children
Wright summarized the following factors bull Medical history bull Maternal anxiety
bull Family and peer influence
bull Dental office environment
bull Growth and development
bull Personal factors
bull Environmental factors
bull Other variables
Role of Dentist in childrsquos behavior
Appearance of dental office Personality of dentist
Time and length of appointment
Maternal influence on Childrsquos Behaviour
Motherrsquos behavior Childrsquos behavior
1 Over protective
a Dominant
b Overindulgent
Submissive shy
anxious aggressive demanding
2 Overindulgent Aggressive spoiled demanding displays temper
3 Under affectionate Usually well behaved but may be unable to
cooperate shy may cry easily
4 Rejecting Aggressive overactive disobedient
5 Authoritarian
6 Identification
Evasive amp dawdling
Cries easily lacks confidence
Behaviour Mangement
Fundamentals of behaviour management
Positive approach
Team attitude
Truthfulness
Organization
Tolerance
Flexiblity
3
Classification of behavior management
Management
Psychological Pharmacological Psychological
Communication
Behavior shaping
Behavior Management
Behavior shaping
Desensitization
Modeling
Contingency management
Disruptive
Voice control
Aversive
HOME
Physical Restraints
Others
Distraction
Audio Analgesia
Bio feed back
Hypnosis
Humor
Coping
Relaxation
COMMUNICATION
communication
Verbal
speech
Non-verbal
Body language
smiling
Eye contact Showing concern
By Touching
Give him a pat
Giving him hug
Expression of feeling
Both
DENTAL TERMINOLOGY WORD SUBSTITUTE
Rubber dam Rain coat
Rubber dam clamp Tooth button
R D frame Coat rack
Sealant Tooth paint
Topical fluoride gel Cavity fighter
Air syringe Wind gun
Suction Vacuum cleaner
Study models Statues
Alginate Pudding
High speeds Whistle
Low speeds Motor cycle
Euphemism Tell Show Do Technique (TSD)
Cornerstone of behaviour management
Given by Addleston in 1959
Objectives
1 Teach the patient imp aspects of the
dental visit amp familiarize the patient with
the dental setting
2 Shape the patientrsquos response to
procedures
through desensitization amp well described
expectations
4
Alternatives to TSD
Tell Play Do
Tell Show Play Doh
Tell Play Do with
Smart Phone Dentist
Game Ask Tell Ask
DESENSITIZATION
Demonstrated by James popularized by Wolpe
Desensitization is a therapeutic technique that pairs an
anxiety- evoking stimulus with a response inhibitory to
anxiety In each situations the percieved link between the
stimulus and the anxiety response is weakened
Involves 3 Stages
1Training the patient to relax
2Constructing a hierarchy of fear
3Introducing each stimulus in the
hierarchy
Modeling
Giver by Bandura (1967) Allowing a pt to observe 1more individual
who demonstrate appropriate behavior in particular situation
Steps in modeling Pt attention obtained Desired behavior is modeled Physical guidance of desired behavior Reinforcement of the guided behavior may be provided Reinforcement of behavior that did not require guidance Reinforcement for appropriate behavior initiated without modeling
Types 1 Live model 2 Symbolic or vicarious model
CONTINGENCY MANAGEMENT
Is a method of modifying the behavior of children by
presentation or withdrawal of reinforcers
Positive reinforcer
Henry W Fields 1984
Contingent presentation
Increases frequency of
behavior
Negative reinforcer
Stokes amp Kennedy1980
Contingent withdrawal
Increases the frequency of
behavior
Material
bull Candies
bull Gums
bull Cookies
bull Toys
Social
bull Praise
bull Facial expressions
bull Nearness
bull Physical contact
Activity
bull TV
bull Camping outdoor
bull Music
Reinforcers
Coping
Defined as the cognitive amp behavioral efforts made by an individual to master tolerate or reduce stressful situations
2types
a) Behavioral physical amp verbal activities
b) Cognitive silent amp thinking in mind to keep calm
It enables
ndash reality-oriented working
- cognitive reappraisal
- emotion cognitions
5
Distraction
Distraction is a tactic designed to divert a patient attention away from their current behavior to focus their interest in something else Types Audio Distraction Audiovisual Distraction
Relaxation
Effective in reducing immediate anxiety and fear
Involves series of basic exercises which may take several months to learn amp practice
Voice control
Given by Pinkham in 1985
Modification of the timbre intensity and pitch of ones voice in an attempt
to dominate the interaction between dentist and child
Objectives
bull To gain the patient attention and
compliance
bull To avoid negative or avoidance
behavior
bull To establish authority
Indications bull Uncoperative and inattentive
patients
Contraindications bull Children who due to age
disability mental or emotional immaturity are unable to understand
Hypnosis
First suggested by Franz A Mesmer in
1773
Altered state of consciousness
characterized by heightened suggestibility
to produce desirable behavioral and
physiological changes
Most effective in the presence of anxiety
Not all patients can be hypnotized
Basic mechanism - relief of pain through
suggestions of relief given in a close
trusting interpersonal situation
Henon outlined following uses
bull To reduce nervousness and
apprehension
bull To eliminate defence mechanisms
that patient use to postpone dental
work
bull To control functional or
psychosomatic grapping
bull To prevent thumb sucking and
bruxism
bull To induce anesthesia
Hand over Mouth Exercise (HOME)
Given by DR EVANGELINE JORDAN (1920)
Evangeline Jordan - If a normal child will not listen but continues to cry
and strugglehellip Hold a folded napkin over the childrsquos mouthhellipand
gently but firmly hold his mouth shut
Other terminologies bull Aversive Conditioning by Lenchner and Wright bull Emotional surprise therapy by Lampshire bull HOM airway restricted (HOMAR) by Levitas (1947) bull Aversion by Crammer (1973)
Children who are
momentarily hysterical
belligerent or defiant
3-6 yrs old
Child who can understands
simple verbal commands
Indications
Contraindications
Very young immature frightened child with serious physical mental or emotional handicap
6
Variationshellip Hand over mouth with airway restricted Towel over mouth
Towel over mouth with airway restricted
Body
Papoose board
Triangular sheet
Pedi wrap
Bean Bag
Safety belt
Extremities
Posey straps
Velco straps
Towel amp Tape
Head
Forearm support
Plastic bowl
Head positioner
Mouth
Tongue blades
Mouth Prop
Bite blocks
Positive Stabilization Mouth
Tongue blade open mouth wide prop Molt mouth prop
Rubber bite blocks
Extremities
Posey Strap
Head
Body
Papoose board
Pedi-wrap
7
1
Impact of Handheld Devices on
Children An Evaluation of Usage amp
Dependency Behaviour
0092
DR MITAKSHARA NIRWAN
Handheld devices
A handheld device is a pocket size
computing device with a display
screen and inputoutput interface like
an external or touchscreen keyboard
For example- smartphones tablet
computers handheld videogame
consoles
Haruki Murakami
ldquoCell Phones are so
convenient that they have
become an inconveniencerdquo
Introduction
The most famouscommonly used and easily accessible type of gadgets are
lsquoHandheld devicesrsquo They are as popular in children as they are in adults
The access and ownership of these devices amongst children has grown
substantially in the past decade Concerns exist regarding excessive usage
and the impact of frequent consumption of mobile media on their health and
behaviour
Aims and Objective
This objective of this study was to asses the level of use of handheld
devices among children aged 0-12 years and their positive and negative
impacts on them It further describes the dependency of these devices
and the behavioral problems associated with it
Materials and Methods An online survey was conducted and a self administered questionnaire
was prepared specially for the parents which included a total of 15
questions regarding the usage and dependency of the device
A total of 100 responses were collected from parents who had children
aged 0-12 years who used these devices on daily basis
2
Level of Usage (Q 123)
Results Purpose (Q7)
Improved
communication and
learning
Using more than
one type of
device
Helped in
Speech
Positive Impacts -
(Q58 amp 9)
P value 0003(s) P value-0007 P value-0006(s)
Reduced parent-
child interaction Disrupted sleep Lack of motivation for academics
Negative Impacts (Q81213)
P value-0001(s) P value-0002(s) P value-0006
Time when children use
the device the most
Isolation of the
child Behavioral impact when gadget is
taken back
Dependency
Behaviour (Q10111415)
P value-002(s) P value 002(s) P value-044
This study was done to evaluate the level of usage of handheld devices and their impact
on the children aged 0-12 years The questionnaire was made such that it asked both the
positive and negative impact and further included the questions regarding the
dependency
784 children had access to smartphone and 17 used tablets
The most common age group in which the devices was used the most was 5-8 years
followed by 9-12 followed by 0-4 (Arlinda et al 2019 )
Another study done by (Rachel Bedford et al 2016) concluded increase usage of mobile
phones 5122 in 6ndash11 monthshy olds through to 9205 by 25ndash36 months
745used these devices several times a day out of which 539 used it for more than
one hourday 255 used it for less than one hour and 206 for more than 2 hours
Various studies follow the same recommendation given by AAP to limit the duration of
gadget amongst children
Discussion
3
Improve of Cognitive Skills
Amongst the positive impacts most parents have answered that the usage of these
devices has helped their child communicate and learn better and it has showed significant
results According to (Sundus M 2018)These devices improve the cognitive skills and
develop their learning skills fasterThe competition skills also get better It gives time for brain to think and process information better Another study which supports this (LF
Jonathan et al 2016)
Motor Physical Exercise
This study has shown that children like to use more than one type of device
sometimesUsing these devices improve fine motor skillshand eye coordination and
hands and fingers become more efficient (Srinahyanti et al 2019) (Sundus M 2018)
Speech Improvement
392 Parents say that maybe usage of the devices has helped improve speech in their
children but Various studies show otherwise as most of them shows that usage of handheld
devices causes delay of speech (Srinahyanti et al 2019)
Reduced parent child interaction
The negative impacts are more when compared to the positive ones Usage of gadgets
has resulted in reduced parent child interaction Less face to face interaction can
cause detachment from family members and value which in turn also causes isolation
of the child as he is more comfortable with the gadget (M Suhana-2017)
Sleep Disorders
This study shows that most parents have agreed that usage of these devices does
cause disruption of sleep Various studies have shown that children get fewer hours of
sleepdrowsiness during the day and dramatic increase in day time sleep because of
the screen usage (Acc to National Sleep Foundation) ( Cain N et al 2010)
In this study most number of parents have
agreed that their children might be dependent on
these devices and also had showed restless and
violent behavior if the gadget is snatched from
them
Most number of kids (667) are heavily
dependent as they like to use the device during
their meal time
Various other studies have assessed the screen
time dependency and have concluded that
various kids suffer from SDD
Conclusion The study conclusively shows that the impact of handheld devices is akin to the
importance of table salt in our meals most significant for our growth and
development in moderate amounts and hazardous in excess The negatives clearly
outweigh the positives with the latter too few and far in between This study also
points towards further extensive research on the subject because we need to find ways and also educate parents to optimise the role of these devices in their
childrenrsquos life taking advantage of their positive attributes and minimising their
negative ones
References 1Wahyuni AS Siahaan FB Arfa M Alona I Nerdy N The Relationship between the Duration of Playing
Gadget and Mental Emotional State of Elementary School Students Open Access Maced J Med Sci
20197(1)148ndash151
2Sundus M Department of Computer Science Lahore-The Impacts of using Gadgets on ChildrenJournal of Depression and Anxiety 2018vol 7(1)296
3Amawi SO Subki AH Khatib HA et al Use of Electronic Entertainment and Communication Devices Among
a Saudi Pediatric Population Cross-Sectional Study Interact J Med Res 20187(2)e13
4Julia ldquoHandheld Screen Time Linked with Speech Delays in Young Childrenrdquo Present Pediatric Acad Soc
Meet 2017
5C Rowan ldquoThe Impact of Technology on Child Sensory Motor Developmentrdquo 2003
6Impact of media use on children and youth Paediatr Child Health 20038(5)301ndash317
7Naik SV Children and their gadgets A pedodontist perspective Int J Oral Health Sci 2018857-8
8Roberts DF Foehr UG Rideout V Generation M Media in the lives of 8‐18 year‐olds A Kaiser Family
Foundation Study 2005
9Arya K Time spent on television viewing and its effect on changing values of school going children Anthropologist 20046269‐71
10 Lerner C Barr R Screen Sense Setting the Record StraightResearch‐Based Guidelines for Screen
Use for Children Under 3 Years Old Early learning project at Georgetown university 2014 p 1‐10
11SrinahyantiYasaratodo Wau Imelda Free Unita Manurung Nur Arjani-Influence of gadget A positive
and Negative Impact of Smartphone Usage for Early Child2019
4
THANK YOU
1
Morankar Rahul Aditi Kapur Krishan Gauba Ashima Goyal
MANAGEMENT OF ENDODONTIC INSTRUMENT SEPARATION IN
PRIMARY TEETH
CASE REPORT
Journal of South Asian Association of Pediatric Dentistry 2020
DR MITAKSHARA NIRWAN
bull Introduction
bull Aims amp Objectives
bull Case report
bull Discussion
bull Conclusion
bull Pros amp Cons
bull References
CONTENTS
Separation of endodontic instrument is an unexpected complication and its prevalence is not known It is a common belief among the dental professionals that rotary nickelndashtitanium (NiTi) instruments separate more frequently than stainless steel hand instruments
However literature revealed that in permanent teeth the reported prevalence of separated endodontics manual instruments is in the range of 07-74 whereas for rotary NiTI instruments it is
approximately 04-5
Fractured root canal instruments may include endodontic files Gates Glidden burs finger spreaders
and paste fillers
INTRODUCTION
The aim of this study is to describe the management strategies for endodontic
instrument separation in a root canal of primary teeth with emphasis on factors
requiring consideration in different clinical situations
AIMS amp OBJECTIVES
CASE 1
A 6-year-old male child reported with the chief complaint of spontaneous toothache in mandibular left second primary molar since few days It has aggravated following dental treatment at a private dental clinic Clinical examination revealed an underprepared access cavity with 75 and incomplete caries removal
which was sealed with glass ionomer cement
An intraoral periapical radiograph revealed a separated instrument of about 6ndash7 mm size in the distal root
2
The separated instrument was lodged firmly in distobuccal root canal 2ndash3 mm below the cementoenamel junction The instrument was bypassed successfully with no 15 and no 20 H-files but attempts for its retrieval were not successful
GatesndashGlidden (GG) drills no 2 (07 mm) and no 3 (09 mm) were used to drill around the instrument after which it was retrieved successfully using no 25 H-file
All the canals were instrumented till size 30 k-file followed by obturation with metapex and restoration with glass ionomer cement amp followed by placement of a crown and loop space maintainer for missing 74 The instrument retrieved was a manual reamer measuring 6 mm in length
The patient was asymptomatic since then and is under regular follow-up
CASE 2
A 5-year-old female child reported with the chief complaint of spontaneous toothache in mandibular left second
primary molar Clinical examination revealed deep occlusal caries with fractured lingual wall and pain on
percussion An intraoral periapical radiograph revealed caries involving pulp without any furcation or periapical
area of rarefaction and pulpectomy was planned
All the canals were enlarged using NiTi rotary files with a 4 taper operating at 500 rpm with minimum torque
setting An orifice opener [(0825 19 mm) of 8 taper size 25 length 19 mm] and nos 0420 file was used for
instrumentation of root canal This was followed by file nos 0425 which got separated in the distobuccal root
canal The radiograph confirmed a separated instrument of length 3ndash4 mm in the middle third of the root canal
The instrument was bypassed with no 15 k-file but could not get retrieved As instrument separation had occurred with 0425 file the involved root canal was sufficiently debrided before separation and the level of instrument separation was at the mid-root region so it was decided to obturate and seal this tooth with
periodic follow-ups instead of immediate extraction All other canals were enlarged till size 0430 in the sequential manner followed by obturation using metapex and placement of stainless steel crown
3
CASE 3
A 5-year-old female child has complaint of mild intermittent pain with primary mandibular left first molar She
had undergone pulpectomy treatment for the same during which an instrument separation has occurred in
the mesiobuccal root canal by a resident doctor
A radiograph revealed a separated instrument of about 4 mm in size lodged in the apical third but within the
confines of the mesial root An attempt was made for its retrieval but was unsuccessful The extraction of the
involved tooth was carried out under local anesthesia followed by a band and loop space maintainer
CASE 4
A 7-year-old male child reported with a chief complaint of mild intermittent pain on food lodgment with the primary mandibular right first and second molars The patient had a history of dental treatment at a private
dental clinic few months back which he did not continue further
Clinical examination revealed glass ionomer restoration with 85 and proximal caries with 84 leading to food lodgment An intraoral periapical radiograph with 85 revealed empty root canals with a separated
instrument of about 3ndash4 mm size beyond the apex of mesial root close to the developing succedaneous premolar
4
DISCUSSION
Stainless steel files usually separate fracture due to the excessive amounts of torque and overuse or the
preexisting distortion of the instrument whereas in NiTi rotary files it is a combined result of torsional stress and cyclic fatigue
Therapeutic options for the management of separated endodontic instruments include no intervention nonsurgical (orthograde conservative) management surgical management and tooth extraction
Use of ultrasonic scaler Masserann technique Endo extractor and Cavi-Endo ultrasonic instruments are some of the methods popular for retrieval of a separated endodontic instrument in the permanent tooth
In case 1 a 6-mm-long manual reamer was retrieved successfully with the use of GG drill using a manual file and copious irrigation which is the most desired treatment outcome
In case 2 the retrieval of separated rotary file lodged in the middle third of the root canal was unsuccessful in spite of multiple attempts It was therefore managed with routine obturation followed by restoration to maintain the tooth in its physiological functional state It was kept under close periodic follow-up at least
every 3 months This treatment option should be encouraged where it is possible to follow up the patient clinically and radiographically at close periodic intervals as there is the possibility of instrument escaping
into bone due to physiological root resorption
In cases 3 and 4 an instrument has separated in the apical root portion
In case 3 it was within the root canal and thus an attempt was made for its retrieval which was
unsuccessful It was therefore extracted to prevent the fractured instrument from getting exposed in the bone following resorption as there is no accurate and consistent established age for initiation of resorption in primary teeth known per se
In case 4 an immediate extraction of involved tooth was carried out as the separated instrument was beyond the apex of the primary tooth root
Age of the child clinical signs and symptoms and amount of root resorption are the factors which can also influence the management of separated instrument in primary teeth
Moreover if an instrument has separated after initial cleaning and shaping of root canal maintaining a tooth is not a problem as clinical signs and symptoms are not anticipated and the good prognosis is expected
However if an instrument has separated early during the initial cleaning and shaping of the root canal clinical symptoms may compromise the prognosis
Therefore these factors should be kept in mind while planning a suitable management strategy to avoid or at least reduce the burden of extraction and wear of space maintainer for longer period
5
CONCLUSION
The management and prognosis of a primary tooth with a separated instrument is
dependent on the level of instrument fracture within the root age of the child root
resorption and clinical signs and symptoms of the involved tooth
Different management approaches can be tried depending on clinical situations keeping
in mind benefits vs risks in preserving the tooth
PROS amp CONS
PROS
The entire procedure is given
by step by step
Well descriptive xrays and
photographs
CONS
Medical history has not been
given
REFERENCES
1 TOMER ANIL K ET AL ldquoBROKEN FILE RETRIEVAL PUZZLE IN ENDODONTICSrdquo
(2016)
2 SHENOY A MANDAVA P BOLLA N ET AL A NOVEL TECHNIQUE FOR REMOVAL OF
BROKEN INSTRUMENT FROM ROOT CANAL IN MANDIBULAR SECOND MOLAR
INDIAN J DENT RES 201425(1)107ndash110
3 PATEL J MORAWALA A TALATHI R ET AL RETRIEVAL OF A BROKEN INSTRUMENT
FROM ROOT CANAL IN PRIMARY ANTERIOR TEETH UNIV RES J DENT 20155(3)203ndash
206
4 MORANKAR R GOYAL A GAUBA K ET AL MANUAL VERSUS ROTARY
INSTRUMENTATION FOR PRIMARY MOLAR PULPECTOMIES - A 24 MONTHS
RANDOMIZED CLINICAL TRIAL PEDIAT DENT J 201828(2)96ndash102
5 KASHYAP NILOTPOL (2018) RETAINING PRIMARY MOLARS WITH INSTRUMENT
SEPERATION A CASE REPORT AND CLINICAL GUIDE
6
1
IMPACT OF 6 CITRIC ACID AND ENDOACTIVATOR AS IRRIGATION ADJUNCTS ON OBTURATION QUALITY AND PULPECTOMY OUTCOME IN
PRIMARY TEETH
NEETU JAIN SHALINI GARG ABHISHEK DHINDSA SAKSHI JOSHI HARJOY
KHATRIA
PEDIATRIC DENTAL JOURNAL 2019 29
1
DR MITAKSHARA NIRWAN
CONTENTS
bull INTRODUCTION
bull AIMS amp OBJECTIVES
bull CASE REPORT
bull RESULTS
bull DISCUSSION
bull CONCLUSION
bull PROS AND CONS
bull REFERENCES
2
INTRODUCTION
bull ENDODONTIC THERAPY IN PRIMARY TEETH INVOLVES DISINFECTION OF THE ROOT CANAL
SYSTEM AND ITS OBTURATION WITH RESORBABLE PASTE
bull THE CONTENTS OF ROOT CANAL ALONG WITH SMEAR LAYER ARE EXPECTED TO BE REMOVED
DURING THE BIOMECHANICAL PREPARATION
bull IN VITRO AND CLINICAL DOCUMENTS HAVE INDICATED THAT MECHANICAL PREPARATION OF
THE CANAL LEAVES LARGE PORTIONS OF THE CANAL WALLS UNDEBRIDED AND COMPLETE
REMOVAL OF THE BACTERIA BY THIS MECHANICAL PROCEDURE ALONE IS UNLIKELY TO BE SEEN
THEREFORE SOME FORM OF DISINFECTIONIRRIGATION IS MANDATORY TO KILL THE
MICROORGANISMS AND TO REMOVE THE RESIDUAL TISSUES
3
bull THE IDEAL REQUISITES OF A ROOT CANAL IRRIGANT AS GIVEN BY ZEHNDER ARE
1 BROAD ANTIMICROBIAL SPECTRUM
2 HIGH EFFICACY AGAINST ANAEROBIC AND FACULTATIVE MICROORGANISMS ORGANIZED
IN BIOFILMS
3 ABILITY TO DISSOLVE NECROTIC PULP TISSUE REMNANTS
4 ABILITY TO INACTIVATE ENDOTOXIN
5 ABILITY TO PREVENT THE FORMATION OF A SMEAR LAYER DURING INSTRUMENTATION OR
TO DISSOLVE THE LATTER ONCE IT HAS FORMED
6 SYSTEMICALLY NONTOXIC WHEN THEY COME IN CONTACT WITH VITAL TISSUES
NONCAUSTIC TO PERIODONTAL TISSUES AND WITH LITTLE POTENTIAL TO CAUSE AN
ANAPHYLACTIC REACTION
SINCE NO SINGLE IRRIGANT HAS THESE OPTIMAL PROPERTIES STUDIES HAVE REPORTED THE USE
OF TWO OR MORE SOLUTIONS IN A SPECIFIC SEQUENCE OR IN COMBINATIONS FOR BETTER
RESULTS 4
bull SEVERAL IRRIGATING SOLUTIONS ALONG WITH CHELATING AGENTS HAVE BEEN USED
DURING BIOMECHANICAL PREPARATION OF ROOT CANAL BOTH IN PRIMARY AND
PERMANENT TEETH
bull HOWEVER NONE OF THE AVAILABLE IRRIGATING SOLUTIONS HAS BEEN REGARDED CLEARLY
AS OPTIMAL SOLUTION BECAUSE OF THEIR LIMITED EFFECTIVENESS ESPECIALLY IN APICAL
13RD OF THE ROOT CANAL SYSTEM
bull TO OVERCOME SUCH LIMITATIONS USE OF ENDOACTIVATOR HAS BEEN PROPOSED AS AN
IRRIGATION FACILITATOR THAT IS BASED ON SONIC VIBRATION (UP TO 10000 CPM) WHICH
FACILITATES THE IRRIGANT PENETRATION AND ITS RENEWAL WITHIN THE CANAL
bull ACTIVATION SYSTEMS RESULTED IN BETTER REMOVAL OF THE SMEAR LAYER IN THE APICAL
THIRD OF ROOT CANALS IN COMPARISON TO CONVENTIONAL IRRIGATION
5
CITRIC ACID
bull CITRIC ACID IS A WEAK ORGANIC ACID WITH THE APPEARANCE OF WHITE CRYSTALLINE
POWDER AT ROOM TEMPERATURE
bull IT CAN EXIST EITHER IN WATER-FREE FORM (ANHYDROUS) OR MONOHYDRATE FORM THE
WATER-FREE FORM CRYSTALLIZES FROM THE HOT WATER WHEREAS THE MONOHYDRATE
FORMS FROM THE COLD WATER THE LATTER MAY BE CONVERTED TO ANHYDROUS FORM BY
HEATING MORE THAN 78degC
bull CITRIC ACID OCCURS NATURALLY IN THE BODY IN MITOCHONDRIA AND IS USED BY BLOOD
BANKS TO PREVENT COAGULATION OF TRANSFUSED BLOOD CITRIC ACID IS ALSO ESSENTIAL
TO HUMAN METABOLISM AND IS FOUND IN MANY FOODS
6
2
bull THE BIOLOGICAL EFFECTS OF CITRIC ACID ON THE PERIODONTAL STRUCTURE HAS BEEN
EXTENSIVELY STUDIED IN PERIODONTICS
bull NEUMAN AND NEWMAN SHOWED THAT CITRIC ACID IS THE MOST EFFECTIVE ACID IN
ALTERING THE SOLUBILITY OF HYDROXYAPATITE
bull YAMAGUCHI ET AL SHOWED THAT CITRIC ACID SOLUTION HAD ANTIBACTERIAL EFFECTS ON
ALL 12 ROOT CANAL BACTERIA TESTED
bull ARIAS-MOLIZ ET AL SHOWED THAT ETHYLENEDIAMINETETRAACETIC ACID (EDTA) HAS NO
BACTERICIDAL ACTIVITY EVEN AFTER 1 HOUR CONTACT
bull THIS ACID HAS THE ABILITY OF ROOT CANAL IRRIGATION AND ALSO SMEAR LAYER REMOVAL
DIFFERENT CONCENTRATIONS (1ndash50) HAVE BEEN PROPOSED GUTMANN ET AL CONCLUDED
THAT 10 CITRIC ACID IS BETTER THAN ULTRASOUND FOR SMEAR LAYER REMOVAL FROM THE
ROOT END CAVITIES
7
bull STUDIES HAVE SHOWN IRRIGATION WITH 6 CA FOR 15 OR 30 SECONDS IS QUITE
EFFECTIVE IN REMOVING ALL THE COMPONENTS OF THE SMEAR LAYER OF THE PRIMARY
TEETH WHEREAS PERITUBULAR DENTIN DESTRUCTION WAS OBSERVED WHEN HIGHER
CONCENTRATION OF CITRIC ACID WAS USED AS AN IRRIGATING SOLUTION
8
AIMS amp OBJECTIVES
bull THIS STUDY WAS AIMED TO EVALUATE THE CLINICAL AND RADIOGRAPHIC OUTCOME OF
PULPECTOMY ALONG WITH QUALITY OF OBTURATION USING 6 CITRIC ACID AND
ENDOACTIVATOR
9
CASE REPORT
bull 350 CHILDREN (3-9 YEARS) WITH CLINICAL SIGNS AND SYMPTOMS OF CHRONIC IRREVERSIBLE
PULPITIS IN DEEPLY CARIOUS TEETH WERE SCREENED DURING SCHOOL DENTAL HEALTH
PROGRAM FROM MAY 2014-JULY 2014
bull 123 CHILDREN REPORTED TO THE DEPARTMENT AND 67 CHILDREN WERE SELECTED BASED ON
INCLUSION AND EXCLUSION CRITERIA
RECRUITMENT OF PATIENTS
10
INCLUSION CRITERIA
bull HISTORY OF SPONTANEOUS PAIN AND UNCONTROLLED BLEEDING AFTER PULP AMPUTATION
EXCLUSION CRITERIA
bull EVIDENCE OF INTERNAL OR EXTERNAL (PHYSIOLOGICPATHOLOGIC) ROOT RESORPTION OF MORE THAN A THIRD OF ITS LENGTH
bull ROOT CANAL OBLITERATION OR ANATOMIC ANOMALIES
bull INADEQUATE BONE SUPPORT OR NON RESTORABLE TOOTH
bull ONCE PATIENTS ELIGIBILITY WAS CONFIRMED THE TREATMENT PROCEDURE WAS
EXPLAINED TO THE PARENTGUARDIAN AND INFORMED WRITTEN CONSENT WAS
OBTAINED FROM PARENTSGUARDIANS SHOWING WILLINGNESS FOR THEIR
CHILDRENS TREATMENT 11
PROCEDURE
bull PULPECTOMY WAS PERFORMED BY ONE OPERATOR OF PEDIATRIC DENTISTRY DEPARTMENT
USING A STANDARDIZED TREATMENT PROTOCOL FOR ALL THE PATIENTS
bull AFTER ADMINISTRATION OF LOCAL ANESTHESIA RUBBER DAM WAS APPLIED FOR ISOLATION
bull ACCESS CAVITY WAS PREPARED USING AIR-ROTOR HAND PIECE WITH 8 ROUND BUR AND
PULP TISSUE WAS EXTIRPATED WITH THE HELP OF SPOON EXCAVATOR
bull FURTHER THE NEGOTIATION OF THE CANALS WAS DONE WITH 10 K-FILE
bull A DIAGNOSTIC RADIOGRAPH WAS TAKEN FOR ROOT LENGTH DETERMINATION AND
WORKING LENGTH WAS KEPT 1 MM SHORT OF THE RADIOGRAPHICAL APEX
bull ALL ROOT CANALS WERE INSTRUMENTED MANUALLY USING K-FILES AND WERE IRRIGATED
WITH 10 ML 09 NORMAL SALINE AND 1 SODIUM HYPOCHLORITE AS STANDARDIZING
PROTOCOL FOR ROOT CANAL PREPARATION AND DISINFECTION
12
3
GROUP 1 (CA + E) - IRRIGATION WAS DONE
WITH 10 ML OF 6 CITRIC ACID (CITOCID AMMDENT)
AND IRRIGANTS WERE SONICALLY AGITATED WITH
ENDOACTIVATOR (DENTSPLY) FOR 30 S PER CANAL USING REDBLUE
ENDOACTIVATOR TIP
GROUP 2 (CA) - 10 ML OF 6 CITRIC ACID FOR 1 MIN USING
27 GAUZE IRRIGATING NEEDLE
GROUP 3(SH + E) - 10 ML OF 1 SODIUM HYPOCHLORITE
SOLUTION AND SONIC ACTIVATION WITH ENDOACTIVATOR
GROUP 4(SH) - 10 ML OF 1 SODIUM HYPOCHLORITE
SOLUTION USING IRRIGATING NEEDLE (CONTROL GROUP)
bull TEETH UNDERGOING PULPECTOMY WERE RANDOMLY ENROLLED BY CHIT METHOD INTO THREE
STUDY AND ONE CONTROL GROUP
13
bull IN CITRIC ACID GROUPS FINAL RINSE WITH NORMAL SALINE WAS DONE TO REMOVE THE
REMAINING CRYSTALS (CHELATES)
bull FOLLOWING BIOMECHANICAL PREPARATION THE ROOT CANALS WERE DRIED WITH STERILE
ABSORBENT PAPER POINTS AND OBTURATED WITH VITAPEX USING HAND HELD
LENTULOSPIRAL FINAL RESTORATIONS WERE DONE USING COMPOSITE RESIN
14
bull CLINICAL FOLLOW UP WAS DONE AT 24 H1 WEEK 1 MONTH 6 MONTH AND 12
MONTH TO CHECK PAIN PRESENCE AND PAIN FREQUENCY (ONCEMORE THAN ONCE)
SWELLING FISTULA SENSITIVITY TO PERCUSSION
bull RADIOGRAPHIC FOLLOW UP WAS DONE AT 6 MONTH AND 12 MONTH FOR ANY
DEVIATED ERUPTION OF SUCCEDANEOUS TEETH EXCESS FILING MATERIAL AND ITS
RESORPTION EXTERNALINTERNAL ROOT RESORBTION CALCIFIC METAMORPHOSIS
PRESENCE OF FURCATION RADIOLUCENCY
CLINICAL amp RADIOGRAPHIC FOLLOW UP
15
RADIOGRAPHIC ASSESSMENT OF OBTURATION QUALITY
bull POSTOPERATIVE RADIOGRAPHS WERE VISUALLY ASSESSED FOR QUALITY OF OBTURATION BY
TWO INDEPENDENT EXAMINERS (SG AD) WHO WERE BLINDED WITH REGARD TO
IRRIGATION PROTOCOL GROUP TO ENHANCE CALIBRATION EACH EXAMINER ASSESSED THE
RADIOGRAPH INDEPENDENTLY AND LATER REVIEWED TOGETHER FOR FINAL ASSESSMENT
INDIVIDUAL ROOT WAS TAKEN AS UNIT OF ANALYSIS FOR GRADE OF OBTU- RATION AND
SCORING CRITERIA WERE AS GIVEN BY COLL JA 1996
1 UNDER FILLED - FILLING MATERIAL ENDED 1 MM OR MORE SHORT OF THE APEX
2 OPTIMAL FILLING- FILLING MATERIAL APPEARED TO END AT THE RADIOGRAPHICAL APEX
3 OVERFILLED - FILLING MATERIAL EXTRUDED PAST THE RADIOGRAPHIC APEX
4 OPTIMALLY FILLED ROOTS WERE FURTHER ASSESSED FOR THE PRESENCE OF VOIDS AND VOID
AREA (ROOT CANAL SURFACE UNTOUCHED BY THE ROOT CANAL FILLING MATERIAL) IN THREE
VISUALLY DIVIDED SECTIONS OF THE ROOT IE CORONAL MIDDLE AND APICAL 13RD
16
RESULTS
bull OVERALL CLINICAL AND RADIOGRAPHIC SUCCESS RATE OVER A PERIOD OF ONE YEAR WAS
9886 amp 977 RESPECTIVELY
bull ALL GROUPS WERE SIGNIFICANTLY (P = 001) EFFECTIVE IN ALLEVIATING PAIN WITHIN 24 H
OF PULPECTOMY
17 18
4
19
bull IMMEDIATE POST OPERATIVE RADIOGRAPHIC ASSESSMENT REVEALED 68 (102150) ROOTS
WITH OPTIMAL OBTURATION AND 32 (48150) WITH OVERFILLINGUNDERFILLING MAXIMUM
NO OF OPTIMAL FILLINGS WERE OBSERVED IN GROUP1 (CA + E) (3333) FOLLOWED BY
GROUP 2 (CA) (2549) GROUP 3(SH + E) (2549) AND GROUP 4(SH) (1568)
bull CITRIC ACID GROUPS HAD MORE NUMBER OF OPTIMALLY FILLED ROOTS 588 (60102) THAN
NON CITRIC ACID GROUPS 412 (42102)
bull ENDOACTIVATOR CONTRIBUTED TO 18 OF OPTIMAL OBTURATION IRRESPECTIVE OF
CHELATING AGENT USED
20
21
bull MAXIMUM NO OF VOIDS AND VOID AREAS WERE IN NON CITRIC ACID GROUPS
(6419 amp 5384) COMPARED TO CITRIC ACID GROUPS (3580 amp 4615)
RESPECTIVELY
bull ANALYSIS OF ROOT 13RD REVEALED MAXIMUM NO OF VOID AREA IN APICAL
13RD (4755) FOLLOWED BY MIDDLE 13RD (3846) AND CORONAL 13RD
(1398)
bull LEAST NO OF VOIDS amp VOID AREA (1111 amp 1608) WERE OBSERVED WHEN
ENDOACTIVATOR ALONG WITH CHELATING AGENT WAS USED (GROUP 1)
HOWEVER THIS WAS STATISTICALLY INSIGNIFICANT
22
DISCUSSION
bull IN THE PRESENT STUDY 1 SODIUM HYPOCHLORITE WAS USED ALONG WITH 6 CITRIC ACID
(CHELATING AGENT) WHICH IS REPORTED TO BE AS EFFECTIVE AS 17 EDTA
bull CITRIC ACID (BIOLOGICAL ACID) IS FOUND TO BE BIOCOMPATIBLE AND LEAST IRRITATING TO
PERIAPICAL TISSUES THAN OTHER CHELATING AGENTS
bull USE OF SODIUM HYPOCHLORITE SOLUTION FOLLOWING CHELATING AGENT WAS AVOIDED AS IT
RAPIDLY PRODUCES SEVERE EROSION OF ROOT CANAL WALL DENTIN
bull TRADITIONAL APPROACH OF DELIVERING IRRIGANTS INTO THE ROOT CANAL SPACE USING
SYRINGES AND METAL NEEDLES HAS BEEN FOUND TO BE INEFFECTIVE ESPECIALLY IN THE AREAS OF
ANASTOMOSES BETWEEN CANALS AND APICAL 13RD OF ROOT CANAL
23
bull THEREFORE TO ACHIEVE BETTER CLEANING EFFICIENCY IRRIGANT ACTIVATION HAS BEEN
RECOMMENDED SONIC ACTIVATION HAS BEEN REPORTED TO RESULT IN BETTER ROOT CANAL
CLEANLINESS AS COMPARED TO NO ACTIVATION OF IRRIGANT
24
5
CONCLUSION
bull USE OF 6 CITRIC ACID DEFINITELY HELPED IN RAPID ELIMINATION OF PAIN RESOLUTION OF
PERI-RADICULAR RADIOLUCENCY BETTER OBTURATION QUALITY IN TERMS OF LESS VOIDS AND
VOID AREAS ALONG WITH MAXIMUM NO OF OPTIMAL OBTURATION UP TO APICAL AREA
bull 6 CITRIC ACID AND ENDOACTIVATOR IRRIGATION PROTOCOL PROVED TO BE THE BETTER
IRRIGATION PROTOCOL WHICH MAY CONTRIBUTE TO LONG TERM SUCCESS OF PRIMARY
TOOTH AND THE HEALTH OF UNDERLYING PERMANENT TOOTH
bull 6 CITRIC ACID ALONG WITH ENDOACTIVATOR MAY BE RECOMMENDED AS IRRIGATION
ADJUNCTS IN PULPECTOMY PROCEDURE OF PRIMARY TEETH
25
PROS AND CONS
PROS
bull PROPER EXPLANATION OF THE MATERIALS
USED
CONS
bull NO PREOPERATIVE AND POSTOPERATIVE
RADIOGRAPHS
26
REFERENCES
bull RAMACHANDRA JA NIHAL NK NAGARATHNA C VORA MS ROOT CANAL IRRIGANTS IN
PRIMARY TEETH WORLD J DENT 20156(3)229-234
bull MOHAMMADI Z JAFARZADEH H SHALAVI S KINOSHITA JI UNUSUAL ROOT CANAL
IRRIGATION SOLUTIONS J CONTEMP DENT PRACT 201718(5)415-420
bull ZEHNDER M ROOT CANAL IRRIGANTS J ENDOD 2006 32389- 98
bull SMITH JJ amp WAYMAN BE AN EVALUATION OF THE ANTIMICROBIAL EFFECTIVENESS OF
CITRIC ACID AS A ROOT CANAL IRRIGANT JOURNAL OF ENDODONTICS 1986 12(2) 54-58
bull TANNURE PN AZEVEDO CP BARCELOS R GLEISER R PRIMO LG LONG-TERM OUTCOMES OF
PRIMARY TOOTH PULPECTOMY WITH AND WITHOUT SMEAR LAYER REMOVAL A RANDOMIZED
SPLIT-MOUTH CLINICAL TRIAL PEDIATR DENT 201133316E20 27
bull CARON G NHAM K BRONNEC F MACHTOU P EFFECTIVENESS OF DIFFERENT FINAL IRRIGANT
ACTIVATION PROTOCOLS ON SMEAR LAYER REMOVAL IN CURVED CANALS J ENDOD
2010361361E6
bull COLL JA SADRIAN R PREDICTING PULPECTOMY SUCCESS AND ITS RELATIONSHIP TO
EXFOLIATION AND SUCCEDANEOUS DENTITION PEDIATR DENT 19961857E63
28
1
LOCAL
ANESTHESIA
DR MITAKSHARA NIRWAN
CONTENTS
Definition
Methods of inducing local anesthesia
Desirable properties
Electrophysiology of nerve conduction
Impulse propagation and spread
Mode and site of action of local anesthesia
Classification of local anesthetic according to biological site and mode of action
Dissociation of local anaesthetics
Mechanism of action of local anaethetics
Local anaesthetic agent
2
3
DEFINITION
Local anesthesia is defined as a loss of sensation in
a circumscribed area of the body caused by depression
of excitation in nerve endings or an inhibition of the
conduction process in peripheral nerves
An important feature of local anesthesia is that it produces
LOSS OF SENSATION WITHOUT INDUCING LOSS OF
CONSCIOUSNESS
4
METHODS OF INDUCING LOCAL
ANESTHESIA
Low temperature
Mechanical trauma
Anoxia
Neurolytic agents such as alcohol amp phenol
Chemical agents such as local anesthetics
PROPERTIES OF LOCAL
ANESTHESIA
It should not be irritating to tissue to which it is applied
It should not cause any permanent alteration of nerve structure
Its systemic toxicity should be low
Time of onset of anesthesia should be short
It should be effective regardless of whether it is injected into the tissue or applied locally to mucous membranes
The duration of action should be long enough to permit the completion of procedure
5 6
It should have the potency sufficient to give complete
anesthesia with out the use of harmful concentration solutions
It should be free from producing allergic reactions
It should be free in solution and relatively undergo
biotransformation in the body
It should be either sterile or be capable of being sterilized by
heat with out deterioration
2
ELETROPHYSIOLOGY OF
NERVE CONDUCTION
There is an electrical charge across the membrane
This is the membrane potential
The resting potential (when the cell is not firing) is a negative
electrical potential of -70mv that exists across the nerve
membrane produced by different concentrations of either side of
the membrane
The interior of nerve is NEGATIVE in relation to exterior
7 8
inside
outside
Resting potential of neuron = -70mV
+
-
+
-
+
-
+
-
+
-
SLOW DEPOLARIRIZATION
9
RAPID DEPOLARIZATION
The interior of nerve is POSITIVE in relation to exterior
REPOLARIZATION
10
bull Repolarization takes 07 msec
bull Depolarization takes 03 msec
SODIUM PUMP -
energy comes from the oxidative metabolism of ATP
bull The entire process require 1 msec
IMPULSE PROPOGATION
IMPULSE SPREAD
The propagated impulse travels along the nerve
membrane towards CNS The spread of impulse differs
in myelinated and unmyelinated nerve fibers
DEPOLARIZED SEGMENT ADJACENT RESTING AREA
MODE AND SITE OF ACTION OF LOCAL
ANESTHETICS
Local anesthetic agent interferes with excitation
process in a nerve membrane in one of the
following ways
Altering the basic resting potential of nerve
membrane
Altering the threshold potential
Decreasing the rate of depolarization
Prolonging the rate of repolarization
12
3
CLASSIFICATION OF LOCAL ANESTHETIC
SUBSTANCES ACCORDING TO
BIOLOGICAL SITE AND MODE OF ACTION
CLASS A
Agents acting at receptor site on external surface of nerve membrane
Chemical substance Biotoxins (eg tetrodotoxin and saxitoxin)
CLASS B
Agents acting on receptor sites on internal surface of nerve membrane
Chemical substance Quaternary ammonium analogues of lidocaine
scorpion venom 13
CLASS C Agents acting by receptor independent of
physiochemical mechanism
Chemical substance Benzocaine
CLASS D Agents acting by combination of receptors and
receptor independent mechanisms
Chemical substance most clinically useful anesthetic agents
(eg lidocaine mepivacaine prilocaine)
14
BASED ON THE SOURCE
NATUAL
SYNTHETIC
OTHERS
BASED ON MODE OF APPLICATION
bull INJECTABLE
bull TOPICAL
BASED ON DURATION OF ACTION
bull ULTRA SHORT
bull SHORT
bull MEDIEM
bull LONG
BASED ON ONSET OF ACTION SHORT
INTERMEDIATE
LONG
15
DISSOCIATION OF LOCAL
ANESTHETICS
Local anesthetics are available as salts (usually
hydrochlorides) for clinical use
The salts both water soluble and stable is dissolved in
either sterile water or saline
In this solution it exists simultaneously as unchanged
molecule (RN) also called base and positively charged
molecules (RNH+) called cations
RNH+ ==== RN+ H
+
16
The relative concentration of each ionic form in the solution varies
in the pH of the solution or surrounding tissue
In the presence of high concentration of hydrogen ion (low pH) the
equilibrium shifts to left and most of the anesthetic solution exists
in cationic form
RNH+ gt RN
+ + H
+
As hydrogen ion concentration decreases (higher pH) the
equilibrium shifts towards the free base form
RNH+ lt RN + H
+
17
The relative proportion of ionic form also depends on pKa or DISSOCIATION CONSTANT of the specific local anesthetic
The pKa is a measure of molecules affinity for H+
ions
When the pH of the solution has the same value as pKa of the local anesthetic exactly half the drug will exists in the RNH
+ form and
exactly half in RN form
The percentage of drug existing in either form can be determined by Henderson Hasselbalch equation
Log baseacid = pH - pKa
18
4
MECHANISM OF ACTION OF LOCAL
ANESTHETICS
The following sequence is proposed mechanism of action of LA
Displacement of calcium ions from the sodium channel receptor site
Binding of local anesthetic molecule to this receptor site
Blockade of sodium channel
19
Decrease in sodium conductance
Depression of rate of electrical depolarization
Failure to achieve the threshold potential level
Lack of development of propagated action potential
Conduction blockadehellip
20
21
Na + Na +
22
LOCAL ANESTHETIC AGENT
COMERCIALLY PREPARED LOCAL ANESTHESIA
CONSISTS OF
Local anesthetic agent (xylocaine lignocaine 2)
Vasoconstrictor (adrenaline 1 80000)
Reducing agent (sodium metabisulphite)
Preservative (methylparabencapryl
hydrocuprienotoxin)
Fungicide (thymol)
Vehicle (distillde waterNaCl)
LOCAL ANESTHETIC AGENT
The local anesthetics used in dentistry are divided
into two groups
ESTER GROUP
AMIDE GROUP
23 24
ESTER GROUP It is composed of the following
An aromatic lipophilic group
An intermediate chain containing
an ester linkage
A hydrophilic secondary or tertiary
amino group
AMIDE GROUP It is composed of the following
An aromatic lipophilic group
An intermediate chain containing
amide linkage
A hydrophilic secondary or tertiary
amino group
5
25
CLASSIFICATION OF LOCAL ANESTHETICS
ESTERS
Esters of benzoic acid
Butacaine
Cocaine
Benzocaine
Hexylcaine
Piperocaine
Tetracaine
Esters of Para-amino
benzoic acid
Chloroprocain
Procaine
Propoxycaine
26
AMIDES Articaine
Bupivacaine
Dibucaine
Etidocaine
Lidocaine
Mepivacaine
Prilocaine
Ropivacaine
QUINOLINE
Centbucridine
PHARMACOKINETICS OF LOCAL
ANESTHETICS UPTAKE
When injected into soft tissue most local anesthetics produce
dilation of vascular bed
Cocaine is the only local anesthetic that produces
vasoconstriction initially it produces vasodilation which is
followed by prolonged vasoconstriction
Vasodilation is due to increase in the rate of absorption of the
local anesthetic into the blood thus decreasing the duration of
pain control while increasing the anesthetic blood level and
potential for over dose 27
AMIDE LOCAL ANESTHETICS
The metabolism of amide local anesthetics is more
complicated then esters The primary site of
biotransformation of amide drugs is liver
Entire metabolic process occurs in the liver for lidocaine
articaine etidocaine and bupivacaine
Prilocaine undergoes more rapid biotransformation then the
other amides
28
REFERENCES
Handbook of local anesthesia ndash Stanley F Malamed ndash 6th
edition
Essentials of Local Anesthetic Pharmacology Daniel E
Becker Anesth Prog 2006 Fall 53(3) 98ndash109
WIKIPEDIEA
29
THANK YOU
30
1
Pharmacological Methods of Behavior
Management
DR MITAKSHARA NIRWAN
DEFINITIONS
bull Conscious Sedation ndash A minimally depressed level of consciousness that retains
the patients ability to independently and continuously maintain an airway and respond appropriately to physical stimulation or verbal command
(American Dental Association House Of Delegates 2000)
bull Deep Sedation ndash An induced state of depressed consciousness
accompanied by partial loss of protective reflexes including the inability to continuously maintain an airway independently and or to respond purposefully to physical stimulation or verbal command
bull General Anesthesia (G A) ndash An induced state of unconsciousness or complete loss of
protective reflexes including the inability to continually maintain an airway independently and respond purposefully to physical stimulation or verbal command
Conscious sedation
ADVANTAGES
Conscious
Protective reflexes active amp intact
Stable vital signs
Operating dentist may perform sedation
Minimum amount of equipment required
Prolong detainment in recovery room not required
Risk of complication very low
Excellent choice for poor ndash risk pt in dental office
Cost effective
General anesthesia
ADVANTAGES Not absolutely
essential May be the only
method Not necessary (no
pain reaction) Amnesia always
present
Conscious sedation
DISADVANTAGES
Pt cooperation is essential
Extremely difficult or mentally handicapped pt cannot always be managed
Use of local anesthesia is a must
Amnesia may or may not be present
General anesthesia DISADVANTAGES
Pt unconscious
Protective reflexes are depressed
Depressed
Advanced training required Dentist must not act also as anesthetist
Special equipment necessary
Detainment in recovery area necessary
High IOP amp postoperative complications
Not indicated in dental office
More expensive
Fundamental Concepts
bull Techniques that utilize drugs to induce co-operative yet conscious state in an otherwise uncooperative child ndash CONSCIOUS SEDATION
2
GOALS
1 To facilitate the provision of quality care
2 To minimize the extremes of disruptive behavior
3 To promote a positive psychologic response to treatment
4 To promote patient welfare amp safety
5 To return the patient to physiologic state
OBJECTIVES
1 The pt mood must be altered
2 The pt must remain conscious at all times
3 The pt must be cooperative
4 All protective reflexes must remain intact and active
5 Vital signs must remain stable and with in normal limits
6 The ptrsquos pain threshold should be elevated
7 Amnesia may be present
Indications
1 Preschool children
2 Lack of Psychological Emotional maturity
3 Lack of Cognitive Physical Medical disability
4 Fearful amp anxious pts
5 Pt who require extensive amp complicated dental care amp would require or benefit from prolonged visits
6 Acute pain
7 Traumatic injuries
Operating Facilities amp Equipment
A positive pressure O2 delivery system capable of administering gt than 90 O2 at 10L min flow for 60 min (650L ldquoErdquo cylinder)
OR
Self inflating bag valve mask device (15L min)
A functional suction apparatus with appropriate suction catheters
Monitoring equipment - PO BPC PC or Capno
Inhalation sedation unit
100 O2 amp never less than 25
A fail safe mechanism that is checked and calibrated annually
Must have appropriate scavenging system
Emergency drugs
Techniques of sedation
Routes for drug administration
bull Oral
bull Rectal
bull Inhalational
bull Transmucosal
ndash Sublingual
ndash Intranasal
bull Parenteral
ndash IM
ndash sub mucosal
ndash IV
3
Oral Sedation
Advantages
1 Almost universally accepted and the easiest method
2 Decreased incidence and severity of adverse reaction
3 Low cost
Disadvantages
1 Absorption is variable
2 Prolonged latent period(30 min)
3 Reversal of any unwanted effect is also difficult
4 Inability to readily lighten or deepen the level of sedation
5 Prolonged duration of action
Rectal Sedation
Advantages 1 Incidence and intensity of
drug related side effects is minimized
2 Drug absorption occurs from the large intestine directly into the circulation
3 The lack of a needle syringe or other equipment
4 The ease of administration
5 The low cost
Disadvantages
1 Inconvenience to the administrator amp pt
2 The variable absorption of drugs from the large intestine
3 The slow onset of action amp the relatively long duration of action
4 Inability to titrate the drug dosage
5 The inability to reverse the action of the drug the prolonged recovery
Intranasal sedation
Advantages
Rapid onset (10 ndash 15 min)
Simple amp relatively painless
Less pt cooperation is required
Absorbed directly into the C V S
Intranasal sedation
Disadvantages
1 Dependence on nasal mucous membrane
2 Shorter duration of action(40-60min)
3 Multiple dosage may be necessary
Drugs
Midazolam ndash 02mgkg
Sufentanil ndash 15 ndash 3 mcgkg
Ketamine ndash 3-6mg kg
Sublingual sedation
Advantages
1 Pt acceptance
2 Rapid onset
3 High bioavailability
Drugs
Oral Transmucosal Fentanyl Citrate (OTFC)
Intramuscular Sedation
Advantages
1 More rapid onset of action
2 Absorbed directly into the C V system
3 More reliable absorption of drug
4 Pt cooperation is not as essential
Disadvantages
1 Time factor ndash its 15 min latent period
2 Pt may not be willing to accept the injection
3 The prolonged duration of action(2-4 hrs more)
4 Possibility of injury to the tissues at the site of injection caused by either the drug or the needle
4
Sites of I M administration
1 Gluteal area
2 Vastus lateralis
3 Mid ndash deltoid area
Drugs
Diazepam
Midazolam
Hydroxyzine
Inhalation Sedation
Advantages
1 The onset of action is more rapid
2 Peak clinical level is achieved rapidly(3-5min) - permit titration
3 Administrator has complete control over the actions of the drug - safety feature
4 No significant over dosage
5 Flexible duration of action
6 Recovery time is rapid amp most complete
7 No injection is required
8 With N2O- O2 it is safe with very few side effects
Disadvantages
1 The initial cost of the equipment is high 2 The continuing cost of the gases is high 3 The equipment occupies considerable space 4 N2O is not a potent agent 5 A degree of cooperation is required from the pt 6 Chronic exposure to N2O is deleterious to the health of
dental personnel
Contraindications
1 Nasal obstruction 2 Cyanosis at rest 3 Poor cooperation 4 1st trimester of pregnancy 5 Fear of masks
I V Sedation
Advantages
1 The onset of action is the most rapid 2 The dosage may be titrated 3 Suitable level of sedation can be provided 4 The recovery period is shorter 5 Side effects are extremely uncommon 6 Control of salivary secretions is possible 7 The gag reflex is diminished 8 Effectively diminishes motor disturbances 9 Provides immediate access to CVS in emergency
Disadvantages
1 Venipuncture is necessary
2 Complication may rise at the site of the venipuncture
3 Monitoring must be more intensive
4 Recovery is not complete at the end of the procedure
5 Reversal of sedation is difficult
5
N2O-O2 (Relative Analgesia)
colorless sweet smelling gas
Pharmacokinetics
Absorption through pulmonary epithelium
It is approx 15 times as soluble as is nitrogen It replaces nitrogen in blood
It is carried in solution in plasma of the blood
It is not metabolized by the body
Elimination ndash majorndash lungs minor --- skin
perspiration urine and intestinal gas
Pharmacodynamics
Dose related
10 ndash 25 Lightheaded
Changes in visual amp auditory sensation
Tingling of hands amp feet
Suffusing warmth
Remote from the immediate environment
Reduced anxiety
25-50 max analgesic properties and aberration of vision hearing and proprioception mild drowsiness euphoria amnesia and increased sleepiness and dreams
35 conc will achieve maximum analgesia
bull CNS
ndash Cerebrum-primarily affected
ndash Safe but weak anesthetic agent
bull RESPIRATORY SYSTEM
ndash Increased Tidal and minute volumes
bull CARDIOVASCULAR SYSTEM
ndash 2 studies ndash decreased cardiac output
bull FETAL SYSTEMS
ndash Miscarriage in humans
bull OTHER SYSTEMS
ndash Depression of spinal reflexes increase muscle tone indicates stage of delirium
ndash Muscle rigidity-narcotics + nitrous oxide
ndash Nausea and vomitting - GIT
ndash HEMATOPOIESIS ----- prolonged exposure
Adverse reactions and toxicity
EMOTIONAL REACTIONS
DREAMS HALLUCINATIONS
No acute toxicity
Chronic toxicity ndash bone marrow
depression
PROCEDURE
Diffusion Hypoxia
Sevoflurane
A fluorinated derivative of isopropyl ether ndash synthesized in 1970
Potent anaesthetic agent with rapid uptake amp speedy recovery
Day-case surgery
Problem
Attaching vaporiser to any of the currently available machine
BENZODIAZEPINES
Diazepam 1961 lipid soluble
Uses-alcoholism epilepsy labor tetanus and cerebral palsy
- sedation and amnesia
- varieties of neurosis amp anxiety states
Pharmacokinetics
Orally Rectal IMIV or SC
Well absorbed through GIT
Excretion in urine
6
bull Pharmacodynamics
ndash Depress the brain stem reticular system and the limbic system thalamus and hypothalamus
ndash It is a centrally acting muscle relaxant Has anti-convulsant properties
Adverse reaction amp toxicity
ndash Confusion nausea headache increased appetite decreased salivation and jaundice Thrombophlebitis
ndash Rebound phenomenon
ndash Toxicity drowsiness confusion sleep and coma
Dosage Oral or Rectal ndash 02-05mgkg
Maximum single dose 10mg
IV- 025mgkg
Supplied Tablets 2 5 10 mg
Suspension ndash 5mg
Midazolam Water soluble ndash non-irritant
Oral IM IV
Metabolism- liver
Onset IV 3 -5mins
oral 20 ndash 30mins
Oral administration anxious patients requiring relatively short dental procedure
No rebound phenomenon
Better anxiolysis amp amnesia (retrograde amnesia)
Adverse effects Respiratory depression
dose dependant apnea
Dosage Oral ndash 025 to 1mgkg to maximum single dose 20mg
IM ndash 01 to 015mgkg to a maximum of 10mg
IV ndash slow IV
Supplied Syrup ndash 2mgml
Injectable ndash 1mgml amp 5mgml vials
Flumazenil specific benzodiazepines antagonist
selectively inhibits CNS effects
IV administration amp not recommended below 18yrs of age
02mg over 15 seconds after 45seconds 02mg then after 60seconds to maximum of 1mg
Sedative-Hypnotics
Barbiturates First truly effective drugs for the management of anxiety Generalized CNS depressants Produce dose dependent effects
Sedation ---- sleep ---- GA ---- coma
Suppress the CNS and result in sedation and amnesia Advantages
Rapid onset and short duration Disadvantages
no analgesic effect and possible hypotension Must be used with caution in trauma patients because they may cause
apnea and hypoventilation
DOSE Pentobarbital Sodium 100mg Secobarbital Sodium 100 to 200mg Children 30 to 100mg
bull Chloral Hydrates (Mickey Finn Knock out drops ) First synthesized in 1832 first member of the hypnotic group of drugs
Widely used as conscious sedation agent
Properties
Unpleasant taste
Nausea vomiting
Quite irritating to skin and to mucous membranes
GI irritation
Dosages Individualized for each patient 25 ndash 50mgkg
maximum of 1g
Supplied oral capsule ndash 500mg
oral solution ndash 250 amp 500mg5ml
Rectal suppositories ndash 324 amp 648mg
Narcotics
Do produce sedation amp euphoria greater in children
LA is required but dose should be decreased
Meperidine Synthetic opiate agonist
Very water soluble
Orally SC IM or IV
Peak effect by oral 1 hr amp lasts upto 4 hrs
Adverse reactions
-Seizures
-Extreme caution in hepatic or renal diseases or history of seizures
7
Dosage Oral SC or IM ndash 1to 22mgkg not to exceed 100 mg
Supplied Oral Tablets ndash 50 amp 100mg
Oral Syrup ndash 50mgml
Parental solution ndash 25 50 75 amp 100mgml
Fentanyl
Synthetic opiate narcotic analgesic
Very potent 01mg = 10mg Morophine75mg Meperidine
Pharmacokinetics
IV IM SM
Metabolized in liver Excreted in urine
Fentanyl Onset ndash 7 to 15mins
Duration ndash 1 to 2 hrs
Pharmacodynamics
Respiratory depression RR but returns to normal rapidly Tidal volume amp response to co2 depressed for extended period
Apnea
Less emetic than meperidine
NOT RECOMMENDED IN CHILDREN BELOW 2yrs
Dosage 0002 to 0004mgkg
Supplied 005mgml in 2 amp 5ml ampoules
Reversal drug Naloxone
Semisynthetic opiate antagonist
No agonist activity
Onset 2 to 5mins SC or IM amp 1 to 2mins IV
Reversal 45mins
Pt should be kept under continual surveillance
Adverse reaction nausea vomiting sweating hypotension hypertension ventricular tachycardia fibrillation
Dosage IV SC IM 001mgkg then 01mgkg every 2- 3mins maximum 2mg
Supplied 002 004 1mg solutions
Antihistamines
Hydroxyzine
Oral or IM
Effect ndash 15 ndash 30mins
Half-life ndash 3 hrs
Uses
To relieve anxiety
Used as an anti-histamine
Used to control nausea and vomiting including that associated with motion sickness and pregnancy
Adverse reaction dry mouth drowsiness hypersentivity
Dosage Oral ndash 1 to 2mgkg
IM ndash 11mgkg
Promethazine Oral or IM Onset 15 to 60mins Duration 4 to 6 hrs Uses
To prevent and treat nausea and vomiting associated with motion pregnancy or surgery
Produces sedation and reduce swelling pain and trismus
Lower seizure threshold Adverse reaction dry mouth blurred vision thickening of bronchial secretions Dosage OralIM ndash 05-11mgkg
maximum 25 mg
Diphenhydramine
Oral IM IV
Onset -1hr
Duration ndash 4 to 6 hr
Metabolized in liver
Adverse reaction disturbed coordination thickening of bronchial secretions
Dosage Oral IM IV ndash 1 to 15mgkg
maximum 50mg
Tranquilizers
Major tranquilizer antipsychotic produce calmness control symptoms of psychoses cause reversible extra pyramidal symptoms and do not tend to cause habituation
Minor tranquilizer antianxiety agents also cause calmness do not cause extrapyramidal symptoms Used in conditions like nervous tension and mild depression
8
Classification
Antipsychotics
Phenothiazine derivatives
Chlorpromazine promazine
Butryophenones
Haloperidol
Rauwolfia alkaloids
Reserpine
Antianxiety drugs
Propyl alcohol derivatives
Meprobamate
Benzodiazepine derivatives
Diazepam
Miscellaneous compounds
Hydroxyzine
Meprobamate
White crystalline powder slightly bitter in taste
Only administered orally
Peak blood concentration ----1 to 3hrs
10 ---------excreted unchanged Rest --- excreted as a oxidized derivative or as a glucoronide
Uses
To relieve day time anxiety
Induce sleep in insomniacs
To reduce anxiety associated with dental treatment
Anti-convulsant ndash petit mal epilepsy
Adverse reaction leucopenia acute non-thrombocytopenic purpura ecchymoses eosinophilia edema adenopathy
Dosage Childrengt 6yrs 100 to 200mg
Not recommended for children under 6yrs
Monitoring during sedation
1 Pulse
2 Blood pressure
3 ECG
4 Respiration
5 Temperature
Pulse
Manual Electronic
bull Radial Brachial
bull Facial labial
Blood pressure
ndash Stethoscope amp sphygmomanometer
ndash Automatic devices
ndash Direct cannulation of an artery ndash very accurate
Electrocardiograph
Heart rate rhythm myocardial function
9
Respiration
ndash Monitoring respiratory rate
ndash Observing the rise amp fall of the chest wall
ndash Observing the color of mucous membrane
ndash Observing the inflation amp deflation of the reservoir bag
Devices for monitoring respiration
1 The Precordial pretracheal stethoscope
2 The esophageal stethoscope
ndash Respiratory rate
ndash Heart rate
ndash Any abnormal sounds
Pulse Oximeter
ndash Oxygen saturation
ndash Heart rate
ndash Oxisensor site
ndash Fingers
ndash Toe
ndash Ear lobe
Mechanism
Oxygenated Hb ndash red light
Deoxygenated Hb- infrared light
Tissue pressure from arterial pulse (plethysmography)
Advantages
ndash Safe amp noninvasive
ndash Simple to use
ndash Information is rapidly available for clinical decision
ndash Indirectly indicates respiratory adequacy
Disadvantages
ndash Finger probes can get dislodged
ndash Emitted light source may cause burning
ndash Non reusable probes are expensive
ndash Does not directly determine airway patency
Capnography
1 The presence absence of air flow
2 Indicates depth amp adequacy of respiration
3 Continues analysis of the co2 content of the respired air ndash indicates respiratory adequacy
Temperature
ndash Disposable nondisposable thermometer
ndash Esophageal rectal temp probe
10
Discharge criteria
Cardiovascular function is satisfactory amp stable
Airway patency is uncompromised amp satisfactory
Pt is easily arousable amp protective reflexes intact
State of hydration is adequate
Pt can talk if applicable
Pt can sit unaided if applicable
Pt can ambulate with minimal assistance if applicable
Presedation level of responsiveness achieved
Responsible individual is available
1
PULP THERAPY OF VITAL TEETH
DR MITAKSHARA NIRWAN
Contents
Indirect pulp capping
Direct pulp capping
Medications amp materials used in pulp capping
Pulpotomy
MTA
Apexogenesis
INDIRECT PULP CAPPING
Pieter Van Forest - first to speak about root canal therapy
Glove designed instruments that could prepare a canal to a certain size and taper(1910)
Indirect pulp capping is defined as a procedure where in small amount of carious dentin is retained in
deep areas of cavity to avoid exposure of pulp followed by placement of a suitable medicament and
restorative material that seals off the carious dentin and encourages pulp recovery (Ingle)
A procedure in which only the gross caries is removed from the lesion and the cavity is sealed for a
time with a biocompatible material (McDonald)
Objective of indirect pulp capping
These were given by Eidelman in 1965
bull Arresting the carious process
bull Promoting dentin sclerosis
bull Stimulating formation of tertiary dentin
bull Remineralization of carious dentin
Layers of Carious Dentin Indications of Indirect Pulp Capping
History
Mild pain associated with eating
Negative history of spontaneous extreme pain
Clinical Examination
Deep carious lesion which are close tobut not involving the pulp in vital primary or young
permanent teeth
No mobility
Nominal pulp inflammationdefinite layer of affected dentin after removal of infected dentin
Radiographic examination
Normal lamina dura amp PDL space
No radiolucency around the apices
2
Contraindications of Indirect Pulp Capping
History
Sharp penetrating pulpalgia
Prolonged spontaneous pain especially at night
Clinical examination
Mobility of tooth
Discoloration of tooth
Negative reaction of electric pulp testing
Radiographic examination
Definite pulp exposure
Break in the lamina dura
Radiolucency around the apices
Widened PDL space
Treatment procedure
Sequelae of Indirect Pulp Capping Three distinct types of new dentin formation take place
1 Cellular fibrillar dentinmdashfirst 2 months
2 Globular dentinmdash3 months
3 Tubular dentin (uniform mineralized dentin)
bull 15th of reparative dentin formation begins in less than 30 days
bull After 3 months 01 mm is formed
DIRECT PULP CAPPING Defined by Kopel (1992) as the placement of a medicament or non medicated material on a pulp that
has been exposed in course of excavating the last portions of deep dentinal caries or as a result of
trauma
Objective
To create new dentin in the area of the exposure and subsequent healing of the pulp
Rationale
achieve a biologic closure of the exposure site by deposition of hard tissue barrier (dentin bridge)
between pulp tissue and capping material thus walling off the
INDICATIONS
Small mechanical exposure
Easily controlled haemorrhage
Bright red haemorrhage
True pinpoint exposure
CONTRAINDICATIONS
Severe toothache at night
Spontaneous pain
Tooth mobility
Radiographic appearance of pulp periradicular de- generation
Excess of hemorrhage at the time of exposure Serous exudate from the exposure
Externalinternal root resorption
Swellingfistula
Histological Changes after Pulp Capping
These were illustrated be Glass and Zander in 1949
After 24 hours Necrotic zone adjacent to calcium
hydroxide paste is separated from healthy pulp
tissue by a deep staining basophilic layer
After 7 days Increase in cellular and fibroblastic
activity
After 14 days Partly calcified fibrous tissue lined by
odontoblastic cells is seen below the calcium
proteinate zone disappearance of necrotic zone
After 28 days Zone of new dentin
3
Medications and Materials Used for Pulp Capping Calcium hydroxide
Corticosteroids amp antibiotics
Inert materials
Collagen fibers
4-META adhesive
Direct bonding
Isobutyl cyanoacrylate
Denatured albumin
Mineral trioxide aggregate
Laser
Bone morphogenic protein
PULPOTOMY
Finn (1995) defined it as the complete removal of the coronal portion of the dental pulp
followed by placement of a suitable dressing or medicament that will promote healing and
preserve vitality of the tooth
American Academy of Pediatric Dentistry (1998) defined pulpotomy as the amputation of
affected infected coronal portion of the dental pulp preserving the vitality and function of the
remaining part of radicular pulp
Objectives
bull Removal of inflamed and infected coronal pulp at the site of exposure thus preserving the vitality of the
radicular pulp and allowing it to heal
bull Maintain the tooth in the dental arch
Rationale
bull Radicular pulp is healthy and capable of healing after surgical amputation of the infected coronal pulp
bull Preserves vitality of the radicular pulp
bull Maintains tooth in a physiologic condition
Indications of Pulpotomy bull Mechanical pulp exposure in primary teeth
bull Teeth showing a large carious lesion but free of radicular pulpitis
bull History of only spontaneous pain
bull Hemorrhage from exposure sites bright red and can be controlled
bull Absence of abscess or fistula
bull No interradicular bone loss
bull No interradicular radiolucency
Contraindications of Pulpotomy bull Persistent toothache
bull Tenderness on percussion
bull Root resorption more than 13rd of root length
bull Large carious lesion with nonrestorable crown
bull Highly viscous sluggish hemorrhage from canal orifice which is uncontrollable
bull Medical contradictions like heart disease immuno compromised patient
bull Swelling or fistula
bull External or internal resorption
bull Pathological mobility
bull Calcification of pulp
Classification of pulpotomy
4
Formocresol Pulpotomy
Iby BUCKLEY in 1904
Sweet (1930) Formulated multi visit technique
Doyle (1962) Advocated 2 sitting procedure (complete devitalization)
Spedding (1965) Gave 5 minute protocol (partial devitali- zation)
Venham (1967) Proposed 15 seconds procedure
Current concept uses 4 minutes of application time
Composition of formocresol Buckleyrsquos Formula
bull Cresol ndash 35 percent
bull Glycerol ndash 15 percent
bull Formaldehyde ndash 19 percent
bull Water ndash 31 percent
Mechanism of Action
It prevents tissue autolysis by bonding to the proteins Bonding is of peptide groups of side chain amino acids and is a reversible process accomplished without
changing the basic structure of protein molecules
Histological Changes
bull Demonstrated by Mass and Zilbermann11 in 1933 and also by Massler and Mansokhani in 1959
bull Immediately the pulp becomes fibrous and acidophillic
bull Seven to fourteen days Three zones appear
a broad eosinophilic zone of fixation
b broad pale-staining zone of atrophy with poorcellular definition
c broad zone of inflammation extending apically into normal pulp tissue
bull One yearndash Progressive apical movement of these zones with only acidophillic zone left at the end of 1 year
Modified Formocresol Pulpotomy
Used by TRASK(1972)
The technique is identical to that described for primary teeth except that the formocresol pellet is
sealed permanently in the tooth
Two-visit Devitalization Pulpotomy
Indications
bull There is evidence of sluggish bleeding at the amputation site that is difficult to control
bull Pus in the chamber but none at the amputation site
bull There is thickening of the PDL
bull History of pain
Contraindications
bull Nonrestorable tooth
bull Tooth with necrotic pulp
5
Glutaraldehyde Pulpotomy
It was first suggested by S Gravenmade Introduced by Kopel in 1979
Mechanism of Action
bull Glutaraldehyde produces rapid surface fixation of the underlying pulpal tissue
bull A narrow zone of eosinophilic stained and compressed fixed tissue is found directly beneath the area of application which blends into vital normal appearing tissue apically
bull With time the glutaraldehyde fixed zone is replaced by macrophagic action with dense collagenous tissue thus the entire root canal tissue is vital
Cvekrsquos Pulpotomy
bull This is also called as calcium hydroxide pulpotomy or young permanent partial pulpotomy
bull This was proposed by Mejare and Cvek16 in 1978
bull Indicated in young permanent teeth where the pulp is exposed by mechanical or bacterial means and the
remaining radicular tissue is judged vital by clinical and radiographic criteria whereas the root closure is
notcomplete
MINERAL TRIOXIDE AGGREGATE (MTA) Torabinejad described the physical and chemical properties of MTA in 1995
It is ash colored powder made primarily of fine hydrophilic particles of
1 tricalcium aluminate
2 tricalcium silicate
3 silicate oxide
4 tricalcium oxide
5 bismuth dioxide
Hydration of the powder results in a colloidal gel composed of calcium oxide crystals in an amorphous
structure This gel solidifies into a hard structure in less than three hours
PROPERTIES OF MTA
It is biocompatible material and its sealing ability is better than that of amalgam or ZOE
Initial pH is 102 and set pH is 125
The setting time of cement is 4 hours
The compressive strength is 70 MPA which is comparable with that of IRM
Low cytotoxicity ndash It presents with minimal inflammation if extended beyond the apex
Mineral trioxide aggregate (MTA) has demonstrated the ability to induce hard-tissue formation in
pulpal tissues and it promotes rapid cell growth
APEXOGENESIS
It is defined as the treatment of a vital pulp by capping or pulpotomy in order to permit continued
growth of the root and closure of the open apex
Rationale
Maintenance of integrity of the radicular pulp tissue to allow for continued root growth
Indications
bull Indicated for traumatized or pulpally involved vital permanent tooth when root apex is incompletely formed
bull No history of spontaneous pain
bull No sensitivity on percussion
bull No hemorrhage
bull Normal radiographic appearance
Contraindications
bull Evidence that radicular pulp has undergone degenerative changes
bull Purulent drainage
bull History of prolonged pain bull Necrotic debris in canal
bull Periapical radiolucency
6
1
Gupta A Dhingra R Chaudhari P Gupta A
Department of Paedodontics and Preventive Dentistry Faculty of Dental Sciences SGT University Gurgaon Haryana India
Journal of Indian Society of Pedodontics and Preventive Dentistry
Volume 35 I Issue 3 I July-September 2017
A COMPARISION OF VARIOUS MINIMALLY
INVASIVE TECHNIQUES FOR THE REMOVAL
OF DENTAL FLUOROSIS STAINS IN
CHILDREN
DR MITAKSHARA NIRWAN
CONTENTS
bull Introduction
bull Aims
bull Materials and Methods
bull Results
bull Discussion
bull Conclusion
bull Critical analysis
bull References
INTRODUCTION
bull Dental fluorosis is a developmental disturbance of dental enamel caused by
successive exposure to high concentrations of fluoride during tooth
development
bull Various methods of therapy are advocated for the treatment of fluorosis -
stained teeth which range from invasive ceramic veneer bonding restorations
to abrasive chemical treatments
bull The combination of dental bleaching techniques and microabrasion appears
as an excellent conservative solution to reestablish health in fluorosis
affected teeth
AIMS
bull The aim of the study was to evaluate and compare the effectiveness of
minimally invasive techniques for the removal of dental fluorosis
stains in children in vivo
MATERIALS AND METHODS
Patients visiting the department of Pedodontics and Preventive dentistry
Faculty of Dental Sciences SGT University Gurgaon
bull Sample size 90 patients
bull Age group 10 -17 years
bull Caries cracks or periodontal
disease on anterior teeth
bull Abscess draining sinus
cellulitis
bull Non vital teeth
hypersensitive exposed
crevices
bull Orthodontic appliance
bull Past history of bleaching
bull At least two permanent
maxillary anterior teeth
bull TSIF of score 4
bull Free of systemic diseases
Inclusion criteria Exclusion criteria
2
Groups
Group A In office bleaching with 35 hydrogen peroxide( Pola Office
Bleaching kit) activated by light emitting diode (LED) bleaching unit
(35 HP)
Group B Enamel microabrasion (EM) (PREMA Enamel Microabrasion
System) followed by in-office bleaching with 44 carbamide peroxide
gel (EM)
Group C In-office bleaching with 5 sodium hypochlorite (5
NaOCl)
A baseline colour evaluation was done by taking digital photograph of
the maxillary anterior teeth
RESULTS
Group 1
Colour stability
Group 2 Group 3
Tooth sensitivity
Tooth sensitivity values were taken before the treatment
which was compared to immediate postoperative and follow
up visits It was checked using an electric pulp tester
maximum
moderate
least
immediately
group 2
group 1
group 3
1 month
group 2
group 1
group 3
3 month
group 2
group 1
group 3
Patient satisfaction score
Satisfaction was assessed on visual analog scale
Range 1 to 5
Groups percentage of patients
who were satisfied with
the treatment
Number of patients
who reported slight
reappearance of colour
Group 1
90
7
Group 2
83
8
Group 3
73
7
3
Number of Appointments
Groups One sitting Two sittings Three
sittings
Group 1
25
4
1
group 2
26
3
1
Group 3
30
0
0
DISCUSSION
bull Hydrogen peroxide is capable of penetrating the tooth osmosis and through porosities and cracks subsequently acting directly on the pigmented molecules
bull Gurgan et al investigated 3 different light systems and found out that diode laser system with gave best tooth whitening and least tooth sensitivity
bull In the EM group the surface reflects and refracts light from the surface in such way that mild imperfections in underlying enamel are camouflaged While the highly polished surface of enamel enhances the aesthetic appearance
bull Train et al and Loguercio et al also had the similar results in their studies with EM mild fluorosis showed best results moderate showed moderate results while it had little effect on severe fluorosis
bull NaOCl was only effective on mild stains while moderate and severe
stains could only be lightened to quite an extent but could not be
completely removed
bull When NaOCl comes in contact with hypomineralized and discoloured
enamel it degrades and removes the chromogenic organic material
located on the enamel surface
CONCLUSION
bull It was concluded that esthetic appearance of teeth mild fluorosis can
be achieved by bleaching and microabrasion But in cases of
moderate fluorosis a combination of any of theses modalities can be
used
bull As no special maintenance precautions are required these maybe be
considered as an interesting alternative to conventional operative
treatment
bull Focuses on only TSIF of 4
bull Electric pulp testing is not the
right method to check for
sensitivity
bull Tooth Sensitivity changes
from person to person
bull Food habits can cause
staining of the teeth
bull Minimally invasive
bull Cheaper to veneers
bull Minimal loss of tooth structure
bull 4 parameters checked for the success of treatment
bull Inclusion of specific score of fluorosis for comparing the results
bull Maximum 3 appointments needed
CRITICAL ANALYSIS
Pros Cons
REFERENCES
bull Gurgan S Cakir FY Yazici E Different light-activated in officebleaching
systems Lasers Med Sci 201025817-22
bull Train TE McWhorter AG Seale NSWilson CF Guo IY Examination of
esthetic improvement and surface alteration following microabrasion in
fluorotic human incisors in vivoPediatr dent 199618353-62
bull Loguercio AD Correia LD Zago C Tagliari D Neumann E Gomes OM et al
Clinical effectiveness of two microabrasion materials materials for the
removal of enamel flurosis stains Oper Dent 200732531-8
4
2
I Co-operative behavior (+ve)
1) Cooperative behaviour
2) Lacking co-operative
ability
3) Potentially cooperative
behavior
Wright Classification
II Uncooperative behaviour (-ve)
1Uncontrolled
behaviorhystericalincorrigible
2Defiant behaviorobstinate
3Timid behavior
4Tense cooperative
5Whining behavior
6Stoic behavior
Wilson classification
Normalbold
Tasteful timid
Hysterical rebellious
Nervous fearful
Factors affecting behavior of children
Wright summarized the following factors bull Medical history bull Maternal anxiety
bull Family and peer influence
bull Dental office environment
bull Growth and development
bull Personal factors
bull Environmental factors
bull Other variables
Role of Dentist in childrsquos behavior
Appearance of dental office Personality of dentist
Time and length of appointment
Maternal influence on Childrsquos Behaviour
Motherrsquos behavior Childrsquos behavior
1 Over protective
a Dominant
b Overindulgent
Submissive shy
anxious aggressive demanding
2 Overindulgent Aggressive spoiled demanding displays temper
3 Under affectionate Usually well behaved but may be unable to
cooperate shy may cry easily
4 Rejecting Aggressive overactive disobedient
5 Authoritarian
6 Identification
Evasive amp dawdling
Cries easily lacks confidence
Behaviour Mangement
Fundamentals of behaviour management
Positive approach
Team attitude
Truthfulness
Organization
Tolerance
Flexiblity
3
Classification of behavior management
Management
Psychological Pharmacological Psychological
Communication
Behavior shaping
Behavior Management
Behavior shaping
Desensitization
Modeling
Contingency management
Disruptive
Voice control
Aversive
HOME
Physical Restraints
Others
Distraction
Audio Analgesia
Bio feed back
Hypnosis
Humor
Coping
Relaxation
COMMUNICATION
communication
Verbal
speech
Non-verbal
Body language
smiling
Eye contact Showing concern
By Touching
Give him a pat
Giving him hug
Expression of feeling
Both
DENTAL TERMINOLOGY WORD SUBSTITUTE
Rubber dam Rain coat
Rubber dam clamp Tooth button
R D frame Coat rack
Sealant Tooth paint
Topical fluoride gel Cavity fighter
Air syringe Wind gun
Suction Vacuum cleaner
Study models Statues
Alginate Pudding
High speeds Whistle
Low speeds Motor cycle
Euphemism Tell Show Do Technique (TSD)
Cornerstone of behaviour management
Given by Addleston in 1959
Objectives
1 Teach the patient imp aspects of the
dental visit amp familiarize the patient with
the dental setting
2 Shape the patientrsquos response to
procedures
through desensitization amp well described
expectations
4
Alternatives to TSD
Tell Play Do
Tell Show Play Doh
Tell Play Do with
Smart Phone Dentist
Game Ask Tell Ask
DESENSITIZATION
Demonstrated by James popularized by Wolpe
Desensitization is a therapeutic technique that pairs an
anxiety- evoking stimulus with a response inhibitory to
anxiety In each situations the percieved link between the
stimulus and the anxiety response is weakened
Involves 3 Stages
1Training the patient to relax
2Constructing a hierarchy of fear
3Introducing each stimulus in the
hierarchy
Modeling
Giver by Bandura (1967) Allowing a pt to observe 1more individual
who demonstrate appropriate behavior in particular situation
Steps in modeling Pt attention obtained Desired behavior is modeled Physical guidance of desired behavior Reinforcement of the guided behavior may be provided Reinforcement of behavior that did not require guidance Reinforcement for appropriate behavior initiated without modeling
Types 1 Live model 2 Symbolic or vicarious model
CONTINGENCY MANAGEMENT
Is a method of modifying the behavior of children by
presentation or withdrawal of reinforcers
Positive reinforcer
Henry W Fields 1984
Contingent presentation
Increases frequency of
behavior
Negative reinforcer
Stokes amp Kennedy1980
Contingent withdrawal
Increases the frequency of
behavior
Material
bull Candies
bull Gums
bull Cookies
bull Toys
Social
bull Praise
bull Facial expressions
bull Nearness
bull Physical contact
Activity
bull TV
bull Camping outdoor
bull Music
Reinforcers
Coping
Defined as the cognitive amp behavioral efforts made by an individual to master tolerate or reduce stressful situations
2types
a) Behavioral physical amp verbal activities
b) Cognitive silent amp thinking in mind to keep calm
It enables
ndash reality-oriented working
- cognitive reappraisal
- emotion cognitions
5
Distraction
Distraction is a tactic designed to divert a patient attention away from their current behavior to focus their interest in something else Types Audio Distraction Audiovisual Distraction
Relaxation
Effective in reducing immediate anxiety and fear
Involves series of basic exercises which may take several months to learn amp practice
Voice control
Given by Pinkham in 1985
Modification of the timbre intensity and pitch of ones voice in an attempt
to dominate the interaction between dentist and child
Objectives
bull To gain the patient attention and
compliance
bull To avoid negative or avoidance
behavior
bull To establish authority
Indications bull Uncoperative and inattentive
patients
Contraindications bull Children who due to age
disability mental or emotional immaturity are unable to understand
Hypnosis
First suggested by Franz A Mesmer in
1773
Altered state of consciousness
characterized by heightened suggestibility
to produce desirable behavioral and
physiological changes
Most effective in the presence of anxiety
Not all patients can be hypnotized
Basic mechanism - relief of pain through
suggestions of relief given in a close
trusting interpersonal situation
Henon outlined following uses
bull To reduce nervousness and
apprehension
bull To eliminate defence mechanisms
that patient use to postpone dental
work
bull To control functional or
psychosomatic grapping
bull To prevent thumb sucking and
bruxism
bull To induce anesthesia
Hand over Mouth Exercise (HOME)
Given by DR EVANGELINE JORDAN (1920)
Evangeline Jordan - If a normal child will not listen but continues to cry
and strugglehellip Hold a folded napkin over the childrsquos mouthhellipand
gently but firmly hold his mouth shut
Other terminologies bull Aversive Conditioning by Lenchner and Wright bull Emotional surprise therapy by Lampshire bull HOM airway restricted (HOMAR) by Levitas (1947) bull Aversion by Crammer (1973)
Children who are
momentarily hysterical
belligerent or defiant
3-6 yrs old
Child who can understands
simple verbal commands
Indications
Contraindications
Very young immature frightened child with serious physical mental or emotional handicap
6
Variationshellip Hand over mouth with airway restricted Towel over mouth
Towel over mouth with airway restricted
Body
Papoose board
Triangular sheet
Pedi wrap
Bean Bag
Safety belt
Extremities
Posey straps
Velco straps
Towel amp Tape
Head
Forearm support
Plastic bowl
Head positioner
Mouth
Tongue blades
Mouth Prop
Bite blocks
Positive Stabilization Mouth
Tongue blade open mouth wide prop Molt mouth prop
Rubber bite blocks
Extremities
Posey Strap
Head
Body
Papoose board
Pedi-wrap
7
1
Impact of Handheld Devices on
Children An Evaluation of Usage amp
Dependency Behaviour
0092
DR MITAKSHARA NIRWAN
Handheld devices
A handheld device is a pocket size
computing device with a display
screen and inputoutput interface like
an external or touchscreen keyboard
For example- smartphones tablet
computers handheld videogame
consoles
Haruki Murakami
ldquoCell Phones are so
convenient that they have
become an inconveniencerdquo
Introduction
The most famouscommonly used and easily accessible type of gadgets are
lsquoHandheld devicesrsquo They are as popular in children as they are in adults
The access and ownership of these devices amongst children has grown
substantially in the past decade Concerns exist regarding excessive usage
and the impact of frequent consumption of mobile media on their health and
behaviour
Aims and Objective
This objective of this study was to asses the level of use of handheld
devices among children aged 0-12 years and their positive and negative
impacts on them It further describes the dependency of these devices
and the behavioral problems associated with it
Materials and Methods An online survey was conducted and a self administered questionnaire
was prepared specially for the parents which included a total of 15
questions regarding the usage and dependency of the device
A total of 100 responses were collected from parents who had children
aged 0-12 years who used these devices on daily basis
2
Level of Usage (Q 123)
Results Purpose (Q7)
Improved
communication and
learning
Using more than
one type of
device
Helped in
Speech
Positive Impacts -
(Q58 amp 9)
P value 0003(s) P value-0007 P value-0006(s)
Reduced parent-
child interaction Disrupted sleep Lack of motivation for academics
Negative Impacts (Q81213)
P value-0001(s) P value-0002(s) P value-0006
Time when children use
the device the most
Isolation of the
child Behavioral impact when gadget is
taken back
Dependency
Behaviour (Q10111415)
P value-002(s) P value 002(s) P value-044
This study was done to evaluate the level of usage of handheld devices and their impact
on the children aged 0-12 years The questionnaire was made such that it asked both the
positive and negative impact and further included the questions regarding the
dependency
784 children had access to smartphone and 17 used tablets
The most common age group in which the devices was used the most was 5-8 years
followed by 9-12 followed by 0-4 (Arlinda et al 2019 )
Another study done by (Rachel Bedford et al 2016) concluded increase usage of mobile
phones 5122 in 6ndash11 monthshy olds through to 9205 by 25ndash36 months
745used these devices several times a day out of which 539 used it for more than
one hourday 255 used it for less than one hour and 206 for more than 2 hours
Various studies follow the same recommendation given by AAP to limit the duration of
gadget amongst children
Discussion
3
Improve of Cognitive Skills
Amongst the positive impacts most parents have answered that the usage of these
devices has helped their child communicate and learn better and it has showed significant
results According to (Sundus M 2018)These devices improve the cognitive skills and
develop their learning skills fasterThe competition skills also get better It gives time for brain to think and process information better Another study which supports this (LF
Jonathan et al 2016)
Motor Physical Exercise
This study has shown that children like to use more than one type of device
sometimesUsing these devices improve fine motor skillshand eye coordination and
hands and fingers become more efficient (Srinahyanti et al 2019) (Sundus M 2018)
Speech Improvement
392 Parents say that maybe usage of the devices has helped improve speech in their
children but Various studies show otherwise as most of them shows that usage of handheld
devices causes delay of speech (Srinahyanti et al 2019)
Reduced parent child interaction
The negative impacts are more when compared to the positive ones Usage of gadgets
has resulted in reduced parent child interaction Less face to face interaction can
cause detachment from family members and value which in turn also causes isolation
of the child as he is more comfortable with the gadget (M Suhana-2017)
Sleep Disorders
This study shows that most parents have agreed that usage of these devices does
cause disruption of sleep Various studies have shown that children get fewer hours of
sleepdrowsiness during the day and dramatic increase in day time sleep because of
the screen usage (Acc to National Sleep Foundation) ( Cain N et al 2010)
In this study most number of parents have
agreed that their children might be dependent on
these devices and also had showed restless and
violent behavior if the gadget is snatched from
them
Most number of kids (667) are heavily
dependent as they like to use the device during
their meal time
Various other studies have assessed the screen
time dependency and have concluded that
various kids suffer from SDD
Conclusion The study conclusively shows that the impact of handheld devices is akin to the
importance of table salt in our meals most significant for our growth and
development in moderate amounts and hazardous in excess The negatives clearly
outweigh the positives with the latter too few and far in between This study also
points towards further extensive research on the subject because we need to find ways and also educate parents to optimise the role of these devices in their
childrenrsquos life taking advantage of their positive attributes and minimising their
negative ones
References 1Wahyuni AS Siahaan FB Arfa M Alona I Nerdy N The Relationship between the Duration of Playing
Gadget and Mental Emotional State of Elementary School Students Open Access Maced J Med Sci
20197(1)148ndash151
2Sundus M Department of Computer Science Lahore-The Impacts of using Gadgets on ChildrenJournal of Depression and Anxiety 2018vol 7(1)296
3Amawi SO Subki AH Khatib HA et al Use of Electronic Entertainment and Communication Devices Among
a Saudi Pediatric Population Cross-Sectional Study Interact J Med Res 20187(2)e13
4Julia ldquoHandheld Screen Time Linked with Speech Delays in Young Childrenrdquo Present Pediatric Acad Soc
Meet 2017
5C Rowan ldquoThe Impact of Technology on Child Sensory Motor Developmentrdquo 2003
6Impact of media use on children and youth Paediatr Child Health 20038(5)301ndash317
7Naik SV Children and their gadgets A pedodontist perspective Int J Oral Health Sci 2018857-8
8Roberts DF Foehr UG Rideout V Generation M Media in the lives of 8‐18 year‐olds A Kaiser Family
Foundation Study 2005
9Arya K Time spent on television viewing and its effect on changing values of school going children Anthropologist 20046269‐71
10 Lerner C Barr R Screen Sense Setting the Record StraightResearch‐Based Guidelines for Screen
Use for Children Under 3 Years Old Early learning project at Georgetown university 2014 p 1‐10
11SrinahyantiYasaratodo Wau Imelda Free Unita Manurung Nur Arjani-Influence of gadget A positive
and Negative Impact of Smartphone Usage for Early Child2019
4
THANK YOU
1
Morankar Rahul Aditi Kapur Krishan Gauba Ashima Goyal
MANAGEMENT OF ENDODONTIC INSTRUMENT SEPARATION IN
PRIMARY TEETH
CASE REPORT
Journal of South Asian Association of Pediatric Dentistry 2020
DR MITAKSHARA NIRWAN
bull Introduction
bull Aims amp Objectives
bull Case report
bull Discussion
bull Conclusion
bull Pros amp Cons
bull References
CONTENTS
Separation of endodontic instrument is an unexpected complication and its prevalence is not known It is a common belief among the dental professionals that rotary nickelndashtitanium (NiTi) instruments separate more frequently than stainless steel hand instruments
However literature revealed that in permanent teeth the reported prevalence of separated endodontics manual instruments is in the range of 07-74 whereas for rotary NiTI instruments it is
approximately 04-5
Fractured root canal instruments may include endodontic files Gates Glidden burs finger spreaders
and paste fillers
INTRODUCTION
The aim of this study is to describe the management strategies for endodontic
instrument separation in a root canal of primary teeth with emphasis on factors
requiring consideration in different clinical situations
AIMS amp OBJECTIVES
CASE 1
A 6-year-old male child reported with the chief complaint of spontaneous toothache in mandibular left second primary molar since few days It has aggravated following dental treatment at a private dental clinic Clinical examination revealed an underprepared access cavity with 75 and incomplete caries removal
which was sealed with glass ionomer cement
An intraoral periapical radiograph revealed a separated instrument of about 6ndash7 mm size in the distal root
2
The separated instrument was lodged firmly in distobuccal root canal 2ndash3 mm below the cementoenamel junction The instrument was bypassed successfully with no 15 and no 20 H-files but attempts for its retrieval were not successful
GatesndashGlidden (GG) drills no 2 (07 mm) and no 3 (09 mm) were used to drill around the instrument after which it was retrieved successfully using no 25 H-file
All the canals were instrumented till size 30 k-file followed by obturation with metapex and restoration with glass ionomer cement amp followed by placement of a crown and loop space maintainer for missing 74 The instrument retrieved was a manual reamer measuring 6 mm in length
The patient was asymptomatic since then and is under regular follow-up
CASE 2
A 5-year-old female child reported with the chief complaint of spontaneous toothache in mandibular left second
primary molar Clinical examination revealed deep occlusal caries with fractured lingual wall and pain on
percussion An intraoral periapical radiograph revealed caries involving pulp without any furcation or periapical
area of rarefaction and pulpectomy was planned
All the canals were enlarged using NiTi rotary files with a 4 taper operating at 500 rpm with minimum torque
setting An orifice opener [(0825 19 mm) of 8 taper size 25 length 19 mm] and nos 0420 file was used for
instrumentation of root canal This was followed by file nos 0425 which got separated in the distobuccal root
canal The radiograph confirmed a separated instrument of length 3ndash4 mm in the middle third of the root canal
The instrument was bypassed with no 15 k-file but could not get retrieved As instrument separation had occurred with 0425 file the involved root canal was sufficiently debrided before separation and the level of instrument separation was at the mid-root region so it was decided to obturate and seal this tooth with
periodic follow-ups instead of immediate extraction All other canals were enlarged till size 0430 in the sequential manner followed by obturation using metapex and placement of stainless steel crown
3
CASE 3
A 5-year-old female child has complaint of mild intermittent pain with primary mandibular left first molar She
had undergone pulpectomy treatment for the same during which an instrument separation has occurred in
the mesiobuccal root canal by a resident doctor
A radiograph revealed a separated instrument of about 4 mm in size lodged in the apical third but within the
confines of the mesial root An attempt was made for its retrieval but was unsuccessful The extraction of the
involved tooth was carried out under local anesthesia followed by a band and loop space maintainer
CASE 4
A 7-year-old male child reported with a chief complaint of mild intermittent pain on food lodgment with the primary mandibular right first and second molars The patient had a history of dental treatment at a private
dental clinic few months back which he did not continue further
Clinical examination revealed glass ionomer restoration with 85 and proximal caries with 84 leading to food lodgment An intraoral periapical radiograph with 85 revealed empty root canals with a separated
instrument of about 3ndash4 mm size beyond the apex of mesial root close to the developing succedaneous premolar
4
DISCUSSION
Stainless steel files usually separate fracture due to the excessive amounts of torque and overuse or the
preexisting distortion of the instrument whereas in NiTi rotary files it is a combined result of torsional stress and cyclic fatigue
Therapeutic options for the management of separated endodontic instruments include no intervention nonsurgical (orthograde conservative) management surgical management and tooth extraction
Use of ultrasonic scaler Masserann technique Endo extractor and Cavi-Endo ultrasonic instruments are some of the methods popular for retrieval of a separated endodontic instrument in the permanent tooth
In case 1 a 6-mm-long manual reamer was retrieved successfully with the use of GG drill using a manual file and copious irrigation which is the most desired treatment outcome
In case 2 the retrieval of separated rotary file lodged in the middle third of the root canal was unsuccessful in spite of multiple attempts It was therefore managed with routine obturation followed by restoration to maintain the tooth in its physiological functional state It was kept under close periodic follow-up at least
every 3 months This treatment option should be encouraged where it is possible to follow up the patient clinically and radiographically at close periodic intervals as there is the possibility of instrument escaping
into bone due to physiological root resorption
In cases 3 and 4 an instrument has separated in the apical root portion
In case 3 it was within the root canal and thus an attempt was made for its retrieval which was
unsuccessful It was therefore extracted to prevent the fractured instrument from getting exposed in the bone following resorption as there is no accurate and consistent established age for initiation of resorption in primary teeth known per se
In case 4 an immediate extraction of involved tooth was carried out as the separated instrument was beyond the apex of the primary tooth root
Age of the child clinical signs and symptoms and amount of root resorption are the factors which can also influence the management of separated instrument in primary teeth
Moreover if an instrument has separated after initial cleaning and shaping of root canal maintaining a tooth is not a problem as clinical signs and symptoms are not anticipated and the good prognosis is expected
However if an instrument has separated early during the initial cleaning and shaping of the root canal clinical symptoms may compromise the prognosis
Therefore these factors should be kept in mind while planning a suitable management strategy to avoid or at least reduce the burden of extraction and wear of space maintainer for longer period
5
CONCLUSION
The management and prognosis of a primary tooth with a separated instrument is
dependent on the level of instrument fracture within the root age of the child root
resorption and clinical signs and symptoms of the involved tooth
Different management approaches can be tried depending on clinical situations keeping
in mind benefits vs risks in preserving the tooth
PROS amp CONS
PROS
The entire procedure is given
by step by step
Well descriptive xrays and
photographs
CONS
Medical history has not been
given
REFERENCES
1 TOMER ANIL K ET AL ldquoBROKEN FILE RETRIEVAL PUZZLE IN ENDODONTICSrdquo
(2016)
2 SHENOY A MANDAVA P BOLLA N ET AL A NOVEL TECHNIQUE FOR REMOVAL OF
BROKEN INSTRUMENT FROM ROOT CANAL IN MANDIBULAR SECOND MOLAR
INDIAN J DENT RES 201425(1)107ndash110
3 PATEL J MORAWALA A TALATHI R ET AL RETRIEVAL OF A BROKEN INSTRUMENT
FROM ROOT CANAL IN PRIMARY ANTERIOR TEETH UNIV RES J DENT 20155(3)203ndash
206
4 MORANKAR R GOYAL A GAUBA K ET AL MANUAL VERSUS ROTARY
INSTRUMENTATION FOR PRIMARY MOLAR PULPECTOMIES - A 24 MONTHS
RANDOMIZED CLINICAL TRIAL PEDIAT DENT J 201828(2)96ndash102
5 KASHYAP NILOTPOL (2018) RETAINING PRIMARY MOLARS WITH INSTRUMENT
SEPERATION A CASE REPORT AND CLINICAL GUIDE
6
1
IMPACT OF 6 CITRIC ACID AND ENDOACTIVATOR AS IRRIGATION ADJUNCTS ON OBTURATION QUALITY AND PULPECTOMY OUTCOME IN
PRIMARY TEETH
NEETU JAIN SHALINI GARG ABHISHEK DHINDSA SAKSHI JOSHI HARJOY
KHATRIA
PEDIATRIC DENTAL JOURNAL 2019 29
1
DR MITAKSHARA NIRWAN
CONTENTS
bull INTRODUCTION
bull AIMS amp OBJECTIVES
bull CASE REPORT
bull RESULTS
bull DISCUSSION
bull CONCLUSION
bull PROS AND CONS
bull REFERENCES
2
INTRODUCTION
bull ENDODONTIC THERAPY IN PRIMARY TEETH INVOLVES DISINFECTION OF THE ROOT CANAL
SYSTEM AND ITS OBTURATION WITH RESORBABLE PASTE
bull THE CONTENTS OF ROOT CANAL ALONG WITH SMEAR LAYER ARE EXPECTED TO BE REMOVED
DURING THE BIOMECHANICAL PREPARATION
bull IN VITRO AND CLINICAL DOCUMENTS HAVE INDICATED THAT MECHANICAL PREPARATION OF
THE CANAL LEAVES LARGE PORTIONS OF THE CANAL WALLS UNDEBRIDED AND COMPLETE
REMOVAL OF THE BACTERIA BY THIS MECHANICAL PROCEDURE ALONE IS UNLIKELY TO BE SEEN
THEREFORE SOME FORM OF DISINFECTIONIRRIGATION IS MANDATORY TO KILL THE
MICROORGANISMS AND TO REMOVE THE RESIDUAL TISSUES
3
bull THE IDEAL REQUISITES OF A ROOT CANAL IRRIGANT AS GIVEN BY ZEHNDER ARE
1 BROAD ANTIMICROBIAL SPECTRUM
2 HIGH EFFICACY AGAINST ANAEROBIC AND FACULTATIVE MICROORGANISMS ORGANIZED
IN BIOFILMS
3 ABILITY TO DISSOLVE NECROTIC PULP TISSUE REMNANTS
4 ABILITY TO INACTIVATE ENDOTOXIN
5 ABILITY TO PREVENT THE FORMATION OF A SMEAR LAYER DURING INSTRUMENTATION OR
TO DISSOLVE THE LATTER ONCE IT HAS FORMED
6 SYSTEMICALLY NONTOXIC WHEN THEY COME IN CONTACT WITH VITAL TISSUES
NONCAUSTIC TO PERIODONTAL TISSUES AND WITH LITTLE POTENTIAL TO CAUSE AN
ANAPHYLACTIC REACTION
SINCE NO SINGLE IRRIGANT HAS THESE OPTIMAL PROPERTIES STUDIES HAVE REPORTED THE USE
OF TWO OR MORE SOLUTIONS IN A SPECIFIC SEQUENCE OR IN COMBINATIONS FOR BETTER
RESULTS 4
bull SEVERAL IRRIGATING SOLUTIONS ALONG WITH CHELATING AGENTS HAVE BEEN USED
DURING BIOMECHANICAL PREPARATION OF ROOT CANAL BOTH IN PRIMARY AND
PERMANENT TEETH
bull HOWEVER NONE OF THE AVAILABLE IRRIGATING SOLUTIONS HAS BEEN REGARDED CLEARLY
AS OPTIMAL SOLUTION BECAUSE OF THEIR LIMITED EFFECTIVENESS ESPECIALLY IN APICAL
13RD OF THE ROOT CANAL SYSTEM
bull TO OVERCOME SUCH LIMITATIONS USE OF ENDOACTIVATOR HAS BEEN PROPOSED AS AN
IRRIGATION FACILITATOR THAT IS BASED ON SONIC VIBRATION (UP TO 10000 CPM) WHICH
FACILITATES THE IRRIGANT PENETRATION AND ITS RENEWAL WITHIN THE CANAL
bull ACTIVATION SYSTEMS RESULTED IN BETTER REMOVAL OF THE SMEAR LAYER IN THE APICAL
THIRD OF ROOT CANALS IN COMPARISON TO CONVENTIONAL IRRIGATION
5
CITRIC ACID
bull CITRIC ACID IS A WEAK ORGANIC ACID WITH THE APPEARANCE OF WHITE CRYSTALLINE
POWDER AT ROOM TEMPERATURE
bull IT CAN EXIST EITHER IN WATER-FREE FORM (ANHYDROUS) OR MONOHYDRATE FORM THE
WATER-FREE FORM CRYSTALLIZES FROM THE HOT WATER WHEREAS THE MONOHYDRATE
FORMS FROM THE COLD WATER THE LATTER MAY BE CONVERTED TO ANHYDROUS FORM BY
HEATING MORE THAN 78degC
bull CITRIC ACID OCCURS NATURALLY IN THE BODY IN MITOCHONDRIA AND IS USED BY BLOOD
BANKS TO PREVENT COAGULATION OF TRANSFUSED BLOOD CITRIC ACID IS ALSO ESSENTIAL
TO HUMAN METABOLISM AND IS FOUND IN MANY FOODS
6
2
bull THE BIOLOGICAL EFFECTS OF CITRIC ACID ON THE PERIODONTAL STRUCTURE HAS BEEN
EXTENSIVELY STUDIED IN PERIODONTICS
bull NEUMAN AND NEWMAN SHOWED THAT CITRIC ACID IS THE MOST EFFECTIVE ACID IN
ALTERING THE SOLUBILITY OF HYDROXYAPATITE
bull YAMAGUCHI ET AL SHOWED THAT CITRIC ACID SOLUTION HAD ANTIBACTERIAL EFFECTS ON
ALL 12 ROOT CANAL BACTERIA TESTED
bull ARIAS-MOLIZ ET AL SHOWED THAT ETHYLENEDIAMINETETRAACETIC ACID (EDTA) HAS NO
BACTERICIDAL ACTIVITY EVEN AFTER 1 HOUR CONTACT
bull THIS ACID HAS THE ABILITY OF ROOT CANAL IRRIGATION AND ALSO SMEAR LAYER REMOVAL
DIFFERENT CONCENTRATIONS (1ndash50) HAVE BEEN PROPOSED GUTMANN ET AL CONCLUDED
THAT 10 CITRIC ACID IS BETTER THAN ULTRASOUND FOR SMEAR LAYER REMOVAL FROM THE
ROOT END CAVITIES
7
bull STUDIES HAVE SHOWN IRRIGATION WITH 6 CA FOR 15 OR 30 SECONDS IS QUITE
EFFECTIVE IN REMOVING ALL THE COMPONENTS OF THE SMEAR LAYER OF THE PRIMARY
TEETH WHEREAS PERITUBULAR DENTIN DESTRUCTION WAS OBSERVED WHEN HIGHER
CONCENTRATION OF CITRIC ACID WAS USED AS AN IRRIGATING SOLUTION
8
AIMS amp OBJECTIVES
bull THIS STUDY WAS AIMED TO EVALUATE THE CLINICAL AND RADIOGRAPHIC OUTCOME OF
PULPECTOMY ALONG WITH QUALITY OF OBTURATION USING 6 CITRIC ACID AND
ENDOACTIVATOR
9
CASE REPORT
bull 350 CHILDREN (3-9 YEARS) WITH CLINICAL SIGNS AND SYMPTOMS OF CHRONIC IRREVERSIBLE
PULPITIS IN DEEPLY CARIOUS TEETH WERE SCREENED DURING SCHOOL DENTAL HEALTH
PROGRAM FROM MAY 2014-JULY 2014
bull 123 CHILDREN REPORTED TO THE DEPARTMENT AND 67 CHILDREN WERE SELECTED BASED ON
INCLUSION AND EXCLUSION CRITERIA
RECRUITMENT OF PATIENTS
10
INCLUSION CRITERIA
bull HISTORY OF SPONTANEOUS PAIN AND UNCONTROLLED BLEEDING AFTER PULP AMPUTATION
EXCLUSION CRITERIA
bull EVIDENCE OF INTERNAL OR EXTERNAL (PHYSIOLOGICPATHOLOGIC) ROOT RESORPTION OF MORE THAN A THIRD OF ITS LENGTH
bull ROOT CANAL OBLITERATION OR ANATOMIC ANOMALIES
bull INADEQUATE BONE SUPPORT OR NON RESTORABLE TOOTH
bull ONCE PATIENTS ELIGIBILITY WAS CONFIRMED THE TREATMENT PROCEDURE WAS
EXPLAINED TO THE PARENTGUARDIAN AND INFORMED WRITTEN CONSENT WAS
OBTAINED FROM PARENTSGUARDIANS SHOWING WILLINGNESS FOR THEIR
CHILDRENS TREATMENT 11
PROCEDURE
bull PULPECTOMY WAS PERFORMED BY ONE OPERATOR OF PEDIATRIC DENTISTRY DEPARTMENT
USING A STANDARDIZED TREATMENT PROTOCOL FOR ALL THE PATIENTS
bull AFTER ADMINISTRATION OF LOCAL ANESTHESIA RUBBER DAM WAS APPLIED FOR ISOLATION
bull ACCESS CAVITY WAS PREPARED USING AIR-ROTOR HAND PIECE WITH 8 ROUND BUR AND
PULP TISSUE WAS EXTIRPATED WITH THE HELP OF SPOON EXCAVATOR
bull FURTHER THE NEGOTIATION OF THE CANALS WAS DONE WITH 10 K-FILE
bull A DIAGNOSTIC RADIOGRAPH WAS TAKEN FOR ROOT LENGTH DETERMINATION AND
WORKING LENGTH WAS KEPT 1 MM SHORT OF THE RADIOGRAPHICAL APEX
bull ALL ROOT CANALS WERE INSTRUMENTED MANUALLY USING K-FILES AND WERE IRRIGATED
WITH 10 ML 09 NORMAL SALINE AND 1 SODIUM HYPOCHLORITE AS STANDARDIZING
PROTOCOL FOR ROOT CANAL PREPARATION AND DISINFECTION
12
3
GROUP 1 (CA + E) - IRRIGATION WAS DONE
WITH 10 ML OF 6 CITRIC ACID (CITOCID AMMDENT)
AND IRRIGANTS WERE SONICALLY AGITATED WITH
ENDOACTIVATOR (DENTSPLY) FOR 30 S PER CANAL USING REDBLUE
ENDOACTIVATOR TIP
GROUP 2 (CA) - 10 ML OF 6 CITRIC ACID FOR 1 MIN USING
27 GAUZE IRRIGATING NEEDLE
GROUP 3(SH + E) - 10 ML OF 1 SODIUM HYPOCHLORITE
SOLUTION AND SONIC ACTIVATION WITH ENDOACTIVATOR
GROUP 4(SH) - 10 ML OF 1 SODIUM HYPOCHLORITE
SOLUTION USING IRRIGATING NEEDLE (CONTROL GROUP)
bull TEETH UNDERGOING PULPECTOMY WERE RANDOMLY ENROLLED BY CHIT METHOD INTO THREE
STUDY AND ONE CONTROL GROUP
13
bull IN CITRIC ACID GROUPS FINAL RINSE WITH NORMAL SALINE WAS DONE TO REMOVE THE
REMAINING CRYSTALS (CHELATES)
bull FOLLOWING BIOMECHANICAL PREPARATION THE ROOT CANALS WERE DRIED WITH STERILE
ABSORBENT PAPER POINTS AND OBTURATED WITH VITAPEX USING HAND HELD
LENTULOSPIRAL FINAL RESTORATIONS WERE DONE USING COMPOSITE RESIN
14
bull CLINICAL FOLLOW UP WAS DONE AT 24 H1 WEEK 1 MONTH 6 MONTH AND 12
MONTH TO CHECK PAIN PRESENCE AND PAIN FREQUENCY (ONCEMORE THAN ONCE)
SWELLING FISTULA SENSITIVITY TO PERCUSSION
bull RADIOGRAPHIC FOLLOW UP WAS DONE AT 6 MONTH AND 12 MONTH FOR ANY
DEVIATED ERUPTION OF SUCCEDANEOUS TEETH EXCESS FILING MATERIAL AND ITS
RESORPTION EXTERNALINTERNAL ROOT RESORBTION CALCIFIC METAMORPHOSIS
PRESENCE OF FURCATION RADIOLUCENCY
CLINICAL amp RADIOGRAPHIC FOLLOW UP
15
RADIOGRAPHIC ASSESSMENT OF OBTURATION QUALITY
bull POSTOPERATIVE RADIOGRAPHS WERE VISUALLY ASSESSED FOR QUALITY OF OBTURATION BY
TWO INDEPENDENT EXAMINERS (SG AD) WHO WERE BLINDED WITH REGARD TO
IRRIGATION PROTOCOL GROUP TO ENHANCE CALIBRATION EACH EXAMINER ASSESSED THE
RADIOGRAPH INDEPENDENTLY AND LATER REVIEWED TOGETHER FOR FINAL ASSESSMENT
INDIVIDUAL ROOT WAS TAKEN AS UNIT OF ANALYSIS FOR GRADE OF OBTU- RATION AND
SCORING CRITERIA WERE AS GIVEN BY COLL JA 1996
1 UNDER FILLED - FILLING MATERIAL ENDED 1 MM OR MORE SHORT OF THE APEX
2 OPTIMAL FILLING- FILLING MATERIAL APPEARED TO END AT THE RADIOGRAPHICAL APEX
3 OVERFILLED - FILLING MATERIAL EXTRUDED PAST THE RADIOGRAPHIC APEX
4 OPTIMALLY FILLED ROOTS WERE FURTHER ASSESSED FOR THE PRESENCE OF VOIDS AND VOID
AREA (ROOT CANAL SURFACE UNTOUCHED BY THE ROOT CANAL FILLING MATERIAL) IN THREE
VISUALLY DIVIDED SECTIONS OF THE ROOT IE CORONAL MIDDLE AND APICAL 13RD
16
RESULTS
bull OVERALL CLINICAL AND RADIOGRAPHIC SUCCESS RATE OVER A PERIOD OF ONE YEAR WAS
9886 amp 977 RESPECTIVELY
bull ALL GROUPS WERE SIGNIFICANTLY (P = 001) EFFECTIVE IN ALLEVIATING PAIN WITHIN 24 H
OF PULPECTOMY
17 18
4
19
bull IMMEDIATE POST OPERATIVE RADIOGRAPHIC ASSESSMENT REVEALED 68 (102150) ROOTS
WITH OPTIMAL OBTURATION AND 32 (48150) WITH OVERFILLINGUNDERFILLING MAXIMUM
NO OF OPTIMAL FILLINGS WERE OBSERVED IN GROUP1 (CA + E) (3333) FOLLOWED BY
GROUP 2 (CA) (2549) GROUP 3(SH + E) (2549) AND GROUP 4(SH) (1568)
bull CITRIC ACID GROUPS HAD MORE NUMBER OF OPTIMALLY FILLED ROOTS 588 (60102) THAN
NON CITRIC ACID GROUPS 412 (42102)
bull ENDOACTIVATOR CONTRIBUTED TO 18 OF OPTIMAL OBTURATION IRRESPECTIVE OF
CHELATING AGENT USED
20
21
bull MAXIMUM NO OF VOIDS AND VOID AREAS WERE IN NON CITRIC ACID GROUPS
(6419 amp 5384) COMPARED TO CITRIC ACID GROUPS (3580 amp 4615)
RESPECTIVELY
bull ANALYSIS OF ROOT 13RD REVEALED MAXIMUM NO OF VOID AREA IN APICAL
13RD (4755) FOLLOWED BY MIDDLE 13RD (3846) AND CORONAL 13RD
(1398)
bull LEAST NO OF VOIDS amp VOID AREA (1111 amp 1608) WERE OBSERVED WHEN
ENDOACTIVATOR ALONG WITH CHELATING AGENT WAS USED (GROUP 1)
HOWEVER THIS WAS STATISTICALLY INSIGNIFICANT
22
DISCUSSION
bull IN THE PRESENT STUDY 1 SODIUM HYPOCHLORITE WAS USED ALONG WITH 6 CITRIC ACID
(CHELATING AGENT) WHICH IS REPORTED TO BE AS EFFECTIVE AS 17 EDTA
bull CITRIC ACID (BIOLOGICAL ACID) IS FOUND TO BE BIOCOMPATIBLE AND LEAST IRRITATING TO
PERIAPICAL TISSUES THAN OTHER CHELATING AGENTS
bull USE OF SODIUM HYPOCHLORITE SOLUTION FOLLOWING CHELATING AGENT WAS AVOIDED AS IT
RAPIDLY PRODUCES SEVERE EROSION OF ROOT CANAL WALL DENTIN
bull TRADITIONAL APPROACH OF DELIVERING IRRIGANTS INTO THE ROOT CANAL SPACE USING
SYRINGES AND METAL NEEDLES HAS BEEN FOUND TO BE INEFFECTIVE ESPECIALLY IN THE AREAS OF
ANASTOMOSES BETWEEN CANALS AND APICAL 13RD OF ROOT CANAL
23
bull THEREFORE TO ACHIEVE BETTER CLEANING EFFICIENCY IRRIGANT ACTIVATION HAS BEEN
RECOMMENDED SONIC ACTIVATION HAS BEEN REPORTED TO RESULT IN BETTER ROOT CANAL
CLEANLINESS AS COMPARED TO NO ACTIVATION OF IRRIGANT
24
5
CONCLUSION
bull USE OF 6 CITRIC ACID DEFINITELY HELPED IN RAPID ELIMINATION OF PAIN RESOLUTION OF
PERI-RADICULAR RADIOLUCENCY BETTER OBTURATION QUALITY IN TERMS OF LESS VOIDS AND
VOID AREAS ALONG WITH MAXIMUM NO OF OPTIMAL OBTURATION UP TO APICAL AREA
bull 6 CITRIC ACID AND ENDOACTIVATOR IRRIGATION PROTOCOL PROVED TO BE THE BETTER
IRRIGATION PROTOCOL WHICH MAY CONTRIBUTE TO LONG TERM SUCCESS OF PRIMARY
TOOTH AND THE HEALTH OF UNDERLYING PERMANENT TOOTH
bull 6 CITRIC ACID ALONG WITH ENDOACTIVATOR MAY BE RECOMMENDED AS IRRIGATION
ADJUNCTS IN PULPECTOMY PROCEDURE OF PRIMARY TEETH
25
PROS AND CONS
PROS
bull PROPER EXPLANATION OF THE MATERIALS
USED
CONS
bull NO PREOPERATIVE AND POSTOPERATIVE
RADIOGRAPHS
26
REFERENCES
bull RAMACHANDRA JA NIHAL NK NAGARATHNA C VORA MS ROOT CANAL IRRIGANTS IN
PRIMARY TEETH WORLD J DENT 20156(3)229-234
bull MOHAMMADI Z JAFARZADEH H SHALAVI S KINOSHITA JI UNUSUAL ROOT CANAL
IRRIGATION SOLUTIONS J CONTEMP DENT PRACT 201718(5)415-420
bull ZEHNDER M ROOT CANAL IRRIGANTS J ENDOD 2006 32389- 98
bull SMITH JJ amp WAYMAN BE AN EVALUATION OF THE ANTIMICROBIAL EFFECTIVENESS OF
CITRIC ACID AS A ROOT CANAL IRRIGANT JOURNAL OF ENDODONTICS 1986 12(2) 54-58
bull TANNURE PN AZEVEDO CP BARCELOS R GLEISER R PRIMO LG LONG-TERM OUTCOMES OF
PRIMARY TOOTH PULPECTOMY WITH AND WITHOUT SMEAR LAYER REMOVAL A RANDOMIZED
SPLIT-MOUTH CLINICAL TRIAL PEDIATR DENT 201133316E20 27
bull CARON G NHAM K BRONNEC F MACHTOU P EFFECTIVENESS OF DIFFERENT FINAL IRRIGANT
ACTIVATION PROTOCOLS ON SMEAR LAYER REMOVAL IN CURVED CANALS J ENDOD
2010361361E6
bull COLL JA SADRIAN R PREDICTING PULPECTOMY SUCCESS AND ITS RELATIONSHIP TO
EXFOLIATION AND SUCCEDANEOUS DENTITION PEDIATR DENT 19961857E63
28
1
LOCAL
ANESTHESIA
DR MITAKSHARA NIRWAN
CONTENTS
Definition
Methods of inducing local anesthesia
Desirable properties
Electrophysiology of nerve conduction
Impulse propagation and spread
Mode and site of action of local anesthesia
Classification of local anesthetic according to biological site and mode of action
Dissociation of local anaesthetics
Mechanism of action of local anaethetics
Local anaesthetic agent
2
3
DEFINITION
Local anesthesia is defined as a loss of sensation in
a circumscribed area of the body caused by depression
of excitation in nerve endings or an inhibition of the
conduction process in peripheral nerves
An important feature of local anesthesia is that it produces
LOSS OF SENSATION WITHOUT INDUCING LOSS OF
CONSCIOUSNESS
4
METHODS OF INDUCING LOCAL
ANESTHESIA
Low temperature
Mechanical trauma
Anoxia
Neurolytic agents such as alcohol amp phenol
Chemical agents such as local anesthetics
PROPERTIES OF LOCAL
ANESTHESIA
It should not be irritating to tissue to which it is applied
It should not cause any permanent alteration of nerve structure
Its systemic toxicity should be low
Time of onset of anesthesia should be short
It should be effective regardless of whether it is injected into the tissue or applied locally to mucous membranes
The duration of action should be long enough to permit the completion of procedure
5 6
It should have the potency sufficient to give complete
anesthesia with out the use of harmful concentration solutions
It should be free from producing allergic reactions
It should be free in solution and relatively undergo
biotransformation in the body
It should be either sterile or be capable of being sterilized by
heat with out deterioration
2
ELETROPHYSIOLOGY OF
NERVE CONDUCTION
There is an electrical charge across the membrane
This is the membrane potential
The resting potential (when the cell is not firing) is a negative
electrical potential of -70mv that exists across the nerve
membrane produced by different concentrations of either side of
the membrane
The interior of nerve is NEGATIVE in relation to exterior
7 8
inside
outside
Resting potential of neuron = -70mV
+
-
+
-
+
-
+
-
+
-
SLOW DEPOLARIRIZATION
9
RAPID DEPOLARIZATION
The interior of nerve is POSITIVE in relation to exterior
REPOLARIZATION
10
bull Repolarization takes 07 msec
bull Depolarization takes 03 msec
SODIUM PUMP -
energy comes from the oxidative metabolism of ATP
bull The entire process require 1 msec
IMPULSE PROPOGATION
IMPULSE SPREAD
The propagated impulse travels along the nerve
membrane towards CNS The spread of impulse differs
in myelinated and unmyelinated nerve fibers
DEPOLARIZED SEGMENT ADJACENT RESTING AREA
MODE AND SITE OF ACTION OF LOCAL
ANESTHETICS
Local anesthetic agent interferes with excitation
process in a nerve membrane in one of the
following ways
Altering the basic resting potential of nerve
membrane
Altering the threshold potential
Decreasing the rate of depolarization
Prolonging the rate of repolarization
12
3
CLASSIFICATION OF LOCAL ANESTHETIC
SUBSTANCES ACCORDING TO
BIOLOGICAL SITE AND MODE OF ACTION
CLASS A
Agents acting at receptor site on external surface of nerve membrane
Chemical substance Biotoxins (eg tetrodotoxin and saxitoxin)
CLASS B
Agents acting on receptor sites on internal surface of nerve membrane
Chemical substance Quaternary ammonium analogues of lidocaine
scorpion venom 13
CLASS C Agents acting by receptor independent of
physiochemical mechanism
Chemical substance Benzocaine
CLASS D Agents acting by combination of receptors and
receptor independent mechanisms
Chemical substance most clinically useful anesthetic agents
(eg lidocaine mepivacaine prilocaine)
14
BASED ON THE SOURCE
NATUAL
SYNTHETIC
OTHERS
BASED ON MODE OF APPLICATION
bull INJECTABLE
bull TOPICAL
BASED ON DURATION OF ACTION
bull ULTRA SHORT
bull SHORT
bull MEDIEM
bull LONG
BASED ON ONSET OF ACTION SHORT
INTERMEDIATE
LONG
15
DISSOCIATION OF LOCAL
ANESTHETICS
Local anesthetics are available as salts (usually
hydrochlorides) for clinical use
The salts both water soluble and stable is dissolved in
either sterile water or saline
In this solution it exists simultaneously as unchanged
molecule (RN) also called base and positively charged
molecules (RNH+) called cations
RNH+ ==== RN+ H
+
16
The relative concentration of each ionic form in the solution varies
in the pH of the solution or surrounding tissue
In the presence of high concentration of hydrogen ion (low pH) the
equilibrium shifts to left and most of the anesthetic solution exists
in cationic form
RNH+ gt RN
+ + H
+
As hydrogen ion concentration decreases (higher pH) the
equilibrium shifts towards the free base form
RNH+ lt RN + H
+
17
The relative proportion of ionic form also depends on pKa or DISSOCIATION CONSTANT of the specific local anesthetic
The pKa is a measure of molecules affinity for H+
ions
When the pH of the solution has the same value as pKa of the local anesthetic exactly half the drug will exists in the RNH
+ form and
exactly half in RN form
The percentage of drug existing in either form can be determined by Henderson Hasselbalch equation
Log baseacid = pH - pKa
18
4
MECHANISM OF ACTION OF LOCAL
ANESTHETICS
The following sequence is proposed mechanism of action of LA
Displacement of calcium ions from the sodium channel receptor site
Binding of local anesthetic molecule to this receptor site
Blockade of sodium channel
19
Decrease in sodium conductance
Depression of rate of electrical depolarization
Failure to achieve the threshold potential level
Lack of development of propagated action potential
Conduction blockadehellip
20
21
Na + Na +
22
LOCAL ANESTHETIC AGENT
COMERCIALLY PREPARED LOCAL ANESTHESIA
CONSISTS OF
Local anesthetic agent (xylocaine lignocaine 2)
Vasoconstrictor (adrenaline 1 80000)
Reducing agent (sodium metabisulphite)
Preservative (methylparabencapryl
hydrocuprienotoxin)
Fungicide (thymol)
Vehicle (distillde waterNaCl)
LOCAL ANESTHETIC AGENT
The local anesthetics used in dentistry are divided
into two groups
ESTER GROUP
AMIDE GROUP
23 24
ESTER GROUP It is composed of the following
An aromatic lipophilic group
An intermediate chain containing
an ester linkage
A hydrophilic secondary or tertiary
amino group
AMIDE GROUP It is composed of the following
An aromatic lipophilic group
An intermediate chain containing
amide linkage
A hydrophilic secondary or tertiary
amino group
5
25
CLASSIFICATION OF LOCAL ANESTHETICS
ESTERS
Esters of benzoic acid
Butacaine
Cocaine
Benzocaine
Hexylcaine
Piperocaine
Tetracaine
Esters of Para-amino
benzoic acid
Chloroprocain
Procaine
Propoxycaine
26
AMIDES Articaine
Bupivacaine
Dibucaine
Etidocaine
Lidocaine
Mepivacaine
Prilocaine
Ropivacaine
QUINOLINE
Centbucridine
PHARMACOKINETICS OF LOCAL
ANESTHETICS UPTAKE
When injected into soft tissue most local anesthetics produce
dilation of vascular bed
Cocaine is the only local anesthetic that produces
vasoconstriction initially it produces vasodilation which is
followed by prolonged vasoconstriction
Vasodilation is due to increase in the rate of absorption of the
local anesthetic into the blood thus decreasing the duration of
pain control while increasing the anesthetic blood level and
potential for over dose 27
AMIDE LOCAL ANESTHETICS
The metabolism of amide local anesthetics is more
complicated then esters The primary site of
biotransformation of amide drugs is liver
Entire metabolic process occurs in the liver for lidocaine
articaine etidocaine and bupivacaine
Prilocaine undergoes more rapid biotransformation then the
other amides
28
REFERENCES
Handbook of local anesthesia ndash Stanley F Malamed ndash 6th
edition
Essentials of Local Anesthetic Pharmacology Daniel E
Becker Anesth Prog 2006 Fall 53(3) 98ndash109
WIKIPEDIEA
29
THANK YOU
30
1
Pharmacological Methods of Behavior
Management
DR MITAKSHARA NIRWAN
DEFINITIONS
bull Conscious Sedation ndash A minimally depressed level of consciousness that retains
the patients ability to independently and continuously maintain an airway and respond appropriately to physical stimulation or verbal command
(American Dental Association House Of Delegates 2000)
bull Deep Sedation ndash An induced state of depressed consciousness
accompanied by partial loss of protective reflexes including the inability to continuously maintain an airway independently and or to respond purposefully to physical stimulation or verbal command
bull General Anesthesia (G A) ndash An induced state of unconsciousness or complete loss of
protective reflexes including the inability to continually maintain an airway independently and respond purposefully to physical stimulation or verbal command
Conscious sedation
ADVANTAGES
Conscious
Protective reflexes active amp intact
Stable vital signs
Operating dentist may perform sedation
Minimum amount of equipment required
Prolong detainment in recovery room not required
Risk of complication very low
Excellent choice for poor ndash risk pt in dental office
Cost effective
General anesthesia
ADVANTAGES Not absolutely
essential May be the only
method Not necessary (no
pain reaction) Amnesia always
present
Conscious sedation
DISADVANTAGES
Pt cooperation is essential
Extremely difficult or mentally handicapped pt cannot always be managed
Use of local anesthesia is a must
Amnesia may or may not be present
General anesthesia DISADVANTAGES
Pt unconscious
Protective reflexes are depressed
Depressed
Advanced training required Dentist must not act also as anesthetist
Special equipment necessary
Detainment in recovery area necessary
High IOP amp postoperative complications
Not indicated in dental office
More expensive
Fundamental Concepts
bull Techniques that utilize drugs to induce co-operative yet conscious state in an otherwise uncooperative child ndash CONSCIOUS SEDATION
2
GOALS
1 To facilitate the provision of quality care
2 To minimize the extremes of disruptive behavior
3 To promote a positive psychologic response to treatment
4 To promote patient welfare amp safety
5 To return the patient to physiologic state
OBJECTIVES
1 The pt mood must be altered
2 The pt must remain conscious at all times
3 The pt must be cooperative
4 All protective reflexes must remain intact and active
5 Vital signs must remain stable and with in normal limits
6 The ptrsquos pain threshold should be elevated
7 Amnesia may be present
Indications
1 Preschool children
2 Lack of Psychological Emotional maturity
3 Lack of Cognitive Physical Medical disability
4 Fearful amp anxious pts
5 Pt who require extensive amp complicated dental care amp would require or benefit from prolonged visits
6 Acute pain
7 Traumatic injuries
Operating Facilities amp Equipment
A positive pressure O2 delivery system capable of administering gt than 90 O2 at 10L min flow for 60 min (650L ldquoErdquo cylinder)
OR
Self inflating bag valve mask device (15L min)
A functional suction apparatus with appropriate suction catheters
Monitoring equipment - PO BPC PC or Capno
Inhalation sedation unit
100 O2 amp never less than 25
A fail safe mechanism that is checked and calibrated annually
Must have appropriate scavenging system
Emergency drugs
Techniques of sedation
Routes for drug administration
bull Oral
bull Rectal
bull Inhalational
bull Transmucosal
ndash Sublingual
ndash Intranasal
bull Parenteral
ndash IM
ndash sub mucosal
ndash IV
3
Oral Sedation
Advantages
1 Almost universally accepted and the easiest method
2 Decreased incidence and severity of adverse reaction
3 Low cost
Disadvantages
1 Absorption is variable
2 Prolonged latent period(30 min)
3 Reversal of any unwanted effect is also difficult
4 Inability to readily lighten or deepen the level of sedation
5 Prolonged duration of action
Rectal Sedation
Advantages 1 Incidence and intensity of
drug related side effects is minimized
2 Drug absorption occurs from the large intestine directly into the circulation
3 The lack of a needle syringe or other equipment
4 The ease of administration
5 The low cost
Disadvantages
1 Inconvenience to the administrator amp pt
2 The variable absorption of drugs from the large intestine
3 The slow onset of action amp the relatively long duration of action
4 Inability to titrate the drug dosage
5 The inability to reverse the action of the drug the prolonged recovery
Intranasal sedation
Advantages
Rapid onset (10 ndash 15 min)
Simple amp relatively painless
Less pt cooperation is required
Absorbed directly into the C V S
Intranasal sedation
Disadvantages
1 Dependence on nasal mucous membrane
2 Shorter duration of action(40-60min)
3 Multiple dosage may be necessary
Drugs
Midazolam ndash 02mgkg
Sufentanil ndash 15 ndash 3 mcgkg
Ketamine ndash 3-6mg kg
Sublingual sedation
Advantages
1 Pt acceptance
2 Rapid onset
3 High bioavailability
Drugs
Oral Transmucosal Fentanyl Citrate (OTFC)
Intramuscular Sedation
Advantages
1 More rapid onset of action
2 Absorbed directly into the C V system
3 More reliable absorption of drug
4 Pt cooperation is not as essential
Disadvantages
1 Time factor ndash its 15 min latent period
2 Pt may not be willing to accept the injection
3 The prolonged duration of action(2-4 hrs more)
4 Possibility of injury to the tissues at the site of injection caused by either the drug or the needle
4
Sites of I M administration
1 Gluteal area
2 Vastus lateralis
3 Mid ndash deltoid area
Drugs
Diazepam
Midazolam
Hydroxyzine
Inhalation Sedation
Advantages
1 The onset of action is more rapid
2 Peak clinical level is achieved rapidly(3-5min) - permit titration
3 Administrator has complete control over the actions of the drug - safety feature
4 No significant over dosage
5 Flexible duration of action
6 Recovery time is rapid amp most complete
7 No injection is required
8 With N2O- O2 it is safe with very few side effects
Disadvantages
1 The initial cost of the equipment is high 2 The continuing cost of the gases is high 3 The equipment occupies considerable space 4 N2O is not a potent agent 5 A degree of cooperation is required from the pt 6 Chronic exposure to N2O is deleterious to the health of
dental personnel
Contraindications
1 Nasal obstruction 2 Cyanosis at rest 3 Poor cooperation 4 1st trimester of pregnancy 5 Fear of masks
I V Sedation
Advantages
1 The onset of action is the most rapid 2 The dosage may be titrated 3 Suitable level of sedation can be provided 4 The recovery period is shorter 5 Side effects are extremely uncommon 6 Control of salivary secretions is possible 7 The gag reflex is diminished 8 Effectively diminishes motor disturbances 9 Provides immediate access to CVS in emergency
Disadvantages
1 Venipuncture is necessary
2 Complication may rise at the site of the venipuncture
3 Monitoring must be more intensive
4 Recovery is not complete at the end of the procedure
5 Reversal of sedation is difficult
5
N2O-O2 (Relative Analgesia)
colorless sweet smelling gas
Pharmacokinetics
Absorption through pulmonary epithelium
It is approx 15 times as soluble as is nitrogen It replaces nitrogen in blood
It is carried in solution in plasma of the blood
It is not metabolized by the body
Elimination ndash majorndash lungs minor --- skin
perspiration urine and intestinal gas
Pharmacodynamics
Dose related
10 ndash 25 Lightheaded
Changes in visual amp auditory sensation
Tingling of hands amp feet
Suffusing warmth
Remote from the immediate environment
Reduced anxiety
25-50 max analgesic properties and aberration of vision hearing and proprioception mild drowsiness euphoria amnesia and increased sleepiness and dreams
35 conc will achieve maximum analgesia
bull CNS
ndash Cerebrum-primarily affected
ndash Safe but weak anesthetic agent
bull RESPIRATORY SYSTEM
ndash Increased Tidal and minute volumes
bull CARDIOVASCULAR SYSTEM
ndash 2 studies ndash decreased cardiac output
bull FETAL SYSTEMS
ndash Miscarriage in humans
bull OTHER SYSTEMS
ndash Depression of spinal reflexes increase muscle tone indicates stage of delirium
ndash Muscle rigidity-narcotics + nitrous oxide
ndash Nausea and vomitting - GIT
ndash HEMATOPOIESIS ----- prolonged exposure
Adverse reactions and toxicity
EMOTIONAL REACTIONS
DREAMS HALLUCINATIONS
No acute toxicity
Chronic toxicity ndash bone marrow
depression
PROCEDURE
Diffusion Hypoxia
Sevoflurane
A fluorinated derivative of isopropyl ether ndash synthesized in 1970
Potent anaesthetic agent with rapid uptake amp speedy recovery
Day-case surgery
Problem
Attaching vaporiser to any of the currently available machine
BENZODIAZEPINES
Diazepam 1961 lipid soluble
Uses-alcoholism epilepsy labor tetanus and cerebral palsy
- sedation and amnesia
- varieties of neurosis amp anxiety states
Pharmacokinetics
Orally Rectal IMIV or SC
Well absorbed through GIT
Excretion in urine
6
bull Pharmacodynamics
ndash Depress the brain stem reticular system and the limbic system thalamus and hypothalamus
ndash It is a centrally acting muscle relaxant Has anti-convulsant properties
Adverse reaction amp toxicity
ndash Confusion nausea headache increased appetite decreased salivation and jaundice Thrombophlebitis
ndash Rebound phenomenon
ndash Toxicity drowsiness confusion sleep and coma
Dosage Oral or Rectal ndash 02-05mgkg
Maximum single dose 10mg
IV- 025mgkg
Supplied Tablets 2 5 10 mg
Suspension ndash 5mg
Midazolam Water soluble ndash non-irritant
Oral IM IV
Metabolism- liver
Onset IV 3 -5mins
oral 20 ndash 30mins
Oral administration anxious patients requiring relatively short dental procedure
No rebound phenomenon
Better anxiolysis amp amnesia (retrograde amnesia)
Adverse effects Respiratory depression
dose dependant apnea
Dosage Oral ndash 025 to 1mgkg to maximum single dose 20mg
IM ndash 01 to 015mgkg to a maximum of 10mg
IV ndash slow IV
Supplied Syrup ndash 2mgml
Injectable ndash 1mgml amp 5mgml vials
Flumazenil specific benzodiazepines antagonist
selectively inhibits CNS effects
IV administration amp not recommended below 18yrs of age
02mg over 15 seconds after 45seconds 02mg then after 60seconds to maximum of 1mg
Sedative-Hypnotics
Barbiturates First truly effective drugs for the management of anxiety Generalized CNS depressants Produce dose dependent effects
Sedation ---- sleep ---- GA ---- coma
Suppress the CNS and result in sedation and amnesia Advantages
Rapid onset and short duration Disadvantages
no analgesic effect and possible hypotension Must be used with caution in trauma patients because they may cause
apnea and hypoventilation
DOSE Pentobarbital Sodium 100mg Secobarbital Sodium 100 to 200mg Children 30 to 100mg
bull Chloral Hydrates (Mickey Finn Knock out drops ) First synthesized in 1832 first member of the hypnotic group of drugs
Widely used as conscious sedation agent
Properties
Unpleasant taste
Nausea vomiting
Quite irritating to skin and to mucous membranes
GI irritation
Dosages Individualized for each patient 25 ndash 50mgkg
maximum of 1g
Supplied oral capsule ndash 500mg
oral solution ndash 250 amp 500mg5ml
Rectal suppositories ndash 324 amp 648mg
Narcotics
Do produce sedation amp euphoria greater in children
LA is required but dose should be decreased
Meperidine Synthetic opiate agonist
Very water soluble
Orally SC IM or IV
Peak effect by oral 1 hr amp lasts upto 4 hrs
Adverse reactions
-Seizures
-Extreme caution in hepatic or renal diseases or history of seizures
7
Dosage Oral SC or IM ndash 1to 22mgkg not to exceed 100 mg
Supplied Oral Tablets ndash 50 amp 100mg
Oral Syrup ndash 50mgml
Parental solution ndash 25 50 75 amp 100mgml
Fentanyl
Synthetic opiate narcotic analgesic
Very potent 01mg = 10mg Morophine75mg Meperidine
Pharmacokinetics
IV IM SM
Metabolized in liver Excreted in urine
Fentanyl Onset ndash 7 to 15mins
Duration ndash 1 to 2 hrs
Pharmacodynamics
Respiratory depression RR but returns to normal rapidly Tidal volume amp response to co2 depressed for extended period
Apnea
Less emetic than meperidine
NOT RECOMMENDED IN CHILDREN BELOW 2yrs
Dosage 0002 to 0004mgkg
Supplied 005mgml in 2 amp 5ml ampoules
Reversal drug Naloxone
Semisynthetic opiate antagonist
No agonist activity
Onset 2 to 5mins SC or IM amp 1 to 2mins IV
Reversal 45mins
Pt should be kept under continual surveillance
Adverse reaction nausea vomiting sweating hypotension hypertension ventricular tachycardia fibrillation
Dosage IV SC IM 001mgkg then 01mgkg every 2- 3mins maximum 2mg
Supplied 002 004 1mg solutions
Antihistamines
Hydroxyzine
Oral or IM
Effect ndash 15 ndash 30mins
Half-life ndash 3 hrs
Uses
To relieve anxiety
Used as an anti-histamine
Used to control nausea and vomiting including that associated with motion sickness and pregnancy
Adverse reaction dry mouth drowsiness hypersentivity
Dosage Oral ndash 1 to 2mgkg
IM ndash 11mgkg
Promethazine Oral or IM Onset 15 to 60mins Duration 4 to 6 hrs Uses
To prevent and treat nausea and vomiting associated with motion pregnancy or surgery
Produces sedation and reduce swelling pain and trismus
Lower seizure threshold Adverse reaction dry mouth blurred vision thickening of bronchial secretions Dosage OralIM ndash 05-11mgkg
maximum 25 mg
Diphenhydramine
Oral IM IV
Onset -1hr
Duration ndash 4 to 6 hr
Metabolized in liver
Adverse reaction disturbed coordination thickening of bronchial secretions
Dosage Oral IM IV ndash 1 to 15mgkg
maximum 50mg
Tranquilizers
Major tranquilizer antipsychotic produce calmness control symptoms of psychoses cause reversible extra pyramidal symptoms and do not tend to cause habituation
Minor tranquilizer antianxiety agents also cause calmness do not cause extrapyramidal symptoms Used in conditions like nervous tension and mild depression
8
Classification
Antipsychotics
Phenothiazine derivatives
Chlorpromazine promazine
Butryophenones
Haloperidol
Rauwolfia alkaloids
Reserpine
Antianxiety drugs
Propyl alcohol derivatives
Meprobamate
Benzodiazepine derivatives
Diazepam
Miscellaneous compounds
Hydroxyzine
Meprobamate
White crystalline powder slightly bitter in taste
Only administered orally
Peak blood concentration ----1 to 3hrs
10 ---------excreted unchanged Rest --- excreted as a oxidized derivative or as a glucoronide
Uses
To relieve day time anxiety
Induce sleep in insomniacs
To reduce anxiety associated with dental treatment
Anti-convulsant ndash petit mal epilepsy
Adverse reaction leucopenia acute non-thrombocytopenic purpura ecchymoses eosinophilia edema adenopathy
Dosage Childrengt 6yrs 100 to 200mg
Not recommended for children under 6yrs
Monitoring during sedation
1 Pulse
2 Blood pressure
3 ECG
4 Respiration
5 Temperature
Pulse
Manual Electronic
bull Radial Brachial
bull Facial labial
Blood pressure
ndash Stethoscope amp sphygmomanometer
ndash Automatic devices
ndash Direct cannulation of an artery ndash very accurate
Electrocardiograph
Heart rate rhythm myocardial function
9
Respiration
ndash Monitoring respiratory rate
ndash Observing the rise amp fall of the chest wall
ndash Observing the color of mucous membrane
ndash Observing the inflation amp deflation of the reservoir bag
Devices for monitoring respiration
1 The Precordial pretracheal stethoscope
2 The esophageal stethoscope
ndash Respiratory rate
ndash Heart rate
ndash Any abnormal sounds
Pulse Oximeter
ndash Oxygen saturation
ndash Heart rate
ndash Oxisensor site
ndash Fingers
ndash Toe
ndash Ear lobe
Mechanism
Oxygenated Hb ndash red light
Deoxygenated Hb- infrared light
Tissue pressure from arterial pulse (plethysmography)
Advantages
ndash Safe amp noninvasive
ndash Simple to use
ndash Information is rapidly available for clinical decision
ndash Indirectly indicates respiratory adequacy
Disadvantages
ndash Finger probes can get dislodged
ndash Emitted light source may cause burning
ndash Non reusable probes are expensive
ndash Does not directly determine airway patency
Capnography
1 The presence absence of air flow
2 Indicates depth amp adequacy of respiration
3 Continues analysis of the co2 content of the respired air ndash indicates respiratory adequacy
Temperature
ndash Disposable nondisposable thermometer
ndash Esophageal rectal temp probe
10
Discharge criteria
Cardiovascular function is satisfactory amp stable
Airway patency is uncompromised amp satisfactory
Pt is easily arousable amp protective reflexes intact
State of hydration is adequate
Pt can talk if applicable
Pt can sit unaided if applicable
Pt can ambulate with minimal assistance if applicable
Presedation level of responsiveness achieved
Responsible individual is available
1
PULP THERAPY OF VITAL TEETH
DR MITAKSHARA NIRWAN
Contents
Indirect pulp capping
Direct pulp capping
Medications amp materials used in pulp capping
Pulpotomy
MTA
Apexogenesis
INDIRECT PULP CAPPING
Pieter Van Forest - first to speak about root canal therapy
Glove designed instruments that could prepare a canal to a certain size and taper(1910)
Indirect pulp capping is defined as a procedure where in small amount of carious dentin is retained in
deep areas of cavity to avoid exposure of pulp followed by placement of a suitable medicament and
restorative material that seals off the carious dentin and encourages pulp recovery (Ingle)
A procedure in which only the gross caries is removed from the lesion and the cavity is sealed for a
time with a biocompatible material (McDonald)
Objective of indirect pulp capping
These were given by Eidelman in 1965
bull Arresting the carious process
bull Promoting dentin sclerosis
bull Stimulating formation of tertiary dentin
bull Remineralization of carious dentin
Layers of Carious Dentin Indications of Indirect Pulp Capping
History
Mild pain associated with eating
Negative history of spontaneous extreme pain
Clinical Examination
Deep carious lesion which are close tobut not involving the pulp in vital primary or young
permanent teeth
No mobility
Nominal pulp inflammationdefinite layer of affected dentin after removal of infected dentin
Radiographic examination
Normal lamina dura amp PDL space
No radiolucency around the apices
2
Contraindications of Indirect Pulp Capping
History
Sharp penetrating pulpalgia
Prolonged spontaneous pain especially at night
Clinical examination
Mobility of tooth
Discoloration of tooth
Negative reaction of electric pulp testing
Radiographic examination
Definite pulp exposure
Break in the lamina dura
Radiolucency around the apices
Widened PDL space
Treatment procedure
Sequelae of Indirect Pulp Capping Three distinct types of new dentin formation take place
1 Cellular fibrillar dentinmdashfirst 2 months
2 Globular dentinmdash3 months
3 Tubular dentin (uniform mineralized dentin)
bull 15th of reparative dentin formation begins in less than 30 days
bull After 3 months 01 mm is formed
DIRECT PULP CAPPING Defined by Kopel (1992) as the placement of a medicament or non medicated material on a pulp that
has been exposed in course of excavating the last portions of deep dentinal caries or as a result of
trauma
Objective
To create new dentin in the area of the exposure and subsequent healing of the pulp
Rationale
achieve a biologic closure of the exposure site by deposition of hard tissue barrier (dentin bridge)
between pulp tissue and capping material thus walling off the
INDICATIONS
Small mechanical exposure
Easily controlled haemorrhage
Bright red haemorrhage
True pinpoint exposure
CONTRAINDICATIONS
Severe toothache at night
Spontaneous pain
Tooth mobility
Radiographic appearance of pulp periradicular de- generation
Excess of hemorrhage at the time of exposure Serous exudate from the exposure
Externalinternal root resorption
Swellingfistula
Histological Changes after Pulp Capping
These were illustrated be Glass and Zander in 1949
After 24 hours Necrotic zone adjacent to calcium
hydroxide paste is separated from healthy pulp
tissue by a deep staining basophilic layer
After 7 days Increase in cellular and fibroblastic
activity
After 14 days Partly calcified fibrous tissue lined by
odontoblastic cells is seen below the calcium
proteinate zone disappearance of necrotic zone
After 28 days Zone of new dentin
3
Medications and Materials Used for Pulp Capping Calcium hydroxide
Corticosteroids amp antibiotics
Inert materials
Collagen fibers
4-META adhesive
Direct bonding
Isobutyl cyanoacrylate
Denatured albumin
Mineral trioxide aggregate
Laser
Bone morphogenic protein
PULPOTOMY
Finn (1995) defined it as the complete removal of the coronal portion of the dental pulp
followed by placement of a suitable dressing or medicament that will promote healing and
preserve vitality of the tooth
American Academy of Pediatric Dentistry (1998) defined pulpotomy as the amputation of
affected infected coronal portion of the dental pulp preserving the vitality and function of the
remaining part of radicular pulp
Objectives
bull Removal of inflamed and infected coronal pulp at the site of exposure thus preserving the vitality of the
radicular pulp and allowing it to heal
bull Maintain the tooth in the dental arch
Rationale
bull Radicular pulp is healthy and capable of healing after surgical amputation of the infected coronal pulp
bull Preserves vitality of the radicular pulp
bull Maintains tooth in a physiologic condition
Indications of Pulpotomy bull Mechanical pulp exposure in primary teeth
bull Teeth showing a large carious lesion but free of radicular pulpitis
bull History of only spontaneous pain
bull Hemorrhage from exposure sites bright red and can be controlled
bull Absence of abscess or fistula
bull No interradicular bone loss
bull No interradicular radiolucency
Contraindications of Pulpotomy bull Persistent toothache
bull Tenderness on percussion
bull Root resorption more than 13rd of root length
bull Large carious lesion with nonrestorable crown
bull Highly viscous sluggish hemorrhage from canal orifice which is uncontrollable
bull Medical contradictions like heart disease immuno compromised patient
bull Swelling or fistula
bull External or internal resorption
bull Pathological mobility
bull Calcification of pulp
Classification of pulpotomy
4
Formocresol Pulpotomy
Iby BUCKLEY in 1904
Sweet (1930) Formulated multi visit technique
Doyle (1962) Advocated 2 sitting procedure (complete devitalization)
Spedding (1965) Gave 5 minute protocol (partial devitali- zation)
Venham (1967) Proposed 15 seconds procedure
Current concept uses 4 minutes of application time
Composition of formocresol Buckleyrsquos Formula
bull Cresol ndash 35 percent
bull Glycerol ndash 15 percent
bull Formaldehyde ndash 19 percent
bull Water ndash 31 percent
Mechanism of Action
It prevents tissue autolysis by bonding to the proteins Bonding is of peptide groups of side chain amino acids and is a reversible process accomplished without
changing the basic structure of protein molecules
Histological Changes
bull Demonstrated by Mass and Zilbermann11 in 1933 and also by Massler and Mansokhani in 1959
bull Immediately the pulp becomes fibrous and acidophillic
bull Seven to fourteen days Three zones appear
a broad eosinophilic zone of fixation
b broad pale-staining zone of atrophy with poorcellular definition
c broad zone of inflammation extending apically into normal pulp tissue
bull One yearndash Progressive apical movement of these zones with only acidophillic zone left at the end of 1 year
Modified Formocresol Pulpotomy
Used by TRASK(1972)
The technique is identical to that described for primary teeth except that the formocresol pellet is
sealed permanently in the tooth
Two-visit Devitalization Pulpotomy
Indications
bull There is evidence of sluggish bleeding at the amputation site that is difficult to control
bull Pus in the chamber but none at the amputation site
bull There is thickening of the PDL
bull History of pain
Contraindications
bull Nonrestorable tooth
bull Tooth with necrotic pulp
5
Glutaraldehyde Pulpotomy
It was first suggested by S Gravenmade Introduced by Kopel in 1979
Mechanism of Action
bull Glutaraldehyde produces rapid surface fixation of the underlying pulpal tissue
bull A narrow zone of eosinophilic stained and compressed fixed tissue is found directly beneath the area of application which blends into vital normal appearing tissue apically
bull With time the glutaraldehyde fixed zone is replaced by macrophagic action with dense collagenous tissue thus the entire root canal tissue is vital
Cvekrsquos Pulpotomy
bull This is also called as calcium hydroxide pulpotomy or young permanent partial pulpotomy
bull This was proposed by Mejare and Cvek16 in 1978
bull Indicated in young permanent teeth where the pulp is exposed by mechanical or bacterial means and the
remaining radicular tissue is judged vital by clinical and radiographic criteria whereas the root closure is
notcomplete
MINERAL TRIOXIDE AGGREGATE (MTA) Torabinejad described the physical and chemical properties of MTA in 1995
It is ash colored powder made primarily of fine hydrophilic particles of
1 tricalcium aluminate
2 tricalcium silicate
3 silicate oxide
4 tricalcium oxide
5 bismuth dioxide
Hydration of the powder results in a colloidal gel composed of calcium oxide crystals in an amorphous
structure This gel solidifies into a hard structure in less than three hours
PROPERTIES OF MTA
It is biocompatible material and its sealing ability is better than that of amalgam or ZOE
Initial pH is 102 and set pH is 125
The setting time of cement is 4 hours
The compressive strength is 70 MPA which is comparable with that of IRM
Low cytotoxicity ndash It presents with minimal inflammation if extended beyond the apex
Mineral trioxide aggregate (MTA) has demonstrated the ability to induce hard-tissue formation in
pulpal tissues and it promotes rapid cell growth
APEXOGENESIS
It is defined as the treatment of a vital pulp by capping or pulpotomy in order to permit continued
growth of the root and closure of the open apex
Rationale
Maintenance of integrity of the radicular pulp tissue to allow for continued root growth
Indications
bull Indicated for traumatized or pulpally involved vital permanent tooth when root apex is incompletely formed
bull No history of spontaneous pain
bull No sensitivity on percussion
bull No hemorrhage
bull Normal radiographic appearance
Contraindications
bull Evidence that radicular pulp has undergone degenerative changes
bull Purulent drainage
bull History of prolonged pain bull Necrotic debris in canal
bull Periapical radiolucency
6
1
Gupta A Dhingra R Chaudhari P Gupta A
Department of Paedodontics and Preventive Dentistry Faculty of Dental Sciences SGT University Gurgaon Haryana India
Journal of Indian Society of Pedodontics and Preventive Dentistry
Volume 35 I Issue 3 I July-September 2017
A COMPARISION OF VARIOUS MINIMALLY
INVASIVE TECHNIQUES FOR THE REMOVAL
OF DENTAL FLUOROSIS STAINS IN
CHILDREN
DR MITAKSHARA NIRWAN
CONTENTS
bull Introduction
bull Aims
bull Materials and Methods
bull Results
bull Discussion
bull Conclusion
bull Critical analysis
bull References
INTRODUCTION
bull Dental fluorosis is a developmental disturbance of dental enamel caused by
successive exposure to high concentrations of fluoride during tooth
development
bull Various methods of therapy are advocated for the treatment of fluorosis -
stained teeth which range from invasive ceramic veneer bonding restorations
to abrasive chemical treatments
bull The combination of dental bleaching techniques and microabrasion appears
as an excellent conservative solution to reestablish health in fluorosis
affected teeth
AIMS
bull The aim of the study was to evaluate and compare the effectiveness of
minimally invasive techniques for the removal of dental fluorosis
stains in children in vivo
MATERIALS AND METHODS
Patients visiting the department of Pedodontics and Preventive dentistry
Faculty of Dental Sciences SGT University Gurgaon
bull Sample size 90 patients
bull Age group 10 -17 years
bull Caries cracks or periodontal
disease on anterior teeth
bull Abscess draining sinus
cellulitis
bull Non vital teeth
hypersensitive exposed
crevices
bull Orthodontic appliance
bull Past history of bleaching
bull At least two permanent
maxillary anterior teeth
bull TSIF of score 4
bull Free of systemic diseases
Inclusion criteria Exclusion criteria
2
Groups
Group A In office bleaching with 35 hydrogen peroxide( Pola Office
Bleaching kit) activated by light emitting diode (LED) bleaching unit
(35 HP)
Group B Enamel microabrasion (EM) (PREMA Enamel Microabrasion
System) followed by in-office bleaching with 44 carbamide peroxide
gel (EM)
Group C In-office bleaching with 5 sodium hypochlorite (5
NaOCl)
A baseline colour evaluation was done by taking digital photograph of
the maxillary anterior teeth
RESULTS
Group 1
Colour stability
Group 2 Group 3
Tooth sensitivity
Tooth sensitivity values were taken before the treatment
which was compared to immediate postoperative and follow
up visits It was checked using an electric pulp tester
maximum
moderate
least
immediately
group 2
group 1
group 3
1 month
group 2
group 1
group 3
3 month
group 2
group 1
group 3
Patient satisfaction score
Satisfaction was assessed on visual analog scale
Range 1 to 5
Groups percentage of patients
who were satisfied with
the treatment
Number of patients
who reported slight
reappearance of colour
Group 1
90
7
Group 2
83
8
Group 3
73
7
3
Number of Appointments
Groups One sitting Two sittings Three
sittings
Group 1
25
4
1
group 2
26
3
1
Group 3
30
0
0
DISCUSSION
bull Hydrogen peroxide is capable of penetrating the tooth osmosis and through porosities and cracks subsequently acting directly on the pigmented molecules
bull Gurgan et al investigated 3 different light systems and found out that diode laser system with gave best tooth whitening and least tooth sensitivity
bull In the EM group the surface reflects and refracts light from the surface in such way that mild imperfections in underlying enamel are camouflaged While the highly polished surface of enamel enhances the aesthetic appearance
bull Train et al and Loguercio et al also had the similar results in their studies with EM mild fluorosis showed best results moderate showed moderate results while it had little effect on severe fluorosis
bull NaOCl was only effective on mild stains while moderate and severe
stains could only be lightened to quite an extent but could not be
completely removed
bull When NaOCl comes in contact with hypomineralized and discoloured
enamel it degrades and removes the chromogenic organic material
located on the enamel surface
CONCLUSION
bull It was concluded that esthetic appearance of teeth mild fluorosis can
be achieved by bleaching and microabrasion But in cases of
moderate fluorosis a combination of any of theses modalities can be
used
bull As no special maintenance precautions are required these maybe be
considered as an interesting alternative to conventional operative
treatment
bull Focuses on only TSIF of 4
bull Electric pulp testing is not the
right method to check for
sensitivity
bull Tooth Sensitivity changes
from person to person
bull Food habits can cause
staining of the teeth
bull Minimally invasive
bull Cheaper to veneers
bull Minimal loss of tooth structure
bull 4 parameters checked for the success of treatment
bull Inclusion of specific score of fluorosis for comparing the results
bull Maximum 3 appointments needed
CRITICAL ANALYSIS
Pros Cons
REFERENCES
bull Gurgan S Cakir FY Yazici E Different light-activated in officebleaching
systems Lasers Med Sci 201025817-22
bull Train TE McWhorter AG Seale NSWilson CF Guo IY Examination of
esthetic improvement and surface alteration following microabrasion in
fluorotic human incisors in vivoPediatr dent 199618353-62
bull Loguercio AD Correia LD Zago C Tagliari D Neumann E Gomes OM et al
Clinical effectiveness of two microabrasion materials materials for the
removal of enamel flurosis stains Oper Dent 200732531-8
4
3
Classification of behavior management
Management
Psychological Pharmacological Psychological
Communication
Behavior shaping
Behavior Management
Behavior shaping
Desensitization
Modeling
Contingency management
Disruptive
Voice control
Aversive
HOME
Physical Restraints
Others
Distraction
Audio Analgesia
Bio feed back
Hypnosis
Humor
Coping
Relaxation
COMMUNICATION
communication
Verbal
speech
Non-verbal
Body language
smiling
Eye contact Showing concern
By Touching
Give him a pat
Giving him hug
Expression of feeling
Both
DENTAL TERMINOLOGY WORD SUBSTITUTE
Rubber dam Rain coat
Rubber dam clamp Tooth button
R D frame Coat rack
Sealant Tooth paint
Topical fluoride gel Cavity fighter
Air syringe Wind gun
Suction Vacuum cleaner
Study models Statues
Alginate Pudding
High speeds Whistle
Low speeds Motor cycle
Euphemism Tell Show Do Technique (TSD)
Cornerstone of behaviour management
Given by Addleston in 1959
Objectives
1 Teach the patient imp aspects of the
dental visit amp familiarize the patient with
the dental setting
2 Shape the patientrsquos response to
procedures
through desensitization amp well described
expectations
4
Alternatives to TSD
Tell Play Do
Tell Show Play Doh
Tell Play Do with
Smart Phone Dentist
Game Ask Tell Ask
DESENSITIZATION
Demonstrated by James popularized by Wolpe
Desensitization is a therapeutic technique that pairs an
anxiety- evoking stimulus with a response inhibitory to
anxiety In each situations the percieved link between the
stimulus and the anxiety response is weakened
Involves 3 Stages
1Training the patient to relax
2Constructing a hierarchy of fear
3Introducing each stimulus in the
hierarchy
Modeling
Giver by Bandura (1967) Allowing a pt to observe 1more individual
who demonstrate appropriate behavior in particular situation
Steps in modeling Pt attention obtained Desired behavior is modeled Physical guidance of desired behavior Reinforcement of the guided behavior may be provided Reinforcement of behavior that did not require guidance Reinforcement for appropriate behavior initiated without modeling
Types 1 Live model 2 Symbolic or vicarious model
CONTINGENCY MANAGEMENT
Is a method of modifying the behavior of children by
presentation or withdrawal of reinforcers
Positive reinforcer
Henry W Fields 1984
Contingent presentation
Increases frequency of
behavior
Negative reinforcer
Stokes amp Kennedy1980
Contingent withdrawal
Increases the frequency of
behavior
Material
bull Candies
bull Gums
bull Cookies
bull Toys
Social
bull Praise
bull Facial expressions
bull Nearness
bull Physical contact
Activity
bull TV
bull Camping outdoor
bull Music
Reinforcers
Coping
Defined as the cognitive amp behavioral efforts made by an individual to master tolerate or reduce stressful situations
2types
a) Behavioral physical amp verbal activities
b) Cognitive silent amp thinking in mind to keep calm
It enables
ndash reality-oriented working
- cognitive reappraisal
- emotion cognitions
5
Distraction
Distraction is a tactic designed to divert a patient attention away from their current behavior to focus their interest in something else Types Audio Distraction Audiovisual Distraction
Relaxation
Effective in reducing immediate anxiety and fear
Involves series of basic exercises which may take several months to learn amp practice
Voice control
Given by Pinkham in 1985
Modification of the timbre intensity and pitch of ones voice in an attempt
to dominate the interaction between dentist and child
Objectives
bull To gain the patient attention and
compliance
bull To avoid negative or avoidance
behavior
bull To establish authority
Indications bull Uncoperative and inattentive
patients
Contraindications bull Children who due to age
disability mental or emotional immaturity are unable to understand
Hypnosis
First suggested by Franz A Mesmer in
1773
Altered state of consciousness
characterized by heightened suggestibility
to produce desirable behavioral and
physiological changes
Most effective in the presence of anxiety
Not all patients can be hypnotized
Basic mechanism - relief of pain through
suggestions of relief given in a close
trusting interpersonal situation
Henon outlined following uses
bull To reduce nervousness and
apprehension
bull To eliminate defence mechanisms
that patient use to postpone dental
work
bull To control functional or
psychosomatic grapping
bull To prevent thumb sucking and
bruxism
bull To induce anesthesia
Hand over Mouth Exercise (HOME)
Given by DR EVANGELINE JORDAN (1920)
Evangeline Jordan - If a normal child will not listen but continues to cry
and strugglehellip Hold a folded napkin over the childrsquos mouthhellipand
gently but firmly hold his mouth shut
Other terminologies bull Aversive Conditioning by Lenchner and Wright bull Emotional surprise therapy by Lampshire bull HOM airway restricted (HOMAR) by Levitas (1947) bull Aversion by Crammer (1973)
Children who are
momentarily hysterical
belligerent or defiant
3-6 yrs old
Child who can understands
simple verbal commands
Indications
Contraindications
Very young immature frightened child with serious physical mental or emotional handicap
6
Variationshellip Hand over mouth with airway restricted Towel over mouth
Towel over mouth with airway restricted
Body
Papoose board
Triangular sheet
Pedi wrap
Bean Bag
Safety belt
Extremities
Posey straps
Velco straps
Towel amp Tape
Head
Forearm support
Plastic bowl
Head positioner
Mouth
Tongue blades
Mouth Prop
Bite blocks
Positive Stabilization Mouth
Tongue blade open mouth wide prop Molt mouth prop
Rubber bite blocks
Extremities
Posey Strap
Head
Body
Papoose board
Pedi-wrap
7
1
Impact of Handheld Devices on
Children An Evaluation of Usage amp
Dependency Behaviour
0092
DR MITAKSHARA NIRWAN
Handheld devices
A handheld device is a pocket size
computing device with a display
screen and inputoutput interface like
an external or touchscreen keyboard
For example- smartphones tablet
computers handheld videogame
consoles
Haruki Murakami
ldquoCell Phones are so
convenient that they have
become an inconveniencerdquo
Introduction
The most famouscommonly used and easily accessible type of gadgets are
lsquoHandheld devicesrsquo They are as popular in children as they are in adults
The access and ownership of these devices amongst children has grown
substantially in the past decade Concerns exist regarding excessive usage
and the impact of frequent consumption of mobile media on their health and
behaviour
Aims and Objective
This objective of this study was to asses the level of use of handheld
devices among children aged 0-12 years and their positive and negative
impacts on them It further describes the dependency of these devices
and the behavioral problems associated with it
Materials and Methods An online survey was conducted and a self administered questionnaire
was prepared specially for the parents which included a total of 15
questions regarding the usage and dependency of the device
A total of 100 responses were collected from parents who had children
aged 0-12 years who used these devices on daily basis
2
Level of Usage (Q 123)
Results Purpose (Q7)
Improved
communication and
learning
Using more than
one type of
device
Helped in
Speech
Positive Impacts -
(Q58 amp 9)
P value 0003(s) P value-0007 P value-0006(s)
Reduced parent-
child interaction Disrupted sleep Lack of motivation for academics
Negative Impacts (Q81213)
P value-0001(s) P value-0002(s) P value-0006
Time when children use
the device the most
Isolation of the
child Behavioral impact when gadget is
taken back
Dependency
Behaviour (Q10111415)
P value-002(s) P value 002(s) P value-044
This study was done to evaluate the level of usage of handheld devices and their impact
on the children aged 0-12 years The questionnaire was made such that it asked both the
positive and negative impact and further included the questions regarding the
dependency
784 children had access to smartphone and 17 used tablets
The most common age group in which the devices was used the most was 5-8 years
followed by 9-12 followed by 0-4 (Arlinda et al 2019 )
Another study done by (Rachel Bedford et al 2016) concluded increase usage of mobile
phones 5122 in 6ndash11 monthshy olds through to 9205 by 25ndash36 months
745used these devices several times a day out of which 539 used it for more than
one hourday 255 used it for less than one hour and 206 for more than 2 hours
Various studies follow the same recommendation given by AAP to limit the duration of
gadget amongst children
Discussion
3
Improve of Cognitive Skills
Amongst the positive impacts most parents have answered that the usage of these
devices has helped their child communicate and learn better and it has showed significant
results According to (Sundus M 2018)These devices improve the cognitive skills and
develop their learning skills fasterThe competition skills also get better It gives time for brain to think and process information better Another study which supports this (LF
Jonathan et al 2016)
Motor Physical Exercise
This study has shown that children like to use more than one type of device
sometimesUsing these devices improve fine motor skillshand eye coordination and
hands and fingers become more efficient (Srinahyanti et al 2019) (Sundus M 2018)
Speech Improvement
392 Parents say that maybe usage of the devices has helped improve speech in their
children but Various studies show otherwise as most of them shows that usage of handheld
devices causes delay of speech (Srinahyanti et al 2019)
Reduced parent child interaction
The negative impacts are more when compared to the positive ones Usage of gadgets
has resulted in reduced parent child interaction Less face to face interaction can
cause detachment from family members and value which in turn also causes isolation
of the child as he is more comfortable with the gadget (M Suhana-2017)
Sleep Disorders
This study shows that most parents have agreed that usage of these devices does
cause disruption of sleep Various studies have shown that children get fewer hours of
sleepdrowsiness during the day and dramatic increase in day time sleep because of
the screen usage (Acc to National Sleep Foundation) ( Cain N et al 2010)
In this study most number of parents have
agreed that their children might be dependent on
these devices and also had showed restless and
violent behavior if the gadget is snatched from
them
Most number of kids (667) are heavily
dependent as they like to use the device during
their meal time
Various other studies have assessed the screen
time dependency and have concluded that
various kids suffer from SDD
Conclusion The study conclusively shows that the impact of handheld devices is akin to the
importance of table salt in our meals most significant for our growth and
development in moderate amounts and hazardous in excess The negatives clearly
outweigh the positives with the latter too few and far in between This study also
points towards further extensive research on the subject because we need to find ways and also educate parents to optimise the role of these devices in their
childrenrsquos life taking advantage of their positive attributes and minimising their
negative ones
References 1Wahyuni AS Siahaan FB Arfa M Alona I Nerdy N The Relationship between the Duration of Playing
Gadget and Mental Emotional State of Elementary School Students Open Access Maced J Med Sci
20197(1)148ndash151
2Sundus M Department of Computer Science Lahore-The Impacts of using Gadgets on ChildrenJournal of Depression and Anxiety 2018vol 7(1)296
3Amawi SO Subki AH Khatib HA et al Use of Electronic Entertainment and Communication Devices Among
a Saudi Pediatric Population Cross-Sectional Study Interact J Med Res 20187(2)e13
4Julia ldquoHandheld Screen Time Linked with Speech Delays in Young Childrenrdquo Present Pediatric Acad Soc
Meet 2017
5C Rowan ldquoThe Impact of Technology on Child Sensory Motor Developmentrdquo 2003
6Impact of media use on children and youth Paediatr Child Health 20038(5)301ndash317
7Naik SV Children and their gadgets A pedodontist perspective Int J Oral Health Sci 2018857-8
8Roberts DF Foehr UG Rideout V Generation M Media in the lives of 8‐18 year‐olds A Kaiser Family
Foundation Study 2005
9Arya K Time spent on television viewing and its effect on changing values of school going children Anthropologist 20046269‐71
10 Lerner C Barr R Screen Sense Setting the Record StraightResearch‐Based Guidelines for Screen
Use for Children Under 3 Years Old Early learning project at Georgetown university 2014 p 1‐10
11SrinahyantiYasaratodo Wau Imelda Free Unita Manurung Nur Arjani-Influence of gadget A positive
and Negative Impact of Smartphone Usage for Early Child2019
4
THANK YOU
1
Morankar Rahul Aditi Kapur Krishan Gauba Ashima Goyal
MANAGEMENT OF ENDODONTIC INSTRUMENT SEPARATION IN
PRIMARY TEETH
CASE REPORT
Journal of South Asian Association of Pediatric Dentistry 2020
DR MITAKSHARA NIRWAN
bull Introduction
bull Aims amp Objectives
bull Case report
bull Discussion
bull Conclusion
bull Pros amp Cons
bull References
CONTENTS
Separation of endodontic instrument is an unexpected complication and its prevalence is not known It is a common belief among the dental professionals that rotary nickelndashtitanium (NiTi) instruments separate more frequently than stainless steel hand instruments
However literature revealed that in permanent teeth the reported prevalence of separated endodontics manual instruments is in the range of 07-74 whereas for rotary NiTI instruments it is
approximately 04-5
Fractured root canal instruments may include endodontic files Gates Glidden burs finger spreaders
and paste fillers
INTRODUCTION
The aim of this study is to describe the management strategies for endodontic
instrument separation in a root canal of primary teeth with emphasis on factors
requiring consideration in different clinical situations
AIMS amp OBJECTIVES
CASE 1
A 6-year-old male child reported with the chief complaint of spontaneous toothache in mandibular left second primary molar since few days It has aggravated following dental treatment at a private dental clinic Clinical examination revealed an underprepared access cavity with 75 and incomplete caries removal
which was sealed with glass ionomer cement
An intraoral periapical radiograph revealed a separated instrument of about 6ndash7 mm size in the distal root
2
The separated instrument was lodged firmly in distobuccal root canal 2ndash3 mm below the cementoenamel junction The instrument was bypassed successfully with no 15 and no 20 H-files but attempts for its retrieval were not successful
GatesndashGlidden (GG) drills no 2 (07 mm) and no 3 (09 mm) were used to drill around the instrument after which it was retrieved successfully using no 25 H-file
All the canals were instrumented till size 30 k-file followed by obturation with metapex and restoration with glass ionomer cement amp followed by placement of a crown and loop space maintainer for missing 74 The instrument retrieved was a manual reamer measuring 6 mm in length
The patient was asymptomatic since then and is under regular follow-up
CASE 2
A 5-year-old female child reported with the chief complaint of spontaneous toothache in mandibular left second
primary molar Clinical examination revealed deep occlusal caries with fractured lingual wall and pain on
percussion An intraoral periapical radiograph revealed caries involving pulp without any furcation or periapical
area of rarefaction and pulpectomy was planned
All the canals were enlarged using NiTi rotary files with a 4 taper operating at 500 rpm with minimum torque
setting An orifice opener [(0825 19 mm) of 8 taper size 25 length 19 mm] and nos 0420 file was used for
instrumentation of root canal This was followed by file nos 0425 which got separated in the distobuccal root
canal The radiograph confirmed a separated instrument of length 3ndash4 mm in the middle third of the root canal
The instrument was bypassed with no 15 k-file but could not get retrieved As instrument separation had occurred with 0425 file the involved root canal was sufficiently debrided before separation and the level of instrument separation was at the mid-root region so it was decided to obturate and seal this tooth with
periodic follow-ups instead of immediate extraction All other canals were enlarged till size 0430 in the sequential manner followed by obturation using metapex and placement of stainless steel crown
3
CASE 3
A 5-year-old female child has complaint of mild intermittent pain with primary mandibular left first molar She
had undergone pulpectomy treatment for the same during which an instrument separation has occurred in
the mesiobuccal root canal by a resident doctor
A radiograph revealed a separated instrument of about 4 mm in size lodged in the apical third but within the
confines of the mesial root An attempt was made for its retrieval but was unsuccessful The extraction of the
involved tooth was carried out under local anesthesia followed by a band and loop space maintainer
CASE 4
A 7-year-old male child reported with a chief complaint of mild intermittent pain on food lodgment with the primary mandibular right first and second molars The patient had a history of dental treatment at a private
dental clinic few months back which he did not continue further
Clinical examination revealed glass ionomer restoration with 85 and proximal caries with 84 leading to food lodgment An intraoral periapical radiograph with 85 revealed empty root canals with a separated
instrument of about 3ndash4 mm size beyond the apex of mesial root close to the developing succedaneous premolar
4
DISCUSSION
Stainless steel files usually separate fracture due to the excessive amounts of torque and overuse or the
preexisting distortion of the instrument whereas in NiTi rotary files it is a combined result of torsional stress and cyclic fatigue
Therapeutic options for the management of separated endodontic instruments include no intervention nonsurgical (orthograde conservative) management surgical management and tooth extraction
Use of ultrasonic scaler Masserann technique Endo extractor and Cavi-Endo ultrasonic instruments are some of the methods popular for retrieval of a separated endodontic instrument in the permanent tooth
In case 1 a 6-mm-long manual reamer was retrieved successfully with the use of GG drill using a manual file and copious irrigation which is the most desired treatment outcome
In case 2 the retrieval of separated rotary file lodged in the middle third of the root canal was unsuccessful in spite of multiple attempts It was therefore managed with routine obturation followed by restoration to maintain the tooth in its physiological functional state It was kept under close periodic follow-up at least
every 3 months This treatment option should be encouraged where it is possible to follow up the patient clinically and radiographically at close periodic intervals as there is the possibility of instrument escaping
into bone due to physiological root resorption
In cases 3 and 4 an instrument has separated in the apical root portion
In case 3 it was within the root canal and thus an attempt was made for its retrieval which was
unsuccessful It was therefore extracted to prevent the fractured instrument from getting exposed in the bone following resorption as there is no accurate and consistent established age for initiation of resorption in primary teeth known per se
In case 4 an immediate extraction of involved tooth was carried out as the separated instrument was beyond the apex of the primary tooth root
Age of the child clinical signs and symptoms and amount of root resorption are the factors which can also influence the management of separated instrument in primary teeth
Moreover if an instrument has separated after initial cleaning and shaping of root canal maintaining a tooth is not a problem as clinical signs and symptoms are not anticipated and the good prognosis is expected
However if an instrument has separated early during the initial cleaning and shaping of the root canal clinical symptoms may compromise the prognosis
Therefore these factors should be kept in mind while planning a suitable management strategy to avoid or at least reduce the burden of extraction and wear of space maintainer for longer period
5
CONCLUSION
The management and prognosis of a primary tooth with a separated instrument is
dependent on the level of instrument fracture within the root age of the child root
resorption and clinical signs and symptoms of the involved tooth
Different management approaches can be tried depending on clinical situations keeping
in mind benefits vs risks in preserving the tooth
PROS amp CONS
PROS
The entire procedure is given
by step by step
Well descriptive xrays and
photographs
CONS
Medical history has not been
given
REFERENCES
1 TOMER ANIL K ET AL ldquoBROKEN FILE RETRIEVAL PUZZLE IN ENDODONTICSrdquo
(2016)
2 SHENOY A MANDAVA P BOLLA N ET AL A NOVEL TECHNIQUE FOR REMOVAL OF
BROKEN INSTRUMENT FROM ROOT CANAL IN MANDIBULAR SECOND MOLAR
INDIAN J DENT RES 201425(1)107ndash110
3 PATEL J MORAWALA A TALATHI R ET AL RETRIEVAL OF A BROKEN INSTRUMENT
FROM ROOT CANAL IN PRIMARY ANTERIOR TEETH UNIV RES J DENT 20155(3)203ndash
206
4 MORANKAR R GOYAL A GAUBA K ET AL MANUAL VERSUS ROTARY
INSTRUMENTATION FOR PRIMARY MOLAR PULPECTOMIES - A 24 MONTHS
RANDOMIZED CLINICAL TRIAL PEDIAT DENT J 201828(2)96ndash102
5 KASHYAP NILOTPOL (2018) RETAINING PRIMARY MOLARS WITH INSTRUMENT
SEPERATION A CASE REPORT AND CLINICAL GUIDE
6
1
IMPACT OF 6 CITRIC ACID AND ENDOACTIVATOR AS IRRIGATION ADJUNCTS ON OBTURATION QUALITY AND PULPECTOMY OUTCOME IN
PRIMARY TEETH
NEETU JAIN SHALINI GARG ABHISHEK DHINDSA SAKSHI JOSHI HARJOY
KHATRIA
PEDIATRIC DENTAL JOURNAL 2019 29
1
DR MITAKSHARA NIRWAN
CONTENTS
bull INTRODUCTION
bull AIMS amp OBJECTIVES
bull CASE REPORT
bull RESULTS
bull DISCUSSION
bull CONCLUSION
bull PROS AND CONS
bull REFERENCES
2
INTRODUCTION
bull ENDODONTIC THERAPY IN PRIMARY TEETH INVOLVES DISINFECTION OF THE ROOT CANAL
SYSTEM AND ITS OBTURATION WITH RESORBABLE PASTE
bull THE CONTENTS OF ROOT CANAL ALONG WITH SMEAR LAYER ARE EXPECTED TO BE REMOVED
DURING THE BIOMECHANICAL PREPARATION
bull IN VITRO AND CLINICAL DOCUMENTS HAVE INDICATED THAT MECHANICAL PREPARATION OF
THE CANAL LEAVES LARGE PORTIONS OF THE CANAL WALLS UNDEBRIDED AND COMPLETE
REMOVAL OF THE BACTERIA BY THIS MECHANICAL PROCEDURE ALONE IS UNLIKELY TO BE SEEN
THEREFORE SOME FORM OF DISINFECTIONIRRIGATION IS MANDATORY TO KILL THE
MICROORGANISMS AND TO REMOVE THE RESIDUAL TISSUES
3
bull THE IDEAL REQUISITES OF A ROOT CANAL IRRIGANT AS GIVEN BY ZEHNDER ARE
1 BROAD ANTIMICROBIAL SPECTRUM
2 HIGH EFFICACY AGAINST ANAEROBIC AND FACULTATIVE MICROORGANISMS ORGANIZED
IN BIOFILMS
3 ABILITY TO DISSOLVE NECROTIC PULP TISSUE REMNANTS
4 ABILITY TO INACTIVATE ENDOTOXIN
5 ABILITY TO PREVENT THE FORMATION OF A SMEAR LAYER DURING INSTRUMENTATION OR
TO DISSOLVE THE LATTER ONCE IT HAS FORMED
6 SYSTEMICALLY NONTOXIC WHEN THEY COME IN CONTACT WITH VITAL TISSUES
NONCAUSTIC TO PERIODONTAL TISSUES AND WITH LITTLE POTENTIAL TO CAUSE AN
ANAPHYLACTIC REACTION
SINCE NO SINGLE IRRIGANT HAS THESE OPTIMAL PROPERTIES STUDIES HAVE REPORTED THE USE
OF TWO OR MORE SOLUTIONS IN A SPECIFIC SEQUENCE OR IN COMBINATIONS FOR BETTER
RESULTS 4
bull SEVERAL IRRIGATING SOLUTIONS ALONG WITH CHELATING AGENTS HAVE BEEN USED
DURING BIOMECHANICAL PREPARATION OF ROOT CANAL BOTH IN PRIMARY AND
PERMANENT TEETH
bull HOWEVER NONE OF THE AVAILABLE IRRIGATING SOLUTIONS HAS BEEN REGARDED CLEARLY
AS OPTIMAL SOLUTION BECAUSE OF THEIR LIMITED EFFECTIVENESS ESPECIALLY IN APICAL
13RD OF THE ROOT CANAL SYSTEM
bull TO OVERCOME SUCH LIMITATIONS USE OF ENDOACTIVATOR HAS BEEN PROPOSED AS AN
IRRIGATION FACILITATOR THAT IS BASED ON SONIC VIBRATION (UP TO 10000 CPM) WHICH
FACILITATES THE IRRIGANT PENETRATION AND ITS RENEWAL WITHIN THE CANAL
bull ACTIVATION SYSTEMS RESULTED IN BETTER REMOVAL OF THE SMEAR LAYER IN THE APICAL
THIRD OF ROOT CANALS IN COMPARISON TO CONVENTIONAL IRRIGATION
5
CITRIC ACID
bull CITRIC ACID IS A WEAK ORGANIC ACID WITH THE APPEARANCE OF WHITE CRYSTALLINE
POWDER AT ROOM TEMPERATURE
bull IT CAN EXIST EITHER IN WATER-FREE FORM (ANHYDROUS) OR MONOHYDRATE FORM THE
WATER-FREE FORM CRYSTALLIZES FROM THE HOT WATER WHEREAS THE MONOHYDRATE
FORMS FROM THE COLD WATER THE LATTER MAY BE CONVERTED TO ANHYDROUS FORM BY
HEATING MORE THAN 78degC
bull CITRIC ACID OCCURS NATURALLY IN THE BODY IN MITOCHONDRIA AND IS USED BY BLOOD
BANKS TO PREVENT COAGULATION OF TRANSFUSED BLOOD CITRIC ACID IS ALSO ESSENTIAL
TO HUMAN METABOLISM AND IS FOUND IN MANY FOODS
6
2
bull THE BIOLOGICAL EFFECTS OF CITRIC ACID ON THE PERIODONTAL STRUCTURE HAS BEEN
EXTENSIVELY STUDIED IN PERIODONTICS
bull NEUMAN AND NEWMAN SHOWED THAT CITRIC ACID IS THE MOST EFFECTIVE ACID IN
ALTERING THE SOLUBILITY OF HYDROXYAPATITE
bull YAMAGUCHI ET AL SHOWED THAT CITRIC ACID SOLUTION HAD ANTIBACTERIAL EFFECTS ON
ALL 12 ROOT CANAL BACTERIA TESTED
bull ARIAS-MOLIZ ET AL SHOWED THAT ETHYLENEDIAMINETETRAACETIC ACID (EDTA) HAS NO
BACTERICIDAL ACTIVITY EVEN AFTER 1 HOUR CONTACT
bull THIS ACID HAS THE ABILITY OF ROOT CANAL IRRIGATION AND ALSO SMEAR LAYER REMOVAL
DIFFERENT CONCENTRATIONS (1ndash50) HAVE BEEN PROPOSED GUTMANN ET AL CONCLUDED
THAT 10 CITRIC ACID IS BETTER THAN ULTRASOUND FOR SMEAR LAYER REMOVAL FROM THE
ROOT END CAVITIES
7
bull STUDIES HAVE SHOWN IRRIGATION WITH 6 CA FOR 15 OR 30 SECONDS IS QUITE
EFFECTIVE IN REMOVING ALL THE COMPONENTS OF THE SMEAR LAYER OF THE PRIMARY
TEETH WHEREAS PERITUBULAR DENTIN DESTRUCTION WAS OBSERVED WHEN HIGHER
CONCENTRATION OF CITRIC ACID WAS USED AS AN IRRIGATING SOLUTION
8
AIMS amp OBJECTIVES
bull THIS STUDY WAS AIMED TO EVALUATE THE CLINICAL AND RADIOGRAPHIC OUTCOME OF
PULPECTOMY ALONG WITH QUALITY OF OBTURATION USING 6 CITRIC ACID AND
ENDOACTIVATOR
9
CASE REPORT
bull 350 CHILDREN (3-9 YEARS) WITH CLINICAL SIGNS AND SYMPTOMS OF CHRONIC IRREVERSIBLE
PULPITIS IN DEEPLY CARIOUS TEETH WERE SCREENED DURING SCHOOL DENTAL HEALTH
PROGRAM FROM MAY 2014-JULY 2014
bull 123 CHILDREN REPORTED TO THE DEPARTMENT AND 67 CHILDREN WERE SELECTED BASED ON
INCLUSION AND EXCLUSION CRITERIA
RECRUITMENT OF PATIENTS
10
INCLUSION CRITERIA
bull HISTORY OF SPONTANEOUS PAIN AND UNCONTROLLED BLEEDING AFTER PULP AMPUTATION
EXCLUSION CRITERIA
bull EVIDENCE OF INTERNAL OR EXTERNAL (PHYSIOLOGICPATHOLOGIC) ROOT RESORPTION OF MORE THAN A THIRD OF ITS LENGTH
bull ROOT CANAL OBLITERATION OR ANATOMIC ANOMALIES
bull INADEQUATE BONE SUPPORT OR NON RESTORABLE TOOTH
bull ONCE PATIENTS ELIGIBILITY WAS CONFIRMED THE TREATMENT PROCEDURE WAS
EXPLAINED TO THE PARENTGUARDIAN AND INFORMED WRITTEN CONSENT WAS
OBTAINED FROM PARENTSGUARDIANS SHOWING WILLINGNESS FOR THEIR
CHILDRENS TREATMENT 11
PROCEDURE
bull PULPECTOMY WAS PERFORMED BY ONE OPERATOR OF PEDIATRIC DENTISTRY DEPARTMENT
USING A STANDARDIZED TREATMENT PROTOCOL FOR ALL THE PATIENTS
bull AFTER ADMINISTRATION OF LOCAL ANESTHESIA RUBBER DAM WAS APPLIED FOR ISOLATION
bull ACCESS CAVITY WAS PREPARED USING AIR-ROTOR HAND PIECE WITH 8 ROUND BUR AND
PULP TISSUE WAS EXTIRPATED WITH THE HELP OF SPOON EXCAVATOR
bull FURTHER THE NEGOTIATION OF THE CANALS WAS DONE WITH 10 K-FILE
bull A DIAGNOSTIC RADIOGRAPH WAS TAKEN FOR ROOT LENGTH DETERMINATION AND
WORKING LENGTH WAS KEPT 1 MM SHORT OF THE RADIOGRAPHICAL APEX
bull ALL ROOT CANALS WERE INSTRUMENTED MANUALLY USING K-FILES AND WERE IRRIGATED
WITH 10 ML 09 NORMAL SALINE AND 1 SODIUM HYPOCHLORITE AS STANDARDIZING
PROTOCOL FOR ROOT CANAL PREPARATION AND DISINFECTION
12
3
GROUP 1 (CA + E) - IRRIGATION WAS DONE
WITH 10 ML OF 6 CITRIC ACID (CITOCID AMMDENT)
AND IRRIGANTS WERE SONICALLY AGITATED WITH
ENDOACTIVATOR (DENTSPLY) FOR 30 S PER CANAL USING REDBLUE
ENDOACTIVATOR TIP
GROUP 2 (CA) - 10 ML OF 6 CITRIC ACID FOR 1 MIN USING
27 GAUZE IRRIGATING NEEDLE
GROUP 3(SH + E) - 10 ML OF 1 SODIUM HYPOCHLORITE
SOLUTION AND SONIC ACTIVATION WITH ENDOACTIVATOR
GROUP 4(SH) - 10 ML OF 1 SODIUM HYPOCHLORITE
SOLUTION USING IRRIGATING NEEDLE (CONTROL GROUP)
bull TEETH UNDERGOING PULPECTOMY WERE RANDOMLY ENROLLED BY CHIT METHOD INTO THREE
STUDY AND ONE CONTROL GROUP
13
bull IN CITRIC ACID GROUPS FINAL RINSE WITH NORMAL SALINE WAS DONE TO REMOVE THE
REMAINING CRYSTALS (CHELATES)
bull FOLLOWING BIOMECHANICAL PREPARATION THE ROOT CANALS WERE DRIED WITH STERILE
ABSORBENT PAPER POINTS AND OBTURATED WITH VITAPEX USING HAND HELD
LENTULOSPIRAL FINAL RESTORATIONS WERE DONE USING COMPOSITE RESIN
14
bull CLINICAL FOLLOW UP WAS DONE AT 24 H1 WEEK 1 MONTH 6 MONTH AND 12
MONTH TO CHECK PAIN PRESENCE AND PAIN FREQUENCY (ONCEMORE THAN ONCE)
SWELLING FISTULA SENSITIVITY TO PERCUSSION
bull RADIOGRAPHIC FOLLOW UP WAS DONE AT 6 MONTH AND 12 MONTH FOR ANY
DEVIATED ERUPTION OF SUCCEDANEOUS TEETH EXCESS FILING MATERIAL AND ITS
RESORPTION EXTERNALINTERNAL ROOT RESORBTION CALCIFIC METAMORPHOSIS
PRESENCE OF FURCATION RADIOLUCENCY
CLINICAL amp RADIOGRAPHIC FOLLOW UP
15
RADIOGRAPHIC ASSESSMENT OF OBTURATION QUALITY
bull POSTOPERATIVE RADIOGRAPHS WERE VISUALLY ASSESSED FOR QUALITY OF OBTURATION BY
TWO INDEPENDENT EXAMINERS (SG AD) WHO WERE BLINDED WITH REGARD TO
IRRIGATION PROTOCOL GROUP TO ENHANCE CALIBRATION EACH EXAMINER ASSESSED THE
RADIOGRAPH INDEPENDENTLY AND LATER REVIEWED TOGETHER FOR FINAL ASSESSMENT
INDIVIDUAL ROOT WAS TAKEN AS UNIT OF ANALYSIS FOR GRADE OF OBTU- RATION AND
SCORING CRITERIA WERE AS GIVEN BY COLL JA 1996
1 UNDER FILLED - FILLING MATERIAL ENDED 1 MM OR MORE SHORT OF THE APEX
2 OPTIMAL FILLING- FILLING MATERIAL APPEARED TO END AT THE RADIOGRAPHICAL APEX
3 OVERFILLED - FILLING MATERIAL EXTRUDED PAST THE RADIOGRAPHIC APEX
4 OPTIMALLY FILLED ROOTS WERE FURTHER ASSESSED FOR THE PRESENCE OF VOIDS AND VOID
AREA (ROOT CANAL SURFACE UNTOUCHED BY THE ROOT CANAL FILLING MATERIAL) IN THREE
VISUALLY DIVIDED SECTIONS OF THE ROOT IE CORONAL MIDDLE AND APICAL 13RD
16
RESULTS
bull OVERALL CLINICAL AND RADIOGRAPHIC SUCCESS RATE OVER A PERIOD OF ONE YEAR WAS
9886 amp 977 RESPECTIVELY
bull ALL GROUPS WERE SIGNIFICANTLY (P = 001) EFFECTIVE IN ALLEVIATING PAIN WITHIN 24 H
OF PULPECTOMY
17 18
4
19
bull IMMEDIATE POST OPERATIVE RADIOGRAPHIC ASSESSMENT REVEALED 68 (102150) ROOTS
WITH OPTIMAL OBTURATION AND 32 (48150) WITH OVERFILLINGUNDERFILLING MAXIMUM
NO OF OPTIMAL FILLINGS WERE OBSERVED IN GROUP1 (CA + E) (3333) FOLLOWED BY
GROUP 2 (CA) (2549) GROUP 3(SH + E) (2549) AND GROUP 4(SH) (1568)
bull CITRIC ACID GROUPS HAD MORE NUMBER OF OPTIMALLY FILLED ROOTS 588 (60102) THAN
NON CITRIC ACID GROUPS 412 (42102)
bull ENDOACTIVATOR CONTRIBUTED TO 18 OF OPTIMAL OBTURATION IRRESPECTIVE OF
CHELATING AGENT USED
20
21
bull MAXIMUM NO OF VOIDS AND VOID AREAS WERE IN NON CITRIC ACID GROUPS
(6419 amp 5384) COMPARED TO CITRIC ACID GROUPS (3580 amp 4615)
RESPECTIVELY
bull ANALYSIS OF ROOT 13RD REVEALED MAXIMUM NO OF VOID AREA IN APICAL
13RD (4755) FOLLOWED BY MIDDLE 13RD (3846) AND CORONAL 13RD
(1398)
bull LEAST NO OF VOIDS amp VOID AREA (1111 amp 1608) WERE OBSERVED WHEN
ENDOACTIVATOR ALONG WITH CHELATING AGENT WAS USED (GROUP 1)
HOWEVER THIS WAS STATISTICALLY INSIGNIFICANT
22
DISCUSSION
bull IN THE PRESENT STUDY 1 SODIUM HYPOCHLORITE WAS USED ALONG WITH 6 CITRIC ACID
(CHELATING AGENT) WHICH IS REPORTED TO BE AS EFFECTIVE AS 17 EDTA
bull CITRIC ACID (BIOLOGICAL ACID) IS FOUND TO BE BIOCOMPATIBLE AND LEAST IRRITATING TO
PERIAPICAL TISSUES THAN OTHER CHELATING AGENTS
bull USE OF SODIUM HYPOCHLORITE SOLUTION FOLLOWING CHELATING AGENT WAS AVOIDED AS IT
RAPIDLY PRODUCES SEVERE EROSION OF ROOT CANAL WALL DENTIN
bull TRADITIONAL APPROACH OF DELIVERING IRRIGANTS INTO THE ROOT CANAL SPACE USING
SYRINGES AND METAL NEEDLES HAS BEEN FOUND TO BE INEFFECTIVE ESPECIALLY IN THE AREAS OF
ANASTOMOSES BETWEEN CANALS AND APICAL 13RD OF ROOT CANAL
23
bull THEREFORE TO ACHIEVE BETTER CLEANING EFFICIENCY IRRIGANT ACTIVATION HAS BEEN
RECOMMENDED SONIC ACTIVATION HAS BEEN REPORTED TO RESULT IN BETTER ROOT CANAL
CLEANLINESS AS COMPARED TO NO ACTIVATION OF IRRIGANT
24
5
CONCLUSION
bull USE OF 6 CITRIC ACID DEFINITELY HELPED IN RAPID ELIMINATION OF PAIN RESOLUTION OF
PERI-RADICULAR RADIOLUCENCY BETTER OBTURATION QUALITY IN TERMS OF LESS VOIDS AND
VOID AREAS ALONG WITH MAXIMUM NO OF OPTIMAL OBTURATION UP TO APICAL AREA
bull 6 CITRIC ACID AND ENDOACTIVATOR IRRIGATION PROTOCOL PROVED TO BE THE BETTER
IRRIGATION PROTOCOL WHICH MAY CONTRIBUTE TO LONG TERM SUCCESS OF PRIMARY
TOOTH AND THE HEALTH OF UNDERLYING PERMANENT TOOTH
bull 6 CITRIC ACID ALONG WITH ENDOACTIVATOR MAY BE RECOMMENDED AS IRRIGATION
ADJUNCTS IN PULPECTOMY PROCEDURE OF PRIMARY TEETH
25
PROS AND CONS
PROS
bull PROPER EXPLANATION OF THE MATERIALS
USED
CONS
bull NO PREOPERATIVE AND POSTOPERATIVE
RADIOGRAPHS
26
REFERENCES
bull RAMACHANDRA JA NIHAL NK NAGARATHNA C VORA MS ROOT CANAL IRRIGANTS IN
PRIMARY TEETH WORLD J DENT 20156(3)229-234
bull MOHAMMADI Z JAFARZADEH H SHALAVI S KINOSHITA JI UNUSUAL ROOT CANAL
IRRIGATION SOLUTIONS J CONTEMP DENT PRACT 201718(5)415-420
bull ZEHNDER M ROOT CANAL IRRIGANTS J ENDOD 2006 32389- 98
bull SMITH JJ amp WAYMAN BE AN EVALUATION OF THE ANTIMICROBIAL EFFECTIVENESS OF
CITRIC ACID AS A ROOT CANAL IRRIGANT JOURNAL OF ENDODONTICS 1986 12(2) 54-58
bull TANNURE PN AZEVEDO CP BARCELOS R GLEISER R PRIMO LG LONG-TERM OUTCOMES OF
PRIMARY TOOTH PULPECTOMY WITH AND WITHOUT SMEAR LAYER REMOVAL A RANDOMIZED
SPLIT-MOUTH CLINICAL TRIAL PEDIATR DENT 201133316E20 27
bull CARON G NHAM K BRONNEC F MACHTOU P EFFECTIVENESS OF DIFFERENT FINAL IRRIGANT
ACTIVATION PROTOCOLS ON SMEAR LAYER REMOVAL IN CURVED CANALS J ENDOD
2010361361E6
bull COLL JA SADRIAN R PREDICTING PULPECTOMY SUCCESS AND ITS RELATIONSHIP TO
EXFOLIATION AND SUCCEDANEOUS DENTITION PEDIATR DENT 19961857E63
28
1
LOCAL
ANESTHESIA
DR MITAKSHARA NIRWAN
CONTENTS
Definition
Methods of inducing local anesthesia
Desirable properties
Electrophysiology of nerve conduction
Impulse propagation and spread
Mode and site of action of local anesthesia
Classification of local anesthetic according to biological site and mode of action
Dissociation of local anaesthetics
Mechanism of action of local anaethetics
Local anaesthetic agent
2
3
DEFINITION
Local anesthesia is defined as a loss of sensation in
a circumscribed area of the body caused by depression
of excitation in nerve endings or an inhibition of the
conduction process in peripheral nerves
An important feature of local anesthesia is that it produces
LOSS OF SENSATION WITHOUT INDUCING LOSS OF
CONSCIOUSNESS
4
METHODS OF INDUCING LOCAL
ANESTHESIA
Low temperature
Mechanical trauma
Anoxia
Neurolytic agents such as alcohol amp phenol
Chemical agents such as local anesthetics
PROPERTIES OF LOCAL
ANESTHESIA
It should not be irritating to tissue to which it is applied
It should not cause any permanent alteration of nerve structure
Its systemic toxicity should be low
Time of onset of anesthesia should be short
It should be effective regardless of whether it is injected into the tissue or applied locally to mucous membranes
The duration of action should be long enough to permit the completion of procedure
5 6
It should have the potency sufficient to give complete
anesthesia with out the use of harmful concentration solutions
It should be free from producing allergic reactions
It should be free in solution and relatively undergo
biotransformation in the body
It should be either sterile or be capable of being sterilized by
heat with out deterioration
2
ELETROPHYSIOLOGY OF
NERVE CONDUCTION
There is an electrical charge across the membrane
This is the membrane potential
The resting potential (when the cell is not firing) is a negative
electrical potential of -70mv that exists across the nerve
membrane produced by different concentrations of either side of
the membrane
The interior of nerve is NEGATIVE in relation to exterior
7 8
inside
outside
Resting potential of neuron = -70mV
+
-
+
-
+
-
+
-
+
-
SLOW DEPOLARIRIZATION
9
RAPID DEPOLARIZATION
The interior of nerve is POSITIVE in relation to exterior
REPOLARIZATION
10
bull Repolarization takes 07 msec
bull Depolarization takes 03 msec
SODIUM PUMP -
energy comes from the oxidative metabolism of ATP
bull The entire process require 1 msec
IMPULSE PROPOGATION
IMPULSE SPREAD
The propagated impulse travels along the nerve
membrane towards CNS The spread of impulse differs
in myelinated and unmyelinated nerve fibers
DEPOLARIZED SEGMENT ADJACENT RESTING AREA
MODE AND SITE OF ACTION OF LOCAL
ANESTHETICS
Local anesthetic agent interferes with excitation
process in a nerve membrane in one of the
following ways
Altering the basic resting potential of nerve
membrane
Altering the threshold potential
Decreasing the rate of depolarization
Prolonging the rate of repolarization
12
3
CLASSIFICATION OF LOCAL ANESTHETIC
SUBSTANCES ACCORDING TO
BIOLOGICAL SITE AND MODE OF ACTION
CLASS A
Agents acting at receptor site on external surface of nerve membrane
Chemical substance Biotoxins (eg tetrodotoxin and saxitoxin)
CLASS B
Agents acting on receptor sites on internal surface of nerve membrane
Chemical substance Quaternary ammonium analogues of lidocaine
scorpion venom 13
CLASS C Agents acting by receptor independent of
physiochemical mechanism
Chemical substance Benzocaine
CLASS D Agents acting by combination of receptors and
receptor independent mechanisms
Chemical substance most clinically useful anesthetic agents
(eg lidocaine mepivacaine prilocaine)
14
BASED ON THE SOURCE
NATUAL
SYNTHETIC
OTHERS
BASED ON MODE OF APPLICATION
bull INJECTABLE
bull TOPICAL
BASED ON DURATION OF ACTION
bull ULTRA SHORT
bull SHORT
bull MEDIEM
bull LONG
BASED ON ONSET OF ACTION SHORT
INTERMEDIATE
LONG
15
DISSOCIATION OF LOCAL
ANESTHETICS
Local anesthetics are available as salts (usually
hydrochlorides) for clinical use
The salts both water soluble and stable is dissolved in
either sterile water or saline
In this solution it exists simultaneously as unchanged
molecule (RN) also called base and positively charged
molecules (RNH+) called cations
RNH+ ==== RN+ H
+
16
The relative concentration of each ionic form in the solution varies
in the pH of the solution or surrounding tissue
In the presence of high concentration of hydrogen ion (low pH) the
equilibrium shifts to left and most of the anesthetic solution exists
in cationic form
RNH+ gt RN
+ + H
+
As hydrogen ion concentration decreases (higher pH) the
equilibrium shifts towards the free base form
RNH+ lt RN + H
+
17
The relative proportion of ionic form also depends on pKa or DISSOCIATION CONSTANT of the specific local anesthetic
The pKa is a measure of molecules affinity for H+
ions
When the pH of the solution has the same value as pKa of the local anesthetic exactly half the drug will exists in the RNH
+ form and
exactly half in RN form
The percentage of drug existing in either form can be determined by Henderson Hasselbalch equation
Log baseacid = pH - pKa
18
4
MECHANISM OF ACTION OF LOCAL
ANESTHETICS
The following sequence is proposed mechanism of action of LA
Displacement of calcium ions from the sodium channel receptor site
Binding of local anesthetic molecule to this receptor site
Blockade of sodium channel
19
Decrease in sodium conductance
Depression of rate of electrical depolarization
Failure to achieve the threshold potential level
Lack of development of propagated action potential
Conduction blockadehellip
20
21
Na + Na +
22
LOCAL ANESTHETIC AGENT
COMERCIALLY PREPARED LOCAL ANESTHESIA
CONSISTS OF
Local anesthetic agent (xylocaine lignocaine 2)
Vasoconstrictor (adrenaline 1 80000)
Reducing agent (sodium metabisulphite)
Preservative (methylparabencapryl
hydrocuprienotoxin)
Fungicide (thymol)
Vehicle (distillde waterNaCl)
LOCAL ANESTHETIC AGENT
The local anesthetics used in dentistry are divided
into two groups
ESTER GROUP
AMIDE GROUP
23 24
ESTER GROUP It is composed of the following
An aromatic lipophilic group
An intermediate chain containing
an ester linkage
A hydrophilic secondary or tertiary
amino group
AMIDE GROUP It is composed of the following
An aromatic lipophilic group
An intermediate chain containing
amide linkage
A hydrophilic secondary or tertiary
amino group
5
25
CLASSIFICATION OF LOCAL ANESTHETICS
ESTERS
Esters of benzoic acid
Butacaine
Cocaine
Benzocaine
Hexylcaine
Piperocaine
Tetracaine
Esters of Para-amino
benzoic acid
Chloroprocain
Procaine
Propoxycaine
26
AMIDES Articaine
Bupivacaine
Dibucaine
Etidocaine
Lidocaine
Mepivacaine
Prilocaine
Ropivacaine
QUINOLINE
Centbucridine
PHARMACOKINETICS OF LOCAL
ANESTHETICS UPTAKE
When injected into soft tissue most local anesthetics produce
dilation of vascular bed
Cocaine is the only local anesthetic that produces
vasoconstriction initially it produces vasodilation which is
followed by prolonged vasoconstriction
Vasodilation is due to increase in the rate of absorption of the
local anesthetic into the blood thus decreasing the duration of
pain control while increasing the anesthetic blood level and
potential for over dose 27
AMIDE LOCAL ANESTHETICS
The metabolism of amide local anesthetics is more
complicated then esters The primary site of
biotransformation of amide drugs is liver
Entire metabolic process occurs in the liver for lidocaine
articaine etidocaine and bupivacaine
Prilocaine undergoes more rapid biotransformation then the
other amides
28
REFERENCES
Handbook of local anesthesia ndash Stanley F Malamed ndash 6th
edition
Essentials of Local Anesthetic Pharmacology Daniel E
Becker Anesth Prog 2006 Fall 53(3) 98ndash109
WIKIPEDIEA
29
THANK YOU
30
1
Pharmacological Methods of Behavior
Management
DR MITAKSHARA NIRWAN
DEFINITIONS
bull Conscious Sedation ndash A minimally depressed level of consciousness that retains
the patients ability to independently and continuously maintain an airway and respond appropriately to physical stimulation or verbal command
(American Dental Association House Of Delegates 2000)
bull Deep Sedation ndash An induced state of depressed consciousness
accompanied by partial loss of protective reflexes including the inability to continuously maintain an airway independently and or to respond purposefully to physical stimulation or verbal command
bull General Anesthesia (G A) ndash An induced state of unconsciousness or complete loss of
protective reflexes including the inability to continually maintain an airway independently and respond purposefully to physical stimulation or verbal command
Conscious sedation
ADVANTAGES
Conscious
Protective reflexes active amp intact
Stable vital signs
Operating dentist may perform sedation
Minimum amount of equipment required
Prolong detainment in recovery room not required
Risk of complication very low
Excellent choice for poor ndash risk pt in dental office
Cost effective
General anesthesia
ADVANTAGES Not absolutely
essential May be the only
method Not necessary (no
pain reaction) Amnesia always
present
Conscious sedation
DISADVANTAGES
Pt cooperation is essential
Extremely difficult or mentally handicapped pt cannot always be managed
Use of local anesthesia is a must
Amnesia may or may not be present
General anesthesia DISADVANTAGES
Pt unconscious
Protective reflexes are depressed
Depressed
Advanced training required Dentist must not act also as anesthetist
Special equipment necessary
Detainment in recovery area necessary
High IOP amp postoperative complications
Not indicated in dental office
More expensive
Fundamental Concepts
bull Techniques that utilize drugs to induce co-operative yet conscious state in an otherwise uncooperative child ndash CONSCIOUS SEDATION
2
GOALS
1 To facilitate the provision of quality care
2 To minimize the extremes of disruptive behavior
3 To promote a positive psychologic response to treatment
4 To promote patient welfare amp safety
5 To return the patient to physiologic state
OBJECTIVES
1 The pt mood must be altered
2 The pt must remain conscious at all times
3 The pt must be cooperative
4 All protective reflexes must remain intact and active
5 Vital signs must remain stable and with in normal limits
6 The ptrsquos pain threshold should be elevated
7 Amnesia may be present
Indications
1 Preschool children
2 Lack of Psychological Emotional maturity
3 Lack of Cognitive Physical Medical disability
4 Fearful amp anxious pts
5 Pt who require extensive amp complicated dental care amp would require or benefit from prolonged visits
6 Acute pain
7 Traumatic injuries
Operating Facilities amp Equipment
A positive pressure O2 delivery system capable of administering gt than 90 O2 at 10L min flow for 60 min (650L ldquoErdquo cylinder)
OR
Self inflating bag valve mask device (15L min)
A functional suction apparatus with appropriate suction catheters
Monitoring equipment - PO BPC PC or Capno
Inhalation sedation unit
100 O2 amp never less than 25
A fail safe mechanism that is checked and calibrated annually
Must have appropriate scavenging system
Emergency drugs
Techniques of sedation
Routes for drug administration
bull Oral
bull Rectal
bull Inhalational
bull Transmucosal
ndash Sublingual
ndash Intranasal
bull Parenteral
ndash IM
ndash sub mucosal
ndash IV
3
Oral Sedation
Advantages
1 Almost universally accepted and the easiest method
2 Decreased incidence and severity of adverse reaction
3 Low cost
Disadvantages
1 Absorption is variable
2 Prolonged latent period(30 min)
3 Reversal of any unwanted effect is also difficult
4 Inability to readily lighten or deepen the level of sedation
5 Prolonged duration of action
Rectal Sedation
Advantages 1 Incidence and intensity of
drug related side effects is minimized
2 Drug absorption occurs from the large intestine directly into the circulation
3 The lack of a needle syringe or other equipment
4 The ease of administration
5 The low cost
Disadvantages
1 Inconvenience to the administrator amp pt
2 The variable absorption of drugs from the large intestine
3 The slow onset of action amp the relatively long duration of action
4 Inability to titrate the drug dosage
5 The inability to reverse the action of the drug the prolonged recovery
Intranasal sedation
Advantages
Rapid onset (10 ndash 15 min)
Simple amp relatively painless
Less pt cooperation is required
Absorbed directly into the C V S
Intranasal sedation
Disadvantages
1 Dependence on nasal mucous membrane
2 Shorter duration of action(40-60min)
3 Multiple dosage may be necessary
Drugs
Midazolam ndash 02mgkg
Sufentanil ndash 15 ndash 3 mcgkg
Ketamine ndash 3-6mg kg
Sublingual sedation
Advantages
1 Pt acceptance
2 Rapid onset
3 High bioavailability
Drugs
Oral Transmucosal Fentanyl Citrate (OTFC)
Intramuscular Sedation
Advantages
1 More rapid onset of action
2 Absorbed directly into the C V system
3 More reliable absorption of drug
4 Pt cooperation is not as essential
Disadvantages
1 Time factor ndash its 15 min latent period
2 Pt may not be willing to accept the injection
3 The prolonged duration of action(2-4 hrs more)
4 Possibility of injury to the tissues at the site of injection caused by either the drug or the needle
4
Sites of I M administration
1 Gluteal area
2 Vastus lateralis
3 Mid ndash deltoid area
Drugs
Diazepam
Midazolam
Hydroxyzine
Inhalation Sedation
Advantages
1 The onset of action is more rapid
2 Peak clinical level is achieved rapidly(3-5min) - permit titration
3 Administrator has complete control over the actions of the drug - safety feature
4 No significant over dosage
5 Flexible duration of action
6 Recovery time is rapid amp most complete
7 No injection is required
8 With N2O- O2 it is safe with very few side effects
Disadvantages
1 The initial cost of the equipment is high 2 The continuing cost of the gases is high 3 The equipment occupies considerable space 4 N2O is not a potent agent 5 A degree of cooperation is required from the pt 6 Chronic exposure to N2O is deleterious to the health of
dental personnel
Contraindications
1 Nasal obstruction 2 Cyanosis at rest 3 Poor cooperation 4 1st trimester of pregnancy 5 Fear of masks
I V Sedation
Advantages
1 The onset of action is the most rapid 2 The dosage may be titrated 3 Suitable level of sedation can be provided 4 The recovery period is shorter 5 Side effects are extremely uncommon 6 Control of salivary secretions is possible 7 The gag reflex is diminished 8 Effectively diminishes motor disturbances 9 Provides immediate access to CVS in emergency
Disadvantages
1 Venipuncture is necessary
2 Complication may rise at the site of the venipuncture
3 Monitoring must be more intensive
4 Recovery is not complete at the end of the procedure
5 Reversal of sedation is difficult
5
N2O-O2 (Relative Analgesia)
colorless sweet smelling gas
Pharmacokinetics
Absorption through pulmonary epithelium
It is approx 15 times as soluble as is nitrogen It replaces nitrogen in blood
It is carried in solution in plasma of the blood
It is not metabolized by the body
Elimination ndash majorndash lungs minor --- skin
perspiration urine and intestinal gas
Pharmacodynamics
Dose related
10 ndash 25 Lightheaded
Changes in visual amp auditory sensation
Tingling of hands amp feet
Suffusing warmth
Remote from the immediate environment
Reduced anxiety
25-50 max analgesic properties and aberration of vision hearing and proprioception mild drowsiness euphoria amnesia and increased sleepiness and dreams
35 conc will achieve maximum analgesia
bull CNS
ndash Cerebrum-primarily affected
ndash Safe but weak anesthetic agent
bull RESPIRATORY SYSTEM
ndash Increased Tidal and minute volumes
bull CARDIOVASCULAR SYSTEM
ndash 2 studies ndash decreased cardiac output
bull FETAL SYSTEMS
ndash Miscarriage in humans
bull OTHER SYSTEMS
ndash Depression of spinal reflexes increase muscle tone indicates stage of delirium
ndash Muscle rigidity-narcotics + nitrous oxide
ndash Nausea and vomitting - GIT
ndash HEMATOPOIESIS ----- prolonged exposure
Adverse reactions and toxicity
EMOTIONAL REACTIONS
DREAMS HALLUCINATIONS
No acute toxicity
Chronic toxicity ndash bone marrow
depression
PROCEDURE
Diffusion Hypoxia
Sevoflurane
A fluorinated derivative of isopropyl ether ndash synthesized in 1970
Potent anaesthetic agent with rapid uptake amp speedy recovery
Day-case surgery
Problem
Attaching vaporiser to any of the currently available machine
BENZODIAZEPINES
Diazepam 1961 lipid soluble
Uses-alcoholism epilepsy labor tetanus and cerebral palsy
- sedation and amnesia
- varieties of neurosis amp anxiety states
Pharmacokinetics
Orally Rectal IMIV or SC
Well absorbed through GIT
Excretion in urine
6
bull Pharmacodynamics
ndash Depress the brain stem reticular system and the limbic system thalamus and hypothalamus
ndash It is a centrally acting muscle relaxant Has anti-convulsant properties
Adverse reaction amp toxicity
ndash Confusion nausea headache increased appetite decreased salivation and jaundice Thrombophlebitis
ndash Rebound phenomenon
ndash Toxicity drowsiness confusion sleep and coma
Dosage Oral or Rectal ndash 02-05mgkg
Maximum single dose 10mg
IV- 025mgkg
Supplied Tablets 2 5 10 mg
Suspension ndash 5mg
Midazolam Water soluble ndash non-irritant
Oral IM IV
Metabolism- liver
Onset IV 3 -5mins
oral 20 ndash 30mins
Oral administration anxious patients requiring relatively short dental procedure
No rebound phenomenon
Better anxiolysis amp amnesia (retrograde amnesia)
Adverse effects Respiratory depression
dose dependant apnea
Dosage Oral ndash 025 to 1mgkg to maximum single dose 20mg
IM ndash 01 to 015mgkg to a maximum of 10mg
IV ndash slow IV
Supplied Syrup ndash 2mgml
Injectable ndash 1mgml amp 5mgml vials
Flumazenil specific benzodiazepines antagonist
selectively inhibits CNS effects
IV administration amp not recommended below 18yrs of age
02mg over 15 seconds after 45seconds 02mg then after 60seconds to maximum of 1mg
Sedative-Hypnotics
Barbiturates First truly effective drugs for the management of anxiety Generalized CNS depressants Produce dose dependent effects
Sedation ---- sleep ---- GA ---- coma
Suppress the CNS and result in sedation and amnesia Advantages
Rapid onset and short duration Disadvantages
no analgesic effect and possible hypotension Must be used with caution in trauma patients because they may cause
apnea and hypoventilation
DOSE Pentobarbital Sodium 100mg Secobarbital Sodium 100 to 200mg Children 30 to 100mg
bull Chloral Hydrates (Mickey Finn Knock out drops ) First synthesized in 1832 first member of the hypnotic group of drugs
Widely used as conscious sedation agent
Properties
Unpleasant taste
Nausea vomiting
Quite irritating to skin and to mucous membranes
GI irritation
Dosages Individualized for each patient 25 ndash 50mgkg
maximum of 1g
Supplied oral capsule ndash 500mg
oral solution ndash 250 amp 500mg5ml
Rectal suppositories ndash 324 amp 648mg
Narcotics
Do produce sedation amp euphoria greater in children
LA is required but dose should be decreased
Meperidine Synthetic opiate agonist
Very water soluble
Orally SC IM or IV
Peak effect by oral 1 hr amp lasts upto 4 hrs
Adverse reactions
-Seizures
-Extreme caution in hepatic or renal diseases or history of seizures
7
Dosage Oral SC or IM ndash 1to 22mgkg not to exceed 100 mg
Supplied Oral Tablets ndash 50 amp 100mg
Oral Syrup ndash 50mgml
Parental solution ndash 25 50 75 amp 100mgml
Fentanyl
Synthetic opiate narcotic analgesic
Very potent 01mg = 10mg Morophine75mg Meperidine
Pharmacokinetics
IV IM SM
Metabolized in liver Excreted in urine
Fentanyl Onset ndash 7 to 15mins
Duration ndash 1 to 2 hrs
Pharmacodynamics
Respiratory depression RR but returns to normal rapidly Tidal volume amp response to co2 depressed for extended period
Apnea
Less emetic than meperidine
NOT RECOMMENDED IN CHILDREN BELOW 2yrs
Dosage 0002 to 0004mgkg
Supplied 005mgml in 2 amp 5ml ampoules
Reversal drug Naloxone
Semisynthetic opiate antagonist
No agonist activity
Onset 2 to 5mins SC or IM amp 1 to 2mins IV
Reversal 45mins
Pt should be kept under continual surveillance
Adverse reaction nausea vomiting sweating hypotension hypertension ventricular tachycardia fibrillation
Dosage IV SC IM 001mgkg then 01mgkg every 2- 3mins maximum 2mg
Supplied 002 004 1mg solutions
Antihistamines
Hydroxyzine
Oral or IM
Effect ndash 15 ndash 30mins
Half-life ndash 3 hrs
Uses
To relieve anxiety
Used as an anti-histamine
Used to control nausea and vomiting including that associated with motion sickness and pregnancy
Adverse reaction dry mouth drowsiness hypersentivity
Dosage Oral ndash 1 to 2mgkg
IM ndash 11mgkg
Promethazine Oral or IM Onset 15 to 60mins Duration 4 to 6 hrs Uses
To prevent and treat nausea and vomiting associated with motion pregnancy or surgery
Produces sedation and reduce swelling pain and trismus
Lower seizure threshold Adverse reaction dry mouth blurred vision thickening of bronchial secretions Dosage OralIM ndash 05-11mgkg
maximum 25 mg
Diphenhydramine
Oral IM IV
Onset -1hr
Duration ndash 4 to 6 hr
Metabolized in liver
Adverse reaction disturbed coordination thickening of bronchial secretions
Dosage Oral IM IV ndash 1 to 15mgkg
maximum 50mg
Tranquilizers
Major tranquilizer antipsychotic produce calmness control symptoms of psychoses cause reversible extra pyramidal symptoms and do not tend to cause habituation
Minor tranquilizer antianxiety agents also cause calmness do not cause extrapyramidal symptoms Used in conditions like nervous tension and mild depression
8
Classification
Antipsychotics
Phenothiazine derivatives
Chlorpromazine promazine
Butryophenones
Haloperidol
Rauwolfia alkaloids
Reserpine
Antianxiety drugs
Propyl alcohol derivatives
Meprobamate
Benzodiazepine derivatives
Diazepam
Miscellaneous compounds
Hydroxyzine
Meprobamate
White crystalline powder slightly bitter in taste
Only administered orally
Peak blood concentration ----1 to 3hrs
10 ---------excreted unchanged Rest --- excreted as a oxidized derivative or as a glucoronide
Uses
To relieve day time anxiety
Induce sleep in insomniacs
To reduce anxiety associated with dental treatment
Anti-convulsant ndash petit mal epilepsy
Adverse reaction leucopenia acute non-thrombocytopenic purpura ecchymoses eosinophilia edema adenopathy
Dosage Childrengt 6yrs 100 to 200mg
Not recommended for children under 6yrs
Monitoring during sedation
1 Pulse
2 Blood pressure
3 ECG
4 Respiration
5 Temperature
Pulse
Manual Electronic
bull Radial Brachial
bull Facial labial
Blood pressure
ndash Stethoscope amp sphygmomanometer
ndash Automatic devices
ndash Direct cannulation of an artery ndash very accurate
Electrocardiograph
Heart rate rhythm myocardial function
9
Respiration
ndash Monitoring respiratory rate
ndash Observing the rise amp fall of the chest wall
ndash Observing the color of mucous membrane
ndash Observing the inflation amp deflation of the reservoir bag
Devices for monitoring respiration
1 The Precordial pretracheal stethoscope
2 The esophageal stethoscope
ndash Respiratory rate
ndash Heart rate
ndash Any abnormal sounds
Pulse Oximeter
ndash Oxygen saturation
ndash Heart rate
ndash Oxisensor site
ndash Fingers
ndash Toe
ndash Ear lobe
Mechanism
Oxygenated Hb ndash red light
Deoxygenated Hb- infrared light
Tissue pressure from arterial pulse (plethysmography)
Advantages
ndash Safe amp noninvasive
ndash Simple to use
ndash Information is rapidly available for clinical decision
ndash Indirectly indicates respiratory adequacy
Disadvantages
ndash Finger probes can get dislodged
ndash Emitted light source may cause burning
ndash Non reusable probes are expensive
ndash Does not directly determine airway patency
Capnography
1 The presence absence of air flow
2 Indicates depth amp adequacy of respiration
3 Continues analysis of the co2 content of the respired air ndash indicates respiratory adequacy
Temperature
ndash Disposable nondisposable thermometer
ndash Esophageal rectal temp probe
10
Discharge criteria
Cardiovascular function is satisfactory amp stable
Airway patency is uncompromised amp satisfactory
Pt is easily arousable amp protective reflexes intact
State of hydration is adequate
Pt can talk if applicable
Pt can sit unaided if applicable
Pt can ambulate with minimal assistance if applicable
Presedation level of responsiveness achieved
Responsible individual is available
1
PULP THERAPY OF VITAL TEETH
DR MITAKSHARA NIRWAN
Contents
Indirect pulp capping
Direct pulp capping
Medications amp materials used in pulp capping
Pulpotomy
MTA
Apexogenesis
INDIRECT PULP CAPPING
Pieter Van Forest - first to speak about root canal therapy
Glove designed instruments that could prepare a canal to a certain size and taper(1910)
Indirect pulp capping is defined as a procedure where in small amount of carious dentin is retained in
deep areas of cavity to avoid exposure of pulp followed by placement of a suitable medicament and
restorative material that seals off the carious dentin and encourages pulp recovery (Ingle)
A procedure in which only the gross caries is removed from the lesion and the cavity is sealed for a
time with a biocompatible material (McDonald)
Objective of indirect pulp capping
These were given by Eidelman in 1965
bull Arresting the carious process
bull Promoting dentin sclerosis
bull Stimulating formation of tertiary dentin
bull Remineralization of carious dentin
Layers of Carious Dentin Indications of Indirect Pulp Capping
History
Mild pain associated with eating
Negative history of spontaneous extreme pain
Clinical Examination
Deep carious lesion which are close tobut not involving the pulp in vital primary or young
permanent teeth
No mobility
Nominal pulp inflammationdefinite layer of affected dentin after removal of infected dentin
Radiographic examination
Normal lamina dura amp PDL space
No radiolucency around the apices
2
Contraindications of Indirect Pulp Capping
History
Sharp penetrating pulpalgia
Prolonged spontaneous pain especially at night
Clinical examination
Mobility of tooth
Discoloration of tooth
Negative reaction of electric pulp testing
Radiographic examination
Definite pulp exposure
Break in the lamina dura
Radiolucency around the apices
Widened PDL space
Treatment procedure
Sequelae of Indirect Pulp Capping Three distinct types of new dentin formation take place
1 Cellular fibrillar dentinmdashfirst 2 months
2 Globular dentinmdash3 months
3 Tubular dentin (uniform mineralized dentin)
bull 15th of reparative dentin formation begins in less than 30 days
bull After 3 months 01 mm is formed
DIRECT PULP CAPPING Defined by Kopel (1992) as the placement of a medicament or non medicated material on a pulp that
has been exposed in course of excavating the last portions of deep dentinal caries or as a result of
trauma
Objective
To create new dentin in the area of the exposure and subsequent healing of the pulp
Rationale
achieve a biologic closure of the exposure site by deposition of hard tissue barrier (dentin bridge)
between pulp tissue and capping material thus walling off the
INDICATIONS
Small mechanical exposure
Easily controlled haemorrhage
Bright red haemorrhage
True pinpoint exposure
CONTRAINDICATIONS
Severe toothache at night
Spontaneous pain
Tooth mobility
Radiographic appearance of pulp periradicular de- generation
Excess of hemorrhage at the time of exposure Serous exudate from the exposure
Externalinternal root resorption
Swellingfistula
Histological Changes after Pulp Capping
These were illustrated be Glass and Zander in 1949
After 24 hours Necrotic zone adjacent to calcium
hydroxide paste is separated from healthy pulp
tissue by a deep staining basophilic layer
After 7 days Increase in cellular and fibroblastic
activity
After 14 days Partly calcified fibrous tissue lined by
odontoblastic cells is seen below the calcium
proteinate zone disappearance of necrotic zone
After 28 days Zone of new dentin
3
Medications and Materials Used for Pulp Capping Calcium hydroxide
Corticosteroids amp antibiotics
Inert materials
Collagen fibers
4-META adhesive
Direct bonding
Isobutyl cyanoacrylate
Denatured albumin
Mineral trioxide aggregate
Laser
Bone morphogenic protein
PULPOTOMY
Finn (1995) defined it as the complete removal of the coronal portion of the dental pulp
followed by placement of a suitable dressing or medicament that will promote healing and
preserve vitality of the tooth
American Academy of Pediatric Dentistry (1998) defined pulpotomy as the amputation of
affected infected coronal portion of the dental pulp preserving the vitality and function of the
remaining part of radicular pulp
Objectives
bull Removal of inflamed and infected coronal pulp at the site of exposure thus preserving the vitality of the
radicular pulp and allowing it to heal
bull Maintain the tooth in the dental arch
Rationale
bull Radicular pulp is healthy and capable of healing after surgical amputation of the infected coronal pulp
bull Preserves vitality of the radicular pulp
bull Maintains tooth in a physiologic condition
Indications of Pulpotomy bull Mechanical pulp exposure in primary teeth
bull Teeth showing a large carious lesion but free of radicular pulpitis
bull History of only spontaneous pain
bull Hemorrhage from exposure sites bright red and can be controlled
bull Absence of abscess or fistula
bull No interradicular bone loss
bull No interradicular radiolucency
Contraindications of Pulpotomy bull Persistent toothache
bull Tenderness on percussion
bull Root resorption more than 13rd of root length
bull Large carious lesion with nonrestorable crown
bull Highly viscous sluggish hemorrhage from canal orifice which is uncontrollable
bull Medical contradictions like heart disease immuno compromised patient
bull Swelling or fistula
bull External or internal resorption
bull Pathological mobility
bull Calcification of pulp
Classification of pulpotomy
4
Formocresol Pulpotomy
Iby BUCKLEY in 1904
Sweet (1930) Formulated multi visit technique
Doyle (1962) Advocated 2 sitting procedure (complete devitalization)
Spedding (1965) Gave 5 minute protocol (partial devitali- zation)
Venham (1967) Proposed 15 seconds procedure
Current concept uses 4 minutes of application time
Composition of formocresol Buckleyrsquos Formula
bull Cresol ndash 35 percent
bull Glycerol ndash 15 percent
bull Formaldehyde ndash 19 percent
bull Water ndash 31 percent
Mechanism of Action
It prevents tissue autolysis by bonding to the proteins Bonding is of peptide groups of side chain amino acids and is a reversible process accomplished without
changing the basic structure of protein molecules
Histological Changes
bull Demonstrated by Mass and Zilbermann11 in 1933 and also by Massler and Mansokhani in 1959
bull Immediately the pulp becomes fibrous and acidophillic
bull Seven to fourteen days Three zones appear
a broad eosinophilic zone of fixation
b broad pale-staining zone of atrophy with poorcellular definition
c broad zone of inflammation extending apically into normal pulp tissue
bull One yearndash Progressive apical movement of these zones with only acidophillic zone left at the end of 1 year
Modified Formocresol Pulpotomy
Used by TRASK(1972)
The technique is identical to that described for primary teeth except that the formocresol pellet is
sealed permanently in the tooth
Two-visit Devitalization Pulpotomy
Indications
bull There is evidence of sluggish bleeding at the amputation site that is difficult to control
bull Pus in the chamber but none at the amputation site
bull There is thickening of the PDL
bull History of pain
Contraindications
bull Nonrestorable tooth
bull Tooth with necrotic pulp
5
Glutaraldehyde Pulpotomy
It was first suggested by S Gravenmade Introduced by Kopel in 1979
Mechanism of Action
bull Glutaraldehyde produces rapid surface fixation of the underlying pulpal tissue
bull A narrow zone of eosinophilic stained and compressed fixed tissue is found directly beneath the area of application which blends into vital normal appearing tissue apically
bull With time the glutaraldehyde fixed zone is replaced by macrophagic action with dense collagenous tissue thus the entire root canal tissue is vital
Cvekrsquos Pulpotomy
bull This is also called as calcium hydroxide pulpotomy or young permanent partial pulpotomy
bull This was proposed by Mejare and Cvek16 in 1978
bull Indicated in young permanent teeth where the pulp is exposed by mechanical or bacterial means and the
remaining radicular tissue is judged vital by clinical and radiographic criteria whereas the root closure is
notcomplete
MINERAL TRIOXIDE AGGREGATE (MTA) Torabinejad described the physical and chemical properties of MTA in 1995
It is ash colored powder made primarily of fine hydrophilic particles of
1 tricalcium aluminate
2 tricalcium silicate
3 silicate oxide
4 tricalcium oxide
5 bismuth dioxide
Hydration of the powder results in a colloidal gel composed of calcium oxide crystals in an amorphous
structure This gel solidifies into a hard structure in less than three hours
PROPERTIES OF MTA
It is biocompatible material and its sealing ability is better than that of amalgam or ZOE
Initial pH is 102 and set pH is 125
The setting time of cement is 4 hours
The compressive strength is 70 MPA which is comparable with that of IRM
Low cytotoxicity ndash It presents with minimal inflammation if extended beyond the apex
Mineral trioxide aggregate (MTA) has demonstrated the ability to induce hard-tissue formation in
pulpal tissues and it promotes rapid cell growth
APEXOGENESIS
It is defined as the treatment of a vital pulp by capping or pulpotomy in order to permit continued
growth of the root and closure of the open apex
Rationale
Maintenance of integrity of the radicular pulp tissue to allow for continued root growth
Indications
bull Indicated for traumatized or pulpally involved vital permanent tooth when root apex is incompletely formed
bull No history of spontaneous pain
bull No sensitivity on percussion
bull No hemorrhage
bull Normal radiographic appearance
Contraindications
bull Evidence that radicular pulp has undergone degenerative changes
bull Purulent drainage
bull History of prolonged pain bull Necrotic debris in canal
bull Periapical radiolucency
6
1
Gupta A Dhingra R Chaudhari P Gupta A
Department of Paedodontics and Preventive Dentistry Faculty of Dental Sciences SGT University Gurgaon Haryana India
Journal of Indian Society of Pedodontics and Preventive Dentistry
Volume 35 I Issue 3 I July-September 2017
A COMPARISION OF VARIOUS MINIMALLY
INVASIVE TECHNIQUES FOR THE REMOVAL
OF DENTAL FLUOROSIS STAINS IN
CHILDREN
DR MITAKSHARA NIRWAN
CONTENTS
bull Introduction
bull Aims
bull Materials and Methods
bull Results
bull Discussion
bull Conclusion
bull Critical analysis
bull References
INTRODUCTION
bull Dental fluorosis is a developmental disturbance of dental enamel caused by
successive exposure to high concentrations of fluoride during tooth
development
bull Various methods of therapy are advocated for the treatment of fluorosis -
stained teeth which range from invasive ceramic veneer bonding restorations
to abrasive chemical treatments
bull The combination of dental bleaching techniques and microabrasion appears
as an excellent conservative solution to reestablish health in fluorosis
affected teeth
AIMS
bull The aim of the study was to evaluate and compare the effectiveness of
minimally invasive techniques for the removal of dental fluorosis
stains in children in vivo
MATERIALS AND METHODS
Patients visiting the department of Pedodontics and Preventive dentistry
Faculty of Dental Sciences SGT University Gurgaon
bull Sample size 90 patients
bull Age group 10 -17 years
bull Caries cracks or periodontal
disease on anterior teeth
bull Abscess draining sinus
cellulitis
bull Non vital teeth
hypersensitive exposed
crevices
bull Orthodontic appliance
bull Past history of bleaching
bull At least two permanent
maxillary anterior teeth
bull TSIF of score 4
bull Free of systemic diseases
Inclusion criteria Exclusion criteria
2
Groups
Group A In office bleaching with 35 hydrogen peroxide( Pola Office
Bleaching kit) activated by light emitting diode (LED) bleaching unit
(35 HP)
Group B Enamel microabrasion (EM) (PREMA Enamel Microabrasion
System) followed by in-office bleaching with 44 carbamide peroxide
gel (EM)
Group C In-office bleaching with 5 sodium hypochlorite (5
NaOCl)
A baseline colour evaluation was done by taking digital photograph of
the maxillary anterior teeth
RESULTS
Group 1
Colour stability
Group 2 Group 3
Tooth sensitivity
Tooth sensitivity values were taken before the treatment
which was compared to immediate postoperative and follow
up visits It was checked using an electric pulp tester
maximum
moderate
least
immediately
group 2
group 1
group 3
1 month
group 2
group 1
group 3
3 month
group 2
group 1
group 3
Patient satisfaction score
Satisfaction was assessed on visual analog scale
Range 1 to 5
Groups percentage of patients
who were satisfied with
the treatment
Number of patients
who reported slight
reappearance of colour
Group 1
90
7
Group 2
83
8
Group 3
73
7
3
Number of Appointments
Groups One sitting Two sittings Three
sittings
Group 1
25
4
1
group 2
26
3
1
Group 3
30
0
0
DISCUSSION
bull Hydrogen peroxide is capable of penetrating the tooth osmosis and through porosities and cracks subsequently acting directly on the pigmented molecules
bull Gurgan et al investigated 3 different light systems and found out that diode laser system with gave best tooth whitening and least tooth sensitivity
bull In the EM group the surface reflects and refracts light from the surface in such way that mild imperfections in underlying enamel are camouflaged While the highly polished surface of enamel enhances the aesthetic appearance
bull Train et al and Loguercio et al also had the similar results in their studies with EM mild fluorosis showed best results moderate showed moderate results while it had little effect on severe fluorosis
bull NaOCl was only effective on mild stains while moderate and severe
stains could only be lightened to quite an extent but could not be
completely removed
bull When NaOCl comes in contact with hypomineralized and discoloured
enamel it degrades and removes the chromogenic organic material
located on the enamel surface
CONCLUSION
bull It was concluded that esthetic appearance of teeth mild fluorosis can
be achieved by bleaching and microabrasion But in cases of
moderate fluorosis a combination of any of theses modalities can be
used
bull As no special maintenance precautions are required these maybe be
considered as an interesting alternative to conventional operative
treatment
bull Focuses on only TSIF of 4
bull Electric pulp testing is not the
right method to check for
sensitivity
bull Tooth Sensitivity changes
from person to person
bull Food habits can cause
staining of the teeth
bull Minimally invasive
bull Cheaper to veneers
bull Minimal loss of tooth structure
bull 4 parameters checked for the success of treatment
bull Inclusion of specific score of fluorosis for comparing the results
bull Maximum 3 appointments needed
CRITICAL ANALYSIS
Pros Cons
REFERENCES
bull Gurgan S Cakir FY Yazici E Different light-activated in officebleaching
systems Lasers Med Sci 201025817-22
bull Train TE McWhorter AG Seale NSWilson CF Guo IY Examination of
esthetic improvement and surface alteration following microabrasion in
fluorotic human incisors in vivoPediatr dent 199618353-62
bull Loguercio AD Correia LD Zago C Tagliari D Neumann E Gomes OM et al
Clinical effectiveness of two microabrasion materials materials for the
removal of enamel flurosis stains Oper Dent 200732531-8
4
4
Alternatives to TSD
Tell Play Do
Tell Show Play Doh
Tell Play Do with
Smart Phone Dentist
Game Ask Tell Ask
DESENSITIZATION
Demonstrated by James popularized by Wolpe
Desensitization is a therapeutic technique that pairs an
anxiety- evoking stimulus with a response inhibitory to
anxiety In each situations the percieved link between the
stimulus and the anxiety response is weakened
Involves 3 Stages
1Training the patient to relax
2Constructing a hierarchy of fear
3Introducing each stimulus in the
hierarchy
Modeling
Giver by Bandura (1967) Allowing a pt to observe 1more individual
who demonstrate appropriate behavior in particular situation
Steps in modeling Pt attention obtained Desired behavior is modeled Physical guidance of desired behavior Reinforcement of the guided behavior may be provided Reinforcement of behavior that did not require guidance Reinforcement for appropriate behavior initiated without modeling
Types 1 Live model 2 Symbolic or vicarious model
CONTINGENCY MANAGEMENT
Is a method of modifying the behavior of children by
presentation or withdrawal of reinforcers
Positive reinforcer
Henry W Fields 1984
Contingent presentation
Increases frequency of
behavior
Negative reinforcer
Stokes amp Kennedy1980
Contingent withdrawal
Increases the frequency of
behavior
Material
bull Candies
bull Gums
bull Cookies
bull Toys
Social
bull Praise
bull Facial expressions
bull Nearness
bull Physical contact
Activity
bull TV
bull Camping outdoor
bull Music
Reinforcers
Coping
Defined as the cognitive amp behavioral efforts made by an individual to master tolerate or reduce stressful situations
2types
a) Behavioral physical amp verbal activities
b) Cognitive silent amp thinking in mind to keep calm
It enables
ndash reality-oriented working
- cognitive reappraisal
- emotion cognitions
5
Distraction
Distraction is a tactic designed to divert a patient attention away from their current behavior to focus their interest in something else Types Audio Distraction Audiovisual Distraction
Relaxation
Effective in reducing immediate anxiety and fear
Involves series of basic exercises which may take several months to learn amp practice
Voice control
Given by Pinkham in 1985
Modification of the timbre intensity and pitch of ones voice in an attempt
to dominate the interaction between dentist and child
Objectives
bull To gain the patient attention and
compliance
bull To avoid negative or avoidance
behavior
bull To establish authority
Indications bull Uncoperative and inattentive
patients
Contraindications bull Children who due to age
disability mental or emotional immaturity are unable to understand
Hypnosis
First suggested by Franz A Mesmer in
1773
Altered state of consciousness
characterized by heightened suggestibility
to produce desirable behavioral and
physiological changes
Most effective in the presence of anxiety
Not all patients can be hypnotized
Basic mechanism - relief of pain through
suggestions of relief given in a close
trusting interpersonal situation
Henon outlined following uses
bull To reduce nervousness and
apprehension
bull To eliminate defence mechanisms
that patient use to postpone dental
work
bull To control functional or
psychosomatic grapping
bull To prevent thumb sucking and
bruxism
bull To induce anesthesia
Hand over Mouth Exercise (HOME)
Given by DR EVANGELINE JORDAN (1920)
Evangeline Jordan - If a normal child will not listen but continues to cry
and strugglehellip Hold a folded napkin over the childrsquos mouthhellipand
gently but firmly hold his mouth shut
Other terminologies bull Aversive Conditioning by Lenchner and Wright bull Emotional surprise therapy by Lampshire bull HOM airway restricted (HOMAR) by Levitas (1947) bull Aversion by Crammer (1973)
Children who are
momentarily hysterical
belligerent or defiant
3-6 yrs old
Child who can understands
simple verbal commands
Indications
Contraindications
Very young immature frightened child with serious physical mental or emotional handicap
6
Variationshellip Hand over mouth with airway restricted Towel over mouth
Towel over mouth with airway restricted
Body
Papoose board
Triangular sheet
Pedi wrap
Bean Bag
Safety belt
Extremities
Posey straps
Velco straps
Towel amp Tape
Head
Forearm support
Plastic bowl
Head positioner
Mouth
Tongue blades
Mouth Prop
Bite blocks
Positive Stabilization Mouth
Tongue blade open mouth wide prop Molt mouth prop
Rubber bite blocks
Extremities
Posey Strap
Head
Body
Papoose board
Pedi-wrap
7
1
Impact of Handheld Devices on
Children An Evaluation of Usage amp
Dependency Behaviour
0092
DR MITAKSHARA NIRWAN
Handheld devices
A handheld device is a pocket size
computing device with a display
screen and inputoutput interface like
an external or touchscreen keyboard
For example- smartphones tablet
computers handheld videogame
consoles
Haruki Murakami
ldquoCell Phones are so
convenient that they have
become an inconveniencerdquo
Introduction
The most famouscommonly used and easily accessible type of gadgets are
lsquoHandheld devicesrsquo They are as popular in children as they are in adults
The access and ownership of these devices amongst children has grown
substantially in the past decade Concerns exist regarding excessive usage
and the impact of frequent consumption of mobile media on their health and
behaviour
Aims and Objective
This objective of this study was to asses the level of use of handheld
devices among children aged 0-12 years and their positive and negative
impacts on them It further describes the dependency of these devices
and the behavioral problems associated with it
Materials and Methods An online survey was conducted and a self administered questionnaire
was prepared specially for the parents which included a total of 15
questions regarding the usage and dependency of the device
A total of 100 responses were collected from parents who had children
aged 0-12 years who used these devices on daily basis
2
Level of Usage (Q 123)
Results Purpose (Q7)
Improved
communication and
learning
Using more than
one type of
device
Helped in
Speech
Positive Impacts -
(Q58 amp 9)
P value 0003(s) P value-0007 P value-0006(s)
Reduced parent-
child interaction Disrupted sleep Lack of motivation for academics
Negative Impacts (Q81213)
P value-0001(s) P value-0002(s) P value-0006
Time when children use
the device the most
Isolation of the
child Behavioral impact when gadget is
taken back
Dependency
Behaviour (Q10111415)
P value-002(s) P value 002(s) P value-044
This study was done to evaluate the level of usage of handheld devices and their impact
on the children aged 0-12 years The questionnaire was made such that it asked both the
positive and negative impact and further included the questions regarding the
dependency
784 children had access to smartphone and 17 used tablets
The most common age group in which the devices was used the most was 5-8 years
followed by 9-12 followed by 0-4 (Arlinda et al 2019 )
Another study done by (Rachel Bedford et al 2016) concluded increase usage of mobile
phones 5122 in 6ndash11 monthshy olds through to 9205 by 25ndash36 months
745used these devices several times a day out of which 539 used it for more than
one hourday 255 used it for less than one hour and 206 for more than 2 hours
Various studies follow the same recommendation given by AAP to limit the duration of
gadget amongst children
Discussion
3
Improve of Cognitive Skills
Amongst the positive impacts most parents have answered that the usage of these
devices has helped their child communicate and learn better and it has showed significant
results According to (Sundus M 2018)These devices improve the cognitive skills and
develop their learning skills fasterThe competition skills also get better It gives time for brain to think and process information better Another study which supports this (LF
Jonathan et al 2016)
Motor Physical Exercise
This study has shown that children like to use more than one type of device
sometimesUsing these devices improve fine motor skillshand eye coordination and
hands and fingers become more efficient (Srinahyanti et al 2019) (Sundus M 2018)
Speech Improvement
392 Parents say that maybe usage of the devices has helped improve speech in their
children but Various studies show otherwise as most of them shows that usage of handheld
devices causes delay of speech (Srinahyanti et al 2019)
Reduced parent child interaction
The negative impacts are more when compared to the positive ones Usage of gadgets
has resulted in reduced parent child interaction Less face to face interaction can
cause detachment from family members and value which in turn also causes isolation
of the child as he is more comfortable with the gadget (M Suhana-2017)
Sleep Disorders
This study shows that most parents have agreed that usage of these devices does
cause disruption of sleep Various studies have shown that children get fewer hours of
sleepdrowsiness during the day and dramatic increase in day time sleep because of
the screen usage (Acc to National Sleep Foundation) ( Cain N et al 2010)
In this study most number of parents have
agreed that their children might be dependent on
these devices and also had showed restless and
violent behavior if the gadget is snatched from
them
Most number of kids (667) are heavily
dependent as they like to use the device during
their meal time
Various other studies have assessed the screen
time dependency and have concluded that
various kids suffer from SDD
Conclusion The study conclusively shows that the impact of handheld devices is akin to the
importance of table salt in our meals most significant for our growth and
development in moderate amounts and hazardous in excess The negatives clearly
outweigh the positives with the latter too few and far in between This study also
points towards further extensive research on the subject because we need to find ways and also educate parents to optimise the role of these devices in their
childrenrsquos life taking advantage of their positive attributes and minimising their
negative ones
References 1Wahyuni AS Siahaan FB Arfa M Alona I Nerdy N The Relationship between the Duration of Playing
Gadget and Mental Emotional State of Elementary School Students Open Access Maced J Med Sci
20197(1)148ndash151
2Sundus M Department of Computer Science Lahore-The Impacts of using Gadgets on ChildrenJournal of Depression and Anxiety 2018vol 7(1)296
3Amawi SO Subki AH Khatib HA et al Use of Electronic Entertainment and Communication Devices Among
a Saudi Pediatric Population Cross-Sectional Study Interact J Med Res 20187(2)e13
4Julia ldquoHandheld Screen Time Linked with Speech Delays in Young Childrenrdquo Present Pediatric Acad Soc
Meet 2017
5C Rowan ldquoThe Impact of Technology on Child Sensory Motor Developmentrdquo 2003
6Impact of media use on children and youth Paediatr Child Health 20038(5)301ndash317
7Naik SV Children and their gadgets A pedodontist perspective Int J Oral Health Sci 2018857-8
8Roberts DF Foehr UG Rideout V Generation M Media in the lives of 8‐18 year‐olds A Kaiser Family
Foundation Study 2005
9Arya K Time spent on television viewing and its effect on changing values of school going children Anthropologist 20046269‐71
10 Lerner C Barr R Screen Sense Setting the Record StraightResearch‐Based Guidelines for Screen
Use for Children Under 3 Years Old Early learning project at Georgetown university 2014 p 1‐10
11SrinahyantiYasaratodo Wau Imelda Free Unita Manurung Nur Arjani-Influence of gadget A positive
and Negative Impact of Smartphone Usage for Early Child2019
4
THANK YOU
1
Morankar Rahul Aditi Kapur Krishan Gauba Ashima Goyal
MANAGEMENT OF ENDODONTIC INSTRUMENT SEPARATION IN
PRIMARY TEETH
CASE REPORT
Journal of South Asian Association of Pediatric Dentistry 2020
DR MITAKSHARA NIRWAN
bull Introduction
bull Aims amp Objectives
bull Case report
bull Discussion
bull Conclusion
bull Pros amp Cons
bull References
CONTENTS
Separation of endodontic instrument is an unexpected complication and its prevalence is not known It is a common belief among the dental professionals that rotary nickelndashtitanium (NiTi) instruments separate more frequently than stainless steel hand instruments
However literature revealed that in permanent teeth the reported prevalence of separated endodontics manual instruments is in the range of 07-74 whereas for rotary NiTI instruments it is
approximately 04-5
Fractured root canal instruments may include endodontic files Gates Glidden burs finger spreaders
and paste fillers
INTRODUCTION
The aim of this study is to describe the management strategies for endodontic
instrument separation in a root canal of primary teeth with emphasis on factors
requiring consideration in different clinical situations
AIMS amp OBJECTIVES
CASE 1
A 6-year-old male child reported with the chief complaint of spontaneous toothache in mandibular left second primary molar since few days It has aggravated following dental treatment at a private dental clinic Clinical examination revealed an underprepared access cavity with 75 and incomplete caries removal
which was sealed with glass ionomer cement
An intraoral periapical radiograph revealed a separated instrument of about 6ndash7 mm size in the distal root
2
The separated instrument was lodged firmly in distobuccal root canal 2ndash3 mm below the cementoenamel junction The instrument was bypassed successfully with no 15 and no 20 H-files but attempts for its retrieval were not successful
GatesndashGlidden (GG) drills no 2 (07 mm) and no 3 (09 mm) were used to drill around the instrument after which it was retrieved successfully using no 25 H-file
All the canals were instrumented till size 30 k-file followed by obturation with metapex and restoration with glass ionomer cement amp followed by placement of a crown and loop space maintainer for missing 74 The instrument retrieved was a manual reamer measuring 6 mm in length
The patient was asymptomatic since then and is under regular follow-up
CASE 2
A 5-year-old female child reported with the chief complaint of spontaneous toothache in mandibular left second
primary molar Clinical examination revealed deep occlusal caries with fractured lingual wall and pain on
percussion An intraoral periapical radiograph revealed caries involving pulp without any furcation or periapical
area of rarefaction and pulpectomy was planned
All the canals were enlarged using NiTi rotary files with a 4 taper operating at 500 rpm with minimum torque
setting An orifice opener [(0825 19 mm) of 8 taper size 25 length 19 mm] and nos 0420 file was used for
instrumentation of root canal This was followed by file nos 0425 which got separated in the distobuccal root
canal The radiograph confirmed a separated instrument of length 3ndash4 mm in the middle third of the root canal
The instrument was bypassed with no 15 k-file but could not get retrieved As instrument separation had occurred with 0425 file the involved root canal was sufficiently debrided before separation and the level of instrument separation was at the mid-root region so it was decided to obturate and seal this tooth with
periodic follow-ups instead of immediate extraction All other canals were enlarged till size 0430 in the sequential manner followed by obturation using metapex and placement of stainless steel crown
3
CASE 3
A 5-year-old female child has complaint of mild intermittent pain with primary mandibular left first molar She
had undergone pulpectomy treatment for the same during which an instrument separation has occurred in
the mesiobuccal root canal by a resident doctor
A radiograph revealed a separated instrument of about 4 mm in size lodged in the apical third but within the
confines of the mesial root An attempt was made for its retrieval but was unsuccessful The extraction of the
involved tooth was carried out under local anesthesia followed by a band and loop space maintainer
CASE 4
A 7-year-old male child reported with a chief complaint of mild intermittent pain on food lodgment with the primary mandibular right first and second molars The patient had a history of dental treatment at a private
dental clinic few months back which he did not continue further
Clinical examination revealed glass ionomer restoration with 85 and proximal caries with 84 leading to food lodgment An intraoral periapical radiograph with 85 revealed empty root canals with a separated
instrument of about 3ndash4 mm size beyond the apex of mesial root close to the developing succedaneous premolar
4
DISCUSSION
Stainless steel files usually separate fracture due to the excessive amounts of torque and overuse or the
preexisting distortion of the instrument whereas in NiTi rotary files it is a combined result of torsional stress and cyclic fatigue
Therapeutic options for the management of separated endodontic instruments include no intervention nonsurgical (orthograde conservative) management surgical management and tooth extraction
Use of ultrasonic scaler Masserann technique Endo extractor and Cavi-Endo ultrasonic instruments are some of the methods popular for retrieval of a separated endodontic instrument in the permanent tooth
In case 1 a 6-mm-long manual reamer was retrieved successfully with the use of GG drill using a manual file and copious irrigation which is the most desired treatment outcome
In case 2 the retrieval of separated rotary file lodged in the middle third of the root canal was unsuccessful in spite of multiple attempts It was therefore managed with routine obturation followed by restoration to maintain the tooth in its physiological functional state It was kept under close periodic follow-up at least
every 3 months This treatment option should be encouraged where it is possible to follow up the patient clinically and radiographically at close periodic intervals as there is the possibility of instrument escaping
into bone due to physiological root resorption
In cases 3 and 4 an instrument has separated in the apical root portion
In case 3 it was within the root canal and thus an attempt was made for its retrieval which was
unsuccessful It was therefore extracted to prevent the fractured instrument from getting exposed in the bone following resorption as there is no accurate and consistent established age for initiation of resorption in primary teeth known per se
In case 4 an immediate extraction of involved tooth was carried out as the separated instrument was beyond the apex of the primary tooth root
Age of the child clinical signs and symptoms and amount of root resorption are the factors which can also influence the management of separated instrument in primary teeth
Moreover if an instrument has separated after initial cleaning and shaping of root canal maintaining a tooth is not a problem as clinical signs and symptoms are not anticipated and the good prognosis is expected
However if an instrument has separated early during the initial cleaning and shaping of the root canal clinical symptoms may compromise the prognosis
Therefore these factors should be kept in mind while planning a suitable management strategy to avoid or at least reduce the burden of extraction and wear of space maintainer for longer period
5
CONCLUSION
The management and prognosis of a primary tooth with a separated instrument is
dependent on the level of instrument fracture within the root age of the child root
resorption and clinical signs and symptoms of the involved tooth
Different management approaches can be tried depending on clinical situations keeping
in mind benefits vs risks in preserving the tooth
PROS amp CONS
PROS
The entire procedure is given
by step by step
Well descriptive xrays and
photographs
CONS
Medical history has not been
given
REFERENCES
1 TOMER ANIL K ET AL ldquoBROKEN FILE RETRIEVAL PUZZLE IN ENDODONTICSrdquo
(2016)
2 SHENOY A MANDAVA P BOLLA N ET AL A NOVEL TECHNIQUE FOR REMOVAL OF
BROKEN INSTRUMENT FROM ROOT CANAL IN MANDIBULAR SECOND MOLAR
INDIAN J DENT RES 201425(1)107ndash110
3 PATEL J MORAWALA A TALATHI R ET AL RETRIEVAL OF A BROKEN INSTRUMENT
FROM ROOT CANAL IN PRIMARY ANTERIOR TEETH UNIV RES J DENT 20155(3)203ndash
206
4 MORANKAR R GOYAL A GAUBA K ET AL MANUAL VERSUS ROTARY
INSTRUMENTATION FOR PRIMARY MOLAR PULPECTOMIES - A 24 MONTHS
RANDOMIZED CLINICAL TRIAL PEDIAT DENT J 201828(2)96ndash102
5 KASHYAP NILOTPOL (2018) RETAINING PRIMARY MOLARS WITH INSTRUMENT
SEPERATION A CASE REPORT AND CLINICAL GUIDE
6
1
IMPACT OF 6 CITRIC ACID AND ENDOACTIVATOR AS IRRIGATION ADJUNCTS ON OBTURATION QUALITY AND PULPECTOMY OUTCOME IN
PRIMARY TEETH
NEETU JAIN SHALINI GARG ABHISHEK DHINDSA SAKSHI JOSHI HARJOY
KHATRIA
PEDIATRIC DENTAL JOURNAL 2019 29
1
DR MITAKSHARA NIRWAN
CONTENTS
bull INTRODUCTION
bull AIMS amp OBJECTIVES
bull CASE REPORT
bull RESULTS
bull DISCUSSION
bull CONCLUSION
bull PROS AND CONS
bull REFERENCES
2
INTRODUCTION
bull ENDODONTIC THERAPY IN PRIMARY TEETH INVOLVES DISINFECTION OF THE ROOT CANAL
SYSTEM AND ITS OBTURATION WITH RESORBABLE PASTE
bull THE CONTENTS OF ROOT CANAL ALONG WITH SMEAR LAYER ARE EXPECTED TO BE REMOVED
DURING THE BIOMECHANICAL PREPARATION
bull IN VITRO AND CLINICAL DOCUMENTS HAVE INDICATED THAT MECHANICAL PREPARATION OF
THE CANAL LEAVES LARGE PORTIONS OF THE CANAL WALLS UNDEBRIDED AND COMPLETE
REMOVAL OF THE BACTERIA BY THIS MECHANICAL PROCEDURE ALONE IS UNLIKELY TO BE SEEN
THEREFORE SOME FORM OF DISINFECTIONIRRIGATION IS MANDATORY TO KILL THE
MICROORGANISMS AND TO REMOVE THE RESIDUAL TISSUES
3
bull THE IDEAL REQUISITES OF A ROOT CANAL IRRIGANT AS GIVEN BY ZEHNDER ARE
1 BROAD ANTIMICROBIAL SPECTRUM
2 HIGH EFFICACY AGAINST ANAEROBIC AND FACULTATIVE MICROORGANISMS ORGANIZED
IN BIOFILMS
3 ABILITY TO DISSOLVE NECROTIC PULP TISSUE REMNANTS
4 ABILITY TO INACTIVATE ENDOTOXIN
5 ABILITY TO PREVENT THE FORMATION OF A SMEAR LAYER DURING INSTRUMENTATION OR
TO DISSOLVE THE LATTER ONCE IT HAS FORMED
6 SYSTEMICALLY NONTOXIC WHEN THEY COME IN CONTACT WITH VITAL TISSUES
NONCAUSTIC TO PERIODONTAL TISSUES AND WITH LITTLE POTENTIAL TO CAUSE AN
ANAPHYLACTIC REACTION
SINCE NO SINGLE IRRIGANT HAS THESE OPTIMAL PROPERTIES STUDIES HAVE REPORTED THE USE
OF TWO OR MORE SOLUTIONS IN A SPECIFIC SEQUENCE OR IN COMBINATIONS FOR BETTER
RESULTS 4
bull SEVERAL IRRIGATING SOLUTIONS ALONG WITH CHELATING AGENTS HAVE BEEN USED
DURING BIOMECHANICAL PREPARATION OF ROOT CANAL BOTH IN PRIMARY AND
PERMANENT TEETH
bull HOWEVER NONE OF THE AVAILABLE IRRIGATING SOLUTIONS HAS BEEN REGARDED CLEARLY
AS OPTIMAL SOLUTION BECAUSE OF THEIR LIMITED EFFECTIVENESS ESPECIALLY IN APICAL
13RD OF THE ROOT CANAL SYSTEM
bull TO OVERCOME SUCH LIMITATIONS USE OF ENDOACTIVATOR HAS BEEN PROPOSED AS AN
IRRIGATION FACILITATOR THAT IS BASED ON SONIC VIBRATION (UP TO 10000 CPM) WHICH
FACILITATES THE IRRIGANT PENETRATION AND ITS RENEWAL WITHIN THE CANAL
bull ACTIVATION SYSTEMS RESULTED IN BETTER REMOVAL OF THE SMEAR LAYER IN THE APICAL
THIRD OF ROOT CANALS IN COMPARISON TO CONVENTIONAL IRRIGATION
5
CITRIC ACID
bull CITRIC ACID IS A WEAK ORGANIC ACID WITH THE APPEARANCE OF WHITE CRYSTALLINE
POWDER AT ROOM TEMPERATURE
bull IT CAN EXIST EITHER IN WATER-FREE FORM (ANHYDROUS) OR MONOHYDRATE FORM THE
WATER-FREE FORM CRYSTALLIZES FROM THE HOT WATER WHEREAS THE MONOHYDRATE
FORMS FROM THE COLD WATER THE LATTER MAY BE CONVERTED TO ANHYDROUS FORM BY
HEATING MORE THAN 78degC
bull CITRIC ACID OCCURS NATURALLY IN THE BODY IN MITOCHONDRIA AND IS USED BY BLOOD
BANKS TO PREVENT COAGULATION OF TRANSFUSED BLOOD CITRIC ACID IS ALSO ESSENTIAL
TO HUMAN METABOLISM AND IS FOUND IN MANY FOODS
6
2
bull THE BIOLOGICAL EFFECTS OF CITRIC ACID ON THE PERIODONTAL STRUCTURE HAS BEEN
EXTENSIVELY STUDIED IN PERIODONTICS
bull NEUMAN AND NEWMAN SHOWED THAT CITRIC ACID IS THE MOST EFFECTIVE ACID IN
ALTERING THE SOLUBILITY OF HYDROXYAPATITE
bull YAMAGUCHI ET AL SHOWED THAT CITRIC ACID SOLUTION HAD ANTIBACTERIAL EFFECTS ON
ALL 12 ROOT CANAL BACTERIA TESTED
bull ARIAS-MOLIZ ET AL SHOWED THAT ETHYLENEDIAMINETETRAACETIC ACID (EDTA) HAS NO
BACTERICIDAL ACTIVITY EVEN AFTER 1 HOUR CONTACT
bull THIS ACID HAS THE ABILITY OF ROOT CANAL IRRIGATION AND ALSO SMEAR LAYER REMOVAL
DIFFERENT CONCENTRATIONS (1ndash50) HAVE BEEN PROPOSED GUTMANN ET AL CONCLUDED
THAT 10 CITRIC ACID IS BETTER THAN ULTRASOUND FOR SMEAR LAYER REMOVAL FROM THE
ROOT END CAVITIES
7
bull STUDIES HAVE SHOWN IRRIGATION WITH 6 CA FOR 15 OR 30 SECONDS IS QUITE
EFFECTIVE IN REMOVING ALL THE COMPONENTS OF THE SMEAR LAYER OF THE PRIMARY
TEETH WHEREAS PERITUBULAR DENTIN DESTRUCTION WAS OBSERVED WHEN HIGHER
CONCENTRATION OF CITRIC ACID WAS USED AS AN IRRIGATING SOLUTION
8
AIMS amp OBJECTIVES
bull THIS STUDY WAS AIMED TO EVALUATE THE CLINICAL AND RADIOGRAPHIC OUTCOME OF
PULPECTOMY ALONG WITH QUALITY OF OBTURATION USING 6 CITRIC ACID AND
ENDOACTIVATOR
9
CASE REPORT
bull 350 CHILDREN (3-9 YEARS) WITH CLINICAL SIGNS AND SYMPTOMS OF CHRONIC IRREVERSIBLE
PULPITIS IN DEEPLY CARIOUS TEETH WERE SCREENED DURING SCHOOL DENTAL HEALTH
PROGRAM FROM MAY 2014-JULY 2014
bull 123 CHILDREN REPORTED TO THE DEPARTMENT AND 67 CHILDREN WERE SELECTED BASED ON
INCLUSION AND EXCLUSION CRITERIA
RECRUITMENT OF PATIENTS
10
INCLUSION CRITERIA
bull HISTORY OF SPONTANEOUS PAIN AND UNCONTROLLED BLEEDING AFTER PULP AMPUTATION
EXCLUSION CRITERIA
bull EVIDENCE OF INTERNAL OR EXTERNAL (PHYSIOLOGICPATHOLOGIC) ROOT RESORPTION OF MORE THAN A THIRD OF ITS LENGTH
bull ROOT CANAL OBLITERATION OR ANATOMIC ANOMALIES
bull INADEQUATE BONE SUPPORT OR NON RESTORABLE TOOTH
bull ONCE PATIENTS ELIGIBILITY WAS CONFIRMED THE TREATMENT PROCEDURE WAS
EXPLAINED TO THE PARENTGUARDIAN AND INFORMED WRITTEN CONSENT WAS
OBTAINED FROM PARENTSGUARDIANS SHOWING WILLINGNESS FOR THEIR
CHILDRENS TREATMENT 11
PROCEDURE
bull PULPECTOMY WAS PERFORMED BY ONE OPERATOR OF PEDIATRIC DENTISTRY DEPARTMENT
USING A STANDARDIZED TREATMENT PROTOCOL FOR ALL THE PATIENTS
bull AFTER ADMINISTRATION OF LOCAL ANESTHESIA RUBBER DAM WAS APPLIED FOR ISOLATION
bull ACCESS CAVITY WAS PREPARED USING AIR-ROTOR HAND PIECE WITH 8 ROUND BUR AND
PULP TISSUE WAS EXTIRPATED WITH THE HELP OF SPOON EXCAVATOR
bull FURTHER THE NEGOTIATION OF THE CANALS WAS DONE WITH 10 K-FILE
bull A DIAGNOSTIC RADIOGRAPH WAS TAKEN FOR ROOT LENGTH DETERMINATION AND
WORKING LENGTH WAS KEPT 1 MM SHORT OF THE RADIOGRAPHICAL APEX
bull ALL ROOT CANALS WERE INSTRUMENTED MANUALLY USING K-FILES AND WERE IRRIGATED
WITH 10 ML 09 NORMAL SALINE AND 1 SODIUM HYPOCHLORITE AS STANDARDIZING
PROTOCOL FOR ROOT CANAL PREPARATION AND DISINFECTION
12
3
GROUP 1 (CA + E) - IRRIGATION WAS DONE
WITH 10 ML OF 6 CITRIC ACID (CITOCID AMMDENT)
AND IRRIGANTS WERE SONICALLY AGITATED WITH
ENDOACTIVATOR (DENTSPLY) FOR 30 S PER CANAL USING REDBLUE
ENDOACTIVATOR TIP
GROUP 2 (CA) - 10 ML OF 6 CITRIC ACID FOR 1 MIN USING
27 GAUZE IRRIGATING NEEDLE
GROUP 3(SH + E) - 10 ML OF 1 SODIUM HYPOCHLORITE
SOLUTION AND SONIC ACTIVATION WITH ENDOACTIVATOR
GROUP 4(SH) - 10 ML OF 1 SODIUM HYPOCHLORITE
SOLUTION USING IRRIGATING NEEDLE (CONTROL GROUP)
bull TEETH UNDERGOING PULPECTOMY WERE RANDOMLY ENROLLED BY CHIT METHOD INTO THREE
STUDY AND ONE CONTROL GROUP
13
bull IN CITRIC ACID GROUPS FINAL RINSE WITH NORMAL SALINE WAS DONE TO REMOVE THE
REMAINING CRYSTALS (CHELATES)
bull FOLLOWING BIOMECHANICAL PREPARATION THE ROOT CANALS WERE DRIED WITH STERILE
ABSORBENT PAPER POINTS AND OBTURATED WITH VITAPEX USING HAND HELD
LENTULOSPIRAL FINAL RESTORATIONS WERE DONE USING COMPOSITE RESIN
14
bull CLINICAL FOLLOW UP WAS DONE AT 24 H1 WEEK 1 MONTH 6 MONTH AND 12
MONTH TO CHECK PAIN PRESENCE AND PAIN FREQUENCY (ONCEMORE THAN ONCE)
SWELLING FISTULA SENSITIVITY TO PERCUSSION
bull RADIOGRAPHIC FOLLOW UP WAS DONE AT 6 MONTH AND 12 MONTH FOR ANY
DEVIATED ERUPTION OF SUCCEDANEOUS TEETH EXCESS FILING MATERIAL AND ITS
RESORPTION EXTERNALINTERNAL ROOT RESORBTION CALCIFIC METAMORPHOSIS
PRESENCE OF FURCATION RADIOLUCENCY
CLINICAL amp RADIOGRAPHIC FOLLOW UP
15
RADIOGRAPHIC ASSESSMENT OF OBTURATION QUALITY
bull POSTOPERATIVE RADIOGRAPHS WERE VISUALLY ASSESSED FOR QUALITY OF OBTURATION BY
TWO INDEPENDENT EXAMINERS (SG AD) WHO WERE BLINDED WITH REGARD TO
IRRIGATION PROTOCOL GROUP TO ENHANCE CALIBRATION EACH EXAMINER ASSESSED THE
RADIOGRAPH INDEPENDENTLY AND LATER REVIEWED TOGETHER FOR FINAL ASSESSMENT
INDIVIDUAL ROOT WAS TAKEN AS UNIT OF ANALYSIS FOR GRADE OF OBTU- RATION AND
SCORING CRITERIA WERE AS GIVEN BY COLL JA 1996
1 UNDER FILLED - FILLING MATERIAL ENDED 1 MM OR MORE SHORT OF THE APEX
2 OPTIMAL FILLING- FILLING MATERIAL APPEARED TO END AT THE RADIOGRAPHICAL APEX
3 OVERFILLED - FILLING MATERIAL EXTRUDED PAST THE RADIOGRAPHIC APEX
4 OPTIMALLY FILLED ROOTS WERE FURTHER ASSESSED FOR THE PRESENCE OF VOIDS AND VOID
AREA (ROOT CANAL SURFACE UNTOUCHED BY THE ROOT CANAL FILLING MATERIAL) IN THREE
VISUALLY DIVIDED SECTIONS OF THE ROOT IE CORONAL MIDDLE AND APICAL 13RD
16
RESULTS
bull OVERALL CLINICAL AND RADIOGRAPHIC SUCCESS RATE OVER A PERIOD OF ONE YEAR WAS
9886 amp 977 RESPECTIVELY
bull ALL GROUPS WERE SIGNIFICANTLY (P = 001) EFFECTIVE IN ALLEVIATING PAIN WITHIN 24 H
OF PULPECTOMY
17 18
4
19
bull IMMEDIATE POST OPERATIVE RADIOGRAPHIC ASSESSMENT REVEALED 68 (102150) ROOTS
WITH OPTIMAL OBTURATION AND 32 (48150) WITH OVERFILLINGUNDERFILLING MAXIMUM
NO OF OPTIMAL FILLINGS WERE OBSERVED IN GROUP1 (CA + E) (3333) FOLLOWED BY
GROUP 2 (CA) (2549) GROUP 3(SH + E) (2549) AND GROUP 4(SH) (1568)
bull CITRIC ACID GROUPS HAD MORE NUMBER OF OPTIMALLY FILLED ROOTS 588 (60102) THAN
NON CITRIC ACID GROUPS 412 (42102)
bull ENDOACTIVATOR CONTRIBUTED TO 18 OF OPTIMAL OBTURATION IRRESPECTIVE OF
CHELATING AGENT USED
20
21
bull MAXIMUM NO OF VOIDS AND VOID AREAS WERE IN NON CITRIC ACID GROUPS
(6419 amp 5384) COMPARED TO CITRIC ACID GROUPS (3580 amp 4615)
RESPECTIVELY
bull ANALYSIS OF ROOT 13RD REVEALED MAXIMUM NO OF VOID AREA IN APICAL
13RD (4755) FOLLOWED BY MIDDLE 13RD (3846) AND CORONAL 13RD
(1398)
bull LEAST NO OF VOIDS amp VOID AREA (1111 amp 1608) WERE OBSERVED WHEN
ENDOACTIVATOR ALONG WITH CHELATING AGENT WAS USED (GROUP 1)
HOWEVER THIS WAS STATISTICALLY INSIGNIFICANT
22
DISCUSSION
bull IN THE PRESENT STUDY 1 SODIUM HYPOCHLORITE WAS USED ALONG WITH 6 CITRIC ACID
(CHELATING AGENT) WHICH IS REPORTED TO BE AS EFFECTIVE AS 17 EDTA
bull CITRIC ACID (BIOLOGICAL ACID) IS FOUND TO BE BIOCOMPATIBLE AND LEAST IRRITATING TO
PERIAPICAL TISSUES THAN OTHER CHELATING AGENTS
bull USE OF SODIUM HYPOCHLORITE SOLUTION FOLLOWING CHELATING AGENT WAS AVOIDED AS IT
RAPIDLY PRODUCES SEVERE EROSION OF ROOT CANAL WALL DENTIN
bull TRADITIONAL APPROACH OF DELIVERING IRRIGANTS INTO THE ROOT CANAL SPACE USING
SYRINGES AND METAL NEEDLES HAS BEEN FOUND TO BE INEFFECTIVE ESPECIALLY IN THE AREAS OF
ANASTOMOSES BETWEEN CANALS AND APICAL 13RD OF ROOT CANAL
23
bull THEREFORE TO ACHIEVE BETTER CLEANING EFFICIENCY IRRIGANT ACTIVATION HAS BEEN
RECOMMENDED SONIC ACTIVATION HAS BEEN REPORTED TO RESULT IN BETTER ROOT CANAL
CLEANLINESS AS COMPARED TO NO ACTIVATION OF IRRIGANT
24
5
CONCLUSION
bull USE OF 6 CITRIC ACID DEFINITELY HELPED IN RAPID ELIMINATION OF PAIN RESOLUTION OF
PERI-RADICULAR RADIOLUCENCY BETTER OBTURATION QUALITY IN TERMS OF LESS VOIDS AND
VOID AREAS ALONG WITH MAXIMUM NO OF OPTIMAL OBTURATION UP TO APICAL AREA
bull 6 CITRIC ACID AND ENDOACTIVATOR IRRIGATION PROTOCOL PROVED TO BE THE BETTER
IRRIGATION PROTOCOL WHICH MAY CONTRIBUTE TO LONG TERM SUCCESS OF PRIMARY
TOOTH AND THE HEALTH OF UNDERLYING PERMANENT TOOTH
bull 6 CITRIC ACID ALONG WITH ENDOACTIVATOR MAY BE RECOMMENDED AS IRRIGATION
ADJUNCTS IN PULPECTOMY PROCEDURE OF PRIMARY TEETH
25
PROS AND CONS
PROS
bull PROPER EXPLANATION OF THE MATERIALS
USED
CONS
bull NO PREOPERATIVE AND POSTOPERATIVE
RADIOGRAPHS
26
REFERENCES
bull RAMACHANDRA JA NIHAL NK NAGARATHNA C VORA MS ROOT CANAL IRRIGANTS IN
PRIMARY TEETH WORLD J DENT 20156(3)229-234
bull MOHAMMADI Z JAFARZADEH H SHALAVI S KINOSHITA JI UNUSUAL ROOT CANAL
IRRIGATION SOLUTIONS J CONTEMP DENT PRACT 201718(5)415-420
bull ZEHNDER M ROOT CANAL IRRIGANTS J ENDOD 2006 32389- 98
bull SMITH JJ amp WAYMAN BE AN EVALUATION OF THE ANTIMICROBIAL EFFECTIVENESS OF
CITRIC ACID AS A ROOT CANAL IRRIGANT JOURNAL OF ENDODONTICS 1986 12(2) 54-58
bull TANNURE PN AZEVEDO CP BARCELOS R GLEISER R PRIMO LG LONG-TERM OUTCOMES OF
PRIMARY TOOTH PULPECTOMY WITH AND WITHOUT SMEAR LAYER REMOVAL A RANDOMIZED
SPLIT-MOUTH CLINICAL TRIAL PEDIATR DENT 201133316E20 27
bull CARON G NHAM K BRONNEC F MACHTOU P EFFECTIVENESS OF DIFFERENT FINAL IRRIGANT
ACTIVATION PROTOCOLS ON SMEAR LAYER REMOVAL IN CURVED CANALS J ENDOD
2010361361E6
bull COLL JA SADRIAN R PREDICTING PULPECTOMY SUCCESS AND ITS RELATIONSHIP TO
EXFOLIATION AND SUCCEDANEOUS DENTITION PEDIATR DENT 19961857E63
28
1
LOCAL
ANESTHESIA
DR MITAKSHARA NIRWAN
CONTENTS
Definition
Methods of inducing local anesthesia
Desirable properties
Electrophysiology of nerve conduction
Impulse propagation and spread
Mode and site of action of local anesthesia
Classification of local anesthetic according to biological site and mode of action
Dissociation of local anaesthetics
Mechanism of action of local anaethetics
Local anaesthetic agent
2
3
DEFINITION
Local anesthesia is defined as a loss of sensation in
a circumscribed area of the body caused by depression
of excitation in nerve endings or an inhibition of the
conduction process in peripheral nerves
An important feature of local anesthesia is that it produces
LOSS OF SENSATION WITHOUT INDUCING LOSS OF
CONSCIOUSNESS
4
METHODS OF INDUCING LOCAL
ANESTHESIA
Low temperature
Mechanical trauma
Anoxia
Neurolytic agents such as alcohol amp phenol
Chemical agents such as local anesthetics
PROPERTIES OF LOCAL
ANESTHESIA
It should not be irritating to tissue to which it is applied
It should not cause any permanent alteration of nerve structure
Its systemic toxicity should be low
Time of onset of anesthesia should be short
It should be effective regardless of whether it is injected into the tissue or applied locally to mucous membranes
The duration of action should be long enough to permit the completion of procedure
5 6
It should have the potency sufficient to give complete
anesthesia with out the use of harmful concentration solutions
It should be free from producing allergic reactions
It should be free in solution and relatively undergo
biotransformation in the body
It should be either sterile or be capable of being sterilized by
heat with out deterioration
2
ELETROPHYSIOLOGY OF
NERVE CONDUCTION
There is an electrical charge across the membrane
This is the membrane potential
The resting potential (when the cell is not firing) is a negative
electrical potential of -70mv that exists across the nerve
membrane produced by different concentrations of either side of
the membrane
The interior of nerve is NEGATIVE in relation to exterior
7 8
inside
outside
Resting potential of neuron = -70mV
+
-
+
-
+
-
+
-
+
-
SLOW DEPOLARIRIZATION
9
RAPID DEPOLARIZATION
The interior of nerve is POSITIVE in relation to exterior
REPOLARIZATION
10
bull Repolarization takes 07 msec
bull Depolarization takes 03 msec
SODIUM PUMP -
energy comes from the oxidative metabolism of ATP
bull The entire process require 1 msec
IMPULSE PROPOGATION
IMPULSE SPREAD
The propagated impulse travels along the nerve
membrane towards CNS The spread of impulse differs
in myelinated and unmyelinated nerve fibers
DEPOLARIZED SEGMENT ADJACENT RESTING AREA
MODE AND SITE OF ACTION OF LOCAL
ANESTHETICS
Local anesthetic agent interferes with excitation
process in a nerve membrane in one of the
following ways
Altering the basic resting potential of nerve
membrane
Altering the threshold potential
Decreasing the rate of depolarization
Prolonging the rate of repolarization
12
3
CLASSIFICATION OF LOCAL ANESTHETIC
SUBSTANCES ACCORDING TO
BIOLOGICAL SITE AND MODE OF ACTION
CLASS A
Agents acting at receptor site on external surface of nerve membrane
Chemical substance Biotoxins (eg tetrodotoxin and saxitoxin)
CLASS B
Agents acting on receptor sites on internal surface of nerve membrane
Chemical substance Quaternary ammonium analogues of lidocaine
scorpion venom 13
CLASS C Agents acting by receptor independent of
physiochemical mechanism
Chemical substance Benzocaine
CLASS D Agents acting by combination of receptors and
receptor independent mechanisms
Chemical substance most clinically useful anesthetic agents
(eg lidocaine mepivacaine prilocaine)
14
BASED ON THE SOURCE
NATUAL
SYNTHETIC
OTHERS
BASED ON MODE OF APPLICATION
bull INJECTABLE
bull TOPICAL
BASED ON DURATION OF ACTION
bull ULTRA SHORT
bull SHORT
bull MEDIEM
bull LONG
BASED ON ONSET OF ACTION SHORT
INTERMEDIATE
LONG
15
DISSOCIATION OF LOCAL
ANESTHETICS
Local anesthetics are available as salts (usually
hydrochlorides) for clinical use
The salts both water soluble and stable is dissolved in
either sterile water or saline
In this solution it exists simultaneously as unchanged
molecule (RN) also called base and positively charged
molecules (RNH+) called cations
RNH+ ==== RN+ H
+
16
The relative concentration of each ionic form in the solution varies
in the pH of the solution or surrounding tissue
In the presence of high concentration of hydrogen ion (low pH) the
equilibrium shifts to left and most of the anesthetic solution exists
in cationic form
RNH+ gt RN
+ + H
+
As hydrogen ion concentration decreases (higher pH) the
equilibrium shifts towards the free base form
RNH+ lt RN + H
+
17
The relative proportion of ionic form also depends on pKa or DISSOCIATION CONSTANT of the specific local anesthetic
The pKa is a measure of molecules affinity for H+
ions
When the pH of the solution has the same value as pKa of the local anesthetic exactly half the drug will exists in the RNH
+ form and
exactly half in RN form
The percentage of drug existing in either form can be determined by Henderson Hasselbalch equation
Log baseacid = pH - pKa
18
4
MECHANISM OF ACTION OF LOCAL
ANESTHETICS
The following sequence is proposed mechanism of action of LA
Displacement of calcium ions from the sodium channel receptor site
Binding of local anesthetic molecule to this receptor site
Blockade of sodium channel
19
Decrease in sodium conductance
Depression of rate of electrical depolarization
Failure to achieve the threshold potential level
Lack of development of propagated action potential
Conduction blockadehellip
20
21
Na + Na +
22
LOCAL ANESTHETIC AGENT
COMERCIALLY PREPARED LOCAL ANESTHESIA
CONSISTS OF
Local anesthetic agent (xylocaine lignocaine 2)
Vasoconstrictor (adrenaline 1 80000)
Reducing agent (sodium metabisulphite)
Preservative (methylparabencapryl
hydrocuprienotoxin)
Fungicide (thymol)
Vehicle (distillde waterNaCl)
LOCAL ANESTHETIC AGENT
The local anesthetics used in dentistry are divided
into two groups
ESTER GROUP
AMIDE GROUP
23 24
ESTER GROUP It is composed of the following
An aromatic lipophilic group
An intermediate chain containing
an ester linkage
A hydrophilic secondary or tertiary
amino group
AMIDE GROUP It is composed of the following
An aromatic lipophilic group
An intermediate chain containing
amide linkage
A hydrophilic secondary or tertiary
amino group
5
25
CLASSIFICATION OF LOCAL ANESTHETICS
ESTERS
Esters of benzoic acid
Butacaine
Cocaine
Benzocaine
Hexylcaine
Piperocaine
Tetracaine
Esters of Para-amino
benzoic acid
Chloroprocain
Procaine
Propoxycaine
26
AMIDES Articaine
Bupivacaine
Dibucaine
Etidocaine
Lidocaine
Mepivacaine
Prilocaine
Ropivacaine
QUINOLINE
Centbucridine
PHARMACOKINETICS OF LOCAL
ANESTHETICS UPTAKE
When injected into soft tissue most local anesthetics produce
dilation of vascular bed
Cocaine is the only local anesthetic that produces
vasoconstriction initially it produces vasodilation which is
followed by prolonged vasoconstriction
Vasodilation is due to increase in the rate of absorption of the
local anesthetic into the blood thus decreasing the duration of
pain control while increasing the anesthetic blood level and
potential for over dose 27
AMIDE LOCAL ANESTHETICS
The metabolism of amide local anesthetics is more
complicated then esters The primary site of
biotransformation of amide drugs is liver
Entire metabolic process occurs in the liver for lidocaine
articaine etidocaine and bupivacaine
Prilocaine undergoes more rapid biotransformation then the
other amides
28
REFERENCES
Handbook of local anesthesia ndash Stanley F Malamed ndash 6th
edition
Essentials of Local Anesthetic Pharmacology Daniel E
Becker Anesth Prog 2006 Fall 53(3) 98ndash109
WIKIPEDIEA
29
THANK YOU
30
1
Pharmacological Methods of Behavior
Management
DR MITAKSHARA NIRWAN
DEFINITIONS
bull Conscious Sedation ndash A minimally depressed level of consciousness that retains
the patients ability to independently and continuously maintain an airway and respond appropriately to physical stimulation or verbal command
(American Dental Association House Of Delegates 2000)
bull Deep Sedation ndash An induced state of depressed consciousness
accompanied by partial loss of protective reflexes including the inability to continuously maintain an airway independently and or to respond purposefully to physical stimulation or verbal command
bull General Anesthesia (G A) ndash An induced state of unconsciousness or complete loss of
protective reflexes including the inability to continually maintain an airway independently and respond purposefully to physical stimulation or verbal command
Conscious sedation
ADVANTAGES
Conscious
Protective reflexes active amp intact
Stable vital signs
Operating dentist may perform sedation
Minimum amount of equipment required
Prolong detainment in recovery room not required
Risk of complication very low
Excellent choice for poor ndash risk pt in dental office
Cost effective
General anesthesia
ADVANTAGES Not absolutely
essential May be the only
method Not necessary (no
pain reaction) Amnesia always
present
Conscious sedation
DISADVANTAGES
Pt cooperation is essential
Extremely difficult or mentally handicapped pt cannot always be managed
Use of local anesthesia is a must
Amnesia may or may not be present
General anesthesia DISADVANTAGES
Pt unconscious
Protective reflexes are depressed
Depressed
Advanced training required Dentist must not act also as anesthetist
Special equipment necessary
Detainment in recovery area necessary
High IOP amp postoperative complications
Not indicated in dental office
More expensive
Fundamental Concepts
bull Techniques that utilize drugs to induce co-operative yet conscious state in an otherwise uncooperative child ndash CONSCIOUS SEDATION
2
GOALS
1 To facilitate the provision of quality care
2 To minimize the extremes of disruptive behavior
3 To promote a positive psychologic response to treatment
4 To promote patient welfare amp safety
5 To return the patient to physiologic state
OBJECTIVES
1 The pt mood must be altered
2 The pt must remain conscious at all times
3 The pt must be cooperative
4 All protective reflexes must remain intact and active
5 Vital signs must remain stable and with in normal limits
6 The ptrsquos pain threshold should be elevated
7 Amnesia may be present
Indications
1 Preschool children
2 Lack of Psychological Emotional maturity
3 Lack of Cognitive Physical Medical disability
4 Fearful amp anxious pts
5 Pt who require extensive amp complicated dental care amp would require or benefit from prolonged visits
6 Acute pain
7 Traumatic injuries
Operating Facilities amp Equipment
A positive pressure O2 delivery system capable of administering gt than 90 O2 at 10L min flow for 60 min (650L ldquoErdquo cylinder)
OR
Self inflating bag valve mask device (15L min)
A functional suction apparatus with appropriate suction catheters
Monitoring equipment - PO BPC PC or Capno
Inhalation sedation unit
100 O2 amp never less than 25
A fail safe mechanism that is checked and calibrated annually
Must have appropriate scavenging system
Emergency drugs
Techniques of sedation
Routes for drug administration
bull Oral
bull Rectal
bull Inhalational
bull Transmucosal
ndash Sublingual
ndash Intranasal
bull Parenteral
ndash IM
ndash sub mucosal
ndash IV
3
Oral Sedation
Advantages
1 Almost universally accepted and the easiest method
2 Decreased incidence and severity of adverse reaction
3 Low cost
Disadvantages
1 Absorption is variable
2 Prolonged latent period(30 min)
3 Reversal of any unwanted effect is also difficult
4 Inability to readily lighten or deepen the level of sedation
5 Prolonged duration of action
Rectal Sedation
Advantages 1 Incidence and intensity of
drug related side effects is minimized
2 Drug absorption occurs from the large intestine directly into the circulation
3 The lack of a needle syringe or other equipment
4 The ease of administration
5 The low cost
Disadvantages
1 Inconvenience to the administrator amp pt
2 The variable absorption of drugs from the large intestine
3 The slow onset of action amp the relatively long duration of action
4 Inability to titrate the drug dosage
5 The inability to reverse the action of the drug the prolonged recovery
Intranasal sedation
Advantages
Rapid onset (10 ndash 15 min)
Simple amp relatively painless
Less pt cooperation is required
Absorbed directly into the C V S
Intranasal sedation
Disadvantages
1 Dependence on nasal mucous membrane
2 Shorter duration of action(40-60min)
3 Multiple dosage may be necessary
Drugs
Midazolam ndash 02mgkg
Sufentanil ndash 15 ndash 3 mcgkg
Ketamine ndash 3-6mg kg
Sublingual sedation
Advantages
1 Pt acceptance
2 Rapid onset
3 High bioavailability
Drugs
Oral Transmucosal Fentanyl Citrate (OTFC)
Intramuscular Sedation
Advantages
1 More rapid onset of action
2 Absorbed directly into the C V system
3 More reliable absorption of drug
4 Pt cooperation is not as essential
Disadvantages
1 Time factor ndash its 15 min latent period
2 Pt may not be willing to accept the injection
3 The prolonged duration of action(2-4 hrs more)
4 Possibility of injury to the tissues at the site of injection caused by either the drug or the needle
4
Sites of I M administration
1 Gluteal area
2 Vastus lateralis
3 Mid ndash deltoid area
Drugs
Diazepam
Midazolam
Hydroxyzine
Inhalation Sedation
Advantages
1 The onset of action is more rapid
2 Peak clinical level is achieved rapidly(3-5min) - permit titration
3 Administrator has complete control over the actions of the drug - safety feature
4 No significant over dosage
5 Flexible duration of action
6 Recovery time is rapid amp most complete
7 No injection is required
8 With N2O- O2 it is safe with very few side effects
Disadvantages
1 The initial cost of the equipment is high 2 The continuing cost of the gases is high 3 The equipment occupies considerable space 4 N2O is not a potent agent 5 A degree of cooperation is required from the pt 6 Chronic exposure to N2O is deleterious to the health of
dental personnel
Contraindications
1 Nasal obstruction 2 Cyanosis at rest 3 Poor cooperation 4 1st trimester of pregnancy 5 Fear of masks
I V Sedation
Advantages
1 The onset of action is the most rapid 2 The dosage may be titrated 3 Suitable level of sedation can be provided 4 The recovery period is shorter 5 Side effects are extremely uncommon 6 Control of salivary secretions is possible 7 The gag reflex is diminished 8 Effectively diminishes motor disturbances 9 Provides immediate access to CVS in emergency
Disadvantages
1 Venipuncture is necessary
2 Complication may rise at the site of the venipuncture
3 Monitoring must be more intensive
4 Recovery is not complete at the end of the procedure
5 Reversal of sedation is difficult
5
N2O-O2 (Relative Analgesia)
colorless sweet smelling gas
Pharmacokinetics
Absorption through pulmonary epithelium
It is approx 15 times as soluble as is nitrogen It replaces nitrogen in blood
It is carried in solution in plasma of the blood
It is not metabolized by the body
Elimination ndash majorndash lungs minor --- skin
perspiration urine and intestinal gas
Pharmacodynamics
Dose related
10 ndash 25 Lightheaded
Changes in visual amp auditory sensation
Tingling of hands amp feet
Suffusing warmth
Remote from the immediate environment
Reduced anxiety
25-50 max analgesic properties and aberration of vision hearing and proprioception mild drowsiness euphoria amnesia and increased sleepiness and dreams
35 conc will achieve maximum analgesia
bull CNS
ndash Cerebrum-primarily affected
ndash Safe but weak anesthetic agent
bull RESPIRATORY SYSTEM
ndash Increased Tidal and minute volumes
bull CARDIOVASCULAR SYSTEM
ndash 2 studies ndash decreased cardiac output
bull FETAL SYSTEMS
ndash Miscarriage in humans
bull OTHER SYSTEMS
ndash Depression of spinal reflexes increase muscle tone indicates stage of delirium
ndash Muscle rigidity-narcotics + nitrous oxide
ndash Nausea and vomitting - GIT
ndash HEMATOPOIESIS ----- prolonged exposure
Adverse reactions and toxicity
EMOTIONAL REACTIONS
DREAMS HALLUCINATIONS
No acute toxicity
Chronic toxicity ndash bone marrow
depression
PROCEDURE
Diffusion Hypoxia
Sevoflurane
A fluorinated derivative of isopropyl ether ndash synthesized in 1970
Potent anaesthetic agent with rapid uptake amp speedy recovery
Day-case surgery
Problem
Attaching vaporiser to any of the currently available machine
BENZODIAZEPINES
Diazepam 1961 lipid soluble
Uses-alcoholism epilepsy labor tetanus and cerebral palsy
- sedation and amnesia
- varieties of neurosis amp anxiety states
Pharmacokinetics
Orally Rectal IMIV or SC
Well absorbed through GIT
Excretion in urine
6
bull Pharmacodynamics
ndash Depress the brain stem reticular system and the limbic system thalamus and hypothalamus
ndash It is a centrally acting muscle relaxant Has anti-convulsant properties
Adverse reaction amp toxicity
ndash Confusion nausea headache increased appetite decreased salivation and jaundice Thrombophlebitis
ndash Rebound phenomenon
ndash Toxicity drowsiness confusion sleep and coma
Dosage Oral or Rectal ndash 02-05mgkg
Maximum single dose 10mg
IV- 025mgkg
Supplied Tablets 2 5 10 mg
Suspension ndash 5mg
Midazolam Water soluble ndash non-irritant
Oral IM IV
Metabolism- liver
Onset IV 3 -5mins
oral 20 ndash 30mins
Oral administration anxious patients requiring relatively short dental procedure
No rebound phenomenon
Better anxiolysis amp amnesia (retrograde amnesia)
Adverse effects Respiratory depression
dose dependant apnea
Dosage Oral ndash 025 to 1mgkg to maximum single dose 20mg
IM ndash 01 to 015mgkg to a maximum of 10mg
IV ndash slow IV
Supplied Syrup ndash 2mgml
Injectable ndash 1mgml amp 5mgml vials
Flumazenil specific benzodiazepines antagonist
selectively inhibits CNS effects
IV administration amp not recommended below 18yrs of age
02mg over 15 seconds after 45seconds 02mg then after 60seconds to maximum of 1mg
Sedative-Hypnotics
Barbiturates First truly effective drugs for the management of anxiety Generalized CNS depressants Produce dose dependent effects
Sedation ---- sleep ---- GA ---- coma
Suppress the CNS and result in sedation and amnesia Advantages
Rapid onset and short duration Disadvantages
no analgesic effect and possible hypotension Must be used with caution in trauma patients because they may cause
apnea and hypoventilation
DOSE Pentobarbital Sodium 100mg Secobarbital Sodium 100 to 200mg Children 30 to 100mg
bull Chloral Hydrates (Mickey Finn Knock out drops ) First synthesized in 1832 first member of the hypnotic group of drugs
Widely used as conscious sedation agent
Properties
Unpleasant taste
Nausea vomiting
Quite irritating to skin and to mucous membranes
GI irritation
Dosages Individualized for each patient 25 ndash 50mgkg
maximum of 1g
Supplied oral capsule ndash 500mg
oral solution ndash 250 amp 500mg5ml
Rectal suppositories ndash 324 amp 648mg
Narcotics
Do produce sedation amp euphoria greater in children
LA is required but dose should be decreased
Meperidine Synthetic opiate agonist
Very water soluble
Orally SC IM or IV
Peak effect by oral 1 hr amp lasts upto 4 hrs
Adverse reactions
-Seizures
-Extreme caution in hepatic or renal diseases or history of seizures
7
Dosage Oral SC or IM ndash 1to 22mgkg not to exceed 100 mg
Supplied Oral Tablets ndash 50 amp 100mg
Oral Syrup ndash 50mgml
Parental solution ndash 25 50 75 amp 100mgml
Fentanyl
Synthetic opiate narcotic analgesic
Very potent 01mg = 10mg Morophine75mg Meperidine
Pharmacokinetics
IV IM SM
Metabolized in liver Excreted in urine
Fentanyl Onset ndash 7 to 15mins
Duration ndash 1 to 2 hrs
Pharmacodynamics
Respiratory depression RR but returns to normal rapidly Tidal volume amp response to co2 depressed for extended period
Apnea
Less emetic than meperidine
NOT RECOMMENDED IN CHILDREN BELOW 2yrs
Dosage 0002 to 0004mgkg
Supplied 005mgml in 2 amp 5ml ampoules
Reversal drug Naloxone
Semisynthetic opiate antagonist
No agonist activity
Onset 2 to 5mins SC or IM amp 1 to 2mins IV
Reversal 45mins
Pt should be kept under continual surveillance
Adverse reaction nausea vomiting sweating hypotension hypertension ventricular tachycardia fibrillation
Dosage IV SC IM 001mgkg then 01mgkg every 2- 3mins maximum 2mg
Supplied 002 004 1mg solutions
Antihistamines
Hydroxyzine
Oral or IM
Effect ndash 15 ndash 30mins
Half-life ndash 3 hrs
Uses
To relieve anxiety
Used as an anti-histamine
Used to control nausea and vomiting including that associated with motion sickness and pregnancy
Adverse reaction dry mouth drowsiness hypersentivity
Dosage Oral ndash 1 to 2mgkg
IM ndash 11mgkg
Promethazine Oral or IM Onset 15 to 60mins Duration 4 to 6 hrs Uses
To prevent and treat nausea and vomiting associated with motion pregnancy or surgery
Produces sedation and reduce swelling pain and trismus
Lower seizure threshold Adverse reaction dry mouth blurred vision thickening of bronchial secretions Dosage OralIM ndash 05-11mgkg
maximum 25 mg
Diphenhydramine
Oral IM IV
Onset -1hr
Duration ndash 4 to 6 hr
Metabolized in liver
Adverse reaction disturbed coordination thickening of bronchial secretions
Dosage Oral IM IV ndash 1 to 15mgkg
maximum 50mg
Tranquilizers
Major tranquilizer antipsychotic produce calmness control symptoms of psychoses cause reversible extra pyramidal symptoms and do not tend to cause habituation
Minor tranquilizer antianxiety agents also cause calmness do not cause extrapyramidal symptoms Used in conditions like nervous tension and mild depression
8
Classification
Antipsychotics
Phenothiazine derivatives
Chlorpromazine promazine
Butryophenones
Haloperidol
Rauwolfia alkaloids
Reserpine
Antianxiety drugs
Propyl alcohol derivatives
Meprobamate
Benzodiazepine derivatives
Diazepam
Miscellaneous compounds
Hydroxyzine
Meprobamate
White crystalline powder slightly bitter in taste
Only administered orally
Peak blood concentration ----1 to 3hrs
10 ---------excreted unchanged Rest --- excreted as a oxidized derivative or as a glucoronide
Uses
To relieve day time anxiety
Induce sleep in insomniacs
To reduce anxiety associated with dental treatment
Anti-convulsant ndash petit mal epilepsy
Adverse reaction leucopenia acute non-thrombocytopenic purpura ecchymoses eosinophilia edema adenopathy
Dosage Childrengt 6yrs 100 to 200mg
Not recommended for children under 6yrs
Monitoring during sedation
1 Pulse
2 Blood pressure
3 ECG
4 Respiration
5 Temperature
Pulse
Manual Electronic
bull Radial Brachial
bull Facial labial
Blood pressure
ndash Stethoscope amp sphygmomanometer
ndash Automatic devices
ndash Direct cannulation of an artery ndash very accurate
Electrocardiograph
Heart rate rhythm myocardial function
9
Respiration
ndash Monitoring respiratory rate
ndash Observing the rise amp fall of the chest wall
ndash Observing the color of mucous membrane
ndash Observing the inflation amp deflation of the reservoir bag
Devices for monitoring respiration
1 The Precordial pretracheal stethoscope
2 The esophageal stethoscope
ndash Respiratory rate
ndash Heart rate
ndash Any abnormal sounds
Pulse Oximeter
ndash Oxygen saturation
ndash Heart rate
ndash Oxisensor site
ndash Fingers
ndash Toe
ndash Ear lobe
Mechanism
Oxygenated Hb ndash red light
Deoxygenated Hb- infrared light
Tissue pressure from arterial pulse (plethysmography)
Advantages
ndash Safe amp noninvasive
ndash Simple to use
ndash Information is rapidly available for clinical decision
ndash Indirectly indicates respiratory adequacy
Disadvantages
ndash Finger probes can get dislodged
ndash Emitted light source may cause burning
ndash Non reusable probes are expensive
ndash Does not directly determine airway patency
Capnography
1 The presence absence of air flow
2 Indicates depth amp adequacy of respiration
3 Continues analysis of the co2 content of the respired air ndash indicates respiratory adequacy
Temperature
ndash Disposable nondisposable thermometer
ndash Esophageal rectal temp probe
10
Discharge criteria
Cardiovascular function is satisfactory amp stable
Airway patency is uncompromised amp satisfactory
Pt is easily arousable amp protective reflexes intact
State of hydration is adequate
Pt can talk if applicable
Pt can sit unaided if applicable
Pt can ambulate with minimal assistance if applicable
Presedation level of responsiveness achieved
Responsible individual is available
1
PULP THERAPY OF VITAL TEETH
DR MITAKSHARA NIRWAN
Contents
Indirect pulp capping
Direct pulp capping
Medications amp materials used in pulp capping
Pulpotomy
MTA
Apexogenesis
INDIRECT PULP CAPPING
Pieter Van Forest - first to speak about root canal therapy
Glove designed instruments that could prepare a canal to a certain size and taper(1910)
Indirect pulp capping is defined as a procedure where in small amount of carious dentin is retained in
deep areas of cavity to avoid exposure of pulp followed by placement of a suitable medicament and
restorative material that seals off the carious dentin and encourages pulp recovery (Ingle)
A procedure in which only the gross caries is removed from the lesion and the cavity is sealed for a
time with a biocompatible material (McDonald)
Objective of indirect pulp capping
These were given by Eidelman in 1965
bull Arresting the carious process
bull Promoting dentin sclerosis
bull Stimulating formation of tertiary dentin
bull Remineralization of carious dentin
Layers of Carious Dentin Indications of Indirect Pulp Capping
History
Mild pain associated with eating
Negative history of spontaneous extreme pain
Clinical Examination
Deep carious lesion which are close tobut not involving the pulp in vital primary or young
permanent teeth
No mobility
Nominal pulp inflammationdefinite layer of affected dentin after removal of infected dentin
Radiographic examination
Normal lamina dura amp PDL space
No radiolucency around the apices
2
Contraindications of Indirect Pulp Capping
History
Sharp penetrating pulpalgia
Prolonged spontaneous pain especially at night
Clinical examination
Mobility of tooth
Discoloration of tooth
Negative reaction of electric pulp testing
Radiographic examination
Definite pulp exposure
Break in the lamina dura
Radiolucency around the apices
Widened PDL space
Treatment procedure
Sequelae of Indirect Pulp Capping Three distinct types of new dentin formation take place
1 Cellular fibrillar dentinmdashfirst 2 months
2 Globular dentinmdash3 months
3 Tubular dentin (uniform mineralized dentin)
bull 15th of reparative dentin formation begins in less than 30 days
bull After 3 months 01 mm is formed
DIRECT PULP CAPPING Defined by Kopel (1992) as the placement of a medicament or non medicated material on a pulp that
has been exposed in course of excavating the last portions of deep dentinal caries or as a result of
trauma
Objective
To create new dentin in the area of the exposure and subsequent healing of the pulp
Rationale
achieve a biologic closure of the exposure site by deposition of hard tissue barrier (dentin bridge)
between pulp tissue and capping material thus walling off the
INDICATIONS
Small mechanical exposure
Easily controlled haemorrhage
Bright red haemorrhage
True pinpoint exposure
CONTRAINDICATIONS
Severe toothache at night
Spontaneous pain
Tooth mobility
Radiographic appearance of pulp periradicular de- generation
Excess of hemorrhage at the time of exposure Serous exudate from the exposure
Externalinternal root resorption
Swellingfistula
Histological Changes after Pulp Capping
These were illustrated be Glass and Zander in 1949
After 24 hours Necrotic zone adjacent to calcium
hydroxide paste is separated from healthy pulp
tissue by a deep staining basophilic layer
After 7 days Increase in cellular and fibroblastic
activity
After 14 days Partly calcified fibrous tissue lined by
odontoblastic cells is seen below the calcium
proteinate zone disappearance of necrotic zone
After 28 days Zone of new dentin
3
Medications and Materials Used for Pulp Capping Calcium hydroxide
Corticosteroids amp antibiotics
Inert materials
Collagen fibers
4-META adhesive
Direct bonding
Isobutyl cyanoacrylate
Denatured albumin
Mineral trioxide aggregate
Laser
Bone morphogenic protein
PULPOTOMY
Finn (1995) defined it as the complete removal of the coronal portion of the dental pulp
followed by placement of a suitable dressing or medicament that will promote healing and
preserve vitality of the tooth
American Academy of Pediatric Dentistry (1998) defined pulpotomy as the amputation of
affected infected coronal portion of the dental pulp preserving the vitality and function of the
remaining part of radicular pulp
Objectives
bull Removal of inflamed and infected coronal pulp at the site of exposure thus preserving the vitality of the
radicular pulp and allowing it to heal
bull Maintain the tooth in the dental arch
Rationale
bull Radicular pulp is healthy and capable of healing after surgical amputation of the infected coronal pulp
bull Preserves vitality of the radicular pulp
bull Maintains tooth in a physiologic condition
Indications of Pulpotomy bull Mechanical pulp exposure in primary teeth
bull Teeth showing a large carious lesion but free of radicular pulpitis
bull History of only spontaneous pain
bull Hemorrhage from exposure sites bright red and can be controlled
bull Absence of abscess or fistula
bull No interradicular bone loss
bull No interradicular radiolucency
Contraindications of Pulpotomy bull Persistent toothache
bull Tenderness on percussion
bull Root resorption more than 13rd of root length
bull Large carious lesion with nonrestorable crown
bull Highly viscous sluggish hemorrhage from canal orifice which is uncontrollable
bull Medical contradictions like heart disease immuno compromised patient
bull Swelling or fistula
bull External or internal resorption
bull Pathological mobility
bull Calcification of pulp
Classification of pulpotomy
4
Formocresol Pulpotomy
Iby BUCKLEY in 1904
Sweet (1930) Formulated multi visit technique
Doyle (1962) Advocated 2 sitting procedure (complete devitalization)
Spedding (1965) Gave 5 minute protocol (partial devitali- zation)
Venham (1967) Proposed 15 seconds procedure
Current concept uses 4 minutes of application time
Composition of formocresol Buckleyrsquos Formula
bull Cresol ndash 35 percent
bull Glycerol ndash 15 percent
bull Formaldehyde ndash 19 percent
bull Water ndash 31 percent
Mechanism of Action
It prevents tissue autolysis by bonding to the proteins Bonding is of peptide groups of side chain amino acids and is a reversible process accomplished without
changing the basic structure of protein molecules
Histological Changes
bull Demonstrated by Mass and Zilbermann11 in 1933 and also by Massler and Mansokhani in 1959
bull Immediately the pulp becomes fibrous and acidophillic
bull Seven to fourteen days Three zones appear
a broad eosinophilic zone of fixation
b broad pale-staining zone of atrophy with poorcellular definition
c broad zone of inflammation extending apically into normal pulp tissue
bull One yearndash Progressive apical movement of these zones with only acidophillic zone left at the end of 1 year
Modified Formocresol Pulpotomy
Used by TRASK(1972)
The technique is identical to that described for primary teeth except that the formocresol pellet is
sealed permanently in the tooth
Two-visit Devitalization Pulpotomy
Indications
bull There is evidence of sluggish bleeding at the amputation site that is difficult to control
bull Pus in the chamber but none at the amputation site
bull There is thickening of the PDL
bull History of pain
Contraindications
bull Nonrestorable tooth
bull Tooth with necrotic pulp
5
Glutaraldehyde Pulpotomy
It was first suggested by S Gravenmade Introduced by Kopel in 1979
Mechanism of Action
bull Glutaraldehyde produces rapid surface fixation of the underlying pulpal tissue
bull A narrow zone of eosinophilic stained and compressed fixed tissue is found directly beneath the area of application which blends into vital normal appearing tissue apically
bull With time the glutaraldehyde fixed zone is replaced by macrophagic action with dense collagenous tissue thus the entire root canal tissue is vital
Cvekrsquos Pulpotomy
bull This is also called as calcium hydroxide pulpotomy or young permanent partial pulpotomy
bull This was proposed by Mejare and Cvek16 in 1978
bull Indicated in young permanent teeth where the pulp is exposed by mechanical or bacterial means and the
remaining radicular tissue is judged vital by clinical and radiographic criteria whereas the root closure is
notcomplete
MINERAL TRIOXIDE AGGREGATE (MTA) Torabinejad described the physical and chemical properties of MTA in 1995
It is ash colored powder made primarily of fine hydrophilic particles of
1 tricalcium aluminate
2 tricalcium silicate
3 silicate oxide
4 tricalcium oxide
5 bismuth dioxide
Hydration of the powder results in a colloidal gel composed of calcium oxide crystals in an amorphous
structure This gel solidifies into a hard structure in less than three hours
PROPERTIES OF MTA
It is biocompatible material and its sealing ability is better than that of amalgam or ZOE
Initial pH is 102 and set pH is 125
The setting time of cement is 4 hours
The compressive strength is 70 MPA which is comparable with that of IRM
Low cytotoxicity ndash It presents with minimal inflammation if extended beyond the apex
Mineral trioxide aggregate (MTA) has demonstrated the ability to induce hard-tissue formation in
pulpal tissues and it promotes rapid cell growth
APEXOGENESIS
It is defined as the treatment of a vital pulp by capping or pulpotomy in order to permit continued
growth of the root and closure of the open apex
Rationale
Maintenance of integrity of the radicular pulp tissue to allow for continued root growth
Indications
bull Indicated for traumatized or pulpally involved vital permanent tooth when root apex is incompletely formed
bull No history of spontaneous pain
bull No sensitivity on percussion
bull No hemorrhage
bull Normal radiographic appearance
Contraindications
bull Evidence that radicular pulp has undergone degenerative changes
bull Purulent drainage
bull History of prolonged pain bull Necrotic debris in canal
bull Periapical radiolucency
6
1
Gupta A Dhingra R Chaudhari P Gupta A
Department of Paedodontics and Preventive Dentistry Faculty of Dental Sciences SGT University Gurgaon Haryana India
Journal of Indian Society of Pedodontics and Preventive Dentistry
Volume 35 I Issue 3 I July-September 2017
A COMPARISION OF VARIOUS MINIMALLY
INVASIVE TECHNIQUES FOR THE REMOVAL
OF DENTAL FLUOROSIS STAINS IN
CHILDREN
DR MITAKSHARA NIRWAN
CONTENTS
bull Introduction
bull Aims
bull Materials and Methods
bull Results
bull Discussion
bull Conclusion
bull Critical analysis
bull References
INTRODUCTION
bull Dental fluorosis is a developmental disturbance of dental enamel caused by
successive exposure to high concentrations of fluoride during tooth
development
bull Various methods of therapy are advocated for the treatment of fluorosis -
stained teeth which range from invasive ceramic veneer bonding restorations
to abrasive chemical treatments
bull The combination of dental bleaching techniques and microabrasion appears
as an excellent conservative solution to reestablish health in fluorosis
affected teeth
AIMS
bull The aim of the study was to evaluate and compare the effectiveness of
minimally invasive techniques for the removal of dental fluorosis
stains in children in vivo
MATERIALS AND METHODS
Patients visiting the department of Pedodontics and Preventive dentistry
Faculty of Dental Sciences SGT University Gurgaon
bull Sample size 90 patients
bull Age group 10 -17 years
bull Caries cracks or periodontal
disease on anterior teeth
bull Abscess draining sinus
cellulitis
bull Non vital teeth
hypersensitive exposed
crevices
bull Orthodontic appliance
bull Past history of bleaching
bull At least two permanent
maxillary anterior teeth
bull TSIF of score 4
bull Free of systemic diseases
Inclusion criteria Exclusion criteria
2
Groups
Group A In office bleaching with 35 hydrogen peroxide( Pola Office
Bleaching kit) activated by light emitting diode (LED) bleaching unit
(35 HP)
Group B Enamel microabrasion (EM) (PREMA Enamel Microabrasion
System) followed by in-office bleaching with 44 carbamide peroxide
gel (EM)
Group C In-office bleaching with 5 sodium hypochlorite (5
NaOCl)
A baseline colour evaluation was done by taking digital photograph of
the maxillary anterior teeth
RESULTS
Group 1
Colour stability
Group 2 Group 3
Tooth sensitivity
Tooth sensitivity values were taken before the treatment
which was compared to immediate postoperative and follow
up visits It was checked using an electric pulp tester
maximum
moderate
least
immediately
group 2
group 1
group 3
1 month
group 2
group 1
group 3
3 month
group 2
group 1
group 3
Patient satisfaction score
Satisfaction was assessed on visual analog scale
Range 1 to 5
Groups percentage of patients
who were satisfied with
the treatment
Number of patients
who reported slight
reappearance of colour
Group 1
90
7
Group 2
83
8
Group 3
73
7
3
Number of Appointments
Groups One sitting Two sittings Three
sittings
Group 1
25
4
1
group 2
26
3
1
Group 3
30
0
0
DISCUSSION
bull Hydrogen peroxide is capable of penetrating the tooth osmosis and through porosities and cracks subsequently acting directly on the pigmented molecules
bull Gurgan et al investigated 3 different light systems and found out that diode laser system with gave best tooth whitening and least tooth sensitivity
bull In the EM group the surface reflects and refracts light from the surface in such way that mild imperfections in underlying enamel are camouflaged While the highly polished surface of enamel enhances the aesthetic appearance
bull Train et al and Loguercio et al also had the similar results in their studies with EM mild fluorosis showed best results moderate showed moderate results while it had little effect on severe fluorosis
bull NaOCl was only effective on mild stains while moderate and severe
stains could only be lightened to quite an extent but could not be
completely removed
bull When NaOCl comes in contact with hypomineralized and discoloured
enamel it degrades and removes the chromogenic organic material
located on the enamel surface
CONCLUSION
bull It was concluded that esthetic appearance of teeth mild fluorosis can
be achieved by bleaching and microabrasion But in cases of
moderate fluorosis a combination of any of theses modalities can be
used
bull As no special maintenance precautions are required these maybe be
considered as an interesting alternative to conventional operative
treatment
bull Focuses on only TSIF of 4
bull Electric pulp testing is not the
right method to check for
sensitivity
bull Tooth Sensitivity changes
from person to person
bull Food habits can cause
staining of the teeth
bull Minimally invasive
bull Cheaper to veneers
bull Minimal loss of tooth structure
bull 4 parameters checked for the success of treatment
bull Inclusion of specific score of fluorosis for comparing the results
bull Maximum 3 appointments needed
CRITICAL ANALYSIS
Pros Cons
REFERENCES
bull Gurgan S Cakir FY Yazici E Different light-activated in officebleaching
systems Lasers Med Sci 201025817-22
bull Train TE McWhorter AG Seale NSWilson CF Guo IY Examination of
esthetic improvement and surface alteration following microabrasion in
fluorotic human incisors in vivoPediatr dent 199618353-62
bull Loguercio AD Correia LD Zago C Tagliari D Neumann E Gomes OM et al
Clinical effectiveness of two microabrasion materials materials for the
removal of enamel flurosis stains Oper Dent 200732531-8
4
5
Distraction
Distraction is a tactic designed to divert a patient attention away from their current behavior to focus their interest in something else Types Audio Distraction Audiovisual Distraction
Relaxation
Effective in reducing immediate anxiety and fear
Involves series of basic exercises which may take several months to learn amp practice
Voice control
Given by Pinkham in 1985
Modification of the timbre intensity and pitch of ones voice in an attempt
to dominate the interaction between dentist and child
Objectives
bull To gain the patient attention and
compliance
bull To avoid negative or avoidance
behavior
bull To establish authority
Indications bull Uncoperative and inattentive
patients
Contraindications bull Children who due to age
disability mental or emotional immaturity are unable to understand
Hypnosis
First suggested by Franz A Mesmer in
1773
Altered state of consciousness
characterized by heightened suggestibility
to produce desirable behavioral and
physiological changes
Most effective in the presence of anxiety
Not all patients can be hypnotized
Basic mechanism - relief of pain through
suggestions of relief given in a close
trusting interpersonal situation
Henon outlined following uses
bull To reduce nervousness and
apprehension
bull To eliminate defence mechanisms
that patient use to postpone dental
work
bull To control functional or
psychosomatic grapping
bull To prevent thumb sucking and
bruxism
bull To induce anesthesia
Hand over Mouth Exercise (HOME)
Given by DR EVANGELINE JORDAN (1920)
Evangeline Jordan - If a normal child will not listen but continues to cry
and strugglehellip Hold a folded napkin over the childrsquos mouthhellipand
gently but firmly hold his mouth shut
Other terminologies bull Aversive Conditioning by Lenchner and Wright bull Emotional surprise therapy by Lampshire bull HOM airway restricted (HOMAR) by Levitas (1947) bull Aversion by Crammer (1973)
Children who are
momentarily hysterical
belligerent or defiant
3-6 yrs old
Child who can understands
simple verbal commands
Indications
Contraindications
Very young immature frightened child with serious physical mental or emotional handicap
6
Variationshellip Hand over mouth with airway restricted Towel over mouth
Towel over mouth with airway restricted
Body
Papoose board
Triangular sheet
Pedi wrap
Bean Bag
Safety belt
Extremities
Posey straps
Velco straps
Towel amp Tape
Head
Forearm support
Plastic bowl
Head positioner
Mouth
Tongue blades
Mouth Prop
Bite blocks
Positive Stabilization Mouth
Tongue blade open mouth wide prop Molt mouth prop
Rubber bite blocks
Extremities
Posey Strap
Head
Body
Papoose board
Pedi-wrap
7
1
Impact of Handheld Devices on
Children An Evaluation of Usage amp
Dependency Behaviour
0092
DR MITAKSHARA NIRWAN
Handheld devices
A handheld device is a pocket size
computing device with a display
screen and inputoutput interface like
an external or touchscreen keyboard
For example- smartphones tablet
computers handheld videogame
consoles
Haruki Murakami
ldquoCell Phones are so
convenient that they have
become an inconveniencerdquo
Introduction
The most famouscommonly used and easily accessible type of gadgets are
lsquoHandheld devicesrsquo They are as popular in children as they are in adults
The access and ownership of these devices amongst children has grown
substantially in the past decade Concerns exist regarding excessive usage
and the impact of frequent consumption of mobile media on their health and
behaviour
Aims and Objective
This objective of this study was to asses the level of use of handheld
devices among children aged 0-12 years and their positive and negative
impacts on them It further describes the dependency of these devices
and the behavioral problems associated with it
Materials and Methods An online survey was conducted and a self administered questionnaire
was prepared specially for the parents which included a total of 15
questions regarding the usage and dependency of the device
A total of 100 responses were collected from parents who had children
aged 0-12 years who used these devices on daily basis
2
Level of Usage (Q 123)
Results Purpose (Q7)
Improved
communication and
learning
Using more than
one type of
device
Helped in
Speech
Positive Impacts -
(Q58 amp 9)
P value 0003(s) P value-0007 P value-0006(s)
Reduced parent-
child interaction Disrupted sleep Lack of motivation for academics
Negative Impacts (Q81213)
P value-0001(s) P value-0002(s) P value-0006
Time when children use
the device the most
Isolation of the
child Behavioral impact when gadget is
taken back
Dependency
Behaviour (Q10111415)
P value-002(s) P value 002(s) P value-044
This study was done to evaluate the level of usage of handheld devices and their impact
on the children aged 0-12 years The questionnaire was made such that it asked both the
positive and negative impact and further included the questions regarding the
dependency
784 children had access to smartphone and 17 used tablets
The most common age group in which the devices was used the most was 5-8 years
followed by 9-12 followed by 0-4 (Arlinda et al 2019 )
Another study done by (Rachel Bedford et al 2016) concluded increase usage of mobile
phones 5122 in 6ndash11 monthshy olds through to 9205 by 25ndash36 months
745used these devices several times a day out of which 539 used it for more than
one hourday 255 used it for less than one hour and 206 for more than 2 hours
Various studies follow the same recommendation given by AAP to limit the duration of
gadget amongst children
Discussion
3
Improve of Cognitive Skills
Amongst the positive impacts most parents have answered that the usage of these
devices has helped their child communicate and learn better and it has showed significant
results According to (Sundus M 2018)These devices improve the cognitive skills and
develop their learning skills fasterThe competition skills also get better It gives time for brain to think and process information better Another study which supports this (LF
Jonathan et al 2016)
Motor Physical Exercise
This study has shown that children like to use more than one type of device
sometimesUsing these devices improve fine motor skillshand eye coordination and
hands and fingers become more efficient (Srinahyanti et al 2019) (Sundus M 2018)
Speech Improvement
392 Parents say that maybe usage of the devices has helped improve speech in their
children but Various studies show otherwise as most of them shows that usage of handheld
devices causes delay of speech (Srinahyanti et al 2019)
Reduced parent child interaction
The negative impacts are more when compared to the positive ones Usage of gadgets
has resulted in reduced parent child interaction Less face to face interaction can
cause detachment from family members and value which in turn also causes isolation
of the child as he is more comfortable with the gadget (M Suhana-2017)
Sleep Disorders
This study shows that most parents have agreed that usage of these devices does
cause disruption of sleep Various studies have shown that children get fewer hours of
sleepdrowsiness during the day and dramatic increase in day time sleep because of
the screen usage (Acc to National Sleep Foundation) ( Cain N et al 2010)
In this study most number of parents have
agreed that their children might be dependent on
these devices and also had showed restless and
violent behavior if the gadget is snatched from
them
Most number of kids (667) are heavily
dependent as they like to use the device during
their meal time
Various other studies have assessed the screen
time dependency and have concluded that
various kids suffer from SDD
Conclusion The study conclusively shows that the impact of handheld devices is akin to the
importance of table salt in our meals most significant for our growth and
development in moderate amounts and hazardous in excess The negatives clearly
outweigh the positives with the latter too few and far in between This study also
points towards further extensive research on the subject because we need to find ways and also educate parents to optimise the role of these devices in their
childrenrsquos life taking advantage of their positive attributes and minimising their
negative ones
References 1Wahyuni AS Siahaan FB Arfa M Alona I Nerdy N The Relationship between the Duration of Playing
Gadget and Mental Emotional State of Elementary School Students Open Access Maced J Med Sci
20197(1)148ndash151
2Sundus M Department of Computer Science Lahore-The Impacts of using Gadgets on ChildrenJournal of Depression and Anxiety 2018vol 7(1)296
3Amawi SO Subki AH Khatib HA et al Use of Electronic Entertainment and Communication Devices Among
a Saudi Pediatric Population Cross-Sectional Study Interact J Med Res 20187(2)e13
4Julia ldquoHandheld Screen Time Linked with Speech Delays in Young Childrenrdquo Present Pediatric Acad Soc
Meet 2017
5C Rowan ldquoThe Impact of Technology on Child Sensory Motor Developmentrdquo 2003
6Impact of media use on children and youth Paediatr Child Health 20038(5)301ndash317
7Naik SV Children and their gadgets A pedodontist perspective Int J Oral Health Sci 2018857-8
8Roberts DF Foehr UG Rideout V Generation M Media in the lives of 8‐18 year‐olds A Kaiser Family
Foundation Study 2005
9Arya K Time spent on television viewing and its effect on changing values of school going children Anthropologist 20046269‐71
10 Lerner C Barr R Screen Sense Setting the Record StraightResearch‐Based Guidelines for Screen
Use for Children Under 3 Years Old Early learning project at Georgetown university 2014 p 1‐10
11SrinahyantiYasaratodo Wau Imelda Free Unita Manurung Nur Arjani-Influence of gadget A positive
and Negative Impact of Smartphone Usage for Early Child2019
4
THANK YOU
1
Morankar Rahul Aditi Kapur Krishan Gauba Ashima Goyal
MANAGEMENT OF ENDODONTIC INSTRUMENT SEPARATION IN
PRIMARY TEETH
CASE REPORT
Journal of South Asian Association of Pediatric Dentistry 2020
DR MITAKSHARA NIRWAN
bull Introduction
bull Aims amp Objectives
bull Case report
bull Discussion
bull Conclusion
bull Pros amp Cons
bull References
CONTENTS
Separation of endodontic instrument is an unexpected complication and its prevalence is not known It is a common belief among the dental professionals that rotary nickelndashtitanium (NiTi) instruments separate more frequently than stainless steel hand instruments
However literature revealed that in permanent teeth the reported prevalence of separated endodontics manual instruments is in the range of 07-74 whereas for rotary NiTI instruments it is
approximately 04-5
Fractured root canal instruments may include endodontic files Gates Glidden burs finger spreaders
and paste fillers
INTRODUCTION
The aim of this study is to describe the management strategies for endodontic
instrument separation in a root canal of primary teeth with emphasis on factors
requiring consideration in different clinical situations
AIMS amp OBJECTIVES
CASE 1
A 6-year-old male child reported with the chief complaint of spontaneous toothache in mandibular left second primary molar since few days It has aggravated following dental treatment at a private dental clinic Clinical examination revealed an underprepared access cavity with 75 and incomplete caries removal
which was sealed with glass ionomer cement
An intraoral periapical radiograph revealed a separated instrument of about 6ndash7 mm size in the distal root
2
The separated instrument was lodged firmly in distobuccal root canal 2ndash3 mm below the cementoenamel junction The instrument was bypassed successfully with no 15 and no 20 H-files but attempts for its retrieval were not successful
GatesndashGlidden (GG) drills no 2 (07 mm) and no 3 (09 mm) were used to drill around the instrument after which it was retrieved successfully using no 25 H-file
All the canals were instrumented till size 30 k-file followed by obturation with metapex and restoration with glass ionomer cement amp followed by placement of a crown and loop space maintainer for missing 74 The instrument retrieved was a manual reamer measuring 6 mm in length
The patient was asymptomatic since then and is under regular follow-up
CASE 2
A 5-year-old female child reported with the chief complaint of spontaneous toothache in mandibular left second
primary molar Clinical examination revealed deep occlusal caries with fractured lingual wall and pain on
percussion An intraoral periapical radiograph revealed caries involving pulp without any furcation or periapical
area of rarefaction and pulpectomy was planned
All the canals were enlarged using NiTi rotary files with a 4 taper operating at 500 rpm with minimum torque
setting An orifice opener [(0825 19 mm) of 8 taper size 25 length 19 mm] and nos 0420 file was used for
instrumentation of root canal This was followed by file nos 0425 which got separated in the distobuccal root
canal The radiograph confirmed a separated instrument of length 3ndash4 mm in the middle third of the root canal
The instrument was bypassed with no 15 k-file but could not get retrieved As instrument separation had occurred with 0425 file the involved root canal was sufficiently debrided before separation and the level of instrument separation was at the mid-root region so it was decided to obturate and seal this tooth with
periodic follow-ups instead of immediate extraction All other canals were enlarged till size 0430 in the sequential manner followed by obturation using metapex and placement of stainless steel crown
3
CASE 3
A 5-year-old female child has complaint of mild intermittent pain with primary mandibular left first molar She
had undergone pulpectomy treatment for the same during which an instrument separation has occurred in
the mesiobuccal root canal by a resident doctor
A radiograph revealed a separated instrument of about 4 mm in size lodged in the apical third but within the
confines of the mesial root An attempt was made for its retrieval but was unsuccessful The extraction of the
involved tooth was carried out under local anesthesia followed by a band and loop space maintainer
CASE 4
A 7-year-old male child reported with a chief complaint of mild intermittent pain on food lodgment with the primary mandibular right first and second molars The patient had a history of dental treatment at a private
dental clinic few months back which he did not continue further
Clinical examination revealed glass ionomer restoration with 85 and proximal caries with 84 leading to food lodgment An intraoral periapical radiograph with 85 revealed empty root canals with a separated
instrument of about 3ndash4 mm size beyond the apex of mesial root close to the developing succedaneous premolar
4
DISCUSSION
Stainless steel files usually separate fracture due to the excessive amounts of torque and overuse or the
preexisting distortion of the instrument whereas in NiTi rotary files it is a combined result of torsional stress and cyclic fatigue
Therapeutic options for the management of separated endodontic instruments include no intervention nonsurgical (orthograde conservative) management surgical management and tooth extraction
Use of ultrasonic scaler Masserann technique Endo extractor and Cavi-Endo ultrasonic instruments are some of the methods popular for retrieval of a separated endodontic instrument in the permanent tooth
In case 1 a 6-mm-long manual reamer was retrieved successfully with the use of GG drill using a manual file and copious irrigation which is the most desired treatment outcome
In case 2 the retrieval of separated rotary file lodged in the middle third of the root canal was unsuccessful in spite of multiple attempts It was therefore managed with routine obturation followed by restoration to maintain the tooth in its physiological functional state It was kept under close periodic follow-up at least
every 3 months This treatment option should be encouraged where it is possible to follow up the patient clinically and radiographically at close periodic intervals as there is the possibility of instrument escaping
into bone due to physiological root resorption
In cases 3 and 4 an instrument has separated in the apical root portion
In case 3 it was within the root canal and thus an attempt was made for its retrieval which was
unsuccessful It was therefore extracted to prevent the fractured instrument from getting exposed in the bone following resorption as there is no accurate and consistent established age for initiation of resorption in primary teeth known per se
In case 4 an immediate extraction of involved tooth was carried out as the separated instrument was beyond the apex of the primary tooth root
Age of the child clinical signs and symptoms and amount of root resorption are the factors which can also influence the management of separated instrument in primary teeth
Moreover if an instrument has separated after initial cleaning and shaping of root canal maintaining a tooth is not a problem as clinical signs and symptoms are not anticipated and the good prognosis is expected
However if an instrument has separated early during the initial cleaning and shaping of the root canal clinical symptoms may compromise the prognosis
Therefore these factors should be kept in mind while planning a suitable management strategy to avoid or at least reduce the burden of extraction and wear of space maintainer for longer period
5
CONCLUSION
The management and prognosis of a primary tooth with a separated instrument is
dependent on the level of instrument fracture within the root age of the child root
resorption and clinical signs and symptoms of the involved tooth
Different management approaches can be tried depending on clinical situations keeping
in mind benefits vs risks in preserving the tooth
PROS amp CONS
PROS
The entire procedure is given
by step by step
Well descriptive xrays and
photographs
CONS
Medical history has not been
given
REFERENCES
1 TOMER ANIL K ET AL ldquoBROKEN FILE RETRIEVAL PUZZLE IN ENDODONTICSrdquo
(2016)
2 SHENOY A MANDAVA P BOLLA N ET AL A NOVEL TECHNIQUE FOR REMOVAL OF
BROKEN INSTRUMENT FROM ROOT CANAL IN MANDIBULAR SECOND MOLAR
INDIAN J DENT RES 201425(1)107ndash110
3 PATEL J MORAWALA A TALATHI R ET AL RETRIEVAL OF A BROKEN INSTRUMENT
FROM ROOT CANAL IN PRIMARY ANTERIOR TEETH UNIV RES J DENT 20155(3)203ndash
206
4 MORANKAR R GOYAL A GAUBA K ET AL MANUAL VERSUS ROTARY
INSTRUMENTATION FOR PRIMARY MOLAR PULPECTOMIES - A 24 MONTHS
RANDOMIZED CLINICAL TRIAL PEDIAT DENT J 201828(2)96ndash102
5 KASHYAP NILOTPOL (2018) RETAINING PRIMARY MOLARS WITH INSTRUMENT
SEPERATION A CASE REPORT AND CLINICAL GUIDE
6
1
IMPACT OF 6 CITRIC ACID AND ENDOACTIVATOR AS IRRIGATION ADJUNCTS ON OBTURATION QUALITY AND PULPECTOMY OUTCOME IN
PRIMARY TEETH
NEETU JAIN SHALINI GARG ABHISHEK DHINDSA SAKSHI JOSHI HARJOY
KHATRIA
PEDIATRIC DENTAL JOURNAL 2019 29
1
DR MITAKSHARA NIRWAN
CONTENTS
bull INTRODUCTION
bull AIMS amp OBJECTIVES
bull CASE REPORT
bull RESULTS
bull DISCUSSION
bull CONCLUSION
bull PROS AND CONS
bull REFERENCES
2
INTRODUCTION
bull ENDODONTIC THERAPY IN PRIMARY TEETH INVOLVES DISINFECTION OF THE ROOT CANAL
SYSTEM AND ITS OBTURATION WITH RESORBABLE PASTE
bull THE CONTENTS OF ROOT CANAL ALONG WITH SMEAR LAYER ARE EXPECTED TO BE REMOVED
DURING THE BIOMECHANICAL PREPARATION
bull IN VITRO AND CLINICAL DOCUMENTS HAVE INDICATED THAT MECHANICAL PREPARATION OF
THE CANAL LEAVES LARGE PORTIONS OF THE CANAL WALLS UNDEBRIDED AND COMPLETE
REMOVAL OF THE BACTERIA BY THIS MECHANICAL PROCEDURE ALONE IS UNLIKELY TO BE SEEN
THEREFORE SOME FORM OF DISINFECTIONIRRIGATION IS MANDATORY TO KILL THE
MICROORGANISMS AND TO REMOVE THE RESIDUAL TISSUES
3
bull THE IDEAL REQUISITES OF A ROOT CANAL IRRIGANT AS GIVEN BY ZEHNDER ARE
1 BROAD ANTIMICROBIAL SPECTRUM
2 HIGH EFFICACY AGAINST ANAEROBIC AND FACULTATIVE MICROORGANISMS ORGANIZED
IN BIOFILMS
3 ABILITY TO DISSOLVE NECROTIC PULP TISSUE REMNANTS
4 ABILITY TO INACTIVATE ENDOTOXIN
5 ABILITY TO PREVENT THE FORMATION OF A SMEAR LAYER DURING INSTRUMENTATION OR
TO DISSOLVE THE LATTER ONCE IT HAS FORMED
6 SYSTEMICALLY NONTOXIC WHEN THEY COME IN CONTACT WITH VITAL TISSUES
NONCAUSTIC TO PERIODONTAL TISSUES AND WITH LITTLE POTENTIAL TO CAUSE AN
ANAPHYLACTIC REACTION
SINCE NO SINGLE IRRIGANT HAS THESE OPTIMAL PROPERTIES STUDIES HAVE REPORTED THE USE
OF TWO OR MORE SOLUTIONS IN A SPECIFIC SEQUENCE OR IN COMBINATIONS FOR BETTER
RESULTS 4
bull SEVERAL IRRIGATING SOLUTIONS ALONG WITH CHELATING AGENTS HAVE BEEN USED
DURING BIOMECHANICAL PREPARATION OF ROOT CANAL BOTH IN PRIMARY AND
PERMANENT TEETH
bull HOWEVER NONE OF THE AVAILABLE IRRIGATING SOLUTIONS HAS BEEN REGARDED CLEARLY
AS OPTIMAL SOLUTION BECAUSE OF THEIR LIMITED EFFECTIVENESS ESPECIALLY IN APICAL
13RD OF THE ROOT CANAL SYSTEM
bull TO OVERCOME SUCH LIMITATIONS USE OF ENDOACTIVATOR HAS BEEN PROPOSED AS AN
IRRIGATION FACILITATOR THAT IS BASED ON SONIC VIBRATION (UP TO 10000 CPM) WHICH
FACILITATES THE IRRIGANT PENETRATION AND ITS RENEWAL WITHIN THE CANAL
bull ACTIVATION SYSTEMS RESULTED IN BETTER REMOVAL OF THE SMEAR LAYER IN THE APICAL
THIRD OF ROOT CANALS IN COMPARISON TO CONVENTIONAL IRRIGATION
5
CITRIC ACID
bull CITRIC ACID IS A WEAK ORGANIC ACID WITH THE APPEARANCE OF WHITE CRYSTALLINE
POWDER AT ROOM TEMPERATURE
bull IT CAN EXIST EITHER IN WATER-FREE FORM (ANHYDROUS) OR MONOHYDRATE FORM THE
WATER-FREE FORM CRYSTALLIZES FROM THE HOT WATER WHEREAS THE MONOHYDRATE
FORMS FROM THE COLD WATER THE LATTER MAY BE CONVERTED TO ANHYDROUS FORM BY
HEATING MORE THAN 78degC
bull CITRIC ACID OCCURS NATURALLY IN THE BODY IN MITOCHONDRIA AND IS USED BY BLOOD
BANKS TO PREVENT COAGULATION OF TRANSFUSED BLOOD CITRIC ACID IS ALSO ESSENTIAL
TO HUMAN METABOLISM AND IS FOUND IN MANY FOODS
6
2
bull THE BIOLOGICAL EFFECTS OF CITRIC ACID ON THE PERIODONTAL STRUCTURE HAS BEEN
EXTENSIVELY STUDIED IN PERIODONTICS
bull NEUMAN AND NEWMAN SHOWED THAT CITRIC ACID IS THE MOST EFFECTIVE ACID IN
ALTERING THE SOLUBILITY OF HYDROXYAPATITE
bull YAMAGUCHI ET AL SHOWED THAT CITRIC ACID SOLUTION HAD ANTIBACTERIAL EFFECTS ON
ALL 12 ROOT CANAL BACTERIA TESTED
bull ARIAS-MOLIZ ET AL SHOWED THAT ETHYLENEDIAMINETETRAACETIC ACID (EDTA) HAS NO
BACTERICIDAL ACTIVITY EVEN AFTER 1 HOUR CONTACT
bull THIS ACID HAS THE ABILITY OF ROOT CANAL IRRIGATION AND ALSO SMEAR LAYER REMOVAL
DIFFERENT CONCENTRATIONS (1ndash50) HAVE BEEN PROPOSED GUTMANN ET AL CONCLUDED
THAT 10 CITRIC ACID IS BETTER THAN ULTRASOUND FOR SMEAR LAYER REMOVAL FROM THE
ROOT END CAVITIES
7
bull STUDIES HAVE SHOWN IRRIGATION WITH 6 CA FOR 15 OR 30 SECONDS IS QUITE
EFFECTIVE IN REMOVING ALL THE COMPONENTS OF THE SMEAR LAYER OF THE PRIMARY
TEETH WHEREAS PERITUBULAR DENTIN DESTRUCTION WAS OBSERVED WHEN HIGHER
CONCENTRATION OF CITRIC ACID WAS USED AS AN IRRIGATING SOLUTION
8
AIMS amp OBJECTIVES
bull THIS STUDY WAS AIMED TO EVALUATE THE CLINICAL AND RADIOGRAPHIC OUTCOME OF
PULPECTOMY ALONG WITH QUALITY OF OBTURATION USING 6 CITRIC ACID AND
ENDOACTIVATOR
9
CASE REPORT
bull 350 CHILDREN (3-9 YEARS) WITH CLINICAL SIGNS AND SYMPTOMS OF CHRONIC IRREVERSIBLE
PULPITIS IN DEEPLY CARIOUS TEETH WERE SCREENED DURING SCHOOL DENTAL HEALTH
PROGRAM FROM MAY 2014-JULY 2014
bull 123 CHILDREN REPORTED TO THE DEPARTMENT AND 67 CHILDREN WERE SELECTED BASED ON
INCLUSION AND EXCLUSION CRITERIA
RECRUITMENT OF PATIENTS
10
INCLUSION CRITERIA
bull HISTORY OF SPONTANEOUS PAIN AND UNCONTROLLED BLEEDING AFTER PULP AMPUTATION
EXCLUSION CRITERIA
bull EVIDENCE OF INTERNAL OR EXTERNAL (PHYSIOLOGICPATHOLOGIC) ROOT RESORPTION OF MORE THAN A THIRD OF ITS LENGTH
bull ROOT CANAL OBLITERATION OR ANATOMIC ANOMALIES
bull INADEQUATE BONE SUPPORT OR NON RESTORABLE TOOTH
bull ONCE PATIENTS ELIGIBILITY WAS CONFIRMED THE TREATMENT PROCEDURE WAS
EXPLAINED TO THE PARENTGUARDIAN AND INFORMED WRITTEN CONSENT WAS
OBTAINED FROM PARENTSGUARDIANS SHOWING WILLINGNESS FOR THEIR
CHILDRENS TREATMENT 11
PROCEDURE
bull PULPECTOMY WAS PERFORMED BY ONE OPERATOR OF PEDIATRIC DENTISTRY DEPARTMENT
USING A STANDARDIZED TREATMENT PROTOCOL FOR ALL THE PATIENTS
bull AFTER ADMINISTRATION OF LOCAL ANESTHESIA RUBBER DAM WAS APPLIED FOR ISOLATION
bull ACCESS CAVITY WAS PREPARED USING AIR-ROTOR HAND PIECE WITH 8 ROUND BUR AND
PULP TISSUE WAS EXTIRPATED WITH THE HELP OF SPOON EXCAVATOR
bull FURTHER THE NEGOTIATION OF THE CANALS WAS DONE WITH 10 K-FILE
bull A DIAGNOSTIC RADIOGRAPH WAS TAKEN FOR ROOT LENGTH DETERMINATION AND
WORKING LENGTH WAS KEPT 1 MM SHORT OF THE RADIOGRAPHICAL APEX
bull ALL ROOT CANALS WERE INSTRUMENTED MANUALLY USING K-FILES AND WERE IRRIGATED
WITH 10 ML 09 NORMAL SALINE AND 1 SODIUM HYPOCHLORITE AS STANDARDIZING
PROTOCOL FOR ROOT CANAL PREPARATION AND DISINFECTION
12
3
GROUP 1 (CA + E) - IRRIGATION WAS DONE
WITH 10 ML OF 6 CITRIC ACID (CITOCID AMMDENT)
AND IRRIGANTS WERE SONICALLY AGITATED WITH
ENDOACTIVATOR (DENTSPLY) FOR 30 S PER CANAL USING REDBLUE
ENDOACTIVATOR TIP
GROUP 2 (CA) - 10 ML OF 6 CITRIC ACID FOR 1 MIN USING
27 GAUZE IRRIGATING NEEDLE
GROUP 3(SH + E) - 10 ML OF 1 SODIUM HYPOCHLORITE
SOLUTION AND SONIC ACTIVATION WITH ENDOACTIVATOR
GROUP 4(SH) - 10 ML OF 1 SODIUM HYPOCHLORITE
SOLUTION USING IRRIGATING NEEDLE (CONTROL GROUP)
bull TEETH UNDERGOING PULPECTOMY WERE RANDOMLY ENROLLED BY CHIT METHOD INTO THREE
STUDY AND ONE CONTROL GROUP
13
bull IN CITRIC ACID GROUPS FINAL RINSE WITH NORMAL SALINE WAS DONE TO REMOVE THE
REMAINING CRYSTALS (CHELATES)
bull FOLLOWING BIOMECHANICAL PREPARATION THE ROOT CANALS WERE DRIED WITH STERILE
ABSORBENT PAPER POINTS AND OBTURATED WITH VITAPEX USING HAND HELD
LENTULOSPIRAL FINAL RESTORATIONS WERE DONE USING COMPOSITE RESIN
14
bull CLINICAL FOLLOW UP WAS DONE AT 24 H1 WEEK 1 MONTH 6 MONTH AND 12
MONTH TO CHECK PAIN PRESENCE AND PAIN FREQUENCY (ONCEMORE THAN ONCE)
SWELLING FISTULA SENSITIVITY TO PERCUSSION
bull RADIOGRAPHIC FOLLOW UP WAS DONE AT 6 MONTH AND 12 MONTH FOR ANY
DEVIATED ERUPTION OF SUCCEDANEOUS TEETH EXCESS FILING MATERIAL AND ITS
RESORPTION EXTERNALINTERNAL ROOT RESORBTION CALCIFIC METAMORPHOSIS
PRESENCE OF FURCATION RADIOLUCENCY
CLINICAL amp RADIOGRAPHIC FOLLOW UP
15
RADIOGRAPHIC ASSESSMENT OF OBTURATION QUALITY
bull POSTOPERATIVE RADIOGRAPHS WERE VISUALLY ASSESSED FOR QUALITY OF OBTURATION BY
TWO INDEPENDENT EXAMINERS (SG AD) WHO WERE BLINDED WITH REGARD TO
IRRIGATION PROTOCOL GROUP TO ENHANCE CALIBRATION EACH EXAMINER ASSESSED THE
RADIOGRAPH INDEPENDENTLY AND LATER REVIEWED TOGETHER FOR FINAL ASSESSMENT
INDIVIDUAL ROOT WAS TAKEN AS UNIT OF ANALYSIS FOR GRADE OF OBTU- RATION AND
SCORING CRITERIA WERE AS GIVEN BY COLL JA 1996
1 UNDER FILLED - FILLING MATERIAL ENDED 1 MM OR MORE SHORT OF THE APEX
2 OPTIMAL FILLING- FILLING MATERIAL APPEARED TO END AT THE RADIOGRAPHICAL APEX
3 OVERFILLED - FILLING MATERIAL EXTRUDED PAST THE RADIOGRAPHIC APEX
4 OPTIMALLY FILLED ROOTS WERE FURTHER ASSESSED FOR THE PRESENCE OF VOIDS AND VOID
AREA (ROOT CANAL SURFACE UNTOUCHED BY THE ROOT CANAL FILLING MATERIAL) IN THREE
VISUALLY DIVIDED SECTIONS OF THE ROOT IE CORONAL MIDDLE AND APICAL 13RD
16
RESULTS
bull OVERALL CLINICAL AND RADIOGRAPHIC SUCCESS RATE OVER A PERIOD OF ONE YEAR WAS
9886 amp 977 RESPECTIVELY
bull ALL GROUPS WERE SIGNIFICANTLY (P = 001) EFFECTIVE IN ALLEVIATING PAIN WITHIN 24 H
OF PULPECTOMY
17 18
4
19
bull IMMEDIATE POST OPERATIVE RADIOGRAPHIC ASSESSMENT REVEALED 68 (102150) ROOTS
WITH OPTIMAL OBTURATION AND 32 (48150) WITH OVERFILLINGUNDERFILLING MAXIMUM
NO OF OPTIMAL FILLINGS WERE OBSERVED IN GROUP1 (CA + E) (3333) FOLLOWED BY
GROUP 2 (CA) (2549) GROUP 3(SH + E) (2549) AND GROUP 4(SH) (1568)
bull CITRIC ACID GROUPS HAD MORE NUMBER OF OPTIMALLY FILLED ROOTS 588 (60102) THAN
NON CITRIC ACID GROUPS 412 (42102)
bull ENDOACTIVATOR CONTRIBUTED TO 18 OF OPTIMAL OBTURATION IRRESPECTIVE OF
CHELATING AGENT USED
20
21
bull MAXIMUM NO OF VOIDS AND VOID AREAS WERE IN NON CITRIC ACID GROUPS
(6419 amp 5384) COMPARED TO CITRIC ACID GROUPS (3580 amp 4615)
RESPECTIVELY
bull ANALYSIS OF ROOT 13RD REVEALED MAXIMUM NO OF VOID AREA IN APICAL
13RD (4755) FOLLOWED BY MIDDLE 13RD (3846) AND CORONAL 13RD
(1398)
bull LEAST NO OF VOIDS amp VOID AREA (1111 amp 1608) WERE OBSERVED WHEN
ENDOACTIVATOR ALONG WITH CHELATING AGENT WAS USED (GROUP 1)
HOWEVER THIS WAS STATISTICALLY INSIGNIFICANT
22
DISCUSSION
bull IN THE PRESENT STUDY 1 SODIUM HYPOCHLORITE WAS USED ALONG WITH 6 CITRIC ACID
(CHELATING AGENT) WHICH IS REPORTED TO BE AS EFFECTIVE AS 17 EDTA
bull CITRIC ACID (BIOLOGICAL ACID) IS FOUND TO BE BIOCOMPATIBLE AND LEAST IRRITATING TO
PERIAPICAL TISSUES THAN OTHER CHELATING AGENTS
bull USE OF SODIUM HYPOCHLORITE SOLUTION FOLLOWING CHELATING AGENT WAS AVOIDED AS IT
RAPIDLY PRODUCES SEVERE EROSION OF ROOT CANAL WALL DENTIN
bull TRADITIONAL APPROACH OF DELIVERING IRRIGANTS INTO THE ROOT CANAL SPACE USING
SYRINGES AND METAL NEEDLES HAS BEEN FOUND TO BE INEFFECTIVE ESPECIALLY IN THE AREAS OF
ANASTOMOSES BETWEEN CANALS AND APICAL 13RD OF ROOT CANAL
23
bull THEREFORE TO ACHIEVE BETTER CLEANING EFFICIENCY IRRIGANT ACTIVATION HAS BEEN
RECOMMENDED SONIC ACTIVATION HAS BEEN REPORTED TO RESULT IN BETTER ROOT CANAL
CLEANLINESS AS COMPARED TO NO ACTIVATION OF IRRIGANT
24
5
CONCLUSION
bull USE OF 6 CITRIC ACID DEFINITELY HELPED IN RAPID ELIMINATION OF PAIN RESOLUTION OF
PERI-RADICULAR RADIOLUCENCY BETTER OBTURATION QUALITY IN TERMS OF LESS VOIDS AND
VOID AREAS ALONG WITH MAXIMUM NO OF OPTIMAL OBTURATION UP TO APICAL AREA
bull 6 CITRIC ACID AND ENDOACTIVATOR IRRIGATION PROTOCOL PROVED TO BE THE BETTER
IRRIGATION PROTOCOL WHICH MAY CONTRIBUTE TO LONG TERM SUCCESS OF PRIMARY
TOOTH AND THE HEALTH OF UNDERLYING PERMANENT TOOTH
bull 6 CITRIC ACID ALONG WITH ENDOACTIVATOR MAY BE RECOMMENDED AS IRRIGATION
ADJUNCTS IN PULPECTOMY PROCEDURE OF PRIMARY TEETH
25
PROS AND CONS
PROS
bull PROPER EXPLANATION OF THE MATERIALS
USED
CONS
bull NO PREOPERATIVE AND POSTOPERATIVE
RADIOGRAPHS
26
REFERENCES
bull RAMACHANDRA JA NIHAL NK NAGARATHNA C VORA MS ROOT CANAL IRRIGANTS IN
PRIMARY TEETH WORLD J DENT 20156(3)229-234
bull MOHAMMADI Z JAFARZADEH H SHALAVI S KINOSHITA JI UNUSUAL ROOT CANAL
IRRIGATION SOLUTIONS J CONTEMP DENT PRACT 201718(5)415-420
bull ZEHNDER M ROOT CANAL IRRIGANTS J ENDOD 2006 32389- 98
bull SMITH JJ amp WAYMAN BE AN EVALUATION OF THE ANTIMICROBIAL EFFECTIVENESS OF
CITRIC ACID AS A ROOT CANAL IRRIGANT JOURNAL OF ENDODONTICS 1986 12(2) 54-58
bull TANNURE PN AZEVEDO CP BARCELOS R GLEISER R PRIMO LG LONG-TERM OUTCOMES OF
PRIMARY TOOTH PULPECTOMY WITH AND WITHOUT SMEAR LAYER REMOVAL A RANDOMIZED
SPLIT-MOUTH CLINICAL TRIAL PEDIATR DENT 201133316E20 27
bull CARON G NHAM K BRONNEC F MACHTOU P EFFECTIVENESS OF DIFFERENT FINAL IRRIGANT
ACTIVATION PROTOCOLS ON SMEAR LAYER REMOVAL IN CURVED CANALS J ENDOD
2010361361E6
bull COLL JA SADRIAN R PREDICTING PULPECTOMY SUCCESS AND ITS RELATIONSHIP TO
EXFOLIATION AND SUCCEDANEOUS DENTITION PEDIATR DENT 19961857E63
28
1
LOCAL
ANESTHESIA
DR MITAKSHARA NIRWAN
CONTENTS
Definition
Methods of inducing local anesthesia
Desirable properties
Electrophysiology of nerve conduction
Impulse propagation and spread
Mode and site of action of local anesthesia
Classification of local anesthetic according to biological site and mode of action
Dissociation of local anaesthetics
Mechanism of action of local anaethetics
Local anaesthetic agent
2
3
DEFINITION
Local anesthesia is defined as a loss of sensation in
a circumscribed area of the body caused by depression
of excitation in nerve endings or an inhibition of the
conduction process in peripheral nerves
An important feature of local anesthesia is that it produces
LOSS OF SENSATION WITHOUT INDUCING LOSS OF
CONSCIOUSNESS
4
METHODS OF INDUCING LOCAL
ANESTHESIA
Low temperature
Mechanical trauma
Anoxia
Neurolytic agents such as alcohol amp phenol
Chemical agents such as local anesthetics
PROPERTIES OF LOCAL
ANESTHESIA
It should not be irritating to tissue to which it is applied
It should not cause any permanent alteration of nerve structure
Its systemic toxicity should be low
Time of onset of anesthesia should be short
It should be effective regardless of whether it is injected into the tissue or applied locally to mucous membranes
The duration of action should be long enough to permit the completion of procedure
5 6
It should have the potency sufficient to give complete
anesthesia with out the use of harmful concentration solutions
It should be free from producing allergic reactions
It should be free in solution and relatively undergo
biotransformation in the body
It should be either sterile or be capable of being sterilized by
heat with out deterioration
2
ELETROPHYSIOLOGY OF
NERVE CONDUCTION
There is an electrical charge across the membrane
This is the membrane potential
The resting potential (when the cell is not firing) is a negative
electrical potential of -70mv that exists across the nerve
membrane produced by different concentrations of either side of
the membrane
The interior of nerve is NEGATIVE in relation to exterior
7 8
inside
outside
Resting potential of neuron = -70mV
+
-
+
-
+
-
+
-
+
-
SLOW DEPOLARIRIZATION
9
RAPID DEPOLARIZATION
The interior of nerve is POSITIVE in relation to exterior
REPOLARIZATION
10
bull Repolarization takes 07 msec
bull Depolarization takes 03 msec
SODIUM PUMP -
energy comes from the oxidative metabolism of ATP
bull The entire process require 1 msec
IMPULSE PROPOGATION
IMPULSE SPREAD
The propagated impulse travels along the nerve
membrane towards CNS The spread of impulse differs
in myelinated and unmyelinated nerve fibers
DEPOLARIZED SEGMENT ADJACENT RESTING AREA
MODE AND SITE OF ACTION OF LOCAL
ANESTHETICS
Local anesthetic agent interferes with excitation
process in a nerve membrane in one of the
following ways
Altering the basic resting potential of nerve
membrane
Altering the threshold potential
Decreasing the rate of depolarization
Prolonging the rate of repolarization
12
3
CLASSIFICATION OF LOCAL ANESTHETIC
SUBSTANCES ACCORDING TO
BIOLOGICAL SITE AND MODE OF ACTION
CLASS A
Agents acting at receptor site on external surface of nerve membrane
Chemical substance Biotoxins (eg tetrodotoxin and saxitoxin)
CLASS B
Agents acting on receptor sites on internal surface of nerve membrane
Chemical substance Quaternary ammonium analogues of lidocaine
scorpion venom 13
CLASS C Agents acting by receptor independent of
physiochemical mechanism
Chemical substance Benzocaine
CLASS D Agents acting by combination of receptors and
receptor independent mechanisms
Chemical substance most clinically useful anesthetic agents
(eg lidocaine mepivacaine prilocaine)
14
BASED ON THE SOURCE
NATUAL
SYNTHETIC
OTHERS
BASED ON MODE OF APPLICATION
bull INJECTABLE
bull TOPICAL
BASED ON DURATION OF ACTION
bull ULTRA SHORT
bull SHORT
bull MEDIEM
bull LONG
BASED ON ONSET OF ACTION SHORT
INTERMEDIATE
LONG
15
DISSOCIATION OF LOCAL
ANESTHETICS
Local anesthetics are available as salts (usually
hydrochlorides) for clinical use
The salts both water soluble and stable is dissolved in
either sterile water or saline
In this solution it exists simultaneously as unchanged
molecule (RN) also called base and positively charged
molecules (RNH+) called cations
RNH+ ==== RN+ H
+
16
The relative concentration of each ionic form in the solution varies
in the pH of the solution or surrounding tissue
In the presence of high concentration of hydrogen ion (low pH) the
equilibrium shifts to left and most of the anesthetic solution exists
in cationic form
RNH+ gt RN
+ + H
+
As hydrogen ion concentration decreases (higher pH) the
equilibrium shifts towards the free base form
RNH+ lt RN + H
+
17
The relative proportion of ionic form also depends on pKa or DISSOCIATION CONSTANT of the specific local anesthetic
The pKa is a measure of molecules affinity for H+
ions
When the pH of the solution has the same value as pKa of the local anesthetic exactly half the drug will exists in the RNH
+ form and
exactly half in RN form
The percentage of drug existing in either form can be determined by Henderson Hasselbalch equation
Log baseacid = pH - pKa
18
4
MECHANISM OF ACTION OF LOCAL
ANESTHETICS
The following sequence is proposed mechanism of action of LA
Displacement of calcium ions from the sodium channel receptor site
Binding of local anesthetic molecule to this receptor site
Blockade of sodium channel
19
Decrease in sodium conductance
Depression of rate of electrical depolarization
Failure to achieve the threshold potential level
Lack of development of propagated action potential
Conduction blockadehellip
20
21
Na + Na +
22
LOCAL ANESTHETIC AGENT
COMERCIALLY PREPARED LOCAL ANESTHESIA
CONSISTS OF
Local anesthetic agent (xylocaine lignocaine 2)
Vasoconstrictor (adrenaline 1 80000)
Reducing agent (sodium metabisulphite)
Preservative (methylparabencapryl
hydrocuprienotoxin)
Fungicide (thymol)
Vehicle (distillde waterNaCl)
LOCAL ANESTHETIC AGENT
The local anesthetics used in dentistry are divided
into two groups
ESTER GROUP
AMIDE GROUP
23 24
ESTER GROUP It is composed of the following
An aromatic lipophilic group
An intermediate chain containing
an ester linkage
A hydrophilic secondary or tertiary
amino group
AMIDE GROUP It is composed of the following
An aromatic lipophilic group
An intermediate chain containing
amide linkage
A hydrophilic secondary or tertiary
amino group
5
25
CLASSIFICATION OF LOCAL ANESTHETICS
ESTERS
Esters of benzoic acid
Butacaine
Cocaine
Benzocaine
Hexylcaine
Piperocaine
Tetracaine
Esters of Para-amino
benzoic acid
Chloroprocain
Procaine
Propoxycaine
26
AMIDES Articaine
Bupivacaine
Dibucaine
Etidocaine
Lidocaine
Mepivacaine
Prilocaine
Ropivacaine
QUINOLINE
Centbucridine
PHARMACOKINETICS OF LOCAL
ANESTHETICS UPTAKE
When injected into soft tissue most local anesthetics produce
dilation of vascular bed
Cocaine is the only local anesthetic that produces
vasoconstriction initially it produces vasodilation which is
followed by prolonged vasoconstriction
Vasodilation is due to increase in the rate of absorption of the
local anesthetic into the blood thus decreasing the duration of
pain control while increasing the anesthetic blood level and
potential for over dose 27
AMIDE LOCAL ANESTHETICS
The metabolism of amide local anesthetics is more
complicated then esters The primary site of
biotransformation of amide drugs is liver
Entire metabolic process occurs in the liver for lidocaine
articaine etidocaine and bupivacaine
Prilocaine undergoes more rapid biotransformation then the
other amides
28
REFERENCES
Handbook of local anesthesia ndash Stanley F Malamed ndash 6th
edition
Essentials of Local Anesthetic Pharmacology Daniel E
Becker Anesth Prog 2006 Fall 53(3) 98ndash109
WIKIPEDIEA
29
THANK YOU
30
1
Pharmacological Methods of Behavior
Management
DR MITAKSHARA NIRWAN
DEFINITIONS
bull Conscious Sedation ndash A minimally depressed level of consciousness that retains
the patients ability to independently and continuously maintain an airway and respond appropriately to physical stimulation or verbal command
(American Dental Association House Of Delegates 2000)
bull Deep Sedation ndash An induced state of depressed consciousness
accompanied by partial loss of protective reflexes including the inability to continuously maintain an airway independently and or to respond purposefully to physical stimulation or verbal command
bull General Anesthesia (G A) ndash An induced state of unconsciousness or complete loss of
protective reflexes including the inability to continually maintain an airway independently and respond purposefully to physical stimulation or verbal command
Conscious sedation
ADVANTAGES
Conscious
Protective reflexes active amp intact
Stable vital signs
Operating dentist may perform sedation
Minimum amount of equipment required
Prolong detainment in recovery room not required
Risk of complication very low
Excellent choice for poor ndash risk pt in dental office
Cost effective
General anesthesia
ADVANTAGES Not absolutely
essential May be the only
method Not necessary (no
pain reaction) Amnesia always
present
Conscious sedation
DISADVANTAGES
Pt cooperation is essential
Extremely difficult or mentally handicapped pt cannot always be managed
Use of local anesthesia is a must
Amnesia may or may not be present
General anesthesia DISADVANTAGES
Pt unconscious
Protective reflexes are depressed
Depressed
Advanced training required Dentist must not act also as anesthetist
Special equipment necessary
Detainment in recovery area necessary
High IOP amp postoperative complications
Not indicated in dental office
More expensive
Fundamental Concepts
bull Techniques that utilize drugs to induce co-operative yet conscious state in an otherwise uncooperative child ndash CONSCIOUS SEDATION
2
GOALS
1 To facilitate the provision of quality care
2 To minimize the extremes of disruptive behavior
3 To promote a positive psychologic response to treatment
4 To promote patient welfare amp safety
5 To return the patient to physiologic state
OBJECTIVES
1 The pt mood must be altered
2 The pt must remain conscious at all times
3 The pt must be cooperative
4 All protective reflexes must remain intact and active
5 Vital signs must remain stable and with in normal limits
6 The ptrsquos pain threshold should be elevated
7 Amnesia may be present
Indications
1 Preschool children
2 Lack of Psychological Emotional maturity
3 Lack of Cognitive Physical Medical disability
4 Fearful amp anxious pts
5 Pt who require extensive amp complicated dental care amp would require or benefit from prolonged visits
6 Acute pain
7 Traumatic injuries
Operating Facilities amp Equipment
A positive pressure O2 delivery system capable of administering gt than 90 O2 at 10L min flow for 60 min (650L ldquoErdquo cylinder)
OR
Self inflating bag valve mask device (15L min)
A functional suction apparatus with appropriate suction catheters
Monitoring equipment - PO BPC PC or Capno
Inhalation sedation unit
100 O2 amp never less than 25
A fail safe mechanism that is checked and calibrated annually
Must have appropriate scavenging system
Emergency drugs
Techniques of sedation
Routes for drug administration
bull Oral
bull Rectal
bull Inhalational
bull Transmucosal
ndash Sublingual
ndash Intranasal
bull Parenteral
ndash IM
ndash sub mucosal
ndash IV
3
Oral Sedation
Advantages
1 Almost universally accepted and the easiest method
2 Decreased incidence and severity of adverse reaction
3 Low cost
Disadvantages
1 Absorption is variable
2 Prolonged latent period(30 min)
3 Reversal of any unwanted effect is also difficult
4 Inability to readily lighten or deepen the level of sedation
5 Prolonged duration of action
Rectal Sedation
Advantages 1 Incidence and intensity of
drug related side effects is minimized
2 Drug absorption occurs from the large intestine directly into the circulation
3 The lack of a needle syringe or other equipment
4 The ease of administration
5 The low cost
Disadvantages
1 Inconvenience to the administrator amp pt
2 The variable absorption of drugs from the large intestine
3 The slow onset of action amp the relatively long duration of action
4 Inability to titrate the drug dosage
5 The inability to reverse the action of the drug the prolonged recovery
Intranasal sedation
Advantages
Rapid onset (10 ndash 15 min)
Simple amp relatively painless
Less pt cooperation is required
Absorbed directly into the C V S
Intranasal sedation
Disadvantages
1 Dependence on nasal mucous membrane
2 Shorter duration of action(40-60min)
3 Multiple dosage may be necessary
Drugs
Midazolam ndash 02mgkg
Sufentanil ndash 15 ndash 3 mcgkg
Ketamine ndash 3-6mg kg
Sublingual sedation
Advantages
1 Pt acceptance
2 Rapid onset
3 High bioavailability
Drugs
Oral Transmucosal Fentanyl Citrate (OTFC)
Intramuscular Sedation
Advantages
1 More rapid onset of action
2 Absorbed directly into the C V system
3 More reliable absorption of drug
4 Pt cooperation is not as essential
Disadvantages
1 Time factor ndash its 15 min latent period
2 Pt may not be willing to accept the injection
3 The prolonged duration of action(2-4 hrs more)
4 Possibility of injury to the tissues at the site of injection caused by either the drug or the needle
4
Sites of I M administration
1 Gluteal area
2 Vastus lateralis
3 Mid ndash deltoid area
Drugs
Diazepam
Midazolam
Hydroxyzine
Inhalation Sedation
Advantages
1 The onset of action is more rapid
2 Peak clinical level is achieved rapidly(3-5min) - permit titration
3 Administrator has complete control over the actions of the drug - safety feature
4 No significant over dosage
5 Flexible duration of action
6 Recovery time is rapid amp most complete
7 No injection is required
8 With N2O- O2 it is safe with very few side effects
Disadvantages
1 The initial cost of the equipment is high 2 The continuing cost of the gases is high 3 The equipment occupies considerable space 4 N2O is not a potent agent 5 A degree of cooperation is required from the pt 6 Chronic exposure to N2O is deleterious to the health of
dental personnel
Contraindications
1 Nasal obstruction 2 Cyanosis at rest 3 Poor cooperation 4 1st trimester of pregnancy 5 Fear of masks
I V Sedation
Advantages
1 The onset of action is the most rapid 2 The dosage may be titrated 3 Suitable level of sedation can be provided 4 The recovery period is shorter 5 Side effects are extremely uncommon 6 Control of salivary secretions is possible 7 The gag reflex is diminished 8 Effectively diminishes motor disturbances 9 Provides immediate access to CVS in emergency
Disadvantages
1 Venipuncture is necessary
2 Complication may rise at the site of the venipuncture
3 Monitoring must be more intensive
4 Recovery is not complete at the end of the procedure
5 Reversal of sedation is difficult
5
N2O-O2 (Relative Analgesia)
colorless sweet smelling gas
Pharmacokinetics
Absorption through pulmonary epithelium
It is approx 15 times as soluble as is nitrogen It replaces nitrogen in blood
It is carried in solution in plasma of the blood
It is not metabolized by the body
Elimination ndash majorndash lungs minor --- skin
perspiration urine and intestinal gas
Pharmacodynamics
Dose related
10 ndash 25 Lightheaded
Changes in visual amp auditory sensation
Tingling of hands amp feet
Suffusing warmth
Remote from the immediate environment
Reduced anxiety
25-50 max analgesic properties and aberration of vision hearing and proprioception mild drowsiness euphoria amnesia and increased sleepiness and dreams
35 conc will achieve maximum analgesia
bull CNS
ndash Cerebrum-primarily affected
ndash Safe but weak anesthetic agent
bull RESPIRATORY SYSTEM
ndash Increased Tidal and minute volumes
bull CARDIOVASCULAR SYSTEM
ndash 2 studies ndash decreased cardiac output
bull FETAL SYSTEMS
ndash Miscarriage in humans
bull OTHER SYSTEMS
ndash Depression of spinal reflexes increase muscle tone indicates stage of delirium
ndash Muscle rigidity-narcotics + nitrous oxide
ndash Nausea and vomitting - GIT
ndash HEMATOPOIESIS ----- prolonged exposure
Adverse reactions and toxicity
EMOTIONAL REACTIONS
DREAMS HALLUCINATIONS
No acute toxicity
Chronic toxicity ndash bone marrow
depression
PROCEDURE
Diffusion Hypoxia
Sevoflurane
A fluorinated derivative of isopropyl ether ndash synthesized in 1970
Potent anaesthetic agent with rapid uptake amp speedy recovery
Day-case surgery
Problem
Attaching vaporiser to any of the currently available machine
BENZODIAZEPINES
Diazepam 1961 lipid soluble
Uses-alcoholism epilepsy labor tetanus and cerebral palsy
- sedation and amnesia
- varieties of neurosis amp anxiety states
Pharmacokinetics
Orally Rectal IMIV or SC
Well absorbed through GIT
Excretion in urine
6
bull Pharmacodynamics
ndash Depress the brain stem reticular system and the limbic system thalamus and hypothalamus
ndash It is a centrally acting muscle relaxant Has anti-convulsant properties
Adverse reaction amp toxicity
ndash Confusion nausea headache increased appetite decreased salivation and jaundice Thrombophlebitis
ndash Rebound phenomenon
ndash Toxicity drowsiness confusion sleep and coma
Dosage Oral or Rectal ndash 02-05mgkg
Maximum single dose 10mg
IV- 025mgkg
Supplied Tablets 2 5 10 mg
Suspension ndash 5mg
Midazolam Water soluble ndash non-irritant
Oral IM IV
Metabolism- liver
Onset IV 3 -5mins
oral 20 ndash 30mins
Oral administration anxious patients requiring relatively short dental procedure
No rebound phenomenon
Better anxiolysis amp amnesia (retrograde amnesia)
Adverse effects Respiratory depression
dose dependant apnea
Dosage Oral ndash 025 to 1mgkg to maximum single dose 20mg
IM ndash 01 to 015mgkg to a maximum of 10mg
IV ndash slow IV
Supplied Syrup ndash 2mgml
Injectable ndash 1mgml amp 5mgml vials
Flumazenil specific benzodiazepines antagonist
selectively inhibits CNS effects
IV administration amp not recommended below 18yrs of age
02mg over 15 seconds after 45seconds 02mg then after 60seconds to maximum of 1mg
Sedative-Hypnotics
Barbiturates First truly effective drugs for the management of anxiety Generalized CNS depressants Produce dose dependent effects
Sedation ---- sleep ---- GA ---- coma
Suppress the CNS and result in sedation and amnesia Advantages
Rapid onset and short duration Disadvantages
no analgesic effect and possible hypotension Must be used with caution in trauma patients because they may cause
apnea and hypoventilation
DOSE Pentobarbital Sodium 100mg Secobarbital Sodium 100 to 200mg Children 30 to 100mg
bull Chloral Hydrates (Mickey Finn Knock out drops ) First synthesized in 1832 first member of the hypnotic group of drugs
Widely used as conscious sedation agent
Properties
Unpleasant taste
Nausea vomiting
Quite irritating to skin and to mucous membranes
GI irritation
Dosages Individualized for each patient 25 ndash 50mgkg
maximum of 1g
Supplied oral capsule ndash 500mg
oral solution ndash 250 amp 500mg5ml
Rectal suppositories ndash 324 amp 648mg
Narcotics
Do produce sedation amp euphoria greater in children
LA is required but dose should be decreased
Meperidine Synthetic opiate agonist
Very water soluble
Orally SC IM or IV
Peak effect by oral 1 hr amp lasts upto 4 hrs
Adverse reactions
-Seizures
-Extreme caution in hepatic or renal diseases or history of seizures
7
Dosage Oral SC or IM ndash 1to 22mgkg not to exceed 100 mg
Supplied Oral Tablets ndash 50 amp 100mg
Oral Syrup ndash 50mgml
Parental solution ndash 25 50 75 amp 100mgml
Fentanyl
Synthetic opiate narcotic analgesic
Very potent 01mg = 10mg Morophine75mg Meperidine
Pharmacokinetics
IV IM SM
Metabolized in liver Excreted in urine
Fentanyl Onset ndash 7 to 15mins
Duration ndash 1 to 2 hrs
Pharmacodynamics
Respiratory depression RR but returns to normal rapidly Tidal volume amp response to co2 depressed for extended period
Apnea
Less emetic than meperidine
NOT RECOMMENDED IN CHILDREN BELOW 2yrs
Dosage 0002 to 0004mgkg
Supplied 005mgml in 2 amp 5ml ampoules
Reversal drug Naloxone
Semisynthetic opiate antagonist
No agonist activity
Onset 2 to 5mins SC or IM amp 1 to 2mins IV
Reversal 45mins
Pt should be kept under continual surveillance
Adverse reaction nausea vomiting sweating hypotension hypertension ventricular tachycardia fibrillation
Dosage IV SC IM 001mgkg then 01mgkg every 2- 3mins maximum 2mg
Supplied 002 004 1mg solutions
Antihistamines
Hydroxyzine
Oral or IM
Effect ndash 15 ndash 30mins
Half-life ndash 3 hrs
Uses
To relieve anxiety
Used as an anti-histamine
Used to control nausea and vomiting including that associated with motion sickness and pregnancy
Adverse reaction dry mouth drowsiness hypersentivity
Dosage Oral ndash 1 to 2mgkg
IM ndash 11mgkg
Promethazine Oral or IM Onset 15 to 60mins Duration 4 to 6 hrs Uses
To prevent and treat nausea and vomiting associated with motion pregnancy or surgery
Produces sedation and reduce swelling pain and trismus
Lower seizure threshold Adverse reaction dry mouth blurred vision thickening of bronchial secretions Dosage OralIM ndash 05-11mgkg
maximum 25 mg
Diphenhydramine
Oral IM IV
Onset -1hr
Duration ndash 4 to 6 hr
Metabolized in liver
Adverse reaction disturbed coordination thickening of bronchial secretions
Dosage Oral IM IV ndash 1 to 15mgkg
maximum 50mg
Tranquilizers
Major tranquilizer antipsychotic produce calmness control symptoms of psychoses cause reversible extra pyramidal symptoms and do not tend to cause habituation
Minor tranquilizer antianxiety agents also cause calmness do not cause extrapyramidal symptoms Used in conditions like nervous tension and mild depression
8
Classification
Antipsychotics
Phenothiazine derivatives
Chlorpromazine promazine
Butryophenones
Haloperidol
Rauwolfia alkaloids
Reserpine
Antianxiety drugs
Propyl alcohol derivatives
Meprobamate
Benzodiazepine derivatives
Diazepam
Miscellaneous compounds
Hydroxyzine
Meprobamate
White crystalline powder slightly bitter in taste
Only administered orally
Peak blood concentration ----1 to 3hrs
10 ---------excreted unchanged Rest --- excreted as a oxidized derivative or as a glucoronide
Uses
To relieve day time anxiety
Induce sleep in insomniacs
To reduce anxiety associated with dental treatment
Anti-convulsant ndash petit mal epilepsy
Adverse reaction leucopenia acute non-thrombocytopenic purpura ecchymoses eosinophilia edema adenopathy
Dosage Childrengt 6yrs 100 to 200mg
Not recommended for children under 6yrs
Monitoring during sedation
1 Pulse
2 Blood pressure
3 ECG
4 Respiration
5 Temperature
Pulse
Manual Electronic
bull Radial Brachial
bull Facial labial
Blood pressure
ndash Stethoscope amp sphygmomanometer
ndash Automatic devices
ndash Direct cannulation of an artery ndash very accurate
Electrocardiograph
Heart rate rhythm myocardial function
9
Respiration
ndash Monitoring respiratory rate
ndash Observing the rise amp fall of the chest wall
ndash Observing the color of mucous membrane
ndash Observing the inflation amp deflation of the reservoir bag
Devices for monitoring respiration
1 The Precordial pretracheal stethoscope
2 The esophageal stethoscope
ndash Respiratory rate
ndash Heart rate
ndash Any abnormal sounds
Pulse Oximeter
ndash Oxygen saturation
ndash Heart rate
ndash Oxisensor site
ndash Fingers
ndash Toe
ndash Ear lobe
Mechanism
Oxygenated Hb ndash red light
Deoxygenated Hb- infrared light
Tissue pressure from arterial pulse (plethysmography)
Advantages
ndash Safe amp noninvasive
ndash Simple to use
ndash Information is rapidly available for clinical decision
ndash Indirectly indicates respiratory adequacy
Disadvantages
ndash Finger probes can get dislodged
ndash Emitted light source may cause burning
ndash Non reusable probes are expensive
ndash Does not directly determine airway patency
Capnography
1 The presence absence of air flow
2 Indicates depth amp adequacy of respiration
3 Continues analysis of the co2 content of the respired air ndash indicates respiratory adequacy
Temperature
ndash Disposable nondisposable thermometer
ndash Esophageal rectal temp probe
10
Discharge criteria
Cardiovascular function is satisfactory amp stable
Airway patency is uncompromised amp satisfactory
Pt is easily arousable amp protective reflexes intact
State of hydration is adequate
Pt can talk if applicable
Pt can sit unaided if applicable
Pt can ambulate with minimal assistance if applicable
Presedation level of responsiveness achieved
Responsible individual is available
1
PULP THERAPY OF VITAL TEETH
DR MITAKSHARA NIRWAN
Contents
Indirect pulp capping
Direct pulp capping
Medications amp materials used in pulp capping
Pulpotomy
MTA
Apexogenesis
INDIRECT PULP CAPPING
Pieter Van Forest - first to speak about root canal therapy
Glove designed instruments that could prepare a canal to a certain size and taper(1910)
Indirect pulp capping is defined as a procedure where in small amount of carious dentin is retained in
deep areas of cavity to avoid exposure of pulp followed by placement of a suitable medicament and
restorative material that seals off the carious dentin and encourages pulp recovery (Ingle)
A procedure in which only the gross caries is removed from the lesion and the cavity is sealed for a
time with a biocompatible material (McDonald)
Objective of indirect pulp capping
These were given by Eidelman in 1965
bull Arresting the carious process
bull Promoting dentin sclerosis
bull Stimulating formation of tertiary dentin
bull Remineralization of carious dentin
Layers of Carious Dentin Indications of Indirect Pulp Capping
History
Mild pain associated with eating
Negative history of spontaneous extreme pain
Clinical Examination
Deep carious lesion which are close tobut not involving the pulp in vital primary or young
permanent teeth
No mobility
Nominal pulp inflammationdefinite layer of affected dentin after removal of infected dentin
Radiographic examination
Normal lamina dura amp PDL space
No radiolucency around the apices
2
Contraindications of Indirect Pulp Capping
History
Sharp penetrating pulpalgia
Prolonged spontaneous pain especially at night
Clinical examination
Mobility of tooth
Discoloration of tooth
Negative reaction of electric pulp testing
Radiographic examination
Definite pulp exposure
Break in the lamina dura
Radiolucency around the apices
Widened PDL space
Treatment procedure
Sequelae of Indirect Pulp Capping Three distinct types of new dentin formation take place
1 Cellular fibrillar dentinmdashfirst 2 months
2 Globular dentinmdash3 months
3 Tubular dentin (uniform mineralized dentin)
bull 15th of reparative dentin formation begins in less than 30 days
bull After 3 months 01 mm is formed
DIRECT PULP CAPPING Defined by Kopel (1992) as the placement of a medicament or non medicated material on a pulp that
has been exposed in course of excavating the last portions of deep dentinal caries or as a result of
trauma
Objective
To create new dentin in the area of the exposure and subsequent healing of the pulp
Rationale
achieve a biologic closure of the exposure site by deposition of hard tissue barrier (dentin bridge)
between pulp tissue and capping material thus walling off the
INDICATIONS
Small mechanical exposure
Easily controlled haemorrhage
Bright red haemorrhage
True pinpoint exposure
CONTRAINDICATIONS
Severe toothache at night
Spontaneous pain
Tooth mobility
Radiographic appearance of pulp periradicular de- generation
Excess of hemorrhage at the time of exposure Serous exudate from the exposure
Externalinternal root resorption
Swellingfistula
Histological Changes after Pulp Capping
These were illustrated be Glass and Zander in 1949
After 24 hours Necrotic zone adjacent to calcium
hydroxide paste is separated from healthy pulp
tissue by a deep staining basophilic layer
After 7 days Increase in cellular and fibroblastic
activity
After 14 days Partly calcified fibrous tissue lined by
odontoblastic cells is seen below the calcium
proteinate zone disappearance of necrotic zone
After 28 days Zone of new dentin
3
Medications and Materials Used for Pulp Capping Calcium hydroxide
Corticosteroids amp antibiotics
Inert materials
Collagen fibers
4-META adhesive
Direct bonding
Isobutyl cyanoacrylate
Denatured albumin
Mineral trioxide aggregate
Laser
Bone morphogenic protein
PULPOTOMY
Finn (1995) defined it as the complete removal of the coronal portion of the dental pulp
followed by placement of a suitable dressing or medicament that will promote healing and
preserve vitality of the tooth
American Academy of Pediatric Dentistry (1998) defined pulpotomy as the amputation of
affected infected coronal portion of the dental pulp preserving the vitality and function of the
remaining part of radicular pulp
Objectives
bull Removal of inflamed and infected coronal pulp at the site of exposure thus preserving the vitality of the
radicular pulp and allowing it to heal
bull Maintain the tooth in the dental arch
Rationale
bull Radicular pulp is healthy and capable of healing after surgical amputation of the infected coronal pulp
bull Preserves vitality of the radicular pulp
bull Maintains tooth in a physiologic condition
Indications of Pulpotomy bull Mechanical pulp exposure in primary teeth
bull Teeth showing a large carious lesion but free of radicular pulpitis
bull History of only spontaneous pain
bull Hemorrhage from exposure sites bright red and can be controlled
bull Absence of abscess or fistula
bull No interradicular bone loss
bull No interradicular radiolucency
Contraindications of Pulpotomy bull Persistent toothache
bull Tenderness on percussion
bull Root resorption more than 13rd of root length
bull Large carious lesion with nonrestorable crown
bull Highly viscous sluggish hemorrhage from canal orifice which is uncontrollable
bull Medical contradictions like heart disease immuno compromised patient
bull Swelling or fistula
bull External or internal resorption
bull Pathological mobility
bull Calcification of pulp
Classification of pulpotomy
4
Formocresol Pulpotomy
Iby BUCKLEY in 1904
Sweet (1930) Formulated multi visit technique
Doyle (1962) Advocated 2 sitting procedure (complete devitalization)
Spedding (1965) Gave 5 minute protocol (partial devitali- zation)
Venham (1967) Proposed 15 seconds procedure
Current concept uses 4 minutes of application time
Composition of formocresol Buckleyrsquos Formula
bull Cresol ndash 35 percent
bull Glycerol ndash 15 percent
bull Formaldehyde ndash 19 percent
bull Water ndash 31 percent
Mechanism of Action
It prevents tissue autolysis by bonding to the proteins Bonding is of peptide groups of side chain amino acids and is a reversible process accomplished without
changing the basic structure of protein molecules
Histological Changes
bull Demonstrated by Mass and Zilbermann11 in 1933 and also by Massler and Mansokhani in 1959
bull Immediately the pulp becomes fibrous and acidophillic
bull Seven to fourteen days Three zones appear
a broad eosinophilic zone of fixation
b broad pale-staining zone of atrophy with poorcellular definition
c broad zone of inflammation extending apically into normal pulp tissue
bull One yearndash Progressive apical movement of these zones with only acidophillic zone left at the end of 1 year
Modified Formocresol Pulpotomy
Used by TRASK(1972)
The technique is identical to that described for primary teeth except that the formocresol pellet is
sealed permanently in the tooth
Two-visit Devitalization Pulpotomy
Indications
bull There is evidence of sluggish bleeding at the amputation site that is difficult to control
bull Pus in the chamber but none at the amputation site
bull There is thickening of the PDL
bull History of pain
Contraindications
bull Nonrestorable tooth
bull Tooth with necrotic pulp
5
Glutaraldehyde Pulpotomy
It was first suggested by S Gravenmade Introduced by Kopel in 1979
Mechanism of Action
bull Glutaraldehyde produces rapid surface fixation of the underlying pulpal tissue
bull A narrow zone of eosinophilic stained and compressed fixed tissue is found directly beneath the area of application which blends into vital normal appearing tissue apically
bull With time the glutaraldehyde fixed zone is replaced by macrophagic action with dense collagenous tissue thus the entire root canal tissue is vital
Cvekrsquos Pulpotomy
bull This is also called as calcium hydroxide pulpotomy or young permanent partial pulpotomy
bull This was proposed by Mejare and Cvek16 in 1978
bull Indicated in young permanent teeth where the pulp is exposed by mechanical or bacterial means and the
remaining radicular tissue is judged vital by clinical and radiographic criteria whereas the root closure is
notcomplete
MINERAL TRIOXIDE AGGREGATE (MTA) Torabinejad described the physical and chemical properties of MTA in 1995
It is ash colored powder made primarily of fine hydrophilic particles of
1 tricalcium aluminate
2 tricalcium silicate
3 silicate oxide
4 tricalcium oxide
5 bismuth dioxide
Hydration of the powder results in a colloidal gel composed of calcium oxide crystals in an amorphous
structure This gel solidifies into a hard structure in less than three hours
PROPERTIES OF MTA
It is biocompatible material and its sealing ability is better than that of amalgam or ZOE
Initial pH is 102 and set pH is 125
The setting time of cement is 4 hours
The compressive strength is 70 MPA which is comparable with that of IRM
Low cytotoxicity ndash It presents with minimal inflammation if extended beyond the apex
Mineral trioxide aggregate (MTA) has demonstrated the ability to induce hard-tissue formation in
pulpal tissues and it promotes rapid cell growth
APEXOGENESIS
It is defined as the treatment of a vital pulp by capping or pulpotomy in order to permit continued
growth of the root and closure of the open apex
Rationale
Maintenance of integrity of the radicular pulp tissue to allow for continued root growth
Indications
bull Indicated for traumatized or pulpally involved vital permanent tooth when root apex is incompletely formed
bull No history of spontaneous pain
bull No sensitivity on percussion
bull No hemorrhage
bull Normal radiographic appearance
Contraindications
bull Evidence that radicular pulp has undergone degenerative changes
bull Purulent drainage
bull History of prolonged pain bull Necrotic debris in canal
bull Periapical radiolucency
6
1
Gupta A Dhingra R Chaudhari P Gupta A
Department of Paedodontics and Preventive Dentistry Faculty of Dental Sciences SGT University Gurgaon Haryana India
Journal of Indian Society of Pedodontics and Preventive Dentistry
Volume 35 I Issue 3 I July-September 2017
A COMPARISION OF VARIOUS MINIMALLY
INVASIVE TECHNIQUES FOR THE REMOVAL
OF DENTAL FLUOROSIS STAINS IN
CHILDREN
DR MITAKSHARA NIRWAN
CONTENTS
bull Introduction
bull Aims
bull Materials and Methods
bull Results
bull Discussion
bull Conclusion
bull Critical analysis
bull References
INTRODUCTION
bull Dental fluorosis is a developmental disturbance of dental enamel caused by
successive exposure to high concentrations of fluoride during tooth
development
bull Various methods of therapy are advocated for the treatment of fluorosis -
stained teeth which range from invasive ceramic veneer bonding restorations
to abrasive chemical treatments
bull The combination of dental bleaching techniques and microabrasion appears
as an excellent conservative solution to reestablish health in fluorosis
affected teeth
AIMS
bull The aim of the study was to evaluate and compare the effectiveness of
minimally invasive techniques for the removal of dental fluorosis
stains in children in vivo
MATERIALS AND METHODS
Patients visiting the department of Pedodontics and Preventive dentistry
Faculty of Dental Sciences SGT University Gurgaon
bull Sample size 90 patients
bull Age group 10 -17 years
bull Caries cracks or periodontal
disease on anterior teeth
bull Abscess draining sinus
cellulitis
bull Non vital teeth
hypersensitive exposed
crevices
bull Orthodontic appliance
bull Past history of bleaching
bull At least two permanent
maxillary anterior teeth
bull TSIF of score 4
bull Free of systemic diseases
Inclusion criteria Exclusion criteria
2
Groups
Group A In office bleaching with 35 hydrogen peroxide( Pola Office
Bleaching kit) activated by light emitting diode (LED) bleaching unit
(35 HP)
Group B Enamel microabrasion (EM) (PREMA Enamel Microabrasion
System) followed by in-office bleaching with 44 carbamide peroxide
gel (EM)
Group C In-office bleaching with 5 sodium hypochlorite (5
NaOCl)
A baseline colour evaluation was done by taking digital photograph of
the maxillary anterior teeth
RESULTS
Group 1
Colour stability
Group 2 Group 3
Tooth sensitivity
Tooth sensitivity values were taken before the treatment
which was compared to immediate postoperative and follow
up visits It was checked using an electric pulp tester
maximum
moderate
least
immediately
group 2
group 1
group 3
1 month
group 2
group 1
group 3
3 month
group 2
group 1
group 3
Patient satisfaction score
Satisfaction was assessed on visual analog scale
Range 1 to 5
Groups percentage of patients
who were satisfied with
the treatment
Number of patients
who reported slight
reappearance of colour
Group 1
90
7
Group 2
83
8
Group 3
73
7
3
Number of Appointments
Groups One sitting Two sittings Three
sittings
Group 1
25
4
1
group 2
26
3
1
Group 3
30
0
0
DISCUSSION
bull Hydrogen peroxide is capable of penetrating the tooth osmosis and through porosities and cracks subsequently acting directly on the pigmented molecules
bull Gurgan et al investigated 3 different light systems and found out that diode laser system with gave best tooth whitening and least tooth sensitivity
bull In the EM group the surface reflects and refracts light from the surface in such way that mild imperfections in underlying enamel are camouflaged While the highly polished surface of enamel enhances the aesthetic appearance
bull Train et al and Loguercio et al also had the similar results in their studies with EM mild fluorosis showed best results moderate showed moderate results while it had little effect on severe fluorosis
bull NaOCl was only effective on mild stains while moderate and severe
stains could only be lightened to quite an extent but could not be
completely removed
bull When NaOCl comes in contact with hypomineralized and discoloured
enamel it degrades and removes the chromogenic organic material
located on the enamel surface
CONCLUSION
bull It was concluded that esthetic appearance of teeth mild fluorosis can
be achieved by bleaching and microabrasion But in cases of
moderate fluorosis a combination of any of theses modalities can be
used
bull As no special maintenance precautions are required these maybe be
considered as an interesting alternative to conventional operative
treatment
bull Focuses on only TSIF of 4
bull Electric pulp testing is not the
right method to check for
sensitivity
bull Tooth Sensitivity changes
from person to person
bull Food habits can cause
staining of the teeth
bull Minimally invasive
bull Cheaper to veneers
bull Minimal loss of tooth structure
bull 4 parameters checked for the success of treatment
bull Inclusion of specific score of fluorosis for comparing the results
bull Maximum 3 appointments needed
CRITICAL ANALYSIS
Pros Cons
REFERENCES
bull Gurgan S Cakir FY Yazici E Different light-activated in officebleaching
systems Lasers Med Sci 201025817-22
bull Train TE McWhorter AG Seale NSWilson CF Guo IY Examination of
esthetic improvement and surface alteration following microabrasion in
fluorotic human incisors in vivoPediatr dent 199618353-62
bull Loguercio AD Correia LD Zago C Tagliari D Neumann E Gomes OM et al
Clinical effectiveness of two microabrasion materials materials for the
removal of enamel flurosis stains Oper Dent 200732531-8
4
6
Variationshellip Hand over mouth with airway restricted Towel over mouth
Towel over mouth with airway restricted
Body
Papoose board
Triangular sheet
Pedi wrap
Bean Bag
Safety belt
Extremities
Posey straps
Velco straps
Towel amp Tape
Head
Forearm support
Plastic bowl
Head positioner
Mouth
Tongue blades
Mouth Prop
Bite blocks
Positive Stabilization Mouth
Tongue blade open mouth wide prop Molt mouth prop
Rubber bite blocks
Extremities
Posey Strap
Head
Body
Papoose board
Pedi-wrap
7
1
Impact of Handheld Devices on
Children An Evaluation of Usage amp
Dependency Behaviour
0092
DR MITAKSHARA NIRWAN
Handheld devices
A handheld device is a pocket size
computing device with a display
screen and inputoutput interface like
an external or touchscreen keyboard
For example- smartphones tablet
computers handheld videogame
consoles
Haruki Murakami
ldquoCell Phones are so
convenient that they have
become an inconveniencerdquo
Introduction
The most famouscommonly used and easily accessible type of gadgets are
lsquoHandheld devicesrsquo They are as popular in children as they are in adults
The access and ownership of these devices amongst children has grown
substantially in the past decade Concerns exist regarding excessive usage
and the impact of frequent consumption of mobile media on their health and
behaviour
Aims and Objective
This objective of this study was to asses the level of use of handheld
devices among children aged 0-12 years and their positive and negative
impacts on them It further describes the dependency of these devices
and the behavioral problems associated with it
Materials and Methods An online survey was conducted and a self administered questionnaire
was prepared specially for the parents which included a total of 15
questions regarding the usage and dependency of the device
A total of 100 responses were collected from parents who had children
aged 0-12 years who used these devices on daily basis
2
Level of Usage (Q 123)
Results Purpose (Q7)
Improved
communication and
learning
Using more than
one type of
device
Helped in
Speech
Positive Impacts -
(Q58 amp 9)
P value 0003(s) P value-0007 P value-0006(s)
Reduced parent-
child interaction Disrupted sleep Lack of motivation for academics
Negative Impacts (Q81213)
P value-0001(s) P value-0002(s) P value-0006
Time when children use
the device the most
Isolation of the
child Behavioral impact when gadget is
taken back
Dependency
Behaviour (Q10111415)
P value-002(s) P value 002(s) P value-044
This study was done to evaluate the level of usage of handheld devices and their impact
on the children aged 0-12 years The questionnaire was made such that it asked both the
positive and negative impact and further included the questions regarding the
dependency
784 children had access to smartphone and 17 used tablets
The most common age group in which the devices was used the most was 5-8 years
followed by 9-12 followed by 0-4 (Arlinda et al 2019 )
Another study done by (Rachel Bedford et al 2016) concluded increase usage of mobile
phones 5122 in 6ndash11 monthshy olds through to 9205 by 25ndash36 months
745used these devices several times a day out of which 539 used it for more than
one hourday 255 used it for less than one hour and 206 for more than 2 hours
Various studies follow the same recommendation given by AAP to limit the duration of
gadget amongst children
Discussion
3
Improve of Cognitive Skills
Amongst the positive impacts most parents have answered that the usage of these
devices has helped their child communicate and learn better and it has showed significant
results According to (Sundus M 2018)These devices improve the cognitive skills and
develop their learning skills fasterThe competition skills also get better It gives time for brain to think and process information better Another study which supports this (LF
Jonathan et al 2016)
Motor Physical Exercise
This study has shown that children like to use more than one type of device
sometimesUsing these devices improve fine motor skillshand eye coordination and
hands and fingers become more efficient (Srinahyanti et al 2019) (Sundus M 2018)
Speech Improvement
392 Parents say that maybe usage of the devices has helped improve speech in their
children but Various studies show otherwise as most of them shows that usage of handheld
devices causes delay of speech (Srinahyanti et al 2019)
Reduced parent child interaction
The negative impacts are more when compared to the positive ones Usage of gadgets
has resulted in reduced parent child interaction Less face to face interaction can
cause detachment from family members and value which in turn also causes isolation
of the child as he is more comfortable with the gadget (M Suhana-2017)
Sleep Disorders
This study shows that most parents have agreed that usage of these devices does
cause disruption of sleep Various studies have shown that children get fewer hours of
sleepdrowsiness during the day and dramatic increase in day time sleep because of
the screen usage (Acc to National Sleep Foundation) ( Cain N et al 2010)
In this study most number of parents have
agreed that their children might be dependent on
these devices and also had showed restless and
violent behavior if the gadget is snatched from
them
Most number of kids (667) are heavily
dependent as they like to use the device during
their meal time
Various other studies have assessed the screen
time dependency and have concluded that
various kids suffer from SDD
Conclusion The study conclusively shows that the impact of handheld devices is akin to the
importance of table salt in our meals most significant for our growth and
development in moderate amounts and hazardous in excess The negatives clearly
outweigh the positives with the latter too few and far in between This study also
points towards further extensive research on the subject because we need to find ways and also educate parents to optimise the role of these devices in their
childrenrsquos life taking advantage of their positive attributes and minimising their
negative ones
References 1Wahyuni AS Siahaan FB Arfa M Alona I Nerdy N The Relationship between the Duration of Playing
Gadget and Mental Emotional State of Elementary School Students Open Access Maced J Med Sci
20197(1)148ndash151
2Sundus M Department of Computer Science Lahore-The Impacts of using Gadgets on ChildrenJournal of Depression and Anxiety 2018vol 7(1)296
3Amawi SO Subki AH Khatib HA et al Use of Electronic Entertainment and Communication Devices Among
a Saudi Pediatric Population Cross-Sectional Study Interact J Med Res 20187(2)e13
4Julia ldquoHandheld Screen Time Linked with Speech Delays in Young Childrenrdquo Present Pediatric Acad Soc
Meet 2017
5C Rowan ldquoThe Impact of Technology on Child Sensory Motor Developmentrdquo 2003
6Impact of media use on children and youth Paediatr Child Health 20038(5)301ndash317
7Naik SV Children and their gadgets A pedodontist perspective Int J Oral Health Sci 2018857-8
8Roberts DF Foehr UG Rideout V Generation M Media in the lives of 8‐18 year‐olds A Kaiser Family
Foundation Study 2005
9Arya K Time spent on television viewing and its effect on changing values of school going children Anthropologist 20046269‐71
10 Lerner C Barr R Screen Sense Setting the Record StraightResearch‐Based Guidelines for Screen
Use for Children Under 3 Years Old Early learning project at Georgetown university 2014 p 1‐10
11SrinahyantiYasaratodo Wau Imelda Free Unita Manurung Nur Arjani-Influence of gadget A positive
and Negative Impact of Smartphone Usage for Early Child2019
4
THANK YOU
1
Morankar Rahul Aditi Kapur Krishan Gauba Ashima Goyal
MANAGEMENT OF ENDODONTIC INSTRUMENT SEPARATION IN
PRIMARY TEETH
CASE REPORT
Journal of South Asian Association of Pediatric Dentistry 2020
DR MITAKSHARA NIRWAN
bull Introduction
bull Aims amp Objectives
bull Case report
bull Discussion
bull Conclusion
bull Pros amp Cons
bull References
CONTENTS
Separation of endodontic instrument is an unexpected complication and its prevalence is not known It is a common belief among the dental professionals that rotary nickelndashtitanium (NiTi) instruments separate more frequently than stainless steel hand instruments
However literature revealed that in permanent teeth the reported prevalence of separated endodontics manual instruments is in the range of 07-74 whereas for rotary NiTI instruments it is
approximately 04-5
Fractured root canal instruments may include endodontic files Gates Glidden burs finger spreaders
and paste fillers
INTRODUCTION
The aim of this study is to describe the management strategies for endodontic
instrument separation in a root canal of primary teeth with emphasis on factors
requiring consideration in different clinical situations
AIMS amp OBJECTIVES
CASE 1
A 6-year-old male child reported with the chief complaint of spontaneous toothache in mandibular left second primary molar since few days It has aggravated following dental treatment at a private dental clinic Clinical examination revealed an underprepared access cavity with 75 and incomplete caries removal
which was sealed with glass ionomer cement
An intraoral periapical radiograph revealed a separated instrument of about 6ndash7 mm size in the distal root
2
The separated instrument was lodged firmly in distobuccal root canal 2ndash3 mm below the cementoenamel junction The instrument was bypassed successfully with no 15 and no 20 H-files but attempts for its retrieval were not successful
GatesndashGlidden (GG) drills no 2 (07 mm) and no 3 (09 mm) were used to drill around the instrument after which it was retrieved successfully using no 25 H-file
All the canals were instrumented till size 30 k-file followed by obturation with metapex and restoration with glass ionomer cement amp followed by placement of a crown and loop space maintainer for missing 74 The instrument retrieved was a manual reamer measuring 6 mm in length
The patient was asymptomatic since then and is under regular follow-up
CASE 2
A 5-year-old female child reported with the chief complaint of spontaneous toothache in mandibular left second
primary molar Clinical examination revealed deep occlusal caries with fractured lingual wall and pain on
percussion An intraoral periapical radiograph revealed caries involving pulp without any furcation or periapical
area of rarefaction and pulpectomy was planned
All the canals were enlarged using NiTi rotary files with a 4 taper operating at 500 rpm with minimum torque
setting An orifice opener [(0825 19 mm) of 8 taper size 25 length 19 mm] and nos 0420 file was used for
instrumentation of root canal This was followed by file nos 0425 which got separated in the distobuccal root
canal The radiograph confirmed a separated instrument of length 3ndash4 mm in the middle third of the root canal
The instrument was bypassed with no 15 k-file but could not get retrieved As instrument separation had occurred with 0425 file the involved root canal was sufficiently debrided before separation and the level of instrument separation was at the mid-root region so it was decided to obturate and seal this tooth with
periodic follow-ups instead of immediate extraction All other canals were enlarged till size 0430 in the sequential manner followed by obturation using metapex and placement of stainless steel crown
3
CASE 3
A 5-year-old female child has complaint of mild intermittent pain with primary mandibular left first molar She
had undergone pulpectomy treatment for the same during which an instrument separation has occurred in
the mesiobuccal root canal by a resident doctor
A radiograph revealed a separated instrument of about 4 mm in size lodged in the apical third but within the
confines of the mesial root An attempt was made for its retrieval but was unsuccessful The extraction of the
involved tooth was carried out under local anesthesia followed by a band and loop space maintainer
CASE 4
A 7-year-old male child reported with a chief complaint of mild intermittent pain on food lodgment with the primary mandibular right first and second molars The patient had a history of dental treatment at a private
dental clinic few months back which he did not continue further
Clinical examination revealed glass ionomer restoration with 85 and proximal caries with 84 leading to food lodgment An intraoral periapical radiograph with 85 revealed empty root canals with a separated
instrument of about 3ndash4 mm size beyond the apex of mesial root close to the developing succedaneous premolar
4
DISCUSSION
Stainless steel files usually separate fracture due to the excessive amounts of torque and overuse or the
preexisting distortion of the instrument whereas in NiTi rotary files it is a combined result of torsional stress and cyclic fatigue
Therapeutic options for the management of separated endodontic instruments include no intervention nonsurgical (orthograde conservative) management surgical management and tooth extraction
Use of ultrasonic scaler Masserann technique Endo extractor and Cavi-Endo ultrasonic instruments are some of the methods popular for retrieval of a separated endodontic instrument in the permanent tooth
In case 1 a 6-mm-long manual reamer was retrieved successfully with the use of GG drill using a manual file and copious irrigation which is the most desired treatment outcome
In case 2 the retrieval of separated rotary file lodged in the middle third of the root canal was unsuccessful in spite of multiple attempts It was therefore managed with routine obturation followed by restoration to maintain the tooth in its physiological functional state It was kept under close periodic follow-up at least
every 3 months This treatment option should be encouraged where it is possible to follow up the patient clinically and radiographically at close periodic intervals as there is the possibility of instrument escaping
into bone due to physiological root resorption
In cases 3 and 4 an instrument has separated in the apical root portion
In case 3 it was within the root canal and thus an attempt was made for its retrieval which was
unsuccessful It was therefore extracted to prevent the fractured instrument from getting exposed in the bone following resorption as there is no accurate and consistent established age for initiation of resorption in primary teeth known per se
In case 4 an immediate extraction of involved tooth was carried out as the separated instrument was beyond the apex of the primary tooth root
Age of the child clinical signs and symptoms and amount of root resorption are the factors which can also influence the management of separated instrument in primary teeth
Moreover if an instrument has separated after initial cleaning and shaping of root canal maintaining a tooth is not a problem as clinical signs and symptoms are not anticipated and the good prognosis is expected
However if an instrument has separated early during the initial cleaning and shaping of the root canal clinical symptoms may compromise the prognosis
Therefore these factors should be kept in mind while planning a suitable management strategy to avoid or at least reduce the burden of extraction and wear of space maintainer for longer period
5
CONCLUSION
The management and prognosis of a primary tooth with a separated instrument is
dependent on the level of instrument fracture within the root age of the child root
resorption and clinical signs and symptoms of the involved tooth
Different management approaches can be tried depending on clinical situations keeping
in mind benefits vs risks in preserving the tooth
PROS amp CONS
PROS
The entire procedure is given
by step by step
Well descriptive xrays and
photographs
CONS
Medical history has not been
given
REFERENCES
1 TOMER ANIL K ET AL ldquoBROKEN FILE RETRIEVAL PUZZLE IN ENDODONTICSrdquo
(2016)
2 SHENOY A MANDAVA P BOLLA N ET AL A NOVEL TECHNIQUE FOR REMOVAL OF
BROKEN INSTRUMENT FROM ROOT CANAL IN MANDIBULAR SECOND MOLAR
INDIAN J DENT RES 201425(1)107ndash110
3 PATEL J MORAWALA A TALATHI R ET AL RETRIEVAL OF A BROKEN INSTRUMENT
FROM ROOT CANAL IN PRIMARY ANTERIOR TEETH UNIV RES J DENT 20155(3)203ndash
206
4 MORANKAR R GOYAL A GAUBA K ET AL MANUAL VERSUS ROTARY
INSTRUMENTATION FOR PRIMARY MOLAR PULPECTOMIES - A 24 MONTHS
RANDOMIZED CLINICAL TRIAL PEDIAT DENT J 201828(2)96ndash102
5 KASHYAP NILOTPOL (2018) RETAINING PRIMARY MOLARS WITH INSTRUMENT
SEPERATION A CASE REPORT AND CLINICAL GUIDE
6
1
IMPACT OF 6 CITRIC ACID AND ENDOACTIVATOR AS IRRIGATION ADJUNCTS ON OBTURATION QUALITY AND PULPECTOMY OUTCOME IN
PRIMARY TEETH
NEETU JAIN SHALINI GARG ABHISHEK DHINDSA SAKSHI JOSHI HARJOY
KHATRIA
PEDIATRIC DENTAL JOURNAL 2019 29
1
DR MITAKSHARA NIRWAN
CONTENTS
bull INTRODUCTION
bull AIMS amp OBJECTIVES
bull CASE REPORT
bull RESULTS
bull DISCUSSION
bull CONCLUSION
bull PROS AND CONS
bull REFERENCES
2
INTRODUCTION
bull ENDODONTIC THERAPY IN PRIMARY TEETH INVOLVES DISINFECTION OF THE ROOT CANAL
SYSTEM AND ITS OBTURATION WITH RESORBABLE PASTE
bull THE CONTENTS OF ROOT CANAL ALONG WITH SMEAR LAYER ARE EXPECTED TO BE REMOVED
DURING THE BIOMECHANICAL PREPARATION
bull IN VITRO AND CLINICAL DOCUMENTS HAVE INDICATED THAT MECHANICAL PREPARATION OF
THE CANAL LEAVES LARGE PORTIONS OF THE CANAL WALLS UNDEBRIDED AND COMPLETE
REMOVAL OF THE BACTERIA BY THIS MECHANICAL PROCEDURE ALONE IS UNLIKELY TO BE SEEN
THEREFORE SOME FORM OF DISINFECTIONIRRIGATION IS MANDATORY TO KILL THE
MICROORGANISMS AND TO REMOVE THE RESIDUAL TISSUES
3
bull THE IDEAL REQUISITES OF A ROOT CANAL IRRIGANT AS GIVEN BY ZEHNDER ARE
1 BROAD ANTIMICROBIAL SPECTRUM
2 HIGH EFFICACY AGAINST ANAEROBIC AND FACULTATIVE MICROORGANISMS ORGANIZED
IN BIOFILMS
3 ABILITY TO DISSOLVE NECROTIC PULP TISSUE REMNANTS
4 ABILITY TO INACTIVATE ENDOTOXIN
5 ABILITY TO PREVENT THE FORMATION OF A SMEAR LAYER DURING INSTRUMENTATION OR
TO DISSOLVE THE LATTER ONCE IT HAS FORMED
6 SYSTEMICALLY NONTOXIC WHEN THEY COME IN CONTACT WITH VITAL TISSUES
NONCAUSTIC TO PERIODONTAL TISSUES AND WITH LITTLE POTENTIAL TO CAUSE AN
ANAPHYLACTIC REACTION
SINCE NO SINGLE IRRIGANT HAS THESE OPTIMAL PROPERTIES STUDIES HAVE REPORTED THE USE
OF TWO OR MORE SOLUTIONS IN A SPECIFIC SEQUENCE OR IN COMBINATIONS FOR BETTER
RESULTS 4
bull SEVERAL IRRIGATING SOLUTIONS ALONG WITH CHELATING AGENTS HAVE BEEN USED
DURING BIOMECHANICAL PREPARATION OF ROOT CANAL BOTH IN PRIMARY AND
PERMANENT TEETH
bull HOWEVER NONE OF THE AVAILABLE IRRIGATING SOLUTIONS HAS BEEN REGARDED CLEARLY
AS OPTIMAL SOLUTION BECAUSE OF THEIR LIMITED EFFECTIVENESS ESPECIALLY IN APICAL
13RD OF THE ROOT CANAL SYSTEM
bull TO OVERCOME SUCH LIMITATIONS USE OF ENDOACTIVATOR HAS BEEN PROPOSED AS AN
IRRIGATION FACILITATOR THAT IS BASED ON SONIC VIBRATION (UP TO 10000 CPM) WHICH
FACILITATES THE IRRIGANT PENETRATION AND ITS RENEWAL WITHIN THE CANAL
bull ACTIVATION SYSTEMS RESULTED IN BETTER REMOVAL OF THE SMEAR LAYER IN THE APICAL
THIRD OF ROOT CANALS IN COMPARISON TO CONVENTIONAL IRRIGATION
5
CITRIC ACID
bull CITRIC ACID IS A WEAK ORGANIC ACID WITH THE APPEARANCE OF WHITE CRYSTALLINE
POWDER AT ROOM TEMPERATURE
bull IT CAN EXIST EITHER IN WATER-FREE FORM (ANHYDROUS) OR MONOHYDRATE FORM THE
WATER-FREE FORM CRYSTALLIZES FROM THE HOT WATER WHEREAS THE MONOHYDRATE
FORMS FROM THE COLD WATER THE LATTER MAY BE CONVERTED TO ANHYDROUS FORM BY
HEATING MORE THAN 78degC
bull CITRIC ACID OCCURS NATURALLY IN THE BODY IN MITOCHONDRIA AND IS USED BY BLOOD
BANKS TO PREVENT COAGULATION OF TRANSFUSED BLOOD CITRIC ACID IS ALSO ESSENTIAL
TO HUMAN METABOLISM AND IS FOUND IN MANY FOODS
6
2
bull THE BIOLOGICAL EFFECTS OF CITRIC ACID ON THE PERIODONTAL STRUCTURE HAS BEEN
EXTENSIVELY STUDIED IN PERIODONTICS
bull NEUMAN AND NEWMAN SHOWED THAT CITRIC ACID IS THE MOST EFFECTIVE ACID IN
ALTERING THE SOLUBILITY OF HYDROXYAPATITE
bull YAMAGUCHI ET AL SHOWED THAT CITRIC ACID SOLUTION HAD ANTIBACTERIAL EFFECTS ON
ALL 12 ROOT CANAL BACTERIA TESTED
bull ARIAS-MOLIZ ET AL SHOWED THAT ETHYLENEDIAMINETETRAACETIC ACID (EDTA) HAS NO
BACTERICIDAL ACTIVITY EVEN AFTER 1 HOUR CONTACT
bull THIS ACID HAS THE ABILITY OF ROOT CANAL IRRIGATION AND ALSO SMEAR LAYER REMOVAL
DIFFERENT CONCENTRATIONS (1ndash50) HAVE BEEN PROPOSED GUTMANN ET AL CONCLUDED
THAT 10 CITRIC ACID IS BETTER THAN ULTRASOUND FOR SMEAR LAYER REMOVAL FROM THE
ROOT END CAVITIES
7
bull STUDIES HAVE SHOWN IRRIGATION WITH 6 CA FOR 15 OR 30 SECONDS IS QUITE
EFFECTIVE IN REMOVING ALL THE COMPONENTS OF THE SMEAR LAYER OF THE PRIMARY
TEETH WHEREAS PERITUBULAR DENTIN DESTRUCTION WAS OBSERVED WHEN HIGHER
CONCENTRATION OF CITRIC ACID WAS USED AS AN IRRIGATING SOLUTION
8
AIMS amp OBJECTIVES
bull THIS STUDY WAS AIMED TO EVALUATE THE CLINICAL AND RADIOGRAPHIC OUTCOME OF
PULPECTOMY ALONG WITH QUALITY OF OBTURATION USING 6 CITRIC ACID AND
ENDOACTIVATOR
9
CASE REPORT
bull 350 CHILDREN (3-9 YEARS) WITH CLINICAL SIGNS AND SYMPTOMS OF CHRONIC IRREVERSIBLE
PULPITIS IN DEEPLY CARIOUS TEETH WERE SCREENED DURING SCHOOL DENTAL HEALTH
PROGRAM FROM MAY 2014-JULY 2014
bull 123 CHILDREN REPORTED TO THE DEPARTMENT AND 67 CHILDREN WERE SELECTED BASED ON
INCLUSION AND EXCLUSION CRITERIA
RECRUITMENT OF PATIENTS
10
INCLUSION CRITERIA
bull HISTORY OF SPONTANEOUS PAIN AND UNCONTROLLED BLEEDING AFTER PULP AMPUTATION
EXCLUSION CRITERIA
bull EVIDENCE OF INTERNAL OR EXTERNAL (PHYSIOLOGICPATHOLOGIC) ROOT RESORPTION OF MORE THAN A THIRD OF ITS LENGTH
bull ROOT CANAL OBLITERATION OR ANATOMIC ANOMALIES
bull INADEQUATE BONE SUPPORT OR NON RESTORABLE TOOTH
bull ONCE PATIENTS ELIGIBILITY WAS CONFIRMED THE TREATMENT PROCEDURE WAS
EXPLAINED TO THE PARENTGUARDIAN AND INFORMED WRITTEN CONSENT WAS
OBTAINED FROM PARENTSGUARDIANS SHOWING WILLINGNESS FOR THEIR
CHILDRENS TREATMENT 11
PROCEDURE
bull PULPECTOMY WAS PERFORMED BY ONE OPERATOR OF PEDIATRIC DENTISTRY DEPARTMENT
USING A STANDARDIZED TREATMENT PROTOCOL FOR ALL THE PATIENTS
bull AFTER ADMINISTRATION OF LOCAL ANESTHESIA RUBBER DAM WAS APPLIED FOR ISOLATION
bull ACCESS CAVITY WAS PREPARED USING AIR-ROTOR HAND PIECE WITH 8 ROUND BUR AND
PULP TISSUE WAS EXTIRPATED WITH THE HELP OF SPOON EXCAVATOR
bull FURTHER THE NEGOTIATION OF THE CANALS WAS DONE WITH 10 K-FILE
bull A DIAGNOSTIC RADIOGRAPH WAS TAKEN FOR ROOT LENGTH DETERMINATION AND
WORKING LENGTH WAS KEPT 1 MM SHORT OF THE RADIOGRAPHICAL APEX
bull ALL ROOT CANALS WERE INSTRUMENTED MANUALLY USING K-FILES AND WERE IRRIGATED
WITH 10 ML 09 NORMAL SALINE AND 1 SODIUM HYPOCHLORITE AS STANDARDIZING
PROTOCOL FOR ROOT CANAL PREPARATION AND DISINFECTION
12
3
GROUP 1 (CA + E) - IRRIGATION WAS DONE
WITH 10 ML OF 6 CITRIC ACID (CITOCID AMMDENT)
AND IRRIGANTS WERE SONICALLY AGITATED WITH
ENDOACTIVATOR (DENTSPLY) FOR 30 S PER CANAL USING REDBLUE
ENDOACTIVATOR TIP
GROUP 2 (CA) - 10 ML OF 6 CITRIC ACID FOR 1 MIN USING
27 GAUZE IRRIGATING NEEDLE
GROUP 3(SH + E) - 10 ML OF 1 SODIUM HYPOCHLORITE
SOLUTION AND SONIC ACTIVATION WITH ENDOACTIVATOR
GROUP 4(SH) - 10 ML OF 1 SODIUM HYPOCHLORITE
SOLUTION USING IRRIGATING NEEDLE (CONTROL GROUP)
bull TEETH UNDERGOING PULPECTOMY WERE RANDOMLY ENROLLED BY CHIT METHOD INTO THREE
STUDY AND ONE CONTROL GROUP
13
bull IN CITRIC ACID GROUPS FINAL RINSE WITH NORMAL SALINE WAS DONE TO REMOVE THE
REMAINING CRYSTALS (CHELATES)
bull FOLLOWING BIOMECHANICAL PREPARATION THE ROOT CANALS WERE DRIED WITH STERILE
ABSORBENT PAPER POINTS AND OBTURATED WITH VITAPEX USING HAND HELD
LENTULOSPIRAL FINAL RESTORATIONS WERE DONE USING COMPOSITE RESIN
14
bull CLINICAL FOLLOW UP WAS DONE AT 24 H1 WEEK 1 MONTH 6 MONTH AND 12
MONTH TO CHECK PAIN PRESENCE AND PAIN FREQUENCY (ONCEMORE THAN ONCE)
SWELLING FISTULA SENSITIVITY TO PERCUSSION
bull RADIOGRAPHIC FOLLOW UP WAS DONE AT 6 MONTH AND 12 MONTH FOR ANY
DEVIATED ERUPTION OF SUCCEDANEOUS TEETH EXCESS FILING MATERIAL AND ITS
RESORPTION EXTERNALINTERNAL ROOT RESORBTION CALCIFIC METAMORPHOSIS
PRESENCE OF FURCATION RADIOLUCENCY
CLINICAL amp RADIOGRAPHIC FOLLOW UP
15
RADIOGRAPHIC ASSESSMENT OF OBTURATION QUALITY
bull POSTOPERATIVE RADIOGRAPHS WERE VISUALLY ASSESSED FOR QUALITY OF OBTURATION BY
TWO INDEPENDENT EXAMINERS (SG AD) WHO WERE BLINDED WITH REGARD TO
IRRIGATION PROTOCOL GROUP TO ENHANCE CALIBRATION EACH EXAMINER ASSESSED THE
RADIOGRAPH INDEPENDENTLY AND LATER REVIEWED TOGETHER FOR FINAL ASSESSMENT
INDIVIDUAL ROOT WAS TAKEN AS UNIT OF ANALYSIS FOR GRADE OF OBTU- RATION AND
SCORING CRITERIA WERE AS GIVEN BY COLL JA 1996
1 UNDER FILLED - FILLING MATERIAL ENDED 1 MM OR MORE SHORT OF THE APEX
2 OPTIMAL FILLING- FILLING MATERIAL APPEARED TO END AT THE RADIOGRAPHICAL APEX
3 OVERFILLED - FILLING MATERIAL EXTRUDED PAST THE RADIOGRAPHIC APEX
4 OPTIMALLY FILLED ROOTS WERE FURTHER ASSESSED FOR THE PRESENCE OF VOIDS AND VOID
AREA (ROOT CANAL SURFACE UNTOUCHED BY THE ROOT CANAL FILLING MATERIAL) IN THREE
VISUALLY DIVIDED SECTIONS OF THE ROOT IE CORONAL MIDDLE AND APICAL 13RD
16
RESULTS
bull OVERALL CLINICAL AND RADIOGRAPHIC SUCCESS RATE OVER A PERIOD OF ONE YEAR WAS
9886 amp 977 RESPECTIVELY
bull ALL GROUPS WERE SIGNIFICANTLY (P = 001) EFFECTIVE IN ALLEVIATING PAIN WITHIN 24 H
OF PULPECTOMY
17 18
4
19
bull IMMEDIATE POST OPERATIVE RADIOGRAPHIC ASSESSMENT REVEALED 68 (102150) ROOTS
WITH OPTIMAL OBTURATION AND 32 (48150) WITH OVERFILLINGUNDERFILLING MAXIMUM
NO OF OPTIMAL FILLINGS WERE OBSERVED IN GROUP1 (CA + E) (3333) FOLLOWED BY
GROUP 2 (CA) (2549) GROUP 3(SH + E) (2549) AND GROUP 4(SH) (1568)
bull CITRIC ACID GROUPS HAD MORE NUMBER OF OPTIMALLY FILLED ROOTS 588 (60102) THAN
NON CITRIC ACID GROUPS 412 (42102)
bull ENDOACTIVATOR CONTRIBUTED TO 18 OF OPTIMAL OBTURATION IRRESPECTIVE OF
CHELATING AGENT USED
20
21
bull MAXIMUM NO OF VOIDS AND VOID AREAS WERE IN NON CITRIC ACID GROUPS
(6419 amp 5384) COMPARED TO CITRIC ACID GROUPS (3580 amp 4615)
RESPECTIVELY
bull ANALYSIS OF ROOT 13RD REVEALED MAXIMUM NO OF VOID AREA IN APICAL
13RD (4755) FOLLOWED BY MIDDLE 13RD (3846) AND CORONAL 13RD
(1398)
bull LEAST NO OF VOIDS amp VOID AREA (1111 amp 1608) WERE OBSERVED WHEN
ENDOACTIVATOR ALONG WITH CHELATING AGENT WAS USED (GROUP 1)
HOWEVER THIS WAS STATISTICALLY INSIGNIFICANT
22
DISCUSSION
bull IN THE PRESENT STUDY 1 SODIUM HYPOCHLORITE WAS USED ALONG WITH 6 CITRIC ACID
(CHELATING AGENT) WHICH IS REPORTED TO BE AS EFFECTIVE AS 17 EDTA
bull CITRIC ACID (BIOLOGICAL ACID) IS FOUND TO BE BIOCOMPATIBLE AND LEAST IRRITATING TO
PERIAPICAL TISSUES THAN OTHER CHELATING AGENTS
bull USE OF SODIUM HYPOCHLORITE SOLUTION FOLLOWING CHELATING AGENT WAS AVOIDED AS IT
RAPIDLY PRODUCES SEVERE EROSION OF ROOT CANAL WALL DENTIN
bull TRADITIONAL APPROACH OF DELIVERING IRRIGANTS INTO THE ROOT CANAL SPACE USING
SYRINGES AND METAL NEEDLES HAS BEEN FOUND TO BE INEFFECTIVE ESPECIALLY IN THE AREAS OF
ANASTOMOSES BETWEEN CANALS AND APICAL 13RD OF ROOT CANAL
23
bull THEREFORE TO ACHIEVE BETTER CLEANING EFFICIENCY IRRIGANT ACTIVATION HAS BEEN
RECOMMENDED SONIC ACTIVATION HAS BEEN REPORTED TO RESULT IN BETTER ROOT CANAL
CLEANLINESS AS COMPARED TO NO ACTIVATION OF IRRIGANT
24
5
CONCLUSION
bull USE OF 6 CITRIC ACID DEFINITELY HELPED IN RAPID ELIMINATION OF PAIN RESOLUTION OF
PERI-RADICULAR RADIOLUCENCY BETTER OBTURATION QUALITY IN TERMS OF LESS VOIDS AND
VOID AREAS ALONG WITH MAXIMUM NO OF OPTIMAL OBTURATION UP TO APICAL AREA
bull 6 CITRIC ACID AND ENDOACTIVATOR IRRIGATION PROTOCOL PROVED TO BE THE BETTER
IRRIGATION PROTOCOL WHICH MAY CONTRIBUTE TO LONG TERM SUCCESS OF PRIMARY
TOOTH AND THE HEALTH OF UNDERLYING PERMANENT TOOTH
bull 6 CITRIC ACID ALONG WITH ENDOACTIVATOR MAY BE RECOMMENDED AS IRRIGATION
ADJUNCTS IN PULPECTOMY PROCEDURE OF PRIMARY TEETH
25
PROS AND CONS
PROS
bull PROPER EXPLANATION OF THE MATERIALS
USED
CONS
bull NO PREOPERATIVE AND POSTOPERATIVE
RADIOGRAPHS
26
REFERENCES
bull RAMACHANDRA JA NIHAL NK NAGARATHNA C VORA MS ROOT CANAL IRRIGANTS IN
PRIMARY TEETH WORLD J DENT 20156(3)229-234
bull MOHAMMADI Z JAFARZADEH H SHALAVI S KINOSHITA JI UNUSUAL ROOT CANAL
IRRIGATION SOLUTIONS J CONTEMP DENT PRACT 201718(5)415-420
bull ZEHNDER M ROOT CANAL IRRIGANTS J ENDOD 2006 32389- 98
bull SMITH JJ amp WAYMAN BE AN EVALUATION OF THE ANTIMICROBIAL EFFECTIVENESS OF
CITRIC ACID AS A ROOT CANAL IRRIGANT JOURNAL OF ENDODONTICS 1986 12(2) 54-58
bull TANNURE PN AZEVEDO CP BARCELOS R GLEISER R PRIMO LG LONG-TERM OUTCOMES OF
PRIMARY TOOTH PULPECTOMY WITH AND WITHOUT SMEAR LAYER REMOVAL A RANDOMIZED
SPLIT-MOUTH CLINICAL TRIAL PEDIATR DENT 201133316E20 27
bull CARON G NHAM K BRONNEC F MACHTOU P EFFECTIVENESS OF DIFFERENT FINAL IRRIGANT
ACTIVATION PROTOCOLS ON SMEAR LAYER REMOVAL IN CURVED CANALS J ENDOD
2010361361E6
bull COLL JA SADRIAN R PREDICTING PULPECTOMY SUCCESS AND ITS RELATIONSHIP TO
EXFOLIATION AND SUCCEDANEOUS DENTITION PEDIATR DENT 19961857E63
28
1
LOCAL
ANESTHESIA
DR MITAKSHARA NIRWAN
CONTENTS
Definition
Methods of inducing local anesthesia
Desirable properties
Electrophysiology of nerve conduction
Impulse propagation and spread
Mode and site of action of local anesthesia
Classification of local anesthetic according to biological site and mode of action
Dissociation of local anaesthetics
Mechanism of action of local anaethetics
Local anaesthetic agent
2
3
DEFINITION
Local anesthesia is defined as a loss of sensation in
a circumscribed area of the body caused by depression
of excitation in nerve endings or an inhibition of the
conduction process in peripheral nerves
An important feature of local anesthesia is that it produces
LOSS OF SENSATION WITHOUT INDUCING LOSS OF
CONSCIOUSNESS
4
METHODS OF INDUCING LOCAL
ANESTHESIA
Low temperature
Mechanical trauma
Anoxia
Neurolytic agents such as alcohol amp phenol
Chemical agents such as local anesthetics
PROPERTIES OF LOCAL
ANESTHESIA
It should not be irritating to tissue to which it is applied
It should not cause any permanent alteration of nerve structure
Its systemic toxicity should be low
Time of onset of anesthesia should be short
It should be effective regardless of whether it is injected into the tissue or applied locally to mucous membranes
The duration of action should be long enough to permit the completion of procedure
5 6
It should have the potency sufficient to give complete
anesthesia with out the use of harmful concentration solutions
It should be free from producing allergic reactions
It should be free in solution and relatively undergo
biotransformation in the body
It should be either sterile or be capable of being sterilized by
heat with out deterioration
2
ELETROPHYSIOLOGY OF
NERVE CONDUCTION
There is an electrical charge across the membrane
This is the membrane potential
The resting potential (when the cell is not firing) is a negative
electrical potential of -70mv that exists across the nerve
membrane produced by different concentrations of either side of
the membrane
The interior of nerve is NEGATIVE in relation to exterior
7 8
inside
outside
Resting potential of neuron = -70mV
+
-
+
-
+
-
+
-
+
-
SLOW DEPOLARIRIZATION
9
RAPID DEPOLARIZATION
The interior of nerve is POSITIVE in relation to exterior
REPOLARIZATION
10
bull Repolarization takes 07 msec
bull Depolarization takes 03 msec
SODIUM PUMP -
energy comes from the oxidative metabolism of ATP
bull The entire process require 1 msec
IMPULSE PROPOGATION
IMPULSE SPREAD
The propagated impulse travels along the nerve
membrane towards CNS The spread of impulse differs
in myelinated and unmyelinated nerve fibers
DEPOLARIZED SEGMENT ADJACENT RESTING AREA
MODE AND SITE OF ACTION OF LOCAL
ANESTHETICS
Local anesthetic agent interferes with excitation
process in a nerve membrane in one of the
following ways
Altering the basic resting potential of nerve
membrane
Altering the threshold potential
Decreasing the rate of depolarization
Prolonging the rate of repolarization
12
3
CLASSIFICATION OF LOCAL ANESTHETIC
SUBSTANCES ACCORDING TO
BIOLOGICAL SITE AND MODE OF ACTION
CLASS A
Agents acting at receptor site on external surface of nerve membrane
Chemical substance Biotoxins (eg tetrodotoxin and saxitoxin)
CLASS B
Agents acting on receptor sites on internal surface of nerve membrane
Chemical substance Quaternary ammonium analogues of lidocaine
scorpion venom 13
CLASS C Agents acting by receptor independent of
physiochemical mechanism
Chemical substance Benzocaine
CLASS D Agents acting by combination of receptors and
receptor independent mechanisms
Chemical substance most clinically useful anesthetic agents
(eg lidocaine mepivacaine prilocaine)
14
BASED ON THE SOURCE
NATUAL
SYNTHETIC
OTHERS
BASED ON MODE OF APPLICATION
bull INJECTABLE
bull TOPICAL
BASED ON DURATION OF ACTION
bull ULTRA SHORT
bull SHORT
bull MEDIEM
bull LONG
BASED ON ONSET OF ACTION SHORT
INTERMEDIATE
LONG
15
DISSOCIATION OF LOCAL
ANESTHETICS
Local anesthetics are available as salts (usually
hydrochlorides) for clinical use
The salts both water soluble and stable is dissolved in
either sterile water or saline
In this solution it exists simultaneously as unchanged
molecule (RN) also called base and positively charged
molecules (RNH+) called cations
RNH+ ==== RN+ H
+
16
The relative concentration of each ionic form in the solution varies
in the pH of the solution or surrounding tissue
In the presence of high concentration of hydrogen ion (low pH) the
equilibrium shifts to left and most of the anesthetic solution exists
in cationic form
RNH+ gt RN
+ + H
+
As hydrogen ion concentration decreases (higher pH) the
equilibrium shifts towards the free base form
RNH+ lt RN + H
+
17
The relative proportion of ionic form also depends on pKa or DISSOCIATION CONSTANT of the specific local anesthetic
The pKa is a measure of molecules affinity for H+
ions
When the pH of the solution has the same value as pKa of the local anesthetic exactly half the drug will exists in the RNH
+ form and
exactly half in RN form
The percentage of drug existing in either form can be determined by Henderson Hasselbalch equation
Log baseacid = pH - pKa
18
4
MECHANISM OF ACTION OF LOCAL
ANESTHETICS
The following sequence is proposed mechanism of action of LA
Displacement of calcium ions from the sodium channel receptor site
Binding of local anesthetic molecule to this receptor site
Blockade of sodium channel
19
Decrease in sodium conductance
Depression of rate of electrical depolarization
Failure to achieve the threshold potential level
Lack of development of propagated action potential
Conduction blockadehellip
20
21
Na + Na +
22
LOCAL ANESTHETIC AGENT
COMERCIALLY PREPARED LOCAL ANESTHESIA
CONSISTS OF
Local anesthetic agent (xylocaine lignocaine 2)
Vasoconstrictor (adrenaline 1 80000)
Reducing agent (sodium metabisulphite)
Preservative (methylparabencapryl
hydrocuprienotoxin)
Fungicide (thymol)
Vehicle (distillde waterNaCl)
LOCAL ANESTHETIC AGENT
The local anesthetics used in dentistry are divided
into two groups
ESTER GROUP
AMIDE GROUP
23 24
ESTER GROUP It is composed of the following
An aromatic lipophilic group
An intermediate chain containing
an ester linkage
A hydrophilic secondary or tertiary
amino group
AMIDE GROUP It is composed of the following
An aromatic lipophilic group
An intermediate chain containing
amide linkage
A hydrophilic secondary or tertiary
amino group
5
25
CLASSIFICATION OF LOCAL ANESTHETICS
ESTERS
Esters of benzoic acid
Butacaine
Cocaine
Benzocaine
Hexylcaine
Piperocaine
Tetracaine
Esters of Para-amino
benzoic acid
Chloroprocain
Procaine
Propoxycaine
26
AMIDES Articaine
Bupivacaine
Dibucaine
Etidocaine
Lidocaine
Mepivacaine
Prilocaine
Ropivacaine
QUINOLINE
Centbucridine
PHARMACOKINETICS OF LOCAL
ANESTHETICS UPTAKE
When injected into soft tissue most local anesthetics produce
dilation of vascular bed
Cocaine is the only local anesthetic that produces
vasoconstriction initially it produces vasodilation which is
followed by prolonged vasoconstriction
Vasodilation is due to increase in the rate of absorption of the
local anesthetic into the blood thus decreasing the duration of
pain control while increasing the anesthetic blood level and
potential for over dose 27
AMIDE LOCAL ANESTHETICS
The metabolism of amide local anesthetics is more
complicated then esters The primary site of
biotransformation of amide drugs is liver
Entire metabolic process occurs in the liver for lidocaine
articaine etidocaine and bupivacaine
Prilocaine undergoes more rapid biotransformation then the
other amides
28
REFERENCES
Handbook of local anesthesia ndash Stanley F Malamed ndash 6th
edition
Essentials of Local Anesthetic Pharmacology Daniel E
Becker Anesth Prog 2006 Fall 53(3) 98ndash109
WIKIPEDIEA
29
THANK YOU
30
1
Pharmacological Methods of Behavior
Management
DR MITAKSHARA NIRWAN
DEFINITIONS
bull Conscious Sedation ndash A minimally depressed level of consciousness that retains
the patients ability to independently and continuously maintain an airway and respond appropriately to physical stimulation or verbal command
(American Dental Association House Of Delegates 2000)
bull Deep Sedation ndash An induced state of depressed consciousness
accompanied by partial loss of protective reflexes including the inability to continuously maintain an airway independently and or to respond purposefully to physical stimulation or verbal command
bull General Anesthesia (G A) ndash An induced state of unconsciousness or complete loss of
protective reflexes including the inability to continually maintain an airway independently and respond purposefully to physical stimulation or verbal command
Conscious sedation
ADVANTAGES
Conscious
Protective reflexes active amp intact
Stable vital signs
Operating dentist may perform sedation
Minimum amount of equipment required
Prolong detainment in recovery room not required
Risk of complication very low
Excellent choice for poor ndash risk pt in dental office
Cost effective
General anesthesia
ADVANTAGES Not absolutely
essential May be the only
method Not necessary (no
pain reaction) Amnesia always
present
Conscious sedation
DISADVANTAGES
Pt cooperation is essential
Extremely difficult or mentally handicapped pt cannot always be managed
Use of local anesthesia is a must
Amnesia may or may not be present
General anesthesia DISADVANTAGES
Pt unconscious
Protective reflexes are depressed
Depressed
Advanced training required Dentist must not act also as anesthetist
Special equipment necessary
Detainment in recovery area necessary
High IOP amp postoperative complications
Not indicated in dental office
More expensive
Fundamental Concepts
bull Techniques that utilize drugs to induce co-operative yet conscious state in an otherwise uncooperative child ndash CONSCIOUS SEDATION
2
GOALS
1 To facilitate the provision of quality care
2 To minimize the extremes of disruptive behavior
3 To promote a positive psychologic response to treatment
4 To promote patient welfare amp safety
5 To return the patient to physiologic state
OBJECTIVES
1 The pt mood must be altered
2 The pt must remain conscious at all times
3 The pt must be cooperative
4 All protective reflexes must remain intact and active
5 Vital signs must remain stable and with in normal limits
6 The ptrsquos pain threshold should be elevated
7 Amnesia may be present
Indications
1 Preschool children
2 Lack of Psychological Emotional maturity
3 Lack of Cognitive Physical Medical disability
4 Fearful amp anxious pts
5 Pt who require extensive amp complicated dental care amp would require or benefit from prolonged visits
6 Acute pain
7 Traumatic injuries
Operating Facilities amp Equipment
A positive pressure O2 delivery system capable of administering gt than 90 O2 at 10L min flow for 60 min (650L ldquoErdquo cylinder)
OR
Self inflating bag valve mask device (15L min)
A functional suction apparatus with appropriate suction catheters
Monitoring equipment - PO BPC PC or Capno
Inhalation sedation unit
100 O2 amp never less than 25
A fail safe mechanism that is checked and calibrated annually
Must have appropriate scavenging system
Emergency drugs
Techniques of sedation
Routes for drug administration
bull Oral
bull Rectal
bull Inhalational
bull Transmucosal
ndash Sublingual
ndash Intranasal
bull Parenteral
ndash IM
ndash sub mucosal
ndash IV
3
Oral Sedation
Advantages
1 Almost universally accepted and the easiest method
2 Decreased incidence and severity of adverse reaction
3 Low cost
Disadvantages
1 Absorption is variable
2 Prolonged latent period(30 min)
3 Reversal of any unwanted effect is also difficult
4 Inability to readily lighten or deepen the level of sedation
5 Prolonged duration of action
Rectal Sedation
Advantages 1 Incidence and intensity of
drug related side effects is minimized
2 Drug absorption occurs from the large intestine directly into the circulation
3 The lack of a needle syringe or other equipment
4 The ease of administration
5 The low cost
Disadvantages
1 Inconvenience to the administrator amp pt
2 The variable absorption of drugs from the large intestine
3 The slow onset of action amp the relatively long duration of action
4 Inability to titrate the drug dosage
5 The inability to reverse the action of the drug the prolonged recovery
Intranasal sedation
Advantages
Rapid onset (10 ndash 15 min)
Simple amp relatively painless
Less pt cooperation is required
Absorbed directly into the C V S
Intranasal sedation
Disadvantages
1 Dependence on nasal mucous membrane
2 Shorter duration of action(40-60min)
3 Multiple dosage may be necessary
Drugs
Midazolam ndash 02mgkg
Sufentanil ndash 15 ndash 3 mcgkg
Ketamine ndash 3-6mg kg
Sublingual sedation
Advantages
1 Pt acceptance
2 Rapid onset
3 High bioavailability
Drugs
Oral Transmucosal Fentanyl Citrate (OTFC)
Intramuscular Sedation
Advantages
1 More rapid onset of action
2 Absorbed directly into the C V system
3 More reliable absorption of drug
4 Pt cooperation is not as essential
Disadvantages
1 Time factor ndash its 15 min latent period
2 Pt may not be willing to accept the injection
3 The prolonged duration of action(2-4 hrs more)
4 Possibility of injury to the tissues at the site of injection caused by either the drug or the needle
4
Sites of I M administration
1 Gluteal area
2 Vastus lateralis
3 Mid ndash deltoid area
Drugs
Diazepam
Midazolam
Hydroxyzine
Inhalation Sedation
Advantages
1 The onset of action is more rapid
2 Peak clinical level is achieved rapidly(3-5min) - permit titration
3 Administrator has complete control over the actions of the drug - safety feature
4 No significant over dosage
5 Flexible duration of action
6 Recovery time is rapid amp most complete
7 No injection is required
8 With N2O- O2 it is safe with very few side effects
Disadvantages
1 The initial cost of the equipment is high 2 The continuing cost of the gases is high 3 The equipment occupies considerable space 4 N2O is not a potent agent 5 A degree of cooperation is required from the pt 6 Chronic exposure to N2O is deleterious to the health of
dental personnel
Contraindications
1 Nasal obstruction 2 Cyanosis at rest 3 Poor cooperation 4 1st trimester of pregnancy 5 Fear of masks
I V Sedation
Advantages
1 The onset of action is the most rapid 2 The dosage may be titrated 3 Suitable level of sedation can be provided 4 The recovery period is shorter 5 Side effects are extremely uncommon 6 Control of salivary secretions is possible 7 The gag reflex is diminished 8 Effectively diminishes motor disturbances 9 Provides immediate access to CVS in emergency
Disadvantages
1 Venipuncture is necessary
2 Complication may rise at the site of the venipuncture
3 Monitoring must be more intensive
4 Recovery is not complete at the end of the procedure
5 Reversal of sedation is difficult
5
N2O-O2 (Relative Analgesia)
colorless sweet smelling gas
Pharmacokinetics
Absorption through pulmonary epithelium
It is approx 15 times as soluble as is nitrogen It replaces nitrogen in blood
It is carried in solution in plasma of the blood
It is not metabolized by the body
Elimination ndash majorndash lungs minor --- skin
perspiration urine and intestinal gas
Pharmacodynamics
Dose related
10 ndash 25 Lightheaded
Changes in visual amp auditory sensation
Tingling of hands amp feet
Suffusing warmth
Remote from the immediate environment
Reduced anxiety
25-50 max analgesic properties and aberration of vision hearing and proprioception mild drowsiness euphoria amnesia and increased sleepiness and dreams
35 conc will achieve maximum analgesia
bull CNS
ndash Cerebrum-primarily affected
ndash Safe but weak anesthetic agent
bull RESPIRATORY SYSTEM
ndash Increased Tidal and minute volumes
bull CARDIOVASCULAR SYSTEM
ndash 2 studies ndash decreased cardiac output
bull FETAL SYSTEMS
ndash Miscarriage in humans
bull OTHER SYSTEMS
ndash Depression of spinal reflexes increase muscle tone indicates stage of delirium
ndash Muscle rigidity-narcotics + nitrous oxide
ndash Nausea and vomitting - GIT
ndash HEMATOPOIESIS ----- prolonged exposure
Adverse reactions and toxicity
EMOTIONAL REACTIONS
DREAMS HALLUCINATIONS
No acute toxicity
Chronic toxicity ndash bone marrow
depression
PROCEDURE
Diffusion Hypoxia
Sevoflurane
A fluorinated derivative of isopropyl ether ndash synthesized in 1970
Potent anaesthetic agent with rapid uptake amp speedy recovery
Day-case surgery
Problem
Attaching vaporiser to any of the currently available machine
BENZODIAZEPINES
Diazepam 1961 lipid soluble
Uses-alcoholism epilepsy labor tetanus and cerebral palsy
- sedation and amnesia
- varieties of neurosis amp anxiety states
Pharmacokinetics
Orally Rectal IMIV or SC
Well absorbed through GIT
Excretion in urine
6
bull Pharmacodynamics
ndash Depress the brain stem reticular system and the limbic system thalamus and hypothalamus
ndash It is a centrally acting muscle relaxant Has anti-convulsant properties
Adverse reaction amp toxicity
ndash Confusion nausea headache increased appetite decreased salivation and jaundice Thrombophlebitis
ndash Rebound phenomenon
ndash Toxicity drowsiness confusion sleep and coma
Dosage Oral or Rectal ndash 02-05mgkg
Maximum single dose 10mg
IV- 025mgkg
Supplied Tablets 2 5 10 mg
Suspension ndash 5mg
Midazolam Water soluble ndash non-irritant
Oral IM IV
Metabolism- liver
Onset IV 3 -5mins
oral 20 ndash 30mins
Oral administration anxious patients requiring relatively short dental procedure
No rebound phenomenon
Better anxiolysis amp amnesia (retrograde amnesia)
Adverse effects Respiratory depression
dose dependant apnea
Dosage Oral ndash 025 to 1mgkg to maximum single dose 20mg
IM ndash 01 to 015mgkg to a maximum of 10mg
IV ndash slow IV
Supplied Syrup ndash 2mgml
Injectable ndash 1mgml amp 5mgml vials
Flumazenil specific benzodiazepines antagonist
selectively inhibits CNS effects
IV administration amp not recommended below 18yrs of age
02mg over 15 seconds after 45seconds 02mg then after 60seconds to maximum of 1mg
Sedative-Hypnotics
Barbiturates First truly effective drugs for the management of anxiety Generalized CNS depressants Produce dose dependent effects
Sedation ---- sleep ---- GA ---- coma
Suppress the CNS and result in sedation and amnesia Advantages
Rapid onset and short duration Disadvantages
no analgesic effect and possible hypotension Must be used with caution in trauma patients because they may cause
apnea and hypoventilation
DOSE Pentobarbital Sodium 100mg Secobarbital Sodium 100 to 200mg Children 30 to 100mg
bull Chloral Hydrates (Mickey Finn Knock out drops ) First synthesized in 1832 first member of the hypnotic group of drugs
Widely used as conscious sedation agent
Properties
Unpleasant taste
Nausea vomiting
Quite irritating to skin and to mucous membranes
GI irritation
Dosages Individualized for each patient 25 ndash 50mgkg
maximum of 1g
Supplied oral capsule ndash 500mg
oral solution ndash 250 amp 500mg5ml
Rectal suppositories ndash 324 amp 648mg
Narcotics
Do produce sedation amp euphoria greater in children
LA is required but dose should be decreased
Meperidine Synthetic opiate agonist
Very water soluble
Orally SC IM or IV
Peak effect by oral 1 hr amp lasts upto 4 hrs
Adverse reactions
-Seizures
-Extreme caution in hepatic or renal diseases or history of seizures
7
Dosage Oral SC or IM ndash 1to 22mgkg not to exceed 100 mg
Supplied Oral Tablets ndash 50 amp 100mg
Oral Syrup ndash 50mgml
Parental solution ndash 25 50 75 amp 100mgml
Fentanyl
Synthetic opiate narcotic analgesic
Very potent 01mg = 10mg Morophine75mg Meperidine
Pharmacokinetics
IV IM SM
Metabolized in liver Excreted in urine
Fentanyl Onset ndash 7 to 15mins
Duration ndash 1 to 2 hrs
Pharmacodynamics
Respiratory depression RR but returns to normal rapidly Tidal volume amp response to co2 depressed for extended period
Apnea
Less emetic than meperidine
NOT RECOMMENDED IN CHILDREN BELOW 2yrs
Dosage 0002 to 0004mgkg
Supplied 005mgml in 2 amp 5ml ampoules
Reversal drug Naloxone
Semisynthetic opiate antagonist
No agonist activity
Onset 2 to 5mins SC or IM amp 1 to 2mins IV
Reversal 45mins
Pt should be kept under continual surveillance
Adverse reaction nausea vomiting sweating hypotension hypertension ventricular tachycardia fibrillation
Dosage IV SC IM 001mgkg then 01mgkg every 2- 3mins maximum 2mg
Supplied 002 004 1mg solutions
Antihistamines
Hydroxyzine
Oral or IM
Effect ndash 15 ndash 30mins
Half-life ndash 3 hrs
Uses
To relieve anxiety
Used as an anti-histamine
Used to control nausea and vomiting including that associated with motion sickness and pregnancy
Adverse reaction dry mouth drowsiness hypersentivity
Dosage Oral ndash 1 to 2mgkg
IM ndash 11mgkg
Promethazine Oral or IM Onset 15 to 60mins Duration 4 to 6 hrs Uses
To prevent and treat nausea and vomiting associated with motion pregnancy or surgery
Produces sedation and reduce swelling pain and trismus
Lower seizure threshold Adverse reaction dry mouth blurred vision thickening of bronchial secretions Dosage OralIM ndash 05-11mgkg
maximum 25 mg
Diphenhydramine
Oral IM IV
Onset -1hr
Duration ndash 4 to 6 hr
Metabolized in liver
Adverse reaction disturbed coordination thickening of bronchial secretions
Dosage Oral IM IV ndash 1 to 15mgkg
maximum 50mg
Tranquilizers
Major tranquilizer antipsychotic produce calmness control symptoms of psychoses cause reversible extra pyramidal symptoms and do not tend to cause habituation
Minor tranquilizer antianxiety agents also cause calmness do not cause extrapyramidal symptoms Used in conditions like nervous tension and mild depression
8
Classification
Antipsychotics
Phenothiazine derivatives
Chlorpromazine promazine
Butryophenones
Haloperidol
Rauwolfia alkaloids
Reserpine
Antianxiety drugs
Propyl alcohol derivatives
Meprobamate
Benzodiazepine derivatives
Diazepam
Miscellaneous compounds
Hydroxyzine
Meprobamate
White crystalline powder slightly bitter in taste
Only administered orally
Peak blood concentration ----1 to 3hrs
10 ---------excreted unchanged Rest --- excreted as a oxidized derivative or as a glucoronide
Uses
To relieve day time anxiety
Induce sleep in insomniacs
To reduce anxiety associated with dental treatment
Anti-convulsant ndash petit mal epilepsy
Adverse reaction leucopenia acute non-thrombocytopenic purpura ecchymoses eosinophilia edema adenopathy
Dosage Childrengt 6yrs 100 to 200mg
Not recommended for children under 6yrs
Monitoring during sedation
1 Pulse
2 Blood pressure
3 ECG
4 Respiration
5 Temperature
Pulse
Manual Electronic
bull Radial Brachial
bull Facial labial
Blood pressure
ndash Stethoscope amp sphygmomanometer
ndash Automatic devices
ndash Direct cannulation of an artery ndash very accurate
Electrocardiograph
Heart rate rhythm myocardial function
9
Respiration
ndash Monitoring respiratory rate
ndash Observing the rise amp fall of the chest wall
ndash Observing the color of mucous membrane
ndash Observing the inflation amp deflation of the reservoir bag
Devices for monitoring respiration
1 The Precordial pretracheal stethoscope
2 The esophageal stethoscope
ndash Respiratory rate
ndash Heart rate
ndash Any abnormal sounds
Pulse Oximeter
ndash Oxygen saturation
ndash Heart rate
ndash Oxisensor site
ndash Fingers
ndash Toe
ndash Ear lobe
Mechanism
Oxygenated Hb ndash red light
Deoxygenated Hb- infrared light
Tissue pressure from arterial pulse (plethysmography)
Advantages
ndash Safe amp noninvasive
ndash Simple to use
ndash Information is rapidly available for clinical decision
ndash Indirectly indicates respiratory adequacy
Disadvantages
ndash Finger probes can get dislodged
ndash Emitted light source may cause burning
ndash Non reusable probes are expensive
ndash Does not directly determine airway patency
Capnography
1 The presence absence of air flow
2 Indicates depth amp adequacy of respiration
3 Continues analysis of the co2 content of the respired air ndash indicates respiratory adequacy
Temperature
ndash Disposable nondisposable thermometer
ndash Esophageal rectal temp probe
10
Discharge criteria
Cardiovascular function is satisfactory amp stable
Airway patency is uncompromised amp satisfactory
Pt is easily arousable amp protective reflexes intact
State of hydration is adequate
Pt can talk if applicable
Pt can sit unaided if applicable
Pt can ambulate with minimal assistance if applicable
Presedation level of responsiveness achieved
Responsible individual is available
1
PULP THERAPY OF VITAL TEETH
DR MITAKSHARA NIRWAN
Contents
Indirect pulp capping
Direct pulp capping
Medications amp materials used in pulp capping
Pulpotomy
MTA
Apexogenesis
INDIRECT PULP CAPPING
Pieter Van Forest - first to speak about root canal therapy
Glove designed instruments that could prepare a canal to a certain size and taper(1910)
Indirect pulp capping is defined as a procedure where in small amount of carious dentin is retained in
deep areas of cavity to avoid exposure of pulp followed by placement of a suitable medicament and
restorative material that seals off the carious dentin and encourages pulp recovery (Ingle)
A procedure in which only the gross caries is removed from the lesion and the cavity is sealed for a
time with a biocompatible material (McDonald)
Objective of indirect pulp capping
These were given by Eidelman in 1965
bull Arresting the carious process
bull Promoting dentin sclerosis
bull Stimulating formation of tertiary dentin
bull Remineralization of carious dentin
Layers of Carious Dentin Indications of Indirect Pulp Capping
History
Mild pain associated with eating
Negative history of spontaneous extreme pain
Clinical Examination
Deep carious lesion which are close tobut not involving the pulp in vital primary or young
permanent teeth
No mobility
Nominal pulp inflammationdefinite layer of affected dentin after removal of infected dentin
Radiographic examination
Normal lamina dura amp PDL space
No radiolucency around the apices
2
Contraindications of Indirect Pulp Capping
History
Sharp penetrating pulpalgia
Prolonged spontaneous pain especially at night
Clinical examination
Mobility of tooth
Discoloration of tooth
Negative reaction of electric pulp testing
Radiographic examination
Definite pulp exposure
Break in the lamina dura
Radiolucency around the apices
Widened PDL space
Treatment procedure
Sequelae of Indirect Pulp Capping Three distinct types of new dentin formation take place
1 Cellular fibrillar dentinmdashfirst 2 months
2 Globular dentinmdash3 months
3 Tubular dentin (uniform mineralized dentin)
bull 15th of reparative dentin formation begins in less than 30 days
bull After 3 months 01 mm is formed
DIRECT PULP CAPPING Defined by Kopel (1992) as the placement of a medicament or non medicated material on a pulp that
has been exposed in course of excavating the last portions of deep dentinal caries or as a result of
trauma
Objective
To create new dentin in the area of the exposure and subsequent healing of the pulp
Rationale
achieve a biologic closure of the exposure site by deposition of hard tissue barrier (dentin bridge)
between pulp tissue and capping material thus walling off the
INDICATIONS
Small mechanical exposure
Easily controlled haemorrhage
Bright red haemorrhage
True pinpoint exposure
CONTRAINDICATIONS
Severe toothache at night
Spontaneous pain
Tooth mobility
Radiographic appearance of pulp periradicular de- generation
Excess of hemorrhage at the time of exposure Serous exudate from the exposure
Externalinternal root resorption
Swellingfistula
Histological Changes after Pulp Capping
These were illustrated be Glass and Zander in 1949
After 24 hours Necrotic zone adjacent to calcium
hydroxide paste is separated from healthy pulp
tissue by a deep staining basophilic layer
After 7 days Increase in cellular and fibroblastic
activity
After 14 days Partly calcified fibrous tissue lined by
odontoblastic cells is seen below the calcium
proteinate zone disappearance of necrotic zone
After 28 days Zone of new dentin
3
Medications and Materials Used for Pulp Capping Calcium hydroxide
Corticosteroids amp antibiotics
Inert materials
Collagen fibers
4-META adhesive
Direct bonding
Isobutyl cyanoacrylate
Denatured albumin
Mineral trioxide aggregate
Laser
Bone morphogenic protein
PULPOTOMY
Finn (1995) defined it as the complete removal of the coronal portion of the dental pulp
followed by placement of a suitable dressing or medicament that will promote healing and
preserve vitality of the tooth
American Academy of Pediatric Dentistry (1998) defined pulpotomy as the amputation of
affected infected coronal portion of the dental pulp preserving the vitality and function of the
remaining part of radicular pulp
Objectives
bull Removal of inflamed and infected coronal pulp at the site of exposure thus preserving the vitality of the
radicular pulp and allowing it to heal
bull Maintain the tooth in the dental arch
Rationale
bull Radicular pulp is healthy and capable of healing after surgical amputation of the infected coronal pulp
bull Preserves vitality of the radicular pulp
bull Maintains tooth in a physiologic condition
Indications of Pulpotomy bull Mechanical pulp exposure in primary teeth
bull Teeth showing a large carious lesion but free of radicular pulpitis
bull History of only spontaneous pain
bull Hemorrhage from exposure sites bright red and can be controlled
bull Absence of abscess or fistula
bull No interradicular bone loss
bull No interradicular radiolucency
Contraindications of Pulpotomy bull Persistent toothache
bull Tenderness on percussion
bull Root resorption more than 13rd of root length
bull Large carious lesion with nonrestorable crown
bull Highly viscous sluggish hemorrhage from canal orifice which is uncontrollable
bull Medical contradictions like heart disease immuno compromised patient
bull Swelling or fistula
bull External or internal resorption
bull Pathological mobility
bull Calcification of pulp
Classification of pulpotomy
4
Formocresol Pulpotomy
Iby BUCKLEY in 1904
Sweet (1930) Formulated multi visit technique
Doyle (1962) Advocated 2 sitting procedure (complete devitalization)
Spedding (1965) Gave 5 minute protocol (partial devitali- zation)
Venham (1967) Proposed 15 seconds procedure
Current concept uses 4 minutes of application time
Composition of formocresol Buckleyrsquos Formula
bull Cresol ndash 35 percent
bull Glycerol ndash 15 percent
bull Formaldehyde ndash 19 percent
bull Water ndash 31 percent
Mechanism of Action
It prevents tissue autolysis by bonding to the proteins Bonding is of peptide groups of side chain amino acids and is a reversible process accomplished without
changing the basic structure of protein molecules
Histological Changes
bull Demonstrated by Mass and Zilbermann11 in 1933 and also by Massler and Mansokhani in 1959
bull Immediately the pulp becomes fibrous and acidophillic
bull Seven to fourteen days Three zones appear
a broad eosinophilic zone of fixation
b broad pale-staining zone of atrophy with poorcellular definition
c broad zone of inflammation extending apically into normal pulp tissue
bull One yearndash Progressive apical movement of these zones with only acidophillic zone left at the end of 1 year
Modified Formocresol Pulpotomy
Used by TRASK(1972)
The technique is identical to that described for primary teeth except that the formocresol pellet is
sealed permanently in the tooth
Two-visit Devitalization Pulpotomy
Indications
bull There is evidence of sluggish bleeding at the amputation site that is difficult to control
bull Pus in the chamber but none at the amputation site
bull There is thickening of the PDL
bull History of pain
Contraindications
bull Nonrestorable tooth
bull Tooth with necrotic pulp
5
Glutaraldehyde Pulpotomy
It was first suggested by S Gravenmade Introduced by Kopel in 1979
Mechanism of Action
bull Glutaraldehyde produces rapid surface fixation of the underlying pulpal tissue
bull A narrow zone of eosinophilic stained and compressed fixed tissue is found directly beneath the area of application which blends into vital normal appearing tissue apically
bull With time the glutaraldehyde fixed zone is replaced by macrophagic action with dense collagenous tissue thus the entire root canal tissue is vital
Cvekrsquos Pulpotomy
bull This is also called as calcium hydroxide pulpotomy or young permanent partial pulpotomy
bull This was proposed by Mejare and Cvek16 in 1978
bull Indicated in young permanent teeth where the pulp is exposed by mechanical or bacterial means and the
remaining radicular tissue is judged vital by clinical and radiographic criteria whereas the root closure is
notcomplete
MINERAL TRIOXIDE AGGREGATE (MTA) Torabinejad described the physical and chemical properties of MTA in 1995
It is ash colored powder made primarily of fine hydrophilic particles of
1 tricalcium aluminate
2 tricalcium silicate
3 silicate oxide
4 tricalcium oxide
5 bismuth dioxide
Hydration of the powder results in a colloidal gel composed of calcium oxide crystals in an amorphous
structure This gel solidifies into a hard structure in less than three hours
PROPERTIES OF MTA
It is biocompatible material and its sealing ability is better than that of amalgam or ZOE
Initial pH is 102 and set pH is 125
The setting time of cement is 4 hours
The compressive strength is 70 MPA which is comparable with that of IRM
Low cytotoxicity ndash It presents with minimal inflammation if extended beyond the apex
Mineral trioxide aggregate (MTA) has demonstrated the ability to induce hard-tissue formation in
pulpal tissues and it promotes rapid cell growth
APEXOGENESIS
It is defined as the treatment of a vital pulp by capping or pulpotomy in order to permit continued
growth of the root and closure of the open apex
Rationale
Maintenance of integrity of the radicular pulp tissue to allow for continued root growth
Indications
bull Indicated for traumatized or pulpally involved vital permanent tooth when root apex is incompletely formed
bull No history of spontaneous pain
bull No sensitivity on percussion
bull No hemorrhage
bull Normal radiographic appearance
Contraindications
bull Evidence that radicular pulp has undergone degenerative changes
bull Purulent drainage
bull History of prolonged pain bull Necrotic debris in canal
bull Periapical radiolucency
6
1
Gupta A Dhingra R Chaudhari P Gupta A
Department of Paedodontics and Preventive Dentistry Faculty of Dental Sciences SGT University Gurgaon Haryana India
Journal of Indian Society of Pedodontics and Preventive Dentistry
Volume 35 I Issue 3 I July-September 2017
A COMPARISION OF VARIOUS MINIMALLY
INVASIVE TECHNIQUES FOR THE REMOVAL
OF DENTAL FLUOROSIS STAINS IN
CHILDREN
DR MITAKSHARA NIRWAN
CONTENTS
bull Introduction
bull Aims
bull Materials and Methods
bull Results
bull Discussion
bull Conclusion
bull Critical analysis
bull References
INTRODUCTION
bull Dental fluorosis is a developmental disturbance of dental enamel caused by
successive exposure to high concentrations of fluoride during tooth
development
bull Various methods of therapy are advocated for the treatment of fluorosis -
stained teeth which range from invasive ceramic veneer bonding restorations
to abrasive chemical treatments
bull The combination of dental bleaching techniques and microabrasion appears
as an excellent conservative solution to reestablish health in fluorosis
affected teeth
AIMS
bull The aim of the study was to evaluate and compare the effectiveness of
minimally invasive techniques for the removal of dental fluorosis
stains in children in vivo
MATERIALS AND METHODS
Patients visiting the department of Pedodontics and Preventive dentistry
Faculty of Dental Sciences SGT University Gurgaon
bull Sample size 90 patients
bull Age group 10 -17 years
bull Caries cracks or periodontal
disease on anterior teeth
bull Abscess draining sinus
cellulitis
bull Non vital teeth
hypersensitive exposed
crevices
bull Orthodontic appliance
bull Past history of bleaching
bull At least two permanent
maxillary anterior teeth
bull TSIF of score 4
bull Free of systemic diseases
Inclusion criteria Exclusion criteria
2
Groups
Group A In office bleaching with 35 hydrogen peroxide( Pola Office
Bleaching kit) activated by light emitting diode (LED) bleaching unit
(35 HP)
Group B Enamel microabrasion (EM) (PREMA Enamel Microabrasion
System) followed by in-office bleaching with 44 carbamide peroxide
gel (EM)
Group C In-office bleaching with 5 sodium hypochlorite (5
NaOCl)
A baseline colour evaluation was done by taking digital photograph of
the maxillary anterior teeth
RESULTS
Group 1
Colour stability
Group 2 Group 3
Tooth sensitivity
Tooth sensitivity values were taken before the treatment
which was compared to immediate postoperative and follow
up visits It was checked using an electric pulp tester
maximum
moderate
least
immediately
group 2
group 1
group 3
1 month
group 2
group 1
group 3
3 month
group 2
group 1
group 3
Patient satisfaction score
Satisfaction was assessed on visual analog scale
Range 1 to 5
Groups percentage of patients
who were satisfied with
the treatment
Number of patients
who reported slight
reappearance of colour
Group 1
90
7
Group 2
83
8
Group 3
73
7
3
Number of Appointments
Groups One sitting Two sittings Three
sittings
Group 1
25
4
1
group 2
26
3
1
Group 3
30
0
0
DISCUSSION
bull Hydrogen peroxide is capable of penetrating the tooth osmosis and through porosities and cracks subsequently acting directly on the pigmented molecules
bull Gurgan et al investigated 3 different light systems and found out that diode laser system with gave best tooth whitening and least tooth sensitivity
bull In the EM group the surface reflects and refracts light from the surface in such way that mild imperfections in underlying enamel are camouflaged While the highly polished surface of enamel enhances the aesthetic appearance
bull Train et al and Loguercio et al also had the similar results in their studies with EM mild fluorosis showed best results moderate showed moderate results while it had little effect on severe fluorosis
bull NaOCl was only effective on mild stains while moderate and severe
stains could only be lightened to quite an extent but could not be
completely removed
bull When NaOCl comes in contact with hypomineralized and discoloured
enamel it degrades and removes the chromogenic organic material
located on the enamel surface
CONCLUSION
bull It was concluded that esthetic appearance of teeth mild fluorosis can
be achieved by bleaching and microabrasion But in cases of
moderate fluorosis a combination of any of theses modalities can be
used
bull As no special maintenance precautions are required these maybe be
considered as an interesting alternative to conventional operative
treatment
bull Focuses on only TSIF of 4
bull Electric pulp testing is not the
right method to check for
sensitivity
bull Tooth Sensitivity changes
from person to person
bull Food habits can cause
staining of the teeth
bull Minimally invasive
bull Cheaper to veneers
bull Minimal loss of tooth structure
bull 4 parameters checked for the success of treatment
bull Inclusion of specific score of fluorosis for comparing the results
bull Maximum 3 appointments needed
CRITICAL ANALYSIS
Pros Cons
REFERENCES
bull Gurgan S Cakir FY Yazici E Different light-activated in officebleaching
systems Lasers Med Sci 201025817-22
bull Train TE McWhorter AG Seale NSWilson CF Guo IY Examination of
esthetic improvement and surface alteration following microabrasion in
fluorotic human incisors in vivoPediatr dent 199618353-62
bull Loguercio AD Correia LD Zago C Tagliari D Neumann E Gomes OM et al
Clinical effectiveness of two microabrasion materials materials for the
removal of enamel flurosis stains Oper Dent 200732531-8
4
7
1
Impact of Handheld Devices on
Children An Evaluation of Usage amp
Dependency Behaviour
0092
DR MITAKSHARA NIRWAN
Handheld devices
A handheld device is a pocket size
computing device with a display
screen and inputoutput interface like
an external or touchscreen keyboard
For example- smartphones tablet
computers handheld videogame
consoles
Haruki Murakami
ldquoCell Phones are so
convenient that they have
become an inconveniencerdquo
Introduction
The most famouscommonly used and easily accessible type of gadgets are
lsquoHandheld devicesrsquo They are as popular in children as they are in adults
The access and ownership of these devices amongst children has grown
substantially in the past decade Concerns exist regarding excessive usage
and the impact of frequent consumption of mobile media on their health and
behaviour
Aims and Objective
This objective of this study was to asses the level of use of handheld
devices among children aged 0-12 years and their positive and negative
impacts on them It further describes the dependency of these devices
and the behavioral problems associated with it
Materials and Methods An online survey was conducted and a self administered questionnaire
was prepared specially for the parents which included a total of 15
questions regarding the usage and dependency of the device
A total of 100 responses were collected from parents who had children
aged 0-12 years who used these devices on daily basis
2
Level of Usage (Q 123)
Results Purpose (Q7)
Improved
communication and
learning
Using more than
one type of
device
Helped in
Speech
Positive Impacts -
(Q58 amp 9)
P value 0003(s) P value-0007 P value-0006(s)
Reduced parent-
child interaction Disrupted sleep Lack of motivation for academics
Negative Impacts (Q81213)
P value-0001(s) P value-0002(s) P value-0006
Time when children use
the device the most
Isolation of the
child Behavioral impact when gadget is
taken back
Dependency
Behaviour (Q10111415)
P value-002(s) P value 002(s) P value-044
This study was done to evaluate the level of usage of handheld devices and their impact
on the children aged 0-12 years The questionnaire was made such that it asked both the
positive and negative impact and further included the questions regarding the
dependency
784 children had access to smartphone and 17 used tablets
The most common age group in which the devices was used the most was 5-8 years
followed by 9-12 followed by 0-4 (Arlinda et al 2019 )
Another study done by (Rachel Bedford et al 2016) concluded increase usage of mobile
phones 5122 in 6ndash11 monthshy olds through to 9205 by 25ndash36 months
745used these devices several times a day out of which 539 used it for more than
one hourday 255 used it for less than one hour and 206 for more than 2 hours
Various studies follow the same recommendation given by AAP to limit the duration of
gadget amongst children
Discussion
3
Improve of Cognitive Skills
Amongst the positive impacts most parents have answered that the usage of these
devices has helped their child communicate and learn better and it has showed significant
results According to (Sundus M 2018)These devices improve the cognitive skills and
develop their learning skills fasterThe competition skills also get better It gives time for brain to think and process information better Another study which supports this (LF
Jonathan et al 2016)
Motor Physical Exercise
This study has shown that children like to use more than one type of device
sometimesUsing these devices improve fine motor skillshand eye coordination and
hands and fingers become more efficient (Srinahyanti et al 2019) (Sundus M 2018)
Speech Improvement
392 Parents say that maybe usage of the devices has helped improve speech in their
children but Various studies show otherwise as most of them shows that usage of handheld
devices causes delay of speech (Srinahyanti et al 2019)
Reduced parent child interaction
The negative impacts are more when compared to the positive ones Usage of gadgets
has resulted in reduced parent child interaction Less face to face interaction can
cause detachment from family members and value which in turn also causes isolation
of the child as he is more comfortable with the gadget (M Suhana-2017)
Sleep Disorders
This study shows that most parents have agreed that usage of these devices does
cause disruption of sleep Various studies have shown that children get fewer hours of
sleepdrowsiness during the day and dramatic increase in day time sleep because of
the screen usage (Acc to National Sleep Foundation) ( Cain N et al 2010)
In this study most number of parents have
agreed that their children might be dependent on
these devices and also had showed restless and
violent behavior if the gadget is snatched from
them
Most number of kids (667) are heavily
dependent as they like to use the device during
their meal time
Various other studies have assessed the screen
time dependency and have concluded that
various kids suffer from SDD
Conclusion The study conclusively shows that the impact of handheld devices is akin to the
importance of table salt in our meals most significant for our growth and
development in moderate amounts and hazardous in excess The negatives clearly
outweigh the positives with the latter too few and far in between This study also
points towards further extensive research on the subject because we need to find ways and also educate parents to optimise the role of these devices in their
childrenrsquos life taking advantage of their positive attributes and minimising their
negative ones
References 1Wahyuni AS Siahaan FB Arfa M Alona I Nerdy N The Relationship between the Duration of Playing
Gadget and Mental Emotional State of Elementary School Students Open Access Maced J Med Sci
20197(1)148ndash151
2Sundus M Department of Computer Science Lahore-The Impacts of using Gadgets on ChildrenJournal of Depression and Anxiety 2018vol 7(1)296
3Amawi SO Subki AH Khatib HA et al Use of Electronic Entertainment and Communication Devices Among
a Saudi Pediatric Population Cross-Sectional Study Interact J Med Res 20187(2)e13
4Julia ldquoHandheld Screen Time Linked with Speech Delays in Young Childrenrdquo Present Pediatric Acad Soc
Meet 2017
5C Rowan ldquoThe Impact of Technology on Child Sensory Motor Developmentrdquo 2003
6Impact of media use on children and youth Paediatr Child Health 20038(5)301ndash317
7Naik SV Children and their gadgets A pedodontist perspective Int J Oral Health Sci 2018857-8
8Roberts DF Foehr UG Rideout V Generation M Media in the lives of 8‐18 year‐olds A Kaiser Family
Foundation Study 2005
9Arya K Time spent on television viewing and its effect on changing values of school going children Anthropologist 20046269‐71
10 Lerner C Barr R Screen Sense Setting the Record StraightResearch‐Based Guidelines for Screen
Use for Children Under 3 Years Old Early learning project at Georgetown university 2014 p 1‐10
11SrinahyantiYasaratodo Wau Imelda Free Unita Manurung Nur Arjani-Influence of gadget A positive
and Negative Impact of Smartphone Usage for Early Child2019
4
THANK YOU
1
Morankar Rahul Aditi Kapur Krishan Gauba Ashima Goyal
MANAGEMENT OF ENDODONTIC INSTRUMENT SEPARATION IN
PRIMARY TEETH
CASE REPORT
Journal of South Asian Association of Pediatric Dentistry 2020
DR MITAKSHARA NIRWAN
bull Introduction
bull Aims amp Objectives
bull Case report
bull Discussion
bull Conclusion
bull Pros amp Cons
bull References
CONTENTS
Separation of endodontic instrument is an unexpected complication and its prevalence is not known It is a common belief among the dental professionals that rotary nickelndashtitanium (NiTi) instruments separate more frequently than stainless steel hand instruments
However literature revealed that in permanent teeth the reported prevalence of separated endodontics manual instruments is in the range of 07-74 whereas for rotary NiTI instruments it is
approximately 04-5
Fractured root canal instruments may include endodontic files Gates Glidden burs finger spreaders
and paste fillers
INTRODUCTION
The aim of this study is to describe the management strategies for endodontic
instrument separation in a root canal of primary teeth with emphasis on factors
requiring consideration in different clinical situations
AIMS amp OBJECTIVES
CASE 1
A 6-year-old male child reported with the chief complaint of spontaneous toothache in mandibular left second primary molar since few days It has aggravated following dental treatment at a private dental clinic Clinical examination revealed an underprepared access cavity with 75 and incomplete caries removal
which was sealed with glass ionomer cement
An intraoral periapical radiograph revealed a separated instrument of about 6ndash7 mm size in the distal root
2
The separated instrument was lodged firmly in distobuccal root canal 2ndash3 mm below the cementoenamel junction The instrument was bypassed successfully with no 15 and no 20 H-files but attempts for its retrieval were not successful
GatesndashGlidden (GG) drills no 2 (07 mm) and no 3 (09 mm) were used to drill around the instrument after which it was retrieved successfully using no 25 H-file
All the canals were instrumented till size 30 k-file followed by obturation with metapex and restoration with glass ionomer cement amp followed by placement of a crown and loop space maintainer for missing 74 The instrument retrieved was a manual reamer measuring 6 mm in length
The patient was asymptomatic since then and is under regular follow-up
CASE 2
A 5-year-old female child reported with the chief complaint of spontaneous toothache in mandibular left second
primary molar Clinical examination revealed deep occlusal caries with fractured lingual wall and pain on
percussion An intraoral periapical radiograph revealed caries involving pulp without any furcation or periapical
area of rarefaction and pulpectomy was planned
All the canals were enlarged using NiTi rotary files with a 4 taper operating at 500 rpm with minimum torque
setting An orifice opener [(0825 19 mm) of 8 taper size 25 length 19 mm] and nos 0420 file was used for
instrumentation of root canal This was followed by file nos 0425 which got separated in the distobuccal root
canal The radiograph confirmed a separated instrument of length 3ndash4 mm in the middle third of the root canal
The instrument was bypassed with no 15 k-file but could not get retrieved As instrument separation had occurred with 0425 file the involved root canal was sufficiently debrided before separation and the level of instrument separation was at the mid-root region so it was decided to obturate and seal this tooth with
periodic follow-ups instead of immediate extraction All other canals were enlarged till size 0430 in the sequential manner followed by obturation using metapex and placement of stainless steel crown
3
CASE 3
A 5-year-old female child has complaint of mild intermittent pain with primary mandibular left first molar She
had undergone pulpectomy treatment for the same during which an instrument separation has occurred in
the mesiobuccal root canal by a resident doctor
A radiograph revealed a separated instrument of about 4 mm in size lodged in the apical third but within the
confines of the mesial root An attempt was made for its retrieval but was unsuccessful The extraction of the
involved tooth was carried out under local anesthesia followed by a band and loop space maintainer
CASE 4
A 7-year-old male child reported with a chief complaint of mild intermittent pain on food lodgment with the primary mandibular right first and second molars The patient had a history of dental treatment at a private
dental clinic few months back which he did not continue further
Clinical examination revealed glass ionomer restoration with 85 and proximal caries with 84 leading to food lodgment An intraoral periapical radiograph with 85 revealed empty root canals with a separated
instrument of about 3ndash4 mm size beyond the apex of mesial root close to the developing succedaneous premolar
4
DISCUSSION
Stainless steel files usually separate fracture due to the excessive amounts of torque and overuse or the
preexisting distortion of the instrument whereas in NiTi rotary files it is a combined result of torsional stress and cyclic fatigue
Therapeutic options for the management of separated endodontic instruments include no intervention nonsurgical (orthograde conservative) management surgical management and tooth extraction
Use of ultrasonic scaler Masserann technique Endo extractor and Cavi-Endo ultrasonic instruments are some of the methods popular for retrieval of a separated endodontic instrument in the permanent tooth
In case 1 a 6-mm-long manual reamer was retrieved successfully with the use of GG drill using a manual file and copious irrigation which is the most desired treatment outcome
In case 2 the retrieval of separated rotary file lodged in the middle third of the root canal was unsuccessful in spite of multiple attempts It was therefore managed with routine obturation followed by restoration to maintain the tooth in its physiological functional state It was kept under close periodic follow-up at least
every 3 months This treatment option should be encouraged where it is possible to follow up the patient clinically and radiographically at close periodic intervals as there is the possibility of instrument escaping
into bone due to physiological root resorption
In cases 3 and 4 an instrument has separated in the apical root portion
In case 3 it was within the root canal and thus an attempt was made for its retrieval which was
unsuccessful It was therefore extracted to prevent the fractured instrument from getting exposed in the bone following resorption as there is no accurate and consistent established age for initiation of resorption in primary teeth known per se
In case 4 an immediate extraction of involved tooth was carried out as the separated instrument was beyond the apex of the primary tooth root
Age of the child clinical signs and symptoms and amount of root resorption are the factors which can also influence the management of separated instrument in primary teeth
Moreover if an instrument has separated after initial cleaning and shaping of root canal maintaining a tooth is not a problem as clinical signs and symptoms are not anticipated and the good prognosis is expected
However if an instrument has separated early during the initial cleaning and shaping of the root canal clinical symptoms may compromise the prognosis
Therefore these factors should be kept in mind while planning a suitable management strategy to avoid or at least reduce the burden of extraction and wear of space maintainer for longer period
5
CONCLUSION
The management and prognosis of a primary tooth with a separated instrument is
dependent on the level of instrument fracture within the root age of the child root
resorption and clinical signs and symptoms of the involved tooth
Different management approaches can be tried depending on clinical situations keeping
in mind benefits vs risks in preserving the tooth
PROS amp CONS
PROS
The entire procedure is given
by step by step
Well descriptive xrays and
photographs
CONS
Medical history has not been
given
REFERENCES
1 TOMER ANIL K ET AL ldquoBROKEN FILE RETRIEVAL PUZZLE IN ENDODONTICSrdquo
(2016)
2 SHENOY A MANDAVA P BOLLA N ET AL A NOVEL TECHNIQUE FOR REMOVAL OF
BROKEN INSTRUMENT FROM ROOT CANAL IN MANDIBULAR SECOND MOLAR
INDIAN J DENT RES 201425(1)107ndash110
3 PATEL J MORAWALA A TALATHI R ET AL RETRIEVAL OF A BROKEN INSTRUMENT
FROM ROOT CANAL IN PRIMARY ANTERIOR TEETH UNIV RES J DENT 20155(3)203ndash
206
4 MORANKAR R GOYAL A GAUBA K ET AL MANUAL VERSUS ROTARY
INSTRUMENTATION FOR PRIMARY MOLAR PULPECTOMIES - A 24 MONTHS
RANDOMIZED CLINICAL TRIAL PEDIAT DENT J 201828(2)96ndash102
5 KASHYAP NILOTPOL (2018) RETAINING PRIMARY MOLARS WITH INSTRUMENT
SEPERATION A CASE REPORT AND CLINICAL GUIDE
6
1
IMPACT OF 6 CITRIC ACID AND ENDOACTIVATOR AS IRRIGATION ADJUNCTS ON OBTURATION QUALITY AND PULPECTOMY OUTCOME IN
PRIMARY TEETH
NEETU JAIN SHALINI GARG ABHISHEK DHINDSA SAKSHI JOSHI HARJOY
KHATRIA
PEDIATRIC DENTAL JOURNAL 2019 29
1
DR MITAKSHARA NIRWAN
CONTENTS
bull INTRODUCTION
bull AIMS amp OBJECTIVES
bull CASE REPORT
bull RESULTS
bull DISCUSSION
bull CONCLUSION
bull PROS AND CONS
bull REFERENCES
2
INTRODUCTION
bull ENDODONTIC THERAPY IN PRIMARY TEETH INVOLVES DISINFECTION OF THE ROOT CANAL
SYSTEM AND ITS OBTURATION WITH RESORBABLE PASTE
bull THE CONTENTS OF ROOT CANAL ALONG WITH SMEAR LAYER ARE EXPECTED TO BE REMOVED
DURING THE BIOMECHANICAL PREPARATION
bull IN VITRO AND CLINICAL DOCUMENTS HAVE INDICATED THAT MECHANICAL PREPARATION OF
THE CANAL LEAVES LARGE PORTIONS OF THE CANAL WALLS UNDEBRIDED AND COMPLETE
REMOVAL OF THE BACTERIA BY THIS MECHANICAL PROCEDURE ALONE IS UNLIKELY TO BE SEEN
THEREFORE SOME FORM OF DISINFECTIONIRRIGATION IS MANDATORY TO KILL THE
MICROORGANISMS AND TO REMOVE THE RESIDUAL TISSUES
3
bull THE IDEAL REQUISITES OF A ROOT CANAL IRRIGANT AS GIVEN BY ZEHNDER ARE
1 BROAD ANTIMICROBIAL SPECTRUM
2 HIGH EFFICACY AGAINST ANAEROBIC AND FACULTATIVE MICROORGANISMS ORGANIZED
IN BIOFILMS
3 ABILITY TO DISSOLVE NECROTIC PULP TISSUE REMNANTS
4 ABILITY TO INACTIVATE ENDOTOXIN
5 ABILITY TO PREVENT THE FORMATION OF A SMEAR LAYER DURING INSTRUMENTATION OR
TO DISSOLVE THE LATTER ONCE IT HAS FORMED
6 SYSTEMICALLY NONTOXIC WHEN THEY COME IN CONTACT WITH VITAL TISSUES
NONCAUSTIC TO PERIODONTAL TISSUES AND WITH LITTLE POTENTIAL TO CAUSE AN
ANAPHYLACTIC REACTION
SINCE NO SINGLE IRRIGANT HAS THESE OPTIMAL PROPERTIES STUDIES HAVE REPORTED THE USE
OF TWO OR MORE SOLUTIONS IN A SPECIFIC SEQUENCE OR IN COMBINATIONS FOR BETTER
RESULTS 4
bull SEVERAL IRRIGATING SOLUTIONS ALONG WITH CHELATING AGENTS HAVE BEEN USED
DURING BIOMECHANICAL PREPARATION OF ROOT CANAL BOTH IN PRIMARY AND
PERMANENT TEETH
bull HOWEVER NONE OF THE AVAILABLE IRRIGATING SOLUTIONS HAS BEEN REGARDED CLEARLY
AS OPTIMAL SOLUTION BECAUSE OF THEIR LIMITED EFFECTIVENESS ESPECIALLY IN APICAL
13RD OF THE ROOT CANAL SYSTEM
bull TO OVERCOME SUCH LIMITATIONS USE OF ENDOACTIVATOR HAS BEEN PROPOSED AS AN
IRRIGATION FACILITATOR THAT IS BASED ON SONIC VIBRATION (UP TO 10000 CPM) WHICH
FACILITATES THE IRRIGANT PENETRATION AND ITS RENEWAL WITHIN THE CANAL
bull ACTIVATION SYSTEMS RESULTED IN BETTER REMOVAL OF THE SMEAR LAYER IN THE APICAL
THIRD OF ROOT CANALS IN COMPARISON TO CONVENTIONAL IRRIGATION
5
CITRIC ACID
bull CITRIC ACID IS A WEAK ORGANIC ACID WITH THE APPEARANCE OF WHITE CRYSTALLINE
POWDER AT ROOM TEMPERATURE
bull IT CAN EXIST EITHER IN WATER-FREE FORM (ANHYDROUS) OR MONOHYDRATE FORM THE
WATER-FREE FORM CRYSTALLIZES FROM THE HOT WATER WHEREAS THE MONOHYDRATE
FORMS FROM THE COLD WATER THE LATTER MAY BE CONVERTED TO ANHYDROUS FORM BY
HEATING MORE THAN 78degC
bull CITRIC ACID OCCURS NATURALLY IN THE BODY IN MITOCHONDRIA AND IS USED BY BLOOD
BANKS TO PREVENT COAGULATION OF TRANSFUSED BLOOD CITRIC ACID IS ALSO ESSENTIAL
TO HUMAN METABOLISM AND IS FOUND IN MANY FOODS
6
2
bull THE BIOLOGICAL EFFECTS OF CITRIC ACID ON THE PERIODONTAL STRUCTURE HAS BEEN
EXTENSIVELY STUDIED IN PERIODONTICS
bull NEUMAN AND NEWMAN SHOWED THAT CITRIC ACID IS THE MOST EFFECTIVE ACID IN
ALTERING THE SOLUBILITY OF HYDROXYAPATITE
bull YAMAGUCHI ET AL SHOWED THAT CITRIC ACID SOLUTION HAD ANTIBACTERIAL EFFECTS ON
ALL 12 ROOT CANAL BACTERIA TESTED
bull ARIAS-MOLIZ ET AL SHOWED THAT ETHYLENEDIAMINETETRAACETIC ACID (EDTA) HAS NO
BACTERICIDAL ACTIVITY EVEN AFTER 1 HOUR CONTACT
bull THIS ACID HAS THE ABILITY OF ROOT CANAL IRRIGATION AND ALSO SMEAR LAYER REMOVAL
DIFFERENT CONCENTRATIONS (1ndash50) HAVE BEEN PROPOSED GUTMANN ET AL CONCLUDED
THAT 10 CITRIC ACID IS BETTER THAN ULTRASOUND FOR SMEAR LAYER REMOVAL FROM THE
ROOT END CAVITIES
7
bull STUDIES HAVE SHOWN IRRIGATION WITH 6 CA FOR 15 OR 30 SECONDS IS QUITE
EFFECTIVE IN REMOVING ALL THE COMPONENTS OF THE SMEAR LAYER OF THE PRIMARY
TEETH WHEREAS PERITUBULAR DENTIN DESTRUCTION WAS OBSERVED WHEN HIGHER
CONCENTRATION OF CITRIC ACID WAS USED AS AN IRRIGATING SOLUTION
8
AIMS amp OBJECTIVES
bull THIS STUDY WAS AIMED TO EVALUATE THE CLINICAL AND RADIOGRAPHIC OUTCOME OF
PULPECTOMY ALONG WITH QUALITY OF OBTURATION USING 6 CITRIC ACID AND
ENDOACTIVATOR
9
CASE REPORT
bull 350 CHILDREN (3-9 YEARS) WITH CLINICAL SIGNS AND SYMPTOMS OF CHRONIC IRREVERSIBLE
PULPITIS IN DEEPLY CARIOUS TEETH WERE SCREENED DURING SCHOOL DENTAL HEALTH
PROGRAM FROM MAY 2014-JULY 2014
bull 123 CHILDREN REPORTED TO THE DEPARTMENT AND 67 CHILDREN WERE SELECTED BASED ON
INCLUSION AND EXCLUSION CRITERIA
RECRUITMENT OF PATIENTS
10
INCLUSION CRITERIA
bull HISTORY OF SPONTANEOUS PAIN AND UNCONTROLLED BLEEDING AFTER PULP AMPUTATION
EXCLUSION CRITERIA
bull EVIDENCE OF INTERNAL OR EXTERNAL (PHYSIOLOGICPATHOLOGIC) ROOT RESORPTION OF MORE THAN A THIRD OF ITS LENGTH
bull ROOT CANAL OBLITERATION OR ANATOMIC ANOMALIES
bull INADEQUATE BONE SUPPORT OR NON RESTORABLE TOOTH
bull ONCE PATIENTS ELIGIBILITY WAS CONFIRMED THE TREATMENT PROCEDURE WAS
EXPLAINED TO THE PARENTGUARDIAN AND INFORMED WRITTEN CONSENT WAS
OBTAINED FROM PARENTSGUARDIANS SHOWING WILLINGNESS FOR THEIR
CHILDRENS TREATMENT 11
PROCEDURE
bull PULPECTOMY WAS PERFORMED BY ONE OPERATOR OF PEDIATRIC DENTISTRY DEPARTMENT
USING A STANDARDIZED TREATMENT PROTOCOL FOR ALL THE PATIENTS
bull AFTER ADMINISTRATION OF LOCAL ANESTHESIA RUBBER DAM WAS APPLIED FOR ISOLATION
bull ACCESS CAVITY WAS PREPARED USING AIR-ROTOR HAND PIECE WITH 8 ROUND BUR AND
PULP TISSUE WAS EXTIRPATED WITH THE HELP OF SPOON EXCAVATOR
bull FURTHER THE NEGOTIATION OF THE CANALS WAS DONE WITH 10 K-FILE
bull A DIAGNOSTIC RADIOGRAPH WAS TAKEN FOR ROOT LENGTH DETERMINATION AND
WORKING LENGTH WAS KEPT 1 MM SHORT OF THE RADIOGRAPHICAL APEX
bull ALL ROOT CANALS WERE INSTRUMENTED MANUALLY USING K-FILES AND WERE IRRIGATED
WITH 10 ML 09 NORMAL SALINE AND 1 SODIUM HYPOCHLORITE AS STANDARDIZING
PROTOCOL FOR ROOT CANAL PREPARATION AND DISINFECTION
12
3
GROUP 1 (CA + E) - IRRIGATION WAS DONE
WITH 10 ML OF 6 CITRIC ACID (CITOCID AMMDENT)
AND IRRIGANTS WERE SONICALLY AGITATED WITH
ENDOACTIVATOR (DENTSPLY) FOR 30 S PER CANAL USING REDBLUE
ENDOACTIVATOR TIP
GROUP 2 (CA) - 10 ML OF 6 CITRIC ACID FOR 1 MIN USING
27 GAUZE IRRIGATING NEEDLE
GROUP 3(SH + E) - 10 ML OF 1 SODIUM HYPOCHLORITE
SOLUTION AND SONIC ACTIVATION WITH ENDOACTIVATOR
GROUP 4(SH) - 10 ML OF 1 SODIUM HYPOCHLORITE
SOLUTION USING IRRIGATING NEEDLE (CONTROL GROUP)
bull TEETH UNDERGOING PULPECTOMY WERE RANDOMLY ENROLLED BY CHIT METHOD INTO THREE
STUDY AND ONE CONTROL GROUP
13
bull IN CITRIC ACID GROUPS FINAL RINSE WITH NORMAL SALINE WAS DONE TO REMOVE THE
REMAINING CRYSTALS (CHELATES)
bull FOLLOWING BIOMECHANICAL PREPARATION THE ROOT CANALS WERE DRIED WITH STERILE
ABSORBENT PAPER POINTS AND OBTURATED WITH VITAPEX USING HAND HELD
LENTULOSPIRAL FINAL RESTORATIONS WERE DONE USING COMPOSITE RESIN
14
bull CLINICAL FOLLOW UP WAS DONE AT 24 H1 WEEK 1 MONTH 6 MONTH AND 12
MONTH TO CHECK PAIN PRESENCE AND PAIN FREQUENCY (ONCEMORE THAN ONCE)
SWELLING FISTULA SENSITIVITY TO PERCUSSION
bull RADIOGRAPHIC FOLLOW UP WAS DONE AT 6 MONTH AND 12 MONTH FOR ANY
DEVIATED ERUPTION OF SUCCEDANEOUS TEETH EXCESS FILING MATERIAL AND ITS
RESORPTION EXTERNALINTERNAL ROOT RESORBTION CALCIFIC METAMORPHOSIS
PRESENCE OF FURCATION RADIOLUCENCY
CLINICAL amp RADIOGRAPHIC FOLLOW UP
15
RADIOGRAPHIC ASSESSMENT OF OBTURATION QUALITY
bull POSTOPERATIVE RADIOGRAPHS WERE VISUALLY ASSESSED FOR QUALITY OF OBTURATION BY
TWO INDEPENDENT EXAMINERS (SG AD) WHO WERE BLINDED WITH REGARD TO
IRRIGATION PROTOCOL GROUP TO ENHANCE CALIBRATION EACH EXAMINER ASSESSED THE
RADIOGRAPH INDEPENDENTLY AND LATER REVIEWED TOGETHER FOR FINAL ASSESSMENT
INDIVIDUAL ROOT WAS TAKEN AS UNIT OF ANALYSIS FOR GRADE OF OBTU- RATION AND
SCORING CRITERIA WERE AS GIVEN BY COLL JA 1996
1 UNDER FILLED - FILLING MATERIAL ENDED 1 MM OR MORE SHORT OF THE APEX
2 OPTIMAL FILLING- FILLING MATERIAL APPEARED TO END AT THE RADIOGRAPHICAL APEX
3 OVERFILLED - FILLING MATERIAL EXTRUDED PAST THE RADIOGRAPHIC APEX
4 OPTIMALLY FILLED ROOTS WERE FURTHER ASSESSED FOR THE PRESENCE OF VOIDS AND VOID
AREA (ROOT CANAL SURFACE UNTOUCHED BY THE ROOT CANAL FILLING MATERIAL) IN THREE
VISUALLY DIVIDED SECTIONS OF THE ROOT IE CORONAL MIDDLE AND APICAL 13RD
16
RESULTS
bull OVERALL CLINICAL AND RADIOGRAPHIC SUCCESS RATE OVER A PERIOD OF ONE YEAR WAS
9886 amp 977 RESPECTIVELY
bull ALL GROUPS WERE SIGNIFICANTLY (P = 001) EFFECTIVE IN ALLEVIATING PAIN WITHIN 24 H
OF PULPECTOMY
17 18
4
19
bull IMMEDIATE POST OPERATIVE RADIOGRAPHIC ASSESSMENT REVEALED 68 (102150) ROOTS
WITH OPTIMAL OBTURATION AND 32 (48150) WITH OVERFILLINGUNDERFILLING MAXIMUM
NO OF OPTIMAL FILLINGS WERE OBSERVED IN GROUP1 (CA + E) (3333) FOLLOWED BY
GROUP 2 (CA) (2549) GROUP 3(SH + E) (2549) AND GROUP 4(SH) (1568)
bull CITRIC ACID GROUPS HAD MORE NUMBER OF OPTIMALLY FILLED ROOTS 588 (60102) THAN
NON CITRIC ACID GROUPS 412 (42102)
bull ENDOACTIVATOR CONTRIBUTED TO 18 OF OPTIMAL OBTURATION IRRESPECTIVE OF
CHELATING AGENT USED
20
21
bull MAXIMUM NO OF VOIDS AND VOID AREAS WERE IN NON CITRIC ACID GROUPS
(6419 amp 5384) COMPARED TO CITRIC ACID GROUPS (3580 amp 4615)
RESPECTIVELY
bull ANALYSIS OF ROOT 13RD REVEALED MAXIMUM NO OF VOID AREA IN APICAL
13RD (4755) FOLLOWED BY MIDDLE 13RD (3846) AND CORONAL 13RD
(1398)
bull LEAST NO OF VOIDS amp VOID AREA (1111 amp 1608) WERE OBSERVED WHEN
ENDOACTIVATOR ALONG WITH CHELATING AGENT WAS USED (GROUP 1)
HOWEVER THIS WAS STATISTICALLY INSIGNIFICANT
22
DISCUSSION
bull IN THE PRESENT STUDY 1 SODIUM HYPOCHLORITE WAS USED ALONG WITH 6 CITRIC ACID
(CHELATING AGENT) WHICH IS REPORTED TO BE AS EFFECTIVE AS 17 EDTA
bull CITRIC ACID (BIOLOGICAL ACID) IS FOUND TO BE BIOCOMPATIBLE AND LEAST IRRITATING TO
PERIAPICAL TISSUES THAN OTHER CHELATING AGENTS
bull USE OF SODIUM HYPOCHLORITE SOLUTION FOLLOWING CHELATING AGENT WAS AVOIDED AS IT
RAPIDLY PRODUCES SEVERE EROSION OF ROOT CANAL WALL DENTIN
bull TRADITIONAL APPROACH OF DELIVERING IRRIGANTS INTO THE ROOT CANAL SPACE USING
SYRINGES AND METAL NEEDLES HAS BEEN FOUND TO BE INEFFECTIVE ESPECIALLY IN THE AREAS OF
ANASTOMOSES BETWEEN CANALS AND APICAL 13RD OF ROOT CANAL
23
bull THEREFORE TO ACHIEVE BETTER CLEANING EFFICIENCY IRRIGANT ACTIVATION HAS BEEN
RECOMMENDED SONIC ACTIVATION HAS BEEN REPORTED TO RESULT IN BETTER ROOT CANAL
CLEANLINESS AS COMPARED TO NO ACTIVATION OF IRRIGANT
24
5
CONCLUSION
bull USE OF 6 CITRIC ACID DEFINITELY HELPED IN RAPID ELIMINATION OF PAIN RESOLUTION OF
PERI-RADICULAR RADIOLUCENCY BETTER OBTURATION QUALITY IN TERMS OF LESS VOIDS AND
VOID AREAS ALONG WITH MAXIMUM NO OF OPTIMAL OBTURATION UP TO APICAL AREA
bull 6 CITRIC ACID AND ENDOACTIVATOR IRRIGATION PROTOCOL PROVED TO BE THE BETTER
IRRIGATION PROTOCOL WHICH MAY CONTRIBUTE TO LONG TERM SUCCESS OF PRIMARY
TOOTH AND THE HEALTH OF UNDERLYING PERMANENT TOOTH
bull 6 CITRIC ACID ALONG WITH ENDOACTIVATOR MAY BE RECOMMENDED AS IRRIGATION
ADJUNCTS IN PULPECTOMY PROCEDURE OF PRIMARY TEETH
25
PROS AND CONS
PROS
bull PROPER EXPLANATION OF THE MATERIALS
USED
CONS
bull NO PREOPERATIVE AND POSTOPERATIVE
RADIOGRAPHS
26
REFERENCES
bull RAMACHANDRA JA NIHAL NK NAGARATHNA C VORA MS ROOT CANAL IRRIGANTS IN
PRIMARY TEETH WORLD J DENT 20156(3)229-234
bull MOHAMMADI Z JAFARZADEH H SHALAVI S KINOSHITA JI UNUSUAL ROOT CANAL
IRRIGATION SOLUTIONS J CONTEMP DENT PRACT 201718(5)415-420
bull ZEHNDER M ROOT CANAL IRRIGANTS J ENDOD 2006 32389- 98
bull SMITH JJ amp WAYMAN BE AN EVALUATION OF THE ANTIMICROBIAL EFFECTIVENESS OF
CITRIC ACID AS A ROOT CANAL IRRIGANT JOURNAL OF ENDODONTICS 1986 12(2) 54-58
bull TANNURE PN AZEVEDO CP BARCELOS R GLEISER R PRIMO LG LONG-TERM OUTCOMES OF
PRIMARY TOOTH PULPECTOMY WITH AND WITHOUT SMEAR LAYER REMOVAL A RANDOMIZED
SPLIT-MOUTH CLINICAL TRIAL PEDIATR DENT 201133316E20 27
bull CARON G NHAM K BRONNEC F MACHTOU P EFFECTIVENESS OF DIFFERENT FINAL IRRIGANT
ACTIVATION PROTOCOLS ON SMEAR LAYER REMOVAL IN CURVED CANALS J ENDOD
2010361361E6
bull COLL JA SADRIAN R PREDICTING PULPECTOMY SUCCESS AND ITS RELATIONSHIP TO
EXFOLIATION AND SUCCEDANEOUS DENTITION PEDIATR DENT 19961857E63
28
1
LOCAL
ANESTHESIA
DR MITAKSHARA NIRWAN
CONTENTS
Definition
Methods of inducing local anesthesia
Desirable properties
Electrophysiology of nerve conduction
Impulse propagation and spread
Mode and site of action of local anesthesia
Classification of local anesthetic according to biological site and mode of action
Dissociation of local anaesthetics
Mechanism of action of local anaethetics
Local anaesthetic agent
2
3
DEFINITION
Local anesthesia is defined as a loss of sensation in
a circumscribed area of the body caused by depression
of excitation in nerve endings or an inhibition of the
conduction process in peripheral nerves
An important feature of local anesthesia is that it produces
LOSS OF SENSATION WITHOUT INDUCING LOSS OF
CONSCIOUSNESS
4
METHODS OF INDUCING LOCAL
ANESTHESIA
Low temperature
Mechanical trauma
Anoxia
Neurolytic agents such as alcohol amp phenol
Chemical agents such as local anesthetics
PROPERTIES OF LOCAL
ANESTHESIA
It should not be irritating to tissue to which it is applied
It should not cause any permanent alteration of nerve structure
Its systemic toxicity should be low
Time of onset of anesthesia should be short
It should be effective regardless of whether it is injected into the tissue or applied locally to mucous membranes
The duration of action should be long enough to permit the completion of procedure
5 6
It should have the potency sufficient to give complete
anesthesia with out the use of harmful concentration solutions
It should be free from producing allergic reactions
It should be free in solution and relatively undergo
biotransformation in the body
It should be either sterile or be capable of being sterilized by
heat with out deterioration
2
ELETROPHYSIOLOGY OF
NERVE CONDUCTION
There is an electrical charge across the membrane
This is the membrane potential
The resting potential (when the cell is not firing) is a negative
electrical potential of -70mv that exists across the nerve
membrane produced by different concentrations of either side of
the membrane
The interior of nerve is NEGATIVE in relation to exterior
7 8
inside
outside
Resting potential of neuron = -70mV
+
-
+
-
+
-
+
-
+
-
SLOW DEPOLARIRIZATION
9
RAPID DEPOLARIZATION
The interior of nerve is POSITIVE in relation to exterior
REPOLARIZATION
10
bull Repolarization takes 07 msec
bull Depolarization takes 03 msec
SODIUM PUMP -
energy comes from the oxidative metabolism of ATP
bull The entire process require 1 msec
IMPULSE PROPOGATION
IMPULSE SPREAD
The propagated impulse travels along the nerve
membrane towards CNS The spread of impulse differs
in myelinated and unmyelinated nerve fibers
DEPOLARIZED SEGMENT ADJACENT RESTING AREA
MODE AND SITE OF ACTION OF LOCAL
ANESTHETICS
Local anesthetic agent interferes with excitation
process in a nerve membrane in one of the
following ways
Altering the basic resting potential of nerve
membrane
Altering the threshold potential
Decreasing the rate of depolarization
Prolonging the rate of repolarization
12
3
CLASSIFICATION OF LOCAL ANESTHETIC
SUBSTANCES ACCORDING TO
BIOLOGICAL SITE AND MODE OF ACTION
CLASS A
Agents acting at receptor site on external surface of nerve membrane
Chemical substance Biotoxins (eg tetrodotoxin and saxitoxin)
CLASS B
Agents acting on receptor sites on internal surface of nerve membrane
Chemical substance Quaternary ammonium analogues of lidocaine
scorpion venom 13
CLASS C Agents acting by receptor independent of
physiochemical mechanism
Chemical substance Benzocaine
CLASS D Agents acting by combination of receptors and
receptor independent mechanisms
Chemical substance most clinically useful anesthetic agents
(eg lidocaine mepivacaine prilocaine)
14
BASED ON THE SOURCE
NATUAL
SYNTHETIC
OTHERS
BASED ON MODE OF APPLICATION
bull INJECTABLE
bull TOPICAL
BASED ON DURATION OF ACTION
bull ULTRA SHORT
bull SHORT
bull MEDIEM
bull LONG
BASED ON ONSET OF ACTION SHORT
INTERMEDIATE
LONG
15
DISSOCIATION OF LOCAL
ANESTHETICS
Local anesthetics are available as salts (usually
hydrochlorides) for clinical use
The salts both water soluble and stable is dissolved in
either sterile water or saline
In this solution it exists simultaneously as unchanged
molecule (RN) also called base and positively charged
molecules (RNH+) called cations
RNH+ ==== RN+ H
+
16
The relative concentration of each ionic form in the solution varies
in the pH of the solution or surrounding tissue
In the presence of high concentration of hydrogen ion (low pH) the
equilibrium shifts to left and most of the anesthetic solution exists
in cationic form
RNH+ gt RN
+ + H
+
As hydrogen ion concentration decreases (higher pH) the
equilibrium shifts towards the free base form
RNH+ lt RN + H
+
17
The relative proportion of ionic form also depends on pKa or DISSOCIATION CONSTANT of the specific local anesthetic
The pKa is a measure of molecules affinity for H+
ions
When the pH of the solution has the same value as pKa of the local anesthetic exactly half the drug will exists in the RNH
+ form and
exactly half in RN form
The percentage of drug existing in either form can be determined by Henderson Hasselbalch equation
Log baseacid = pH - pKa
18
4
MECHANISM OF ACTION OF LOCAL
ANESTHETICS
The following sequence is proposed mechanism of action of LA
Displacement of calcium ions from the sodium channel receptor site
Binding of local anesthetic molecule to this receptor site
Blockade of sodium channel
19
Decrease in sodium conductance
Depression of rate of electrical depolarization
Failure to achieve the threshold potential level
Lack of development of propagated action potential
Conduction blockadehellip
20
21
Na + Na +
22
LOCAL ANESTHETIC AGENT
COMERCIALLY PREPARED LOCAL ANESTHESIA
CONSISTS OF
Local anesthetic agent (xylocaine lignocaine 2)
Vasoconstrictor (adrenaline 1 80000)
Reducing agent (sodium metabisulphite)
Preservative (methylparabencapryl
hydrocuprienotoxin)
Fungicide (thymol)
Vehicle (distillde waterNaCl)
LOCAL ANESTHETIC AGENT
The local anesthetics used in dentistry are divided
into two groups
ESTER GROUP
AMIDE GROUP
23 24
ESTER GROUP It is composed of the following
An aromatic lipophilic group
An intermediate chain containing
an ester linkage
A hydrophilic secondary or tertiary
amino group
AMIDE GROUP It is composed of the following
An aromatic lipophilic group
An intermediate chain containing
amide linkage
A hydrophilic secondary or tertiary
amino group
5
25
CLASSIFICATION OF LOCAL ANESTHETICS
ESTERS
Esters of benzoic acid
Butacaine
Cocaine
Benzocaine
Hexylcaine
Piperocaine
Tetracaine
Esters of Para-amino
benzoic acid
Chloroprocain
Procaine
Propoxycaine
26
AMIDES Articaine
Bupivacaine
Dibucaine
Etidocaine
Lidocaine
Mepivacaine
Prilocaine
Ropivacaine
QUINOLINE
Centbucridine
PHARMACOKINETICS OF LOCAL
ANESTHETICS UPTAKE
When injected into soft tissue most local anesthetics produce
dilation of vascular bed
Cocaine is the only local anesthetic that produces
vasoconstriction initially it produces vasodilation which is
followed by prolonged vasoconstriction
Vasodilation is due to increase in the rate of absorption of the
local anesthetic into the blood thus decreasing the duration of
pain control while increasing the anesthetic blood level and
potential for over dose 27
AMIDE LOCAL ANESTHETICS
The metabolism of amide local anesthetics is more
complicated then esters The primary site of
biotransformation of amide drugs is liver
Entire metabolic process occurs in the liver for lidocaine
articaine etidocaine and bupivacaine
Prilocaine undergoes more rapid biotransformation then the
other amides
28
REFERENCES
Handbook of local anesthesia ndash Stanley F Malamed ndash 6th
edition
Essentials of Local Anesthetic Pharmacology Daniel E
Becker Anesth Prog 2006 Fall 53(3) 98ndash109
WIKIPEDIEA
29
THANK YOU
30
1
Pharmacological Methods of Behavior
Management
DR MITAKSHARA NIRWAN
DEFINITIONS
bull Conscious Sedation ndash A minimally depressed level of consciousness that retains
the patients ability to independently and continuously maintain an airway and respond appropriately to physical stimulation or verbal command
(American Dental Association House Of Delegates 2000)
bull Deep Sedation ndash An induced state of depressed consciousness
accompanied by partial loss of protective reflexes including the inability to continuously maintain an airway independently and or to respond purposefully to physical stimulation or verbal command
bull General Anesthesia (G A) ndash An induced state of unconsciousness or complete loss of
protective reflexes including the inability to continually maintain an airway independently and respond purposefully to physical stimulation or verbal command
Conscious sedation
ADVANTAGES
Conscious
Protective reflexes active amp intact
Stable vital signs
Operating dentist may perform sedation
Minimum amount of equipment required
Prolong detainment in recovery room not required
Risk of complication very low
Excellent choice for poor ndash risk pt in dental office
Cost effective
General anesthesia
ADVANTAGES Not absolutely
essential May be the only
method Not necessary (no
pain reaction) Amnesia always
present
Conscious sedation
DISADVANTAGES
Pt cooperation is essential
Extremely difficult or mentally handicapped pt cannot always be managed
Use of local anesthesia is a must
Amnesia may or may not be present
General anesthesia DISADVANTAGES
Pt unconscious
Protective reflexes are depressed
Depressed
Advanced training required Dentist must not act also as anesthetist
Special equipment necessary
Detainment in recovery area necessary
High IOP amp postoperative complications
Not indicated in dental office
More expensive
Fundamental Concepts
bull Techniques that utilize drugs to induce co-operative yet conscious state in an otherwise uncooperative child ndash CONSCIOUS SEDATION
2
GOALS
1 To facilitate the provision of quality care
2 To minimize the extremes of disruptive behavior
3 To promote a positive psychologic response to treatment
4 To promote patient welfare amp safety
5 To return the patient to physiologic state
OBJECTIVES
1 The pt mood must be altered
2 The pt must remain conscious at all times
3 The pt must be cooperative
4 All protective reflexes must remain intact and active
5 Vital signs must remain stable and with in normal limits
6 The ptrsquos pain threshold should be elevated
7 Amnesia may be present
Indications
1 Preschool children
2 Lack of Psychological Emotional maturity
3 Lack of Cognitive Physical Medical disability
4 Fearful amp anxious pts
5 Pt who require extensive amp complicated dental care amp would require or benefit from prolonged visits
6 Acute pain
7 Traumatic injuries
Operating Facilities amp Equipment
A positive pressure O2 delivery system capable of administering gt than 90 O2 at 10L min flow for 60 min (650L ldquoErdquo cylinder)
OR
Self inflating bag valve mask device (15L min)
A functional suction apparatus with appropriate suction catheters
Monitoring equipment - PO BPC PC or Capno
Inhalation sedation unit
100 O2 amp never less than 25
A fail safe mechanism that is checked and calibrated annually
Must have appropriate scavenging system
Emergency drugs
Techniques of sedation
Routes for drug administration
bull Oral
bull Rectal
bull Inhalational
bull Transmucosal
ndash Sublingual
ndash Intranasal
bull Parenteral
ndash IM
ndash sub mucosal
ndash IV
3
Oral Sedation
Advantages
1 Almost universally accepted and the easiest method
2 Decreased incidence and severity of adverse reaction
3 Low cost
Disadvantages
1 Absorption is variable
2 Prolonged latent period(30 min)
3 Reversal of any unwanted effect is also difficult
4 Inability to readily lighten or deepen the level of sedation
5 Prolonged duration of action
Rectal Sedation
Advantages 1 Incidence and intensity of
drug related side effects is minimized
2 Drug absorption occurs from the large intestine directly into the circulation
3 The lack of a needle syringe or other equipment
4 The ease of administration
5 The low cost
Disadvantages
1 Inconvenience to the administrator amp pt
2 The variable absorption of drugs from the large intestine
3 The slow onset of action amp the relatively long duration of action
4 Inability to titrate the drug dosage
5 The inability to reverse the action of the drug the prolonged recovery
Intranasal sedation
Advantages
Rapid onset (10 ndash 15 min)
Simple amp relatively painless
Less pt cooperation is required
Absorbed directly into the C V S
Intranasal sedation
Disadvantages
1 Dependence on nasal mucous membrane
2 Shorter duration of action(40-60min)
3 Multiple dosage may be necessary
Drugs
Midazolam ndash 02mgkg
Sufentanil ndash 15 ndash 3 mcgkg
Ketamine ndash 3-6mg kg
Sublingual sedation
Advantages
1 Pt acceptance
2 Rapid onset
3 High bioavailability
Drugs
Oral Transmucosal Fentanyl Citrate (OTFC)
Intramuscular Sedation
Advantages
1 More rapid onset of action
2 Absorbed directly into the C V system
3 More reliable absorption of drug
4 Pt cooperation is not as essential
Disadvantages
1 Time factor ndash its 15 min latent period
2 Pt may not be willing to accept the injection
3 The prolonged duration of action(2-4 hrs more)
4 Possibility of injury to the tissues at the site of injection caused by either the drug or the needle
4
Sites of I M administration
1 Gluteal area
2 Vastus lateralis
3 Mid ndash deltoid area
Drugs
Diazepam
Midazolam
Hydroxyzine
Inhalation Sedation
Advantages
1 The onset of action is more rapid
2 Peak clinical level is achieved rapidly(3-5min) - permit titration
3 Administrator has complete control over the actions of the drug - safety feature
4 No significant over dosage
5 Flexible duration of action
6 Recovery time is rapid amp most complete
7 No injection is required
8 With N2O- O2 it is safe with very few side effects
Disadvantages
1 The initial cost of the equipment is high 2 The continuing cost of the gases is high 3 The equipment occupies considerable space 4 N2O is not a potent agent 5 A degree of cooperation is required from the pt 6 Chronic exposure to N2O is deleterious to the health of
dental personnel
Contraindications
1 Nasal obstruction 2 Cyanosis at rest 3 Poor cooperation 4 1st trimester of pregnancy 5 Fear of masks
I V Sedation
Advantages
1 The onset of action is the most rapid 2 The dosage may be titrated 3 Suitable level of sedation can be provided 4 The recovery period is shorter 5 Side effects are extremely uncommon 6 Control of salivary secretions is possible 7 The gag reflex is diminished 8 Effectively diminishes motor disturbances 9 Provides immediate access to CVS in emergency
Disadvantages
1 Venipuncture is necessary
2 Complication may rise at the site of the venipuncture
3 Monitoring must be more intensive
4 Recovery is not complete at the end of the procedure
5 Reversal of sedation is difficult
5
N2O-O2 (Relative Analgesia)
colorless sweet smelling gas
Pharmacokinetics
Absorption through pulmonary epithelium
It is approx 15 times as soluble as is nitrogen It replaces nitrogen in blood
It is carried in solution in plasma of the blood
It is not metabolized by the body
Elimination ndash majorndash lungs minor --- skin
perspiration urine and intestinal gas
Pharmacodynamics
Dose related
10 ndash 25 Lightheaded
Changes in visual amp auditory sensation
Tingling of hands amp feet
Suffusing warmth
Remote from the immediate environment
Reduced anxiety
25-50 max analgesic properties and aberration of vision hearing and proprioception mild drowsiness euphoria amnesia and increased sleepiness and dreams
35 conc will achieve maximum analgesia
bull CNS
ndash Cerebrum-primarily affected
ndash Safe but weak anesthetic agent
bull RESPIRATORY SYSTEM
ndash Increased Tidal and minute volumes
bull CARDIOVASCULAR SYSTEM
ndash 2 studies ndash decreased cardiac output
bull FETAL SYSTEMS
ndash Miscarriage in humans
bull OTHER SYSTEMS
ndash Depression of spinal reflexes increase muscle tone indicates stage of delirium
ndash Muscle rigidity-narcotics + nitrous oxide
ndash Nausea and vomitting - GIT
ndash HEMATOPOIESIS ----- prolonged exposure
Adverse reactions and toxicity
EMOTIONAL REACTIONS
DREAMS HALLUCINATIONS
No acute toxicity
Chronic toxicity ndash bone marrow
depression
PROCEDURE
Diffusion Hypoxia
Sevoflurane
A fluorinated derivative of isopropyl ether ndash synthesized in 1970
Potent anaesthetic agent with rapid uptake amp speedy recovery
Day-case surgery
Problem
Attaching vaporiser to any of the currently available machine
BENZODIAZEPINES
Diazepam 1961 lipid soluble
Uses-alcoholism epilepsy labor tetanus and cerebral palsy
- sedation and amnesia
- varieties of neurosis amp anxiety states
Pharmacokinetics
Orally Rectal IMIV or SC
Well absorbed through GIT
Excretion in urine
6
bull Pharmacodynamics
ndash Depress the brain stem reticular system and the limbic system thalamus and hypothalamus
ndash It is a centrally acting muscle relaxant Has anti-convulsant properties
Adverse reaction amp toxicity
ndash Confusion nausea headache increased appetite decreased salivation and jaundice Thrombophlebitis
ndash Rebound phenomenon
ndash Toxicity drowsiness confusion sleep and coma
Dosage Oral or Rectal ndash 02-05mgkg
Maximum single dose 10mg
IV- 025mgkg
Supplied Tablets 2 5 10 mg
Suspension ndash 5mg
Midazolam Water soluble ndash non-irritant
Oral IM IV
Metabolism- liver
Onset IV 3 -5mins
oral 20 ndash 30mins
Oral administration anxious patients requiring relatively short dental procedure
No rebound phenomenon
Better anxiolysis amp amnesia (retrograde amnesia)
Adverse effects Respiratory depression
dose dependant apnea
Dosage Oral ndash 025 to 1mgkg to maximum single dose 20mg
IM ndash 01 to 015mgkg to a maximum of 10mg
IV ndash slow IV
Supplied Syrup ndash 2mgml
Injectable ndash 1mgml amp 5mgml vials
Flumazenil specific benzodiazepines antagonist
selectively inhibits CNS effects
IV administration amp not recommended below 18yrs of age
02mg over 15 seconds after 45seconds 02mg then after 60seconds to maximum of 1mg
Sedative-Hypnotics
Barbiturates First truly effective drugs for the management of anxiety Generalized CNS depressants Produce dose dependent effects
Sedation ---- sleep ---- GA ---- coma
Suppress the CNS and result in sedation and amnesia Advantages
Rapid onset and short duration Disadvantages
no analgesic effect and possible hypotension Must be used with caution in trauma patients because they may cause
apnea and hypoventilation
DOSE Pentobarbital Sodium 100mg Secobarbital Sodium 100 to 200mg Children 30 to 100mg
bull Chloral Hydrates (Mickey Finn Knock out drops ) First synthesized in 1832 first member of the hypnotic group of drugs
Widely used as conscious sedation agent
Properties
Unpleasant taste
Nausea vomiting
Quite irritating to skin and to mucous membranes
GI irritation
Dosages Individualized for each patient 25 ndash 50mgkg
maximum of 1g
Supplied oral capsule ndash 500mg
oral solution ndash 250 amp 500mg5ml
Rectal suppositories ndash 324 amp 648mg
Narcotics
Do produce sedation amp euphoria greater in children
LA is required but dose should be decreased
Meperidine Synthetic opiate agonist
Very water soluble
Orally SC IM or IV
Peak effect by oral 1 hr amp lasts upto 4 hrs
Adverse reactions
-Seizures
-Extreme caution in hepatic or renal diseases or history of seizures
7
Dosage Oral SC or IM ndash 1to 22mgkg not to exceed 100 mg
Supplied Oral Tablets ndash 50 amp 100mg
Oral Syrup ndash 50mgml
Parental solution ndash 25 50 75 amp 100mgml
Fentanyl
Synthetic opiate narcotic analgesic
Very potent 01mg = 10mg Morophine75mg Meperidine
Pharmacokinetics
IV IM SM
Metabolized in liver Excreted in urine
Fentanyl Onset ndash 7 to 15mins
Duration ndash 1 to 2 hrs
Pharmacodynamics
Respiratory depression RR but returns to normal rapidly Tidal volume amp response to co2 depressed for extended period
Apnea
Less emetic than meperidine
NOT RECOMMENDED IN CHILDREN BELOW 2yrs
Dosage 0002 to 0004mgkg
Supplied 005mgml in 2 amp 5ml ampoules
Reversal drug Naloxone
Semisynthetic opiate antagonist
No agonist activity
Onset 2 to 5mins SC or IM amp 1 to 2mins IV
Reversal 45mins
Pt should be kept under continual surveillance
Adverse reaction nausea vomiting sweating hypotension hypertension ventricular tachycardia fibrillation
Dosage IV SC IM 001mgkg then 01mgkg every 2- 3mins maximum 2mg
Supplied 002 004 1mg solutions
Antihistamines
Hydroxyzine
Oral or IM
Effect ndash 15 ndash 30mins
Half-life ndash 3 hrs
Uses
To relieve anxiety
Used as an anti-histamine
Used to control nausea and vomiting including that associated with motion sickness and pregnancy
Adverse reaction dry mouth drowsiness hypersentivity
Dosage Oral ndash 1 to 2mgkg
IM ndash 11mgkg
Promethazine Oral or IM Onset 15 to 60mins Duration 4 to 6 hrs Uses
To prevent and treat nausea and vomiting associated with motion pregnancy or surgery
Produces sedation and reduce swelling pain and trismus
Lower seizure threshold Adverse reaction dry mouth blurred vision thickening of bronchial secretions Dosage OralIM ndash 05-11mgkg
maximum 25 mg
Diphenhydramine
Oral IM IV
Onset -1hr
Duration ndash 4 to 6 hr
Metabolized in liver
Adverse reaction disturbed coordination thickening of bronchial secretions
Dosage Oral IM IV ndash 1 to 15mgkg
maximum 50mg
Tranquilizers
Major tranquilizer antipsychotic produce calmness control symptoms of psychoses cause reversible extra pyramidal symptoms and do not tend to cause habituation
Minor tranquilizer antianxiety agents also cause calmness do not cause extrapyramidal symptoms Used in conditions like nervous tension and mild depression
8
Classification
Antipsychotics
Phenothiazine derivatives
Chlorpromazine promazine
Butryophenones
Haloperidol
Rauwolfia alkaloids
Reserpine
Antianxiety drugs
Propyl alcohol derivatives
Meprobamate
Benzodiazepine derivatives
Diazepam
Miscellaneous compounds
Hydroxyzine
Meprobamate
White crystalline powder slightly bitter in taste
Only administered orally
Peak blood concentration ----1 to 3hrs
10 ---------excreted unchanged Rest --- excreted as a oxidized derivative or as a glucoronide
Uses
To relieve day time anxiety
Induce sleep in insomniacs
To reduce anxiety associated with dental treatment
Anti-convulsant ndash petit mal epilepsy
Adverse reaction leucopenia acute non-thrombocytopenic purpura ecchymoses eosinophilia edema adenopathy
Dosage Childrengt 6yrs 100 to 200mg
Not recommended for children under 6yrs
Monitoring during sedation
1 Pulse
2 Blood pressure
3 ECG
4 Respiration
5 Temperature
Pulse
Manual Electronic
bull Radial Brachial
bull Facial labial
Blood pressure
ndash Stethoscope amp sphygmomanometer
ndash Automatic devices
ndash Direct cannulation of an artery ndash very accurate
Electrocardiograph
Heart rate rhythm myocardial function
9
Respiration
ndash Monitoring respiratory rate
ndash Observing the rise amp fall of the chest wall
ndash Observing the color of mucous membrane
ndash Observing the inflation amp deflation of the reservoir bag
Devices for monitoring respiration
1 The Precordial pretracheal stethoscope
2 The esophageal stethoscope
ndash Respiratory rate
ndash Heart rate
ndash Any abnormal sounds
Pulse Oximeter
ndash Oxygen saturation
ndash Heart rate
ndash Oxisensor site
ndash Fingers
ndash Toe
ndash Ear lobe
Mechanism
Oxygenated Hb ndash red light
Deoxygenated Hb- infrared light
Tissue pressure from arterial pulse (plethysmography)
Advantages
ndash Safe amp noninvasive
ndash Simple to use
ndash Information is rapidly available for clinical decision
ndash Indirectly indicates respiratory adequacy
Disadvantages
ndash Finger probes can get dislodged
ndash Emitted light source may cause burning
ndash Non reusable probes are expensive
ndash Does not directly determine airway patency
Capnography
1 The presence absence of air flow
2 Indicates depth amp adequacy of respiration
3 Continues analysis of the co2 content of the respired air ndash indicates respiratory adequacy
Temperature
ndash Disposable nondisposable thermometer
ndash Esophageal rectal temp probe
10
Discharge criteria
Cardiovascular function is satisfactory amp stable
Airway patency is uncompromised amp satisfactory
Pt is easily arousable amp protective reflexes intact
State of hydration is adequate
Pt can talk if applicable
Pt can sit unaided if applicable
Pt can ambulate with minimal assistance if applicable
Presedation level of responsiveness achieved
Responsible individual is available
1
PULP THERAPY OF VITAL TEETH
DR MITAKSHARA NIRWAN
Contents
Indirect pulp capping
Direct pulp capping
Medications amp materials used in pulp capping
Pulpotomy
MTA
Apexogenesis
INDIRECT PULP CAPPING
Pieter Van Forest - first to speak about root canal therapy
Glove designed instruments that could prepare a canal to a certain size and taper(1910)
Indirect pulp capping is defined as a procedure where in small amount of carious dentin is retained in
deep areas of cavity to avoid exposure of pulp followed by placement of a suitable medicament and
restorative material that seals off the carious dentin and encourages pulp recovery (Ingle)
A procedure in which only the gross caries is removed from the lesion and the cavity is sealed for a
time with a biocompatible material (McDonald)
Objective of indirect pulp capping
These were given by Eidelman in 1965
bull Arresting the carious process
bull Promoting dentin sclerosis
bull Stimulating formation of tertiary dentin
bull Remineralization of carious dentin
Layers of Carious Dentin Indications of Indirect Pulp Capping
History
Mild pain associated with eating
Negative history of spontaneous extreme pain
Clinical Examination
Deep carious lesion which are close tobut not involving the pulp in vital primary or young
permanent teeth
No mobility
Nominal pulp inflammationdefinite layer of affected dentin after removal of infected dentin
Radiographic examination
Normal lamina dura amp PDL space
No radiolucency around the apices
2
Contraindications of Indirect Pulp Capping
History
Sharp penetrating pulpalgia
Prolonged spontaneous pain especially at night
Clinical examination
Mobility of tooth
Discoloration of tooth
Negative reaction of electric pulp testing
Radiographic examination
Definite pulp exposure
Break in the lamina dura
Radiolucency around the apices
Widened PDL space
Treatment procedure
Sequelae of Indirect Pulp Capping Three distinct types of new dentin formation take place
1 Cellular fibrillar dentinmdashfirst 2 months
2 Globular dentinmdash3 months
3 Tubular dentin (uniform mineralized dentin)
bull 15th of reparative dentin formation begins in less than 30 days
bull After 3 months 01 mm is formed
DIRECT PULP CAPPING Defined by Kopel (1992) as the placement of a medicament or non medicated material on a pulp that
has been exposed in course of excavating the last portions of deep dentinal caries or as a result of
trauma
Objective
To create new dentin in the area of the exposure and subsequent healing of the pulp
Rationale
achieve a biologic closure of the exposure site by deposition of hard tissue barrier (dentin bridge)
between pulp tissue and capping material thus walling off the
INDICATIONS
Small mechanical exposure
Easily controlled haemorrhage
Bright red haemorrhage
True pinpoint exposure
CONTRAINDICATIONS
Severe toothache at night
Spontaneous pain
Tooth mobility
Radiographic appearance of pulp periradicular de- generation
Excess of hemorrhage at the time of exposure Serous exudate from the exposure
Externalinternal root resorption
Swellingfistula
Histological Changes after Pulp Capping
These were illustrated be Glass and Zander in 1949
After 24 hours Necrotic zone adjacent to calcium
hydroxide paste is separated from healthy pulp
tissue by a deep staining basophilic layer
After 7 days Increase in cellular and fibroblastic
activity
After 14 days Partly calcified fibrous tissue lined by
odontoblastic cells is seen below the calcium
proteinate zone disappearance of necrotic zone
After 28 days Zone of new dentin
3
Medications and Materials Used for Pulp Capping Calcium hydroxide
Corticosteroids amp antibiotics
Inert materials
Collagen fibers
4-META adhesive
Direct bonding
Isobutyl cyanoacrylate
Denatured albumin
Mineral trioxide aggregate
Laser
Bone morphogenic protein
PULPOTOMY
Finn (1995) defined it as the complete removal of the coronal portion of the dental pulp
followed by placement of a suitable dressing or medicament that will promote healing and
preserve vitality of the tooth
American Academy of Pediatric Dentistry (1998) defined pulpotomy as the amputation of
affected infected coronal portion of the dental pulp preserving the vitality and function of the
remaining part of radicular pulp
Objectives
bull Removal of inflamed and infected coronal pulp at the site of exposure thus preserving the vitality of the
radicular pulp and allowing it to heal
bull Maintain the tooth in the dental arch
Rationale
bull Radicular pulp is healthy and capable of healing after surgical amputation of the infected coronal pulp
bull Preserves vitality of the radicular pulp
bull Maintains tooth in a physiologic condition
Indications of Pulpotomy bull Mechanical pulp exposure in primary teeth
bull Teeth showing a large carious lesion but free of radicular pulpitis
bull History of only spontaneous pain
bull Hemorrhage from exposure sites bright red and can be controlled
bull Absence of abscess or fistula
bull No interradicular bone loss
bull No interradicular radiolucency
Contraindications of Pulpotomy bull Persistent toothache
bull Tenderness on percussion
bull Root resorption more than 13rd of root length
bull Large carious lesion with nonrestorable crown
bull Highly viscous sluggish hemorrhage from canal orifice which is uncontrollable
bull Medical contradictions like heart disease immuno compromised patient
bull Swelling or fistula
bull External or internal resorption
bull Pathological mobility
bull Calcification of pulp
Classification of pulpotomy
4
Formocresol Pulpotomy
Iby BUCKLEY in 1904
Sweet (1930) Formulated multi visit technique
Doyle (1962) Advocated 2 sitting procedure (complete devitalization)
Spedding (1965) Gave 5 minute protocol (partial devitali- zation)
Venham (1967) Proposed 15 seconds procedure
Current concept uses 4 minutes of application time
Composition of formocresol Buckleyrsquos Formula
bull Cresol ndash 35 percent
bull Glycerol ndash 15 percent
bull Formaldehyde ndash 19 percent
bull Water ndash 31 percent
Mechanism of Action
It prevents tissue autolysis by bonding to the proteins Bonding is of peptide groups of side chain amino acids and is a reversible process accomplished without
changing the basic structure of protein molecules
Histological Changes
bull Demonstrated by Mass and Zilbermann11 in 1933 and also by Massler and Mansokhani in 1959
bull Immediately the pulp becomes fibrous and acidophillic
bull Seven to fourteen days Three zones appear
a broad eosinophilic zone of fixation
b broad pale-staining zone of atrophy with poorcellular definition
c broad zone of inflammation extending apically into normal pulp tissue
bull One yearndash Progressive apical movement of these zones with only acidophillic zone left at the end of 1 year
Modified Formocresol Pulpotomy
Used by TRASK(1972)
The technique is identical to that described for primary teeth except that the formocresol pellet is
sealed permanently in the tooth
Two-visit Devitalization Pulpotomy
Indications
bull There is evidence of sluggish bleeding at the amputation site that is difficult to control
bull Pus in the chamber but none at the amputation site
bull There is thickening of the PDL
bull History of pain
Contraindications
bull Nonrestorable tooth
bull Tooth with necrotic pulp
5
Glutaraldehyde Pulpotomy
It was first suggested by S Gravenmade Introduced by Kopel in 1979
Mechanism of Action
bull Glutaraldehyde produces rapid surface fixation of the underlying pulpal tissue
bull A narrow zone of eosinophilic stained and compressed fixed tissue is found directly beneath the area of application which blends into vital normal appearing tissue apically
bull With time the glutaraldehyde fixed zone is replaced by macrophagic action with dense collagenous tissue thus the entire root canal tissue is vital
Cvekrsquos Pulpotomy
bull This is also called as calcium hydroxide pulpotomy or young permanent partial pulpotomy
bull This was proposed by Mejare and Cvek16 in 1978
bull Indicated in young permanent teeth where the pulp is exposed by mechanical or bacterial means and the
remaining radicular tissue is judged vital by clinical and radiographic criteria whereas the root closure is
notcomplete
MINERAL TRIOXIDE AGGREGATE (MTA) Torabinejad described the physical and chemical properties of MTA in 1995
It is ash colored powder made primarily of fine hydrophilic particles of
1 tricalcium aluminate
2 tricalcium silicate
3 silicate oxide
4 tricalcium oxide
5 bismuth dioxide
Hydration of the powder results in a colloidal gel composed of calcium oxide crystals in an amorphous
structure This gel solidifies into a hard structure in less than three hours
PROPERTIES OF MTA
It is biocompatible material and its sealing ability is better than that of amalgam or ZOE
Initial pH is 102 and set pH is 125
The setting time of cement is 4 hours
The compressive strength is 70 MPA which is comparable with that of IRM
Low cytotoxicity ndash It presents with minimal inflammation if extended beyond the apex
Mineral trioxide aggregate (MTA) has demonstrated the ability to induce hard-tissue formation in
pulpal tissues and it promotes rapid cell growth
APEXOGENESIS
It is defined as the treatment of a vital pulp by capping or pulpotomy in order to permit continued
growth of the root and closure of the open apex
Rationale
Maintenance of integrity of the radicular pulp tissue to allow for continued root growth
Indications
bull Indicated for traumatized or pulpally involved vital permanent tooth when root apex is incompletely formed
bull No history of spontaneous pain
bull No sensitivity on percussion
bull No hemorrhage
bull Normal radiographic appearance
Contraindications
bull Evidence that radicular pulp has undergone degenerative changes
bull Purulent drainage
bull History of prolonged pain bull Necrotic debris in canal
bull Periapical radiolucency
6
1
Gupta A Dhingra R Chaudhari P Gupta A
Department of Paedodontics and Preventive Dentistry Faculty of Dental Sciences SGT University Gurgaon Haryana India
Journal of Indian Society of Pedodontics and Preventive Dentistry
Volume 35 I Issue 3 I July-September 2017
A COMPARISION OF VARIOUS MINIMALLY
INVASIVE TECHNIQUES FOR THE REMOVAL
OF DENTAL FLUOROSIS STAINS IN
CHILDREN
DR MITAKSHARA NIRWAN
CONTENTS
bull Introduction
bull Aims
bull Materials and Methods
bull Results
bull Discussion
bull Conclusion
bull Critical analysis
bull References
INTRODUCTION
bull Dental fluorosis is a developmental disturbance of dental enamel caused by
successive exposure to high concentrations of fluoride during tooth
development
bull Various methods of therapy are advocated for the treatment of fluorosis -
stained teeth which range from invasive ceramic veneer bonding restorations
to abrasive chemical treatments
bull The combination of dental bleaching techniques and microabrasion appears
as an excellent conservative solution to reestablish health in fluorosis
affected teeth
AIMS
bull The aim of the study was to evaluate and compare the effectiveness of
minimally invasive techniques for the removal of dental fluorosis
stains in children in vivo
MATERIALS AND METHODS
Patients visiting the department of Pedodontics and Preventive dentistry
Faculty of Dental Sciences SGT University Gurgaon
bull Sample size 90 patients
bull Age group 10 -17 years
bull Caries cracks or periodontal
disease on anterior teeth
bull Abscess draining sinus
cellulitis
bull Non vital teeth
hypersensitive exposed
crevices
bull Orthodontic appliance
bull Past history of bleaching
bull At least two permanent
maxillary anterior teeth
bull TSIF of score 4
bull Free of systemic diseases
Inclusion criteria Exclusion criteria
2
Groups
Group A In office bleaching with 35 hydrogen peroxide( Pola Office
Bleaching kit) activated by light emitting diode (LED) bleaching unit
(35 HP)
Group B Enamel microabrasion (EM) (PREMA Enamel Microabrasion
System) followed by in-office bleaching with 44 carbamide peroxide
gel (EM)
Group C In-office bleaching with 5 sodium hypochlorite (5
NaOCl)
A baseline colour evaluation was done by taking digital photograph of
the maxillary anterior teeth
RESULTS
Group 1
Colour stability
Group 2 Group 3
Tooth sensitivity
Tooth sensitivity values were taken before the treatment
which was compared to immediate postoperative and follow
up visits It was checked using an electric pulp tester
maximum
moderate
least
immediately
group 2
group 1
group 3
1 month
group 2
group 1
group 3
3 month
group 2
group 1
group 3
Patient satisfaction score
Satisfaction was assessed on visual analog scale
Range 1 to 5
Groups percentage of patients
who were satisfied with
the treatment
Number of patients
who reported slight
reappearance of colour
Group 1
90
7
Group 2
83
8
Group 3
73
7
3
Number of Appointments
Groups One sitting Two sittings Three
sittings
Group 1
25
4
1
group 2
26
3
1
Group 3
30
0
0
DISCUSSION
bull Hydrogen peroxide is capable of penetrating the tooth osmosis and through porosities and cracks subsequently acting directly on the pigmented molecules
bull Gurgan et al investigated 3 different light systems and found out that diode laser system with gave best tooth whitening and least tooth sensitivity
bull In the EM group the surface reflects and refracts light from the surface in such way that mild imperfections in underlying enamel are camouflaged While the highly polished surface of enamel enhances the aesthetic appearance
bull Train et al and Loguercio et al also had the similar results in their studies with EM mild fluorosis showed best results moderate showed moderate results while it had little effect on severe fluorosis
bull NaOCl was only effective on mild stains while moderate and severe
stains could only be lightened to quite an extent but could not be
completely removed
bull When NaOCl comes in contact with hypomineralized and discoloured
enamel it degrades and removes the chromogenic organic material
located on the enamel surface
CONCLUSION
bull It was concluded that esthetic appearance of teeth mild fluorosis can
be achieved by bleaching and microabrasion But in cases of
moderate fluorosis a combination of any of theses modalities can be
used
bull As no special maintenance precautions are required these maybe be
considered as an interesting alternative to conventional operative
treatment
bull Focuses on only TSIF of 4
bull Electric pulp testing is not the
right method to check for
sensitivity
bull Tooth Sensitivity changes
from person to person
bull Food habits can cause
staining of the teeth
bull Minimally invasive
bull Cheaper to veneers
bull Minimal loss of tooth structure
bull 4 parameters checked for the success of treatment
bull Inclusion of specific score of fluorosis for comparing the results
bull Maximum 3 appointments needed
CRITICAL ANALYSIS
Pros Cons
REFERENCES
bull Gurgan S Cakir FY Yazici E Different light-activated in officebleaching
systems Lasers Med Sci 201025817-22
bull Train TE McWhorter AG Seale NSWilson CF Guo IY Examination of
esthetic improvement and surface alteration following microabrasion in
fluorotic human incisors in vivoPediatr dent 199618353-62
bull Loguercio AD Correia LD Zago C Tagliari D Neumann E Gomes OM et al
Clinical effectiveness of two microabrasion materials materials for the
removal of enamel flurosis stains Oper Dent 200732531-8
4
1
Impact of Handheld Devices on
Children An Evaluation of Usage amp
Dependency Behaviour
0092
DR MITAKSHARA NIRWAN
Handheld devices
A handheld device is a pocket size
computing device with a display
screen and inputoutput interface like
an external or touchscreen keyboard
For example- smartphones tablet
computers handheld videogame
consoles
Haruki Murakami
ldquoCell Phones are so
convenient that they have
become an inconveniencerdquo
Introduction
The most famouscommonly used and easily accessible type of gadgets are
lsquoHandheld devicesrsquo They are as popular in children as they are in adults
The access and ownership of these devices amongst children has grown
substantially in the past decade Concerns exist regarding excessive usage
and the impact of frequent consumption of mobile media on their health and
behaviour
Aims and Objective
This objective of this study was to asses the level of use of handheld
devices among children aged 0-12 years and their positive and negative
impacts on them It further describes the dependency of these devices
and the behavioral problems associated with it
Materials and Methods An online survey was conducted and a self administered questionnaire
was prepared specially for the parents which included a total of 15
questions regarding the usage and dependency of the device
A total of 100 responses were collected from parents who had children
aged 0-12 years who used these devices on daily basis
2
Level of Usage (Q 123)
Results Purpose (Q7)
Improved
communication and
learning
Using more than
one type of
device
Helped in
Speech
Positive Impacts -
(Q58 amp 9)
P value 0003(s) P value-0007 P value-0006(s)
Reduced parent-
child interaction Disrupted sleep Lack of motivation for academics
Negative Impacts (Q81213)
P value-0001(s) P value-0002(s) P value-0006
Time when children use
the device the most
Isolation of the
child Behavioral impact when gadget is
taken back
Dependency
Behaviour (Q10111415)
P value-002(s) P value 002(s) P value-044
This study was done to evaluate the level of usage of handheld devices and their impact
on the children aged 0-12 years The questionnaire was made such that it asked both the
positive and negative impact and further included the questions regarding the
dependency
784 children had access to smartphone and 17 used tablets
The most common age group in which the devices was used the most was 5-8 years
followed by 9-12 followed by 0-4 (Arlinda et al 2019 )
Another study done by (Rachel Bedford et al 2016) concluded increase usage of mobile
phones 5122 in 6ndash11 monthshy olds through to 9205 by 25ndash36 months
745used these devices several times a day out of which 539 used it for more than
one hourday 255 used it for less than one hour and 206 for more than 2 hours
Various studies follow the same recommendation given by AAP to limit the duration of
gadget amongst children
Discussion
3
Improve of Cognitive Skills
Amongst the positive impacts most parents have answered that the usage of these
devices has helped their child communicate and learn better and it has showed significant
results According to (Sundus M 2018)These devices improve the cognitive skills and
develop their learning skills fasterThe competition skills also get better It gives time for brain to think and process information better Another study which supports this (LF
Jonathan et al 2016)
Motor Physical Exercise
This study has shown that children like to use more than one type of device
sometimesUsing these devices improve fine motor skillshand eye coordination and
hands and fingers become more efficient (Srinahyanti et al 2019) (Sundus M 2018)
Speech Improvement
392 Parents say that maybe usage of the devices has helped improve speech in their
children but Various studies show otherwise as most of them shows that usage of handheld
devices causes delay of speech (Srinahyanti et al 2019)
Reduced parent child interaction
The negative impacts are more when compared to the positive ones Usage of gadgets
has resulted in reduced parent child interaction Less face to face interaction can
cause detachment from family members and value which in turn also causes isolation
of the child as he is more comfortable with the gadget (M Suhana-2017)
Sleep Disorders
This study shows that most parents have agreed that usage of these devices does
cause disruption of sleep Various studies have shown that children get fewer hours of
sleepdrowsiness during the day and dramatic increase in day time sleep because of
the screen usage (Acc to National Sleep Foundation) ( Cain N et al 2010)
In this study most number of parents have
agreed that their children might be dependent on
these devices and also had showed restless and
violent behavior if the gadget is snatched from
them
Most number of kids (667) are heavily
dependent as they like to use the device during
their meal time
Various other studies have assessed the screen
time dependency and have concluded that
various kids suffer from SDD
Conclusion The study conclusively shows that the impact of handheld devices is akin to the
importance of table salt in our meals most significant for our growth and
development in moderate amounts and hazardous in excess The negatives clearly
outweigh the positives with the latter too few and far in between This study also
points towards further extensive research on the subject because we need to find ways and also educate parents to optimise the role of these devices in their
childrenrsquos life taking advantage of their positive attributes and minimising their
negative ones
References 1Wahyuni AS Siahaan FB Arfa M Alona I Nerdy N The Relationship between the Duration of Playing
Gadget and Mental Emotional State of Elementary School Students Open Access Maced J Med Sci
20197(1)148ndash151
2Sundus M Department of Computer Science Lahore-The Impacts of using Gadgets on ChildrenJournal of Depression and Anxiety 2018vol 7(1)296
3Amawi SO Subki AH Khatib HA et al Use of Electronic Entertainment and Communication Devices Among
a Saudi Pediatric Population Cross-Sectional Study Interact J Med Res 20187(2)e13
4Julia ldquoHandheld Screen Time Linked with Speech Delays in Young Childrenrdquo Present Pediatric Acad Soc
Meet 2017
5C Rowan ldquoThe Impact of Technology on Child Sensory Motor Developmentrdquo 2003
6Impact of media use on children and youth Paediatr Child Health 20038(5)301ndash317
7Naik SV Children and their gadgets A pedodontist perspective Int J Oral Health Sci 2018857-8
8Roberts DF Foehr UG Rideout V Generation M Media in the lives of 8‐18 year‐olds A Kaiser Family
Foundation Study 2005
9Arya K Time spent on television viewing and its effect on changing values of school going children Anthropologist 20046269‐71
10 Lerner C Barr R Screen Sense Setting the Record StraightResearch‐Based Guidelines for Screen
Use for Children Under 3 Years Old Early learning project at Georgetown university 2014 p 1‐10
11SrinahyantiYasaratodo Wau Imelda Free Unita Manurung Nur Arjani-Influence of gadget A positive
and Negative Impact of Smartphone Usage for Early Child2019
4
THANK YOU
1
Morankar Rahul Aditi Kapur Krishan Gauba Ashima Goyal
MANAGEMENT OF ENDODONTIC INSTRUMENT SEPARATION IN
PRIMARY TEETH
CASE REPORT
Journal of South Asian Association of Pediatric Dentistry 2020
DR MITAKSHARA NIRWAN
bull Introduction
bull Aims amp Objectives
bull Case report
bull Discussion
bull Conclusion
bull Pros amp Cons
bull References
CONTENTS
Separation of endodontic instrument is an unexpected complication and its prevalence is not known It is a common belief among the dental professionals that rotary nickelndashtitanium (NiTi) instruments separate more frequently than stainless steel hand instruments
However literature revealed that in permanent teeth the reported prevalence of separated endodontics manual instruments is in the range of 07-74 whereas for rotary NiTI instruments it is
approximately 04-5
Fractured root canal instruments may include endodontic files Gates Glidden burs finger spreaders
and paste fillers
INTRODUCTION
The aim of this study is to describe the management strategies for endodontic
instrument separation in a root canal of primary teeth with emphasis on factors
requiring consideration in different clinical situations
AIMS amp OBJECTIVES
CASE 1
A 6-year-old male child reported with the chief complaint of spontaneous toothache in mandibular left second primary molar since few days It has aggravated following dental treatment at a private dental clinic Clinical examination revealed an underprepared access cavity with 75 and incomplete caries removal
which was sealed with glass ionomer cement
An intraoral periapical radiograph revealed a separated instrument of about 6ndash7 mm size in the distal root
2
The separated instrument was lodged firmly in distobuccal root canal 2ndash3 mm below the cementoenamel junction The instrument was bypassed successfully with no 15 and no 20 H-files but attempts for its retrieval were not successful
GatesndashGlidden (GG) drills no 2 (07 mm) and no 3 (09 mm) were used to drill around the instrument after which it was retrieved successfully using no 25 H-file
All the canals were instrumented till size 30 k-file followed by obturation with metapex and restoration with glass ionomer cement amp followed by placement of a crown and loop space maintainer for missing 74 The instrument retrieved was a manual reamer measuring 6 mm in length
The patient was asymptomatic since then and is under regular follow-up
CASE 2
A 5-year-old female child reported with the chief complaint of spontaneous toothache in mandibular left second
primary molar Clinical examination revealed deep occlusal caries with fractured lingual wall and pain on
percussion An intraoral periapical radiograph revealed caries involving pulp without any furcation or periapical
area of rarefaction and pulpectomy was planned
All the canals were enlarged using NiTi rotary files with a 4 taper operating at 500 rpm with minimum torque
setting An orifice opener [(0825 19 mm) of 8 taper size 25 length 19 mm] and nos 0420 file was used for
instrumentation of root canal This was followed by file nos 0425 which got separated in the distobuccal root
canal The radiograph confirmed a separated instrument of length 3ndash4 mm in the middle third of the root canal
The instrument was bypassed with no 15 k-file but could not get retrieved As instrument separation had occurred with 0425 file the involved root canal was sufficiently debrided before separation and the level of instrument separation was at the mid-root region so it was decided to obturate and seal this tooth with
periodic follow-ups instead of immediate extraction All other canals were enlarged till size 0430 in the sequential manner followed by obturation using metapex and placement of stainless steel crown
3
CASE 3
A 5-year-old female child has complaint of mild intermittent pain with primary mandibular left first molar She
had undergone pulpectomy treatment for the same during which an instrument separation has occurred in
the mesiobuccal root canal by a resident doctor
A radiograph revealed a separated instrument of about 4 mm in size lodged in the apical third but within the
confines of the mesial root An attempt was made for its retrieval but was unsuccessful The extraction of the
involved tooth was carried out under local anesthesia followed by a band and loop space maintainer
CASE 4
A 7-year-old male child reported with a chief complaint of mild intermittent pain on food lodgment with the primary mandibular right first and second molars The patient had a history of dental treatment at a private
dental clinic few months back which he did not continue further
Clinical examination revealed glass ionomer restoration with 85 and proximal caries with 84 leading to food lodgment An intraoral periapical radiograph with 85 revealed empty root canals with a separated
instrument of about 3ndash4 mm size beyond the apex of mesial root close to the developing succedaneous premolar
4
DISCUSSION
Stainless steel files usually separate fracture due to the excessive amounts of torque and overuse or the
preexisting distortion of the instrument whereas in NiTi rotary files it is a combined result of torsional stress and cyclic fatigue
Therapeutic options for the management of separated endodontic instruments include no intervention nonsurgical (orthograde conservative) management surgical management and tooth extraction
Use of ultrasonic scaler Masserann technique Endo extractor and Cavi-Endo ultrasonic instruments are some of the methods popular for retrieval of a separated endodontic instrument in the permanent tooth
In case 1 a 6-mm-long manual reamer was retrieved successfully with the use of GG drill using a manual file and copious irrigation which is the most desired treatment outcome
In case 2 the retrieval of separated rotary file lodged in the middle third of the root canal was unsuccessful in spite of multiple attempts It was therefore managed with routine obturation followed by restoration to maintain the tooth in its physiological functional state It was kept under close periodic follow-up at least
every 3 months This treatment option should be encouraged where it is possible to follow up the patient clinically and radiographically at close periodic intervals as there is the possibility of instrument escaping
into bone due to physiological root resorption
In cases 3 and 4 an instrument has separated in the apical root portion
In case 3 it was within the root canal and thus an attempt was made for its retrieval which was
unsuccessful It was therefore extracted to prevent the fractured instrument from getting exposed in the bone following resorption as there is no accurate and consistent established age for initiation of resorption in primary teeth known per se
In case 4 an immediate extraction of involved tooth was carried out as the separated instrument was beyond the apex of the primary tooth root
Age of the child clinical signs and symptoms and amount of root resorption are the factors which can also influence the management of separated instrument in primary teeth
Moreover if an instrument has separated after initial cleaning and shaping of root canal maintaining a tooth is not a problem as clinical signs and symptoms are not anticipated and the good prognosis is expected
However if an instrument has separated early during the initial cleaning and shaping of the root canal clinical symptoms may compromise the prognosis
Therefore these factors should be kept in mind while planning a suitable management strategy to avoid or at least reduce the burden of extraction and wear of space maintainer for longer period
5
CONCLUSION
The management and prognosis of a primary tooth with a separated instrument is
dependent on the level of instrument fracture within the root age of the child root
resorption and clinical signs and symptoms of the involved tooth
Different management approaches can be tried depending on clinical situations keeping
in mind benefits vs risks in preserving the tooth
PROS amp CONS
PROS
The entire procedure is given
by step by step
Well descriptive xrays and
photographs
CONS
Medical history has not been
given
REFERENCES
1 TOMER ANIL K ET AL ldquoBROKEN FILE RETRIEVAL PUZZLE IN ENDODONTICSrdquo
(2016)
2 SHENOY A MANDAVA P BOLLA N ET AL A NOVEL TECHNIQUE FOR REMOVAL OF
BROKEN INSTRUMENT FROM ROOT CANAL IN MANDIBULAR SECOND MOLAR
INDIAN J DENT RES 201425(1)107ndash110
3 PATEL J MORAWALA A TALATHI R ET AL RETRIEVAL OF A BROKEN INSTRUMENT
FROM ROOT CANAL IN PRIMARY ANTERIOR TEETH UNIV RES J DENT 20155(3)203ndash
206
4 MORANKAR R GOYAL A GAUBA K ET AL MANUAL VERSUS ROTARY
INSTRUMENTATION FOR PRIMARY MOLAR PULPECTOMIES - A 24 MONTHS
RANDOMIZED CLINICAL TRIAL PEDIAT DENT J 201828(2)96ndash102
5 KASHYAP NILOTPOL (2018) RETAINING PRIMARY MOLARS WITH INSTRUMENT
SEPERATION A CASE REPORT AND CLINICAL GUIDE
6
1
IMPACT OF 6 CITRIC ACID AND ENDOACTIVATOR AS IRRIGATION ADJUNCTS ON OBTURATION QUALITY AND PULPECTOMY OUTCOME IN
PRIMARY TEETH
NEETU JAIN SHALINI GARG ABHISHEK DHINDSA SAKSHI JOSHI HARJOY
KHATRIA
PEDIATRIC DENTAL JOURNAL 2019 29
1
DR MITAKSHARA NIRWAN
CONTENTS
bull INTRODUCTION
bull AIMS amp OBJECTIVES
bull CASE REPORT
bull RESULTS
bull DISCUSSION
bull CONCLUSION
bull PROS AND CONS
bull REFERENCES
2
INTRODUCTION
bull ENDODONTIC THERAPY IN PRIMARY TEETH INVOLVES DISINFECTION OF THE ROOT CANAL
SYSTEM AND ITS OBTURATION WITH RESORBABLE PASTE
bull THE CONTENTS OF ROOT CANAL ALONG WITH SMEAR LAYER ARE EXPECTED TO BE REMOVED
DURING THE BIOMECHANICAL PREPARATION
bull IN VITRO AND CLINICAL DOCUMENTS HAVE INDICATED THAT MECHANICAL PREPARATION OF
THE CANAL LEAVES LARGE PORTIONS OF THE CANAL WALLS UNDEBRIDED AND COMPLETE
REMOVAL OF THE BACTERIA BY THIS MECHANICAL PROCEDURE ALONE IS UNLIKELY TO BE SEEN
THEREFORE SOME FORM OF DISINFECTIONIRRIGATION IS MANDATORY TO KILL THE
MICROORGANISMS AND TO REMOVE THE RESIDUAL TISSUES
3
bull THE IDEAL REQUISITES OF A ROOT CANAL IRRIGANT AS GIVEN BY ZEHNDER ARE
1 BROAD ANTIMICROBIAL SPECTRUM
2 HIGH EFFICACY AGAINST ANAEROBIC AND FACULTATIVE MICROORGANISMS ORGANIZED
IN BIOFILMS
3 ABILITY TO DISSOLVE NECROTIC PULP TISSUE REMNANTS
4 ABILITY TO INACTIVATE ENDOTOXIN
5 ABILITY TO PREVENT THE FORMATION OF A SMEAR LAYER DURING INSTRUMENTATION OR
TO DISSOLVE THE LATTER ONCE IT HAS FORMED
6 SYSTEMICALLY NONTOXIC WHEN THEY COME IN CONTACT WITH VITAL TISSUES
NONCAUSTIC TO PERIODONTAL TISSUES AND WITH LITTLE POTENTIAL TO CAUSE AN
ANAPHYLACTIC REACTION
SINCE NO SINGLE IRRIGANT HAS THESE OPTIMAL PROPERTIES STUDIES HAVE REPORTED THE USE
OF TWO OR MORE SOLUTIONS IN A SPECIFIC SEQUENCE OR IN COMBINATIONS FOR BETTER
RESULTS 4
bull SEVERAL IRRIGATING SOLUTIONS ALONG WITH CHELATING AGENTS HAVE BEEN USED
DURING BIOMECHANICAL PREPARATION OF ROOT CANAL BOTH IN PRIMARY AND
PERMANENT TEETH
bull HOWEVER NONE OF THE AVAILABLE IRRIGATING SOLUTIONS HAS BEEN REGARDED CLEARLY
AS OPTIMAL SOLUTION BECAUSE OF THEIR LIMITED EFFECTIVENESS ESPECIALLY IN APICAL
13RD OF THE ROOT CANAL SYSTEM
bull TO OVERCOME SUCH LIMITATIONS USE OF ENDOACTIVATOR HAS BEEN PROPOSED AS AN
IRRIGATION FACILITATOR THAT IS BASED ON SONIC VIBRATION (UP TO 10000 CPM) WHICH
FACILITATES THE IRRIGANT PENETRATION AND ITS RENEWAL WITHIN THE CANAL
bull ACTIVATION SYSTEMS RESULTED IN BETTER REMOVAL OF THE SMEAR LAYER IN THE APICAL
THIRD OF ROOT CANALS IN COMPARISON TO CONVENTIONAL IRRIGATION
5
CITRIC ACID
bull CITRIC ACID IS A WEAK ORGANIC ACID WITH THE APPEARANCE OF WHITE CRYSTALLINE
POWDER AT ROOM TEMPERATURE
bull IT CAN EXIST EITHER IN WATER-FREE FORM (ANHYDROUS) OR MONOHYDRATE FORM THE
WATER-FREE FORM CRYSTALLIZES FROM THE HOT WATER WHEREAS THE MONOHYDRATE
FORMS FROM THE COLD WATER THE LATTER MAY BE CONVERTED TO ANHYDROUS FORM BY
HEATING MORE THAN 78degC
bull CITRIC ACID OCCURS NATURALLY IN THE BODY IN MITOCHONDRIA AND IS USED BY BLOOD
BANKS TO PREVENT COAGULATION OF TRANSFUSED BLOOD CITRIC ACID IS ALSO ESSENTIAL
TO HUMAN METABOLISM AND IS FOUND IN MANY FOODS
6
2
bull THE BIOLOGICAL EFFECTS OF CITRIC ACID ON THE PERIODONTAL STRUCTURE HAS BEEN
EXTENSIVELY STUDIED IN PERIODONTICS
bull NEUMAN AND NEWMAN SHOWED THAT CITRIC ACID IS THE MOST EFFECTIVE ACID IN
ALTERING THE SOLUBILITY OF HYDROXYAPATITE
bull YAMAGUCHI ET AL SHOWED THAT CITRIC ACID SOLUTION HAD ANTIBACTERIAL EFFECTS ON
ALL 12 ROOT CANAL BACTERIA TESTED
bull ARIAS-MOLIZ ET AL SHOWED THAT ETHYLENEDIAMINETETRAACETIC ACID (EDTA) HAS NO
BACTERICIDAL ACTIVITY EVEN AFTER 1 HOUR CONTACT
bull THIS ACID HAS THE ABILITY OF ROOT CANAL IRRIGATION AND ALSO SMEAR LAYER REMOVAL
DIFFERENT CONCENTRATIONS (1ndash50) HAVE BEEN PROPOSED GUTMANN ET AL CONCLUDED
THAT 10 CITRIC ACID IS BETTER THAN ULTRASOUND FOR SMEAR LAYER REMOVAL FROM THE
ROOT END CAVITIES
7
bull STUDIES HAVE SHOWN IRRIGATION WITH 6 CA FOR 15 OR 30 SECONDS IS QUITE
EFFECTIVE IN REMOVING ALL THE COMPONENTS OF THE SMEAR LAYER OF THE PRIMARY
TEETH WHEREAS PERITUBULAR DENTIN DESTRUCTION WAS OBSERVED WHEN HIGHER
CONCENTRATION OF CITRIC ACID WAS USED AS AN IRRIGATING SOLUTION
8
AIMS amp OBJECTIVES
bull THIS STUDY WAS AIMED TO EVALUATE THE CLINICAL AND RADIOGRAPHIC OUTCOME OF
PULPECTOMY ALONG WITH QUALITY OF OBTURATION USING 6 CITRIC ACID AND
ENDOACTIVATOR
9
CASE REPORT
bull 350 CHILDREN (3-9 YEARS) WITH CLINICAL SIGNS AND SYMPTOMS OF CHRONIC IRREVERSIBLE
PULPITIS IN DEEPLY CARIOUS TEETH WERE SCREENED DURING SCHOOL DENTAL HEALTH
PROGRAM FROM MAY 2014-JULY 2014
bull 123 CHILDREN REPORTED TO THE DEPARTMENT AND 67 CHILDREN WERE SELECTED BASED ON
INCLUSION AND EXCLUSION CRITERIA
RECRUITMENT OF PATIENTS
10
INCLUSION CRITERIA
bull HISTORY OF SPONTANEOUS PAIN AND UNCONTROLLED BLEEDING AFTER PULP AMPUTATION
EXCLUSION CRITERIA
bull EVIDENCE OF INTERNAL OR EXTERNAL (PHYSIOLOGICPATHOLOGIC) ROOT RESORPTION OF MORE THAN A THIRD OF ITS LENGTH
bull ROOT CANAL OBLITERATION OR ANATOMIC ANOMALIES
bull INADEQUATE BONE SUPPORT OR NON RESTORABLE TOOTH
bull ONCE PATIENTS ELIGIBILITY WAS CONFIRMED THE TREATMENT PROCEDURE WAS
EXPLAINED TO THE PARENTGUARDIAN AND INFORMED WRITTEN CONSENT WAS
OBTAINED FROM PARENTSGUARDIANS SHOWING WILLINGNESS FOR THEIR
CHILDRENS TREATMENT 11
PROCEDURE
bull PULPECTOMY WAS PERFORMED BY ONE OPERATOR OF PEDIATRIC DENTISTRY DEPARTMENT
USING A STANDARDIZED TREATMENT PROTOCOL FOR ALL THE PATIENTS
bull AFTER ADMINISTRATION OF LOCAL ANESTHESIA RUBBER DAM WAS APPLIED FOR ISOLATION
bull ACCESS CAVITY WAS PREPARED USING AIR-ROTOR HAND PIECE WITH 8 ROUND BUR AND
PULP TISSUE WAS EXTIRPATED WITH THE HELP OF SPOON EXCAVATOR
bull FURTHER THE NEGOTIATION OF THE CANALS WAS DONE WITH 10 K-FILE
bull A DIAGNOSTIC RADIOGRAPH WAS TAKEN FOR ROOT LENGTH DETERMINATION AND
WORKING LENGTH WAS KEPT 1 MM SHORT OF THE RADIOGRAPHICAL APEX
bull ALL ROOT CANALS WERE INSTRUMENTED MANUALLY USING K-FILES AND WERE IRRIGATED
WITH 10 ML 09 NORMAL SALINE AND 1 SODIUM HYPOCHLORITE AS STANDARDIZING
PROTOCOL FOR ROOT CANAL PREPARATION AND DISINFECTION
12
3
GROUP 1 (CA + E) - IRRIGATION WAS DONE
WITH 10 ML OF 6 CITRIC ACID (CITOCID AMMDENT)
AND IRRIGANTS WERE SONICALLY AGITATED WITH
ENDOACTIVATOR (DENTSPLY) FOR 30 S PER CANAL USING REDBLUE
ENDOACTIVATOR TIP
GROUP 2 (CA) - 10 ML OF 6 CITRIC ACID FOR 1 MIN USING
27 GAUZE IRRIGATING NEEDLE
GROUP 3(SH + E) - 10 ML OF 1 SODIUM HYPOCHLORITE
SOLUTION AND SONIC ACTIVATION WITH ENDOACTIVATOR
GROUP 4(SH) - 10 ML OF 1 SODIUM HYPOCHLORITE
SOLUTION USING IRRIGATING NEEDLE (CONTROL GROUP)
bull TEETH UNDERGOING PULPECTOMY WERE RANDOMLY ENROLLED BY CHIT METHOD INTO THREE
STUDY AND ONE CONTROL GROUP
13
bull IN CITRIC ACID GROUPS FINAL RINSE WITH NORMAL SALINE WAS DONE TO REMOVE THE
REMAINING CRYSTALS (CHELATES)
bull FOLLOWING BIOMECHANICAL PREPARATION THE ROOT CANALS WERE DRIED WITH STERILE
ABSORBENT PAPER POINTS AND OBTURATED WITH VITAPEX USING HAND HELD
LENTULOSPIRAL FINAL RESTORATIONS WERE DONE USING COMPOSITE RESIN
14
bull CLINICAL FOLLOW UP WAS DONE AT 24 H1 WEEK 1 MONTH 6 MONTH AND 12
MONTH TO CHECK PAIN PRESENCE AND PAIN FREQUENCY (ONCEMORE THAN ONCE)
SWELLING FISTULA SENSITIVITY TO PERCUSSION
bull RADIOGRAPHIC FOLLOW UP WAS DONE AT 6 MONTH AND 12 MONTH FOR ANY
DEVIATED ERUPTION OF SUCCEDANEOUS TEETH EXCESS FILING MATERIAL AND ITS
RESORPTION EXTERNALINTERNAL ROOT RESORBTION CALCIFIC METAMORPHOSIS
PRESENCE OF FURCATION RADIOLUCENCY
CLINICAL amp RADIOGRAPHIC FOLLOW UP
15
RADIOGRAPHIC ASSESSMENT OF OBTURATION QUALITY
bull POSTOPERATIVE RADIOGRAPHS WERE VISUALLY ASSESSED FOR QUALITY OF OBTURATION BY
TWO INDEPENDENT EXAMINERS (SG AD) WHO WERE BLINDED WITH REGARD TO
IRRIGATION PROTOCOL GROUP TO ENHANCE CALIBRATION EACH EXAMINER ASSESSED THE
RADIOGRAPH INDEPENDENTLY AND LATER REVIEWED TOGETHER FOR FINAL ASSESSMENT
INDIVIDUAL ROOT WAS TAKEN AS UNIT OF ANALYSIS FOR GRADE OF OBTU- RATION AND
SCORING CRITERIA WERE AS GIVEN BY COLL JA 1996
1 UNDER FILLED - FILLING MATERIAL ENDED 1 MM OR MORE SHORT OF THE APEX
2 OPTIMAL FILLING- FILLING MATERIAL APPEARED TO END AT THE RADIOGRAPHICAL APEX
3 OVERFILLED - FILLING MATERIAL EXTRUDED PAST THE RADIOGRAPHIC APEX
4 OPTIMALLY FILLED ROOTS WERE FURTHER ASSESSED FOR THE PRESENCE OF VOIDS AND VOID
AREA (ROOT CANAL SURFACE UNTOUCHED BY THE ROOT CANAL FILLING MATERIAL) IN THREE
VISUALLY DIVIDED SECTIONS OF THE ROOT IE CORONAL MIDDLE AND APICAL 13RD
16
RESULTS
bull OVERALL CLINICAL AND RADIOGRAPHIC SUCCESS RATE OVER A PERIOD OF ONE YEAR WAS
9886 amp 977 RESPECTIVELY
bull ALL GROUPS WERE SIGNIFICANTLY (P = 001) EFFECTIVE IN ALLEVIATING PAIN WITHIN 24 H
OF PULPECTOMY
17 18
4
19
bull IMMEDIATE POST OPERATIVE RADIOGRAPHIC ASSESSMENT REVEALED 68 (102150) ROOTS
WITH OPTIMAL OBTURATION AND 32 (48150) WITH OVERFILLINGUNDERFILLING MAXIMUM
NO OF OPTIMAL FILLINGS WERE OBSERVED IN GROUP1 (CA + E) (3333) FOLLOWED BY
GROUP 2 (CA) (2549) GROUP 3(SH + E) (2549) AND GROUP 4(SH) (1568)
bull CITRIC ACID GROUPS HAD MORE NUMBER OF OPTIMALLY FILLED ROOTS 588 (60102) THAN
NON CITRIC ACID GROUPS 412 (42102)
bull ENDOACTIVATOR CONTRIBUTED TO 18 OF OPTIMAL OBTURATION IRRESPECTIVE OF
CHELATING AGENT USED
20
21
bull MAXIMUM NO OF VOIDS AND VOID AREAS WERE IN NON CITRIC ACID GROUPS
(6419 amp 5384) COMPARED TO CITRIC ACID GROUPS (3580 amp 4615)
RESPECTIVELY
bull ANALYSIS OF ROOT 13RD REVEALED MAXIMUM NO OF VOID AREA IN APICAL
13RD (4755) FOLLOWED BY MIDDLE 13RD (3846) AND CORONAL 13RD
(1398)
bull LEAST NO OF VOIDS amp VOID AREA (1111 amp 1608) WERE OBSERVED WHEN
ENDOACTIVATOR ALONG WITH CHELATING AGENT WAS USED (GROUP 1)
HOWEVER THIS WAS STATISTICALLY INSIGNIFICANT
22
DISCUSSION
bull IN THE PRESENT STUDY 1 SODIUM HYPOCHLORITE WAS USED ALONG WITH 6 CITRIC ACID
(CHELATING AGENT) WHICH IS REPORTED TO BE AS EFFECTIVE AS 17 EDTA
bull CITRIC ACID (BIOLOGICAL ACID) IS FOUND TO BE BIOCOMPATIBLE AND LEAST IRRITATING TO
PERIAPICAL TISSUES THAN OTHER CHELATING AGENTS
bull USE OF SODIUM HYPOCHLORITE SOLUTION FOLLOWING CHELATING AGENT WAS AVOIDED AS IT
RAPIDLY PRODUCES SEVERE EROSION OF ROOT CANAL WALL DENTIN
bull TRADITIONAL APPROACH OF DELIVERING IRRIGANTS INTO THE ROOT CANAL SPACE USING
SYRINGES AND METAL NEEDLES HAS BEEN FOUND TO BE INEFFECTIVE ESPECIALLY IN THE AREAS OF
ANASTOMOSES BETWEEN CANALS AND APICAL 13RD OF ROOT CANAL
23
bull THEREFORE TO ACHIEVE BETTER CLEANING EFFICIENCY IRRIGANT ACTIVATION HAS BEEN
RECOMMENDED SONIC ACTIVATION HAS BEEN REPORTED TO RESULT IN BETTER ROOT CANAL
CLEANLINESS AS COMPARED TO NO ACTIVATION OF IRRIGANT
24
5
CONCLUSION
bull USE OF 6 CITRIC ACID DEFINITELY HELPED IN RAPID ELIMINATION OF PAIN RESOLUTION OF
PERI-RADICULAR RADIOLUCENCY BETTER OBTURATION QUALITY IN TERMS OF LESS VOIDS AND
VOID AREAS ALONG WITH MAXIMUM NO OF OPTIMAL OBTURATION UP TO APICAL AREA
bull 6 CITRIC ACID AND ENDOACTIVATOR IRRIGATION PROTOCOL PROVED TO BE THE BETTER
IRRIGATION PROTOCOL WHICH MAY CONTRIBUTE TO LONG TERM SUCCESS OF PRIMARY
TOOTH AND THE HEALTH OF UNDERLYING PERMANENT TOOTH
bull 6 CITRIC ACID ALONG WITH ENDOACTIVATOR MAY BE RECOMMENDED AS IRRIGATION
ADJUNCTS IN PULPECTOMY PROCEDURE OF PRIMARY TEETH
25
PROS AND CONS
PROS
bull PROPER EXPLANATION OF THE MATERIALS
USED
CONS
bull NO PREOPERATIVE AND POSTOPERATIVE
RADIOGRAPHS
26
REFERENCES
bull RAMACHANDRA JA NIHAL NK NAGARATHNA C VORA MS ROOT CANAL IRRIGANTS IN
PRIMARY TEETH WORLD J DENT 20156(3)229-234
bull MOHAMMADI Z JAFARZADEH H SHALAVI S KINOSHITA JI UNUSUAL ROOT CANAL
IRRIGATION SOLUTIONS J CONTEMP DENT PRACT 201718(5)415-420
bull ZEHNDER M ROOT CANAL IRRIGANTS J ENDOD 2006 32389- 98
bull SMITH JJ amp WAYMAN BE AN EVALUATION OF THE ANTIMICROBIAL EFFECTIVENESS OF
CITRIC ACID AS A ROOT CANAL IRRIGANT JOURNAL OF ENDODONTICS 1986 12(2) 54-58
bull TANNURE PN AZEVEDO CP BARCELOS R GLEISER R PRIMO LG LONG-TERM OUTCOMES OF
PRIMARY TOOTH PULPECTOMY WITH AND WITHOUT SMEAR LAYER REMOVAL A RANDOMIZED
SPLIT-MOUTH CLINICAL TRIAL PEDIATR DENT 201133316E20 27
bull CARON G NHAM K BRONNEC F MACHTOU P EFFECTIVENESS OF DIFFERENT FINAL IRRIGANT
ACTIVATION PROTOCOLS ON SMEAR LAYER REMOVAL IN CURVED CANALS J ENDOD
2010361361E6
bull COLL JA SADRIAN R PREDICTING PULPECTOMY SUCCESS AND ITS RELATIONSHIP TO
EXFOLIATION AND SUCCEDANEOUS DENTITION PEDIATR DENT 19961857E63
28
1
LOCAL
ANESTHESIA
DR MITAKSHARA NIRWAN
CONTENTS
Definition
Methods of inducing local anesthesia
Desirable properties
Electrophysiology of nerve conduction
Impulse propagation and spread
Mode and site of action of local anesthesia
Classification of local anesthetic according to biological site and mode of action
Dissociation of local anaesthetics
Mechanism of action of local anaethetics
Local anaesthetic agent
2
3
DEFINITION
Local anesthesia is defined as a loss of sensation in
a circumscribed area of the body caused by depression
of excitation in nerve endings or an inhibition of the
conduction process in peripheral nerves
An important feature of local anesthesia is that it produces
LOSS OF SENSATION WITHOUT INDUCING LOSS OF
CONSCIOUSNESS
4
METHODS OF INDUCING LOCAL
ANESTHESIA
Low temperature
Mechanical trauma
Anoxia
Neurolytic agents such as alcohol amp phenol
Chemical agents such as local anesthetics
PROPERTIES OF LOCAL
ANESTHESIA
It should not be irritating to tissue to which it is applied
It should not cause any permanent alteration of nerve structure
Its systemic toxicity should be low
Time of onset of anesthesia should be short
It should be effective regardless of whether it is injected into the tissue or applied locally to mucous membranes
The duration of action should be long enough to permit the completion of procedure
5 6
It should have the potency sufficient to give complete
anesthesia with out the use of harmful concentration solutions
It should be free from producing allergic reactions
It should be free in solution and relatively undergo
biotransformation in the body
It should be either sterile or be capable of being sterilized by
heat with out deterioration
2
ELETROPHYSIOLOGY OF
NERVE CONDUCTION
There is an electrical charge across the membrane
This is the membrane potential
The resting potential (when the cell is not firing) is a negative
electrical potential of -70mv that exists across the nerve
membrane produced by different concentrations of either side of
the membrane
The interior of nerve is NEGATIVE in relation to exterior
7 8
inside
outside
Resting potential of neuron = -70mV
+
-
+
-
+
-
+
-
+
-
SLOW DEPOLARIRIZATION
9
RAPID DEPOLARIZATION
The interior of nerve is POSITIVE in relation to exterior
REPOLARIZATION
10
bull Repolarization takes 07 msec
bull Depolarization takes 03 msec
SODIUM PUMP -
energy comes from the oxidative metabolism of ATP
bull The entire process require 1 msec
IMPULSE PROPOGATION
IMPULSE SPREAD
The propagated impulse travels along the nerve
membrane towards CNS The spread of impulse differs
in myelinated and unmyelinated nerve fibers
DEPOLARIZED SEGMENT ADJACENT RESTING AREA
MODE AND SITE OF ACTION OF LOCAL
ANESTHETICS
Local anesthetic agent interferes with excitation
process in a nerve membrane in one of the
following ways
Altering the basic resting potential of nerve
membrane
Altering the threshold potential
Decreasing the rate of depolarization
Prolonging the rate of repolarization
12
3
CLASSIFICATION OF LOCAL ANESTHETIC
SUBSTANCES ACCORDING TO
BIOLOGICAL SITE AND MODE OF ACTION
CLASS A
Agents acting at receptor site on external surface of nerve membrane
Chemical substance Biotoxins (eg tetrodotoxin and saxitoxin)
CLASS B
Agents acting on receptor sites on internal surface of nerve membrane
Chemical substance Quaternary ammonium analogues of lidocaine
scorpion venom 13
CLASS C Agents acting by receptor independent of
physiochemical mechanism
Chemical substance Benzocaine
CLASS D Agents acting by combination of receptors and
receptor independent mechanisms
Chemical substance most clinically useful anesthetic agents
(eg lidocaine mepivacaine prilocaine)
14
BASED ON THE SOURCE
NATUAL
SYNTHETIC
OTHERS
BASED ON MODE OF APPLICATION
bull INJECTABLE
bull TOPICAL
BASED ON DURATION OF ACTION
bull ULTRA SHORT
bull SHORT
bull MEDIEM
bull LONG
BASED ON ONSET OF ACTION SHORT
INTERMEDIATE
LONG
15
DISSOCIATION OF LOCAL
ANESTHETICS
Local anesthetics are available as salts (usually
hydrochlorides) for clinical use
The salts both water soluble and stable is dissolved in
either sterile water or saline
In this solution it exists simultaneously as unchanged
molecule (RN) also called base and positively charged
molecules (RNH+) called cations
RNH+ ==== RN+ H
+
16
The relative concentration of each ionic form in the solution varies
in the pH of the solution or surrounding tissue
In the presence of high concentration of hydrogen ion (low pH) the
equilibrium shifts to left and most of the anesthetic solution exists
in cationic form
RNH+ gt RN
+ + H
+
As hydrogen ion concentration decreases (higher pH) the
equilibrium shifts towards the free base form
RNH+ lt RN + H
+
17
The relative proportion of ionic form also depends on pKa or DISSOCIATION CONSTANT of the specific local anesthetic
The pKa is a measure of molecules affinity for H+
ions
When the pH of the solution has the same value as pKa of the local anesthetic exactly half the drug will exists in the RNH
+ form and
exactly half in RN form
The percentage of drug existing in either form can be determined by Henderson Hasselbalch equation
Log baseacid = pH - pKa
18
4
MECHANISM OF ACTION OF LOCAL
ANESTHETICS
The following sequence is proposed mechanism of action of LA
Displacement of calcium ions from the sodium channel receptor site
Binding of local anesthetic molecule to this receptor site
Blockade of sodium channel
19
Decrease in sodium conductance
Depression of rate of electrical depolarization
Failure to achieve the threshold potential level
Lack of development of propagated action potential
Conduction blockadehellip
20
21
Na + Na +
22
LOCAL ANESTHETIC AGENT
COMERCIALLY PREPARED LOCAL ANESTHESIA
CONSISTS OF
Local anesthetic agent (xylocaine lignocaine 2)
Vasoconstrictor (adrenaline 1 80000)
Reducing agent (sodium metabisulphite)
Preservative (methylparabencapryl
hydrocuprienotoxin)
Fungicide (thymol)
Vehicle (distillde waterNaCl)
LOCAL ANESTHETIC AGENT
The local anesthetics used in dentistry are divided
into two groups
ESTER GROUP
AMIDE GROUP
23 24
ESTER GROUP It is composed of the following
An aromatic lipophilic group
An intermediate chain containing
an ester linkage
A hydrophilic secondary or tertiary
amino group
AMIDE GROUP It is composed of the following
An aromatic lipophilic group
An intermediate chain containing
amide linkage
A hydrophilic secondary or tertiary
amino group
5
25
CLASSIFICATION OF LOCAL ANESTHETICS
ESTERS
Esters of benzoic acid
Butacaine
Cocaine
Benzocaine
Hexylcaine
Piperocaine
Tetracaine
Esters of Para-amino
benzoic acid
Chloroprocain
Procaine
Propoxycaine
26
AMIDES Articaine
Bupivacaine
Dibucaine
Etidocaine
Lidocaine
Mepivacaine
Prilocaine
Ropivacaine
QUINOLINE
Centbucridine
PHARMACOKINETICS OF LOCAL
ANESTHETICS UPTAKE
When injected into soft tissue most local anesthetics produce
dilation of vascular bed
Cocaine is the only local anesthetic that produces
vasoconstriction initially it produces vasodilation which is
followed by prolonged vasoconstriction
Vasodilation is due to increase in the rate of absorption of the
local anesthetic into the blood thus decreasing the duration of
pain control while increasing the anesthetic blood level and
potential for over dose 27
AMIDE LOCAL ANESTHETICS
The metabolism of amide local anesthetics is more
complicated then esters The primary site of
biotransformation of amide drugs is liver
Entire metabolic process occurs in the liver for lidocaine
articaine etidocaine and bupivacaine
Prilocaine undergoes more rapid biotransformation then the
other amides
28
REFERENCES
Handbook of local anesthesia ndash Stanley F Malamed ndash 6th
edition
Essentials of Local Anesthetic Pharmacology Daniel E
Becker Anesth Prog 2006 Fall 53(3) 98ndash109
WIKIPEDIEA
29
THANK YOU
30
1
Pharmacological Methods of Behavior
Management
DR MITAKSHARA NIRWAN
DEFINITIONS
bull Conscious Sedation ndash A minimally depressed level of consciousness that retains
the patients ability to independently and continuously maintain an airway and respond appropriately to physical stimulation or verbal command
(American Dental Association House Of Delegates 2000)
bull Deep Sedation ndash An induced state of depressed consciousness
accompanied by partial loss of protective reflexes including the inability to continuously maintain an airway independently and or to respond purposefully to physical stimulation or verbal command
bull General Anesthesia (G A) ndash An induced state of unconsciousness or complete loss of
protective reflexes including the inability to continually maintain an airway independently and respond purposefully to physical stimulation or verbal command
Conscious sedation
ADVANTAGES
Conscious
Protective reflexes active amp intact
Stable vital signs
Operating dentist may perform sedation
Minimum amount of equipment required
Prolong detainment in recovery room not required
Risk of complication very low
Excellent choice for poor ndash risk pt in dental office
Cost effective
General anesthesia
ADVANTAGES Not absolutely
essential May be the only
method Not necessary (no
pain reaction) Amnesia always
present
Conscious sedation
DISADVANTAGES
Pt cooperation is essential
Extremely difficult or mentally handicapped pt cannot always be managed
Use of local anesthesia is a must
Amnesia may or may not be present
General anesthesia DISADVANTAGES
Pt unconscious
Protective reflexes are depressed
Depressed
Advanced training required Dentist must not act also as anesthetist
Special equipment necessary
Detainment in recovery area necessary
High IOP amp postoperative complications
Not indicated in dental office
More expensive
Fundamental Concepts
bull Techniques that utilize drugs to induce co-operative yet conscious state in an otherwise uncooperative child ndash CONSCIOUS SEDATION
2
GOALS
1 To facilitate the provision of quality care
2 To minimize the extremes of disruptive behavior
3 To promote a positive psychologic response to treatment
4 To promote patient welfare amp safety
5 To return the patient to physiologic state
OBJECTIVES
1 The pt mood must be altered
2 The pt must remain conscious at all times
3 The pt must be cooperative
4 All protective reflexes must remain intact and active
5 Vital signs must remain stable and with in normal limits
6 The ptrsquos pain threshold should be elevated
7 Amnesia may be present
Indications
1 Preschool children
2 Lack of Psychological Emotional maturity
3 Lack of Cognitive Physical Medical disability
4 Fearful amp anxious pts
5 Pt who require extensive amp complicated dental care amp would require or benefit from prolonged visits
6 Acute pain
7 Traumatic injuries
Operating Facilities amp Equipment
A positive pressure O2 delivery system capable of administering gt than 90 O2 at 10L min flow for 60 min (650L ldquoErdquo cylinder)
OR
Self inflating bag valve mask device (15L min)
A functional suction apparatus with appropriate suction catheters
Monitoring equipment - PO BPC PC or Capno
Inhalation sedation unit
100 O2 amp never less than 25
A fail safe mechanism that is checked and calibrated annually
Must have appropriate scavenging system
Emergency drugs
Techniques of sedation
Routes for drug administration
bull Oral
bull Rectal
bull Inhalational
bull Transmucosal
ndash Sublingual
ndash Intranasal
bull Parenteral
ndash IM
ndash sub mucosal
ndash IV
3
Oral Sedation
Advantages
1 Almost universally accepted and the easiest method
2 Decreased incidence and severity of adverse reaction
3 Low cost
Disadvantages
1 Absorption is variable
2 Prolonged latent period(30 min)
3 Reversal of any unwanted effect is also difficult
4 Inability to readily lighten or deepen the level of sedation
5 Prolonged duration of action
Rectal Sedation
Advantages 1 Incidence and intensity of
drug related side effects is minimized
2 Drug absorption occurs from the large intestine directly into the circulation
3 The lack of a needle syringe or other equipment
4 The ease of administration
5 The low cost
Disadvantages
1 Inconvenience to the administrator amp pt
2 The variable absorption of drugs from the large intestine
3 The slow onset of action amp the relatively long duration of action
4 Inability to titrate the drug dosage
5 The inability to reverse the action of the drug the prolonged recovery
Intranasal sedation
Advantages
Rapid onset (10 ndash 15 min)
Simple amp relatively painless
Less pt cooperation is required
Absorbed directly into the C V S
Intranasal sedation
Disadvantages
1 Dependence on nasal mucous membrane
2 Shorter duration of action(40-60min)
3 Multiple dosage may be necessary
Drugs
Midazolam ndash 02mgkg
Sufentanil ndash 15 ndash 3 mcgkg
Ketamine ndash 3-6mg kg
Sublingual sedation
Advantages
1 Pt acceptance
2 Rapid onset
3 High bioavailability
Drugs
Oral Transmucosal Fentanyl Citrate (OTFC)
Intramuscular Sedation
Advantages
1 More rapid onset of action
2 Absorbed directly into the C V system
3 More reliable absorption of drug
4 Pt cooperation is not as essential
Disadvantages
1 Time factor ndash its 15 min latent period
2 Pt may not be willing to accept the injection
3 The prolonged duration of action(2-4 hrs more)
4 Possibility of injury to the tissues at the site of injection caused by either the drug or the needle
4
Sites of I M administration
1 Gluteal area
2 Vastus lateralis
3 Mid ndash deltoid area
Drugs
Diazepam
Midazolam
Hydroxyzine
Inhalation Sedation
Advantages
1 The onset of action is more rapid
2 Peak clinical level is achieved rapidly(3-5min) - permit titration
3 Administrator has complete control over the actions of the drug - safety feature
4 No significant over dosage
5 Flexible duration of action
6 Recovery time is rapid amp most complete
7 No injection is required
8 With N2O- O2 it is safe with very few side effects
Disadvantages
1 The initial cost of the equipment is high 2 The continuing cost of the gases is high 3 The equipment occupies considerable space 4 N2O is not a potent agent 5 A degree of cooperation is required from the pt 6 Chronic exposure to N2O is deleterious to the health of
dental personnel
Contraindications
1 Nasal obstruction 2 Cyanosis at rest 3 Poor cooperation 4 1st trimester of pregnancy 5 Fear of masks
I V Sedation
Advantages
1 The onset of action is the most rapid 2 The dosage may be titrated 3 Suitable level of sedation can be provided 4 The recovery period is shorter 5 Side effects are extremely uncommon 6 Control of salivary secretions is possible 7 The gag reflex is diminished 8 Effectively diminishes motor disturbances 9 Provides immediate access to CVS in emergency
Disadvantages
1 Venipuncture is necessary
2 Complication may rise at the site of the venipuncture
3 Monitoring must be more intensive
4 Recovery is not complete at the end of the procedure
5 Reversal of sedation is difficult
5
N2O-O2 (Relative Analgesia)
colorless sweet smelling gas
Pharmacokinetics
Absorption through pulmonary epithelium
It is approx 15 times as soluble as is nitrogen It replaces nitrogen in blood
It is carried in solution in plasma of the blood
It is not metabolized by the body
Elimination ndash majorndash lungs minor --- skin
perspiration urine and intestinal gas
Pharmacodynamics
Dose related
10 ndash 25 Lightheaded
Changes in visual amp auditory sensation
Tingling of hands amp feet
Suffusing warmth
Remote from the immediate environment
Reduced anxiety
25-50 max analgesic properties and aberration of vision hearing and proprioception mild drowsiness euphoria amnesia and increased sleepiness and dreams
35 conc will achieve maximum analgesia
bull CNS
ndash Cerebrum-primarily affected
ndash Safe but weak anesthetic agent
bull RESPIRATORY SYSTEM
ndash Increased Tidal and minute volumes
bull CARDIOVASCULAR SYSTEM
ndash 2 studies ndash decreased cardiac output
bull FETAL SYSTEMS
ndash Miscarriage in humans
bull OTHER SYSTEMS
ndash Depression of spinal reflexes increase muscle tone indicates stage of delirium
ndash Muscle rigidity-narcotics + nitrous oxide
ndash Nausea and vomitting - GIT
ndash HEMATOPOIESIS ----- prolonged exposure
Adverse reactions and toxicity
EMOTIONAL REACTIONS
DREAMS HALLUCINATIONS
No acute toxicity
Chronic toxicity ndash bone marrow
depression
PROCEDURE
Diffusion Hypoxia
Sevoflurane
A fluorinated derivative of isopropyl ether ndash synthesized in 1970
Potent anaesthetic agent with rapid uptake amp speedy recovery
Day-case surgery
Problem
Attaching vaporiser to any of the currently available machine
BENZODIAZEPINES
Diazepam 1961 lipid soluble
Uses-alcoholism epilepsy labor tetanus and cerebral palsy
- sedation and amnesia
- varieties of neurosis amp anxiety states
Pharmacokinetics
Orally Rectal IMIV or SC
Well absorbed through GIT
Excretion in urine
6
bull Pharmacodynamics
ndash Depress the brain stem reticular system and the limbic system thalamus and hypothalamus
ndash It is a centrally acting muscle relaxant Has anti-convulsant properties
Adverse reaction amp toxicity
ndash Confusion nausea headache increased appetite decreased salivation and jaundice Thrombophlebitis
ndash Rebound phenomenon
ndash Toxicity drowsiness confusion sleep and coma
Dosage Oral or Rectal ndash 02-05mgkg
Maximum single dose 10mg
IV- 025mgkg
Supplied Tablets 2 5 10 mg
Suspension ndash 5mg
Midazolam Water soluble ndash non-irritant
Oral IM IV
Metabolism- liver
Onset IV 3 -5mins
oral 20 ndash 30mins
Oral administration anxious patients requiring relatively short dental procedure
No rebound phenomenon
Better anxiolysis amp amnesia (retrograde amnesia)
Adverse effects Respiratory depression
dose dependant apnea
Dosage Oral ndash 025 to 1mgkg to maximum single dose 20mg
IM ndash 01 to 015mgkg to a maximum of 10mg
IV ndash slow IV
Supplied Syrup ndash 2mgml
Injectable ndash 1mgml amp 5mgml vials
Flumazenil specific benzodiazepines antagonist
selectively inhibits CNS effects
IV administration amp not recommended below 18yrs of age
02mg over 15 seconds after 45seconds 02mg then after 60seconds to maximum of 1mg
Sedative-Hypnotics
Barbiturates First truly effective drugs for the management of anxiety Generalized CNS depressants Produce dose dependent effects
Sedation ---- sleep ---- GA ---- coma
Suppress the CNS and result in sedation and amnesia Advantages
Rapid onset and short duration Disadvantages
no analgesic effect and possible hypotension Must be used with caution in trauma patients because they may cause
apnea and hypoventilation
DOSE Pentobarbital Sodium 100mg Secobarbital Sodium 100 to 200mg Children 30 to 100mg
bull Chloral Hydrates (Mickey Finn Knock out drops ) First synthesized in 1832 first member of the hypnotic group of drugs
Widely used as conscious sedation agent
Properties
Unpleasant taste
Nausea vomiting
Quite irritating to skin and to mucous membranes
GI irritation
Dosages Individualized for each patient 25 ndash 50mgkg
maximum of 1g
Supplied oral capsule ndash 500mg
oral solution ndash 250 amp 500mg5ml
Rectal suppositories ndash 324 amp 648mg
Narcotics
Do produce sedation amp euphoria greater in children
LA is required but dose should be decreased
Meperidine Synthetic opiate agonist
Very water soluble
Orally SC IM or IV
Peak effect by oral 1 hr amp lasts upto 4 hrs
Adverse reactions
-Seizures
-Extreme caution in hepatic or renal diseases or history of seizures
7
Dosage Oral SC or IM ndash 1to 22mgkg not to exceed 100 mg
Supplied Oral Tablets ndash 50 amp 100mg
Oral Syrup ndash 50mgml
Parental solution ndash 25 50 75 amp 100mgml
Fentanyl
Synthetic opiate narcotic analgesic
Very potent 01mg = 10mg Morophine75mg Meperidine
Pharmacokinetics
IV IM SM
Metabolized in liver Excreted in urine
Fentanyl Onset ndash 7 to 15mins
Duration ndash 1 to 2 hrs
Pharmacodynamics
Respiratory depression RR but returns to normal rapidly Tidal volume amp response to co2 depressed for extended period
Apnea
Less emetic than meperidine
NOT RECOMMENDED IN CHILDREN BELOW 2yrs
Dosage 0002 to 0004mgkg
Supplied 005mgml in 2 amp 5ml ampoules
Reversal drug Naloxone
Semisynthetic opiate antagonist
No agonist activity
Onset 2 to 5mins SC or IM amp 1 to 2mins IV
Reversal 45mins
Pt should be kept under continual surveillance
Adverse reaction nausea vomiting sweating hypotension hypertension ventricular tachycardia fibrillation
Dosage IV SC IM 001mgkg then 01mgkg every 2- 3mins maximum 2mg
Supplied 002 004 1mg solutions
Antihistamines
Hydroxyzine
Oral or IM
Effect ndash 15 ndash 30mins
Half-life ndash 3 hrs
Uses
To relieve anxiety
Used as an anti-histamine
Used to control nausea and vomiting including that associated with motion sickness and pregnancy
Adverse reaction dry mouth drowsiness hypersentivity
Dosage Oral ndash 1 to 2mgkg
IM ndash 11mgkg
Promethazine Oral or IM Onset 15 to 60mins Duration 4 to 6 hrs Uses
To prevent and treat nausea and vomiting associated with motion pregnancy or surgery
Produces sedation and reduce swelling pain and trismus
Lower seizure threshold Adverse reaction dry mouth blurred vision thickening of bronchial secretions Dosage OralIM ndash 05-11mgkg
maximum 25 mg
Diphenhydramine
Oral IM IV
Onset -1hr
Duration ndash 4 to 6 hr
Metabolized in liver
Adverse reaction disturbed coordination thickening of bronchial secretions
Dosage Oral IM IV ndash 1 to 15mgkg
maximum 50mg
Tranquilizers
Major tranquilizer antipsychotic produce calmness control symptoms of psychoses cause reversible extra pyramidal symptoms and do not tend to cause habituation
Minor tranquilizer antianxiety agents also cause calmness do not cause extrapyramidal symptoms Used in conditions like nervous tension and mild depression
8
Classification
Antipsychotics
Phenothiazine derivatives
Chlorpromazine promazine
Butryophenones
Haloperidol
Rauwolfia alkaloids
Reserpine
Antianxiety drugs
Propyl alcohol derivatives
Meprobamate
Benzodiazepine derivatives
Diazepam
Miscellaneous compounds
Hydroxyzine
Meprobamate
White crystalline powder slightly bitter in taste
Only administered orally
Peak blood concentration ----1 to 3hrs
10 ---------excreted unchanged Rest --- excreted as a oxidized derivative or as a glucoronide
Uses
To relieve day time anxiety
Induce sleep in insomniacs
To reduce anxiety associated with dental treatment
Anti-convulsant ndash petit mal epilepsy
Adverse reaction leucopenia acute non-thrombocytopenic purpura ecchymoses eosinophilia edema adenopathy
Dosage Childrengt 6yrs 100 to 200mg
Not recommended for children under 6yrs
Monitoring during sedation
1 Pulse
2 Blood pressure
3 ECG
4 Respiration
5 Temperature
Pulse
Manual Electronic
bull Radial Brachial
bull Facial labial
Blood pressure
ndash Stethoscope amp sphygmomanometer
ndash Automatic devices
ndash Direct cannulation of an artery ndash very accurate
Electrocardiograph
Heart rate rhythm myocardial function
9
Respiration
ndash Monitoring respiratory rate
ndash Observing the rise amp fall of the chest wall
ndash Observing the color of mucous membrane
ndash Observing the inflation amp deflation of the reservoir bag
Devices for monitoring respiration
1 The Precordial pretracheal stethoscope
2 The esophageal stethoscope
ndash Respiratory rate
ndash Heart rate
ndash Any abnormal sounds
Pulse Oximeter
ndash Oxygen saturation
ndash Heart rate
ndash Oxisensor site
ndash Fingers
ndash Toe
ndash Ear lobe
Mechanism
Oxygenated Hb ndash red light
Deoxygenated Hb- infrared light
Tissue pressure from arterial pulse (plethysmography)
Advantages
ndash Safe amp noninvasive
ndash Simple to use
ndash Information is rapidly available for clinical decision
ndash Indirectly indicates respiratory adequacy
Disadvantages
ndash Finger probes can get dislodged
ndash Emitted light source may cause burning
ndash Non reusable probes are expensive
ndash Does not directly determine airway patency
Capnography
1 The presence absence of air flow
2 Indicates depth amp adequacy of respiration
3 Continues analysis of the co2 content of the respired air ndash indicates respiratory adequacy
Temperature
ndash Disposable nondisposable thermometer
ndash Esophageal rectal temp probe
10
Discharge criteria
Cardiovascular function is satisfactory amp stable
Airway patency is uncompromised amp satisfactory
Pt is easily arousable amp protective reflexes intact
State of hydration is adequate
Pt can talk if applicable
Pt can sit unaided if applicable
Pt can ambulate with minimal assistance if applicable
Presedation level of responsiveness achieved
Responsible individual is available
1
PULP THERAPY OF VITAL TEETH
DR MITAKSHARA NIRWAN
Contents
Indirect pulp capping
Direct pulp capping
Medications amp materials used in pulp capping
Pulpotomy
MTA
Apexogenesis
INDIRECT PULP CAPPING
Pieter Van Forest - first to speak about root canal therapy
Glove designed instruments that could prepare a canal to a certain size and taper(1910)
Indirect pulp capping is defined as a procedure where in small amount of carious dentin is retained in
deep areas of cavity to avoid exposure of pulp followed by placement of a suitable medicament and
restorative material that seals off the carious dentin and encourages pulp recovery (Ingle)
A procedure in which only the gross caries is removed from the lesion and the cavity is sealed for a
time with a biocompatible material (McDonald)
Objective of indirect pulp capping
These were given by Eidelman in 1965
bull Arresting the carious process
bull Promoting dentin sclerosis
bull Stimulating formation of tertiary dentin
bull Remineralization of carious dentin
Layers of Carious Dentin Indications of Indirect Pulp Capping
History
Mild pain associated with eating
Negative history of spontaneous extreme pain
Clinical Examination
Deep carious lesion which are close tobut not involving the pulp in vital primary or young
permanent teeth
No mobility
Nominal pulp inflammationdefinite layer of affected dentin after removal of infected dentin
Radiographic examination
Normal lamina dura amp PDL space
No radiolucency around the apices
2
Contraindications of Indirect Pulp Capping
History
Sharp penetrating pulpalgia
Prolonged spontaneous pain especially at night
Clinical examination
Mobility of tooth
Discoloration of tooth
Negative reaction of electric pulp testing
Radiographic examination
Definite pulp exposure
Break in the lamina dura
Radiolucency around the apices
Widened PDL space
Treatment procedure
Sequelae of Indirect Pulp Capping Three distinct types of new dentin formation take place
1 Cellular fibrillar dentinmdashfirst 2 months
2 Globular dentinmdash3 months
3 Tubular dentin (uniform mineralized dentin)
bull 15th of reparative dentin formation begins in less than 30 days
bull After 3 months 01 mm is formed
DIRECT PULP CAPPING Defined by Kopel (1992) as the placement of a medicament or non medicated material on a pulp that
has been exposed in course of excavating the last portions of deep dentinal caries or as a result of
trauma
Objective
To create new dentin in the area of the exposure and subsequent healing of the pulp
Rationale
achieve a biologic closure of the exposure site by deposition of hard tissue barrier (dentin bridge)
between pulp tissue and capping material thus walling off the
INDICATIONS
Small mechanical exposure
Easily controlled haemorrhage
Bright red haemorrhage
True pinpoint exposure
CONTRAINDICATIONS
Severe toothache at night
Spontaneous pain
Tooth mobility
Radiographic appearance of pulp periradicular de- generation
Excess of hemorrhage at the time of exposure Serous exudate from the exposure
Externalinternal root resorption
Swellingfistula
Histological Changes after Pulp Capping
These were illustrated be Glass and Zander in 1949
After 24 hours Necrotic zone adjacent to calcium
hydroxide paste is separated from healthy pulp
tissue by a deep staining basophilic layer
After 7 days Increase in cellular and fibroblastic
activity
After 14 days Partly calcified fibrous tissue lined by
odontoblastic cells is seen below the calcium
proteinate zone disappearance of necrotic zone
After 28 days Zone of new dentin
3
Medications and Materials Used for Pulp Capping Calcium hydroxide
Corticosteroids amp antibiotics
Inert materials
Collagen fibers
4-META adhesive
Direct bonding
Isobutyl cyanoacrylate
Denatured albumin
Mineral trioxide aggregate
Laser
Bone morphogenic protein
PULPOTOMY
Finn (1995) defined it as the complete removal of the coronal portion of the dental pulp
followed by placement of a suitable dressing or medicament that will promote healing and
preserve vitality of the tooth
American Academy of Pediatric Dentistry (1998) defined pulpotomy as the amputation of
affected infected coronal portion of the dental pulp preserving the vitality and function of the
remaining part of radicular pulp
Objectives
bull Removal of inflamed and infected coronal pulp at the site of exposure thus preserving the vitality of the
radicular pulp and allowing it to heal
bull Maintain the tooth in the dental arch
Rationale
bull Radicular pulp is healthy and capable of healing after surgical amputation of the infected coronal pulp
bull Preserves vitality of the radicular pulp
bull Maintains tooth in a physiologic condition
Indications of Pulpotomy bull Mechanical pulp exposure in primary teeth
bull Teeth showing a large carious lesion but free of radicular pulpitis
bull History of only spontaneous pain
bull Hemorrhage from exposure sites bright red and can be controlled
bull Absence of abscess or fistula
bull No interradicular bone loss
bull No interradicular radiolucency
Contraindications of Pulpotomy bull Persistent toothache
bull Tenderness on percussion
bull Root resorption more than 13rd of root length
bull Large carious lesion with nonrestorable crown
bull Highly viscous sluggish hemorrhage from canal orifice which is uncontrollable
bull Medical contradictions like heart disease immuno compromised patient
bull Swelling or fistula
bull External or internal resorption
bull Pathological mobility
bull Calcification of pulp
Classification of pulpotomy
4
Formocresol Pulpotomy
Iby BUCKLEY in 1904
Sweet (1930) Formulated multi visit technique
Doyle (1962) Advocated 2 sitting procedure (complete devitalization)
Spedding (1965) Gave 5 minute protocol (partial devitali- zation)
Venham (1967) Proposed 15 seconds procedure
Current concept uses 4 minutes of application time
Composition of formocresol Buckleyrsquos Formula
bull Cresol ndash 35 percent
bull Glycerol ndash 15 percent
bull Formaldehyde ndash 19 percent
bull Water ndash 31 percent
Mechanism of Action
It prevents tissue autolysis by bonding to the proteins Bonding is of peptide groups of side chain amino acids and is a reversible process accomplished without
changing the basic structure of protein molecules
Histological Changes
bull Demonstrated by Mass and Zilbermann11 in 1933 and also by Massler and Mansokhani in 1959
bull Immediately the pulp becomes fibrous and acidophillic
bull Seven to fourteen days Three zones appear
a broad eosinophilic zone of fixation
b broad pale-staining zone of atrophy with poorcellular definition
c broad zone of inflammation extending apically into normal pulp tissue
bull One yearndash Progressive apical movement of these zones with only acidophillic zone left at the end of 1 year
Modified Formocresol Pulpotomy
Used by TRASK(1972)
The technique is identical to that described for primary teeth except that the formocresol pellet is
sealed permanently in the tooth
Two-visit Devitalization Pulpotomy
Indications
bull There is evidence of sluggish bleeding at the amputation site that is difficult to control
bull Pus in the chamber but none at the amputation site
bull There is thickening of the PDL
bull History of pain
Contraindications
bull Nonrestorable tooth
bull Tooth with necrotic pulp
5
Glutaraldehyde Pulpotomy
It was first suggested by S Gravenmade Introduced by Kopel in 1979
Mechanism of Action
bull Glutaraldehyde produces rapid surface fixation of the underlying pulpal tissue
bull A narrow zone of eosinophilic stained and compressed fixed tissue is found directly beneath the area of application which blends into vital normal appearing tissue apically
bull With time the glutaraldehyde fixed zone is replaced by macrophagic action with dense collagenous tissue thus the entire root canal tissue is vital
Cvekrsquos Pulpotomy
bull This is also called as calcium hydroxide pulpotomy or young permanent partial pulpotomy
bull This was proposed by Mejare and Cvek16 in 1978
bull Indicated in young permanent teeth where the pulp is exposed by mechanical or bacterial means and the
remaining radicular tissue is judged vital by clinical and radiographic criteria whereas the root closure is
notcomplete
MINERAL TRIOXIDE AGGREGATE (MTA) Torabinejad described the physical and chemical properties of MTA in 1995
It is ash colored powder made primarily of fine hydrophilic particles of
1 tricalcium aluminate
2 tricalcium silicate
3 silicate oxide
4 tricalcium oxide
5 bismuth dioxide
Hydration of the powder results in a colloidal gel composed of calcium oxide crystals in an amorphous
structure This gel solidifies into a hard structure in less than three hours
PROPERTIES OF MTA
It is biocompatible material and its sealing ability is better than that of amalgam or ZOE
Initial pH is 102 and set pH is 125
The setting time of cement is 4 hours
The compressive strength is 70 MPA which is comparable with that of IRM
Low cytotoxicity ndash It presents with minimal inflammation if extended beyond the apex
Mineral trioxide aggregate (MTA) has demonstrated the ability to induce hard-tissue formation in
pulpal tissues and it promotes rapid cell growth
APEXOGENESIS
It is defined as the treatment of a vital pulp by capping or pulpotomy in order to permit continued
growth of the root and closure of the open apex
Rationale
Maintenance of integrity of the radicular pulp tissue to allow for continued root growth
Indications
bull Indicated for traumatized or pulpally involved vital permanent tooth when root apex is incompletely formed
bull No history of spontaneous pain
bull No sensitivity on percussion
bull No hemorrhage
bull Normal radiographic appearance
Contraindications
bull Evidence that radicular pulp has undergone degenerative changes
bull Purulent drainage
bull History of prolonged pain bull Necrotic debris in canal
bull Periapical radiolucency
6
1
Gupta A Dhingra R Chaudhari P Gupta A
Department of Paedodontics and Preventive Dentistry Faculty of Dental Sciences SGT University Gurgaon Haryana India
Journal of Indian Society of Pedodontics and Preventive Dentistry
Volume 35 I Issue 3 I July-September 2017
A COMPARISION OF VARIOUS MINIMALLY
INVASIVE TECHNIQUES FOR THE REMOVAL
OF DENTAL FLUOROSIS STAINS IN
CHILDREN
DR MITAKSHARA NIRWAN
CONTENTS
bull Introduction
bull Aims
bull Materials and Methods
bull Results
bull Discussion
bull Conclusion
bull Critical analysis
bull References
INTRODUCTION
bull Dental fluorosis is a developmental disturbance of dental enamel caused by
successive exposure to high concentrations of fluoride during tooth
development
bull Various methods of therapy are advocated for the treatment of fluorosis -
stained teeth which range from invasive ceramic veneer bonding restorations
to abrasive chemical treatments
bull The combination of dental bleaching techniques and microabrasion appears
as an excellent conservative solution to reestablish health in fluorosis
affected teeth
AIMS
bull The aim of the study was to evaluate and compare the effectiveness of
minimally invasive techniques for the removal of dental fluorosis
stains in children in vivo
MATERIALS AND METHODS
Patients visiting the department of Pedodontics and Preventive dentistry
Faculty of Dental Sciences SGT University Gurgaon
bull Sample size 90 patients
bull Age group 10 -17 years
bull Caries cracks or periodontal
disease on anterior teeth
bull Abscess draining sinus
cellulitis
bull Non vital teeth
hypersensitive exposed
crevices
bull Orthodontic appliance
bull Past history of bleaching
bull At least two permanent
maxillary anterior teeth
bull TSIF of score 4
bull Free of systemic diseases
Inclusion criteria Exclusion criteria
2
Groups
Group A In office bleaching with 35 hydrogen peroxide( Pola Office
Bleaching kit) activated by light emitting diode (LED) bleaching unit
(35 HP)
Group B Enamel microabrasion (EM) (PREMA Enamel Microabrasion
System) followed by in-office bleaching with 44 carbamide peroxide
gel (EM)
Group C In-office bleaching with 5 sodium hypochlorite (5
NaOCl)
A baseline colour evaluation was done by taking digital photograph of
the maxillary anterior teeth
RESULTS
Group 1
Colour stability
Group 2 Group 3
Tooth sensitivity
Tooth sensitivity values were taken before the treatment
which was compared to immediate postoperative and follow
up visits It was checked using an electric pulp tester
maximum
moderate
least
immediately
group 2
group 1
group 3
1 month
group 2
group 1
group 3
3 month
group 2
group 1
group 3
Patient satisfaction score
Satisfaction was assessed on visual analog scale
Range 1 to 5
Groups percentage of patients
who were satisfied with
the treatment
Number of patients
who reported slight
reappearance of colour
Group 1
90
7
Group 2
83
8
Group 3
73
7
3
Number of Appointments
Groups One sitting Two sittings Three
sittings
Group 1
25
4
1
group 2
26
3
1
Group 3
30
0
0
DISCUSSION
bull Hydrogen peroxide is capable of penetrating the tooth osmosis and through porosities and cracks subsequently acting directly on the pigmented molecules
bull Gurgan et al investigated 3 different light systems and found out that diode laser system with gave best tooth whitening and least tooth sensitivity
bull In the EM group the surface reflects and refracts light from the surface in such way that mild imperfections in underlying enamel are camouflaged While the highly polished surface of enamel enhances the aesthetic appearance
bull Train et al and Loguercio et al also had the similar results in their studies with EM mild fluorosis showed best results moderate showed moderate results while it had little effect on severe fluorosis
bull NaOCl was only effective on mild stains while moderate and severe
stains could only be lightened to quite an extent but could not be
completely removed
bull When NaOCl comes in contact with hypomineralized and discoloured
enamel it degrades and removes the chromogenic organic material
located on the enamel surface
CONCLUSION
bull It was concluded that esthetic appearance of teeth mild fluorosis can
be achieved by bleaching and microabrasion But in cases of
moderate fluorosis a combination of any of theses modalities can be
used
bull As no special maintenance precautions are required these maybe be
considered as an interesting alternative to conventional operative
treatment
bull Focuses on only TSIF of 4
bull Electric pulp testing is not the
right method to check for
sensitivity
bull Tooth Sensitivity changes
from person to person
bull Food habits can cause
staining of the teeth
bull Minimally invasive
bull Cheaper to veneers
bull Minimal loss of tooth structure
bull 4 parameters checked for the success of treatment
bull Inclusion of specific score of fluorosis for comparing the results
bull Maximum 3 appointments needed
CRITICAL ANALYSIS
Pros Cons
REFERENCES
bull Gurgan S Cakir FY Yazici E Different light-activated in officebleaching
systems Lasers Med Sci 201025817-22
bull Train TE McWhorter AG Seale NSWilson CF Guo IY Examination of
esthetic improvement and surface alteration following microabrasion in
fluorotic human incisors in vivoPediatr dent 199618353-62
bull Loguercio AD Correia LD Zago C Tagliari D Neumann E Gomes OM et al
Clinical effectiveness of two microabrasion materials materials for the
removal of enamel flurosis stains Oper Dent 200732531-8
4
2
Level of Usage (Q 123)
Results Purpose (Q7)
Improved
communication and
learning
Using more than
one type of
device
Helped in
Speech
Positive Impacts -
(Q58 amp 9)
P value 0003(s) P value-0007 P value-0006(s)
Reduced parent-
child interaction Disrupted sleep Lack of motivation for academics
Negative Impacts (Q81213)
P value-0001(s) P value-0002(s) P value-0006
Time when children use
the device the most
Isolation of the
child Behavioral impact when gadget is
taken back
Dependency
Behaviour (Q10111415)
P value-002(s) P value 002(s) P value-044
This study was done to evaluate the level of usage of handheld devices and their impact
on the children aged 0-12 years The questionnaire was made such that it asked both the
positive and negative impact and further included the questions regarding the
dependency
784 children had access to smartphone and 17 used tablets
The most common age group in which the devices was used the most was 5-8 years
followed by 9-12 followed by 0-4 (Arlinda et al 2019 )
Another study done by (Rachel Bedford et al 2016) concluded increase usage of mobile
phones 5122 in 6ndash11 monthshy olds through to 9205 by 25ndash36 months
745used these devices several times a day out of which 539 used it for more than
one hourday 255 used it for less than one hour and 206 for more than 2 hours
Various studies follow the same recommendation given by AAP to limit the duration of
gadget amongst children
Discussion
3
Improve of Cognitive Skills
Amongst the positive impacts most parents have answered that the usage of these
devices has helped their child communicate and learn better and it has showed significant
results According to (Sundus M 2018)These devices improve the cognitive skills and
develop their learning skills fasterThe competition skills also get better It gives time for brain to think and process information better Another study which supports this (LF
Jonathan et al 2016)
Motor Physical Exercise
This study has shown that children like to use more than one type of device
sometimesUsing these devices improve fine motor skillshand eye coordination and
hands and fingers become more efficient (Srinahyanti et al 2019) (Sundus M 2018)
Speech Improvement
392 Parents say that maybe usage of the devices has helped improve speech in their
children but Various studies show otherwise as most of them shows that usage of handheld
devices causes delay of speech (Srinahyanti et al 2019)
Reduced parent child interaction
The negative impacts are more when compared to the positive ones Usage of gadgets
has resulted in reduced parent child interaction Less face to face interaction can
cause detachment from family members and value which in turn also causes isolation
of the child as he is more comfortable with the gadget (M Suhana-2017)
Sleep Disorders
This study shows that most parents have agreed that usage of these devices does
cause disruption of sleep Various studies have shown that children get fewer hours of
sleepdrowsiness during the day and dramatic increase in day time sleep because of
the screen usage (Acc to National Sleep Foundation) ( Cain N et al 2010)
In this study most number of parents have
agreed that their children might be dependent on
these devices and also had showed restless and
violent behavior if the gadget is snatched from
them
Most number of kids (667) are heavily
dependent as they like to use the device during
their meal time
Various other studies have assessed the screen
time dependency and have concluded that
various kids suffer from SDD
Conclusion The study conclusively shows that the impact of handheld devices is akin to the
importance of table salt in our meals most significant for our growth and
development in moderate amounts and hazardous in excess The negatives clearly
outweigh the positives with the latter too few and far in between This study also
points towards further extensive research on the subject because we need to find ways and also educate parents to optimise the role of these devices in their
childrenrsquos life taking advantage of their positive attributes and minimising their
negative ones
References 1Wahyuni AS Siahaan FB Arfa M Alona I Nerdy N The Relationship between the Duration of Playing
Gadget and Mental Emotional State of Elementary School Students Open Access Maced J Med Sci
20197(1)148ndash151
2Sundus M Department of Computer Science Lahore-The Impacts of using Gadgets on ChildrenJournal of Depression and Anxiety 2018vol 7(1)296
3Amawi SO Subki AH Khatib HA et al Use of Electronic Entertainment and Communication Devices Among
a Saudi Pediatric Population Cross-Sectional Study Interact J Med Res 20187(2)e13
4Julia ldquoHandheld Screen Time Linked with Speech Delays in Young Childrenrdquo Present Pediatric Acad Soc
Meet 2017
5C Rowan ldquoThe Impact of Technology on Child Sensory Motor Developmentrdquo 2003
6Impact of media use on children and youth Paediatr Child Health 20038(5)301ndash317
7Naik SV Children and their gadgets A pedodontist perspective Int J Oral Health Sci 2018857-8
8Roberts DF Foehr UG Rideout V Generation M Media in the lives of 8‐18 year‐olds A Kaiser Family
Foundation Study 2005
9Arya K Time spent on television viewing and its effect on changing values of school going children Anthropologist 20046269‐71
10 Lerner C Barr R Screen Sense Setting the Record StraightResearch‐Based Guidelines for Screen
Use for Children Under 3 Years Old Early learning project at Georgetown university 2014 p 1‐10
11SrinahyantiYasaratodo Wau Imelda Free Unita Manurung Nur Arjani-Influence of gadget A positive
and Negative Impact of Smartphone Usage for Early Child2019
4
THANK YOU
1
Morankar Rahul Aditi Kapur Krishan Gauba Ashima Goyal
MANAGEMENT OF ENDODONTIC INSTRUMENT SEPARATION IN
PRIMARY TEETH
CASE REPORT
Journal of South Asian Association of Pediatric Dentistry 2020
DR MITAKSHARA NIRWAN
bull Introduction
bull Aims amp Objectives
bull Case report
bull Discussion
bull Conclusion
bull Pros amp Cons
bull References
CONTENTS
Separation of endodontic instrument is an unexpected complication and its prevalence is not known It is a common belief among the dental professionals that rotary nickelndashtitanium (NiTi) instruments separate more frequently than stainless steel hand instruments
However literature revealed that in permanent teeth the reported prevalence of separated endodontics manual instruments is in the range of 07-74 whereas for rotary NiTI instruments it is
approximately 04-5
Fractured root canal instruments may include endodontic files Gates Glidden burs finger spreaders
and paste fillers
INTRODUCTION
The aim of this study is to describe the management strategies for endodontic
instrument separation in a root canal of primary teeth with emphasis on factors
requiring consideration in different clinical situations
AIMS amp OBJECTIVES
CASE 1
A 6-year-old male child reported with the chief complaint of spontaneous toothache in mandibular left second primary molar since few days It has aggravated following dental treatment at a private dental clinic Clinical examination revealed an underprepared access cavity with 75 and incomplete caries removal
which was sealed with glass ionomer cement
An intraoral periapical radiograph revealed a separated instrument of about 6ndash7 mm size in the distal root
2
The separated instrument was lodged firmly in distobuccal root canal 2ndash3 mm below the cementoenamel junction The instrument was bypassed successfully with no 15 and no 20 H-files but attempts for its retrieval were not successful
GatesndashGlidden (GG) drills no 2 (07 mm) and no 3 (09 mm) were used to drill around the instrument after which it was retrieved successfully using no 25 H-file
All the canals were instrumented till size 30 k-file followed by obturation with metapex and restoration with glass ionomer cement amp followed by placement of a crown and loop space maintainer for missing 74 The instrument retrieved was a manual reamer measuring 6 mm in length
The patient was asymptomatic since then and is under regular follow-up
CASE 2
A 5-year-old female child reported with the chief complaint of spontaneous toothache in mandibular left second
primary molar Clinical examination revealed deep occlusal caries with fractured lingual wall and pain on
percussion An intraoral periapical radiograph revealed caries involving pulp without any furcation or periapical
area of rarefaction and pulpectomy was planned
All the canals were enlarged using NiTi rotary files with a 4 taper operating at 500 rpm with minimum torque
setting An orifice opener [(0825 19 mm) of 8 taper size 25 length 19 mm] and nos 0420 file was used for
instrumentation of root canal This was followed by file nos 0425 which got separated in the distobuccal root
canal The radiograph confirmed a separated instrument of length 3ndash4 mm in the middle third of the root canal
The instrument was bypassed with no 15 k-file but could not get retrieved As instrument separation had occurred with 0425 file the involved root canal was sufficiently debrided before separation and the level of instrument separation was at the mid-root region so it was decided to obturate and seal this tooth with
periodic follow-ups instead of immediate extraction All other canals were enlarged till size 0430 in the sequential manner followed by obturation using metapex and placement of stainless steel crown
3
CASE 3
A 5-year-old female child has complaint of mild intermittent pain with primary mandibular left first molar She
had undergone pulpectomy treatment for the same during which an instrument separation has occurred in
the mesiobuccal root canal by a resident doctor
A radiograph revealed a separated instrument of about 4 mm in size lodged in the apical third but within the
confines of the mesial root An attempt was made for its retrieval but was unsuccessful The extraction of the
involved tooth was carried out under local anesthesia followed by a band and loop space maintainer
CASE 4
A 7-year-old male child reported with a chief complaint of mild intermittent pain on food lodgment with the primary mandibular right first and second molars The patient had a history of dental treatment at a private
dental clinic few months back which he did not continue further
Clinical examination revealed glass ionomer restoration with 85 and proximal caries with 84 leading to food lodgment An intraoral periapical radiograph with 85 revealed empty root canals with a separated
instrument of about 3ndash4 mm size beyond the apex of mesial root close to the developing succedaneous premolar
4
DISCUSSION
Stainless steel files usually separate fracture due to the excessive amounts of torque and overuse or the
preexisting distortion of the instrument whereas in NiTi rotary files it is a combined result of torsional stress and cyclic fatigue
Therapeutic options for the management of separated endodontic instruments include no intervention nonsurgical (orthograde conservative) management surgical management and tooth extraction
Use of ultrasonic scaler Masserann technique Endo extractor and Cavi-Endo ultrasonic instruments are some of the methods popular for retrieval of a separated endodontic instrument in the permanent tooth
In case 1 a 6-mm-long manual reamer was retrieved successfully with the use of GG drill using a manual file and copious irrigation which is the most desired treatment outcome
In case 2 the retrieval of separated rotary file lodged in the middle third of the root canal was unsuccessful in spite of multiple attempts It was therefore managed with routine obturation followed by restoration to maintain the tooth in its physiological functional state It was kept under close periodic follow-up at least
every 3 months This treatment option should be encouraged where it is possible to follow up the patient clinically and radiographically at close periodic intervals as there is the possibility of instrument escaping
into bone due to physiological root resorption
In cases 3 and 4 an instrument has separated in the apical root portion
In case 3 it was within the root canal and thus an attempt was made for its retrieval which was
unsuccessful It was therefore extracted to prevent the fractured instrument from getting exposed in the bone following resorption as there is no accurate and consistent established age for initiation of resorption in primary teeth known per se
In case 4 an immediate extraction of involved tooth was carried out as the separated instrument was beyond the apex of the primary tooth root
Age of the child clinical signs and symptoms and amount of root resorption are the factors which can also influence the management of separated instrument in primary teeth
Moreover if an instrument has separated after initial cleaning and shaping of root canal maintaining a tooth is not a problem as clinical signs and symptoms are not anticipated and the good prognosis is expected
However if an instrument has separated early during the initial cleaning and shaping of the root canal clinical symptoms may compromise the prognosis
Therefore these factors should be kept in mind while planning a suitable management strategy to avoid or at least reduce the burden of extraction and wear of space maintainer for longer period
5
CONCLUSION
The management and prognosis of a primary tooth with a separated instrument is
dependent on the level of instrument fracture within the root age of the child root
resorption and clinical signs and symptoms of the involved tooth
Different management approaches can be tried depending on clinical situations keeping
in mind benefits vs risks in preserving the tooth
PROS amp CONS
PROS
The entire procedure is given
by step by step
Well descriptive xrays and
photographs
CONS
Medical history has not been
given
REFERENCES
1 TOMER ANIL K ET AL ldquoBROKEN FILE RETRIEVAL PUZZLE IN ENDODONTICSrdquo
(2016)
2 SHENOY A MANDAVA P BOLLA N ET AL A NOVEL TECHNIQUE FOR REMOVAL OF
BROKEN INSTRUMENT FROM ROOT CANAL IN MANDIBULAR SECOND MOLAR
INDIAN J DENT RES 201425(1)107ndash110
3 PATEL J MORAWALA A TALATHI R ET AL RETRIEVAL OF A BROKEN INSTRUMENT
FROM ROOT CANAL IN PRIMARY ANTERIOR TEETH UNIV RES J DENT 20155(3)203ndash
206
4 MORANKAR R GOYAL A GAUBA K ET AL MANUAL VERSUS ROTARY
INSTRUMENTATION FOR PRIMARY MOLAR PULPECTOMIES - A 24 MONTHS
RANDOMIZED CLINICAL TRIAL PEDIAT DENT J 201828(2)96ndash102
5 KASHYAP NILOTPOL (2018) RETAINING PRIMARY MOLARS WITH INSTRUMENT
SEPERATION A CASE REPORT AND CLINICAL GUIDE
6
1
IMPACT OF 6 CITRIC ACID AND ENDOACTIVATOR AS IRRIGATION ADJUNCTS ON OBTURATION QUALITY AND PULPECTOMY OUTCOME IN
PRIMARY TEETH
NEETU JAIN SHALINI GARG ABHISHEK DHINDSA SAKSHI JOSHI HARJOY
KHATRIA
PEDIATRIC DENTAL JOURNAL 2019 29
1
DR MITAKSHARA NIRWAN
CONTENTS
bull INTRODUCTION
bull AIMS amp OBJECTIVES
bull CASE REPORT
bull RESULTS
bull DISCUSSION
bull CONCLUSION
bull PROS AND CONS
bull REFERENCES
2
INTRODUCTION
bull ENDODONTIC THERAPY IN PRIMARY TEETH INVOLVES DISINFECTION OF THE ROOT CANAL
SYSTEM AND ITS OBTURATION WITH RESORBABLE PASTE
bull THE CONTENTS OF ROOT CANAL ALONG WITH SMEAR LAYER ARE EXPECTED TO BE REMOVED
DURING THE BIOMECHANICAL PREPARATION
bull IN VITRO AND CLINICAL DOCUMENTS HAVE INDICATED THAT MECHANICAL PREPARATION OF
THE CANAL LEAVES LARGE PORTIONS OF THE CANAL WALLS UNDEBRIDED AND COMPLETE
REMOVAL OF THE BACTERIA BY THIS MECHANICAL PROCEDURE ALONE IS UNLIKELY TO BE SEEN
THEREFORE SOME FORM OF DISINFECTIONIRRIGATION IS MANDATORY TO KILL THE
MICROORGANISMS AND TO REMOVE THE RESIDUAL TISSUES
3
bull THE IDEAL REQUISITES OF A ROOT CANAL IRRIGANT AS GIVEN BY ZEHNDER ARE
1 BROAD ANTIMICROBIAL SPECTRUM
2 HIGH EFFICACY AGAINST ANAEROBIC AND FACULTATIVE MICROORGANISMS ORGANIZED
IN BIOFILMS
3 ABILITY TO DISSOLVE NECROTIC PULP TISSUE REMNANTS
4 ABILITY TO INACTIVATE ENDOTOXIN
5 ABILITY TO PREVENT THE FORMATION OF A SMEAR LAYER DURING INSTRUMENTATION OR
TO DISSOLVE THE LATTER ONCE IT HAS FORMED
6 SYSTEMICALLY NONTOXIC WHEN THEY COME IN CONTACT WITH VITAL TISSUES
NONCAUSTIC TO PERIODONTAL TISSUES AND WITH LITTLE POTENTIAL TO CAUSE AN
ANAPHYLACTIC REACTION
SINCE NO SINGLE IRRIGANT HAS THESE OPTIMAL PROPERTIES STUDIES HAVE REPORTED THE USE
OF TWO OR MORE SOLUTIONS IN A SPECIFIC SEQUENCE OR IN COMBINATIONS FOR BETTER
RESULTS 4
bull SEVERAL IRRIGATING SOLUTIONS ALONG WITH CHELATING AGENTS HAVE BEEN USED
DURING BIOMECHANICAL PREPARATION OF ROOT CANAL BOTH IN PRIMARY AND
PERMANENT TEETH
bull HOWEVER NONE OF THE AVAILABLE IRRIGATING SOLUTIONS HAS BEEN REGARDED CLEARLY
AS OPTIMAL SOLUTION BECAUSE OF THEIR LIMITED EFFECTIVENESS ESPECIALLY IN APICAL
13RD OF THE ROOT CANAL SYSTEM
bull TO OVERCOME SUCH LIMITATIONS USE OF ENDOACTIVATOR HAS BEEN PROPOSED AS AN
IRRIGATION FACILITATOR THAT IS BASED ON SONIC VIBRATION (UP TO 10000 CPM) WHICH
FACILITATES THE IRRIGANT PENETRATION AND ITS RENEWAL WITHIN THE CANAL
bull ACTIVATION SYSTEMS RESULTED IN BETTER REMOVAL OF THE SMEAR LAYER IN THE APICAL
THIRD OF ROOT CANALS IN COMPARISON TO CONVENTIONAL IRRIGATION
5
CITRIC ACID
bull CITRIC ACID IS A WEAK ORGANIC ACID WITH THE APPEARANCE OF WHITE CRYSTALLINE
POWDER AT ROOM TEMPERATURE
bull IT CAN EXIST EITHER IN WATER-FREE FORM (ANHYDROUS) OR MONOHYDRATE FORM THE
WATER-FREE FORM CRYSTALLIZES FROM THE HOT WATER WHEREAS THE MONOHYDRATE
FORMS FROM THE COLD WATER THE LATTER MAY BE CONVERTED TO ANHYDROUS FORM BY
HEATING MORE THAN 78degC
bull CITRIC ACID OCCURS NATURALLY IN THE BODY IN MITOCHONDRIA AND IS USED BY BLOOD
BANKS TO PREVENT COAGULATION OF TRANSFUSED BLOOD CITRIC ACID IS ALSO ESSENTIAL
TO HUMAN METABOLISM AND IS FOUND IN MANY FOODS
6
2
bull THE BIOLOGICAL EFFECTS OF CITRIC ACID ON THE PERIODONTAL STRUCTURE HAS BEEN
EXTENSIVELY STUDIED IN PERIODONTICS
bull NEUMAN AND NEWMAN SHOWED THAT CITRIC ACID IS THE MOST EFFECTIVE ACID IN
ALTERING THE SOLUBILITY OF HYDROXYAPATITE
bull YAMAGUCHI ET AL SHOWED THAT CITRIC ACID SOLUTION HAD ANTIBACTERIAL EFFECTS ON
ALL 12 ROOT CANAL BACTERIA TESTED
bull ARIAS-MOLIZ ET AL SHOWED THAT ETHYLENEDIAMINETETRAACETIC ACID (EDTA) HAS NO
BACTERICIDAL ACTIVITY EVEN AFTER 1 HOUR CONTACT
bull THIS ACID HAS THE ABILITY OF ROOT CANAL IRRIGATION AND ALSO SMEAR LAYER REMOVAL
DIFFERENT CONCENTRATIONS (1ndash50) HAVE BEEN PROPOSED GUTMANN ET AL CONCLUDED
THAT 10 CITRIC ACID IS BETTER THAN ULTRASOUND FOR SMEAR LAYER REMOVAL FROM THE
ROOT END CAVITIES
7
bull STUDIES HAVE SHOWN IRRIGATION WITH 6 CA FOR 15 OR 30 SECONDS IS QUITE
EFFECTIVE IN REMOVING ALL THE COMPONENTS OF THE SMEAR LAYER OF THE PRIMARY
TEETH WHEREAS PERITUBULAR DENTIN DESTRUCTION WAS OBSERVED WHEN HIGHER
CONCENTRATION OF CITRIC ACID WAS USED AS AN IRRIGATING SOLUTION
8
AIMS amp OBJECTIVES
bull THIS STUDY WAS AIMED TO EVALUATE THE CLINICAL AND RADIOGRAPHIC OUTCOME OF
PULPECTOMY ALONG WITH QUALITY OF OBTURATION USING 6 CITRIC ACID AND
ENDOACTIVATOR
9
CASE REPORT
bull 350 CHILDREN (3-9 YEARS) WITH CLINICAL SIGNS AND SYMPTOMS OF CHRONIC IRREVERSIBLE
PULPITIS IN DEEPLY CARIOUS TEETH WERE SCREENED DURING SCHOOL DENTAL HEALTH
PROGRAM FROM MAY 2014-JULY 2014
bull 123 CHILDREN REPORTED TO THE DEPARTMENT AND 67 CHILDREN WERE SELECTED BASED ON
INCLUSION AND EXCLUSION CRITERIA
RECRUITMENT OF PATIENTS
10
INCLUSION CRITERIA
bull HISTORY OF SPONTANEOUS PAIN AND UNCONTROLLED BLEEDING AFTER PULP AMPUTATION
EXCLUSION CRITERIA
bull EVIDENCE OF INTERNAL OR EXTERNAL (PHYSIOLOGICPATHOLOGIC) ROOT RESORPTION OF MORE THAN A THIRD OF ITS LENGTH
bull ROOT CANAL OBLITERATION OR ANATOMIC ANOMALIES
bull INADEQUATE BONE SUPPORT OR NON RESTORABLE TOOTH
bull ONCE PATIENTS ELIGIBILITY WAS CONFIRMED THE TREATMENT PROCEDURE WAS
EXPLAINED TO THE PARENTGUARDIAN AND INFORMED WRITTEN CONSENT WAS
OBTAINED FROM PARENTSGUARDIANS SHOWING WILLINGNESS FOR THEIR
CHILDRENS TREATMENT 11
PROCEDURE
bull PULPECTOMY WAS PERFORMED BY ONE OPERATOR OF PEDIATRIC DENTISTRY DEPARTMENT
USING A STANDARDIZED TREATMENT PROTOCOL FOR ALL THE PATIENTS
bull AFTER ADMINISTRATION OF LOCAL ANESTHESIA RUBBER DAM WAS APPLIED FOR ISOLATION
bull ACCESS CAVITY WAS PREPARED USING AIR-ROTOR HAND PIECE WITH 8 ROUND BUR AND
PULP TISSUE WAS EXTIRPATED WITH THE HELP OF SPOON EXCAVATOR
bull FURTHER THE NEGOTIATION OF THE CANALS WAS DONE WITH 10 K-FILE
bull A DIAGNOSTIC RADIOGRAPH WAS TAKEN FOR ROOT LENGTH DETERMINATION AND
WORKING LENGTH WAS KEPT 1 MM SHORT OF THE RADIOGRAPHICAL APEX
bull ALL ROOT CANALS WERE INSTRUMENTED MANUALLY USING K-FILES AND WERE IRRIGATED
WITH 10 ML 09 NORMAL SALINE AND 1 SODIUM HYPOCHLORITE AS STANDARDIZING
PROTOCOL FOR ROOT CANAL PREPARATION AND DISINFECTION
12
3
GROUP 1 (CA + E) - IRRIGATION WAS DONE
WITH 10 ML OF 6 CITRIC ACID (CITOCID AMMDENT)
AND IRRIGANTS WERE SONICALLY AGITATED WITH
ENDOACTIVATOR (DENTSPLY) FOR 30 S PER CANAL USING REDBLUE
ENDOACTIVATOR TIP
GROUP 2 (CA) - 10 ML OF 6 CITRIC ACID FOR 1 MIN USING
27 GAUZE IRRIGATING NEEDLE
GROUP 3(SH + E) - 10 ML OF 1 SODIUM HYPOCHLORITE
SOLUTION AND SONIC ACTIVATION WITH ENDOACTIVATOR
GROUP 4(SH) - 10 ML OF 1 SODIUM HYPOCHLORITE
SOLUTION USING IRRIGATING NEEDLE (CONTROL GROUP)
bull TEETH UNDERGOING PULPECTOMY WERE RANDOMLY ENROLLED BY CHIT METHOD INTO THREE
STUDY AND ONE CONTROL GROUP
13
bull IN CITRIC ACID GROUPS FINAL RINSE WITH NORMAL SALINE WAS DONE TO REMOVE THE
REMAINING CRYSTALS (CHELATES)
bull FOLLOWING BIOMECHANICAL PREPARATION THE ROOT CANALS WERE DRIED WITH STERILE
ABSORBENT PAPER POINTS AND OBTURATED WITH VITAPEX USING HAND HELD
LENTULOSPIRAL FINAL RESTORATIONS WERE DONE USING COMPOSITE RESIN
14
bull CLINICAL FOLLOW UP WAS DONE AT 24 H1 WEEK 1 MONTH 6 MONTH AND 12
MONTH TO CHECK PAIN PRESENCE AND PAIN FREQUENCY (ONCEMORE THAN ONCE)
SWELLING FISTULA SENSITIVITY TO PERCUSSION
bull RADIOGRAPHIC FOLLOW UP WAS DONE AT 6 MONTH AND 12 MONTH FOR ANY
DEVIATED ERUPTION OF SUCCEDANEOUS TEETH EXCESS FILING MATERIAL AND ITS
RESORPTION EXTERNALINTERNAL ROOT RESORBTION CALCIFIC METAMORPHOSIS
PRESENCE OF FURCATION RADIOLUCENCY
CLINICAL amp RADIOGRAPHIC FOLLOW UP
15
RADIOGRAPHIC ASSESSMENT OF OBTURATION QUALITY
bull POSTOPERATIVE RADIOGRAPHS WERE VISUALLY ASSESSED FOR QUALITY OF OBTURATION BY
TWO INDEPENDENT EXAMINERS (SG AD) WHO WERE BLINDED WITH REGARD TO
IRRIGATION PROTOCOL GROUP TO ENHANCE CALIBRATION EACH EXAMINER ASSESSED THE
RADIOGRAPH INDEPENDENTLY AND LATER REVIEWED TOGETHER FOR FINAL ASSESSMENT
INDIVIDUAL ROOT WAS TAKEN AS UNIT OF ANALYSIS FOR GRADE OF OBTU- RATION AND
SCORING CRITERIA WERE AS GIVEN BY COLL JA 1996
1 UNDER FILLED - FILLING MATERIAL ENDED 1 MM OR MORE SHORT OF THE APEX
2 OPTIMAL FILLING- FILLING MATERIAL APPEARED TO END AT THE RADIOGRAPHICAL APEX
3 OVERFILLED - FILLING MATERIAL EXTRUDED PAST THE RADIOGRAPHIC APEX
4 OPTIMALLY FILLED ROOTS WERE FURTHER ASSESSED FOR THE PRESENCE OF VOIDS AND VOID
AREA (ROOT CANAL SURFACE UNTOUCHED BY THE ROOT CANAL FILLING MATERIAL) IN THREE
VISUALLY DIVIDED SECTIONS OF THE ROOT IE CORONAL MIDDLE AND APICAL 13RD
16
RESULTS
bull OVERALL CLINICAL AND RADIOGRAPHIC SUCCESS RATE OVER A PERIOD OF ONE YEAR WAS
9886 amp 977 RESPECTIVELY
bull ALL GROUPS WERE SIGNIFICANTLY (P = 001) EFFECTIVE IN ALLEVIATING PAIN WITHIN 24 H
OF PULPECTOMY
17 18
4
19
bull IMMEDIATE POST OPERATIVE RADIOGRAPHIC ASSESSMENT REVEALED 68 (102150) ROOTS
WITH OPTIMAL OBTURATION AND 32 (48150) WITH OVERFILLINGUNDERFILLING MAXIMUM
NO OF OPTIMAL FILLINGS WERE OBSERVED IN GROUP1 (CA + E) (3333) FOLLOWED BY
GROUP 2 (CA) (2549) GROUP 3(SH + E) (2549) AND GROUP 4(SH) (1568)
bull CITRIC ACID GROUPS HAD MORE NUMBER OF OPTIMALLY FILLED ROOTS 588 (60102) THAN
NON CITRIC ACID GROUPS 412 (42102)
bull ENDOACTIVATOR CONTRIBUTED TO 18 OF OPTIMAL OBTURATION IRRESPECTIVE OF
CHELATING AGENT USED
20
21
bull MAXIMUM NO OF VOIDS AND VOID AREAS WERE IN NON CITRIC ACID GROUPS
(6419 amp 5384) COMPARED TO CITRIC ACID GROUPS (3580 amp 4615)
RESPECTIVELY
bull ANALYSIS OF ROOT 13RD REVEALED MAXIMUM NO OF VOID AREA IN APICAL
13RD (4755) FOLLOWED BY MIDDLE 13RD (3846) AND CORONAL 13RD
(1398)
bull LEAST NO OF VOIDS amp VOID AREA (1111 amp 1608) WERE OBSERVED WHEN
ENDOACTIVATOR ALONG WITH CHELATING AGENT WAS USED (GROUP 1)
HOWEVER THIS WAS STATISTICALLY INSIGNIFICANT
22
DISCUSSION
bull IN THE PRESENT STUDY 1 SODIUM HYPOCHLORITE WAS USED ALONG WITH 6 CITRIC ACID
(CHELATING AGENT) WHICH IS REPORTED TO BE AS EFFECTIVE AS 17 EDTA
bull CITRIC ACID (BIOLOGICAL ACID) IS FOUND TO BE BIOCOMPATIBLE AND LEAST IRRITATING TO
PERIAPICAL TISSUES THAN OTHER CHELATING AGENTS
bull USE OF SODIUM HYPOCHLORITE SOLUTION FOLLOWING CHELATING AGENT WAS AVOIDED AS IT
RAPIDLY PRODUCES SEVERE EROSION OF ROOT CANAL WALL DENTIN
bull TRADITIONAL APPROACH OF DELIVERING IRRIGANTS INTO THE ROOT CANAL SPACE USING
SYRINGES AND METAL NEEDLES HAS BEEN FOUND TO BE INEFFECTIVE ESPECIALLY IN THE AREAS OF
ANASTOMOSES BETWEEN CANALS AND APICAL 13RD OF ROOT CANAL
23
bull THEREFORE TO ACHIEVE BETTER CLEANING EFFICIENCY IRRIGANT ACTIVATION HAS BEEN
RECOMMENDED SONIC ACTIVATION HAS BEEN REPORTED TO RESULT IN BETTER ROOT CANAL
CLEANLINESS AS COMPARED TO NO ACTIVATION OF IRRIGANT
24
5
CONCLUSION
bull USE OF 6 CITRIC ACID DEFINITELY HELPED IN RAPID ELIMINATION OF PAIN RESOLUTION OF
PERI-RADICULAR RADIOLUCENCY BETTER OBTURATION QUALITY IN TERMS OF LESS VOIDS AND
VOID AREAS ALONG WITH MAXIMUM NO OF OPTIMAL OBTURATION UP TO APICAL AREA
bull 6 CITRIC ACID AND ENDOACTIVATOR IRRIGATION PROTOCOL PROVED TO BE THE BETTER
IRRIGATION PROTOCOL WHICH MAY CONTRIBUTE TO LONG TERM SUCCESS OF PRIMARY
TOOTH AND THE HEALTH OF UNDERLYING PERMANENT TOOTH
bull 6 CITRIC ACID ALONG WITH ENDOACTIVATOR MAY BE RECOMMENDED AS IRRIGATION
ADJUNCTS IN PULPECTOMY PROCEDURE OF PRIMARY TEETH
25
PROS AND CONS
PROS
bull PROPER EXPLANATION OF THE MATERIALS
USED
CONS
bull NO PREOPERATIVE AND POSTOPERATIVE
RADIOGRAPHS
26
REFERENCES
bull RAMACHANDRA JA NIHAL NK NAGARATHNA C VORA MS ROOT CANAL IRRIGANTS IN
PRIMARY TEETH WORLD J DENT 20156(3)229-234
bull MOHAMMADI Z JAFARZADEH H SHALAVI S KINOSHITA JI UNUSUAL ROOT CANAL
IRRIGATION SOLUTIONS J CONTEMP DENT PRACT 201718(5)415-420
bull ZEHNDER M ROOT CANAL IRRIGANTS J ENDOD 2006 32389- 98
bull SMITH JJ amp WAYMAN BE AN EVALUATION OF THE ANTIMICROBIAL EFFECTIVENESS OF
CITRIC ACID AS A ROOT CANAL IRRIGANT JOURNAL OF ENDODONTICS 1986 12(2) 54-58
bull TANNURE PN AZEVEDO CP BARCELOS R GLEISER R PRIMO LG LONG-TERM OUTCOMES OF
PRIMARY TOOTH PULPECTOMY WITH AND WITHOUT SMEAR LAYER REMOVAL A RANDOMIZED
SPLIT-MOUTH CLINICAL TRIAL PEDIATR DENT 201133316E20 27
bull CARON G NHAM K BRONNEC F MACHTOU P EFFECTIVENESS OF DIFFERENT FINAL IRRIGANT
ACTIVATION PROTOCOLS ON SMEAR LAYER REMOVAL IN CURVED CANALS J ENDOD
2010361361E6
bull COLL JA SADRIAN R PREDICTING PULPECTOMY SUCCESS AND ITS RELATIONSHIP TO
EXFOLIATION AND SUCCEDANEOUS DENTITION PEDIATR DENT 19961857E63
28
1
LOCAL
ANESTHESIA
DR MITAKSHARA NIRWAN
CONTENTS
Definition
Methods of inducing local anesthesia
Desirable properties
Electrophysiology of nerve conduction
Impulse propagation and spread
Mode and site of action of local anesthesia
Classification of local anesthetic according to biological site and mode of action
Dissociation of local anaesthetics
Mechanism of action of local anaethetics
Local anaesthetic agent
2
3
DEFINITION
Local anesthesia is defined as a loss of sensation in
a circumscribed area of the body caused by depression
of excitation in nerve endings or an inhibition of the
conduction process in peripheral nerves
An important feature of local anesthesia is that it produces
LOSS OF SENSATION WITHOUT INDUCING LOSS OF
CONSCIOUSNESS
4
METHODS OF INDUCING LOCAL
ANESTHESIA
Low temperature
Mechanical trauma
Anoxia
Neurolytic agents such as alcohol amp phenol
Chemical agents such as local anesthetics
PROPERTIES OF LOCAL
ANESTHESIA
It should not be irritating to tissue to which it is applied
It should not cause any permanent alteration of nerve structure
Its systemic toxicity should be low
Time of onset of anesthesia should be short
It should be effective regardless of whether it is injected into the tissue or applied locally to mucous membranes
The duration of action should be long enough to permit the completion of procedure
5 6
It should have the potency sufficient to give complete
anesthesia with out the use of harmful concentration solutions
It should be free from producing allergic reactions
It should be free in solution and relatively undergo
biotransformation in the body
It should be either sterile or be capable of being sterilized by
heat with out deterioration
2
ELETROPHYSIOLOGY OF
NERVE CONDUCTION
There is an electrical charge across the membrane
This is the membrane potential
The resting potential (when the cell is not firing) is a negative
electrical potential of -70mv that exists across the nerve
membrane produced by different concentrations of either side of
the membrane
The interior of nerve is NEGATIVE in relation to exterior
7 8
inside
outside
Resting potential of neuron = -70mV
+
-
+
-
+
-
+
-
+
-
SLOW DEPOLARIRIZATION
9
RAPID DEPOLARIZATION
The interior of nerve is POSITIVE in relation to exterior
REPOLARIZATION
10
bull Repolarization takes 07 msec
bull Depolarization takes 03 msec
SODIUM PUMP -
energy comes from the oxidative metabolism of ATP
bull The entire process require 1 msec
IMPULSE PROPOGATION
IMPULSE SPREAD
The propagated impulse travels along the nerve
membrane towards CNS The spread of impulse differs
in myelinated and unmyelinated nerve fibers
DEPOLARIZED SEGMENT ADJACENT RESTING AREA
MODE AND SITE OF ACTION OF LOCAL
ANESTHETICS
Local anesthetic agent interferes with excitation
process in a nerve membrane in one of the
following ways
Altering the basic resting potential of nerve
membrane
Altering the threshold potential
Decreasing the rate of depolarization
Prolonging the rate of repolarization
12
3
CLASSIFICATION OF LOCAL ANESTHETIC
SUBSTANCES ACCORDING TO
BIOLOGICAL SITE AND MODE OF ACTION
CLASS A
Agents acting at receptor site on external surface of nerve membrane
Chemical substance Biotoxins (eg tetrodotoxin and saxitoxin)
CLASS B
Agents acting on receptor sites on internal surface of nerve membrane
Chemical substance Quaternary ammonium analogues of lidocaine
scorpion venom 13
CLASS C Agents acting by receptor independent of
physiochemical mechanism
Chemical substance Benzocaine
CLASS D Agents acting by combination of receptors and
receptor independent mechanisms
Chemical substance most clinically useful anesthetic agents
(eg lidocaine mepivacaine prilocaine)
14
BASED ON THE SOURCE
NATUAL
SYNTHETIC
OTHERS
BASED ON MODE OF APPLICATION
bull INJECTABLE
bull TOPICAL
BASED ON DURATION OF ACTION
bull ULTRA SHORT
bull SHORT
bull MEDIEM
bull LONG
BASED ON ONSET OF ACTION SHORT
INTERMEDIATE
LONG
15
DISSOCIATION OF LOCAL
ANESTHETICS
Local anesthetics are available as salts (usually
hydrochlorides) for clinical use
The salts both water soluble and stable is dissolved in
either sterile water or saline
In this solution it exists simultaneously as unchanged
molecule (RN) also called base and positively charged
molecules (RNH+) called cations
RNH+ ==== RN+ H
+
16
The relative concentration of each ionic form in the solution varies
in the pH of the solution or surrounding tissue
In the presence of high concentration of hydrogen ion (low pH) the
equilibrium shifts to left and most of the anesthetic solution exists
in cationic form
RNH+ gt RN
+ + H
+
As hydrogen ion concentration decreases (higher pH) the
equilibrium shifts towards the free base form
RNH+ lt RN + H
+
17
The relative proportion of ionic form also depends on pKa or DISSOCIATION CONSTANT of the specific local anesthetic
The pKa is a measure of molecules affinity for H+
ions
When the pH of the solution has the same value as pKa of the local anesthetic exactly half the drug will exists in the RNH
+ form and
exactly half in RN form
The percentage of drug existing in either form can be determined by Henderson Hasselbalch equation
Log baseacid = pH - pKa
18
4
MECHANISM OF ACTION OF LOCAL
ANESTHETICS
The following sequence is proposed mechanism of action of LA
Displacement of calcium ions from the sodium channel receptor site
Binding of local anesthetic molecule to this receptor site
Blockade of sodium channel
19
Decrease in sodium conductance
Depression of rate of electrical depolarization
Failure to achieve the threshold potential level
Lack of development of propagated action potential
Conduction blockadehellip
20
21
Na + Na +
22
LOCAL ANESTHETIC AGENT
COMERCIALLY PREPARED LOCAL ANESTHESIA
CONSISTS OF
Local anesthetic agent (xylocaine lignocaine 2)
Vasoconstrictor (adrenaline 1 80000)
Reducing agent (sodium metabisulphite)
Preservative (methylparabencapryl
hydrocuprienotoxin)
Fungicide (thymol)
Vehicle (distillde waterNaCl)
LOCAL ANESTHETIC AGENT
The local anesthetics used in dentistry are divided
into two groups
ESTER GROUP
AMIDE GROUP
23 24
ESTER GROUP It is composed of the following
An aromatic lipophilic group
An intermediate chain containing
an ester linkage
A hydrophilic secondary or tertiary
amino group
AMIDE GROUP It is composed of the following
An aromatic lipophilic group
An intermediate chain containing
amide linkage
A hydrophilic secondary or tertiary
amino group
5
25
CLASSIFICATION OF LOCAL ANESTHETICS
ESTERS
Esters of benzoic acid
Butacaine
Cocaine
Benzocaine
Hexylcaine
Piperocaine
Tetracaine
Esters of Para-amino
benzoic acid
Chloroprocain
Procaine
Propoxycaine
26
AMIDES Articaine
Bupivacaine
Dibucaine
Etidocaine
Lidocaine
Mepivacaine
Prilocaine
Ropivacaine
QUINOLINE
Centbucridine
PHARMACOKINETICS OF LOCAL
ANESTHETICS UPTAKE
When injected into soft tissue most local anesthetics produce
dilation of vascular bed
Cocaine is the only local anesthetic that produces
vasoconstriction initially it produces vasodilation which is
followed by prolonged vasoconstriction
Vasodilation is due to increase in the rate of absorption of the
local anesthetic into the blood thus decreasing the duration of
pain control while increasing the anesthetic blood level and
potential for over dose 27
AMIDE LOCAL ANESTHETICS
The metabolism of amide local anesthetics is more
complicated then esters The primary site of
biotransformation of amide drugs is liver
Entire metabolic process occurs in the liver for lidocaine
articaine etidocaine and bupivacaine
Prilocaine undergoes more rapid biotransformation then the
other amides
28
REFERENCES
Handbook of local anesthesia ndash Stanley F Malamed ndash 6th
edition
Essentials of Local Anesthetic Pharmacology Daniel E
Becker Anesth Prog 2006 Fall 53(3) 98ndash109
WIKIPEDIEA
29
THANK YOU
30
1
Pharmacological Methods of Behavior
Management
DR MITAKSHARA NIRWAN
DEFINITIONS
bull Conscious Sedation ndash A minimally depressed level of consciousness that retains
the patients ability to independently and continuously maintain an airway and respond appropriately to physical stimulation or verbal command
(American Dental Association House Of Delegates 2000)
bull Deep Sedation ndash An induced state of depressed consciousness
accompanied by partial loss of protective reflexes including the inability to continuously maintain an airway independently and or to respond purposefully to physical stimulation or verbal command
bull General Anesthesia (G A) ndash An induced state of unconsciousness or complete loss of
protective reflexes including the inability to continually maintain an airway independently and respond purposefully to physical stimulation or verbal command
Conscious sedation
ADVANTAGES
Conscious
Protective reflexes active amp intact
Stable vital signs
Operating dentist may perform sedation
Minimum amount of equipment required
Prolong detainment in recovery room not required
Risk of complication very low
Excellent choice for poor ndash risk pt in dental office
Cost effective
General anesthesia
ADVANTAGES Not absolutely
essential May be the only
method Not necessary (no
pain reaction) Amnesia always
present
Conscious sedation
DISADVANTAGES
Pt cooperation is essential
Extremely difficult or mentally handicapped pt cannot always be managed
Use of local anesthesia is a must
Amnesia may or may not be present
General anesthesia DISADVANTAGES
Pt unconscious
Protective reflexes are depressed
Depressed
Advanced training required Dentist must not act also as anesthetist
Special equipment necessary
Detainment in recovery area necessary
High IOP amp postoperative complications
Not indicated in dental office
More expensive
Fundamental Concepts
bull Techniques that utilize drugs to induce co-operative yet conscious state in an otherwise uncooperative child ndash CONSCIOUS SEDATION
2
GOALS
1 To facilitate the provision of quality care
2 To minimize the extremes of disruptive behavior
3 To promote a positive psychologic response to treatment
4 To promote patient welfare amp safety
5 To return the patient to physiologic state
OBJECTIVES
1 The pt mood must be altered
2 The pt must remain conscious at all times
3 The pt must be cooperative
4 All protective reflexes must remain intact and active
5 Vital signs must remain stable and with in normal limits
6 The ptrsquos pain threshold should be elevated
7 Amnesia may be present
Indications
1 Preschool children
2 Lack of Psychological Emotional maturity
3 Lack of Cognitive Physical Medical disability
4 Fearful amp anxious pts
5 Pt who require extensive amp complicated dental care amp would require or benefit from prolonged visits
6 Acute pain
7 Traumatic injuries
Operating Facilities amp Equipment
A positive pressure O2 delivery system capable of administering gt than 90 O2 at 10L min flow for 60 min (650L ldquoErdquo cylinder)
OR
Self inflating bag valve mask device (15L min)
A functional suction apparatus with appropriate suction catheters
Monitoring equipment - PO BPC PC or Capno
Inhalation sedation unit
100 O2 amp never less than 25
A fail safe mechanism that is checked and calibrated annually
Must have appropriate scavenging system
Emergency drugs
Techniques of sedation
Routes for drug administration
bull Oral
bull Rectal
bull Inhalational
bull Transmucosal
ndash Sublingual
ndash Intranasal
bull Parenteral
ndash IM
ndash sub mucosal
ndash IV
3
Oral Sedation
Advantages
1 Almost universally accepted and the easiest method
2 Decreased incidence and severity of adverse reaction
3 Low cost
Disadvantages
1 Absorption is variable
2 Prolonged latent period(30 min)
3 Reversal of any unwanted effect is also difficult
4 Inability to readily lighten or deepen the level of sedation
5 Prolonged duration of action
Rectal Sedation
Advantages 1 Incidence and intensity of
drug related side effects is minimized
2 Drug absorption occurs from the large intestine directly into the circulation
3 The lack of a needle syringe or other equipment
4 The ease of administration
5 The low cost
Disadvantages
1 Inconvenience to the administrator amp pt
2 The variable absorption of drugs from the large intestine
3 The slow onset of action amp the relatively long duration of action
4 Inability to titrate the drug dosage
5 The inability to reverse the action of the drug the prolonged recovery
Intranasal sedation
Advantages
Rapid onset (10 ndash 15 min)
Simple amp relatively painless
Less pt cooperation is required
Absorbed directly into the C V S
Intranasal sedation
Disadvantages
1 Dependence on nasal mucous membrane
2 Shorter duration of action(40-60min)
3 Multiple dosage may be necessary
Drugs
Midazolam ndash 02mgkg
Sufentanil ndash 15 ndash 3 mcgkg
Ketamine ndash 3-6mg kg
Sublingual sedation
Advantages
1 Pt acceptance
2 Rapid onset
3 High bioavailability
Drugs
Oral Transmucosal Fentanyl Citrate (OTFC)
Intramuscular Sedation
Advantages
1 More rapid onset of action
2 Absorbed directly into the C V system
3 More reliable absorption of drug
4 Pt cooperation is not as essential
Disadvantages
1 Time factor ndash its 15 min latent period
2 Pt may not be willing to accept the injection
3 The prolonged duration of action(2-4 hrs more)
4 Possibility of injury to the tissues at the site of injection caused by either the drug or the needle
4
Sites of I M administration
1 Gluteal area
2 Vastus lateralis
3 Mid ndash deltoid area
Drugs
Diazepam
Midazolam
Hydroxyzine
Inhalation Sedation
Advantages
1 The onset of action is more rapid
2 Peak clinical level is achieved rapidly(3-5min) - permit titration
3 Administrator has complete control over the actions of the drug - safety feature
4 No significant over dosage
5 Flexible duration of action
6 Recovery time is rapid amp most complete
7 No injection is required
8 With N2O- O2 it is safe with very few side effects
Disadvantages
1 The initial cost of the equipment is high 2 The continuing cost of the gases is high 3 The equipment occupies considerable space 4 N2O is not a potent agent 5 A degree of cooperation is required from the pt 6 Chronic exposure to N2O is deleterious to the health of
dental personnel
Contraindications
1 Nasal obstruction 2 Cyanosis at rest 3 Poor cooperation 4 1st trimester of pregnancy 5 Fear of masks
I V Sedation
Advantages
1 The onset of action is the most rapid 2 The dosage may be titrated 3 Suitable level of sedation can be provided 4 The recovery period is shorter 5 Side effects are extremely uncommon 6 Control of salivary secretions is possible 7 The gag reflex is diminished 8 Effectively diminishes motor disturbances 9 Provides immediate access to CVS in emergency
Disadvantages
1 Venipuncture is necessary
2 Complication may rise at the site of the venipuncture
3 Monitoring must be more intensive
4 Recovery is not complete at the end of the procedure
5 Reversal of sedation is difficult
5
N2O-O2 (Relative Analgesia)
colorless sweet smelling gas
Pharmacokinetics
Absorption through pulmonary epithelium
It is approx 15 times as soluble as is nitrogen It replaces nitrogen in blood
It is carried in solution in plasma of the blood
It is not metabolized by the body
Elimination ndash majorndash lungs minor --- skin
perspiration urine and intestinal gas
Pharmacodynamics
Dose related
10 ndash 25 Lightheaded
Changes in visual amp auditory sensation
Tingling of hands amp feet
Suffusing warmth
Remote from the immediate environment
Reduced anxiety
25-50 max analgesic properties and aberration of vision hearing and proprioception mild drowsiness euphoria amnesia and increased sleepiness and dreams
35 conc will achieve maximum analgesia
bull CNS
ndash Cerebrum-primarily affected
ndash Safe but weak anesthetic agent
bull RESPIRATORY SYSTEM
ndash Increased Tidal and minute volumes
bull CARDIOVASCULAR SYSTEM
ndash 2 studies ndash decreased cardiac output
bull FETAL SYSTEMS
ndash Miscarriage in humans
bull OTHER SYSTEMS
ndash Depression of spinal reflexes increase muscle tone indicates stage of delirium
ndash Muscle rigidity-narcotics + nitrous oxide
ndash Nausea and vomitting - GIT
ndash HEMATOPOIESIS ----- prolonged exposure
Adverse reactions and toxicity
EMOTIONAL REACTIONS
DREAMS HALLUCINATIONS
No acute toxicity
Chronic toxicity ndash bone marrow
depression
PROCEDURE
Diffusion Hypoxia
Sevoflurane
A fluorinated derivative of isopropyl ether ndash synthesized in 1970
Potent anaesthetic agent with rapid uptake amp speedy recovery
Day-case surgery
Problem
Attaching vaporiser to any of the currently available machine
BENZODIAZEPINES
Diazepam 1961 lipid soluble
Uses-alcoholism epilepsy labor tetanus and cerebral palsy
- sedation and amnesia
- varieties of neurosis amp anxiety states
Pharmacokinetics
Orally Rectal IMIV or SC
Well absorbed through GIT
Excretion in urine
6
bull Pharmacodynamics
ndash Depress the brain stem reticular system and the limbic system thalamus and hypothalamus
ndash It is a centrally acting muscle relaxant Has anti-convulsant properties
Adverse reaction amp toxicity
ndash Confusion nausea headache increased appetite decreased salivation and jaundice Thrombophlebitis
ndash Rebound phenomenon
ndash Toxicity drowsiness confusion sleep and coma
Dosage Oral or Rectal ndash 02-05mgkg
Maximum single dose 10mg
IV- 025mgkg
Supplied Tablets 2 5 10 mg
Suspension ndash 5mg
Midazolam Water soluble ndash non-irritant
Oral IM IV
Metabolism- liver
Onset IV 3 -5mins
oral 20 ndash 30mins
Oral administration anxious patients requiring relatively short dental procedure
No rebound phenomenon
Better anxiolysis amp amnesia (retrograde amnesia)
Adverse effects Respiratory depression
dose dependant apnea
Dosage Oral ndash 025 to 1mgkg to maximum single dose 20mg
IM ndash 01 to 015mgkg to a maximum of 10mg
IV ndash slow IV
Supplied Syrup ndash 2mgml
Injectable ndash 1mgml amp 5mgml vials
Flumazenil specific benzodiazepines antagonist
selectively inhibits CNS effects
IV administration amp not recommended below 18yrs of age
02mg over 15 seconds after 45seconds 02mg then after 60seconds to maximum of 1mg
Sedative-Hypnotics
Barbiturates First truly effective drugs for the management of anxiety Generalized CNS depressants Produce dose dependent effects
Sedation ---- sleep ---- GA ---- coma
Suppress the CNS and result in sedation and amnesia Advantages
Rapid onset and short duration Disadvantages
no analgesic effect and possible hypotension Must be used with caution in trauma patients because they may cause
apnea and hypoventilation
DOSE Pentobarbital Sodium 100mg Secobarbital Sodium 100 to 200mg Children 30 to 100mg
bull Chloral Hydrates (Mickey Finn Knock out drops ) First synthesized in 1832 first member of the hypnotic group of drugs
Widely used as conscious sedation agent
Properties
Unpleasant taste
Nausea vomiting
Quite irritating to skin and to mucous membranes
GI irritation
Dosages Individualized for each patient 25 ndash 50mgkg
maximum of 1g
Supplied oral capsule ndash 500mg
oral solution ndash 250 amp 500mg5ml
Rectal suppositories ndash 324 amp 648mg
Narcotics
Do produce sedation amp euphoria greater in children
LA is required but dose should be decreased
Meperidine Synthetic opiate agonist
Very water soluble
Orally SC IM or IV
Peak effect by oral 1 hr amp lasts upto 4 hrs
Adverse reactions
-Seizures
-Extreme caution in hepatic or renal diseases or history of seizures
7
Dosage Oral SC or IM ndash 1to 22mgkg not to exceed 100 mg
Supplied Oral Tablets ndash 50 amp 100mg
Oral Syrup ndash 50mgml
Parental solution ndash 25 50 75 amp 100mgml
Fentanyl
Synthetic opiate narcotic analgesic
Very potent 01mg = 10mg Morophine75mg Meperidine
Pharmacokinetics
IV IM SM
Metabolized in liver Excreted in urine
Fentanyl Onset ndash 7 to 15mins
Duration ndash 1 to 2 hrs
Pharmacodynamics
Respiratory depression RR but returns to normal rapidly Tidal volume amp response to co2 depressed for extended period
Apnea
Less emetic than meperidine
NOT RECOMMENDED IN CHILDREN BELOW 2yrs
Dosage 0002 to 0004mgkg
Supplied 005mgml in 2 amp 5ml ampoules
Reversal drug Naloxone
Semisynthetic opiate antagonist
No agonist activity
Onset 2 to 5mins SC or IM amp 1 to 2mins IV
Reversal 45mins
Pt should be kept under continual surveillance
Adverse reaction nausea vomiting sweating hypotension hypertension ventricular tachycardia fibrillation
Dosage IV SC IM 001mgkg then 01mgkg every 2- 3mins maximum 2mg
Supplied 002 004 1mg solutions
Antihistamines
Hydroxyzine
Oral or IM
Effect ndash 15 ndash 30mins
Half-life ndash 3 hrs
Uses
To relieve anxiety
Used as an anti-histamine
Used to control nausea and vomiting including that associated with motion sickness and pregnancy
Adverse reaction dry mouth drowsiness hypersentivity
Dosage Oral ndash 1 to 2mgkg
IM ndash 11mgkg
Promethazine Oral or IM Onset 15 to 60mins Duration 4 to 6 hrs Uses
To prevent and treat nausea and vomiting associated with motion pregnancy or surgery
Produces sedation and reduce swelling pain and trismus
Lower seizure threshold Adverse reaction dry mouth blurred vision thickening of bronchial secretions Dosage OralIM ndash 05-11mgkg
maximum 25 mg
Diphenhydramine
Oral IM IV
Onset -1hr
Duration ndash 4 to 6 hr
Metabolized in liver
Adverse reaction disturbed coordination thickening of bronchial secretions
Dosage Oral IM IV ndash 1 to 15mgkg
maximum 50mg
Tranquilizers
Major tranquilizer antipsychotic produce calmness control symptoms of psychoses cause reversible extra pyramidal symptoms and do not tend to cause habituation
Minor tranquilizer antianxiety agents also cause calmness do not cause extrapyramidal symptoms Used in conditions like nervous tension and mild depression
8
Classification
Antipsychotics
Phenothiazine derivatives
Chlorpromazine promazine
Butryophenones
Haloperidol
Rauwolfia alkaloids
Reserpine
Antianxiety drugs
Propyl alcohol derivatives
Meprobamate
Benzodiazepine derivatives
Diazepam
Miscellaneous compounds
Hydroxyzine
Meprobamate
White crystalline powder slightly bitter in taste
Only administered orally
Peak blood concentration ----1 to 3hrs
10 ---------excreted unchanged Rest --- excreted as a oxidized derivative or as a glucoronide
Uses
To relieve day time anxiety
Induce sleep in insomniacs
To reduce anxiety associated with dental treatment
Anti-convulsant ndash petit mal epilepsy
Adverse reaction leucopenia acute non-thrombocytopenic purpura ecchymoses eosinophilia edema adenopathy
Dosage Childrengt 6yrs 100 to 200mg
Not recommended for children under 6yrs
Monitoring during sedation
1 Pulse
2 Blood pressure
3 ECG
4 Respiration
5 Temperature
Pulse
Manual Electronic
bull Radial Brachial
bull Facial labial
Blood pressure
ndash Stethoscope amp sphygmomanometer
ndash Automatic devices
ndash Direct cannulation of an artery ndash very accurate
Electrocardiograph
Heart rate rhythm myocardial function
9
Respiration
ndash Monitoring respiratory rate
ndash Observing the rise amp fall of the chest wall
ndash Observing the color of mucous membrane
ndash Observing the inflation amp deflation of the reservoir bag
Devices for monitoring respiration
1 The Precordial pretracheal stethoscope
2 The esophageal stethoscope
ndash Respiratory rate
ndash Heart rate
ndash Any abnormal sounds
Pulse Oximeter
ndash Oxygen saturation
ndash Heart rate
ndash Oxisensor site
ndash Fingers
ndash Toe
ndash Ear lobe
Mechanism
Oxygenated Hb ndash red light
Deoxygenated Hb- infrared light
Tissue pressure from arterial pulse (plethysmography)
Advantages
ndash Safe amp noninvasive
ndash Simple to use
ndash Information is rapidly available for clinical decision
ndash Indirectly indicates respiratory adequacy
Disadvantages
ndash Finger probes can get dislodged
ndash Emitted light source may cause burning
ndash Non reusable probes are expensive
ndash Does not directly determine airway patency
Capnography
1 The presence absence of air flow
2 Indicates depth amp adequacy of respiration
3 Continues analysis of the co2 content of the respired air ndash indicates respiratory adequacy
Temperature
ndash Disposable nondisposable thermometer
ndash Esophageal rectal temp probe
10
Discharge criteria
Cardiovascular function is satisfactory amp stable
Airway patency is uncompromised amp satisfactory
Pt is easily arousable amp protective reflexes intact
State of hydration is adequate
Pt can talk if applicable
Pt can sit unaided if applicable
Pt can ambulate with minimal assistance if applicable
Presedation level of responsiveness achieved
Responsible individual is available
1
PULP THERAPY OF VITAL TEETH
DR MITAKSHARA NIRWAN
Contents
Indirect pulp capping
Direct pulp capping
Medications amp materials used in pulp capping
Pulpotomy
MTA
Apexogenesis
INDIRECT PULP CAPPING
Pieter Van Forest - first to speak about root canal therapy
Glove designed instruments that could prepare a canal to a certain size and taper(1910)
Indirect pulp capping is defined as a procedure where in small amount of carious dentin is retained in
deep areas of cavity to avoid exposure of pulp followed by placement of a suitable medicament and
restorative material that seals off the carious dentin and encourages pulp recovery (Ingle)
A procedure in which only the gross caries is removed from the lesion and the cavity is sealed for a
time with a biocompatible material (McDonald)
Objective of indirect pulp capping
These were given by Eidelman in 1965
bull Arresting the carious process
bull Promoting dentin sclerosis
bull Stimulating formation of tertiary dentin
bull Remineralization of carious dentin
Layers of Carious Dentin Indications of Indirect Pulp Capping
History
Mild pain associated with eating
Negative history of spontaneous extreme pain
Clinical Examination
Deep carious lesion which are close tobut not involving the pulp in vital primary or young
permanent teeth
No mobility
Nominal pulp inflammationdefinite layer of affected dentin after removal of infected dentin
Radiographic examination
Normal lamina dura amp PDL space
No radiolucency around the apices
2
Contraindications of Indirect Pulp Capping
History
Sharp penetrating pulpalgia
Prolonged spontaneous pain especially at night
Clinical examination
Mobility of tooth
Discoloration of tooth
Negative reaction of electric pulp testing
Radiographic examination
Definite pulp exposure
Break in the lamina dura
Radiolucency around the apices
Widened PDL space
Treatment procedure
Sequelae of Indirect Pulp Capping Three distinct types of new dentin formation take place
1 Cellular fibrillar dentinmdashfirst 2 months
2 Globular dentinmdash3 months
3 Tubular dentin (uniform mineralized dentin)
bull 15th of reparative dentin formation begins in less than 30 days
bull After 3 months 01 mm is formed
DIRECT PULP CAPPING Defined by Kopel (1992) as the placement of a medicament or non medicated material on a pulp that
has been exposed in course of excavating the last portions of deep dentinal caries or as a result of
trauma
Objective
To create new dentin in the area of the exposure and subsequent healing of the pulp
Rationale
achieve a biologic closure of the exposure site by deposition of hard tissue barrier (dentin bridge)
between pulp tissue and capping material thus walling off the
INDICATIONS
Small mechanical exposure
Easily controlled haemorrhage
Bright red haemorrhage
True pinpoint exposure
CONTRAINDICATIONS
Severe toothache at night
Spontaneous pain
Tooth mobility
Radiographic appearance of pulp periradicular de- generation
Excess of hemorrhage at the time of exposure Serous exudate from the exposure
Externalinternal root resorption
Swellingfistula
Histological Changes after Pulp Capping
These were illustrated be Glass and Zander in 1949
After 24 hours Necrotic zone adjacent to calcium
hydroxide paste is separated from healthy pulp
tissue by a deep staining basophilic layer
After 7 days Increase in cellular and fibroblastic
activity
After 14 days Partly calcified fibrous tissue lined by
odontoblastic cells is seen below the calcium
proteinate zone disappearance of necrotic zone
After 28 days Zone of new dentin
3
Medications and Materials Used for Pulp Capping Calcium hydroxide
Corticosteroids amp antibiotics
Inert materials
Collagen fibers
4-META adhesive
Direct bonding
Isobutyl cyanoacrylate
Denatured albumin
Mineral trioxide aggregate
Laser
Bone morphogenic protein
PULPOTOMY
Finn (1995) defined it as the complete removal of the coronal portion of the dental pulp
followed by placement of a suitable dressing or medicament that will promote healing and
preserve vitality of the tooth
American Academy of Pediatric Dentistry (1998) defined pulpotomy as the amputation of
affected infected coronal portion of the dental pulp preserving the vitality and function of the
remaining part of radicular pulp
Objectives
bull Removal of inflamed and infected coronal pulp at the site of exposure thus preserving the vitality of the
radicular pulp and allowing it to heal
bull Maintain the tooth in the dental arch
Rationale
bull Radicular pulp is healthy and capable of healing after surgical amputation of the infected coronal pulp
bull Preserves vitality of the radicular pulp
bull Maintains tooth in a physiologic condition
Indications of Pulpotomy bull Mechanical pulp exposure in primary teeth
bull Teeth showing a large carious lesion but free of radicular pulpitis
bull History of only spontaneous pain
bull Hemorrhage from exposure sites bright red and can be controlled
bull Absence of abscess or fistula
bull No interradicular bone loss
bull No interradicular radiolucency
Contraindications of Pulpotomy bull Persistent toothache
bull Tenderness on percussion
bull Root resorption more than 13rd of root length
bull Large carious lesion with nonrestorable crown
bull Highly viscous sluggish hemorrhage from canal orifice which is uncontrollable
bull Medical contradictions like heart disease immuno compromised patient
bull Swelling or fistula
bull External or internal resorption
bull Pathological mobility
bull Calcification of pulp
Classification of pulpotomy
4
Formocresol Pulpotomy
Iby BUCKLEY in 1904
Sweet (1930) Formulated multi visit technique
Doyle (1962) Advocated 2 sitting procedure (complete devitalization)
Spedding (1965) Gave 5 minute protocol (partial devitali- zation)
Venham (1967) Proposed 15 seconds procedure
Current concept uses 4 minutes of application time
Composition of formocresol Buckleyrsquos Formula
bull Cresol ndash 35 percent
bull Glycerol ndash 15 percent
bull Formaldehyde ndash 19 percent
bull Water ndash 31 percent
Mechanism of Action
It prevents tissue autolysis by bonding to the proteins Bonding is of peptide groups of side chain amino acids and is a reversible process accomplished without
changing the basic structure of protein molecules
Histological Changes
bull Demonstrated by Mass and Zilbermann11 in 1933 and also by Massler and Mansokhani in 1959
bull Immediately the pulp becomes fibrous and acidophillic
bull Seven to fourteen days Three zones appear
a broad eosinophilic zone of fixation
b broad pale-staining zone of atrophy with poorcellular definition
c broad zone of inflammation extending apically into normal pulp tissue
bull One yearndash Progressive apical movement of these zones with only acidophillic zone left at the end of 1 year
Modified Formocresol Pulpotomy
Used by TRASK(1972)
The technique is identical to that described for primary teeth except that the formocresol pellet is
sealed permanently in the tooth
Two-visit Devitalization Pulpotomy
Indications
bull There is evidence of sluggish bleeding at the amputation site that is difficult to control
bull Pus in the chamber but none at the amputation site
bull There is thickening of the PDL
bull History of pain
Contraindications
bull Nonrestorable tooth
bull Tooth with necrotic pulp
5
Glutaraldehyde Pulpotomy
It was first suggested by S Gravenmade Introduced by Kopel in 1979
Mechanism of Action
bull Glutaraldehyde produces rapid surface fixation of the underlying pulpal tissue
bull A narrow zone of eosinophilic stained and compressed fixed tissue is found directly beneath the area of application which blends into vital normal appearing tissue apically
bull With time the glutaraldehyde fixed zone is replaced by macrophagic action with dense collagenous tissue thus the entire root canal tissue is vital
Cvekrsquos Pulpotomy
bull This is also called as calcium hydroxide pulpotomy or young permanent partial pulpotomy
bull This was proposed by Mejare and Cvek16 in 1978
bull Indicated in young permanent teeth where the pulp is exposed by mechanical or bacterial means and the
remaining radicular tissue is judged vital by clinical and radiographic criteria whereas the root closure is
notcomplete
MINERAL TRIOXIDE AGGREGATE (MTA) Torabinejad described the physical and chemical properties of MTA in 1995
It is ash colored powder made primarily of fine hydrophilic particles of
1 tricalcium aluminate
2 tricalcium silicate
3 silicate oxide
4 tricalcium oxide
5 bismuth dioxide
Hydration of the powder results in a colloidal gel composed of calcium oxide crystals in an amorphous
structure This gel solidifies into a hard structure in less than three hours
PROPERTIES OF MTA
It is biocompatible material and its sealing ability is better than that of amalgam or ZOE
Initial pH is 102 and set pH is 125
The setting time of cement is 4 hours
The compressive strength is 70 MPA which is comparable with that of IRM
Low cytotoxicity ndash It presents with minimal inflammation if extended beyond the apex
Mineral trioxide aggregate (MTA) has demonstrated the ability to induce hard-tissue formation in
pulpal tissues and it promotes rapid cell growth
APEXOGENESIS
It is defined as the treatment of a vital pulp by capping or pulpotomy in order to permit continued
growth of the root and closure of the open apex
Rationale
Maintenance of integrity of the radicular pulp tissue to allow for continued root growth
Indications
bull Indicated for traumatized or pulpally involved vital permanent tooth when root apex is incompletely formed
bull No history of spontaneous pain
bull No sensitivity on percussion
bull No hemorrhage
bull Normal radiographic appearance
Contraindications
bull Evidence that radicular pulp has undergone degenerative changes
bull Purulent drainage
bull History of prolonged pain bull Necrotic debris in canal
bull Periapical radiolucency
6
1
Gupta A Dhingra R Chaudhari P Gupta A
Department of Paedodontics and Preventive Dentistry Faculty of Dental Sciences SGT University Gurgaon Haryana India
Journal of Indian Society of Pedodontics and Preventive Dentistry
Volume 35 I Issue 3 I July-September 2017
A COMPARISION OF VARIOUS MINIMALLY
INVASIVE TECHNIQUES FOR THE REMOVAL
OF DENTAL FLUOROSIS STAINS IN
CHILDREN
DR MITAKSHARA NIRWAN
CONTENTS
bull Introduction
bull Aims
bull Materials and Methods
bull Results
bull Discussion
bull Conclusion
bull Critical analysis
bull References
INTRODUCTION
bull Dental fluorosis is a developmental disturbance of dental enamel caused by
successive exposure to high concentrations of fluoride during tooth
development
bull Various methods of therapy are advocated for the treatment of fluorosis -
stained teeth which range from invasive ceramic veneer bonding restorations
to abrasive chemical treatments
bull The combination of dental bleaching techniques and microabrasion appears
as an excellent conservative solution to reestablish health in fluorosis
affected teeth
AIMS
bull The aim of the study was to evaluate and compare the effectiveness of
minimally invasive techniques for the removal of dental fluorosis
stains in children in vivo
MATERIALS AND METHODS
Patients visiting the department of Pedodontics and Preventive dentistry
Faculty of Dental Sciences SGT University Gurgaon
bull Sample size 90 patients
bull Age group 10 -17 years
bull Caries cracks or periodontal
disease on anterior teeth
bull Abscess draining sinus
cellulitis
bull Non vital teeth
hypersensitive exposed
crevices
bull Orthodontic appliance
bull Past history of bleaching
bull At least two permanent
maxillary anterior teeth
bull TSIF of score 4
bull Free of systemic diseases
Inclusion criteria Exclusion criteria
2
Groups
Group A In office bleaching with 35 hydrogen peroxide( Pola Office
Bleaching kit) activated by light emitting diode (LED) bleaching unit
(35 HP)
Group B Enamel microabrasion (EM) (PREMA Enamel Microabrasion
System) followed by in-office bleaching with 44 carbamide peroxide
gel (EM)
Group C In-office bleaching with 5 sodium hypochlorite (5
NaOCl)
A baseline colour evaluation was done by taking digital photograph of
the maxillary anterior teeth
RESULTS
Group 1
Colour stability
Group 2 Group 3
Tooth sensitivity
Tooth sensitivity values were taken before the treatment
which was compared to immediate postoperative and follow
up visits It was checked using an electric pulp tester
maximum
moderate
least
immediately
group 2
group 1
group 3
1 month
group 2
group 1
group 3
3 month
group 2
group 1
group 3
Patient satisfaction score
Satisfaction was assessed on visual analog scale
Range 1 to 5
Groups percentage of patients
who were satisfied with
the treatment
Number of patients
who reported slight
reappearance of colour
Group 1
90
7
Group 2
83
8
Group 3
73
7
3
Number of Appointments
Groups One sitting Two sittings Three
sittings
Group 1
25
4
1
group 2
26
3
1
Group 3
30
0
0
DISCUSSION
bull Hydrogen peroxide is capable of penetrating the tooth osmosis and through porosities and cracks subsequently acting directly on the pigmented molecules
bull Gurgan et al investigated 3 different light systems and found out that diode laser system with gave best tooth whitening and least tooth sensitivity
bull In the EM group the surface reflects and refracts light from the surface in such way that mild imperfections in underlying enamel are camouflaged While the highly polished surface of enamel enhances the aesthetic appearance
bull Train et al and Loguercio et al also had the similar results in their studies with EM mild fluorosis showed best results moderate showed moderate results while it had little effect on severe fluorosis
bull NaOCl was only effective on mild stains while moderate and severe
stains could only be lightened to quite an extent but could not be
completely removed
bull When NaOCl comes in contact with hypomineralized and discoloured
enamel it degrades and removes the chromogenic organic material
located on the enamel surface
CONCLUSION
bull It was concluded that esthetic appearance of teeth mild fluorosis can
be achieved by bleaching and microabrasion But in cases of
moderate fluorosis a combination of any of theses modalities can be
used
bull As no special maintenance precautions are required these maybe be
considered as an interesting alternative to conventional operative
treatment
bull Focuses on only TSIF of 4
bull Electric pulp testing is not the
right method to check for
sensitivity
bull Tooth Sensitivity changes
from person to person
bull Food habits can cause
staining of the teeth
bull Minimally invasive
bull Cheaper to veneers
bull Minimal loss of tooth structure
bull 4 parameters checked for the success of treatment
bull Inclusion of specific score of fluorosis for comparing the results
bull Maximum 3 appointments needed
CRITICAL ANALYSIS
Pros Cons
REFERENCES
bull Gurgan S Cakir FY Yazici E Different light-activated in officebleaching
systems Lasers Med Sci 201025817-22
bull Train TE McWhorter AG Seale NSWilson CF Guo IY Examination of
esthetic improvement and surface alteration following microabrasion in
fluorotic human incisors in vivoPediatr dent 199618353-62
bull Loguercio AD Correia LD Zago C Tagliari D Neumann E Gomes OM et al
Clinical effectiveness of two microabrasion materials materials for the
removal of enamel flurosis stains Oper Dent 200732531-8
4
3
Improve of Cognitive Skills
Amongst the positive impacts most parents have answered that the usage of these
devices has helped their child communicate and learn better and it has showed significant
results According to (Sundus M 2018)These devices improve the cognitive skills and
develop their learning skills fasterThe competition skills also get better It gives time for brain to think and process information better Another study which supports this (LF
Jonathan et al 2016)
Motor Physical Exercise
This study has shown that children like to use more than one type of device
sometimesUsing these devices improve fine motor skillshand eye coordination and
hands and fingers become more efficient (Srinahyanti et al 2019) (Sundus M 2018)
Speech Improvement
392 Parents say that maybe usage of the devices has helped improve speech in their
children but Various studies show otherwise as most of them shows that usage of handheld
devices causes delay of speech (Srinahyanti et al 2019)
Reduced parent child interaction
The negative impacts are more when compared to the positive ones Usage of gadgets
has resulted in reduced parent child interaction Less face to face interaction can
cause detachment from family members and value which in turn also causes isolation
of the child as he is more comfortable with the gadget (M Suhana-2017)
Sleep Disorders
This study shows that most parents have agreed that usage of these devices does
cause disruption of sleep Various studies have shown that children get fewer hours of
sleepdrowsiness during the day and dramatic increase in day time sleep because of
the screen usage (Acc to National Sleep Foundation) ( Cain N et al 2010)
In this study most number of parents have
agreed that their children might be dependent on
these devices and also had showed restless and
violent behavior if the gadget is snatched from
them
Most number of kids (667) are heavily
dependent as they like to use the device during
their meal time
Various other studies have assessed the screen
time dependency and have concluded that
various kids suffer from SDD
Conclusion The study conclusively shows that the impact of handheld devices is akin to the
importance of table salt in our meals most significant for our growth and
development in moderate amounts and hazardous in excess The negatives clearly
outweigh the positives with the latter too few and far in between This study also
points towards further extensive research on the subject because we need to find ways and also educate parents to optimise the role of these devices in their
childrenrsquos life taking advantage of their positive attributes and minimising their
negative ones
References 1Wahyuni AS Siahaan FB Arfa M Alona I Nerdy N The Relationship between the Duration of Playing
Gadget and Mental Emotional State of Elementary School Students Open Access Maced J Med Sci
20197(1)148ndash151
2Sundus M Department of Computer Science Lahore-The Impacts of using Gadgets on ChildrenJournal of Depression and Anxiety 2018vol 7(1)296
3Amawi SO Subki AH Khatib HA et al Use of Electronic Entertainment and Communication Devices Among
a Saudi Pediatric Population Cross-Sectional Study Interact J Med Res 20187(2)e13
4Julia ldquoHandheld Screen Time Linked with Speech Delays in Young Childrenrdquo Present Pediatric Acad Soc
Meet 2017
5C Rowan ldquoThe Impact of Technology on Child Sensory Motor Developmentrdquo 2003
6Impact of media use on children and youth Paediatr Child Health 20038(5)301ndash317
7Naik SV Children and their gadgets A pedodontist perspective Int J Oral Health Sci 2018857-8
8Roberts DF Foehr UG Rideout V Generation M Media in the lives of 8‐18 year‐olds A Kaiser Family
Foundation Study 2005
9Arya K Time spent on television viewing and its effect on changing values of school going children Anthropologist 20046269‐71
10 Lerner C Barr R Screen Sense Setting the Record StraightResearch‐Based Guidelines for Screen
Use for Children Under 3 Years Old Early learning project at Georgetown university 2014 p 1‐10
11SrinahyantiYasaratodo Wau Imelda Free Unita Manurung Nur Arjani-Influence of gadget A positive
and Negative Impact of Smartphone Usage for Early Child2019
4
THANK YOU
1
Morankar Rahul Aditi Kapur Krishan Gauba Ashima Goyal
MANAGEMENT OF ENDODONTIC INSTRUMENT SEPARATION IN
PRIMARY TEETH
CASE REPORT
Journal of South Asian Association of Pediatric Dentistry 2020
DR MITAKSHARA NIRWAN
bull Introduction
bull Aims amp Objectives
bull Case report
bull Discussion
bull Conclusion
bull Pros amp Cons
bull References
CONTENTS
Separation of endodontic instrument is an unexpected complication and its prevalence is not known It is a common belief among the dental professionals that rotary nickelndashtitanium (NiTi) instruments separate more frequently than stainless steel hand instruments
However literature revealed that in permanent teeth the reported prevalence of separated endodontics manual instruments is in the range of 07-74 whereas for rotary NiTI instruments it is
approximately 04-5
Fractured root canal instruments may include endodontic files Gates Glidden burs finger spreaders
and paste fillers
INTRODUCTION
The aim of this study is to describe the management strategies for endodontic
instrument separation in a root canal of primary teeth with emphasis on factors
requiring consideration in different clinical situations
AIMS amp OBJECTIVES
CASE 1
A 6-year-old male child reported with the chief complaint of spontaneous toothache in mandibular left second primary molar since few days It has aggravated following dental treatment at a private dental clinic Clinical examination revealed an underprepared access cavity with 75 and incomplete caries removal
which was sealed with glass ionomer cement
An intraoral periapical radiograph revealed a separated instrument of about 6ndash7 mm size in the distal root
2
The separated instrument was lodged firmly in distobuccal root canal 2ndash3 mm below the cementoenamel junction The instrument was bypassed successfully with no 15 and no 20 H-files but attempts for its retrieval were not successful
GatesndashGlidden (GG) drills no 2 (07 mm) and no 3 (09 mm) were used to drill around the instrument after which it was retrieved successfully using no 25 H-file
All the canals were instrumented till size 30 k-file followed by obturation with metapex and restoration with glass ionomer cement amp followed by placement of a crown and loop space maintainer for missing 74 The instrument retrieved was a manual reamer measuring 6 mm in length
The patient was asymptomatic since then and is under regular follow-up
CASE 2
A 5-year-old female child reported with the chief complaint of spontaneous toothache in mandibular left second
primary molar Clinical examination revealed deep occlusal caries with fractured lingual wall and pain on
percussion An intraoral periapical radiograph revealed caries involving pulp without any furcation or periapical
area of rarefaction and pulpectomy was planned
All the canals were enlarged using NiTi rotary files with a 4 taper operating at 500 rpm with minimum torque
setting An orifice opener [(0825 19 mm) of 8 taper size 25 length 19 mm] and nos 0420 file was used for
instrumentation of root canal This was followed by file nos 0425 which got separated in the distobuccal root
canal The radiograph confirmed a separated instrument of length 3ndash4 mm in the middle third of the root canal
The instrument was bypassed with no 15 k-file but could not get retrieved As instrument separation had occurred with 0425 file the involved root canal was sufficiently debrided before separation and the level of instrument separation was at the mid-root region so it was decided to obturate and seal this tooth with
periodic follow-ups instead of immediate extraction All other canals were enlarged till size 0430 in the sequential manner followed by obturation using metapex and placement of stainless steel crown
3
CASE 3
A 5-year-old female child has complaint of mild intermittent pain with primary mandibular left first molar She
had undergone pulpectomy treatment for the same during which an instrument separation has occurred in
the mesiobuccal root canal by a resident doctor
A radiograph revealed a separated instrument of about 4 mm in size lodged in the apical third but within the
confines of the mesial root An attempt was made for its retrieval but was unsuccessful The extraction of the
involved tooth was carried out under local anesthesia followed by a band and loop space maintainer
CASE 4
A 7-year-old male child reported with a chief complaint of mild intermittent pain on food lodgment with the primary mandibular right first and second molars The patient had a history of dental treatment at a private
dental clinic few months back which he did not continue further
Clinical examination revealed glass ionomer restoration with 85 and proximal caries with 84 leading to food lodgment An intraoral periapical radiograph with 85 revealed empty root canals with a separated
instrument of about 3ndash4 mm size beyond the apex of mesial root close to the developing succedaneous premolar
4
DISCUSSION
Stainless steel files usually separate fracture due to the excessive amounts of torque and overuse or the
preexisting distortion of the instrument whereas in NiTi rotary files it is a combined result of torsional stress and cyclic fatigue
Therapeutic options for the management of separated endodontic instruments include no intervention nonsurgical (orthograde conservative) management surgical management and tooth extraction
Use of ultrasonic scaler Masserann technique Endo extractor and Cavi-Endo ultrasonic instruments are some of the methods popular for retrieval of a separated endodontic instrument in the permanent tooth
In case 1 a 6-mm-long manual reamer was retrieved successfully with the use of GG drill using a manual file and copious irrigation which is the most desired treatment outcome
In case 2 the retrieval of separated rotary file lodged in the middle third of the root canal was unsuccessful in spite of multiple attempts It was therefore managed with routine obturation followed by restoration to maintain the tooth in its physiological functional state It was kept under close periodic follow-up at least
every 3 months This treatment option should be encouraged where it is possible to follow up the patient clinically and radiographically at close periodic intervals as there is the possibility of instrument escaping
into bone due to physiological root resorption
In cases 3 and 4 an instrument has separated in the apical root portion
In case 3 it was within the root canal and thus an attempt was made for its retrieval which was
unsuccessful It was therefore extracted to prevent the fractured instrument from getting exposed in the bone following resorption as there is no accurate and consistent established age for initiation of resorption in primary teeth known per se
In case 4 an immediate extraction of involved tooth was carried out as the separated instrument was beyond the apex of the primary tooth root
Age of the child clinical signs and symptoms and amount of root resorption are the factors which can also influence the management of separated instrument in primary teeth
Moreover if an instrument has separated after initial cleaning and shaping of root canal maintaining a tooth is not a problem as clinical signs and symptoms are not anticipated and the good prognosis is expected
However if an instrument has separated early during the initial cleaning and shaping of the root canal clinical symptoms may compromise the prognosis
Therefore these factors should be kept in mind while planning a suitable management strategy to avoid or at least reduce the burden of extraction and wear of space maintainer for longer period
5
CONCLUSION
The management and prognosis of a primary tooth with a separated instrument is
dependent on the level of instrument fracture within the root age of the child root
resorption and clinical signs and symptoms of the involved tooth
Different management approaches can be tried depending on clinical situations keeping
in mind benefits vs risks in preserving the tooth
PROS amp CONS
PROS
The entire procedure is given
by step by step
Well descriptive xrays and
photographs
CONS
Medical history has not been
given
REFERENCES
1 TOMER ANIL K ET AL ldquoBROKEN FILE RETRIEVAL PUZZLE IN ENDODONTICSrdquo
(2016)
2 SHENOY A MANDAVA P BOLLA N ET AL A NOVEL TECHNIQUE FOR REMOVAL OF
BROKEN INSTRUMENT FROM ROOT CANAL IN MANDIBULAR SECOND MOLAR
INDIAN J DENT RES 201425(1)107ndash110
3 PATEL J MORAWALA A TALATHI R ET AL RETRIEVAL OF A BROKEN INSTRUMENT
FROM ROOT CANAL IN PRIMARY ANTERIOR TEETH UNIV RES J DENT 20155(3)203ndash
206
4 MORANKAR R GOYAL A GAUBA K ET AL MANUAL VERSUS ROTARY
INSTRUMENTATION FOR PRIMARY MOLAR PULPECTOMIES - A 24 MONTHS
RANDOMIZED CLINICAL TRIAL PEDIAT DENT J 201828(2)96ndash102
5 KASHYAP NILOTPOL (2018) RETAINING PRIMARY MOLARS WITH INSTRUMENT
SEPERATION A CASE REPORT AND CLINICAL GUIDE
6
1
IMPACT OF 6 CITRIC ACID AND ENDOACTIVATOR AS IRRIGATION ADJUNCTS ON OBTURATION QUALITY AND PULPECTOMY OUTCOME IN
PRIMARY TEETH
NEETU JAIN SHALINI GARG ABHISHEK DHINDSA SAKSHI JOSHI HARJOY
KHATRIA
PEDIATRIC DENTAL JOURNAL 2019 29
1
DR MITAKSHARA NIRWAN
CONTENTS
bull INTRODUCTION
bull AIMS amp OBJECTIVES
bull CASE REPORT
bull RESULTS
bull DISCUSSION
bull CONCLUSION
bull PROS AND CONS
bull REFERENCES
2
INTRODUCTION
bull ENDODONTIC THERAPY IN PRIMARY TEETH INVOLVES DISINFECTION OF THE ROOT CANAL
SYSTEM AND ITS OBTURATION WITH RESORBABLE PASTE
bull THE CONTENTS OF ROOT CANAL ALONG WITH SMEAR LAYER ARE EXPECTED TO BE REMOVED
DURING THE BIOMECHANICAL PREPARATION
bull IN VITRO AND CLINICAL DOCUMENTS HAVE INDICATED THAT MECHANICAL PREPARATION OF
THE CANAL LEAVES LARGE PORTIONS OF THE CANAL WALLS UNDEBRIDED AND COMPLETE
REMOVAL OF THE BACTERIA BY THIS MECHANICAL PROCEDURE ALONE IS UNLIKELY TO BE SEEN
THEREFORE SOME FORM OF DISINFECTIONIRRIGATION IS MANDATORY TO KILL THE
MICROORGANISMS AND TO REMOVE THE RESIDUAL TISSUES
3
bull THE IDEAL REQUISITES OF A ROOT CANAL IRRIGANT AS GIVEN BY ZEHNDER ARE
1 BROAD ANTIMICROBIAL SPECTRUM
2 HIGH EFFICACY AGAINST ANAEROBIC AND FACULTATIVE MICROORGANISMS ORGANIZED
IN BIOFILMS
3 ABILITY TO DISSOLVE NECROTIC PULP TISSUE REMNANTS
4 ABILITY TO INACTIVATE ENDOTOXIN
5 ABILITY TO PREVENT THE FORMATION OF A SMEAR LAYER DURING INSTRUMENTATION OR
TO DISSOLVE THE LATTER ONCE IT HAS FORMED
6 SYSTEMICALLY NONTOXIC WHEN THEY COME IN CONTACT WITH VITAL TISSUES
NONCAUSTIC TO PERIODONTAL TISSUES AND WITH LITTLE POTENTIAL TO CAUSE AN
ANAPHYLACTIC REACTION
SINCE NO SINGLE IRRIGANT HAS THESE OPTIMAL PROPERTIES STUDIES HAVE REPORTED THE USE
OF TWO OR MORE SOLUTIONS IN A SPECIFIC SEQUENCE OR IN COMBINATIONS FOR BETTER
RESULTS 4
bull SEVERAL IRRIGATING SOLUTIONS ALONG WITH CHELATING AGENTS HAVE BEEN USED
DURING BIOMECHANICAL PREPARATION OF ROOT CANAL BOTH IN PRIMARY AND
PERMANENT TEETH
bull HOWEVER NONE OF THE AVAILABLE IRRIGATING SOLUTIONS HAS BEEN REGARDED CLEARLY
AS OPTIMAL SOLUTION BECAUSE OF THEIR LIMITED EFFECTIVENESS ESPECIALLY IN APICAL
13RD OF THE ROOT CANAL SYSTEM
bull TO OVERCOME SUCH LIMITATIONS USE OF ENDOACTIVATOR HAS BEEN PROPOSED AS AN
IRRIGATION FACILITATOR THAT IS BASED ON SONIC VIBRATION (UP TO 10000 CPM) WHICH
FACILITATES THE IRRIGANT PENETRATION AND ITS RENEWAL WITHIN THE CANAL
bull ACTIVATION SYSTEMS RESULTED IN BETTER REMOVAL OF THE SMEAR LAYER IN THE APICAL
THIRD OF ROOT CANALS IN COMPARISON TO CONVENTIONAL IRRIGATION
5
CITRIC ACID
bull CITRIC ACID IS A WEAK ORGANIC ACID WITH THE APPEARANCE OF WHITE CRYSTALLINE
POWDER AT ROOM TEMPERATURE
bull IT CAN EXIST EITHER IN WATER-FREE FORM (ANHYDROUS) OR MONOHYDRATE FORM THE
WATER-FREE FORM CRYSTALLIZES FROM THE HOT WATER WHEREAS THE MONOHYDRATE
FORMS FROM THE COLD WATER THE LATTER MAY BE CONVERTED TO ANHYDROUS FORM BY
HEATING MORE THAN 78degC
bull CITRIC ACID OCCURS NATURALLY IN THE BODY IN MITOCHONDRIA AND IS USED BY BLOOD
BANKS TO PREVENT COAGULATION OF TRANSFUSED BLOOD CITRIC ACID IS ALSO ESSENTIAL
TO HUMAN METABOLISM AND IS FOUND IN MANY FOODS
6
2
bull THE BIOLOGICAL EFFECTS OF CITRIC ACID ON THE PERIODONTAL STRUCTURE HAS BEEN
EXTENSIVELY STUDIED IN PERIODONTICS
bull NEUMAN AND NEWMAN SHOWED THAT CITRIC ACID IS THE MOST EFFECTIVE ACID IN
ALTERING THE SOLUBILITY OF HYDROXYAPATITE
bull YAMAGUCHI ET AL SHOWED THAT CITRIC ACID SOLUTION HAD ANTIBACTERIAL EFFECTS ON
ALL 12 ROOT CANAL BACTERIA TESTED
bull ARIAS-MOLIZ ET AL SHOWED THAT ETHYLENEDIAMINETETRAACETIC ACID (EDTA) HAS NO
BACTERICIDAL ACTIVITY EVEN AFTER 1 HOUR CONTACT
bull THIS ACID HAS THE ABILITY OF ROOT CANAL IRRIGATION AND ALSO SMEAR LAYER REMOVAL
DIFFERENT CONCENTRATIONS (1ndash50) HAVE BEEN PROPOSED GUTMANN ET AL CONCLUDED
THAT 10 CITRIC ACID IS BETTER THAN ULTRASOUND FOR SMEAR LAYER REMOVAL FROM THE
ROOT END CAVITIES
7
bull STUDIES HAVE SHOWN IRRIGATION WITH 6 CA FOR 15 OR 30 SECONDS IS QUITE
EFFECTIVE IN REMOVING ALL THE COMPONENTS OF THE SMEAR LAYER OF THE PRIMARY
TEETH WHEREAS PERITUBULAR DENTIN DESTRUCTION WAS OBSERVED WHEN HIGHER
CONCENTRATION OF CITRIC ACID WAS USED AS AN IRRIGATING SOLUTION
8
AIMS amp OBJECTIVES
bull THIS STUDY WAS AIMED TO EVALUATE THE CLINICAL AND RADIOGRAPHIC OUTCOME OF
PULPECTOMY ALONG WITH QUALITY OF OBTURATION USING 6 CITRIC ACID AND
ENDOACTIVATOR
9
CASE REPORT
bull 350 CHILDREN (3-9 YEARS) WITH CLINICAL SIGNS AND SYMPTOMS OF CHRONIC IRREVERSIBLE
PULPITIS IN DEEPLY CARIOUS TEETH WERE SCREENED DURING SCHOOL DENTAL HEALTH
PROGRAM FROM MAY 2014-JULY 2014
bull 123 CHILDREN REPORTED TO THE DEPARTMENT AND 67 CHILDREN WERE SELECTED BASED ON
INCLUSION AND EXCLUSION CRITERIA
RECRUITMENT OF PATIENTS
10
INCLUSION CRITERIA
bull HISTORY OF SPONTANEOUS PAIN AND UNCONTROLLED BLEEDING AFTER PULP AMPUTATION
EXCLUSION CRITERIA
bull EVIDENCE OF INTERNAL OR EXTERNAL (PHYSIOLOGICPATHOLOGIC) ROOT RESORPTION OF MORE THAN A THIRD OF ITS LENGTH
bull ROOT CANAL OBLITERATION OR ANATOMIC ANOMALIES
bull INADEQUATE BONE SUPPORT OR NON RESTORABLE TOOTH
bull ONCE PATIENTS ELIGIBILITY WAS CONFIRMED THE TREATMENT PROCEDURE WAS
EXPLAINED TO THE PARENTGUARDIAN AND INFORMED WRITTEN CONSENT WAS
OBTAINED FROM PARENTSGUARDIANS SHOWING WILLINGNESS FOR THEIR
CHILDRENS TREATMENT 11
PROCEDURE
bull PULPECTOMY WAS PERFORMED BY ONE OPERATOR OF PEDIATRIC DENTISTRY DEPARTMENT
USING A STANDARDIZED TREATMENT PROTOCOL FOR ALL THE PATIENTS
bull AFTER ADMINISTRATION OF LOCAL ANESTHESIA RUBBER DAM WAS APPLIED FOR ISOLATION
bull ACCESS CAVITY WAS PREPARED USING AIR-ROTOR HAND PIECE WITH 8 ROUND BUR AND
PULP TISSUE WAS EXTIRPATED WITH THE HELP OF SPOON EXCAVATOR
bull FURTHER THE NEGOTIATION OF THE CANALS WAS DONE WITH 10 K-FILE
bull A DIAGNOSTIC RADIOGRAPH WAS TAKEN FOR ROOT LENGTH DETERMINATION AND
WORKING LENGTH WAS KEPT 1 MM SHORT OF THE RADIOGRAPHICAL APEX
bull ALL ROOT CANALS WERE INSTRUMENTED MANUALLY USING K-FILES AND WERE IRRIGATED
WITH 10 ML 09 NORMAL SALINE AND 1 SODIUM HYPOCHLORITE AS STANDARDIZING
PROTOCOL FOR ROOT CANAL PREPARATION AND DISINFECTION
12
3
GROUP 1 (CA + E) - IRRIGATION WAS DONE
WITH 10 ML OF 6 CITRIC ACID (CITOCID AMMDENT)
AND IRRIGANTS WERE SONICALLY AGITATED WITH
ENDOACTIVATOR (DENTSPLY) FOR 30 S PER CANAL USING REDBLUE
ENDOACTIVATOR TIP
GROUP 2 (CA) - 10 ML OF 6 CITRIC ACID FOR 1 MIN USING
27 GAUZE IRRIGATING NEEDLE
GROUP 3(SH + E) - 10 ML OF 1 SODIUM HYPOCHLORITE
SOLUTION AND SONIC ACTIVATION WITH ENDOACTIVATOR
GROUP 4(SH) - 10 ML OF 1 SODIUM HYPOCHLORITE
SOLUTION USING IRRIGATING NEEDLE (CONTROL GROUP)
bull TEETH UNDERGOING PULPECTOMY WERE RANDOMLY ENROLLED BY CHIT METHOD INTO THREE
STUDY AND ONE CONTROL GROUP
13
bull IN CITRIC ACID GROUPS FINAL RINSE WITH NORMAL SALINE WAS DONE TO REMOVE THE
REMAINING CRYSTALS (CHELATES)
bull FOLLOWING BIOMECHANICAL PREPARATION THE ROOT CANALS WERE DRIED WITH STERILE
ABSORBENT PAPER POINTS AND OBTURATED WITH VITAPEX USING HAND HELD
LENTULOSPIRAL FINAL RESTORATIONS WERE DONE USING COMPOSITE RESIN
14
bull CLINICAL FOLLOW UP WAS DONE AT 24 H1 WEEK 1 MONTH 6 MONTH AND 12
MONTH TO CHECK PAIN PRESENCE AND PAIN FREQUENCY (ONCEMORE THAN ONCE)
SWELLING FISTULA SENSITIVITY TO PERCUSSION
bull RADIOGRAPHIC FOLLOW UP WAS DONE AT 6 MONTH AND 12 MONTH FOR ANY
DEVIATED ERUPTION OF SUCCEDANEOUS TEETH EXCESS FILING MATERIAL AND ITS
RESORPTION EXTERNALINTERNAL ROOT RESORBTION CALCIFIC METAMORPHOSIS
PRESENCE OF FURCATION RADIOLUCENCY
CLINICAL amp RADIOGRAPHIC FOLLOW UP
15
RADIOGRAPHIC ASSESSMENT OF OBTURATION QUALITY
bull POSTOPERATIVE RADIOGRAPHS WERE VISUALLY ASSESSED FOR QUALITY OF OBTURATION BY
TWO INDEPENDENT EXAMINERS (SG AD) WHO WERE BLINDED WITH REGARD TO
IRRIGATION PROTOCOL GROUP TO ENHANCE CALIBRATION EACH EXAMINER ASSESSED THE
RADIOGRAPH INDEPENDENTLY AND LATER REVIEWED TOGETHER FOR FINAL ASSESSMENT
INDIVIDUAL ROOT WAS TAKEN AS UNIT OF ANALYSIS FOR GRADE OF OBTU- RATION AND
SCORING CRITERIA WERE AS GIVEN BY COLL JA 1996
1 UNDER FILLED - FILLING MATERIAL ENDED 1 MM OR MORE SHORT OF THE APEX
2 OPTIMAL FILLING- FILLING MATERIAL APPEARED TO END AT THE RADIOGRAPHICAL APEX
3 OVERFILLED - FILLING MATERIAL EXTRUDED PAST THE RADIOGRAPHIC APEX
4 OPTIMALLY FILLED ROOTS WERE FURTHER ASSESSED FOR THE PRESENCE OF VOIDS AND VOID
AREA (ROOT CANAL SURFACE UNTOUCHED BY THE ROOT CANAL FILLING MATERIAL) IN THREE
VISUALLY DIVIDED SECTIONS OF THE ROOT IE CORONAL MIDDLE AND APICAL 13RD
16
RESULTS
bull OVERALL CLINICAL AND RADIOGRAPHIC SUCCESS RATE OVER A PERIOD OF ONE YEAR WAS
9886 amp 977 RESPECTIVELY
bull ALL GROUPS WERE SIGNIFICANTLY (P = 001) EFFECTIVE IN ALLEVIATING PAIN WITHIN 24 H
OF PULPECTOMY
17 18
4
19
bull IMMEDIATE POST OPERATIVE RADIOGRAPHIC ASSESSMENT REVEALED 68 (102150) ROOTS
WITH OPTIMAL OBTURATION AND 32 (48150) WITH OVERFILLINGUNDERFILLING MAXIMUM
NO OF OPTIMAL FILLINGS WERE OBSERVED IN GROUP1 (CA + E) (3333) FOLLOWED BY
GROUP 2 (CA) (2549) GROUP 3(SH + E) (2549) AND GROUP 4(SH) (1568)
bull CITRIC ACID GROUPS HAD MORE NUMBER OF OPTIMALLY FILLED ROOTS 588 (60102) THAN
NON CITRIC ACID GROUPS 412 (42102)
bull ENDOACTIVATOR CONTRIBUTED TO 18 OF OPTIMAL OBTURATION IRRESPECTIVE OF
CHELATING AGENT USED
20
21
bull MAXIMUM NO OF VOIDS AND VOID AREAS WERE IN NON CITRIC ACID GROUPS
(6419 amp 5384) COMPARED TO CITRIC ACID GROUPS (3580 amp 4615)
RESPECTIVELY
bull ANALYSIS OF ROOT 13RD REVEALED MAXIMUM NO OF VOID AREA IN APICAL
13RD (4755) FOLLOWED BY MIDDLE 13RD (3846) AND CORONAL 13RD
(1398)
bull LEAST NO OF VOIDS amp VOID AREA (1111 amp 1608) WERE OBSERVED WHEN
ENDOACTIVATOR ALONG WITH CHELATING AGENT WAS USED (GROUP 1)
HOWEVER THIS WAS STATISTICALLY INSIGNIFICANT
22
DISCUSSION
bull IN THE PRESENT STUDY 1 SODIUM HYPOCHLORITE WAS USED ALONG WITH 6 CITRIC ACID
(CHELATING AGENT) WHICH IS REPORTED TO BE AS EFFECTIVE AS 17 EDTA
bull CITRIC ACID (BIOLOGICAL ACID) IS FOUND TO BE BIOCOMPATIBLE AND LEAST IRRITATING TO
PERIAPICAL TISSUES THAN OTHER CHELATING AGENTS
bull USE OF SODIUM HYPOCHLORITE SOLUTION FOLLOWING CHELATING AGENT WAS AVOIDED AS IT
RAPIDLY PRODUCES SEVERE EROSION OF ROOT CANAL WALL DENTIN
bull TRADITIONAL APPROACH OF DELIVERING IRRIGANTS INTO THE ROOT CANAL SPACE USING
SYRINGES AND METAL NEEDLES HAS BEEN FOUND TO BE INEFFECTIVE ESPECIALLY IN THE AREAS OF
ANASTOMOSES BETWEEN CANALS AND APICAL 13RD OF ROOT CANAL
23
bull THEREFORE TO ACHIEVE BETTER CLEANING EFFICIENCY IRRIGANT ACTIVATION HAS BEEN
RECOMMENDED SONIC ACTIVATION HAS BEEN REPORTED TO RESULT IN BETTER ROOT CANAL
CLEANLINESS AS COMPARED TO NO ACTIVATION OF IRRIGANT
24
5
CONCLUSION
bull USE OF 6 CITRIC ACID DEFINITELY HELPED IN RAPID ELIMINATION OF PAIN RESOLUTION OF
PERI-RADICULAR RADIOLUCENCY BETTER OBTURATION QUALITY IN TERMS OF LESS VOIDS AND
VOID AREAS ALONG WITH MAXIMUM NO OF OPTIMAL OBTURATION UP TO APICAL AREA
bull 6 CITRIC ACID AND ENDOACTIVATOR IRRIGATION PROTOCOL PROVED TO BE THE BETTER
IRRIGATION PROTOCOL WHICH MAY CONTRIBUTE TO LONG TERM SUCCESS OF PRIMARY
TOOTH AND THE HEALTH OF UNDERLYING PERMANENT TOOTH
bull 6 CITRIC ACID ALONG WITH ENDOACTIVATOR MAY BE RECOMMENDED AS IRRIGATION
ADJUNCTS IN PULPECTOMY PROCEDURE OF PRIMARY TEETH
25
PROS AND CONS
PROS
bull PROPER EXPLANATION OF THE MATERIALS
USED
CONS
bull NO PREOPERATIVE AND POSTOPERATIVE
RADIOGRAPHS
26
REFERENCES
bull RAMACHANDRA JA NIHAL NK NAGARATHNA C VORA MS ROOT CANAL IRRIGANTS IN
PRIMARY TEETH WORLD J DENT 20156(3)229-234
bull MOHAMMADI Z JAFARZADEH H SHALAVI S KINOSHITA JI UNUSUAL ROOT CANAL
IRRIGATION SOLUTIONS J CONTEMP DENT PRACT 201718(5)415-420
bull ZEHNDER M ROOT CANAL IRRIGANTS J ENDOD 2006 32389- 98
bull SMITH JJ amp WAYMAN BE AN EVALUATION OF THE ANTIMICROBIAL EFFECTIVENESS OF
CITRIC ACID AS A ROOT CANAL IRRIGANT JOURNAL OF ENDODONTICS 1986 12(2) 54-58
bull TANNURE PN AZEVEDO CP BARCELOS R GLEISER R PRIMO LG LONG-TERM OUTCOMES OF
PRIMARY TOOTH PULPECTOMY WITH AND WITHOUT SMEAR LAYER REMOVAL A RANDOMIZED
SPLIT-MOUTH CLINICAL TRIAL PEDIATR DENT 201133316E20 27
bull CARON G NHAM K BRONNEC F MACHTOU P EFFECTIVENESS OF DIFFERENT FINAL IRRIGANT
ACTIVATION PROTOCOLS ON SMEAR LAYER REMOVAL IN CURVED CANALS J ENDOD
2010361361E6
bull COLL JA SADRIAN R PREDICTING PULPECTOMY SUCCESS AND ITS RELATIONSHIP TO
EXFOLIATION AND SUCCEDANEOUS DENTITION PEDIATR DENT 19961857E63
28
1
LOCAL
ANESTHESIA
DR MITAKSHARA NIRWAN
CONTENTS
Definition
Methods of inducing local anesthesia
Desirable properties
Electrophysiology of nerve conduction
Impulse propagation and spread
Mode and site of action of local anesthesia
Classification of local anesthetic according to biological site and mode of action
Dissociation of local anaesthetics
Mechanism of action of local anaethetics
Local anaesthetic agent
2
3
DEFINITION
Local anesthesia is defined as a loss of sensation in
a circumscribed area of the body caused by depression
of excitation in nerve endings or an inhibition of the
conduction process in peripheral nerves
An important feature of local anesthesia is that it produces
LOSS OF SENSATION WITHOUT INDUCING LOSS OF
CONSCIOUSNESS
4
METHODS OF INDUCING LOCAL
ANESTHESIA
Low temperature
Mechanical trauma
Anoxia
Neurolytic agents such as alcohol amp phenol
Chemical agents such as local anesthetics
PROPERTIES OF LOCAL
ANESTHESIA
It should not be irritating to tissue to which it is applied
It should not cause any permanent alteration of nerve structure
Its systemic toxicity should be low
Time of onset of anesthesia should be short
It should be effective regardless of whether it is injected into the tissue or applied locally to mucous membranes
The duration of action should be long enough to permit the completion of procedure
5 6
It should have the potency sufficient to give complete
anesthesia with out the use of harmful concentration solutions
It should be free from producing allergic reactions
It should be free in solution and relatively undergo
biotransformation in the body
It should be either sterile or be capable of being sterilized by
heat with out deterioration
2
ELETROPHYSIOLOGY OF
NERVE CONDUCTION
There is an electrical charge across the membrane
This is the membrane potential
The resting potential (when the cell is not firing) is a negative
electrical potential of -70mv that exists across the nerve
membrane produced by different concentrations of either side of
the membrane
The interior of nerve is NEGATIVE in relation to exterior
7 8
inside
outside
Resting potential of neuron = -70mV
+
-
+
-
+
-
+
-
+
-
SLOW DEPOLARIRIZATION
9
RAPID DEPOLARIZATION
The interior of nerve is POSITIVE in relation to exterior
REPOLARIZATION
10
bull Repolarization takes 07 msec
bull Depolarization takes 03 msec
SODIUM PUMP -
energy comes from the oxidative metabolism of ATP
bull The entire process require 1 msec
IMPULSE PROPOGATION
IMPULSE SPREAD
The propagated impulse travels along the nerve
membrane towards CNS The spread of impulse differs
in myelinated and unmyelinated nerve fibers
DEPOLARIZED SEGMENT ADJACENT RESTING AREA
MODE AND SITE OF ACTION OF LOCAL
ANESTHETICS
Local anesthetic agent interferes with excitation
process in a nerve membrane in one of the
following ways
Altering the basic resting potential of nerve
membrane
Altering the threshold potential
Decreasing the rate of depolarization
Prolonging the rate of repolarization
12
3
CLASSIFICATION OF LOCAL ANESTHETIC
SUBSTANCES ACCORDING TO
BIOLOGICAL SITE AND MODE OF ACTION
CLASS A
Agents acting at receptor site on external surface of nerve membrane
Chemical substance Biotoxins (eg tetrodotoxin and saxitoxin)
CLASS B
Agents acting on receptor sites on internal surface of nerve membrane
Chemical substance Quaternary ammonium analogues of lidocaine
scorpion venom 13
CLASS C Agents acting by receptor independent of
physiochemical mechanism
Chemical substance Benzocaine
CLASS D Agents acting by combination of receptors and
receptor independent mechanisms
Chemical substance most clinically useful anesthetic agents
(eg lidocaine mepivacaine prilocaine)
14
BASED ON THE SOURCE
NATUAL
SYNTHETIC
OTHERS
BASED ON MODE OF APPLICATION
bull INJECTABLE
bull TOPICAL
BASED ON DURATION OF ACTION
bull ULTRA SHORT
bull SHORT
bull MEDIEM
bull LONG
BASED ON ONSET OF ACTION SHORT
INTERMEDIATE
LONG
15
DISSOCIATION OF LOCAL
ANESTHETICS
Local anesthetics are available as salts (usually
hydrochlorides) for clinical use
The salts both water soluble and stable is dissolved in
either sterile water or saline
In this solution it exists simultaneously as unchanged
molecule (RN) also called base and positively charged
molecules (RNH+) called cations
RNH+ ==== RN+ H
+
16
The relative concentration of each ionic form in the solution varies
in the pH of the solution or surrounding tissue
In the presence of high concentration of hydrogen ion (low pH) the
equilibrium shifts to left and most of the anesthetic solution exists
in cationic form
RNH+ gt RN
+ + H
+
As hydrogen ion concentration decreases (higher pH) the
equilibrium shifts towards the free base form
RNH+ lt RN + H
+
17
The relative proportion of ionic form also depends on pKa or DISSOCIATION CONSTANT of the specific local anesthetic
The pKa is a measure of molecules affinity for H+
ions
When the pH of the solution has the same value as pKa of the local anesthetic exactly half the drug will exists in the RNH
+ form and
exactly half in RN form
The percentage of drug existing in either form can be determined by Henderson Hasselbalch equation
Log baseacid = pH - pKa
18
4
MECHANISM OF ACTION OF LOCAL
ANESTHETICS
The following sequence is proposed mechanism of action of LA
Displacement of calcium ions from the sodium channel receptor site
Binding of local anesthetic molecule to this receptor site
Blockade of sodium channel
19
Decrease in sodium conductance
Depression of rate of electrical depolarization
Failure to achieve the threshold potential level
Lack of development of propagated action potential
Conduction blockadehellip
20
21
Na + Na +
22
LOCAL ANESTHETIC AGENT
COMERCIALLY PREPARED LOCAL ANESTHESIA
CONSISTS OF
Local anesthetic agent (xylocaine lignocaine 2)
Vasoconstrictor (adrenaline 1 80000)
Reducing agent (sodium metabisulphite)
Preservative (methylparabencapryl
hydrocuprienotoxin)
Fungicide (thymol)
Vehicle (distillde waterNaCl)
LOCAL ANESTHETIC AGENT
The local anesthetics used in dentistry are divided
into two groups
ESTER GROUP
AMIDE GROUP
23 24
ESTER GROUP It is composed of the following
An aromatic lipophilic group
An intermediate chain containing
an ester linkage
A hydrophilic secondary or tertiary
amino group
AMIDE GROUP It is composed of the following
An aromatic lipophilic group
An intermediate chain containing
amide linkage
A hydrophilic secondary or tertiary
amino group
5
25
CLASSIFICATION OF LOCAL ANESTHETICS
ESTERS
Esters of benzoic acid
Butacaine
Cocaine
Benzocaine
Hexylcaine
Piperocaine
Tetracaine
Esters of Para-amino
benzoic acid
Chloroprocain
Procaine
Propoxycaine
26
AMIDES Articaine
Bupivacaine
Dibucaine
Etidocaine
Lidocaine
Mepivacaine
Prilocaine
Ropivacaine
QUINOLINE
Centbucridine
PHARMACOKINETICS OF LOCAL
ANESTHETICS UPTAKE
When injected into soft tissue most local anesthetics produce
dilation of vascular bed
Cocaine is the only local anesthetic that produces
vasoconstriction initially it produces vasodilation which is
followed by prolonged vasoconstriction
Vasodilation is due to increase in the rate of absorption of the
local anesthetic into the blood thus decreasing the duration of
pain control while increasing the anesthetic blood level and
potential for over dose 27
AMIDE LOCAL ANESTHETICS
The metabolism of amide local anesthetics is more
complicated then esters The primary site of
biotransformation of amide drugs is liver
Entire metabolic process occurs in the liver for lidocaine
articaine etidocaine and bupivacaine
Prilocaine undergoes more rapid biotransformation then the
other amides
28
REFERENCES
Handbook of local anesthesia ndash Stanley F Malamed ndash 6th
edition
Essentials of Local Anesthetic Pharmacology Daniel E
Becker Anesth Prog 2006 Fall 53(3) 98ndash109
WIKIPEDIEA
29
THANK YOU
30
1
Pharmacological Methods of Behavior
Management
DR MITAKSHARA NIRWAN
DEFINITIONS
bull Conscious Sedation ndash A minimally depressed level of consciousness that retains
the patients ability to independently and continuously maintain an airway and respond appropriately to physical stimulation or verbal command
(American Dental Association House Of Delegates 2000)
bull Deep Sedation ndash An induced state of depressed consciousness
accompanied by partial loss of protective reflexes including the inability to continuously maintain an airway independently and or to respond purposefully to physical stimulation or verbal command
bull General Anesthesia (G A) ndash An induced state of unconsciousness or complete loss of
protective reflexes including the inability to continually maintain an airway independently and respond purposefully to physical stimulation or verbal command
Conscious sedation
ADVANTAGES
Conscious
Protective reflexes active amp intact
Stable vital signs
Operating dentist may perform sedation
Minimum amount of equipment required
Prolong detainment in recovery room not required
Risk of complication very low
Excellent choice for poor ndash risk pt in dental office
Cost effective
General anesthesia
ADVANTAGES Not absolutely
essential May be the only
method Not necessary (no
pain reaction) Amnesia always
present
Conscious sedation
DISADVANTAGES
Pt cooperation is essential
Extremely difficult or mentally handicapped pt cannot always be managed
Use of local anesthesia is a must
Amnesia may or may not be present
General anesthesia DISADVANTAGES
Pt unconscious
Protective reflexes are depressed
Depressed
Advanced training required Dentist must not act also as anesthetist
Special equipment necessary
Detainment in recovery area necessary
High IOP amp postoperative complications
Not indicated in dental office
More expensive
Fundamental Concepts
bull Techniques that utilize drugs to induce co-operative yet conscious state in an otherwise uncooperative child ndash CONSCIOUS SEDATION
2
GOALS
1 To facilitate the provision of quality care
2 To minimize the extremes of disruptive behavior
3 To promote a positive psychologic response to treatment
4 To promote patient welfare amp safety
5 To return the patient to physiologic state
OBJECTIVES
1 The pt mood must be altered
2 The pt must remain conscious at all times
3 The pt must be cooperative
4 All protective reflexes must remain intact and active
5 Vital signs must remain stable and with in normal limits
6 The ptrsquos pain threshold should be elevated
7 Amnesia may be present
Indications
1 Preschool children
2 Lack of Psychological Emotional maturity
3 Lack of Cognitive Physical Medical disability
4 Fearful amp anxious pts
5 Pt who require extensive amp complicated dental care amp would require or benefit from prolonged visits
6 Acute pain
7 Traumatic injuries
Operating Facilities amp Equipment
A positive pressure O2 delivery system capable of administering gt than 90 O2 at 10L min flow for 60 min (650L ldquoErdquo cylinder)
OR
Self inflating bag valve mask device (15L min)
A functional suction apparatus with appropriate suction catheters
Monitoring equipment - PO BPC PC or Capno
Inhalation sedation unit
100 O2 amp never less than 25
A fail safe mechanism that is checked and calibrated annually
Must have appropriate scavenging system
Emergency drugs
Techniques of sedation
Routes for drug administration
bull Oral
bull Rectal
bull Inhalational
bull Transmucosal
ndash Sublingual
ndash Intranasal
bull Parenteral
ndash IM
ndash sub mucosal
ndash IV
3
Oral Sedation
Advantages
1 Almost universally accepted and the easiest method
2 Decreased incidence and severity of adverse reaction
3 Low cost
Disadvantages
1 Absorption is variable
2 Prolonged latent period(30 min)
3 Reversal of any unwanted effect is also difficult
4 Inability to readily lighten or deepen the level of sedation
5 Prolonged duration of action
Rectal Sedation
Advantages 1 Incidence and intensity of
drug related side effects is minimized
2 Drug absorption occurs from the large intestine directly into the circulation
3 The lack of a needle syringe or other equipment
4 The ease of administration
5 The low cost
Disadvantages
1 Inconvenience to the administrator amp pt
2 The variable absorption of drugs from the large intestine
3 The slow onset of action amp the relatively long duration of action
4 Inability to titrate the drug dosage
5 The inability to reverse the action of the drug the prolonged recovery
Intranasal sedation
Advantages
Rapid onset (10 ndash 15 min)
Simple amp relatively painless
Less pt cooperation is required
Absorbed directly into the C V S
Intranasal sedation
Disadvantages
1 Dependence on nasal mucous membrane
2 Shorter duration of action(40-60min)
3 Multiple dosage may be necessary
Drugs
Midazolam ndash 02mgkg
Sufentanil ndash 15 ndash 3 mcgkg
Ketamine ndash 3-6mg kg
Sublingual sedation
Advantages
1 Pt acceptance
2 Rapid onset
3 High bioavailability
Drugs
Oral Transmucosal Fentanyl Citrate (OTFC)
Intramuscular Sedation
Advantages
1 More rapid onset of action
2 Absorbed directly into the C V system
3 More reliable absorption of drug
4 Pt cooperation is not as essential
Disadvantages
1 Time factor ndash its 15 min latent period
2 Pt may not be willing to accept the injection
3 The prolonged duration of action(2-4 hrs more)
4 Possibility of injury to the tissues at the site of injection caused by either the drug or the needle
4
Sites of I M administration
1 Gluteal area
2 Vastus lateralis
3 Mid ndash deltoid area
Drugs
Diazepam
Midazolam
Hydroxyzine
Inhalation Sedation
Advantages
1 The onset of action is more rapid
2 Peak clinical level is achieved rapidly(3-5min) - permit titration
3 Administrator has complete control over the actions of the drug - safety feature
4 No significant over dosage
5 Flexible duration of action
6 Recovery time is rapid amp most complete
7 No injection is required
8 With N2O- O2 it is safe with very few side effects
Disadvantages
1 The initial cost of the equipment is high 2 The continuing cost of the gases is high 3 The equipment occupies considerable space 4 N2O is not a potent agent 5 A degree of cooperation is required from the pt 6 Chronic exposure to N2O is deleterious to the health of
dental personnel
Contraindications
1 Nasal obstruction 2 Cyanosis at rest 3 Poor cooperation 4 1st trimester of pregnancy 5 Fear of masks
I V Sedation
Advantages
1 The onset of action is the most rapid 2 The dosage may be titrated 3 Suitable level of sedation can be provided 4 The recovery period is shorter 5 Side effects are extremely uncommon 6 Control of salivary secretions is possible 7 The gag reflex is diminished 8 Effectively diminishes motor disturbances 9 Provides immediate access to CVS in emergency
Disadvantages
1 Venipuncture is necessary
2 Complication may rise at the site of the venipuncture
3 Monitoring must be more intensive
4 Recovery is not complete at the end of the procedure
5 Reversal of sedation is difficult
5
N2O-O2 (Relative Analgesia)
colorless sweet smelling gas
Pharmacokinetics
Absorption through pulmonary epithelium
It is approx 15 times as soluble as is nitrogen It replaces nitrogen in blood
It is carried in solution in plasma of the blood
It is not metabolized by the body
Elimination ndash majorndash lungs minor --- skin
perspiration urine and intestinal gas
Pharmacodynamics
Dose related
10 ndash 25 Lightheaded
Changes in visual amp auditory sensation
Tingling of hands amp feet
Suffusing warmth
Remote from the immediate environment
Reduced anxiety
25-50 max analgesic properties and aberration of vision hearing and proprioception mild drowsiness euphoria amnesia and increased sleepiness and dreams
35 conc will achieve maximum analgesia
bull CNS
ndash Cerebrum-primarily affected
ndash Safe but weak anesthetic agent
bull RESPIRATORY SYSTEM
ndash Increased Tidal and minute volumes
bull CARDIOVASCULAR SYSTEM
ndash 2 studies ndash decreased cardiac output
bull FETAL SYSTEMS
ndash Miscarriage in humans
bull OTHER SYSTEMS
ndash Depression of spinal reflexes increase muscle tone indicates stage of delirium
ndash Muscle rigidity-narcotics + nitrous oxide
ndash Nausea and vomitting - GIT
ndash HEMATOPOIESIS ----- prolonged exposure
Adverse reactions and toxicity
EMOTIONAL REACTIONS
DREAMS HALLUCINATIONS
No acute toxicity
Chronic toxicity ndash bone marrow
depression
PROCEDURE
Diffusion Hypoxia
Sevoflurane
A fluorinated derivative of isopropyl ether ndash synthesized in 1970
Potent anaesthetic agent with rapid uptake amp speedy recovery
Day-case surgery
Problem
Attaching vaporiser to any of the currently available machine
BENZODIAZEPINES
Diazepam 1961 lipid soluble
Uses-alcoholism epilepsy labor tetanus and cerebral palsy
- sedation and amnesia
- varieties of neurosis amp anxiety states
Pharmacokinetics
Orally Rectal IMIV or SC
Well absorbed through GIT
Excretion in urine
6
bull Pharmacodynamics
ndash Depress the brain stem reticular system and the limbic system thalamus and hypothalamus
ndash It is a centrally acting muscle relaxant Has anti-convulsant properties
Adverse reaction amp toxicity
ndash Confusion nausea headache increased appetite decreased salivation and jaundice Thrombophlebitis
ndash Rebound phenomenon
ndash Toxicity drowsiness confusion sleep and coma
Dosage Oral or Rectal ndash 02-05mgkg
Maximum single dose 10mg
IV- 025mgkg
Supplied Tablets 2 5 10 mg
Suspension ndash 5mg
Midazolam Water soluble ndash non-irritant
Oral IM IV
Metabolism- liver
Onset IV 3 -5mins
oral 20 ndash 30mins
Oral administration anxious patients requiring relatively short dental procedure
No rebound phenomenon
Better anxiolysis amp amnesia (retrograde amnesia)
Adverse effects Respiratory depression
dose dependant apnea
Dosage Oral ndash 025 to 1mgkg to maximum single dose 20mg
IM ndash 01 to 015mgkg to a maximum of 10mg
IV ndash slow IV
Supplied Syrup ndash 2mgml
Injectable ndash 1mgml amp 5mgml vials
Flumazenil specific benzodiazepines antagonist
selectively inhibits CNS effects
IV administration amp not recommended below 18yrs of age
02mg over 15 seconds after 45seconds 02mg then after 60seconds to maximum of 1mg
Sedative-Hypnotics
Barbiturates First truly effective drugs for the management of anxiety Generalized CNS depressants Produce dose dependent effects
Sedation ---- sleep ---- GA ---- coma
Suppress the CNS and result in sedation and amnesia Advantages
Rapid onset and short duration Disadvantages
no analgesic effect and possible hypotension Must be used with caution in trauma patients because they may cause
apnea and hypoventilation
DOSE Pentobarbital Sodium 100mg Secobarbital Sodium 100 to 200mg Children 30 to 100mg
bull Chloral Hydrates (Mickey Finn Knock out drops ) First synthesized in 1832 first member of the hypnotic group of drugs
Widely used as conscious sedation agent
Properties
Unpleasant taste
Nausea vomiting
Quite irritating to skin and to mucous membranes
GI irritation
Dosages Individualized for each patient 25 ndash 50mgkg
maximum of 1g
Supplied oral capsule ndash 500mg
oral solution ndash 250 amp 500mg5ml
Rectal suppositories ndash 324 amp 648mg
Narcotics
Do produce sedation amp euphoria greater in children
LA is required but dose should be decreased
Meperidine Synthetic opiate agonist
Very water soluble
Orally SC IM or IV
Peak effect by oral 1 hr amp lasts upto 4 hrs
Adverse reactions
-Seizures
-Extreme caution in hepatic or renal diseases or history of seizures
7
Dosage Oral SC or IM ndash 1to 22mgkg not to exceed 100 mg
Supplied Oral Tablets ndash 50 amp 100mg
Oral Syrup ndash 50mgml
Parental solution ndash 25 50 75 amp 100mgml
Fentanyl
Synthetic opiate narcotic analgesic
Very potent 01mg = 10mg Morophine75mg Meperidine
Pharmacokinetics
IV IM SM
Metabolized in liver Excreted in urine
Fentanyl Onset ndash 7 to 15mins
Duration ndash 1 to 2 hrs
Pharmacodynamics
Respiratory depression RR but returns to normal rapidly Tidal volume amp response to co2 depressed for extended period
Apnea
Less emetic than meperidine
NOT RECOMMENDED IN CHILDREN BELOW 2yrs
Dosage 0002 to 0004mgkg
Supplied 005mgml in 2 amp 5ml ampoules
Reversal drug Naloxone
Semisynthetic opiate antagonist
No agonist activity
Onset 2 to 5mins SC or IM amp 1 to 2mins IV
Reversal 45mins
Pt should be kept under continual surveillance
Adverse reaction nausea vomiting sweating hypotension hypertension ventricular tachycardia fibrillation
Dosage IV SC IM 001mgkg then 01mgkg every 2- 3mins maximum 2mg
Supplied 002 004 1mg solutions
Antihistamines
Hydroxyzine
Oral or IM
Effect ndash 15 ndash 30mins
Half-life ndash 3 hrs
Uses
To relieve anxiety
Used as an anti-histamine
Used to control nausea and vomiting including that associated with motion sickness and pregnancy
Adverse reaction dry mouth drowsiness hypersentivity
Dosage Oral ndash 1 to 2mgkg
IM ndash 11mgkg
Promethazine Oral or IM Onset 15 to 60mins Duration 4 to 6 hrs Uses
To prevent and treat nausea and vomiting associated with motion pregnancy or surgery
Produces sedation and reduce swelling pain and trismus
Lower seizure threshold Adverse reaction dry mouth blurred vision thickening of bronchial secretions Dosage OralIM ndash 05-11mgkg
maximum 25 mg
Diphenhydramine
Oral IM IV
Onset -1hr
Duration ndash 4 to 6 hr
Metabolized in liver
Adverse reaction disturbed coordination thickening of bronchial secretions
Dosage Oral IM IV ndash 1 to 15mgkg
maximum 50mg
Tranquilizers
Major tranquilizer antipsychotic produce calmness control symptoms of psychoses cause reversible extra pyramidal symptoms and do not tend to cause habituation
Minor tranquilizer antianxiety agents also cause calmness do not cause extrapyramidal symptoms Used in conditions like nervous tension and mild depression
8
Classification
Antipsychotics
Phenothiazine derivatives
Chlorpromazine promazine
Butryophenones
Haloperidol
Rauwolfia alkaloids
Reserpine
Antianxiety drugs
Propyl alcohol derivatives
Meprobamate
Benzodiazepine derivatives
Diazepam
Miscellaneous compounds
Hydroxyzine
Meprobamate
White crystalline powder slightly bitter in taste
Only administered orally
Peak blood concentration ----1 to 3hrs
10 ---------excreted unchanged Rest --- excreted as a oxidized derivative or as a glucoronide
Uses
To relieve day time anxiety
Induce sleep in insomniacs
To reduce anxiety associated with dental treatment
Anti-convulsant ndash petit mal epilepsy
Adverse reaction leucopenia acute non-thrombocytopenic purpura ecchymoses eosinophilia edema adenopathy
Dosage Childrengt 6yrs 100 to 200mg
Not recommended for children under 6yrs
Monitoring during sedation
1 Pulse
2 Blood pressure
3 ECG
4 Respiration
5 Temperature
Pulse
Manual Electronic
bull Radial Brachial
bull Facial labial
Blood pressure
ndash Stethoscope amp sphygmomanometer
ndash Automatic devices
ndash Direct cannulation of an artery ndash very accurate
Electrocardiograph
Heart rate rhythm myocardial function
9
Respiration
ndash Monitoring respiratory rate
ndash Observing the rise amp fall of the chest wall
ndash Observing the color of mucous membrane
ndash Observing the inflation amp deflation of the reservoir bag
Devices for monitoring respiration
1 The Precordial pretracheal stethoscope
2 The esophageal stethoscope
ndash Respiratory rate
ndash Heart rate
ndash Any abnormal sounds
Pulse Oximeter
ndash Oxygen saturation
ndash Heart rate
ndash Oxisensor site
ndash Fingers
ndash Toe
ndash Ear lobe
Mechanism
Oxygenated Hb ndash red light
Deoxygenated Hb- infrared light
Tissue pressure from arterial pulse (plethysmography)
Advantages
ndash Safe amp noninvasive
ndash Simple to use
ndash Information is rapidly available for clinical decision
ndash Indirectly indicates respiratory adequacy
Disadvantages
ndash Finger probes can get dislodged
ndash Emitted light source may cause burning
ndash Non reusable probes are expensive
ndash Does not directly determine airway patency
Capnography
1 The presence absence of air flow
2 Indicates depth amp adequacy of respiration
3 Continues analysis of the co2 content of the respired air ndash indicates respiratory adequacy
Temperature
ndash Disposable nondisposable thermometer
ndash Esophageal rectal temp probe
10
Discharge criteria
Cardiovascular function is satisfactory amp stable
Airway patency is uncompromised amp satisfactory
Pt is easily arousable amp protective reflexes intact
State of hydration is adequate
Pt can talk if applicable
Pt can sit unaided if applicable
Pt can ambulate with minimal assistance if applicable
Presedation level of responsiveness achieved
Responsible individual is available
1
PULP THERAPY OF VITAL TEETH
DR MITAKSHARA NIRWAN
Contents
Indirect pulp capping
Direct pulp capping
Medications amp materials used in pulp capping
Pulpotomy
MTA
Apexogenesis
INDIRECT PULP CAPPING
Pieter Van Forest - first to speak about root canal therapy
Glove designed instruments that could prepare a canal to a certain size and taper(1910)
Indirect pulp capping is defined as a procedure where in small amount of carious dentin is retained in
deep areas of cavity to avoid exposure of pulp followed by placement of a suitable medicament and
restorative material that seals off the carious dentin and encourages pulp recovery (Ingle)
A procedure in which only the gross caries is removed from the lesion and the cavity is sealed for a
time with a biocompatible material (McDonald)
Objective of indirect pulp capping
These were given by Eidelman in 1965
bull Arresting the carious process
bull Promoting dentin sclerosis
bull Stimulating formation of tertiary dentin
bull Remineralization of carious dentin
Layers of Carious Dentin Indications of Indirect Pulp Capping
History
Mild pain associated with eating
Negative history of spontaneous extreme pain
Clinical Examination
Deep carious lesion which are close tobut not involving the pulp in vital primary or young
permanent teeth
No mobility
Nominal pulp inflammationdefinite layer of affected dentin after removal of infected dentin
Radiographic examination
Normal lamina dura amp PDL space
No radiolucency around the apices
2
Contraindications of Indirect Pulp Capping
History
Sharp penetrating pulpalgia
Prolonged spontaneous pain especially at night
Clinical examination
Mobility of tooth
Discoloration of tooth
Negative reaction of electric pulp testing
Radiographic examination
Definite pulp exposure
Break in the lamina dura
Radiolucency around the apices
Widened PDL space
Treatment procedure
Sequelae of Indirect Pulp Capping Three distinct types of new dentin formation take place
1 Cellular fibrillar dentinmdashfirst 2 months
2 Globular dentinmdash3 months
3 Tubular dentin (uniform mineralized dentin)
bull 15th of reparative dentin formation begins in less than 30 days
bull After 3 months 01 mm is formed
DIRECT PULP CAPPING Defined by Kopel (1992) as the placement of a medicament or non medicated material on a pulp that
has been exposed in course of excavating the last portions of deep dentinal caries or as a result of
trauma
Objective
To create new dentin in the area of the exposure and subsequent healing of the pulp
Rationale
achieve a biologic closure of the exposure site by deposition of hard tissue barrier (dentin bridge)
between pulp tissue and capping material thus walling off the
INDICATIONS
Small mechanical exposure
Easily controlled haemorrhage
Bright red haemorrhage
True pinpoint exposure
CONTRAINDICATIONS
Severe toothache at night
Spontaneous pain
Tooth mobility
Radiographic appearance of pulp periradicular de- generation
Excess of hemorrhage at the time of exposure Serous exudate from the exposure
Externalinternal root resorption
Swellingfistula
Histological Changes after Pulp Capping
These were illustrated be Glass and Zander in 1949
After 24 hours Necrotic zone adjacent to calcium
hydroxide paste is separated from healthy pulp
tissue by a deep staining basophilic layer
After 7 days Increase in cellular and fibroblastic
activity
After 14 days Partly calcified fibrous tissue lined by
odontoblastic cells is seen below the calcium
proteinate zone disappearance of necrotic zone
After 28 days Zone of new dentin
3
Medications and Materials Used for Pulp Capping Calcium hydroxide
Corticosteroids amp antibiotics
Inert materials
Collagen fibers
4-META adhesive
Direct bonding
Isobutyl cyanoacrylate
Denatured albumin
Mineral trioxide aggregate
Laser
Bone morphogenic protein
PULPOTOMY
Finn (1995) defined it as the complete removal of the coronal portion of the dental pulp
followed by placement of a suitable dressing or medicament that will promote healing and
preserve vitality of the tooth
American Academy of Pediatric Dentistry (1998) defined pulpotomy as the amputation of
affected infected coronal portion of the dental pulp preserving the vitality and function of the
remaining part of radicular pulp
Objectives
bull Removal of inflamed and infected coronal pulp at the site of exposure thus preserving the vitality of the
radicular pulp and allowing it to heal
bull Maintain the tooth in the dental arch
Rationale
bull Radicular pulp is healthy and capable of healing after surgical amputation of the infected coronal pulp
bull Preserves vitality of the radicular pulp
bull Maintains tooth in a physiologic condition
Indications of Pulpotomy bull Mechanical pulp exposure in primary teeth
bull Teeth showing a large carious lesion but free of radicular pulpitis
bull History of only spontaneous pain
bull Hemorrhage from exposure sites bright red and can be controlled
bull Absence of abscess or fistula
bull No interradicular bone loss
bull No interradicular radiolucency
Contraindications of Pulpotomy bull Persistent toothache
bull Tenderness on percussion
bull Root resorption more than 13rd of root length
bull Large carious lesion with nonrestorable crown
bull Highly viscous sluggish hemorrhage from canal orifice which is uncontrollable
bull Medical contradictions like heart disease immuno compromised patient
bull Swelling or fistula
bull External or internal resorption
bull Pathological mobility
bull Calcification of pulp
Classification of pulpotomy
4
Formocresol Pulpotomy
Iby BUCKLEY in 1904
Sweet (1930) Formulated multi visit technique
Doyle (1962) Advocated 2 sitting procedure (complete devitalization)
Spedding (1965) Gave 5 minute protocol (partial devitali- zation)
Venham (1967) Proposed 15 seconds procedure
Current concept uses 4 minutes of application time
Composition of formocresol Buckleyrsquos Formula
bull Cresol ndash 35 percent
bull Glycerol ndash 15 percent
bull Formaldehyde ndash 19 percent
bull Water ndash 31 percent
Mechanism of Action
It prevents tissue autolysis by bonding to the proteins Bonding is of peptide groups of side chain amino acids and is a reversible process accomplished without
changing the basic structure of protein molecules
Histological Changes
bull Demonstrated by Mass and Zilbermann11 in 1933 and also by Massler and Mansokhani in 1959
bull Immediately the pulp becomes fibrous and acidophillic
bull Seven to fourteen days Three zones appear
a broad eosinophilic zone of fixation
b broad pale-staining zone of atrophy with poorcellular definition
c broad zone of inflammation extending apically into normal pulp tissue
bull One yearndash Progressive apical movement of these zones with only acidophillic zone left at the end of 1 year
Modified Formocresol Pulpotomy
Used by TRASK(1972)
The technique is identical to that described for primary teeth except that the formocresol pellet is
sealed permanently in the tooth
Two-visit Devitalization Pulpotomy
Indications
bull There is evidence of sluggish bleeding at the amputation site that is difficult to control
bull Pus in the chamber but none at the amputation site
bull There is thickening of the PDL
bull History of pain
Contraindications
bull Nonrestorable tooth
bull Tooth with necrotic pulp
5
Glutaraldehyde Pulpotomy
It was first suggested by S Gravenmade Introduced by Kopel in 1979
Mechanism of Action
bull Glutaraldehyde produces rapid surface fixation of the underlying pulpal tissue
bull A narrow zone of eosinophilic stained and compressed fixed tissue is found directly beneath the area of application which blends into vital normal appearing tissue apically
bull With time the glutaraldehyde fixed zone is replaced by macrophagic action with dense collagenous tissue thus the entire root canal tissue is vital
Cvekrsquos Pulpotomy
bull This is also called as calcium hydroxide pulpotomy or young permanent partial pulpotomy
bull This was proposed by Mejare and Cvek16 in 1978
bull Indicated in young permanent teeth where the pulp is exposed by mechanical or bacterial means and the
remaining radicular tissue is judged vital by clinical and radiographic criteria whereas the root closure is
notcomplete
MINERAL TRIOXIDE AGGREGATE (MTA) Torabinejad described the physical and chemical properties of MTA in 1995
It is ash colored powder made primarily of fine hydrophilic particles of
1 tricalcium aluminate
2 tricalcium silicate
3 silicate oxide
4 tricalcium oxide
5 bismuth dioxide
Hydration of the powder results in a colloidal gel composed of calcium oxide crystals in an amorphous
structure This gel solidifies into a hard structure in less than three hours
PROPERTIES OF MTA
It is biocompatible material and its sealing ability is better than that of amalgam or ZOE
Initial pH is 102 and set pH is 125
The setting time of cement is 4 hours
The compressive strength is 70 MPA which is comparable with that of IRM
Low cytotoxicity ndash It presents with minimal inflammation if extended beyond the apex
Mineral trioxide aggregate (MTA) has demonstrated the ability to induce hard-tissue formation in
pulpal tissues and it promotes rapid cell growth
APEXOGENESIS
It is defined as the treatment of a vital pulp by capping or pulpotomy in order to permit continued
growth of the root and closure of the open apex
Rationale
Maintenance of integrity of the radicular pulp tissue to allow for continued root growth
Indications
bull Indicated for traumatized or pulpally involved vital permanent tooth when root apex is incompletely formed
bull No history of spontaneous pain
bull No sensitivity on percussion
bull No hemorrhage
bull Normal radiographic appearance
Contraindications
bull Evidence that radicular pulp has undergone degenerative changes
bull Purulent drainage
bull History of prolonged pain bull Necrotic debris in canal
bull Periapical radiolucency
6
1
Gupta A Dhingra R Chaudhari P Gupta A
Department of Paedodontics and Preventive Dentistry Faculty of Dental Sciences SGT University Gurgaon Haryana India
Journal of Indian Society of Pedodontics and Preventive Dentistry
Volume 35 I Issue 3 I July-September 2017
A COMPARISION OF VARIOUS MINIMALLY
INVASIVE TECHNIQUES FOR THE REMOVAL
OF DENTAL FLUOROSIS STAINS IN
CHILDREN
DR MITAKSHARA NIRWAN
CONTENTS
bull Introduction
bull Aims
bull Materials and Methods
bull Results
bull Discussion
bull Conclusion
bull Critical analysis
bull References
INTRODUCTION
bull Dental fluorosis is a developmental disturbance of dental enamel caused by
successive exposure to high concentrations of fluoride during tooth
development
bull Various methods of therapy are advocated for the treatment of fluorosis -
stained teeth which range from invasive ceramic veneer bonding restorations
to abrasive chemical treatments
bull The combination of dental bleaching techniques and microabrasion appears
as an excellent conservative solution to reestablish health in fluorosis
affected teeth
AIMS
bull The aim of the study was to evaluate and compare the effectiveness of
minimally invasive techniques for the removal of dental fluorosis
stains in children in vivo
MATERIALS AND METHODS
Patients visiting the department of Pedodontics and Preventive dentistry
Faculty of Dental Sciences SGT University Gurgaon
bull Sample size 90 patients
bull Age group 10 -17 years
bull Caries cracks or periodontal
disease on anterior teeth
bull Abscess draining sinus
cellulitis
bull Non vital teeth
hypersensitive exposed
crevices
bull Orthodontic appliance
bull Past history of bleaching
bull At least two permanent
maxillary anterior teeth
bull TSIF of score 4
bull Free of systemic diseases
Inclusion criteria Exclusion criteria
2
Groups
Group A In office bleaching with 35 hydrogen peroxide( Pola Office
Bleaching kit) activated by light emitting diode (LED) bleaching unit
(35 HP)
Group B Enamel microabrasion (EM) (PREMA Enamel Microabrasion
System) followed by in-office bleaching with 44 carbamide peroxide
gel (EM)
Group C In-office bleaching with 5 sodium hypochlorite (5
NaOCl)
A baseline colour evaluation was done by taking digital photograph of
the maxillary anterior teeth
RESULTS
Group 1
Colour stability
Group 2 Group 3
Tooth sensitivity
Tooth sensitivity values were taken before the treatment
which was compared to immediate postoperative and follow
up visits It was checked using an electric pulp tester
maximum
moderate
least
immediately
group 2
group 1
group 3
1 month
group 2
group 1
group 3
3 month
group 2
group 1
group 3
Patient satisfaction score
Satisfaction was assessed on visual analog scale
Range 1 to 5
Groups percentage of patients
who were satisfied with
the treatment
Number of patients
who reported slight
reappearance of colour
Group 1
90
7
Group 2
83
8
Group 3
73
7
3
Number of Appointments
Groups One sitting Two sittings Three
sittings
Group 1
25
4
1
group 2
26
3
1
Group 3
30
0
0
DISCUSSION
bull Hydrogen peroxide is capable of penetrating the tooth osmosis and through porosities and cracks subsequently acting directly on the pigmented molecules
bull Gurgan et al investigated 3 different light systems and found out that diode laser system with gave best tooth whitening and least tooth sensitivity
bull In the EM group the surface reflects and refracts light from the surface in such way that mild imperfections in underlying enamel are camouflaged While the highly polished surface of enamel enhances the aesthetic appearance
bull Train et al and Loguercio et al also had the similar results in their studies with EM mild fluorosis showed best results moderate showed moderate results while it had little effect on severe fluorosis
bull NaOCl was only effective on mild stains while moderate and severe
stains could only be lightened to quite an extent but could not be
completely removed
bull When NaOCl comes in contact with hypomineralized and discoloured
enamel it degrades and removes the chromogenic organic material
located on the enamel surface
CONCLUSION
bull It was concluded that esthetic appearance of teeth mild fluorosis can
be achieved by bleaching and microabrasion But in cases of
moderate fluorosis a combination of any of theses modalities can be
used
bull As no special maintenance precautions are required these maybe be
considered as an interesting alternative to conventional operative
treatment
bull Focuses on only TSIF of 4
bull Electric pulp testing is not the
right method to check for
sensitivity
bull Tooth Sensitivity changes
from person to person
bull Food habits can cause
staining of the teeth
bull Minimally invasive
bull Cheaper to veneers
bull Minimal loss of tooth structure
bull 4 parameters checked for the success of treatment
bull Inclusion of specific score of fluorosis for comparing the results
bull Maximum 3 appointments needed
CRITICAL ANALYSIS
Pros Cons
REFERENCES
bull Gurgan S Cakir FY Yazici E Different light-activated in officebleaching
systems Lasers Med Sci 201025817-22
bull Train TE McWhorter AG Seale NSWilson CF Guo IY Examination of
esthetic improvement and surface alteration following microabrasion in
fluorotic human incisors in vivoPediatr dent 199618353-62
bull Loguercio AD Correia LD Zago C Tagliari D Neumann E Gomes OM et al
Clinical effectiveness of two microabrasion materials materials for the
removal of enamel flurosis stains Oper Dent 200732531-8
4
4
THANK YOU
1
Morankar Rahul Aditi Kapur Krishan Gauba Ashima Goyal
MANAGEMENT OF ENDODONTIC INSTRUMENT SEPARATION IN
PRIMARY TEETH
CASE REPORT
Journal of South Asian Association of Pediatric Dentistry 2020
DR MITAKSHARA NIRWAN
bull Introduction
bull Aims amp Objectives
bull Case report
bull Discussion
bull Conclusion
bull Pros amp Cons
bull References
CONTENTS
Separation of endodontic instrument is an unexpected complication and its prevalence is not known It is a common belief among the dental professionals that rotary nickelndashtitanium (NiTi) instruments separate more frequently than stainless steel hand instruments
However literature revealed that in permanent teeth the reported prevalence of separated endodontics manual instruments is in the range of 07-74 whereas for rotary NiTI instruments it is
approximately 04-5
Fractured root canal instruments may include endodontic files Gates Glidden burs finger spreaders
and paste fillers
INTRODUCTION
The aim of this study is to describe the management strategies for endodontic
instrument separation in a root canal of primary teeth with emphasis on factors
requiring consideration in different clinical situations
AIMS amp OBJECTIVES
CASE 1
A 6-year-old male child reported with the chief complaint of spontaneous toothache in mandibular left second primary molar since few days It has aggravated following dental treatment at a private dental clinic Clinical examination revealed an underprepared access cavity with 75 and incomplete caries removal
which was sealed with glass ionomer cement
An intraoral periapical radiograph revealed a separated instrument of about 6ndash7 mm size in the distal root
2
The separated instrument was lodged firmly in distobuccal root canal 2ndash3 mm below the cementoenamel junction The instrument was bypassed successfully with no 15 and no 20 H-files but attempts for its retrieval were not successful
GatesndashGlidden (GG) drills no 2 (07 mm) and no 3 (09 mm) were used to drill around the instrument after which it was retrieved successfully using no 25 H-file
All the canals were instrumented till size 30 k-file followed by obturation with metapex and restoration with glass ionomer cement amp followed by placement of a crown and loop space maintainer for missing 74 The instrument retrieved was a manual reamer measuring 6 mm in length
The patient was asymptomatic since then and is under regular follow-up
CASE 2
A 5-year-old female child reported with the chief complaint of spontaneous toothache in mandibular left second
primary molar Clinical examination revealed deep occlusal caries with fractured lingual wall and pain on
percussion An intraoral periapical radiograph revealed caries involving pulp without any furcation or periapical
area of rarefaction and pulpectomy was planned
All the canals were enlarged using NiTi rotary files with a 4 taper operating at 500 rpm with minimum torque
setting An orifice opener [(0825 19 mm) of 8 taper size 25 length 19 mm] and nos 0420 file was used for
instrumentation of root canal This was followed by file nos 0425 which got separated in the distobuccal root
canal The radiograph confirmed a separated instrument of length 3ndash4 mm in the middle third of the root canal
The instrument was bypassed with no 15 k-file but could not get retrieved As instrument separation had occurred with 0425 file the involved root canal was sufficiently debrided before separation and the level of instrument separation was at the mid-root region so it was decided to obturate and seal this tooth with
periodic follow-ups instead of immediate extraction All other canals were enlarged till size 0430 in the sequential manner followed by obturation using metapex and placement of stainless steel crown
3
CASE 3
A 5-year-old female child has complaint of mild intermittent pain with primary mandibular left first molar She
had undergone pulpectomy treatment for the same during which an instrument separation has occurred in
the mesiobuccal root canal by a resident doctor
A radiograph revealed a separated instrument of about 4 mm in size lodged in the apical third but within the
confines of the mesial root An attempt was made for its retrieval but was unsuccessful The extraction of the
involved tooth was carried out under local anesthesia followed by a band and loop space maintainer
CASE 4
A 7-year-old male child reported with a chief complaint of mild intermittent pain on food lodgment with the primary mandibular right first and second molars The patient had a history of dental treatment at a private
dental clinic few months back which he did not continue further
Clinical examination revealed glass ionomer restoration with 85 and proximal caries with 84 leading to food lodgment An intraoral periapical radiograph with 85 revealed empty root canals with a separated
instrument of about 3ndash4 mm size beyond the apex of mesial root close to the developing succedaneous premolar
4
DISCUSSION
Stainless steel files usually separate fracture due to the excessive amounts of torque and overuse or the
preexisting distortion of the instrument whereas in NiTi rotary files it is a combined result of torsional stress and cyclic fatigue
Therapeutic options for the management of separated endodontic instruments include no intervention nonsurgical (orthograde conservative) management surgical management and tooth extraction
Use of ultrasonic scaler Masserann technique Endo extractor and Cavi-Endo ultrasonic instruments are some of the methods popular for retrieval of a separated endodontic instrument in the permanent tooth
In case 1 a 6-mm-long manual reamer was retrieved successfully with the use of GG drill using a manual file and copious irrigation which is the most desired treatment outcome
In case 2 the retrieval of separated rotary file lodged in the middle third of the root canal was unsuccessful in spite of multiple attempts It was therefore managed with routine obturation followed by restoration to maintain the tooth in its physiological functional state It was kept under close periodic follow-up at least
every 3 months This treatment option should be encouraged where it is possible to follow up the patient clinically and radiographically at close periodic intervals as there is the possibility of instrument escaping
into bone due to physiological root resorption
In cases 3 and 4 an instrument has separated in the apical root portion
In case 3 it was within the root canal and thus an attempt was made for its retrieval which was
unsuccessful It was therefore extracted to prevent the fractured instrument from getting exposed in the bone following resorption as there is no accurate and consistent established age for initiation of resorption in primary teeth known per se
In case 4 an immediate extraction of involved tooth was carried out as the separated instrument was beyond the apex of the primary tooth root
Age of the child clinical signs and symptoms and amount of root resorption are the factors which can also influence the management of separated instrument in primary teeth
Moreover if an instrument has separated after initial cleaning and shaping of root canal maintaining a tooth is not a problem as clinical signs and symptoms are not anticipated and the good prognosis is expected
However if an instrument has separated early during the initial cleaning and shaping of the root canal clinical symptoms may compromise the prognosis
Therefore these factors should be kept in mind while planning a suitable management strategy to avoid or at least reduce the burden of extraction and wear of space maintainer for longer period
5
CONCLUSION
The management and prognosis of a primary tooth with a separated instrument is
dependent on the level of instrument fracture within the root age of the child root
resorption and clinical signs and symptoms of the involved tooth
Different management approaches can be tried depending on clinical situations keeping
in mind benefits vs risks in preserving the tooth
PROS amp CONS
PROS
The entire procedure is given
by step by step
Well descriptive xrays and
photographs
CONS
Medical history has not been
given
REFERENCES
1 TOMER ANIL K ET AL ldquoBROKEN FILE RETRIEVAL PUZZLE IN ENDODONTICSrdquo
(2016)
2 SHENOY A MANDAVA P BOLLA N ET AL A NOVEL TECHNIQUE FOR REMOVAL OF
BROKEN INSTRUMENT FROM ROOT CANAL IN MANDIBULAR SECOND MOLAR
INDIAN J DENT RES 201425(1)107ndash110
3 PATEL J MORAWALA A TALATHI R ET AL RETRIEVAL OF A BROKEN INSTRUMENT
FROM ROOT CANAL IN PRIMARY ANTERIOR TEETH UNIV RES J DENT 20155(3)203ndash
206
4 MORANKAR R GOYAL A GAUBA K ET AL MANUAL VERSUS ROTARY
INSTRUMENTATION FOR PRIMARY MOLAR PULPECTOMIES - A 24 MONTHS
RANDOMIZED CLINICAL TRIAL PEDIAT DENT J 201828(2)96ndash102
5 KASHYAP NILOTPOL (2018) RETAINING PRIMARY MOLARS WITH INSTRUMENT
SEPERATION A CASE REPORT AND CLINICAL GUIDE
6
1
IMPACT OF 6 CITRIC ACID AND ENDOACTIVATOR AS IRRIGATION ADJUNCTS ON OBTURATION QUALITY AND PULPECTOMY OUTCOME IN
PRIMARY TEETH
NEETU JAIN SHALINI GARG ABHISHEK DHINDSA SAKSHI JOSHI HARJOY
KHATRIA
PEDIATRIC DENTAL JOURNAL 2019 29
1
DR MITAKSHARA NIRWAN
CONTENTS
bull INTRODUCTION
bull AIMS amp OBJECTIVES
bull CASE REPORT
bull RESULTS
bull DISCUSSION
bull CONCLUSION
bull PROS AND CONS
bull REFERENCES
2
INTRODUCTION
bull ENDODONTIC THERAPY IN PRIMARY TEETH INVOLVES DISINFECTION OF THE ROOT CANAL
SYSTEM AND ITS OBTURATION WITH RESORBABLE PASTE
bull THE CONTENTS OF ROOT CANAL ALONG WITH SMEAR LAYER ARE EXPECTED TO BE REMOVED
DURING THE BIOMECHANICAL PREPARATION
bull IN VITRO AND CLINICAL DOCUMENTS HAVE INDICATED THAT MECHANICAL PREPARATION OF
THE CANAL LEAVES LARGE PORTIONS OF THE CANAL WALLS UNDEBRIDED AND COMPLETE
REMOVAL OF THE BACTERIA BY THIS MECHANICAL PROCEDURE ALONE IS UNLIKELY TO BE SEEN
THEREFORE SOME FORM OF DISINFECTIONIRRIGATION IS MANDATORY TO KILL THE
MICROORGANISMS AND TO REMOVE THE RESIDUAL TISSUES
3
bull THE IDEAL REQUISITES OF A ROOT CANAL IRRIGANT AS GIVEN BY ZEHNDER ARE
1 BROAD ANTIMICROBIAL SPECTRUM
2 HIGH EFFICACY AGAINST ANAEROBIC AND FACULTATIVE MICROORGANISMS ORGANIZED
IN BIOFILMS
3 ABILITY TO DISSOLVE NECROTIC PULP TISSUE REMNANTS
4 ABILITY TO INACTIVATE ENDOTOXIN
5 ABILITY TO PREVENT THE FORMATION OF A SMEAR LAYER DURING INSTRUMENTATION OR
TO DISSOLVE THE LATTER ONCE IT HAS FORMED
6 SYSTEMICALLY NONTOXIC WHEN THEY COME IN CONTACT WITH VITAL TISSUES
NONCAUSTIC TO PERIODONTAL TISSUES AND WITH LITTLE POTENTIAL TO CAUSE AN
ANAPHYLACTIC REACTION
SINCE NO SINGLE IRRIGANT HAS THESE OPTIMAL PROPERTIES STUDIES HAVE REPORTED THE USE
OF TWO OR MORE SOLUTIONS IN A SPECIFIC SEQUENCE OR IN COMBINATIONS FOR BETTER
RESULTS 4
bull SEVERAL IRRIGATING SOLUTIONS ALONG WITH CHELATING AGENTS HAVE BEEN USED
DURING BIOMECHANICAL PREPARATION OF ROOT CANAL BOTH IN PRIMARY AND
PERMANENT TEETH
bull HOWEVER NONE OF THE AVAILABLE IRRIGATING SOLUTIONS HAS BEEN REGARDED CLEARLY
AS OPTIMAL SOLUTION BECAUSE OF THEIR LIMITED EFFECTIVENESS ESPECIALLY IN APICAL
13RD OF THE ROOT CANAL SYSTEM
bull TO OVERCOME SUCH LIMITATIONS USE OF ENDOACTIVATOR HAS BEEN PROPOSED AS AN
IRRIGATION FACILITATOR THAT IS BASED ON SONIC VIBRATION (UP TO 10000 CPM) WHICH
FACILITATES THE IRRIGANT PENETRATION AND ITS RENEWAL WITHIN THE CANAL
bull ACTIVATION SYSTEMS RESULTED IN BETTER REMOVAL OF THE SMEAR LAYER IN THE APICAL
THIRD OF ROOT CANALS IN COMPARISON TO CONVENTIONAL IRRIGATION
5
CITRIC ACID
bull CITRIC ACID IS A WEAK ORGANIC ACID WITH THE APPEARANCE OF WHITE CRYSTALLINE
POWDER AT ROOM TEMPERATURE
bull IT CAN EXIST EITHER IN WATER-FREE FORM (ANHYDROUS) OR MONOHYDRATE FORM THE
WATER-FREE FORM CRYSTALLIZES FROM THE HOT WATER WHEREAS THE MONOHYDRATE
FORMS FROM THE COLD WATER THE LATTER MAY BE CONVERTED TO ANHYDROUS FORM BY
HEATING MORE THAN 78degC
bull CITRIC ACID OCCURS NATURALLY IN THE BODY IN MITOCHONDRIA AND IS USED BY BLOOD
BANKS TO PREVENT COAGULATION OF TRANSFUSED BLOOD CITRIC ACID IS ALSO ESSENTIAL
TO HUMAN METABOLISM AND IS FOUND IN MANY FOODS
6
2
bull THE BIOLOGICAL EFFECTS OF CITRIC ACID ON THE PERIODONTAL STRUCTURE HAS BEEN
EXTENSIVELY STUDIED IN PERIODONTICS
bull NEUMAN AND NEWMAN SHOWED THAT CITRIC ACID IS THE MOST EFFECTIVE ACID IN
ALTERING THE SOLUBILITY OF HYDROXYAPATITE
bull YAMAGUCHI ET AL SHOWED THAT CITRIC ACID SOLUTION HAD ANTIBACTERIAL EFFECTS ON
ALL 12 ROOT CANAL BACTERIA TESTED
bull ARIAS-MOLIZ ET AL SHOWED THAT ETHYLENEDIAMINETETRAACETIC ACID (EDTA) HAS NO
BACTERICIDAL ACTIVITY EVEN AFTER 1 HOUR CONTACT
bull THIS ACID HAS THE ABILITY OF ROOT CANAL IRRIGATION AND ALSO SMEAR LAYER REMOVAL
DIFFERENT CONCENTRATIONS (1ndash50) HAVE BEEN PROPOSED GUTMANN ET AL CONCLUDED
THAT 10 CITRIC ACID IS BETTER THAN ULTRASOUND FOR SMEAR LAYER REMOVAL FROM THE
ROOT END CAVITIES
7
bull STUDIES HAVE SHOWN IRRIGATION WITH 6 CA FOR 15 OR 30 SECONDS IS QUITE
EFFECTIVE IN REMOVING ALL THE COMPONENTS OF THE SMEAR LAYER OF THE PRIMARY
TEETH WHEREAS PERITUBULAR DENTIN DESTRUCTION WAS OBSERVED WHEN HIGHER
CONCENTRATION OF CITRIC ACID WAS USED AS AN IRRIGATING SOLUTION
8
AIMS amp OBJECTIVES
bull THIS STUDY WAS AIMED TO EVALUATE THE CLINICAL AND RADIOGRAPHIC OUTCOME OF
PULPECTOMY ALONG WITH QUALITY OF OBTURATION USING 6 CITRIC ACID AND
ENDOACTIVATOR
9
CASE REPORT
bull 350 CHILDREN (3-9 YEARS) WITH CLINICAL SIGNS AND SYMPTOMS OF CHRONIC IRREVERSIBLE
PULPITIS IN DEEPLY CARIOUS TEETH WERE SCREENED DURING SCHOOL DENTAL HEALTH
PROGRAM FROM MAY 2014-JULY 2014
bull 123 CHILDREN REPORTED TO THE DEPARTMENT AND 67 CHILDREN WERE SELECTED BASED ON
INCLUSION AND EXCLUSION CRITERIA
RECRUITMENT OF PATIENTS
10
INCLUSION CRITERIA
bull HISTORY OF SPONTANEOUS PAIN AND UNCONTROLLED BLEEDING AFTER PULP AMPUTATION
EXCLUSION CRITERIA
bull EVIDENCE OF INTERNAL OR EXTERNAL (PHYSIOLOGICPATHOLOGIC) ROOT RESORPTION OF MORE THAN A THIRD OF ITS LENGTH
bull ROOT CANAL OBLITERATION OR ANATOMIC ANOMALIES
bull INADEQUATE BONE SUPPORT OR NON RESTORABLE TOOTH
bull ONCE PATIENTS ELIGIBILITY WAS CONFIRMED THE TREATMENT PROCEDURE WAS
EXPLAINED TO THE PARENTGUARDIAN AND INFORMED WRITTEN CONSENT WAS
OBTAINED FROM PARENTSGUARDIANS SHOWING WILLINGNESS FOR THEIR
CHILDRENS TREATMENT 11
PROCEDURE
bull PULPECTOMY WAS PERFORMED BY ONE OPERATOR OF PEDIATRIC DENTISTRY DEPARTMENT
USING A STANDARDIZED TREATMENT PROTOCOL FOR ALL THE PATIENTS
bull AFTER ADMINISTRATION OF LOCAL ANESTHESIA RUBBER DAM WAS APPLIED FOR ISOLATION
bull ACCESS CAVITY WAS PREPARED USING AIR-ROTOR HAND PIECE WITH 8 ROUND BUR AND
PULP TISSUE WAS EXTIRPATED WITH THE HELP OF SPOON EXCAVATOR
bull FURTHER THE NEGOTIATION OF THE CANALS WAS DONE WITH 10 K-FILE
bull A DIAGNOSTIC RADIOGRAPH WAS TAKEN FOR ROOT LENGTH DETERMINATION AND
WORKING LENGTH WAS KEPT 1 MM SHORT OF THE RADIOGRAPHICAL APEX
bull ALL ROOT CANALS WERE INSTRUMENTED MANUALLY USING K-FILES AND WERE IRRIGATED
WITH 10 ML 09 NORMAL SALINE AND 1 SODIUM HYPOCHLORITE AS STANDARDIZING
PROTOCOL FOR ROOT CANAL PREPARATION AND DISINFECTION
12
3
GROUP 1 (CA + E) - IRRIGATION WAS DONE
WITH 10 ML OF 6 CITRIC ACID (CITOCID AMMDENT)
AND IRRIGANTS WERE SONICALLY AGITATED WITH
ENDOACTIVATOR (DENTSPLY) FOR 30 S PER CANAL USING REDBLUE
ENDOACTIVATOR TIP
GROUP 2 (CA) - 10 ML OF 6 CITRIC ACID FOR 1 MIN USING
27 GAUZE IRRIGATING NEEDLE
GROUP 3(SH + E) - 10 ML OF 1 SODIUM HYPOCHLORITE
SOLUTION AND SONIC ACTIVATION WITH ENDOACTIVATOR
GROUP 4(SH) - 10 ML OF 1 SODIUM HYPOCHLORITE
SOLUTION USING IRRIGATING NEEDLE (CONTROL GROUP)
bull TEETH UNDERGOING PULPECTOMY WERE RANDOMLY ENROLLED BY CHIT METHOD INTO THREE
STUDY AND ONE CONTROL GROUP
13
bull IN CITRIC ACID GROUPS FINAL RINSE WITH NORMAL SALINE WAS DONE TO REMOVE THE
REMAINING CRYSTALS (CHELATES)
bull FOLLOWING BIOMECHANICAL PREPARATION THE ROOT CANALS WERE DRIED WITH STERILE
ABSORBENT PAPER POINTS AND OBTURATED WITH VITAPEX USING HAND HELD
LENTULOSPIRAL FINAL RESTORATIONS WERE DONE USING COMPOSITE RESIN
14
bull CLINICAL FOLLOW UP WAS DONE AT 24 H1 WEEK 1 MONTH 6 MONTH AND 12
MONTH TO CHECK PAIN PRESENCE AND PAIN FREQUENCY (ONCEMORE THAN ONCE)
SWELLING FISTULA SENSITIVITY TO PERCUSSION
bull RADIOGRAPHIC FOLLOW UP WAS DONE AT 6 MONTH AND 12 MONTH FOR ANY
DEVIATED ERUPTION OF SUCCEDANEOUS TEETH EXCESS FILING MATERIAL AND ITS
RESORPTION EXTERNALINTERNAL ROOT RESORBTION CALCIFIC METAMORPHOSIS
PRESENCE OF FURCATION RADIOLUCENCY
CLINICAL amp RADIOGRAPHIC FOLLOW UP
15
RADIOGRAPHIC ASSESSMENT OF OBTURATION QUALITY
bull POSTOPERATIVE RADIOGRAPHS WERE VISUALLY ASSESSED FOR QUALITY OF OBTURATION BY
TWO INDEPENDENT EXAMINERS (SG AD) WHO WERE BLINDED WITH REGARD TO
IRRIGATION PROTOCOL GROUP TO ENHANCE CALIBRATION EACH EXAMINER ASSESSED THE
RADIOGRAPH INDEPENDENTLY AND LATER REVIEWED TOGETHER FOR FINAL ASSESSMENT
INDIVIDUAL ROOT WAS TAKEN AS UNIT OF ANALYSIS FOR GRADE OF OBTU- RATION AND
SCORING CRITERIA WERE AS GIVEN BY COLL JA 1996
1 UNDER FILLED - FILLING MATERIAL ENDED 1 MM OR MORE SHORT OF THE APEX
2 OPTIMAL FILLING- FILLING MATERIAL APPEARED TO END AT THE RADIOGRAPHICAL APEX
3 OVERFILLED - FILLING MATERIAL EXTRUDED PAST THE RADIOGRAPHIC APEX
4 OPTIMALLY FILLED ROOTS WERE FURTHER ASSESSED FOR THE PRESENCE OF VOIDS AND VOID
AREA (ROOT CANAL SURFACE UNTOUCHED BY THE ROOT CANAL FILLING MATERIAL) IN THREE
VISUALLY DIVIDED SECTIONS OF THE ROOT IE CORONAL MIDDLE AND APICAL 13RD
16
RESULTS
bull OVERALL CLINICAL AND RADIOGRAPHIC SUCCESS RATE OVER A PERIOD OF ONE YEAR WAS
9886 amp 977 RESPECTIVELY
bull ALL GROUPS WERE SIGNIFICANTLY (P = 001) EFFECTIVE IN ALLEVIATING PAIN WITHIN 24 H
OF PULPECTOMY
17 18
4
19
bull IMMEDIATE POST OPERATIVE RADIOGRAPHIC ASSESSMENT REVEALED 68 (102150) ROOTS
WITH OPTIMAL OBTURATION AND 32 (48150) WITH OVERFILLINGUNDERFILLING MAXIMUM
NO OF OPTIMAL FILLINGS WERE OBSERVED IN GROUP1 (CA + E) (3333) FOLLOWED BY
GROUP 2 (CA) (2549) GROUP 3(SH + E) (2549) AND GROUP 4(SH) (1568)
bull CITRIC ACID GROUPS HAD MORE NUMBER OF OPTIMALLY FILLED ROOTS 588 (60102) THAN
NON CITRIC ACID GROUPS 412 (42102)
bull ENDOACTIVATOR CONTRIBUTED TO 18 OF OPTIMAL OBTURATION IRRESPECTIVE OF
CHELATING AGENT USED
20
21
bull MAXIMUM NO OF VOIDS AND VOID AREAS WERE IN NON CITRIC ACID GROUPS
(6419 amp 5384) COMPARED TO CITRIC ACID GROUPS (3580 amp 4615)
RESPECTIVELY
bull ANALYSIS OF ROOT 13RD REVEALED MAXIMUM NO OF VOID AREA IN APICAL
13RD (4755) FOLLOWED BY MIDDLE 13RD (3846) AND CORONAL 13RD
(1398)
bull LEAST NO OF VOIDS amp VOID AREA (1111 amp 1608) WERE OBSERVED WHEN
ENDOACTIVATOR ALONG WITH CHELATING AGENT WAS USED (GROUP 1)
HOWEVER THIS WAS STATISTICALLY INSIGNIFICANT
22
DISCUSSION
bull IN THE PRESENT STUDY 1 SODIUM HYPOCHLORITE WAS USED ALONG WITH 6 CITRIC ACID
(CHELATING AGENT) WHICH IS REPORTED TO BE AS EFFECTIVE AS 17 EDTA
bull CITRIC ACID (BIOLOGICAL ACID) IS FOUND TO BE BIOCOMPATIBLE AND LEAST IRRITATING TO
PERIAPICAL TISSUES THAN OTHER CHELATING AGENTS
bull USE OF SODIUM HYPOCHLORITE SOLUTION FOLLOWING CHELATING AGENT WAS AVOIDED AS IT
RAPIDLY PRODUCES SEVERE EROSION OF ROOT CANAL WALL DENTIN
bull TRADITIONAL APPROACH OF DELIVERING IRRIGANTS INTO THE ROOT CANAL SPACE USING
SYRINGES AND METAL NEEDLES HAS BEEN FOUND TO BE INEFFECTIVE ESPECIALLY IN THE AREAS OF
ANASTOMOSES BETWEEN CANALS AND APICAL 13RD OF ROOT CANAL
23
bull THEREFORE TO ACHIEVE BETTER CLEANING EFFICIENCY IRRIGANT ACTIVATION HAS BEEN
RECOMMENDED SONIC ACTIVATION HAS BEEN REPORTED TO RESULT IN BETTER ROOT CANAL
CLEANLINESS AS COMPARED TO NO ACTIVATION OF IRRIGANT
24
5
CONCLUSION
bull USE OF 6 CITRIC ACID DEFINITELY HELPED IN RAPID ELIMINATION OF PAIN RESOLUTION OF
PERI-RADICULAR RADIOLUCENCY BETTER OBTURATION QUALITY IN TERMS OF LESS VOIDS AND
VOID AREAS ALONG WITH MAXIMUM NO OF OPTIMAL OBTURATION UP TO APICAL AREA
bull 6 CITRIC ACID AND ENDOACTIVATOR IRRIGATION PROTOCOL PROVED TO BE THE BETTER
IRRIGATION PROTOCOL WHICH MAY CONTRIBUTE TO LONG TERM SUCCESS OF PRIMARY
TOOTH AND THE HEALTH OF UNDERLYING PERMANENT TOOTH
bull 6 CITRIC ACID ALONG WITH ENDOACTIVATOR MAY BE RECOMMENDED AS IRRIGATION
ADJUNCTS IN PULPECTOMY PROCEDURE OF PRIMARY TEETH
25
PROS AND CONS
PROS
bull PROPER EXPLANATION OF THE MATERIALS
USED
CONS
bull NO PREOPERATIVE AND POSTOPERATIVE
RADIOGRAPHS
26
REFERENCES
bull RAMACHANDRA JA NIHAL NK NAGARATHNA C VORA MS ROOT CANAL IRRIGANTS IN
PRIMARY TEETH WORLD J DENT 20156(3)229-234
bull MOHAMMADI Z JAFARZADEH H SHALAVI S KINOSHITA JI UNUSUAL ROOT CANAL
IRRIGATION SOLUTIONS J CONTEMP DENT PRACT 201718(5)415-420
bull ZEHNDER M ROOT CANAL IRRIGANTS J ENDOD 2006 32389- 98
bull SMITH JJ amp WAYMAN BE AN EVALUATION OF THE ANTIMICROBIAL EFFECTIVENESS OF
CITRIC ACID AS A ROOT CANAL IRRIGANT JOURNAL OF ENDODONTICS 1986 12(2) 54-58
bull TANNURE PN AZEVEDO CP BARCELOS R GLEISER R PRIMO LG LONG-TERM OUTCOMES OF
PRIMARY TOOTH PULPECTOMY WITH AND WITHOUT SMEAR LAYER REMOVAL A RANDOMIZED
SPLIT-MOUTH CLINICAL TRIAL PEDIATR DENT 201133316E20 27
bull CARON G NHAM K BRONNEC F MACHTOU P EFFECTIVENESS OF DIFFERENT FINAL IRRIGANT
ACTIVATION PROTOCOLS ON SMEAR LAYER REMOVAL IN CURVED CANALS J ENDOD
2010361361E6
bull COLL JA SADRIAN R PREDICTING PULPECTOMY SUCCESS AND ITS RELATIONSHIP TO
EXFOLIATION AND SUCCEDANEOUS DENTITION PEDIATR DENT 19961857E63
28
1
LOCAL
ANESTHESIA
DR MITAKSHARA NIRWAN
CONTENTS
Definition
Methods of inducing local anesthesia
Desirable properties
Electrophysiology of nerve conduction
Impulse propagation and spread
Mode and site of action of local anesthesia
Classification of local anesthetic according to biological site and mode of action
Dissociation of local anaesthetics
Mechanism of action of local anaethetics
Local anaesthetic agent
2
3
DEFINITION
Local anesthesia is defined as a loss of sensation in
a circumscribed area of the body caused by depression
of excitation in nerve endings or an inhibition of the
conduction process in peripheral nerves
An important feature of local anesthesia is that it produces
LOSS OF SENSATION WITHOUT INDUCING LOSS OF
CONSCIOUSNESS
4
METHODS OF INDUCING LOCAL
ANESTHESIA
Low temperature
Mechanical trauma
Anoxia
Neurolytic agents such as alcohol amp phenol
Chemical agents such as local anesthetics
PROPERTIES OF LOCAL
ANESTHESIA
It should not be irritating to tissue to which it is applied
It should not cause any permanent alteration of nerve structure
Its systemic toxicity should be low
Time of onset of anesthesia should be short
It should be effective regardless of whether it is injected into the tissue or applied locally to mucous membranes
The duration of action should be long enough to permit the completion of procedure
5 6
It should have the potency sufficient to give complete
anesthesia with out the use of harmful concentration solutions
It should be free from producing allergic reactions
It should be free in solution and relatively undergo
biotransformation in the body
It should be either sterile or be capable of being sterilized by
heat with out deterioration
2
ELETROPHYSIOLOGY OF
NERVE CONDUCTION
There is an electrical charge across the membrane
This is the membrane potential
The resting potential (when the cell is not firing) is a negative
electrical potential of -70mv that exists across the nerve
membrane produced by different concentrations of either side of
the membrane
The interior of nerve is NEGATIVE in relation to exterior
7 8
inside
outside
Resting potential of neuron = -70mV
+
-
+
-
+
-
+
-
+
-
SLOW DEPOLARIRIZATION
9
RAPID DEPOLARIZATION
The interior of nerve is POSITIVE in relation to exterior
REPOLARIZATION
10
bull Repolarization takes 07 msec
bull Depolarization takes 03 msec
SODIUM PUMP -
energy comes from the oxidative metabolism of ATP
bull The entire process require 1 msec
IMPULSE PROPOGATION
IMPULSE SPREAD
The propagated impulse travels along the nerve
membrane towards CNS The spread of impulse differs
in myelinated and unmyelinated nerve fibers
DEPOLARIZED SEGMENT ADJACENT RESTING AREA
MODE AND SITE OF ACTION OF LOCAL
ANESTHETICS
Local anesthetic agent interferes with excitation
process in a nerve membrane in one of the
following ways
Altering the basic resting potential of nerve
membrane
Altering the threshold potential
Decreasing the rate of depolarization
Prolonging the rate of repolarization
12
3
CLASSIFICATION OF LOCAL ANESTHETIC
SUBSTANCES ACCORDING TO
BIOLOGICAL SITE AND MODE OF ACTION
CLASS A
Agents acting at receptor site on external surface of nerve membrane
Chemical substance Biotoxins (eg tetrodotoxin and saxitoxin)
CLASS B
Agents acting on receptor sites on internal surface of nerve membrane
Chemical substance Quaternary ammonium analogues of lidocaine
scorpion venom 13
CLASS C Agents acting by receptor independent of
physiochemical mechanism
Chemical substance Benzocaine
CLASS D Agents acting by combination of receptors and
receptor independent mechanisms
Chemical substance most clinically useful anesthetic agents
(eg lidocaine mepivacaine prilocaine)
14
BASED ON THE SOURCE
NATUAL
SYNTHETIC
OTHERS
BASED ON MODE OF APPLICATION
bull INJECTABLE
bull TOPICAL
BASED ON DURATION OF ACTION
bull ULTRA SHORT
bull SHORT
bull MEDIEM
bull LONG
BASED ON ONSET OF ACTION SHORT
INTERMEDIATE
LONG
15
DISSOCIATION OF LOCAL
ANESTHETICS
Local anesthetics are available as salts (usually
hydrochlorides) for clinical use
The salts both water soluble and stable is dissolved in
either sterile water or saline
In this solution it exists simultaneously as unchanged
molecule (RN) also called base and positively charged
molecules (RNH+) called cations
RNH+ ==== RN+ H
+
16
The relative concentration of each ionic form in the solution varies
in the pH of the solution or surrounding tissue
In the presence of high concentration of hydrogen ion (low pH) the
equilibrium shifts to left and most of the anesthetic solution exists
in cationic form
RNH+ gt RN
+ + H
+
As hydrogen ion concentration decreases (higher pH) the
equilibrium shifts towards the free base form
RNH+ lt RN + H
+
17
The relative proportion of ionic form also depends on pKa or DISSOCIATION CONSTANT of the specific local anesthetic
The pKa is a measure of molecules affinity for H+
ions
When the pH of the solution has the same value as pKa of the local anesthetic exactly half the drug will exists in the RNH
+ form and
exactly half in RN form
The percentage of drug existing in either form can be determined by Henderson Hasselbalch equation
Log baseacid = pH - pKa
18
4
MECHANISM OF ACTION OF LOCAL
ANESTHETICS
The following sequence is proposed mechanism of action of LA
Displacement of calcium ions from the sodium channel receptor site
Binding of local anesthetic molecule to this receptor site
Blockade of sodium channel
19
Decrease in sodium conductance
Depression of rate of electrical depolarization
Failure to achieve the threshold potential level
Lack of development of propagated action potential
Conduction blockadehellip
20
21
Na + Na +
22
LOCAL ANESTHETIC AGENT
COMERCIALLY PREPARED LOCAL ANESTHESIA
CONSISTS OF
Local anesthetic agent (xylocaine lignocaine 2)
Vasoconstrictor (adrenaline 1 80000)
Reducing agent (sodium metabisulphite)
Preservative (methylparabencapryl
hydrocuprienotoxin)
Fungicide (thymol)
Vehicle (distillde waterNaCl)
LOCAL ANESTHETIC AGENT
The local anesthetics used in dentistry are divided
into two groups
ESTER GROUP
AMIDE GROUP
23 24
ESTER GROUP It is composed of the following
An aromatic lipophilic group
An intermediate chain containing
an ester linkage
A hydrophilic secondary or tertiary
amino group
AMIDE GROUP It is composed of the following
An aromatic lipophilic group
An intermediate chain containing
amide linkage
A hydrophilic secondary or tertiary
amino group
5
25
CLASSIFICATION OF LOCAL ANESTHETICS
ESTERS
Esters of benzoic acid
Butacaine
Cocaine
Benzocaine
Hexylcaine
Piperocaine
Tetracaine
Esters of Para-amino
benzoic acid
Chloroprocain
Procaine
Propoxycaine
26
AMIDES Articaine
Bupivacaine
Dibucaine
Etidocaine
Lidocaine
Mepivacaine
Prilocaine
Ropivacaine
QUINOLINE
Centbucridine
PHARMACOKINETICS OF LOCAL
ANESTHETICS UPTAKE
When injected into soft tissue most local anesthetics produce
dilation of vascular bed
Cocaine is the only local anesthetic that produces
vasoconstriction initially it produces vasodilation which is
followed by prolonged vasoconstriction
Vasodilation is due to increase in the rate of absorption of the
local anesthetic into the blood thus decreasing the duration of
pain control while increasing the anesthetic blood level and
potential for over dose 27
AMIDE LOCAL ANESTHETICS
The metabolism of amide local anesthetics is more
complicated then esters The primary site of
biotransformation of amide drugs is liver
Entire metabolic process occurs in the liver for lidocaine
articaine etidocaine and bupivacaine
Prilocaine undergoes more rapid biotransformation then the
other amides
28
REFERENCES
Handbook of local anesthesia ndash Stanley F Malamed ndash 6th
edition
Essentials of Local Anesthetic Pharmacology Daniel E
Becker Anesth Prog 2006 Fall 53(3) 98ndash109
WIKIPEDIEA
29
THANK YOU
30
1
Pharmacological Methods of Behavior
Management
DR MITAKSHARA NIRWAN
DEFINITIONS
bull Conscious Sedation ndash A minimally depressed level of consciousness that retains
the patients ability to independently and continuously maintain an airway and respond appropriately to physical stimulation or verbal command
(American Dental Association House Of Delegates 2000)
bull Deep Sedation ndash An induced state of depressed consciousness
accompanied by partial loss of protective reflexes including the inability to continuously maintain an airway independently and or to respond purposefully to physical stimulation or verbal command
bull General Anesthesia (G A) ndash An induced state of unconsciousness or complete loss of
protective reflexes including the inability to continually maintain an airway independently and respond purposefully to physical stimulation or verbal command
Conscious sedation
ADVANTAGES
Conscious
Protective reflexes active amp intact
Stable vital signs
Operating dentist may perform sedation
Minimum amount of equipment required
Prolong detainment in recovery room not required
Risk of complication very low
Excellent choice for poor ndash risk pt in dental office
Cost effective
General anesthesia
ADVANTAGES Not absolutely
essential May be the only
method Not necessary (no
pain reaction) Amnesia always
present
Conscious sedation
DISADVANTAGES
Pt cooperation is essential
Extremely difficult or mentally handicapped pt cannot always be managed
Use of local anesthesia is a must
Amnesia may or may not be present
General anesthesia DISADVANTAGES
Pt unconscious
Protective reflexes are depressed
Depressed
Advanced training required Dentist must not act also as anesthetist
Special equipment necessary
Detainment in recovery area necessary
High IOP amp postoperative complications
Not indicated in dental office
More expensive
Fundamental Concepts
bull Techniques that utilize drugs to induce co-operative yet conscious state in an otherwise uncooperative child ndash CONSCIOUS SEDATION
2
GOALS
1 To facilitate the provision of quality care
2 To minimize the extremes of disruptive behavior
3 To promote a positive psychologic response to treatment
4 To promote patient welfare amp safety
5 To return the patient to physiologic state
OBJECTIVES
1 The pt mood must be altered
2 The pt must remain conscious at all times
3 The pt must be cooperative
4 All protective reflexes must remain intact and active
5 Vital signs must remain stable and with in normal limits
6 The ptrsquos pain threshold should be elevated
7 Amnesia may be present
Indications
1 Preschool children
2 Lack of Psychological Emotional maturity
3 Lack of Cognitive Physical Medical disability
4 Fearful amp anxious pts
5 Pt who require extensive amp complicated dental care amp would require or benefit from prolonged visits
6 Acute pain
7 Traumatic injuries
Operating Facilities amp Equipment
A positive pressure O2 delivery system capable of administering gt than 90 O2 at 10L min flow for 60 min (650L ldquoErdquo cylinder)
OR
Self inflating bag valve mask device (15L min)
A functional suction apparatus with appropriate suction catheters
Monitoring equipment - PO BPC PC or Capno
Inhalation sedation unit
100 O2 amp never less than 25
A fail safe mechanism that is checked and calibrated annually
Must have appropriate scavenging system
Emergency drugs
Techniques of sedation
Routes for drug administration
bull Oral
bull Rectal
bull Inhalational
bull Transmucosal
ndash Sublingual
ndash Intranasal
bull Parenteral
ndash IM
ndash sub mucosal
ndash IV
3
Oral Sedation
Advantages
1 Almost universally accepted and the easiest method
2 Decreased incidence and severity of adverse reaction
3 Low cost
Disadvantages
1 Absorption is variable
2 Prolonged latent period(30 min)
3 Reversal of any unwanted effect is also difficult
4 Inability to readily lighten or deepen the level of sedation
5 Prolonged duration of action
Rectal Sedation
Advantages 1 Incidence and intensity of
drug related side effects is minimized
2 Drug absorption occurs from the large intestine directly into the circulation
3 The lack of a needle syringe or other equipment
4 The ease of administration
5 The low cost
Disadvantages
1 Inconvenience to the administrator amp pt
2 The variable absorption of drugs from the large intestine
3 The slow onset of action amp the relatively long duration of action
4 Inability to titrate the drug dosage
5 The inability to reverse the action of the drug the prolonged recovery
Intranasal sedation
Advantages
Rapid onset (10 ndash 15 min)
Simple amp relatively painless
Less pt cooperation is required
Absorbed directly into the C V S
Intranasal sedation
Disadvantages
1 Dependence on nasal mucous membrane
2 Shorter duration of action(40-60min)
3 Multiple dosage may be necessary
Drugs
Midazolam ndash 02mgkg
Sufentanil ndash 15 ndash 3 mcgkg
Ketamine ndash 3-6mg kg
Sublingual sedation
Advantages
1 Pt acceptance
2 Rapid onset
3 High bioavailability
Drugs
Oral Transmucosal Fentanyl Citrate (OTFC)
Intramuscular Sedation
Advantages
1 More rapid onset of action
2 Absorbed directly into the C V system
3 More reliable absorption of drug
4 Pt cooperation is not as essential
Disadvantages
1 Time factor ndash its 15 min latent period
2 Pt may not be willing to accept the injection
3 The prolonged duration of action(2-4 hrs more)
4 Possibility of injury to the tissues at the site of injection caused by either the drug or the needle
4
Sites of I M administration
1 Gluteal area
2 Vastus lateralis
3 Mid ndash deltoid area
Drugs
Diazepam
Midazolam
Hydroxyzine
Inhalation Sedation
Advantages
1 The onset of action is more rapid
2 Peak clinical level is achieved rapidly(3-5min) - permit titration
3 Administrator has complete control over the actions of the drug - safety feature
4 No significant over dosage
5 Flexible duration of action
6 Recovery time is rapid amp most complete
7 No injection is required
8 With N2O- O2 it is safe with very few side effects
Disadvantages
1 The initial cost of the equipment is high 2 The continuing cost of the gases is high 3 The equipment occupies considerable space 4 N2O is not a potent agent 5 A degree of cooperation is required from the pt 6 Chronic exposure to N2O is deleterious to the health of
dental personnel
Contraindications
1 Nasal obstruction 2 Cyanosis at rest 3 Poor cooperation 4 1st trimester of pregnancy 5 Fear of masks
I V Sedation
Advantages
1 The onset of action is the most rapid 2 The dosage may be titrated 3 Suitable level of sedation can be provided 4 The recovery period is shorter 5 Side effects are extremely uncommon 6 Control of salivary secretions is possible 7 The gag reflex is diminished 8 Effectively diminishes motor disturbances 9 Provides immediate access to CVS in emergency
Disadvantages
1 Venipuncture is necessary
2 Complication may rise at the site of the venipuncture
3 Monitoring must be more intensive
4 Recovery is not complete at the end of the procedure
5 Reversal of sedation is difficult
5
N2O-O2 (Relative Analgesia)
colorless sweet smelling gas
Pharmacokinetics
Absorption through pulmonary epithelium
It is approx 15 times as soluble as is nitrogen It replaces nitrogen in blood
It is carried in solution in plasma of the blood
It is not metabolized by the body
Elimination ndash majorndash lungs minor --- skin
perspiration urine and intestinal gas
Pharmacodynamics
Dose related
10 ndash 25 Lightheaded
Changes in visual amp auditory sensation
Tingling of hands amp feet
Suffusing warmth
Remote from the immediate environment
Reduced anxiety
25-50 max analgesic properties and aberration of vision hearing and proprioception mild drowsiness euphoria amnesia and increased sleepiness and dreams
35 conc will achieve maximum analgesia
bull CNS
ndash Cerebrum-primarily affected
ndash Safe but weak anesthetic agent
bull RESPIRATORY SYSTEM
ndash Increased Tidal and minute volumes
bull CARDIOVASCULAR SYSTEM
ndash 2 studies ndash decreased cardiac output
bull FETAL SYSTEMS
ndash Miscarriage in humans
bull OTHER SYSTEMS
ndash Depression of spinal reflexes increase muscle tone indicates stage of delirium
ndash Muscle rigidity-narcotics + nitrous oxide
ndash Nausea and vomitting - GIT
ndash HEMATOPOIESIS ----- prolonged exposure
Adverse reactions and toxicity
EMOTIONAL REACTIONS
DREAMS HALLUCINATIONS
No acute toxicity
Chronic toxicity ndash bone marrow
depression
PROCEDURE
Diffusion Hypoxia
Sevoflurane
A fluorinated derivative of isopropyl ether ndash synthesized in 1970
Potent anaesthetic agent with rapid uptake amp speedy recovery
Day-case surgery
Problem
Attaching vaporiser to any of the currently available machine
BENZODIAZEPINES
Diazepam 1961 lipid soluble
Uses-alcoholism epilepsy labor tetanus and cerebral palsy
- sedation and amnesia
- varieties of neurosis amp anxiety states
Pharmacokinetics
Orally Rectal IMIV or SC
Well absorbed through GIT
Excretion in urine
6
bull Pharmacodynamics
ndash Depress the brain stem reticular system and the limbic system thalamus and hypothalamus
ndash It is a centrally acting muscle relaxant Has anti-convulsant properties
Adverse reaction amp toxicity
ndash Confusion nausea headache increased appetite decreased salivation and jaundice Thrombophlebitis
ndash Rebound phenomenon
ndash Toxicity drowsiness confusion sleep and coma
Dosage Oral or Rectal ndash 02-05mgkg
Maximum single dose 10mg
IV- 025mgkg
Supplied Tablets 2 5 10 mg
Suspension ndash 5mg
Midazolam Water soluble ndash non-irritant
Oral IM IV
Metabolism- liver
Onset IV 3 -5mins
oral 20 ndash 30mins
Oral administration anxious patients requiring relatively short dental procedure
No rebound phenomenon
Better anxiolysis amp amnesia (retrograde amnesia)
Adverse effects Respiratory depression
dose dependant apnea
Dosage Oral ndash 025 to 1mgkg to maximum single dose 20mg
IM ndash 01 to 015mgkg to a maximum of 10mg
IV ndash slow IV
Supplied Syrup ndash 2mgml
Injectable ndash 1mgml amp 5mgml vials
Flumazenil specific benzodiazepines antagonist
selectively inhibits CNS effects
IV administration amp not recommended below 18yrs of age
02mg over 15 seconds after 45seconds 02mg then after 60seconds to maximum of 1mg
Sedative-Hypnotics
Barbiturates First truly effective drugs for the management of anxiety Generalized CNS depressants Produce dose dependent effects
Sedation ---- sleep ---- GA ---- coma
Suppress the CNS and result in sedation and amnesia Advantages
Rapid onset and short duration Disadvantages
no analgesic effect and possible hypotension Must be used with caution in trauma patients because they may cause
apnea and hypoventilation
DOSE Pentobarbital Sodium 100mg Secobarbital Sodium 100 to 200mg Children 30 to 100mg
bull Chloral Hydrates (Mickey Finn Knock out drops ) First synthesized in 1832 first member of the hypnotic group of drugs
Widely used as conscious sedation agent
Properties
Unpleasant taste
Nausea vomiting
Quite irritating to skin and to mucous membranes
GI irritation
Dosages Individualized for each patient 25 ndash 50mgkg
maximum of 1g
Supplied oral capsule ndash 500mg
oral solution ndash 250 amp 500mg5ml
Rectal suppositories ndash 324 amp 648mg
Narcotics
Do produce sedation amp euphoria greater in children
LA is required but dose should be decreased
Meperidine Synthetic opiate agonist
Very water soluble
Orally SC IM or IV
Peak effect by oral 1 hr amp lasts upto 4 hrs
Adverse reactions
-Seizures
-Extreme caution in hepatic or renal diseases or history of seizures
7
Dosage Oral SC or IM ndash 1to 22mgkg not to exceed 100 mg
Supplied Oral Tablets ndash 50 amp 100mg
Oral Syrup ndash 50mgml
Parental solution ndash 25 50 75 amp 100mgml
Fentanyl
Synthetic opiate narcotic analgesic
Very potent 01mg = 10mg Morophine75mg Meperidine
Pharmacokinetics
IV IM SM
Metabolized in liver Excreted in urine
Fentanyl Onset ndash 7 to 15mins
Duration ndash 1 to 2 hrs
Pharmacodynamics
Respiratory depression RR but returns to normal rapidly Tidal volume amp response to co2 depressed for extended period
Apnea
Less emetic than meperidine
NOT RECOMMENDED IN CHILDREN BELOW 2yrs
Dosage 0002 to 0004mgkg
Supplied 005mgml in 2 amp 5ml ampoules
Reversal drug Naloxone
Semisynthetic opiate antagonist
No agonist activity
Onset 2 to 5mins SC or IM amp 1 to 2mins IV
Reversal 45mins
Pt should be kept under continual surveillance
Adverse reaction nausea vomiting sweating hypotension hypertension ventricular tachycardia fibrillation
Dosage IV SC IM 001mgkg then 01mgkg every 2- 3mins maximum 2mg
Supplied 002 004 1mg solutions
Antihistamines
Hydroxyzine
Oral or IM
Effect ndash 15 ndash 30mins
Half-life ndash 3 hrs
Uses
To relieve anxiety
Used as an anti-histamine
Used to control nausea and vomiting including that associated with motion sickness and pregnancy
Adverse reaction dry mouth drowsiness hypersentivity
Dosage Oral ndash 1 to 2mgkg
IM ndash 11mgkg
Promethazine Oral or IM Onset 15 to 60mins Duration 4 to 6 hrs Uses
To prevent and treat nausea and vomiting associated with motion pregnancy or surgery
Produces sedation and reduce swelling pain and trismus
Lower seizure threshold Adverse reaction dry mouth blurred vision thickening of bronchial secretions Dosage OralIM ndash 05-11mgkg
maximum 25 mg
Diphenhydramine
Oral IM IV
Onset -1hr
Duration ndash 4 to 6 hr
Metabolized in liver
Adverse reaction disturbed coordination thickening of bronchial secretions
Dosage Oral IM IV ndash 1 to 15mgkg
maximum 50mg
Tranquilizers
Major tranquilizer antipsychotic produce calmness control symptoms of psychoses cause reversible extra pyramidal symptoms and do not tend to cause habituation
Minor tranquilizer antianxiety agents also cause calmness do not cause extrapyramidal symptoms Used in conditions like nervous tension and mild depression
8
Classification
Antipsychotics
Phenothiazine derivatives
Chlorpromazine promazine
Butryophenones
Haloperidol
Rauwolfia alkaloids
Reserpine
Antianxiety drugs
Propyl alcohol derivatives
Meprobamate
Benzodiazepine derivatives
Diazepam
Miscellaneous compounds
Hydroxyzine
Meprobamate
White crystalline powder slightly bitter in taste
Only administered orally
Peak blood concentration ----1 to 3hrs
10 ---------excreted unchanged Rest --- excreted as a oxidized derivative or as a glucoronide
Uses
To relieve day time anxiety
Induce sleep in insomniacs
To reduce anxiety associated with dental treatment
Anti-convulsant ndash petit mal epilepsy
Adverse reaction leucopenia acute non-thrombocytopenic purpura ecchymoses eosinophilia edema adenopathy
Dosage Childrengt 6yrs 100 to 200mg
Not recommended for children under 6yrs
Monitoring during sedation
1 Pulse
2 Blood pressure
3 ECG
4 Respiration
5 Temperature
Pulse
Manual Electronic
bull Radial Brachial
bull Facial labial
Blood pressure
ndash Stethoscope amp sphygmomanometer
ndash Automatic devices
ndash Direct cannulation of an artery ndash very accurate
Electrocardiograph
Heart rate rhythm myocardial function
9
Respiration
ndash Monitoring respiratory rate
ndash Observing the rise amp fall of the chest wall
ndash Observing the color of mucous membrane
ndash Observing the inflation amp deflation of the reservoir bag
Devices for monitoring respiration
1 The Precordial pretracheal stethoscope
2 The esophageal stethoscope
ndash Respiratory rate
ndash Heart rate
ndash Any abnormal sounds
Pulse Oximeter
ndash Oxygen saturation
ndash Heart rate
ndash Oxisensor site
ndash Fingers
ndash Toe
ndash Ear lobe
Mechanism
Oxygenated Hb ndash red light
Deoxygenated Hb- infrared light
Tissue pressure from arterial pulse (plethysmography)
Advantages
ndash Safe amp noninvasive
ndash Simple to use
ndash Information is rapidly available for clinical decision
ndash Indirectly indicates respiratory adequacy
Disadvantages
ndash Finger probes can get dislodged
ndash Emitted light source may cause burning
ndash Non reusable probes are expensive
ndash Does not directly determine airway patency
Capnography
1 The presence absence of air flow
2 Indicates depth amp adequacy of respiration
3 Continues analysis of the co2 content of the respired air ndash indicates respiratory adequacy
Temperature
ndash Disposable nondisposable thermometer
ndash Esophageal rectal temp probe
10
Discharge criteria
Cardiovascular function is satisfactory amp stable
Airway patency is uncompromised amp satisfactory
Pt is easily arousable amp protective reflexes intact
State of hydration is adequate
Pt can talk if applicable
Pt can sit unaided if applicable
Pt can ambulate with minimal assistance if applicable
Presedation level of responsiveness achieved
Responsible individual is available
1
PULP THERAPY OF VITAL TEETH
DR MITAKSHARA NIRWAN
Contents
Indirect pulp capping
Direct pulp capping
Medications amp materials used in pulp capping
Pulpotomy
MTA
Apexogenesis
INDIRECT PULP CAPPING
Pieter Van Forest - first to speak about root canal therapy
Glove designed instruments that could prepare a canal to a certain size and taper(1910)
Indirect pulp capping is defined as a procedure where in small amount of carious dentin is retained in
deep areas of cavity to avoid exposure of pulp followed by placement of a suitable medicament and
restorative material that seals off the carious dentin and encourages pulp recovery (Ingle)
A procedure in which only the gross caries is removed from the lesion and the cavity is sealed for a
time with a biocompatible material (McDonald)
Objective of indirect pulp capping
These were given by Eidelman in 1965
bull Arresting the carious process
bull Promoting dentin sclerosis
bull Stimulating formation of tertiary dentin
bull Remineralization of carious dentin
Layers of Carious Dentin Indications of Indirect Pulp Capping
History
Mild pain associated with eating
Negative history of spontaneous extreme pain
Clinical Examination
Deep carious lesion which are close tobut not involving the pulp in vital primary or young
permanent teeth
No mobility
Nominal pulp inflammationdefinite layer of affected dentin after removal of infected dentin
Radiographic examination
Normal lamina dura amp PDL space
No radiolucency around the apices
2
Contraindications of Indirect Pulp Capping
History
Sharp penetrating pulpalgia
Prolonged spontaneous pain especially at night
Clinical examination
Mobility of tooth
Discoloration of tooth
Negative reaction of electric pulp testing
Radiographic examination
Definite pulp exposure
Break in the lamina dura
Radiolucency around the apices
Widened PDL space
Treatment procedure
Sequelae of Indirect Pulp Capping Three distinct types of new dentin formation take place
1 Cellular fibrillar dentinmdashfirst 2 months
2 Globular dentinmdash3 months
3 Tubular dentin (uniform mineralized dentin)
bull 15th of reparative dentin formation begins in less than 30 days
bull After 3 months 01 mm is formed
DIRECT PULP CAPPING Defined by Kopel (1992) as the placement of a medicament or non medicated material on a pulp that
has been exposed in course of excavating the last portions of deep dentinal caries or as a result of
trauma
Objective
To create new dentin in the area of the exposure and subsequent healing of the pulp
Rationale
achieve a biologic closure of the exposure site by deposition of hard tissue barrier (dentin bridge)
between pulp tissue and capping material thus walling off the
INDICATIONS
Small mechanical exposure
Easily controlled haemorrhage
Bright red haemorrhage
True pinpoint exposure
CONTRAINDICATIONS
Severe toothache at night
Spontaneous pain
Tooth mobility
Radiographic appearance of pulp periradicular de- generation
Excess of hemorrhage at the time of exposure Serous exudate from the exposure
Externalinternal root resorption
Swellingfistula
Histological Changes after Pulp Capping
These were illustrated be Glass and Zander in 1949
After 24 hours Necrotic zone adjacent to calcium
hydroxide paste is separated from healthy pulp
tissue by a deep staining basophilic layer
After 7 days Increase in cellular and fibroblastic
activity
After 14 days Partly calcified fibrous tissue lined by
odontoblastic cells is seen below the calcium
proteinate zone disappearance of necrotic zone
After 28 days Zone of new dentin
3
Medications and Materials Used for Pulp Capping Calcium hydroxide
Corticosteroids amp antibiotics
Inert materials
Collagen fibers
4-META adhesive
Direct bonding
Isobutyl cyanoacrylate
Denatured albumin
Mineral trioxide aggregate
Laser
Bone morphogenic protein
PULPOTOMY
Finn (1995) defined it as the complete removal of the coronal portion of the dental pulp
followed by placement of a suitable dressing or medicament that will promote healing and
preserve vitality of the tooth
American Academy of Pediatric Dentistry (1998) defined pulpotomy as the amputation of
affected infected coronal portion of the dental pulp preserving the vitality and function of the
remaining part of radicular pulp
Objectives
bull Removal of inflamed and infected coronal pulp at the site of exposure thus preserving the vitality of the
radicular pulp and allowing it to heal
bull Maintain the tooth in the dental arch
Rationale
bull Radicular pulp is healthy and capable of healing after surgical amputation of the infected coronal pulp
bull Preserves vitality of the radicular pulp
bull Maintains tooth in a physiologic condition
Indications of Pulpotomy bull Mechanical pulp exposure in primary teeth
bull Teeth showing a large carious lesion but free of radicular pulpitis
bull History of only spontaneous pain
bull Hemorrhage from exposure sites bright red and can be controlled
bull Absence of abscess or fistula
bull No interradicular bone loss
bull No interradicular radiolucency
Contraindications of Pulpotomy bull Persistent toothache
bull Tenderness on percussion
bull Root resorption more than 13rd of root length
bull Large carious lesion with nonrestorable crown
bull Highly viscous sluggish hemorrhage from canal orifice which is uncontrollable
bull Medical contradictions like heart disease immuno compromised patient
bull Swelling or fistula
bull External or internal resorption
bull Pathological mobility
bull Calcification of pulp
Classification of pulpotomy
4
Formocresol Pulpotomy
Iby BUCKLEY in 1904
Sweet (1930) Formulated multi visit technique
Doyle (1962) Advocated 2 sitting procedure (complete devitalization)
Spedding (1965) Gave 5 minute protocol (partial devitali- zation)
Venham (1967) Proposed 15 seconds procedure
Current concept uses 4 minutes of application time
Composition of formocresol Buckleyrsquos Formula
bull Cresol ndash 35 percent
bull Glycerol ndash 15 percent
bull Formaldehyde ndash 19 percent
bull Water ndash 31 percent
Mechanism of Action
It prevents tissue autolysis by bonding to the proteins Bonding is of peptide groups of side chain amino acids and is a reversible process accomplished without
changing the basic structure of protein molecules
Histological Changes
bull Demonstrated by Mass and Zilbermann11 in 1933 and also by Massler and Mansokhani in 1959
bull Immediately the pulp becomes fibrous and acidophillic
bull Seven to fourteen days Three zones appear
a broad eosinophilic zone of fixation
b broad pale-staining zone of atrophy with poorcellular definition
c broad zone of inflammation extending apically into normal pulp tissue
bull One yearndash Progressive apical movement of these zones with only acidophillic zone left at the end of 1 year
Modified Formocresol Pulpotomy
Used by TRASK(1972)
The technique is identical to that described for primary teeth except that the formocresol pellet is
sealed permanently in the tooth
Two-visit Devitalization Pulpotomy
Indications
bull There is evidence of sluggish bleeding at the amputation site that is difficult to control
bull Pus in the chamber but none at the amputation site
bull There is thickening of the PDL
bull History of pain
Contraindications
bull Nonrestorable tooth
bull Tooth with necrotic pulp
5
Glutaraldehyde Pulpotomy
It was first suggested by S Gravenmade Introduced by Kopel in 1979
Mechanism of Action
bull Glutaraldehyde produces rapid surface fixation of the underlying pulpal tissue
bull A narrow zone of eosinophilic stained and compressed fixed tissue is found directly beneath the area of application which blends into vital normal appearing tissue apically
bull With time the glutaraldehyde fixed zone is replaced by macrophagic action with dense collagenous tissue thus the entire root canal tissue is vital
Cvekrsquos Pulpotomy
bull This is also called as calcium hydroxide pulpotomy or young permanent partial pulpotomy
bull This was proposed by Mejare and Cvek16 in 1978
bull Indicated in young permanent teeth where the pulp is exposed by mechanical or bacterial means and the
remaining radicular tissue is judged vital by clinical and radiographic criteria whereas the root closure is
notcomplete
MINERAL TRIOXIDE AGGREGATE (MTA) Torabinejad described the physical and chemical properties of MTA in 1995
It is ash colored powder made primarily of fine hydrophilic particles of
1 tricalcium aluminate
2 tricalcium silicate
3 silicate oxide
4 tricalcium oxide
5 bismuth dioxide
Hydration of the powder results in a colloidal gel composed of calcium oxide crystals in an amorphous
structure This gel solidifies into a hard structure in less than three hours
PROPERTIES OF MTA
It is biocompatible material and its sealing ability is better than that of amalgam or ZOE
Initial pH is 102 and set pH is 125
The setting time of cement is 4 hours
The compressive strength is 70 MPA which is comparable with that of IRM
Low cytotoxicity ndash It presents with minimal inflammation if extended beyond the apex
Mineral trioxide aggregate (MTA) has demonstrated the ability to induce hard-tissue formation in
pulpal tissues and it promotes rapid cell growth
APEXOGENESIS
It is defined as the treatment of a vital pulp by capping or pulpotomy in order to permit continued
growth of the root and closure of the open apex
Rationale
Maintenance of integrity of the radicular pulp tissue to allow for continued root growth
Indications
bull Indicated for traumatized or pulpally involved vital permanent tooth when root apex is incompletely formed
bull No history of spontaneous pain
bull No sensitivity on percussion
bull No hemorrhage
bull Normal radiographic appearance
Contraindications
bull Evidence that radicular pulp has undergone degenerative changes
bull Purulent drainage
bull History of prolonged pain bull Necrotic debris in canal
bull Periapical radiolucency
6
1
Gupta A Dhingra R Chaudhari P Gupta A
Department of Paedodontics and Preventive Dentistry Faculty of Dental Sciences SGT University Gurgaon Haryana India
Journal of Indian Society of Pedodontics and Preventive Dentistry
Volume 35 I Issue 3 I July-September 2017
A COMPARISION OF VARIOUS MINIMALLY
INVASIVE TECHNIQUES FOR THE REMOVAL
OF DENTAL FLUOROSIS STAINS IN
CHILDREN
DR MITAKSHARA NIRWAN
CONTENTS
bull Introduction
bull Aims
bull Materials and Methods
bull Results
bull Discussion
bull Conclusion
bull Critical analysis
bull References
INTRODUCTION
bull Dental fluorosis is a developmental disturbance of dental enamel caused by
successive exposure to high concentrations of fluoride during tooth
development
bull Various methods of therapy are advocated for the treatment of fluorosis -
stained teeth which range from invasive ceramic veneer bonding restorations
to abrasive chemical treatments
bull The combination of dental bleaching techniques and microabrasion appears
as an excellent conservative solution to reestablish health in fluorosis
affected teeth
AIMS
bull The aim of the study was to evaluate and compare the effectiveness of
minimally invasive techniques for the removal of dental fluorosis
stains in children in vivo
MATERIALS AND METHODS
Patients visiting the department of Pedodontics and Preventive dentistry
Faculty of Dental Sciences SGT University Gurgaon
bull Sample size 90 patients
bull Age group 10 -17 years
bull Caries cracks or periodontal
disease on anterior teeth
bull Abscess draining sinus
cellulitis
bull Non vital teeth
hypersensitive exposed
crevices
bull Orthodontic appliance
bull Past history of bleaching
bull At least two permanent
maxillary anterior teeth
bull TSIF of score 4
bull Free of systemic diseases
Inclusion criteria Exclusion criteria
2
Groups
Group A In office bleaching with 35 hydrogen peroxide( Pola Office
Bleaching kit) activated by light emitting diode (LED) bleaching unit
(35 HP)
Group B Enamel microabrasion (EM) (PREMA Enamel Microabrasion
System) followed by in-office bleaching with 44 carbamide peroxide
gel (EM)
Group C In-office bleaching with 5 sodium hypochlorite (5
NaOCl)
A baseline colour evaluation was done by taking digital photograph of
the maxillary anterior teeth
RESULTS
Group 1
Colour stability
Group 2 Group 3
Tooth sensitivity
Tooth sensitivity values were taken before the treatment
which was compared to immediate postoperative and follow
up visits It was checked using an electric pulp tester
maximum
moderate
least
immediately
group 2
group 1
group 3
1 month
group 2
group 1
group 3
3 month
group 2
group 1
group 3
Patient satisfaction score
Satisfaction was assessed on visual analog scale
Range 1 to 5
Groups percentage of patients
who were satisfied with
the treatment
Number of patients
who reported slight
reappearance of colour
Group 1
90
7
Group 2
83
8
Group 3
73
7
3
Number of Appointments
Groups One sitting Two sittings Three
sittings
Group 1
25
4
1
group 2
26
3
1
Group 3
30
0
0
DISCUSSION
bull Hydrogen peroxide is capable of penetrating the tooth osmosis and through porosities and cracks subsequently acting directly on the pigmented molecules
bull Gurgan et al investigated 3 different light systems and found out that diode laser system with gave best tooth whitening and least tooth sensitivity
bull In the EM group the surface reflects and refracts light from the surface in such way that mild imperfections in underlying enamel are camouflaged While the highly polished surface of enamel enhances the aesthetic appearance
bull Train et al and Loguercio et al also had the similar results in their studies with EM mild fluorosis showed best results moderate showed moderate results while it had little effect on severe fluorosis
bull NaOCl was only effective on mild stains while moderate and severe
stains could only be lightened to quite an extent but could not be
completely removed
bull When NaOCl comes in contact with hypomineralized and discoloured
enamel it degrades and removes the chromogenic organic material
located on the enamel surface
CONCLUSION
bull It was concluded that esthetic appearance of teeth mild fluorosis can
be achieved by bleaching and microabrasion But in cases of
moderate fluorosis a combination of any of theses modalities can be
used
bull As no special maintenance precautions are required these maybe be
considered as an interesting alternative to conventional operative
treatment
bull Focuses on only TSIF of 4
bull Electric pulp testing is not the
right method to check for
sensitivity
bull Tooth Sensitivity changes
from person to person
bull Food habits can cause
staining of the teeth
bull Minimally invasive
bull Cheaper to veneers
bull Minimal loss of tooth structure
bull 4 parameters checked for the success of treatment
bull Inclusion of specific score of fluorosis for comparing the results
bull Maximum 3 appointments needed
CRITICAL ANALYSIS
Pros Cons
REFERENCES
bull Gurgan S Cakir FY Yazici E Different light-activated in officebleaching
systems Lasers Med Sci 201025817-22
bull Train TE McWhorter AG Seale NSWilson CF Guo IY Examination of
esthetic improvement and surface alteration following microabrasion in
fluorotic human incisors in vivoPediatr dent 199618353-62
bull Loguercio AD Correia LD Zago C Tagliari D Neumann E Gomes OM et al
Clinical effectiveness of two microabrasion materials materials for the
removal of enamel flurosis stains Oper Dent 200732531-8
4
1
Morankar Rahul Aditi Kapur Krishan Gauba Ashima Goyal
MANAGEMENT OF ENDODONTIC INSTRUMENT SEPARATION IN
PRIMARY TEETH
CASE REPORT
Journal of South Asian Association of Pediatric Dentistry 2020
DR MITAKSHARA NIRWAN
bull Introduction
bull Aims amp Objectives
bull Case report
bull Discussion
bull Conclusion
bull Pros amp Cons
bull References
CONTENTS
Separation of endodontic instrument is an unexpected complication and its prevalence is not known It is a common belief among the dental professionals that rotary nickelndashtitanium (NiTi) instruments separate more frequently than stainless steel hand instruments
However literature revealed that in permanent teeth the reported prevalence of separated endodontics manual instruments is in the range of 07-74 whereas for rotary NiTI instruments it is
approximately 04-5
Fractured root canal instruments may include endodontic files Gates Glidden burs finger spreaders
and paste fillers
INTRODUCTION
The aim of this study is to describe the management strategies for endodontic
instrument separation in a root canal of primary teeth with emphasis on factors
requiring consideration in different clinical situations
AIMS amp OBJECTIVES
CASE 1
A 6-year-old male child reported with the chief complaint of spontaneous toothache in mandibular left second primary molar since few days It has aggravated following dental treatment at a private dental clinic Clinical examination revealed an underprepared access cavity with 75 and incomplete caries removal
which was sealed with glass ionomer cement
An intraoral periapical radiograph revealed a separated instrument of about 6ndash7 mm size in the distal root
2
The separated instrument was lodged firmly in distobuccal root canal 2ndash3 mm below the cementoenamel junction The instrument was bypassed successfully with no 15 and no 20 H-files but attempts for its retrieval were not successful
GatesndashGlidden (GG) drills no 2 (07 mm) and no 3 (09 mm) were used to drill around the instrument after which it was retrieved successfully using no 25 H-file
All the canals were instrumented till size 30 k-file followed by obturation with metapex and restoration with glass ionomer cement amp followed by placement of a crown and loop space maintainer for missing 74 The instrument retrieved was a manual reamer measuring 6 mm in length
The patient was asymptomatic since then and is under regular follow-up
CASE 2
A 5-year-old female child reported with the chief complaint of spontaneous toothache in mandibular left second
primary molar Clinical examination revealed deep occlusal caries with fractured lingual wall and pain on
percussion An intraoral periapical radiograph revealed caries involving pulp without any furcation or periapical
area of rarefaction and pulpectomy was planned
All the canals were enlarged using NiTi rotary files with a 4 taper operating at 500 rpm with minimum torque
setting An orifice opener [(0825 19 mm) of 8 taper size 25 length 19 mm] and nos 0420 file was used for
instrumentation of root canal This was followed by file nos 0425 which got separated in the distobuccal root
canal The radiograph confirmed a separated instrument of length 3ndash4 mm in the middle third of the root canal
The instrument was bypassed with no 15 k-file but could not get retrieved As instrument separation had occurred with 0425 file the involved root canal was sufficiently debrided before separation and the level of instrument separation was at the mid-root region so it was decided to obturate and seal this tooth with
periodic follow-ups instead of immediate extraction All other canals were enlarged till size 0430 in the sequential manner followed by obturation using metapex and placement of stainless steel crown
3
CASE 3
A 5-year-old female child has complaint of mild intermittent pain with primary mandibular left first molar She
had undergone pulpectomy treatment for the same during which an instrument separation has occurred in
the mesiobuccal root canal by a resident doctor
A radiograph revealed a separated instrument of about 4 mm in size lodged in the apical third but within the
confines of the mesial root An attempt was made for its retrieval but was unsuccessful The extraction of the
involved tooth was carried out under local anesthesia followed by a band and loop space maintainer
CASE 4
A 7-year-old male child reported with a chief complaint of mild intermittent pain on food lodgment with the primary mandibular right first and second molars The patient had a history of dental treatment at a private
dental clinic few months back which he did not continue further
Clinical examination revealed glass ionomer restoration with 85 and proximal caries with 84 leading to food lodgment An intraoral periapical radiograph with 85 revealed empty root canals with a separated
instrument of about 3ndash4 mm size beyond the apex of mesial root close to the developing succedaneous premolar
4
DISCUSSION
Stainless steel files usually separate fracture due to the excessive amounts of torque and overuse or the
preexisting distortion of the instrument whereas in NiTi rotary files it is a combined result of torsional stress and cyclic fatigue
Therapeutic options for the management of separated endodontic instruments include no intervention nonsurgical (orthograde conservative) management surgical management and tooth extraction
Use of ultrasonic scaler Masserann technique Endo extractor and Cavi-Endo ultrasonic instruments are some of the methods popular for retrieval of a separated endodontic instrument in the permanent tooth
In case 1 a 6-mm-long manual reamer was retrieved successfully with the use of GG drill using a manual file and copious irrigation which is the most desired treatment outcome
In case 2 the retrieval of separated rotary file lodged in the middle third of the root canal was unsuccessful in spite of multiple attempts It was therefore managed with routine obturation followed by restoration to maintain the tooth in its physiological functional state It was kept under close periodic follow-up at least
every 3 months This treatment option should be encouraged where it is possible to follow up the patient clinically and radiographically at close periodic intervals as there is the possibility of instrument escaping
into bone due to physiological root resorption
In cases 3 and 4 an instrument has separated in the apical root portion
In case 3 it was within the root canal and thus an attempt was made for its retrieval which was
unsuccessful It was therefore extracted to prevent the fractured instrument from getting exposed in the bone following resorption as there is no accurate and consistent established age for initiation of resorption in primary teeth known per se
In case 4 an immediate extraction of involved tooth was carried out as the separated instrument was beyond the apex of the primary tooth root
Age of the child clinical signs and symptoms and amount of root resorption are the factors which can also influence the management of separated instrument in primary teeth
Moreover if an instrument has separated after initial cleaning and shaping of root canal maintaining a tooth is not a problem as clinical signs and symptoms are not anticipated and the good prognosis is expected
However if an instrument has separated early during the initial cleaning and shaping of the root canal clinical symptoms may compromise the prognosis
Therefore these factors should be kept in mind while planning a suitable management strategy to avoid or at least reduce the burden of extraction and wear of space maintainer for longer period
5
CONCLUSION
The management and prognosis of a primary tooth with a separated instrument is
dependent on the level of instrument fracture within the root age of the child root
resorption and clinical signs and symptoms of the involved tooth
Different management approaches can be tried depending on clinical situations keeping
in mind benefits vs risks in preserving the tooth
PROS amp CONS
PROS
The entire procedure is given
by step by step
Well descriptive xrays and
photographs
CONS
Medical history has not been
given
REFERENCES
1 TOMER ANIL K ET AL ldquoBROKEN FILE RETRIEVAL PUZZLE IN ENDODONTICSrdquo
(2016)
2 SHENOY A MANDAVA P BOLLA N ET AL A NOVEL TECHNIQUE FOR REMOVAL OF
BROKEN INSTRUMENT FROM ROOT CANAL IN MANDIBULAR SECOND MOLAR
INDIAN J DENT RES 201425(1)107ndash110
3 PATEL J MORAWALA A TALATHI R ET AL RETRIEVAL OF A BROKEN INSTRUMENT
FROM ROOT CANAL IN PRIMARY ANTERIOR TEETH UNIV RES J DENT 20155(3)203ndash
206
4 MORANKAR R GOYAL A GAUBA K ET AL MANUAL VERSUS ROTARY
INSTRUMENTATION FOR PRIMARY MOLAR PULPECTOMIES - A 24 MONTHS
RANDOMIZED CLINICAL TRIAL PEDIAT DENT J 201828(2)96ndash102
5 KASHYAP NILOTPOL (2018) RETAINING PRIMARY MOLARS WITH INSTRUMENT
SEPERATION A CASE REPORT AND CLINICAL GUIDE
6
1
IMPACT OF 6 CITRIC ACID AND ENDOACTIVATOR AS IRRIGATION ADJUNCTS ON OBTURATION QUALITY AND PULPECTOMY OUTCOME IN
PRIMARY TEETH
NEETU JAIN SHALINI GARG ABHISHEK DHINDSA SAKSHI JOSHI HARJOY
KHATRIA
PEDIATRIC DENTAL JOURNAL 2019 29
1
DR MITAKSHARA NIRWAN
CONTENTS
bull INTRODUCTION
bull AIMS amp OBJECTIVES
bull CASE REPORT
bull RESULTS
bull DISCUSSION
bull CONCLUSION
bull PROS AND CONS
bull REFERENCES
2
INTRODUCTION
bull ENDODONTIC THERAPY IN PRIMARY TEETH INVOLVES DISINFECTION OF THE ROOT CANAL
SYSTEM AND ITS OBTURATION WITH RESORBABLE PASTE
bull THE CONTENTS OF ROOT CANAL ALONG WITH SMEAR LAYER ARE EXPECTED TO BE REMOVED
DURING THE BIOMECHANICAL PREPARATION
bull IN VITRO AND CLINICAL DOCUMENTS HAVE INDICATED THAT MECHANICAL PREPARATION OF
THE CANAL LEAVES LARGE PORTIONS OF THE CANAL WALLS UNDEBRIDED AND COMPLETE
REMOVAL OF THE BACTERIA BY THIS MECHANICAL PROCEDURE ALONE IS UNLIKELY TO BE SEEN
THEREFORE SOME FORM OF DISINFECTIONIRRIGATION IS MANDATORY TO KILL THE
MICROORGANISMS AND TO REMOVE THE RESIDUAL TISSUES
3
bull THE IDEAL REQUISITES OF A ROOT CANAL IRRIGANT AS GIVEN BY ZEHNDER ARE
1 BROAD ANTIMICROBIAL SPECTRUM
2 HIGH EFFICACY AGAINST ANAEROBIC AND FACULTATIVE MICROORGANISMS ORGANIZED
IN BIOFILMS
3 ABILITY TO DISSOLVE NECROTIC PULP TISSUE REMNANTS
4 ABILITY TO INACTIVATE ENDOTOXIN
5 ABILITY TO PREVENT THE FORMATION OF A SMEAR LAYER DURING INSTRUMENTATION OR
TO DISSOLVE THE LATTER ONCE IT HAS FORMED
6 SYSTEMICALLY NONTOXIC WHEN THEY COME IN CONTACT WITH VITAL TISSUES
NONCAUSTIC TO PERIODONTAL TISSUES AND WITH LITTLE POTENTIAL TO CAUSE AN
ANAPHYLACTIC REACTION
SINCE NO SINGLE IRRIGANT HAS THESE OPTIMAL PROPERTIES STUDIES HAVE REPORTED THE USE
OF TWO OR MORE SOLUTIONS IN A SPECIFIC SEQUENCE OR IN COMBINATIONS FOR BETTER
RESULTS 4
bull SEVERAL IRRIGATING SOLUTIONS ALONG WITH CHELATING AGENTS HAVE BEEN USED
DURING BIOMECHANICAL PREPARATION OF ROOT CANAL BOTH IN PRIMARY AND
PERMANENT TEETH
bull HOWEVER NONE OF THE AVAILABLE IRRIGATING SOLUTIONS HAS BEEN REGARDED CLEARLY
AS OPTIMAL SOLUTION BECAUSE OF THEIR LIMITED EFFECTIVENESS ESPECIALLY IN APICAL
13RD OF THE ROOT CANAL SYSTEM
bull TO OVERCOME SUCH LIMITATIONS USE OF ENDOACTIVATOR HAS BEEN PROPOSED AS AN
IRRIGATION FACILITATOR THAT IS BASED ON SONIC VIBRATION (UP TO 10000 CPM) WHICH
FACILITATES THE IRRIGANT PENETRATION AND ITS RENEWAL WITHIN THE CANAL
bull ACTIVATION SYSTEMS RESULTED IN BETTER REMOVAL OF THE SMEAR LAYER IN THE APICAL
THIRD OF ROOT CANALS IN COMPARISON TO CONVENTIONAL IRRIGATION
5
CITRIC ACID
bull CITRIC ACID IS A WEAK ORGANIC ACID WITH THE APPEARANCE OF WHITE CRYSTALLINE
POWDER AT ROOM TEMPERATURE
bull IT CAN EXIST EITHER IN WATER-FREE FORM (ANHYDROUS) OR MONOHYDRATE FORM THE
WATER-FREE FORM CRYSTALLIZES FROM THE HOT WATER WHEREAS THE MONOHYDRATE
FORMS FROM THE COLD WATER THE LATTER MAY BE CONVERTED TO ANHYDROUS FORM BY
HEATING MORE THAN 78degC
bull CITRIC ACID OCCURS NATURALLY IN THE BODY IN MITOCHONDRIA AND IS USED BY BLOOD
BANKS TO PREVENT COAGULATION OF TRANSFUSED BLOOD CITRIC ACID IS ALSO ESSENTIAL
TO HUMAN METABOLISM AND IS FOUND IN MANY FOODS
6
2
bull THE BIOLOGICAL EFFECTS OF CITRIC ACID ON THE PERIODONTAL STRUCTURE HAS BEEN
EXTENSIVELY STUDIED IN PERIODONTICS
bull NEUMAN AND NEWMAN SHOWED THAT CITRIC ACID IS THE MOST EFFECTIVE ACID IN
ALTERING THE SOLUBILITY OF HYDROXYAPATITE
bull YAMAGUCHI ET AL SHOWED THAT CITRIC ACID SOLUTION HAD ANTIBACTERIAL EFFECTS ON
ALL 12 ROOT CANAL BACTERIA TESTED
bull ARIAS-MOLIZ ET AL SHOWED THAT ETHYLENEDIAMINETETRAACETIC ACID (EDTA) HAS NO
BACTERICIDAL ACTIVITY EVEN AFTER 1 HOUR CONTACT
bull THIS ACID HAS THE ABILITY OF ROOT CANAL IRRIGATION AND ALSO SMEAR LAYER REMOVAL
DIFFERENT CONCENTRATIONS (1ndash50) HAVE BEEN PROPOSED GUTMANN ET AL CONCLUDED
THAT 10 CITRIC ACID IS BETTER THAN ULTRASOUND FOR SMEAR LAYER REMOVAL FROM THE
ROOT END CAVITIES
7
bull STUDIES HAVE SHOWN IRRIGATION WITH 6 CA FOR 15 OR 30 SECONDS IS QUITE
EFFECTIVE IN REMOVING ALL THE COMPONENTS OF THE SMEAR LAYER OF THE PRIMARY
TEETH WHEREAS PERITUBULAR DENTIN DESTRUCTION WAS OBSERVED WHEN HIGHER
CONCENTRATION OF CITRIC ACID WAS USED AS AN IRRIGATING SOLUTION
8
AIMS amp OBJECTIVES
bull THIS STUDY WAS AIMED TO EVALUATE THE CLINICAL AND RADIOGRAPHIC OUTCOME OF
PULPECTOMY ALONG WITH QUALITY OF OBTURATION USING 6 CITRIC ACID AND
ENDOACTIVATOR
9
CASE REPORT
bull 350 CHILDREN (3-9 YEARS) WITH CLINICAL SIGNS AND SYMPTOMS OF CHRONIC IRREVERSIBLE
PULPITIS IN DEEPLY CARIOUS TEETH WERE SCREENED DURING SCHOOL DENTAL HEALTH
PROGRAM FROM MAY 2014-JULY 2014
bull 123 CHILDREN REPORTED TO THE DEPARTMENT AND 67 CHILDREN WERE SELECTED BASED ON
INCLUSION AND EXCLUSION CRITERIA
RECRUITMENT OF PATIENTS
10
INCLUSION CRITERIA
bull HISTORY OF SPONTANEOUS PAIN AND UNCONTROLLED BLEEDING AFTER PULP AMPUTATION
EXCLUSION CRITERIA
bull EVIDENCE OF INTERNAL OR EXTERNAL (PHYSIOLOGICPATHOLOGIC) ROOT RESORPTION OF MORE THAN A THIRD OF ITS LENGTH
bull ROOT CANAL OBLITERATION OR ANATOMIC ANOMALIES
bull INADEQUATE BONE SUPPORT OR NON RESTORABLE TOOTH
bull ONCE PATIENTS ELIGIBILITY WAS CONFIRMED THE TREATMENT PROCEDURE WAS
EXPLAINED TO THE PARENTGUARDIAN AND INFORMED WRITTEN CONSENT WAS
OBTAINED FROM PARENTSGUARDIANS SHOWING WILLINGNESS FOR THEIR
CHILDRENS TREATMENT 11
PROCEDURE
bull PULPECTOMY WAS PERFORMED BY ONE OPERATOR OF PEDIATRIC DENTISTRY DEPARTMENT
USING A STANDARDIZED TREATMENT PROTOCOL FOR ALL THE PATIENTS
bull AFTER ADMINISTRATION OF LOCAL ANESTHESIA RUBBER DAM WAS APPLIED FOR ISOLATION
bull ACCESS CAVITY WAS PREPARED USING AIR-ROTOR HAND PIECE WITH 8 ROUND BUR AND
PULP TISSUE WAS EXTIRPATED WITH THE HELP OF SPOON EXCAVATOR
bull FURTHER THE NEGOTIATION OF THE CANALS WAS DONE WITH 10 K-FILE
bull A DIAGNOSTIC RADIOGRAPH WAS TAKEN FOR ROOT LENGTH DETERMINATION AND
WORKING LENGTH WAS KEPT 1 MM SHORT OF THE RADIOGRAPHICAL APEX
bull ALL ROOT CANALS WERE INSTRUMENTED MANUALLY USING K-FILES AND WERE IRRIGATED
WITH 10 ML 09 NORMAL SALINE AND 1 SODIUM HYPOCHLORITE AS STANDARDIZING
PROTOCOL FOR ROOT CANAL PREPARATION AND DISINFECTION
12
3
GROUP 1 (CA + E) - IRRIGATION WAS DONE
WITH 10 ML OF 6 CITRIC ACID (CITOCID AMMDENT)
AND IRRIGANTS WERE SONICALLY AGITATED WITH
ENDOACTIVATOR (DENTSPLY) FOR 30 S PER CANAL USING REDBLUE
ENDOACTIVATOR TIP
GROUP 2 (CA) - 10 ML OF 6 CITRIC ACID FOR 1 MIN USING
27 GAUZE IRRIGATING NEEDLE
GROUP 3(SH + E) - 10 ML OF 1 SODIUM HYPOCHLORITE
SOLUTION AND SONIC ACTIVATION WITH ENDOACTIVATOR
GROUP 4(SH) - 10 ML OF 1 SODIUM HYPOCHLORITE
SOLUTION USING IRRIGATING NEEDLE (CONTROL GROUP)
bull TEETH UNDERGOING PULPECTOMY WERE RANDOMLY ENROLLED BY CHIT METHOD INTO THREE
STUDY AND ONE CONTROL GROUP
13
bull IN CITRIC ACID GROUPS FINAL RINSE WITH NORMAL SALINE WAS DONE TO REMOVE THE
REMAINING CRYSTALS (CHELATES)
bull FOLLOWING BIOMECHANICAL PREPARATION THE ROOT CANALS WERE DRIED WITH STERILE
ABSORBENT PAPER POINTS AND OBTURATED WITH VITAPEX USING HAND HELD
LENTULOSPIRAL FINAL RESTORATIONS WERE DONE USING COMPOSITE RESIN
14
bull CLINICAL FOLLOW UP WAS DONE AT 24 H1 WEEK 1 MONTH 6 MONTH AND 12
MONTH TO CHECK PAIN PRESENCE AND PAIN FREQUENCY (ONCEMORE THAN ONCE)
SWELLING FISTULA SENSITIVITY TO PERCUSSION
bull RADIOGRAPHIC FOLLOW UP WAS DONE AT 6 MONTH AND 12 MONTH FOR ANY
DEVIATED ERUPTION OF SUCCEDANEOUS TEETH EXCESS FILING MATERIAL AND ITS
RESORPTION EXTERNALINTERNAL ROOT RESORBTION CALCIFIC METAMORPHOSIS
PRESENCE OF FURCATION RADIOLUCENCY
CLINICAL amp RADIOGRAPHIC FOLLOW UP
15
RADIOGRAPHIC ASSESSMENT OF OBTURATION QUALITY
bull POSTOPERATIVE RADIOGRAPHS WERE VISUALLY ASSESSED FOR QUALITY OF OBTURATION BY
TWO INDEPENDENT EXAMINERS (SG AD) WHO WERE BLINDED WITH REGARD TO
IRRIGATION PROTOCOL GROUP TO ENHANCE CALIBRATION EACH EXAMINER ASSESSED THE
RADIOGRAPH INDEPENDENTLY AND LATER REVIEWED TOGETHER FOR FINAL ASSESSMENT
INDIVIDUAL ROOT WAS TAKEN AS UNIT OF ANALYSIS FOR GRADE OF OBTU- RATION AND
SCORING CRITERIA WERE AS GIVEN BY COLL JA 1996
1 UNDER FILLED - FILLING MATERIAL ENDED 1 MM OR MORE SHORT OF THE APEX
2 OPTIMAL FILLING- FILLING MATERIAL APPEARED TO END AT THE RADIOGRAPHICAL APEX
3 OVERFILLED - FILLING MATERIAL EXTRUDED PAST THE RADIOGRAPHIC APEX
4 OPTIMALLY FILLED ROOTS WERE FURTHER ASSESSED FOR THE PRESENCE OF VOIDS AND VOID
AREA (ROOT CANAL SURFACE UNTOUCHED BY THE ROOT CANAL FILLING MATERIAL) IN THREE
VISUALLY DIVIDED SECTIONS OF THE ROOT IE CORONAL MIDDLE AND APICAL 13RD
16
RESULTS
bull OVERALL CLINICAL AND RADIOGRAPHIC SUCCESS RATE OVER A PERIOD OF ONE YEAR WAS
9886 amp 977 RESPECTIVELY
bull ALL GROUPS WERE SIGNIFICANTLY (P = 001) EFFECTIVE IN ALLEVIATING PAIN WITHIN 24 H
OF PULPECTOMY
17 18
4
19
bull IMMEDIATE POST OPERATIVE RADIOGRAPHIC ASSESSMENT REVEALED 68 (102150) ROOTS
WITH OPTIMAL OBTURATION AND 32 (48150) WITH OVERFILLINGUNDERFILLING MAXIMUM
NO OF OPTIMAL FILLINGS WERE OBSERVED IN GROUP1 (CA + E) (3333) FOLLOWED BY
GROUP 2 (CA) (2549) GROUP 3(SH + E) (2549) AND GROUP 4(SH) (1568)
bull CITRIC ACID GROUPS HAD MORE NUMBER OF OPTIMALLY FILLED ROOTS 588 (60102) THAN
NON CITRIC ACID GROUPS 412 (42102)
bull ENDOACTIVATOR CONTRIBUTED TO 18 OF OPTIMAL OBTURATION IRRESPECTIVE OF
CHELATING AGENT USED
20
21
bull MAXIMUM NO OF VOIDS AND VOID AREAS WERE IN NON CITRIC ACID GROUPS
(6419 amp 5384) COMPARED TO CITRIC ACID GROUPS (3580 amp 4615)
RESPECTIVELY
bull ANALYSIS OF ROOT 13RD REVEALED MAXIMUM NO OF VOID AREA IN APICAL
13RD (4755) FOLLOWED BY MIDDLE 13RD (3846) AND CORONAL 13RD
(1398)
bull LEAST NO OF VOIDS amp VOID AREA (1111 amp 1608) WERE OBSERVED WHEN
ENDOACTIVATOR ALONG WITH CHELATING AGENT WAS USED (GROUP 1)
HOWEVER THIS WAS STATISTICALLY INSIGNIFICANT
22
DISCUSSION
bull IN THE PRESENT STUDY 1 SODIUM HYPOCHLORITE WAS USED ALONG WITH 6 CITRIC ACID
(CHELATING AGENT) WHICH IS REPORTED TO BE AS EFFECTIVE AS 17 EDTA
bull CITRIC ACID (BIOLOGICAL ACID) IS FOUND TO BE BIOCOMPATIBLE AND LEAST IRRITATING TO
PERIAPICAL TISSUES THAN OTHER CHELATING AGENTS
bull USE OF SODIUM HYPOCHLORITE SOLUTION FOLLOWING CHELATING AGENT WAS AVOIDED AS IT
RAPIDLY PRODUCES SEVERE EROSION OF ROOT CANAL WALL DENTIN
bull TRADITIONAL APPROACH OF DELIVERING IRRIGANTS INTO THE ROOT CANAL SPACE USING
SYRINGES AND METAL NEEDLES HAS BEEN FOUND TO BE INEFFECTIVE ESPECIALLY IN THE AREAS OF
ANASTOMOSES BETWEEN CANALS AND APICAL 13RD OF ROOT CANAL
23
bull THEREFORE TO ACHIEVE BETTER CLEANING EFFICIENCY IRRIGANT ACTIVATION HAS BEEN
RECOMMENDED SONIC ACTIVATION HAS BEEN REPORTED TO RESULT IN BETTER ROOT CANAL
CLEANLINESS AS COMPARED TO NO ACTIVATION OF IRRIGANT
24
5
CONCLUSION
bull USE OF 6 CITRIC ACID DEFINITELY HELPED IN RAPID ELIMINATION OF PAIN RESOLUTION OF
PERI-RADICULAR RADIOLUCENCY BETTER OBTURATION QUALITY IN TERMS OF LESS VOIDS AND
VOID AREAS ALONG WITH MAXIMUM NO OF OPTIMAL OBTURATION UP TO APICAL AREA
bull 6 CITRIC ACID AND ENDOACTIVATOR IRRIGATION PROTOCOL PROVED TO BE THE BETTER
IRRIGATION PROTOCOL WHICH MAY CONTRIBUTE TO LONG TERM SUCCESS OF PRIMARY
TOOTH AND THE HEALTH OF UNDERLYING PERMANENT TOOTH
bull 6 CITRIC ACID ALONG WITH ENDOACTIVATOR MAY BE RECOMMENDED AS IRRIGATION
ADJUNCTS IN PULPECTOMY PROCEDURE OF PRIMARY TEETH
25
PROS AND CONS
PROS
bull PROPER EXPLANATION OF THE MATERIALS
USED
CONS
bull NO PREOPERATIVE AND POSTOPERATIVE
RADIOGRAPHS
26
REFERENCES
bull RAMACHANDRA JA NIHAL NK NAGARATHNA C VORA MS ROOT CANAL IRRIGANTS IN
PRIMARY TEETH WORLD J DENT 20156(3)229-234
bull MOHAMMADI Z JAFARZADEH H SHALAVI S KINOSHITA JI UNUSUAL ROOT CANAL
IRRIGATION SOLUTIONS J CONTEMP DENT PRACT 201718(5)415-420
bull ZEHNDER M ROOT CANAL IRRIGANTS J ENDOD 2006 32389- 98
bull SMITH JJ amp WAYMAN BE AN EVALUATION OF THE ANTIMICROBIAL EFFECTIVENESS OF
CITRIC ACID AS A ROOT CANAL IRRIGANT JOURNAL OF ENDODONTICS 1986 12(2) 54-58
bull TANNURE PN AZEVEDO CP BARCELOS R GLEISER R PRIMO LG LONG-TERM OUTCOMES OF
PRIMARY TOOTH PULPECTOMY WITH AND WITHOUT SMEAR LAYER REMOVAL A RANDOMIZED
SPLIT-MOUTH CLINICAL TRIAL PEDIATR DENT 201133316E20 27
bull CARON G NHAM K BRONNEC F MACHTOU P EFFECTIVENESS OF DIFFERENT FINAL IRRIGANT
ACTIVATION PROTOCOLS ON SMEAR LAYER REMOVAL IN CURVED CANALS J ENDOD
2010361361E6
bull COLL JA SADRIAN R PREDICTING PULPECTOMY SUCCESS AND ITS RELATIONSHIP TO
EXFOLIATION AND SUCCEDANEOUS DENTITION PEDIATR DENT 19961857E63
28
1
LOCAL
ANESTHESIA
DR MITAKSHARA NIRWAN
CONTENTS
Definition
Methods of inducing local anesthesia
Desirable properties
Electrophysiology of nerve conduction
Impulse propagation and spread
Mode and site of action of local anesthesia
Classification of local anesthetic according to biological site and mode of action
Dissociation of local anaesthetics
Mechanism of action of local anaethetics
Local anaesthetic agent
2
3
DEFINITION
Local anesthesia is defined as a loss of sensation in
a circumscribed area of the body caused by depression
of excitation in nerve endings or an inhibition of the
conduction process in peripheral nerves
An important feature of local anesthesia is that it produces
LOSS OF SENSATION WITHOUT INDUCING LOSS OF
CONSCIOUSNESS
4
METHODS OF INDUCING LOCAL
ANESTHESIA
Low temperature
Mechanical trauma
Anoxia
Neurolytic agents such as alcohol amp phenol
Chemical agents such as local anesthetics
PROPERTIES OF LOCAL
ANESTHESIA
It should not be irritating to tissue to which it is applied
It should not cause any permanent alteration of nerve structure
Its systemic toxicity should be low
Time of onset of anesthesia should be short
It should be effective regardless of whether it is injected into the tissue or applied locally to mucous membranes
The duration of action should be long enough to permit the completion of procedure
5 6
It should have the potency sufficient to give complete
anesthesia with out the use of harmful concentration solutions
It should be free from producing allergic reactions
It should be free in solution and relatively undergo
biotransformation in the body
It should be either sterile or be capable of being sterilized by
heat with out deterioration
2
ELETROPHYSIOLOGY OF
NERVE CONDUCTION
There is an electrical charge across the membrane
This is the membrane potential
The resting potential (when the cell is not firing) is a negative
electrical potential of -70mv that exists across the nerve
membrane produced by different concentrations of either side of
the membrane
The interior of nerve is NEGATIVE in relation to exterior
7 8
inside
outside
Resting potential of neuron = -70mV
+
-
+
-
+
-
+
-
+
-
SLOW DEPOLARIRIZATION
9
RAPID DEPOLARIZATION
The interior of nerve is POSITIVE in relation to exterior
REPOLARIZATION
10
bull Repolarization takes 07 msec
bull Depolarization takes 03 msec
SODIUM PUMP -
energy comes from the oxidative metabolism of ATP
bull The entire process require 1 msec
IMPULSE PROPOGATION
IMPULSE SPREAD
The propagated impulse travels along the nerve
membrane towards CNS The spread of impulse differs
in myelinated and unmyelinated nerve fibers
DEPOLARIZED SEGMENT ADJACENT RESTING AREA
MODE AND SITE OF ACTION OF LOCAL
ANESTHETICS
Local anesthetic agent interferes with excitation
process in a nerve membrane in one of the
following ways
Altering the basic resting potential of nerve
membrane
Altering the threshold potential
Decreasing the rate of depolarization
Prolonging the rate of repolarization
12
3
CLASSIFICATION OF LOCAL ANESTHETIC
SUBSTANCES ACCORDING TO
BIOLOGICAL SITE AND MODE OF ACTION
CLASS A
Agents acting at receptor site on external surface of nerve membrane
Chemical substance Biotoxins (eg tetrodotoxin and saxitoxin)
CLASS B
Agents acting on receptor sites on internal surface of nerve membrane
Chemical substance Quaternary ammonium analogues of lidocaine
scorpion venom 13
CLASS C Agents acting by receptor independent of
physiochemical mechanism
Chemical substance Benzocaine
CLASS D Agents acting by combination of receptors and
receptor independent mechanisms
Chemical substance most clinically useful anesthetic agents
(eg lidocaine mepivacaine prilocaine)
14
BASED ON THE SOURCE
NATUAL
SYNTHETIC
OTHERS
BASED ON MODE OF APPLICATION
bull INJECTABLE
bull TOPICAL
BASED ON DURATION OF ACTION
bull ULTRA SHORT
bull SHORT
bull MEDIEM
bull LONG
BASED ON ONSET OF ACTION SHORT
INTERMEDIATE
LONG
15
DISSOCIATION OF LOCAL
ANESTHETICS
Local anesthetics are available as salts (usually
hydrochlorides) for clinical use
The salts both water soluble and stable is dissolved in
either sterile water or saline
In this solution it exists simultaneously as unchanged
molecule (RN) also called base and positively charged
molecules (RNH+) called cations
RNH+ ==== RN+ H
+
16
The relative concentration of each ionic form in the solution varies
in the pH of the solution or surrounding tissue
In the presence of high concentration of hydrogen ion (low pH) the
equilibrium shifts to left and most of the anesthetic solution exists
in cationic form
RNH+ gt RN
+ + H
+
As hydrogen ion concentration decreases (higher pH) the
equilibrium shifts towards the free base form
RNH+ lt RN + H
+
17
The relative proportion of ionic form also depends on pKa or DISSOCIATION CONSTANT of the specific local anesthetic
The pKa is a measure of molecules affinity for H+
ions
When the pH of the solution has the same value as pKa of the local anesthetic exactly half the drug will exists in the RNH
+ form and
exactly half in RN form
The percentage of drug existing in either form can be determined by Henderson Hasselbalch equation
Log baseacid = pH - pKa
18
4
MECHANISM OF ACTION OF LOCAL
ANESTHETICS
The following sequence is proposed mechanism of action of LA
Displacement of calcium ions from the sodium channel receptor site
Binding of local anesthetic molecule to this receptor site
Blockade of sodium channel
19
Decrease in sodium conductance
Depression of rate of electrical depolarization
Failure to achieve the threshold potential level
Lack of development of propagated action potential
Conduction blockadehellip
20
21
Na + Na +
22
LOCAL ANESTHETIC AGENT
COMERCIALLY PREPARED LOCAL ANESTHESIA
CONSISTS OF
Local anesthetic agent (xylocaine lignocaine 2)
Vasoconstrictor (adrenaline 1 80000)
Reducing agent (sodium metabisulphite)
Preservative (methylparabencapryl
hydrocuprienotoxin)
Fungicide (thymol)
Vehicle (distillde waterNaCl)
LOCAL ANESTHETIC AGENT
The local anesthetics used in dentistry are divided
into two groups
ESTER GROUP
AMIDE GROUP
23 24
ESTER GROUP It is composed of the following
An aromatic lipophilic group
An intermediate chain containing
an ester linkage
A hydrophilic secondary or tertiary
amino group
AMIDE GROUP It is composed of the following
An aromatic lipophilic group
An intermediate chain containing
amide linkage
A hydrophilic secondary or tertiary
amino group
5
25
CLASSIFICATION OF LOCAL ANESTHETICS
ESTERS
Esters of benzoic acid
Butacaine
Cocaine
Benzocaine
Hexylcaine
Piperocaine
Tetracaine
Esters of Para-amino
benzoic acid
Chloroprocain
Procaine
Propoxycaine
26
AMIDES Articaine
Bupivacaine
Dibucaine
Etidocaine
Lidocaine
Mepivacaine
Prilocaine
Ropivacaine
QUINOLINE
Centbucridine
PHARMACOKINETICS OF LOCAL
ANESTHETICS UPTAKE
When injected into soft tissue most local anesthetics produce
dilation of vascular bed
Cocaine is the only local anesthetic that produces
vasoconstriction initially it produces vasodilation which is
followed by prolonged vasoconstriction
Vasodilation is due to increase in the rate of absorption of the
local anesthetic into the blood thus decreasing the duration of
pain control while increasing the anesthetic blood level and
potential for over dose 27
AMIDE LOCAL ANESTHETICS
The metabolism of amide local anesthetics is more
complicated then esters The primary site of
biotransformation of amide drugs is liver
Entire metabolic process occurs in the liver for lidocaine
articaine etidocaine and bupivacaine
Prilocaine undergoes more rapid biotransformation then the
other amides
28
REFERENCES
Handbook of local anesthesia ndash Stanley F Malamed ndash 6th
edition
Essentials of Local Anesthetic Pharmacology Daniel E
Becker Anesth Prog 2006 Fall 53(3) 98ndash109
WIKIPEDIEA
29
THANK YOU
30
1
Pharmacological Methods of Behavior
Management
DR MITAKSHARA NIRWAN
DEFINITIONS
bull Conscious Sedation ndash A minimally depressed level of consciousness that retains
the patients ability to independently and continuously maintain an airway and respond appropriately to physical stimulation or verbal command
(American Dental Association House Of Delegates 2000)
bull Deep Sedation ndash An induced state of depressed consciousness
accompanied by partial loss of protective reflexes including the inability to continuously maintain an airway independently and or to respond purposefully to physical stimulation or verbal command
bull General Anesthesia (G A) ndash An induced state of unconsciousness or complete loss of
protective reflexes including the inability to continually maintain an airway independently and respond purposefully to physical stimulation or verbal command
Conscious sedation
ADVANTAGES
Conscious
Protective reflexes active amp intact
Stable vital signs
Operating dentist may perform sedation
Minimum amount of equipment required
Prolong detainment in recovery room not required
Risk of complication very low
Excellent choice for poor ndash risk pt in dental office
Cost effective
General anesthesia
ADVANTAGES Not absolutely
essential May be the only
method Not necessary (no
pain reaction) Amnesia always
present
Conscious sedation
DISADVANTAGES
Pt cooperation is essential
Extremely difficult or mentally handicapped pt cannot always be managed
Use of local anesthesia is a must
Amnesia may or may not be present
General anesthesia DISADVANTAGES
Pt unconscious
Protective reflexes are depressed
Depressed
Advanced training required Dentist must not act also as anesthetist
Special equipment necessary
Detainment in recovery area necessary
High IOP amp postoperative complications
Not indicated in dental office
More expensive
Fundamental Concepts
bull Techniques that utilize drugs to induce co-operative yet conscious state in an otherwise uncooperative child ndash CONSCIOUS SEDATION
2
GOALS
1 To facilitate the provision of quality care
2 To minimize the extremes of disruptive behavior
3 To promote a positive psychologic response to treatment
4 To promote patient welfare amp safety
5 To return the patient to physiologic state
OBJECTIVES
1 The pt mood must be altered
2 The pt must remain conscious at all times
3 The pt must be cooperative
4 All protective reflexes must remain intact and active
5 Vital signs must remain stable and with in normal limits
6 The ptrsquos pain threshold should be elevated
7 Amnesia may be present
Indications
1 Preschool children
2 Lack of Psychological Emotional maturity
3 Lack of Cognitive Physical Medical disability
4 Fearful amp anxious pts
5 Pt who require extensive amp complicated dental care amp would require or benefit from prolonged visits
6 Acute pain
7 Traumatic injuries
Operating Facilities amp Equipment
A positive pressure O2 delivery system capable of administering gt than 90 O2 at 10L min flow for 60 min (650L ldquoErdquo cylinder)
OR
Self inflating bag valve mask device (15L min)
A functional suction apparatus with appropriate suction catheters
Monitoring equipment - PO BPC PC or Capno
Inhalation sedation unit
100 O2 amp never less than 25
A fail safe mechanism that is checked and calibrated annually
Must have appropriate scavenging system
Emergency drugs
Techniques of sedation
Routes for drug administration
bull Oral
bull Rectal
bull Inhalational
bull Transmucosal
ndash Sublingual
ndash Intranasal
bull Parenteral
ndash IM
ndash sub mucosal
ndash IV
3
Oral Sedation
Advantages
1 Almost universally accepted and the easiest method
2 Decreased incidence and severity of adverse reaction
3 Low cost
Disadvantages
1 Absorption is variable
2 Prolonged latent period(30 min)
3 Reversal of any unwanted effect is also difficult
4 Inability to readily lighten or deepen the level of sedation
5 Prolonged duration of action
Rectal Sedation
Advantages 1 Incidence and intensity of
drug related side effects is minimized
2 Drug absorption occurs from the large intestine directly into the circulation
3 The lack of a needle syringe or other equipment
4 The ease of administration
5 The low cost
Disadvantages
1 Inconvenience to the administrator amp pt
2 The variable absorption of drugs from the large intestine
3 The slow onset of action amp the relatively long duration of action
4 Inability to titrate the drug dosage
5 The inability to reverse the action of the drug the prolonged recovery
Intranasal sedation
Advantages
Rapid onset (10 ndash 15 min)
Simple amp relatively painless
Less pt cooperation is required
Absorbed directly into the C V S
Intranasal sedation
Disadvantages
1 Dependence on nasal mucous membrane
2 Shorter duration of action(40-60min)
3 Multiple dosage may be necessary
Drugs
Midazolam ndash 02mgkg
Sufentanil ndash 15 ndash 3 mcgkg
Ketamine ndash 3-6mg kg
Sublingual sedation
Advantages
1 Pt acceptance
2 Rapid onset
3 High bioavailability
Drugs
Oral Transmucosal Fentanyl Citrate (OTFC)
Intramuscular Sedation
Advantages
1 More rapid onset of action
2 Absorbed directly into the C V system
3 More reliable absorption of drug
4 Pt cooperation is not as essential
Disadvantages
1 Time factor ndash its 15 min latent period
2 Pt may not be willing to accept the injection
3 The prolonged duration of action(2-4 hrs more)
4 Possibility of injury to the tissues at the site of injection caused by either the drug or the needle
4
Sites of I M administration
1 Gluteal area
2 Vastus lateralis
3 Mid ndash deltoid area
Drugs
Diazepam
Midazolam
Hydroxyzine
Inhalation Sedation
Advantages
1 The onset of action is more rapid
2 Peak clinical level is achieved rapidly(3-5min) - permit titration
3 Administrator has complete control over the actions of the drug - safety feature
4 No significant over dosage
5 Flexible duration of action
6 Recovery time is rapid amp most complete
7 No injection is required
8 With N2O- O2 it is safe with very few side effects
Disadvantages
1 The initial cost of the equipment is high 2 The continuing cost of the gases is high 3 The equipment occupies considerable space 4 N2O is not a potent agent 5 A degree of cooperation is required from the pt 6 Chronic exposure to N2O is deleterious to the health of
dental personnel
Contraindications
1 Nasal obstruction 2 Cyanosis at rest 3 Poor cooperation 4 1st trimester of pregnancy 5 Fear of masks
I V Sedation
Advantages
1 The onset of action is the most rapid 2 The dosage may be titrated 3 Suitable level of sedation can be provided 4 The recovery period is shorter 5 Side effects are extremely uncommon 6 Control of salivary secretions is possible 7 The gag reflex is diminished 8 Effectively diminishes motor disturbances 9 Provides immediate access to CVS in emergency
Disadvantages
1 Venipuncture is necessary
2 Complication may rise at the site of the venipuncture
3 Monitoring must be more intensive
4 Recovery is not complete at the end of the procedure
5 Reversal of sedation is difficult
5
N2O-O2 (Relative Analgesia)
colorless sweet smelling gas
Pharmacokinetics
Absorption through pulmonary epithelium
It is approx 15 times as soluble as is nitrogen It replaces nitrogen in blood
It is carried in solution in plasma of the blood
It is not metabolized by the body
Elimination ndash majorndash lungs minor --- skin
perspiration urine and intestinal gas
Pharmacodynamics
Dose related
10 ndash 25 Lightheaded
Changes in visual amp auditory sensation
Tingling of hands amp feet
Suffusing warmth
Remote from the immediate environment
Reduced anxiety
25-50 max analgesic properties and aberration of vision hearing and proprioception mild drowsiness euphoria amnesia and increased sleepiness and dreams
35 conc will achieve maximum analgesia
bull CNS
ndash Cerebrum-primarily affected
ndash Safe but weak anesthetic agent
bull RESPIRATORY SYSTEM
ndash Increased Tidal and minute volumes
bull CARDIOVASCULAR SYSTEM
ndash 2 studies ndash decreased cardiac output
bull FETAL SYSTEMS
ndash Miscarriage in humans
bull OTHER SYSTEMS
ndash Depression of spinal reflexes increase muscle tone indicates stage of delirium
ndash Muscle rigidity-narcotics + nitrous oxide
ndash Nausea and vomitting - GIT
ndash HEMATOPOIESIS ----- prolonged exposure
Adverse reactions and toxicity
EMOTIONAL REACTIONS
DREAMS HALLUCINATIONS
No acute toxicity
Chronic toxicity ndash bone marrow
depression
PROCEDURE
Diffusion Hypoxia
Sevoflurane
A fluorinated derivative of isopropyl ether ndash synthesized in 1970
Potent anaesthetic agent with rapid uptake amp speedy recovery
Day-case surgery
Problem
Attaching vaporiser to any of the currently available machine
BENZODIAZEPINES
Diazepam 1961 lipid soluble
Uses-alcoholism epilepsy labor tetanus and cerebral palsy
- sedation and amnesia
- varieties of neurosis amp anxiety states
Pharmacokinetics
Orally Rectal IMIV or SC
Well absorbed through GIT
Excretion in urine
6
bull Pharmacodynamics
ndash Depress the brain stem reticular system and the limbic system thalamus and hypothalamus
ndash It is a centrally acting muscle relaxant Has anti-convulsant properties
Adverse reaction amp toxicity
ndash Confusion nausea headache increased appetite decreased salivation and jaundice Thrombophlebitis
ndash Rebound phenomenon
ndash Toxicity drowsiness confusion sleep and coma
Dosage Oral or Rectal ndash 02-05mgkg
Maximum single dose 10mg
IV- 025mgkg
Supplied Tablets 2 5 10 mg
Suspension ndash 5mg
Midazolam Water soluble ndash non-irritant
Oral IM IV
Metabolism- liver
Onset IV 3 -5mins
oral 20 ndash 30mins
Oral administration anxious patients requiring relatively short dental procedure
No rebound phenomenon
Better anxiolysis amp amnesia (retrograde amnesia)
Adverse effects Respiratory depression
dose dependant apnea
Dosage Oral ndash 025 to 1mgkg to maximum single dose 20mg
IM ndash 01 to 015mgkg to a maximum of 10mg
IV ndash slow IV
Supplied Syrup ndash 2mgml
Injectable ndash 1mgml amp 5mgml vials
Flumazenil specific benzodiazepines antagonist
selectively inhibits CNS effects
IV administration amp not recommended below 18yrs of age
02mg over 15 seconds after 45seconds 02mg then after 60seconds to maximum of 1mg
Sedative-Hypnotics
Barbiturates First truly effective drugs for the management of anxiety Generalized CNS depressants Produce dose dependent effects
Sedation ---- sleep ---- GA ---- coma
Suppress the CNS and result in sedation and amnesia Advantages
Rapid onset and short duration Disadvantages
no analgesic effect and possible hypotension Must be used with caution in trauma patients because they may cause
apnea and hypoventilation
DOSE Pentobarbital Sodium 100mg Secobarbital Sodium 100 to 200mg Children 30 to 100mg
bull Chloral Hydrates (Mickey Finn Knock out drops ) First synthesized in 1832 first member of the hypnotic group of drugs
Widely used as conscious sedation agent
Properties
Unpleasant taste
Nausea vomiting
Quite irritating to skin and to mucous membranes
GI irritation
Dosages Individualized for each patient 25 ndash 50mgkg
maximum of 1g
Supplied oral capsule ndash 500mg
oral solution ndash 250 amp 500mg5ml
Rectal suppositories ndash 324 amp 648mg
Narcotics
Do produce sedation amp euphoria greater in children
LA is required but dose should be decreased
Meperidine Synthetic opiate agonist
Very water soluble
Orally SC IM or IV
Peak effect by oral 1 hr amp lasts upto 4 hrs
Adverse reactions
-Seizures
-Extreme caution in hepatic or renal diseases or history of seizures
7
Dosage Oral SC or IM ndash 1to 22mgkg not to exceed 100 mg
Supplied Oral Tablets ndash 50 amp 100mg
Oral Syrup ndash 50mgml
Parental solution ndash 25 50 75 amp 100mgml
Fentanyl
Synthetic opiate narcotic analgesic
Very potent 01mg = 10mg Morophine75mg Meperidine
Pharmacokinetics
IV IM SM
Metabolized in liver Excreted in urine
Fentanyl Onset ndash 7 to 15mins
Duration ndash 1 to 2 hrs
Pharmacodynamics
Respiratory depression RR but returns to normal rapidly Tidal volume amp response to co2 depressed for extended period
Apnea
Less emetic than meperidine
NOT RECOMMENDED IN CHILDREN BELOW 2yrs
Dosage 0002 to 0004mgkg
Supplied 005mgml in 2 amp 5ml ampoules
Reversal drug Naloxone
Semisynthetic opiate antagonist
No agonist activity
Onset 2 to 5mins SC or IM amp 1 to 2mins IV
Reversal 45mins
Pt should be kept under continual surveillance
Adverse reaction nausea vomiting sweating hypotension hypertension ventricular tachycardia fibrillation
Dosage IV SC IM 001mgkg then 01mgkg every 2- 3mins maximum 2mg
Supplied 002 004 1mg solutions
Antihistamines
Hydroxyzine
Oral or IM
Effect ndash 15 ndash 30mins
Half-life ndash 3 hrs
Uses
To relieve anxiety
Used as an anti-histamine
Used to control nausea and vomiting including that associated with motion sickness and pregnancy
Adverse reaction dry mouth drowsiness hypersentivity
Dosage Oral ndash 1 to 2mgkg
IM ndash 11mgkg
Promethazine Oral or IM Onset 15 to 60mins Duration 4 to 6 hrs Uses
To prevent and treat nausea and vomiting associated with motion pregnancy or surgery
Produces sedation and reduce swelling pain and trismus
Lower seizure threshold Adverse reaction dry mouth blurred vision thickening of bronchial secretions Dosage OralIM ndash 05-11mgkg
maximum 25 mg
Diphenhydramine
Oral IM IV
Onset -1hr
Duration ndash 4 to 6 hr
Metabolized in liver
Adverse reaction disturbed coordination thickening of bronchial secretions
Dosage Oral IM IV ndash 1 to 15mgkg
maximum 50mg
Tranquilizers
Major tranquilizer antipsychotic produce calmness control symptoms of psychoses cause reversible extra pyramidal symptoms and do not tend to cause habituation
Minor tranquilizer antianxiety agents also cause calmness do not cause extrapyramidal symptoms Used in conditions like nervous tension and mild depression
8
Classification
Antipsychotics
Phenothiazine derivatives
Chlorpromazine promazine
Butryophenones
Haloperidol
Rauwolfia alkaloids
Reserpine
Antianxiety drugs
Propyl alcohol derivatives
Meprobamate
Benzodiazepine derivatives
Diazepam
Miscellaneous compounds
Hydroxyzine
Meprobamate
White crystalline powder slightly bitter in taste
Only administered orally
Peak blood concentration ----1 to 3hrs
10 ---------excreted unchanged Rest --- excreted as a oxidized derivative or as a glucoronide
Uses
To relieve day time anxiety
Induce sleep in insomniacs
To reduce anxiety associated with dental treatment
Anti-convulsant ndash petit mal epilepsy
Adverse reaction leucopenia acute non-thrombocytopenic purpura ecchymoses eosinophilia edema adenopathy
Dosage Childrengt 6yrs 100 to 200mg
Not recommended for children under 6yrs
Monitoring during sedation
1 Pulse
2 Blood pressure
3 ECG
4 Respiration
5 Temperature
Pulse
Manual Electronic
bull Radial Brachial
bull Facial labial
Blood pressure
ndash Stethoscope amp sphygmomanometer
ndash Automatic devices
ndash Direct cannulation of an artery ndash very accurate
Electrocardiograph
Heart rate rhythm myocardial function
9
Respiration
ndash Monitoring respiratory rate
ndash Observing the rise amp fall of the chest wall
ndash Observing the color of mucous membrane
ndash Observing the inflation amp deflation of the reservoir bag
Devices for monitoring respiration
1 The Precordial pretracheal stethoscope
2 The esophageal stethoscope
ndash Respiratory rate
ndash Heart rate
ndash Any abnormal sounds
Pulse Oximeter
ndash Oxygen saturation
ndash Heart rate
ndash Oxisensor site
ndash Fingers
ndash Toe
ndash Ear lobe
Mechanism
Oxygenated Hb ndash red light
Deoxygenated Hb- infrared light
Tissue pressure from arterial pulse (plethysmography)
Advantages
ndash Safe amp noninvasive
ndash Simple to use
ndash Information is rapidly available for clinical decision
ndash Indirectly indicates respiratory adequacy
Disadvantages
ndash Finger probes can get dislodged
ndash Emitted light source may cause burning
ndash Non reusable probes are expensive
ndash Does not directly determine airway patency
Capnography
1 The presence absence of air flow
2 Indicates depth amp adequacy of respiration
3 Continues analysis of the co2 content of the respired air ndash indicates respiratory adequacy
Temperature
ndash Disposable nondisposable thermometer
ndash Esophageal rectal temp probe
10
Discharge criteria
Cardiovascular function is satisfactory amp stable
Airway patency is uncompromised amp satisfactory
Pt is easily arousable amp protective reflexes intact
State of hydration is adequate
Pt can talk if applicable
Pt can sit unaided if applicable
Pt can ambulate with minimal assistance if applicable
Presedation level of responsiveness achieved
Responsible individual is available
1
PULP THERAPY OF VITAL TEETH
DR MITAKSHARA NIRWAN
Contents
Indirect pulp capping
Direct pulp capping
Medications amp materials used in pulp capping
Pulpotomy
MTA
Apexogenesis
INDIRECT PULP CAPPING
Pieter Van Forest - first to speak about root canal therapy
Glove designed instruments that could prepare a canal to a certain size and taper(1910)
Indirect pulp capping is defined as a procedure where in small amount of carious dentin is retained in
deep areas of cavity to avoid exposure of pulp followed by placement of a suitable medicament and
restorative material that seals off the carious dentin and encourages pulp recovery (Ingle)
A procedure in which only the gross caries is removed from the lesion and the cavity is sealed for a
time with a biocompatible material (McDonald)
Objective of indirect pulp capping
These were given by Eidelman in 1965
bull Arresting the carious process
bull Promoting dentin sclerosis
bull Stimulating formation of tertiary dentin
bull Remineralization of carious dentin
Layers of Carious Dentin Indications of Indirect Pulp Capping
History
Mild pain associated with eating
Negative history of spontaneous extreme pain
Clinical Examination
Deep carious lesion which are close tobut not involving the pulp in vital primary or young
permanent teeth
No mobility
Nominal pulp inflammationdefinite layer of affected dentin after removal of infected dentin
Radiographic examination
Normal lamina dura amp PDL space
No radiolucency around the apices
2
Contraindications of Indirect Pulp Capping
History
Sharp penetrating pulpalgia
Prolonged spontaneous pain especially at night
Clinical examination
Mobility of tooth
Discoloration of tooth
Negative reaction of electric pulp testing
Radiographic examination
Definite pulp exposure
Break in the lamina dura
Radiolucency around the apices
Widened PDL space
Treatment procedure
Sequelae of Indirect Pulp Capping Three distinct types of new dentin formation take place
1 Cellular fibrillar dentinmdashfirst 2 months
2 Globular dentinmdash3 months
3 Tubular dentin (uniform mineralized dentin)
bull 15th of reparative dentin formation begins in less than 30 days
bull After 3 months 01 mm is formed
DIRECT PULP CAPPING Defined by Kopel (1992) as the placement of a medicament or non medicated material on a pulp that
has been exposed in course of excavating the last portions of deep dentinal caries or as a result of
trauma
Objective
To create new dentin in the area of the exposure and subsequent healing of the pulp
Rationale
achieve a biologic closure of the exposure site by deposition of hard tissue barrier (dentin bridge)
between pulp tissue and capping material thus walling off the
INDICATIONS
Small mechanical exposure
Easily controlled haemorrhage
Bright red haemorrhage
True pinpoint exposure
CONTRAINDICATIONS
Severe toothache at night
Spontaneous pain
Tooth mobility
Radiographic appearance of pulp periradicular de- generation
Excess of hemorrhage at the time of exposure Serous exudate from the exposure
Externalinternal root resorption
Swellingfistula
Histological Changes after Pulp Capping
These were illustrated be Glass and Zander in 1949
After 24 hours Necrotic zone adjacent to calcium
hydroxide paste is separated from healthy pulp
tissue by a deep staining basophilic layer
After 7 days Increase in cellular and fibroblastic
activity
After 14 days Partly calcified fibrous tissue lined by
odontoblastic cells is seen below the calcium
proteinate zone disappearance of necrotic zone
After 28 days Zone of new dentin
3
Medications and Materials Used for Pulp Capping Calcium hydroxide
Corticosteroids amp antibiotics
Inert materials
Collagen fibers
4-META adhesive
Direct bonding
Isobutyl cyanoacrylate
Denatured albumin
Mineral trioxide aggregate
Laser
Bone morphogenic protein
PULPOTOMY
Finn (1995) defined it as the complete removal of the coronal portion of the dental pulp
followed by placement of a suitable dressing or medicament that will promote healing and
preserve vitality of the tooth
American Academy of Pediatric Dentistry (1998) defined pulpotomy as the amputation of
affected infected coronal portion of the dental pulp preserving the vitality and function of the
remaining part of radicular pulp
Objectives
bull Removal of inflamed and infected coronal pulp at the site of exposure thus preserving the vitality of the
radicular pulp and allowing it to heal
bull Maintain the tooth in the dental arch
Rationale
bull Radicular pulp is healthy and capable of healing after surgical amputation of the infected coronal pulp
bull Preserves vitality of the radicular pulp
bull Maintains tooth in a physiologic condition
Indications of Pulpotomy bull Mechanical pulp exposure in primary teeth
bull Teeth showing a large carious lesion but free of radicular pulpitis
bull History of only spontaneous pain
bull Hemorrhage from exposure sites bright red and can be controlled
bull Absence of abscess or fistula
bull No interradicular bone loss
bull No interradicular radiolucency
Contraindications of Pulpotomy bull Persistent toothache
bull Tenderness on percussion
bull Root resorption more than 13rd of root length
bull Large carious lesion with nonrestorable crown
bull Highly viscous sluggish hemorrhage from canal orifice which is uncontrollable
bull Medical contradictions like heart disease immuno compromised patient
bull Swelling or fistula
bull External or internal resorption
bull Pathological mobility
bull Calcification of pulp
Classification of pulpotomy
4
Formocresol Pulpotomy
Iby BUCKLEY in 1904
Sweet (1930) Formulated multi visit technique
Doyle (1962) Advocated 2 sitting procedure (complete devitalization)
Spedding (1965) Gave 5 minute protocol (partial devitali- zation)
Venham (1967) Proposed 15 seconds procedure
Current concept uses 4 minutes of application time
Composition of formocresol Buckleyrsquos Formula
bull Cresol ndash 35 percent
bull Glycerol ndash 15 percent
bull Formaldehyde ndash 19 percent
bull Water ndash 31 percent
Mechanism of Action
It prevents tissue autolysis by bonding to the proteins Bonding is of peptide groups of side chain amino acids and is a reversible process accomplished without
changing the basic structure of protein molecules
Histological Changes
bull Demonstrated by Mass and Zilbermann11 in 1933 and also by Massler and Mansokhani in 1959
bull Immediately the pulp becomes fibrous and acidophillic
bull Seven to fourteen days Three zones appear
a broad eosinophilic zone of fixation
b broad pale-staining zone of atrophy with poorcellular definition
c broad zone of inflammation extending apically into normal pulp tissue
bull One yearndash Progressive apical movement of these zones with only acidophillic zone left at the end of 1 year
Modified Formocresol Pulpotomy
Used by TRASK(1972)
The technique is identical to that described for primary teeth except that the formocresol pellet is
sealed permanently in the tooth
Two-visit Devitalization Pulpotomy
Indications
bull There is evidence of sluggish bleeding at the amputation site that is difficult to control
bull Pus in the chamber but none at the amputation site
bull There is thickening of the PDL
bull History of pain
Contraindications
bull Nonrestorable tooth
bull Tooth with necrotic pulp
5
Glutaraldehyde Pulpotomy
It was first suggested by S Gravenmade Introduced by Kopel in 1979
Mechanism of Action
bull Glutaraldehyde produces rapid surface fixation of the underlying pulpal tissue
bull A narrow zone of eosinophilic stained and compressed fixed tissue is found directly beneath the area of application which blends into vital normal appearing tissue apically
bull With time the glutaraldehyde fixed zone is replaced by macrophagic action with dense collagenous tissue thus the entire root canal tissue is vital
Cvekrsquos Pulpotomy
bull This is also called as calcium hydroxide pulpotomy or young permanent partial pulpotomy
bull This was proposed by Mejare and Cvek16 in 1978
bull Indicated in young permanent teeth where the pulp is exposed by mechanical or bacterial means and the
remaining radicular tissue is judged vital by clinical and radiographic criteria whereas the root closure is
notcomplete
MINERAL TRIOXIDE AGGREGATE (MTA) Torabinejad described the physical and chemical properties of MTA in 1995
It is ash colored powder made primarily of fine hydrophilic particles of
1 tricalcium aluminate
2 tricalcium silicate
3 silicate oxide
4 tricalcium oxide
5 bismuth dioxide
Hydration of the powder results in a colloidal gel composed of calcium oxide crystals in an amorphous
structure This gel solidifies into a hard structure in less than three hours
PROPERTIES OF MTA
It is biocompatible material and its sealing ability is better than that of amalgam or ZOE
Initial pH is 102 and set pH is 125
The setting time of cement is 4 hours
The compressive strength is 70 MPA which is comparable with that of IRM
Low cytotoxicity ndash It presents with minimal inflammation if extended beyond the apex
Mineral trioxide aggregate (MTA) has demonstrated the ability to induce hard-tissue formation in
pulpal tissues and it promotes rapid cell growth
APEXOGENESIS
It is defined as the treatment of a vital pulp by capping or pulpotomy in order to permit continued
growth of the root and closure of the open apex
Rationale
Maintenance of integrity of the radicular pulp tissue to allow for continued root growth
Indications
bull Indicated for traumatized or pulpally involved vital permanent tooth when root apex is incompletely formed
bull No history of spontaneous pain
bull No sensitivity on percussion
bull No hemorrhage
bull Normal radiographic appearance
Contraindications
bull Evidence that radicular pulp has undergone degenerative changes
bull Purulent drainage
bull History of prolonged pain bull Necrotic debris in canal
bull Periapical radiolucency
6
1
Gupta A Dhingra R Chaudhari P Gupta A
Department of Paedodontics and Preventive Dentistry Faculty of Dental Sciences SGT University Gurgaon Haryana India
Journal of Indian Society of Pedodontics and Preventive Dentistry
Volume 35 I Issue 3 I July-September 2017
A COMPARISION OF VARIOUS MINIMALLY
INVASIVE TECHNIQUES FOR THE REMOVAL
OF DENTAL FLUOROSIS STAINS IN
CHILDREN
DR MITAKSHARA NIRWAN
CONTENTS
bull Introduction
bull Aims
bull Materials and Methods
bull Results
bull Discussion
bull Conclusion
bull Critical analysis
bull References
INTRODUCTION
bull Dental fluorosis is a developmental disturbance of dental enamel caused by
successive exposure to high concentrations of fluoride during tooth
development
bull Various methods of therapy are advocated for the treatment of fluorosis -
stained teeth which range from invasive ceramic veneer bonding restorations
to abrasive chemical treatments
bull The combination of dental bleaching techniques and microabrasion appears
as an excellent conservative solution to reestablish health in fluorosis
affected teeth
AIMS
bull The aim of the study was to evaluate and compare the effectiveness of
minimally invasive techniques for the removal of dental fluorosis
stains in children in vivo
MATERIALS AND METHODS
Patients visiting the department of Pedodontics and Preventive dentistry
Faculty of Dental Sciences SGT University Gurgaon
bull Sample size 90 patients
bull Age group 10 -17 years
bull Caries cracks or periodontal
disease on anterior teeth
bull Abscess draining sinus
cellulitis
bull Non vital teeth
hypersensitive exposed
crevices
bull Orthodontic appliance
bull Past history of bleaching
bull At least two permanent
maxillary anterior teeth
bull TSIF of score 4
bull Free of systemic diseases
Inclusion criteria Exclusion criteria
2
Groups
Group A In office bleaching with 35 hydrogen peroxide( Pola Office
Bleaching kit) activated by light emitting diode (LED) bleaching unit
(35 HP)
Group B Enamel microabrasion (EM) (PREMA Enamel Microabrasion
System) followed by in-office bleaching with 44 carbamide peroxide
gel (EM)
Group C In-office bleaching with 5 sodium hypochlorite (5
NaOCl)
A baseline colour evaluation was done by taking digital photograph of
the maxillary anterior teeth
RESULTS
Group 1
Colour stability
Group 2 Group 3
Tooth sensitivity
Tooth sensitivity values were taken before the treatment
which was compared to immediate postoperative and follow
up visits It was checked using an electric pulp tester
maximum
moderate
least
immediately
group 2
group 1
group 3
1 month
group 2
group 1
group 3
3 month
group 2
group 1
group 3
Patient satisfaction score
Satisfaction was assessed on visual analog scale
Range 1 to 5
Groups percentage of patients
who were satisfied with
the treatment
Number of patients
who reported slight
reappearance of colour
Group 1
90
7
Group 2
83
8
Group 3
73
7
3
Number of Appointments
Groups One sitting Two sittings Three
sittings
Group 1
25
4
1
group 2
26
3
1
Group 3
30
0
0
DISCUSSION
bull Hydrogen peroxide is capable of penetrating the tooth osmosis and through porosities and cracks subsequently acting directly on the pigmented molecules
bull Gurgan et al investigated 3 different light systems and found out that diode laser system with gave best tooth whitening and least tooth sensitivity
bull In the EM group the surface reflects and refracts light from the surface in such way that mild imperfections in underlying enamel are camouflaged While the highly polished surface of enamel enhances the aesthetic appearance
bull Train et al and Loguercio et al also had the similar results in their studies with EM mild fluorosis showed best results moderate showed moderate results while it had little effect on severe fluorosis
bull NaOCl was only effective on mild stains while moderate and severe
stains could only be lightened to quite an extent but could not be
completely removed
bull When NaOCl comes in contact with hypomineralized and discoloured
enamel it degrades and removes the chromogenic organic material
located on the enamel surface
CONCLUSION
bull It was concluded that esthetic appearance of teeth mild fluorosis can
be achieved by bleaching and microabrasion But in cases of
moderate fluorosis a combination of any of theses modalities can be
used
bull As no special maintenance precautions are required these maybe be
considered as an interesting alternative to conventional operative
treatment
bull Focuses on only TSIF of 4
bull Electric pulp testing is not the
right method to check for
sensitivity
bull Tooth Sensitivity changes
from person to person
bull Food habits can cause
staining of the teeth
bull Minimally invasive
bull Cheaper to veneers
bull Minimal loss of tooth structure
bull 4 parameters checked for the success of treatment
bull Inclusion of specific score of fluorosis for comparing the results
bull Maximum 3 appointments needed
CRITICAL ANALYSIS
Pros Cons
REFERENCES
bull Gurgan S Cakir FY Yazici E Different light-activated in officebleaching
systems Lasers Med Sci 201025817-22
bull Train TE McWhorter AG Seale NSWilson CF Guo IY Examination of
esthetic improvement and surface alteration following microabrasion in
fluorotic human incisors in vivoPediatr dent 199618353-62
bull Loguercio AD Correia LD Zago C Tagliari D Neumann E Gomes OM et al
Clinical effectiveness of two microabrasion materials materials for the
removal of enamel flurosis stains Oper Dent 200732531-8
4
2
The separated instrument was lodged firmly in distobuccal root canal 2ndash3 mm below the cementoenamel junction The instrument was bypassed successfully with no 15 and no 20 H-files but attempts for its retrieval were not successful
GatesndashGlidden (GG) drills no 2 (07 mm) and no 3 (09 mm) were used to drill around the instrument after which it was retrieved successfully using no 25 H-file
All the canals were instrumented till size 30 k-file followed by obturation with metapex and restoration with glass ionomer cement amp followed by placement of a crown and loop space maintainer for missing 74 The instrument retrieved was a manual reamer measuring 6 mm in length
The patient was asymptomatic since then and is under regular follow-up
CASE 2
A 5-year-old female child reported with the chief complaint of spontaneous toothache in mandibular left second
primary molar Clinical examination revealed deep occlusal caries with fractured lingual wall and pain on
percussion An intraoral periapical radiograph revealed caries involving pulp without any furcation or periapical
area of rarefaction and pulpectomy was planned
All the canals were enlarged using NiTi rotary files with a 4 taper operating at 500 rpm with minimum torque
setting An orifice opener [(0825 19 mm) of 8 taper size 25 length 19 mm] and nos 0420 file was used for
instrumentation of root canal This was followed by file nos 0425 which got separated in the distobuccal root
canal The radiograph confirmed a separated instrument of length 3ndash4 mm in the middle third of the root canal
The instrument was bypassed with no 15 k-file but could not get retrieved As instrument separation had occurred with 0425 file the involved root canal was sufficiently debrided before separation and the level of instrument separation was at the mid-root region so it was decided to obturate and seal this tooth with
periodic follow-ups instead of immediate extraction All other canals were enlarged till size 0430 in the sequential manner followed by obturation using metapex and placement of stainless steel crown
3
CASE 3
A 5-year-old female child has complaint of mild intermittent pain with primary mandibular left first molar She
had undergone pulpectomy treatment for the same during which an instrument separation has occurred in
the mesiobuccal root canal by a resident doctor
A radiograph revealed a separated instrument of about 4 mm in size lodged in the apical third but within the
confines of the mesial root An attempt was made for its retrieval but was unsuccessful The extraction of the
involved tooth was carried out under local anesthesia followed by a band and loop space maintainer
CASE 4
A 7-year-old male child reported with a chief complaint of mild intermittent pain on food lodgment with the primary mandibular right first and second molars The patient had a history of dental treatment at a private
dental clinic few months back which he did not continue further
Clinical examination revealed glass ionomer restoration with 85 and proximal caries with 84 leading to food lodgment An intraoral periapical radiograph with 85 revealed empty root canals with a separated
instrument of about 3ndash4 mm size beyond the apex of mesial root close to the developing succedaneous premolar
4
DISCUSSION
Stainless steel files usually separate fracture due to the excessive amounts of torque and overuse or the
preexisting distortion of the instrument whereas in NiTi rotary files it is a combined result of torsional stress and cyclic fatigue
Therapeutic options for the management of separated endodontic instruments include no intervention nonsurgical (orthograde conservative) management surgical management and tooth extraction
Use of ultrasonic scaler Masserann technique Endo extractor and Cavi-Endo ultrasonic instruments are some of the methods popular for retrieval of a separated endodontic instrument in the permanent tooth
In case 1 a 6-mm-long manual reamer was retrieved successfully with the use of GG drill using a manual file and copious irrigation which is the most desired treatment outcome
In case 2 the retrieval of separated rotary file lodged in the middle third of the root canal was unsuccessful in spite of multiple attempts It was therefore managed with routine obturation followed by restoration to maintain the tooth in its physiological functional state It was kept under close periodic follow-up at least
every 3 months This treatment option should be encouraged where it is possible to follow up the patient clinically and radiographically at close periodic intervals as there is the possibility of instrument escaping
into bone due to physiological root resorption
In cases 3 and 4 an instrument has separated in the apical root portion
In case 3 it was within the root canal and thus an attempt was made for its retrieval which was
unsuccessful It was therefore extracted to prevent the fractured instrument from getting exposed in the bone following resorption as there is no accurate and consistent established age for initiation of resorption in primary teeth known per se
In case 4 an immediate extraction of involved tooth was carried out as the separated instrument was beyond the apex of the primary tooth root
Age of the child clinical signs and symptoms and amount of root resorption are the factors which can also influence the management of separated instrument in primary teeth
Moreover if an instrument has separated after initial cleaning and shaping of root canal maintaining a tooth is not a problem as clinical signs and symptoms are not anticipated and the good prognosis is expected
However if an instrument has separated early during the initial cleaning and shaping of the root canal clinical symptoms may compromise the prognosis
Therefore these factors should be kept in mind while planning a suitable management strategy to avoid or at least reduce the burden of extraction and wear of space maintainer for longer period
5
CONCLUSION
The management and prognosis of a primary tooth with a separated instrument is
dependent on the level of instrument fracture within the root age of the child root
resorption and clinical signs and symptoms of the involved tooth
Different management approaches can be tried depending on clinical situations keeping
in mind benefits vs risks in preserving the tooth
PROS amp CONS
PROS
The entire procedure is given
by step by step
Well descriptive xrays and
photographs
CONS
Medical history has not been
given
REFERENCES
1 TOMER ANIL K ET AL ldquoBROKEN FILE RETRIEVAL PUZZLE IN ENDODONTICSrdquo
(2016)
2 SHENOY A MANDAVA P BOLLA N ET AL A NOVEL TECHNIQUE FOR REMOVAL OF
BROKEN INSTRUMENT FROM ROOT CANAL IN MANDIBULAR SECOND MOLAR
INDIAN J DENT RES 201425(1)107ndash110
3 PATEL J MORAWALA A TALATHI R ET AL RETRIEVAL OF A BROKEN INSTRUMENT
FROM ROOT CANAL IN PRIMARY ANTERIOR TEETH UNIV RES J DENT 20155(3)203ndash
206
4 MORANKAR R GOYAL A GAUBA K ET AL MANUAL VERSUS ROTARY
INSTRUMENTATION FOR PRIMARY MOLAR PULPECTOMIES - A 24 MONTHS
RANDOMIZED CLINICAL TRIAL PEDIAT DENT J 201828(2)96ndash102
5 KASHYAP NILOTPOL (2018) RETAINING PRIMARY MOLARS WITH INSTRUMENT
SEPERATION A CASE REPORT AND CLINICAL GUIDE
6
1
IMPACT OF 6 CITRIC ACID AND ENDOACTIVATOR AS IRRIGATION ADJUNCTS ON OBTURATION QUALITY AND PULPECTOMY OUTCOME IN
PRIMARY TEETH
NEETU JAIN SHALINI GARG ABHISHEK DHINDSA SAKSHI JOSHI HARJOY
KHATRIA
PEDIATRIC DENTAL JOURNAL 2019 29
1
DR MITAKSHARA NIRWAN
CONTENTS
bull INTRODUCTION
bull AIMS amp OBJECTIVES
bull CASE REPORT
bull RESULTS
bull DISCUSSION
bull CONCLUSION
bull PROS AND CONS
bull REFERENCES
2
INTRODUCTION
bull ENDODONTIC THERAPY IN PRIMARY TEETH INVOLVES DISINFECTION OF THE ROOT CANAL
SYSTEM AND ITS OBTURATION WITH RESORBABLE PASTE
bull THE CONTENTS OF ROOT CANAL ALONG WITH SMEAR LAYER ARE EXPECTED TO BE REMOVED
DURING THE BIOMECHANICAL PREPARATION
bull IN VITRO AND CLINICAL DOCUMENTS HAVE INDICATED THAT MECHANICAL PREPARATION OF
THE CANAL LEAVES LARGE PORTIONS OF THE CANAL WALLS UNDEBRIDED AND COMPLETE
REMOVAL OF THE BACTERIA BY THIS MECHANICAL PROCEDURE ALONE IS UNLIKELY TO BE SEEN
THEREFORE SOME FORM OF DISINFECTIONIRRIGATION IS MANDATORY TO KILL THE
MICROORGANISMS AND TO REMOVE THE RESIDUAL TISSUES
3
bull THE IDEAL REQUISITES OF A ROOT CANAL IRRIGANT AS GIVEN BY ZEHNDER ARE
1 BROAD ANTIMICROBIAL SPECTRUM
2 HIGH EFFICACY AGAINST ANAEROBIC AND FACULTATIVE MICROORGANISMS ORGANIZED
IN BIOFILMS
3 ABILITY TO DISSOLVE NECROTIC PULP TISSUE REMNANTS
4 ABILITY TO INACTIVATE ENDOTOXIN
5 ABILITY TO PREVENT THE FORMATION OF A SMEAR LAYER DURING INSTRUMENTATION OR
TO DISSOLVE THE LATTER ONCE IT HAS FORMED
6 SYSTEMICALLY NONTOXIC WHEN THEY COME IN CONTACT WITH VITAL TISSUES
NONCAUSTIC TO PERIODONTAL TISSUES AND WITH LITTLE POTENTIAL TO CAUSE AN
ANAPHYLACTIC REACTION
SINCE NO SINGLE IRRIGANT HAS THESE OPTIMAL PROPERTIES STUDIES HAVE REPORTED THE USE
OF TWO OR MORE SOLUTIONS IN A SPECIFIC SEQUENCE OR IN COMBINATIONS FOR BETTER
RESULTS 4
bull SEVERAL IRRIGATING SOLUTIONS ALONG WITH CHELATING AGENTS HAVE BEEN USED
DURING BIOMECHANICAL PREPARATION OF ROOT CANAL BOTH IN PRIMARY AND
PERMANENT TEETH
bull HOWEVER NONE OF THE AVAILABLE IRRIGATING SOLUTIONS HAS BEEN REGARDED CLEARLY
AS OPTIMAL SOLUTION BECAUSE OF THEIR LIMITED EFFECTIVENESS ESPECIALLY IN APICAL
13RD OF THE ROOT CANAL SYSTEM
bull TO OVERCOME SUCH LIMITATIONS USE OF ENDOACTIVATOR HAS BEEN PROPOSED AS AN
IRRIGATION FACILITATOR THAT IS BASED ON SONIC VIBRATION (UP TO 10000 CPM) WHICH
FACILITATES THE IRRIGANT PENETRATION AND ITS RENEWAL WITHIN THE CANAL
bull ACTIVATION SYSTEMS RESULTED IN BETTER REMOVAL OF THE SMEAR LAYER IN THE APICAL
THIRD OF ROOT CANALS IN COMPARISON TO CONVENTIONAL IRRIGATION
5
CITRIC ACID
bull CITRIC ACID IS A WEAK ORGANIC ACID WITH THE APPEARANCE OF WHITE CRYSTALLINE
POWDER AT ROOM TEMPERATURE
bull IT CAN EXIST EITHER IN WATER-FREE FORM (ANHYDROUS) OR MONOHYDRATE FORM THE
WATER-FREE FORM CRYSTALLIZES FROM THE HOT WATER WHEREAS THE MONOHYDRATE
FORMS FROM THE COLD WATER THE LATTER MAY BE CONVERTED TO ANHYDROUS FORM BY
HEATING MORE THAN 78degC
bull CITRIC ACID OCCURS NATURALLY IN THE BODY IN MITOCHONDRIA AND IS USED BY BLOOD
BANKS TO PREVENT COAGULATION OF TRANSFUSED BLOOD CITRIC ACID IS ALSO ESSENTIAL
TO HUMAN METABOLISM AND IS FOUND IN MANY FOODS
6
2
bull THE BIOLOGICAL EFFECTS OF CITRIC ACID ON THE PERIODONTAL STRUCTURE HAS BEEN
EXTENSIVELY STUDIED IN PERIODONTICS
bull NEUMAN AND NEWMAN SHOWED THAT CITRIC ACID IS THE MOST EFFECTIVE ACID IN
ALTERING THE SOLUBILITY OF HYDROXYAPATITE
bull YAMAGUCHI ET AL SHOWED THAT CITRIC ACID SOLUTION HAD ANTIBACTERIAL EFFECTS ON
ALL 12 ROOT CANAL BACTERIA TESTED
bull ARIAS-MOLIZ ET AL SHOWED THAT ETHYLENEDIAMINETETRAACETIC ACID (EDTA) HAS NO
BACTERICIDAL ACTIVITY EVEN AFTER 1 HOUR CONTACT
bull THIS ACID HAS THE ABILITY OF ROOT CANAL IRRIGATION AND ALSO SMEAR LAYER REMOVAL
DIFFERENT CONCENTRATIONS (1ndash50) HAVE BEEN PROPOSED GUTMANN ET AL CONCLUDED
THAT 10 CITRIC ACID IS BETTER THAN ULTRASOUND FOR SMEAR LAYER REMOVAL FROM THE
ROOT END CAVITIES
7
bull STUDIES HAVE SHOWN IRRIGATION WITH 6 CA FOR 15 OR 30 SECONDS IS QUITE
EFFECTIVE IN REMOVING ALL THE COMPONENTS OF THE SMEAR LAYER OF THE PRIMARY
TEETH WHEREAS PERITUBULAR DENTIN DESTRUCTION WAS OBSERVED WHEN HIGHER
CONCENTRATION OF CITRIC ACID WAS USED AS AN IRRIGATING SOLUTION
8
AIMS amp OBJECTIVES
bull THIS STUDY WAS AIMED TO EVALUATE THE CLINICAL AND RADIOGRAPHIC OUTCOME OF
PULPECTOMY ALONG WITH QUALITY OF OBTURATION USING 6 CITRIC ACID AND
ENDOACTIVATOR
9
CASE REPORT
bull 350 CHILDREN (3-9 YEARS) WITH CLINICAL SIGNS AND SYMPTOMS OF CHRONIC IRREVERSIBLE
PULPITIS IN DEEPLY CARIOUS TEETH WERE SCREENED DURING SCHOOL DENTAL HEALTH
PROGRAM FROM MAY 2014-JULY 2014
bull 123 CHILDREN REPORTED TO THE DEPARTMENT AND 67 CHILDREN WERE SELECTED BASED ON
INCLUSION AND EXCLUSION CRITERIA
RECRUITMENT OF PATIENTS
10
INCLUSION CRITERIA
bull HISTORY OF SPONTANEOUS PAIN AND UNCONTROLLED BLEEDING AFTER PULP AMPUTATION
EXCLUSION CRITERIA
bull EVIDENCE OF INTERNAL OR EXTERNAL (PHYSIOLOGICPATHOLOGIC) ROOT RESORPTION OF MORE THAN A THIRD OF ITS LENGTH
bull ROOT CANAL OBLITERATION OR ANATOMIC ANOMALIES
bull INADEQUATE BONE SUPPORT OR NON RESTORABLE TOOTH
bull ONCE PATIENTS ELIGIBILITY WAS CONFIRMED THE TREATMENT PROCEDURE WAS
EXPLAINED TO THE PARENTGUARDIAN AND INFORMED WRITTEN CONSENT WAS
OBTAINED FROM PARENTSGUARDIANS SHOWING WILLINGNESS FOR THEIR
CHILDRENS TREATMENT 11
PROCEDURE
bull PULPECTOMY WAS PERFORMED BY ONE OPERATOR OF PEDIATRIC DENTISTRY DEPARTMENT
USING A STANDARDIZED TREATMENT PROTOCOL FOR ALL THE PATIENTS
bull AFTER ADMINISTRATION OF LOCAL ANESTHESIA RUBBER DAM WAS APPLIED FOR ISOLATION
bull ACCESS CAVITY WAS PREPARED USING AIR-ROTOR HAND PIECE WITH 8 ROUND BUR AND
PULP TISSUE WAS EXTIRPATED WITH THE HELP OF SPOON EXCAVATOR
bull FURTHER THE NEGOTIATION OF THE CANALS WAS DONE WITH 10 K-FILE
bull A DIAGNOSTIC RADIOGRAPH WAS TAKEN FOR ROOT LENGTH DETERMINATION AND
WORKING LENGTH WAS KEPT 1 MM SHORT OF THE RADIOGRAPHICAL APEX
bull ALL ROOT CANALS WERE INSTRUMENTED MANUALLY USING K-FILES AND WERE IRRIGATED
WITH 10 ML 09 NORMAL SALINE AND 1 SODIUM HYPOCHLORITE AS STANDARDIZING
PROTOCOL FOR ROOT CANAL PREPARATION AND DISINFECTION
12
3
GROUP 1 (CA + E) - IRRIGATION WAS DONE
WITH 10 ML OF 6 CITRIC ACID (CITOCID AMMDENT)
AND IRRIGANTS WERE SONICALLY AGITATED WITH
ENDOACTIVATOR (DENTSPLY) FOR 30 S PER CANAL USING REDBLUE
ENDOACTIVATOR TIP
GROUP 2 (CA) - 10 ML OF 6 CITRIC ACID FOR 1 MIN USING
27 GAUZE IRRIGATING NEEDLE
GROUP 3(SH + E) - 10 ML OF 1 SODIUM HYPOCHLORITE
SOLUTION AND SONIC ACTIVATION WITH ENDOACTIVATOR
GROUP 4(SH) - 10 ML OF 1 SODIUM HYPOCHLORITE
SOLUTION USING IRRIGATING NEEDLE (CONTROL GROUP)
bull TEETH UNDERGOING PULPECTOMY WERE RANDOMLY ENROLLED BY CHIT METHOD INTO THREE
STUDY AND ONE CONTROL GROUP
13
bull IN CITRIC ACID GROUPS FINAL RINSE WITH NORMAL SALINE WAS DONE TO REMOVE THE
REMAINING CRYSTALS (CHELATES)
bull FOLLOWING BIOMECHANICAL PREPARATION THE ROOT CANALS WERE DRIED WITH STERILE
ABSORBENT PAPER POINTS AND OBTURATED WITH VITAPEX USING HAND HELD
LENTULOSPIRAL FINAL RESTORATIONS WERE DONE USING COMPOSITE RESIN
14
bull CLINICAL FOLLOW UP WAS DONE AT 24 H1 WEEK 1 MONTH 6 MONTH AND 12
MONTH TO CHECK PAIN PRESENCE AND PAIN FREQUENCY (ONCEMORE THAN ONCE)
SWELLING FISTULA SENSITIVITY TO PERCUSSION
bull RADIOGRAPHIC FOLLOW UP WAS DONE AT 6 MONTH AND 12 MONTH FOR ANY
DEVIATED ERUPTION OF SUCCEDANEOUS TEETH EXCESS FILING MATERIAL AND ITS
RESORPTION EXTERNALINTERNAL ROOT RESORBTION CALCIFIC METAMORPHOSIS
PRESENCE OF FURCATION RADIOLUCENCY
CLINICAL amp RADIOGRAPHIC FOLLOW UP
15
RADIOGRAPHIC ASSESSMENT OF OBTURATION QUALITY
bull POSTOPERATIVE RADIOGRAPHS WERE VISUALLY ASSESSED FOR QUALITY OF OBTURATION BY
TWO INDEPENDENT EXAMINERS (SG AD) WHO WERE BLINDED WITH REGARD TO
IRRIGATION PROTOCOL GROUP TO ENHANCE CALIBRATION EACH EXAMINER ASSESSED THE
RADIOGRAPH INDEPENDENTLY AND LATER REVIEWED TOGETHER FOR FINAL ASSESSMENT
INDIVIDUAL ROOT WAS TAKEN AS UNIT OF ANALYSIS FOR GRADE OF OBTU- RATION AND
SCORING CRITERIA WERE AS GIVEN BY COLL JA 1996
1 UNDER FILLED - FILLING MATERIAL ENDED 1 MM OR MORE SHORT OF THE APEX
2 OPTIMAL FILLING- FILLING MATERIAL APPEARED TO END AT THE RADIOGRAPHICAL APEX
3 OVERFILLED - FILLING MATERIAL EXTRUDED PAST THE RADIOGRAPHIC APEX
4 OPTIMALLY FILLED ROOTS WERE FURTHER ASSESSED FOR THE PRESENCE OF VOIDS AND VOID
AREA (ROOT CANAL SURFACE UNTOUCHED BY THE ROOT CANAL FILLING MATERIAL) IN THREE
VISUALLY DIVIDED SECTIONS OF THE ROOT IE CORONAL MIDDLE AND APICAL 13RD
16
RESULTS
bull OVERALL CLINICAL AND RADIOGRAPHIC SUCCESS RATE OVER A PERIOD OF ONE YEAR WAS
9886 amp 977 RESPECTIVELY
bull ALL GROUPS WERE SIGNIFICANTLY (P = 001) EFFECTIVE IN ALLEVIATING PAIN WITHIN 24 H
OF PULPECTOMY
17 18
4
19
bull IMMEDIATE POST OPERATIVE RADIOGRAPHIC ASSESSMENT REVEALED 68 (102150) ROOTS
WITH OPTIMAL OBTURATION AND 32 (48150) WITH OVERFILLINGUNDERFILLING MAXIMUM
NO OF OPTIMAL FILLINGS WERE OBSERVED IN GROUP1 (CA + E) (3333) FOLLOWED BY
GROUP 2 (CA) (2549) GROUP 3(SH + E) (2549) AND GROUP 4(SH) (1568)
bull CITRIC ACID GROUPS HAD MORE NUMBER OF OPTIMALLY FILLED ROOTS 588 (60102) THAN
NON CITRIC ACID GROUPS 412 (42102)
bull ENDOACTIVATOR CONTRIBUTED TO 18 OF OPTIMAL OBTURATION IRRESPECTIVE OF
CHELATING AGENT USED
20
21
bull MAXIMUM NO OF VOIDS AND VOID AREAS WERE IN NON CITRIC ACID GROUPS
(6419 amp 5384) COMPARED TO CITRIC ACID GROUPS (3580 amp 4615)
RESPECTIVELY
bull ANALYSIS OF ROOT 13RD REVEALED MAXIMUM NO OF VOID AREA IN APICAL
13RD (4755) FOLLOWED BY MIDDLE 13RD (3846) AND CORONAL 13RD
(1398)
bull LEAST NO OF VOIDS amp VOID AREA (1111 amp 1608) WERE OBSERVED WHEN
ENDOACTIVATOR ALONG WITH CHELATING AGENT WAS USED (GROUP 1)
HOWEVER THIS WAS STATISTICALLY INSIGNIFICANT
22
DISCUSSION
bull IN THE PRESENT STUDY 1 SODIUM HYPOCHLORITE WAS USED ALONG WITH 6 CITRIC ACID
(CHELATING AGENT) WHICH IS REPORTED TO BE AS EFFECTIVE AS 17 EDTA
bull CITRIC ACID (BIOLOGICAL ACID) IS FOUND TO BE BIOCOMPATIBLE AND LEAST IRRITATING TO
PERIAPICAL TISSUES THAN OTHER CHELATING AGENTS
bull USE OF SODIUM HYPOCHLORITE SOLUTION FOLLOWING CHELATING AGENT WAS AVOIDED AS IT
RAPIDLY PRODUCES SEVERE EROSION OF ROOT CANAL WALL DENTIN
bull TRADITIONAL APPROACH OF DELIVERING IRRIGANTS INTO THE ROOT CANAL SPACE USING
SYRINGES AND METAL NEEDLES HAS BEEN FOUND TO BE INEFFECTIVE ESPECIALLY IN THE AREAS OF
ANASTOMOSES BETWEEN CANALS AND APICAL 13RD OF ROOT CANAL
23
bull THEREFORE TO ACHIEVE BETTER CLEANING EFFICIENCY IRRIGANT ACTIVATION HAS BEEN
RECOMMENDED SONIC ACTIVATION HAS BEEN REPORTED TO RESULT IN BETTER ROOT CANAL
CLEANLINESS AS COMPARED TO NO ACTIVATION OF IRRIGANT
24
5
CONCLUSION
bull USE OF 6 CITRIC ACID DEFINITELY HELPED IN RAPID ELIMINATION OF PAIN RESOLUTION OF
PERI-RADICULAR RADIOLUCENCY BETTER OBTURATION QUALITY IN TERMS OF LESS VOIDS AND
VOID AREAS ALONG WITH MAXIMUM NO OF OPTIMAL OBTURATION UP TO APICAL AREA
bull 6 CITRIC ACID AND ENDOACTIVATOR IRRIGATION PROTOCOL PROVED TO BE THE BETTER
IRRIGATION PROTOCOL WHICH MAY CONTRIBUTE TO LONG TERM SUCCESS OF PRIMARY
TOOTH AND THE HEALTH OF UNDERLYING PERMANENT TOOTH
bull 6 CITRIC ACID ALONG WITH ENDOACTIVATOR MAY BE RECOMMENDED AS IRRIGATION
ADJUNCTS IN PULPECTOMY PROCEDURE OF PRIMARY TEETH
25
PROS AND CONS
PROS
bull PROPER EXPLANATION OF THE MATERIALS
USED
CONS
bull NO PREOPERATIVE AND POSTOPERATIVE
RADIOGRAPHS
26
REFERENCES
bull RAMACHANDRA JA NIHAL NK NAGARATHNA C VORA MS ROOT CANAL IRRIGANTS IN
PRIMARY TEETH WORLD J DENT 20156(3)229-234
bull MOHAMMADI Z JAFARZADEH H SHALAVI S KINOSHITA JI UNUSUAL ROOT CANAL
IRRIGATION SOLUTIONS J CONTEMP DENT PRACT 201718(5)415-420
bull ZEHNDER M ROOT CANAL IRRIGANTS J ENDOD 2006 32389- 98
bull SMITH JJ amp WAYMAN BE AN EVALUATION OF THE ANTIMICROBIAL EFFECTIVENESS OF
CITRIC ACID AS A ROOT CANAL IRRIGANT JOURNAL OF ENDODONTICS 1986 12(2) 54-58
bull TANNURE PN AZEVEDO CP BARCELOS R GLEISER R PRIMO LG LONG-TERM OUTCOMES OF
PRIMARY TOOTH PULPECTOMY WITH AND WITHOUT SMEAR LAYER REMOVAL A RANDOMIZED
SPLIT-MOUTH CLINICAL TRIAL PEDIATR DENT 201133316E20 27
bull CARON G NHAM K BRONNEC F MACHTOU P EFFECTIVENESS OF DIFFERENT FINAL IRRIGANT
ACTIVATION PROTOCOLS ON SMEAR LAYER REMOVAL IN CURVED CANALS J ENDOD
2010361361E6
bull COLL JA SADRIAN R PREDICTING PULPECTOMY SUCCESS AND ITS RELATIONSHIP TO
EXFOLIATION AND SUCCEDANEOUS DENTITION PEDIATR DENT 19961857E63
28
1
LOCAL
ANESTHESIA
DR MITAKSHARA NIRWAN
CONTENTS
Definition
Methods of inducing local anesthesia
Desirable properties
Electrophysiology of nerve conduction
Impulse propagation and spread
Mode and site of action of local anesthesia
Classification of local anesthetic according to biological site and mode of action
Dissociation of local anaesthetics
Mechanism of action of local anaethetics
Local anaesthetic agent
2
3
DEFINITION
Local anesthesia is defined as a loss of sensation in
a circumscribed area of the body caused by depression
of excitation in nerve endings or an inhibition of the
conduction process in peripheral nerves
An important feature of local anesthesia is that it produces
LOSS OF SENSATION WITHOUT INDUCING LOSS OF
CONSCIOUSNESS
4
METHODS OF INDUCING LOCAL
ANESTHESIA
Low temperature
Mechanical trauma
Anoxia
Neurolytic agents such as alcohol amp phenol
Chemical agents such as local anesthetics
PROPERTIES OF LOCAL
ANESTHESIA
It should not be irritating to tissue to which it is applied
It should not cause any permanent alteration of nerve structure
Its systemic toxicity should be low
Time of onset of anesthesia should be short
It should be effective regardless of whether it is injected into the tissue or applied locally to mucous membranes
The duration of action should be long enough to permit the completion of procedure
5 6
It should have the potency sufficient to give complete
anesthesia with out the use of harmful concentration solutions
It should be free from producing allergic reactions
It should be free in solution and relatively undergo
biotransformation in the body
It should be either sterile or be capable of being sterilized by
heat with out deterioration
2
ELETROPHYSIOLOGY OF
NERVE CONDUCTION
There is an electrical charge across the membrane
This is the membrane potential
The resting potential (when the cell is not firing) is a negative
electrical potential of -70mv that exists across the nerve
membrane produced by different concentrations of either side of
the membrane
The interior of nerve is NEGATIVE in relation to exterior
7 8
inside
outside
Resting potential of neuron = -70mV
+
-
+
-
+
-
+
-
+
-
SLOW DEPOLARIRIZATION
9
RAPID DEPOLARIZATION
The interior of nerve is POSITIVE in relation to exterior
REPOLARIZATION
10
bull Repolarization takes 07 msec
bull Depolarization takes 03 msec
SODIUM PUMP -
energy comes from the oxidative metabolism of ATP
bull The entire process require 1 msec
IMPULSE PROPOGATION
IMPULSE SPREAD
The propagated impulse travels along the nerve
membrane towards CNS The spread of impulse differs
in myelinated and unmyelinated nerve fibers
DEPOLARIZED SEGMENT ADJACENT RESTING AREA
MODE AND SITE OF ACTION OF LOCAL
ANESTHETICS
Local anesthetic agent interferes with excitation
process in a nerve membrane in one of the
following ways
Altering the basic resting potential of nerve
membrane
Altering the threshold potential
Decreasing the rate of depolarization
Prolonging the rate of repolarization
12
3
CLASSIFICATION OF LOCAL ANESTHETIC
SUBSTANCES ACCORDING TO
BIOLOGICAL SITE AND MODE OF ACTION
CLASS A
Agents acting at receptor site on external surface of nerve membrane
Chemical substance Biotoxins (eg tetrodotoxin and saxitoxin)
CLASS B
Agents acting on receptor sites on internal surface of nerve membrane
Chemical substance Quaternary ammonium analogues of lidocaine
scorpion venom 13
CLASS C Agents acting by receptor independent of
physiochemical mechanism
Chemical substance Benzocaine
CLASS D Agents acting by combination of receptors and
receptor independent mechanisms
Chemical substance most clinically useful anesthetic agents
(eg lidocaine mepivacaine prilocaine)
14
BASED ON THE SOURCE
NATUAL
SYNTHETIC
OTHERS
BASED ON MODE OF APPLICATION
bull INJECTABLE
bull TOPICAL
BASED ON DURATION OF ACTION
bull ULTRA SHORT
bull SHORT
bull MEDIEM
bull LONG
BASED ON ONSET OF ACTION SHORT
INTERMEDIATE
LONG
15
DISSOCIATION OF LOCAL
ANESTHETICS
Local anesthetics are available as salts (usually
hydrochlorides) for clinical use
The salts both water soluble and stable is dissolved in
either sterile water or saline
In this solution it exists simultaneously as unchanged
molecule (RN) also called base and positively charged
molecules (RNH+) called cations
RNH+ ==== RN+ H
+
16
The relative concentration of each ionic form in the solution varies
in the pH of the solution or surrounding tissue
In the presence of high concentration of hydrogen ion (low pH) the
equilibrium shifts to left and most of the anesthetic solution exists
in cationic form
RNH+ gt RN
+ + H
+
As hydrogen ion concentration decreases (higher pH) the
equilibrium shifts towards the free base form
RNH+ lt RN + H
+
17
The relative proportion of ionic form also depends on pKa or DISSOCIATION CONSTANT of the specific local anesthetic
The pKa is a measure of molecules affinity for H+
ions
When the pH of the solution has the same value as pKa of the local anesthetic exactly half the drug will exists in the RNH
+ form and
exactly half in RN form
The percentage of drug existing in either form can be determined by Henderson Hasselbalch equation
Log baseacid = pH - pKa
18
4
MECHANISM OF ACTION OF LOCAL
ANESTHETICS
The following sequence is proposed mechanism of action of LA
Displacement of calcium ions from the sodium channel receptor site
Binding of local anesthetic molecule to this receptor site
Blockade of sodium channel
19
Decrease in sodium conductance
Depression of rate of electrical depolarization
Failure to achieve the threshold potential level
Lack of development of propagated action potential
Conduction blockadehellip
20
21
Na + Na +
22
LOCAL ANESTHETIC AGENT
COMERCIALLY PREPARED LOCAL ANESTHESIA
CONSISTS OF
Local anesthetic agent (xylocaine lignocaine 2)
Vasoconstrictor (adrenaline 1 80000)
Reducing agent (sodium metabisulphite)
Preservative (methylparabencapryl
hydrocuprienotoxin)
Fungicide (thymol)
Vehicle (distillde waterNaCl)
LOCAL ANESTHETIC AGENT
The local anesthetics used in dentistry are divided
into two groups
ESTER GROUP
AMIDE GROUP
23 24
ESTER GROUP It is composed of the following
An aromatic lipophilic group
An intermediate chain containing
an ester linkage
A hydrophilic secondary or tertiary
amino group
AMIDE GROUP It is composed of the following
An aromatic lipophilic group
An intermediate chain containing
amide linkage
A hydrophilic secondary or tertiary
amino group
5
25
CLASSIFICATION OF LOCAL ANESTHETICS
ESTERS
Esters of benzoic acid
Butacaine
Cocaine
Benzocaine
Hexylcaine
Piperocaine
Tetracaine
Esters of Para-amino
benzoic acid
Chloroprocain
Procaine
Propoxycaine
26
AMIDES Articaine
Bupivacaine
Dibucaine
Etidocaine
Lidocaine
Mepivacaine
Prilocaine
Ropivacaine
QUINOLINE
Centbucridine
PHARMACOKINETICS OF LOCAL
ANESTHETICS UPTAKE
When injected into soft tissue most local anesthetics produce
dilation of vascular bed
Cocaine is the only local anesthetic that produces
vasoconstriction initially it produces vasodilation which is
followed by prolonged vasoconstriction
Vasodilation is due to increase in the rate of absorption of the
local anesthetic into the blood thus decreasing the duration of
pain control while increasing the anesthetic blood level and
potential for over dose 27
AMIDE LOCAL ANESTHETICS
The metabolism of amide local anesthetics is more
complicated then esters The primary site of
biotransformation of amide drugs is liver
Entire metabolic process occurs in the liver for lidocaine
articaine etidocaine and bupivacaine
Prilocaine undergoes more rapid biotransformation then the
other amides
28
REFERENCES
Handbook of local anesthesia ndash Stanley F Malamed ndash 6th
edition
Essentials of Local Anesthetic Pharmacology Daniel E
Becker Anesth Prog 2006 Fall 53(3) 98ndash109
WIKIPEDIEA
29
THANK YOU
30
1
Pharmacological Methods of Behavior
Management
DR MITAKSHARA NIRWAN
DEFINITIONS
bull Conscious Sedation ndash A minimally depressed level of consciousness that retains
the patients ability to independently and continuously maintain an airway and respond appropriately to physical stimulation or verbal command
(American Dental Association House Of Delegates 2000)
bull Deep Sedation ndash An induced state of depressed consciousness
accompanied by partial loss of protective reflexes including the inability to continuously maintain an airway independently and or to respond purposefully to physical stimulation or verbal command
bull General Anesthesia (G A) ndash An induced state of unconsciousness or complete loss of
protective reflexes including the inability to continually maintain an airway independently and respond purposefully to physical stimulation or verbal command
Conscious sedation
ADVANTAGES
Conscious
Protective reflexes active amp intact
Stable vital signs
Operating dentist may perform sedation
Minimum amount of equipment required
Prolong detainment in recovery room not required
Risk of complication very low
Excellent choice for poor ndash risk pt in dental office
Cost effective
General anesthesia
ADVANTAGES Not absolutely
essential May be the only
method Not necessary (no
pain reaction) Amnesia always
present
Conscious sedation
DISADVANTAGES
Pt cooperation is essential
Extremely difficult or mentally handicapped pt cannot always be managed
Use of local anesthesia is a must
Amnesia may or may not be present
General anesthesia DISADVANTAGES
Pt unconscious
Protective reflexes are depressed
Depressed
Advanced training required Dentist must not act also as anesthetist
Special equipment necessary
Detainment in recovery area necessary
High IOP amp postoperative complications
Not indicated in dental office
More expensive
Fundamental Concepts
bull Techniques that utilize drugs to induce co-operative yet conscious state in an otherwise uncooperative child ndash CONSCIOUS SEDATION
2
GOALS
1 To facilitate the provision of quality care
2 To minimize the extremes of disruptive behavior
3 To promote a positive psychologic response to treatment
4 To promote patient welfare amp safety
5 To return the patient to physiologic state
OBJECTIVES
1 The pt mood must be altered
2 The pt must remain conscious at all times
3 The pt must be cooperative
4 All protective reflexes must remain intact and active
5 Vital signs must remain stable and with in normal limits
6 The ptrsquos pain threshold should be elevated
7 Amnesia may be present
Indications
1 Preschool children
2 Lack of Psychological Emotional maturity
3 Lack of Cognitive Physical Medical disability
4 Fearful amp anxious pts
5 Pt who require extensive amp complicated dental care amp would require or benefit from prolonged visits
6 Acute pain
7 Traumatic injuries
Operating Facilities amp Equipment
A positive pressure O2 delivery system capable of administering gt than 90 O2 at 10L min flow for 60 min (650L ldquoErdquo cylinder)
OR
Self inflating bag valve mask device (15L min)
A functional suction apparatus with appropriate suction catheters
Monitoring equipment - PO BPC PC or Capno
Inhalation sedation unit
100 O2 amp never less than 25
A fail safe mechanism that is checked and calibrated annually
Must have appropriate scavenging system
Emergency drugs
Techniques of sedation
Routes for drug administration
bull Oral
bull Rectal
bull Inhalational
bull Transmucosal
ndash Sublingual
ndash Intranasal
bull Parenteral
ndash IM
ndash sub mucosal
ndash IV
3
Oral Sedation
Advantages
1 Almost universally accepted and the easiest method
2 Decreased incidence and severity of adverse reaction
3 Low cost
Disadvantages
1 Absorption is variable
2 Prolonged latent period(30 min)
3 Reversal of any unwanted effect is also difficult
4 Inability to readily lighten or deepen the level of sedation
5 Prolonged duration of action
Rectal Sedation
Advantages 1 Incidence and intensity of
drug related side effects is minimized
2 Drug absorption occurs from the large intestine directly into the circulation
3 The lack of a needle syringe or other equipment
4 The ease of administration
5 The low cost
Disadvantages
1 Inconvenience to the administrator amp pt
2 The variable absorption of drugs from the large intestine
3 The slow onset of action amp the relatively long duration of action
4 Inability to titrate the drug dosage
5 The inability to reverse the action of the drug the prolonged recovery
Intranasal sedation
Advantages
Rapid onset (10 ndash 15 min)
Simple amp relatively painless
Less pt cooperation is required
Absorbed directly into the C V S
Intranasal sedation
Disadvantages
1 Dependence on nasal mucous membrane
2 Shorter duration of action(40-60min)
3 Multiple dosage may be necessary
Drugs
Midazolam ndash 02mgkg
Sufentanil ndash 15 ndash 3 mcgkg
Ketamine ndash 3-6mg kg
Sublingual sedation
Advantages
1 Pt acceptance
2 Rapid onset
3 High bioavailability
Drugs
Oral Transmucosal Fentanyl Citrate (OTFC)
Intramuscular Sedation
Advantages
1 More rapid onset of action
2 Absorbed directly into the C V system
3 More reliable absorption of drug
4 Pt cooperation is not as essential
Disadvantages
1 Time factor ndash its 15 min latent period
2 Pt may not be willing to accept the injection
3 The prolonged duration of action(2-4 hrs more)
4 Possibility of injury to the tissues at the site of injection caused by either the drug or the needle
4
Sites of I M administration
1 Gluteal area
2 Vastus lateralis
3 Mid ndash deltoid area
Drugs
Diazepam
Midazolam
Hydroxyzine
Inhalation Sedation
Advantages
1 The onset of action is more rapid
2 Peak clinical level is achieved rapidly(3-5min) - permit titration
3 Administrator has complete control over the actions of the drug - safety feature
4 No significant over dosage
5 Flexible duration of action
6 Recovery time is rapid amp most complete
7 No injection is required
8 With N2O- O2 it is safe with very few side effects
Disadvantages
1 The initial cost of the equipment is high 2 The continuing cost of the gases is high 3 The equipment occupies considerable space 4 N2O is not a potent agent 5 A degree of cooperation is required from the pt 6 Chronic exposure to N2O is deleterious to the health of
dental personnel
Contraindications
1 Nasal obstruction 2 Cyanosis at rest 3 Poor cooperation 4 1st trimester of pregnancy 5 Fear of masks
I V Sedation
Advantages
1 The onset of action is the most rapid 2 The dosage may be titrated 3 Suitable level of sedation can be provided 4 The recovery period is shorter 5 Side effects are extremely uncommon 6 Control of salivary secretions is possible 7 The gag reflex is diminished 8 Effectively diminishes motor disturbances 9 Provides immediate access to CVS in emergency
Disadvantages
1 Venipuncture is necessary
2 Complication may rise at the site of the venipuncture
3 Monitoring must be more intensive
4 Recovery is not complete at the end of the procedure
5 Reversal of sedation is difficult
5
N2O-O2 (Relative Analgesia)
colorless sweet smelling gas
Pharmacokinetics
Absorption through pulmonary epithelium
It is approx 15 times as soluble as is nitrogen It replaces nitrogen in blood
It is carried in solution in plasma of the blood
It is not metabolized by the body
Elimination ndash majorndash lungs minor --- skin
perspiration urine and intestinal gas
Pharmacodynamics
Dose related
10 ndash 25 Lightheaded
Changes in visual amp auditory sensation
Tingling of hands amp feet
Suffusing warmth
Remote from the immediate environment
Reduced anxiety
25-50 max analgesic properties and aberration of vision hearing and proprioception mild drowsiness euphoria amnesia and increased sleepiness and dreams
35 conc will achieve maximum analgesia
bull CNS
ndash Cerebrum-primarily affected
ndash Safe but weak anesthetic agent
bull RESPIRATORY SYSTEM
ndash Increased Tidal and minute volumes
bull CARDIOVASCULAR SYSTEM
ndash 2 studies ndash decreased cardiac output
bull FETAL SYSTEMS
ndash Miscarriage in humans
bull OTHER SYSTEMS
ndash Depression of spinal reflexes increase muscle tone indicates stage of delirium
ndash Muscle rigidity-narcotics + nitrous oxide
ndash Nausea and vomitting - GIT
ndash HEMATOPOIESIS ----- prolonged exposure
Adverse reactions and toxicity
EMOTIONAL REACTIONS
DREAMS HALLUCINATIONS
No acute toxicity
Chronic toxicity ndash bone marrow
depression
PROCEDURE
Diffusion Hypoxia
Sevoflurane
A fluorinated derivative of isopropyl ether ndash synthesized in 1970
Potent anaesthetic agent with rapid uptake amp speedy recovery
Day-case surgery
Problem
Attaching vaporiser to any of the currently available machine
BENZODIAZEPINES
Diazepam 1961 lipid soluble
Uses-alcoholism epilepsy labor tetanus and cerebral palsy
- sedation and amnesia
- varieties of neurosis amp anxiety states
Pharmacokinetics
Orally Rectal IMIV or SC
Well absorbed through GIT
Excretion in urine
6
bull Pharmacodynamics
ndash Depress the brain stem reticular system and the limbic system thalamus and hypothalamus
ndash It is a centrally acting muscle relaxant Has anti-convulsant properties
Adverse reaction amp toxicity
ndash Confusion nausea headache increased appetite decreased salivation and jaundice Thrombophlebitis
ndash Rebound phenomenon
ndash Toxicity drowsiness confusion sleep and coma
Dosage Oral or Rectal ndash 02-05mgkg
Maximum single dose 10mg
IV- 025mgkg
Supplied Tablets 2 5 10 mg
Suspension ndash 5mg
Midazolam Water soluble ndash non-irritant
Oral IM IV
Metabolism- liver
Onset IV 3 -5mins
oral 20 ndash 30mins
Oral administration anxious patients requiring relatively short dental procedure
No rebound phenomenon
Better anxiolysis amp amnesia (retrograde amnesia)
Adverse effects Respiratory depression
dose dependant apnea
Dosage Oral ndash 025 to 1mgkg to maximum single dose 20mg
IM ndash 01 to 015mgkg to a maximum of 10mg
IV ndash slow IV
Supplied Syrup ndash 2mgml
Injectable ndash 1mgml amp 5mgml vials
Flumazenil specific benzodiazepines antagonist
selectively inhibits CNS effects
IV administration amp not recommended below 18yrs of age
02mg over 15 seconds after 45seconds 02mg then after 60seconds to maximum of 1mg
Sedative-Hypnotics
Barbiturates First truly effective drugs for the management of anxiety Generalized CNS depressants Produce dose dependent effects
Sedation ---- sleep ---- GA ---- coma
Suppress the CNS and result in sedation and amnesia Advantages
Rapid onset and short duration Disadvantages
no analgesic effect and possible hypotension Must be used with caution in trauma patients because they may cause
apnea and hypoventilation
DOSE Pentobarbital Sodium 100mg Secobarbital Sodium 100 to 200mg Children 30 to 100mg
bull Chloral Hydrates (Mickey Finn Knock out drops ) First synthesized in 1832 first member of the hypnotic group of drugs
Widely used as conscious sedation agent
Properties
Unpleasant taste
Nausea vomiting
Quite irritating to skin and to mucous membranes
GI irritation
Dosages Individualized for each patient 25 ndash 50mgkg
maximum of 1g
Supplied oral capsule ndash 500mg
oral solution ndash 250 amp 500mg5ml
Rectal suppositories ndash 324 amp 648mg
Narcotics
Do produce sedation amp euphoria greater in children
LA is required but dose should be decreased
Meperidine Synthetic opiate agonist
Very water soluble
Orally SC IM or IV
Peak effect by oral 1 hr amp lasts upto 4 hrs
Adverse reactions
-Seizures
-Extreme caution in hepatic or renal diseases or history of seizures
7
Dosage Oral SC or IM ndash 1to 22mgkg not to exceed 100 mg
Supplied Oral Tablets ndash 50 amp 100mg
Oral Syrup ndash 50mgml
Parental solution ndash 25 50 75 amp 100mgml
Fentanyl
Synthetic opiate narcotic analgesic
Very potent 01mg = 10mg Morophine75mg Meperidine
Pharmacokinetics
IV IM SM
Metabolized in liver Excreted in urine
Fentanyl Onset ndash 7 to 15mins
Duration ndash 1 to 2 hrs
Pharmacodynamics
Respiratory depression RR but returns to normal rapidly Tidal volume amp response to co2 depressed for extended period
Apnea
Less emetic than meperidine
NOT RECOMMENDED IN CHILDREN BELOW 2yrs
Dosage 0002 to 0004mgkg
Supplied 005mgml in 2 amp 5ml ampoules
Reversal drug Naloxone
Semisynthetic opiate antagonist
No agonist activity
Onset 2 to 5mins SC or IM amp 1 to 2mins IV
Reversal 45mins
Pt should be kept under continual surveillance
Adverse reaction nausea vomiting sweating hypotension hypertension ventricular tachycardia fibrillation
Dosage IV SC IM 001mgkg then 01mgkg every 2- 3mins maximum 2mg
Supplied 002 004 1mg solutions
Antihistamines
Hydroxyzine
Oral or IM
Effect ndash 15 ndash 30mins
Half-life ndash 3 hrs
Uses
To relieve anxiety
Used as an anti-histamine
Used to control nausea and vomiting including that associated with motion sickness and pregnancy
Adverse reaction dry mouth drowsiness hypersentivity
Dosage Oral ndash 1 to 2mgkg
IM ndash 11mgkg
Promethazine Oral or IM Onset 15 to 60mins Duration 4 to 6 hrs Uses
To prevent and treat nausea and vomiting associated with motion pregnancy or surgery
Produces sedation and reduce swelling pain and trismus
Lower seizure threshold Adverse reaction dry mouth blurred vision thickening of bronchial secretions Dosage OralIM ndash 05-11mgkg
maximum 25 mg
Diphenhydramine
Oral IM IV
Onset -1hr
Duration ndash 4 to 6 hr
Metabolized in liver
Adverse reaction disturbed coordination thickening of bronchial secretions
Dosage Oral IM IV ndash 1 to 15mgkg
maximum 50mg
Tranquilizers
Major tranquilizer antipsychotic produce calmness control symptoms of psychoses cause reversible extra pyramidal symptoms and do not tend to cause habituation
Minor tranquilizer antianxiety agents also cause calmness do not cause extrapyramidal symptoms Used in conditions like nervous tension and mild depression
8
Classification
Antipsychotics
Phenothiazine derivatives
Chlorpromazine promazine
Butryophenones
Haloperidol
Rauwolfia alkaloids
Reserpine
Antianxiety drugs
Propyl alcohol derivatives
Meprobamate
Benzodiazepine derivatives
Diazepam
Miscellaneous compounds
Hydroxyzine
Meprobamate
White crystalline powder slightly bitter in taste
Only administered orally
Peak blood concentration ----1 to 3hrs
10 ---------excreted unchanged Rest --- excreted as a oxidized derivative or as a glucoronide
Uses
To relieve day time anxiety
Induce sleep in insomniacs
To reduce anxiety associated with dental treatment
Anti-convulsant ndash petit mal epilepsy
Adverse reaction leucopenia acute non-thrombocytopenic purpura ecchymoses eosinophilia edema adenopathy
Dosage Childrengt 6yrs 100 to 200mg
Not recommended for children under 6yrs
Monitoring during sedation
1 Pulse
2 Blood pressure
3 ECG
4 Respiration
5 Temperature
Pulse
Manual Electronic
bull Radial Brachial
bull Facial labial
Blood pressure
ndash Stethoscope amp sphygmomanometer
ndash Automatic devices
ndash Direct cannulation of an artery ndash very accurate
Electrocardiograph
Heart rate rhythm myocardial function
9
Respiration
ndash Monitoring respiratory rate
ndash Observing the rise amp fall of the chest wall
ndash Observing the color of mucous membrane
ndash Observing the inflation amp deflation of the reservoir bag
Devices for monitoring respiration
1 The Precordial pretracheal stethoscope
2 The esophageal stethoscope
ndash Respiratory rate
ndash Heart rate
ndash Any abnormal sounds
Pulse Oximeter
ndash Oxygen saturation
ndash Heart rate
ndash Oxisensor site
ndash Fingers
ndash Toe
ndash Ear lobe
Mechanism
Oxygenated Hb ndash red light
Deoxygenated Hb- infrared light
Tissue pressure from arterial pulse (plethysmography)
Advantages
ndash Safe amp noninvasive
ndash Simple to use
ndash Information is rapidly available for clinical decision
ndash Indirectly indicates respiratory adequacy
Disadvantages
ndash Finger probes can get dislodged
ndash Emitted light source may cause burning
ndash Non reusable probes are expensive
ndash Does not directly determine airway patency
Capnography
1 The presence absence of air flow
2 Indicates depth amp adequacy of respiration
3 Continues analysis of the co2 content of the respired air ndash indicates respiratory adequacy
Temperature
ndash Disposable nondisposable thermometer
ndash Esophageal rectal temp probe
10
Discharge criteria
Cardiovascular function is satisfactory amp stable
Airway patency is uncompromised amp satisfactory
Pt is easily arousable amp protective reflexes intact
State of hydration is adequate
Pt can talk if applicable
Pt can sit unaided if applicable
Pt can ambulate with minimal assistance if applicable
Presedation level of responsiveness achieved
Responsible individual is available
1
PULP THERAPY OF VITAL TEETH
DR MITAKSHARA NIRWAN
Contents
Indirect pulp capping
Direct pulp capping
Medications amp materials used in pulp capping
Pulpotomy
MTA
Apexogenesis
INDIRECT PULP CAPPING
Pieter Van Forest - first to speak about root canal therapy
Glove designed instruments that could prepare a canal to a certain size and taper(1910)
Indirect pulp capping is defined as a procedure where in small amount of carious dentin is retained in
deep areas of cavity to avoid exposure of pulp followed by placement of a suitable medicament and
restorative material that seals off the carious dentin and encourages pulp recovery (Ingle)
A procedure in which only the gross caries is removed from the lesion and the cavity is sealed for a
time with a biocompatible material (McDonald)
Objective of indirect pulp capping
These were given by Eidelman in 1965
bull Arresting the carious process
bull Promoting dentin sclerosis
bull Stimulating formation of tertiary dentin
bull Remineralization of carious dentin
Layers of Carious Dentin Indications of Indirect Pulp Capping
History
Mild pain associated with eating
Negative history of spontaneous extreme pain
Clinical Examination
Deep carious lesion which are close tobut not involving the pulp in vital primary or young
permanent teeth
No mobility
Nominal pulp inflammationdefinite layer of affected dentin after removal of infected dentin
Radiographic examination
Normal lamina dura amp PDL space
No radiolucency around the apices
2
Contraindications of Indirect Pulp Capping
History
Sharp penetrating pulpalgia
Prolonged spontaneous pain especially at night
Clinical examination
Mobility of tooth
Discoloration of tooth
Negative reaction of electric pulp testing
Radiographic examination
Definite pulp exposure
Break in the lamina dura
Radiolucency around the apices
Widened PDL space
Treatment procedure
Sequelae of Indirect Pulp Capping Three distinct types of new dentin formation take place
1 Cellular fibrillar dentinmdashfirst 2 months
2 Globular dentinmdash3 months
3 Tubular dentin (uniform mineralized dentin)
bull 15th of reparative dentin formation begins in less than 30 days
bull After 3 months 01 mm is formed
DIRECT PULP CAPPING Defined by Kopel (1992) as the placement of a medicament or non medicated material on a pulp that
has been exposed in course of excavating the last portions of deep dentinal caries or as a result of
trauma
Objective
To create new dentin in the area of the exposure and subsequent healing of the pulp
Rationale
achieve a biologic closure of the exposure site by deposition of hard tissue barrier (dentin bridge)
between pulp tissue and capping material thus walling off the
INDICATIONS
Small mechanical exposure
Easily controlled haemorrhage
Bright red haemorrhage
True pinpoint exposure
CONTRAINDICATIONS
Severe toothache at night
Spontaneous pain
Tooth mobility
Radiographic appearance of pulp periradicular de- generation
Excess of hemorrhage at the time of exposure Serous exudate from the exposure
Externalinternal root resorption
Swellingfistula
Histological Changes after Pulp Capping
These were illustrated be Glass and Zander in 1949
After 24 hours Necrotic zone adjacent to calcium
hydroxide paste is separated from healthy pulp
tissue by a deep staining basophilic layer
After 7 days Increase in cellular and fibroblastic
activity
After 14 days Partly calcified fibrous tissue lined by
odontoblastic cells is seen below the calcium
proteinate zone disappearance of necrotic zone
After 28 days Zone of new dentin
3
Medications and Materials Used for Pulp Capping Calcium hydroxide
Corticosteroids amp antibiotics
Inert materials
Collagen fibers
4-META adhesive
Direct bonding
Isobutyl cyanoacrylate
Denatured albumin
Mineral trioxide aggregate
Laser
Bone morphogenic protein
PULPOTOMY
Finn (1995) defined it as the complete removal of the coronal portion of the dental pulp
followed by placement of a suitable dressing or medicament that will promote healing and
preserve vitality of the tooth
American Academy of Pediatric Dentistry (1998) defined pulpotomy as the amputation of
affected infected coronal portion of the dental pulp preserving the vitality and function of the
remaining part of radicular pulp
Objectives
bull Removal of inflamed and infected coronal pulp at the site of exposure thus preserving the vitality of the
radicular pulp and allowing it to heal
bull Maintain the tooth in the dental arch
Rationale
bull Radicular pulp is healthy and capable of healing after surgical amputation of the infected coronal pulp
bull Preserves vitality of the radicular pulp
bull Maintains tooth in a physiologic condition
Indications of Pulpotomy bull Mechanical pulp exposure in primary teeth
bull Teeth showing a large carious lesion but free of radicular pulpitis
bull History of only spontaneous pain
bull Hemorrhage from exposure sites bright red and can be controlled
bull Absence of abscess or fistula
bull No interradicular bone loss
bull No interradicular radiolucency
Contraindications of Pulpotomy bull Persistent toothache
bull Tenderness on percussion
bull Root resorption more than 13rd of root length
bull Large carious lesion with nonrestorable crown
bull Highly viscous sluggish hemorrhage from canal orifice which is uncontrollable
bull Medical contradictions like heart disease immuno compromised patient
bull Swelling or fistula
bull External or internal resorption
bull Pathological mobility
bull Calcification of pulp
Classification of pulpotomy
4
Formocresol Pulpotomy
Iby BUCKLEY in 1904
Sweet (1930) Formulated multi visit technique
Doyle (1962) Advocated 2 sitting procedure (complete devitalization)
Spedding (1965) Gave 5 minute protocol (partial devitali- zation)
Venham (1967) Proposed 15 seconds procedure
Current concept uses 4 minutes of application time
Composition of formocresol Buckleyrsquos Formula
bull Cresol ndash 35 percent
bull Glycerol ndash 15 percent
bull Formaldehyde ndash 19 percent
bull Water ndash 31 percent
Mechanism of Action
It prevents tissue autolysis by bonding to the proteins Bonding is of peptide groups of side chain amino acids and is a reversible process accomplished without
changing the basic structure of protein molecules
Histological Changes
bull Demonstrated by Mass and Zilbermann11 in 1933 and also by Massler and Mansokhani in 1959
bull Immediately the pulp becomes fibrous and acidophillic
bull Seven to fourteen days Three zones appear
a broad eosinophilic zone of fixation
b broad pale-staining zone of atrophy with poorcellular definition
c broad zone of inflammation extending apically into normal pulp tissue
bull One yearndash Progressive apical movement of these zones with only acidophillic zone left at the end of 1 year
Modified Formocresol Pulpotomy
Used by TRASK(1972)
The technique is identical to that described for primary teeth except that the formocresol pellet is
sealed permanently in the tooth
Two-visit Devitalization Pulpotomy
Indications
bull There is evidence of sluggish bleeding at the amputation site that is difficult to control
bull Pus in the chamber but none at the amputation site
bull There is thickening of the PDL
bull History of pain
Contraindications
bull Nonrestorable tooth
bull Tooth with necrotic pulp
5
Glutaraldehyde Pulpotomy
It was first suggested by S Gravenmade Introduced by Kopel in 1979
Mechanism of Action
bull Glutaraldehyde produces rapid surface fixation of the underlying pulpal tissue
bull A narrow zone of eosinophilic stained and compressed fixed tissue is found directly beneath the area of application which blends into vital normal appearing tissue apically
bull With time the glutaraldehyde fixed zone is replaced by macrophagic action with dense collagenous tissue thus the entire root canal tissue is vital
Cvekrsquos Pulpotomy
bull This is also called as calcium hydroxide pulpotomy or young permanent partial pulpotomy
bull This was proposed by Mejare and Cvek16 in 1978
bull Indicated in young permanent teeth where the pulp is exposed by mechanical or bacterial means and the
remaining radicular tissue is judged vital by clinical and radiographic criteria whereas the root closure is
notcomplete
MINERAL TRIOXIDE AGGREGATE (MTA) Torabinejad described the physical and chemical properties of MTA in 1995
It is ash colored powder made primarily of fine hydrophilic particles of
1 tricalcium aluminate
2 tricalcium silicate
3 silicate oxide
4 tricalcium oxide
5 bismuth dioxide
Hydration of the powder results in a colloidal gel composed of calcium oxide crystals in an amorphous
structure This gel solidifies into a hard structure in less than three hours
PROPERTIES OF MTA
It is biocompatible material and its sealing ability is better than that of amalgam or ZOE
Initial pH is 102 and set pH is 125
The setting time of cement is 4 hours
The compressive strength is 70 MPA which is comparable with that of IRM
Low cytotoxicity ndash It presents with minimal inflammation if extended beyond the apex
Mineral trioxide aggregate (MTA) has demonstrated the ability to induce hard-tissue formation in
pulpal tissues and it promotes rapid cell growth
APEXOGENESIS
It is defined as the treatment of a vital pulp by capping or pulpotomy in order to permit continued
growth of the root and closure of the open apex
Rationale
Maintenance of integrity of the radicular pulp tissue to allow for continued root growth
Indications
bull Indicated for traumatized or pulpally involved vital permanent tooth when root apex is incompletely formed
bull No history of spontaneous pain
bull No sensitivity on percussion
bull No hemorrhage
bull Normal radiographic appearance
Contraindications
bull Evidence that radicular pulp has undergone degenerative changes
bull Purulent drainage
bull History of prolonged pain bull Necrotic debris in canal
bull Periapical radiolucency
6
1
Gupta A Dhingra R Chaudhari P Gupta A
Department of Paedodontics and Preventive Dentistry Faculty of Dental Sciences SGT University Gurgaon Haryana India
Journal of Indian Society of Pedodontics and Preventive Dentistry
Volume 35 I Issue 3 I July-September 2017
A COMPARISION OF VARIOUS MINIMALLY
INVASIVE TECHNIQUES FOR THE REMOVAL
OF DENTAL FLUOROSIS STAINS IN
CHILDREN
DR MITAKSHARA NIRWAN
CONTENTS
bull Introduction
bull Aims
bull Materials and Methods
bull Results
bull Discussion
bull Conclusion
bull Critical analysis
bull References
INTRODUCTION
bull Dental fluorosis is a developmental disturbance of dental enamel caused by
successive exposure to high concentrations of fluoride during tooth
development
bull Various methods of therapy are advocated for the treatment of fluorosis -
stained teeth which range from invasive ceramic veneer bonding restorations
to abrasive chemical treatments
bull The combination of dental bleaching techniques and microabrasion appears
as an excellent conservative solution to reestablish health in fluorosis
affected teeth
AIMS
bull The aim of the study was to evaluate and compare the effectiveness of
minimally invasive techniques for the removal of dental fluorosis
stains in children in vivo
MATERIALS AND METHODS
Patients visiting the department of Pedodontics and Preventive dentistry
Faculty of Dental Sciences SGT University Gurgaon
bull Sample size 90 patients
bull Age group 10 -17 years
bull Caries cracks or periodontal
disease on anterior teeth
bull Abscess draining sinus
cellulitis
bull Non vital teeth
hypersensitive exposed
crevices
bull Orthodontic appliance
bull Past history of bleaching
bull At least two permanent
maxillary anterior teeth
bull TSIF of score 4
bull Free of systemic diseases
Inclusion criteria Exclusion criteria
2
Groups
Group A In office bleaching with 35 hydrogen peroxide( Pola Office
Bleaching kit) activated by light emitting diode (LED) bleaching unit
(35 HP)
Group B Enamel microabrasion (EM) (PREMA Enamel Microabrasion
System) followed by in-office bleaching with 44 carbamide peroxide
gel (EM)
Group C In-office bleaching with 5 sodium hypochlorite (5
NaOCl)
A baseline colour evaluation was done by taking digital photograph of
the maxillary anterior teeth
RESULTS
Group 1
Colour stability
Group 2 Group 3
Tooth sensitivity
Tooth sensitivity values were taken before the treatment
which was compared to immediate postoperative and follow
up visits It was checked using an electric pulp tester
maximum
moderate
least
immediately
group 2
group 1
group 3
1 month
group 2
group 1
group 3
3 month
group 2
group 1
group 3
Patient satisfaction score
Satisfaction was assessed on visual analog scale
Range 1 to 5
Groups percentage of patients
who were satisfied with
the treatment
Number of patients
who reported slight
reappearance of colour
Group 1
90
7
Group 2
83
8
Group 3
73
7
3
Number of Appointments
Groups One sitting Two sittings Three
sittings
Group 1
25
4
1
group 2
26
3
1
Group 3
30
0
0
DISCUSSION
bull Hydrogen peroxide is capable of penetrating the tooth osmosis and through porosities and cracks subsequently acting directly on the pigmented molecules
bull Gurgan et al investigated 3 different light systems and found out that diode laser system with gave best tooth whitening and least tooth sensitivity
bull In the EM group the surface reflects and refracts light from the surface in such way that mild imperfections in underlying enamel are camouflaged While the highly polished surface of enamel enhances the aesthetic appearance
bull Train et al and Loguercio et al also had the similar results in their studies with EM mild fluorosis showed best results moderate showed moderate results while it had little effect on severe fluorosis
bull NaOCl was only effective on mild stains while moderate and severe
stains could only be lightened to quite an extent but could not be
completely removed
bull When NaOCl comes in contact with hypomineralized and discoloured
enamel it degrades and removes the chromogenic organic material
located on the enamel surface
CONCLUSION
bull It was concluded that esthetic appearance of teeth mild fluorosis can
be achieved by bleaching and microabrasion But in cases of
moderate fluorosis a combination of any of theses modalities can be
used
bull As no special maintenance precautions are required these maybe be
considered as an interesting alternative to conventional operative
treatment
bull Focuses on only TSIF of 4
bull Electric pulp testing is not the
right method to check for
sensitivity
bull Tooth Sensitivity changes
from person to person
bull Food habits can cause
staining of the teeth
bull Minimally invasive
bull Cheaper to veneers
bull Minimal loss of tooth structure
bull 4 parameters checked for the success of treatment
bull Inclusion of specific score of fluorosis for comparing the results
bull Maximum 3 appointments needed
CRITICAL ANALYSIS
Pros Cons
REFERENCES
bull Gurgan S Cakir FY Yazici E Different light-activated in officebleaching
systems Lasers Med Sci 201025817-22
bull Train TE McWhorter AG Seale NSWilson CF Guo IY Examination of
esthetic improvement and surface alteration following microabrasion in
fluorotic human incisors in vivoPediatr dent 199618353-62
bull Loguercio AD Correia LD Zago C Tagliari D Neumann E Gomes OM et al
Clinical effectiveness of two microabrasion materials materials for the
removal of enamel flurosis stains Oper Dent 200732531-8
4
3
CASE 3
A 5-year-old female child has complaint of mild intermittent pain with primary mandibular left first molar She
had undergone pulpectomy treatment for the same during which an instrument separation has occurred in
the mesiobuccal root canal by a resident doctor
A radiograph revealed a separated instrument of about 4 mm in size lodged in the apical third but within the
confines of the mesial root An attempt was made for its retrieval but was unsuccessful The extraction of the
involved tooth was carried out under local anesthesia followed by a band and loop space maintainer
CASE 4
A 7-year-old male child reported with a chief complaint of mild intermittent pain on food lodgment with the primary mandibular right first and second molars The patient had a history of dental treatment at a private
dental clinic few months back which he did not continue further
Clinical examination revealed glass ionomer restoration with 85 and proximal caries with 84 leading to food lodgment An intraoral periapical radiograph with 85 revealed empty root canals with a separated
instrument of about 3ndash4 mm size beyond the apex of mesial root close to the developing succedaneous premolar
4
DISCUSSION
Stainless steel files usually separate fracture due to the excessive amounts of torque and overuse or the
preexisting distortion of the instrument whereas in NiTi rotary files it is a combined result of torsional stress and cyclic fatigue
Therapeutic options for the management of separated endodontic instruments include no intervention nonsurgical (orthograde conservative) management surgical management and tooth extraction
Use of ultrasonic scaler Masserann technique Endo extractor and Cavi-Endo ultrasonic instruments are some of the methods popular for retrieval of a separated endodontic instrument in the permanent tooth
In case 1 a 6-mm-long manual reamer was retrieved successfully with the use of GG drill using a manual file and copious irrigation which is the most desired treatment outcome
In case 2 the retrieval of separated rotary file lodged in the middle third of the root canal was unsuccessful in spite of multiple attempts It was therefore managed with routine obturation followed by restoration to maintain the tooth in its physiological functional state It was kept under close periodic follow-up at least
every 3 months This treatment option should be encouraged where it is possible to follow up the patient clinically and radiographically at close periodic intervals as there is the possibility of instrument escaping
into bone due to physiological root resorption
In cases 3 and 4 an instrument has separated in the apical root portion
In case 3 it was within the root canal and thus an attempt was made for its retrieval which was
unsuccessful It was therefore extracted to prevent the fractured instrument from getting exposed in the bone following resorption as there is no accurate and consistent established age for initiation of resorption in primary teeth known per se
In case 4 an immediate extraction of involved tooth was carried out as the separated instrument was beyond the apex of the primary tooth root
Age of the child clinical signs and symptoms and amount of root resorption are the factors which can also influence the management of separated instrument in primary teeth
Moreover if an instrument has separated after initial cleaning and shaping of root canal maintaining a tooth is not a problem as clinical signs and symptoms are not anticipated and the good prognosis is expected
However if an instrument has separated early during the initial cleaning and shaping of the root canal clinical symptoms may compromise the prognosis
Therefore these factors should be kept in mind while planning a suitable management strategy to avoid or at least reduce the burden of extraction and wear of space maintainer for longer period
5
CONCLUSION
The management and prognosis of a primary tooth with a separated instrument is
dependent on the level of instrument fracture within the root age of the child root
resorption and clinical signs and symptoms of the involved tooth
Different management approaches can be tried depending on clinical situations keeping
in mind benefits vs risks in preserving the tooth
PROS amp CONS
PROS
The entire procedure is given
by step by step
Well descriptive xrays and
photographs
CONS
Medical history has not been
given
REFERENCES
1 TOMER ANIL K ET AL ldquoBROKEN FILE RETRIEVAL PUZZLE IN ENDODONTICSrdquo
(2016)
2 SHENOY A MANDAVA P BOLLA N ET AL A NOVEL TECHNIQUE FOR REMOVAL OF
BROKEN INSTRUMENT FROM ROOT CANAL IN MANDIBULAR SECOND MOLAR
INDIAN J DENT RES 201425(1)107ndash110
3 PATEL J MORAWALA A TALATHI R ET AL RETRIEVAL OF A BROKEN INSTRUMENT
FROM ROOT CANAL IN PRIMARY ANTERIOR TEETH UNIV RES J DENT 20155(3)203ndash
206
4 MORANKAR R GOYAL A GAUBA K ET AL MANUAL VERSUS ROTARY
INSTRUMENTATION FOR PRIMARY MOLAR PULPECTOMIES - A 24 MONTHS
RANDOMIZED CLINICAL TRIAL PEDIAT DENT J 201828(2)96ndash102
5 KASHYAP NILOTPOL (2018) RETAINING PRIMARY MOLARS WITH INSTRUMENT
SEPERATION A CASE REPORT AND CLINICAL GUIDE
6
1
IMPACT OF 6 CITRIC ACID AND ENDOACTIVATOR AS IRRIGATION ADJUNCTS ON OBTURATION QUALITY AND PULPECTOMY OUTCOME IN
PRIMARY TEETH
NEETU JAIN SHALINI GARG ABHISHEK DHINDSA SAKSHI JOSHI HARJOY
KHATRIA
PEDIATRIC DENTAL JOURNAL 2019 29
1
DR MITAKSHARA NIRWAN
CONTENTS
bull INTRODUCTION
bull AIMS amp OBJECTIVES
bull CASE REPORT
bull RESULTS
bull DISCUSSION
bull CONCLUSION
bull PROS AND CONS
bull REFERENCES
2
INTRODUCTION
bull ENDODONTIC THERAPY IN PRIMARY TEETH INVOLVES DISINFECTION OF THE ROOT CANAL
SYSTEM AND ITS OBTURATION WITH RESORBABLE PASTE
bull THE CONTENTS OF ROOT CANAL ALONG WITH SMEAR LAYER ARE EXPECTED TO BE REMOVED
DURING THE BIOMECHANICAL PREPARATION
bull IN VITRO AND CLINICAL DOCUMENTS HAVE INDICATED THAT MECHANICAL PREPARATION OF
THE CANAL LEAVES LARGE PORTIONS OF THE CANAL WALLS UNDEBRIDED AND COMPLETE
REMOVAL OF THE BACTERIA BY THIS MECHANICAL PROCEDURE ALONE IS UNLIKELY TO BE SEEN
THEREFORE SOME FORM OF DISINFECTIONIRRIGATION IS MANDATORY TO KILL THE
MICROORGANISMS AND TO REMOVE THE RESIDUAL TISSUES
3
bull THE IDEAL REQUISITES OF A ROOT CANAL IRRIGANT AS GIVEN BY ZEHNDER ARE
1 BROAD ANTIMICROBIAL SPECTRUM
2 HIGH EFFICACY AGAINST ANAEROBIC AND FACULTATIVE MICROORGANISMS ORGANIZED
IN BIOFILMS
3 ABILITY TO DISSOLVE NECROTIC PULP TISSUE REMNANTS
4 ABILITY TO INACTIVATE ENDOTOXIN
5 ABILITY TO PREVENT THE FORMATION OF A SMEAR LAYER DURING INSTRUMENTATION OR
TO DISSOLVE THE LATTER ONCE IT HAS FORMED
6 SYSTEMICALLY NONTOXIC WHEN THEY COME IN CONTACT WITH VITAL TISSUES
NONCAUSTIC TO PERIODONTAL TISSUES AND WITH LITTLE POTENTIAL TO CAUSE AN
ANAPHYLACTIC REACTION
SINCE NO SINGLE IRRIGANT HAS THESE OPTIMAL PROPERTIES STUDIES HAVE REPORTED THE USE
OF TWO OR MORE SOLUTIONS IN A SPECIFIC SEQUENCE OR IN COMBINATIONS FOR BETTER
RESULTS 4
bull SEVERAL IRRIGATING SOLUTIONS ALONG WITH CHELATING AGENTS HAVE BEEN USED
DURING BIOMECHANICAL PREPARATION OF ROOT CANAL BOTH IN PRIMARY AND
PERMANENT TEETH
bull HOWEVER NONE OF THE AVAILABLE IRRIGATING SOLUTIONS HAS BEEN REGARDED CLEARLY
AS OPTIMAL SOLUTION BECAUSE OF THEIR LIMITED EFFECTIVENESS ESPECIALLY IN APICAL
13RD OF THE ROOT CANAL SYSTEM
bull TO OVERCOME SUCH LIMITATIONS USE OF ENDOACTIVATOR HAS BEEN PROPOSED AS AN
IRRIGATION FACILITATOR THAT IS BASED ON SONIC VIBRATION (UP TO 10000 CPM) WHICH
FACILITATES THE IRRIGANT PENETRATION AND ITS RENEWAL WITHIN THE CANAL
bull ACTIVATION SYSTEMS RESULTED IN BETTER REMOVAL OF THE SMEAR LAYER IN THE APICAL
THIRD OF ROOT CANALS IN COMPARISON TO CONVENTIONAL IRRIGATION
5
CITRIC ACID
bull CITRIC ACID IS A WEAK ORGANIC ACID WITH THE APPEARANCE OF WHITE CRYSTALLINE
POWDER AT ROOM TEMPERATURE
bull IT CAN EXIST EITHER IN WATER-FREE FORM (ANHYDROUS) OR MONOHYDRATE FORM THE
WATER-FREE FORM CRYSTALLIZES FROM THE HOT WATER WHEREAS THE MONOHYDRATE
FORMS FROM THE COLD WATER THE LATTER MAY BE CONVERTED TO ANHYDROUS FORM BY
HEATING MORE THAN 78degC
bull CITRIC ACID OCCURS NATURALLY IN THE BODY IN MITOCHONDRIA AND IS USED BY BLOOD
BANKS TO PREVENT COAGULATION OF TRANSFUSED BLOOD CITRIC ACID IS ALSO ESSENTIAL
TO HUMAN METABOLISM AND IS FOUND IN MANY FOODS
6
2
bull THE BIOLOGICAL EFFECTS OF CITRIC ACID ON THE PERIODONTAL STRUCTURE HAS BEEN
EXTENSIVELY STUDIED IN PERIODONTICS
bull NEUMAN AND NEWMAN SHOWED THAT CITRIC ACID IS THE MOST EFFECTIVE ACID IN
ALTERING THE SOLUBILITY OF HYDROXYAPATITE
bull YAMAGUCHI ET AL SHOWED THAT CITRIC ACID SOLUTION HAD ANTIBACTERIAL EFFECTS ON
ALL 12 ROOT CANAL BACTERIA TESTED
bull ARIAS-MOLIZ ET AL SHOWED THAT ETHYLENEDIAMINETETRAACETIC ACID (EDTA) HAS NO
BACTERICIDAL ACTIVITY EVEN AFTER 1 HOUR CONTACT
bull THIS ACID HAS THE ABILITY OF ROOT CANAL IRRIGATION AND ALSO SMEAR LAYER REMOVAL
DIFFERENT CONCENTRATIONS (1ndash50) HAVE BEEN PROPOSED GUTMANN ET AL CONCLUDED
THAT 10 CITRIC ACID IS BETTER THAN ULTRASOUND FOR SMEAR LAYER REMOVAL FROM THE
ROOT END CAVITIES
7
bull STUDIES HAVE SHOWN IRRIGATION WITH 6 CA FOR 15 OR 30 SECONDS IS QUITE
EFFECTIVE IN REMOVING ALL THE COMPONENTS OF THE SMEAR LAYER OF THE PRIMARY
TEETH WHEREAS PERITUBULAR DENTIN DESTRUCTION WAS OBSERVED WHEN HIGHER
CONCENTRATION OF CITRIC ACID WAS USED AS AN IRRIGATING SOLUTION
8
AIMS amp OBJECTIVES
bull THIS STUDY WAS AIMED TO EVALUATE THE CLINICAL AND RADIOGRAPHIC OUTCOME OF
PULPECTOMY ALONG WITH QUALITY OF OBTURATION USING 6 CITRIC ACID AND
ENDOACTIVATOR
9
CASE REPORT
bull 350 CHILDREN (3-9 YEARS) WITH CLINICAL SIGNS AND SYMPTOMS OF CHRONIC IRREVERSIBLE
PULPITIS IN DEEPLY CARIOUS TEETH WERE SCREENED DURING SCHOOL DENTAL HEALTH
PROGRAM FROM MAY 2014-JULY 2014
bull 123 CHILDREN REPORTED TO THE DEPARTMENT AND 67 CHILDREN WERE SELECTED BASED ON
INCLUSION AND EXCLUSION CRITERIA
RECRUITMENT OF PATIENTS
10
INCLUSION CRITERIA
bull HISTORY OF SPONTANEOUS PAIN AND UNCONTROLLED BLEEDING AFTER PULP AMPUTATION
EXCLUSION CRITERIA
bull EVIDENCE OF INTERNAL OR EXTERNAL (PHYSIOLOGICPATHOLOGIC) ROOT RESORPTION OF MORE THAN A THIRD OF ITS LENGTH
bull ROOT CANAL OBLITERATION OR ANATOMIC ANOMALIES
bull INADEQUATE BONE SUPPORT OR NON RESTORABLE TOOTH
bull ONCE PATIENTS ELIGIBILITY WAS CONFIRMED THE TREATMENT PROCEDURE WAS
EXPLAINED TO THE PARENTGUARDIAN AND INFORMED WRITTEN CONSENT WAS
OBTAINED FROM PARENTSGUARDIANS SHOWING WILLINGNESS FOR THEIR
CHILDRENS TREATMENT 11
PROCEDURE
bull PULPECTOMY WAS PERFORMED BY ONE OPERATOR OF PEDIATRIC DENTISTRY DEPARTMENT
USING A STANDARDIZED TREATMENT PROTOCOL FOR ALL THE PATIENTS
bull AFTER ADMINISTRATION OF LOCAL ANESTHESIA RUBBER DAM WAS APPLIED FOR ISOLATION
bull ACCESS CAVITY WAS PREPARED USING AIR-ROTOR HAND PIECE WITH 8 ROUND BUR AND
PULP TISSUE WAS EXTIRPATED WITH THE HELP OF SPOON EXCAVATOR
bull FURTHER THE NEGOTIATION OF THE CANALS WAS DONE WITH 10 K-FILE
bull A DIAGNOSTIC RADIOGRAPH WAS TAKEN FOR ROOT LENGTH DETERMINATION AND
WORKING LENGTH WAS KEPT 1 MM SHORT OF THE RADIOGRAPHICAL APEX
bull ALL ROOT CANALS WERE INSTRUMENTED MANUALLY USING K-FILES AND WERE IRRIGATED
WITH 10 ML 09 NORMAL SALINE AND 1 SODIUM HYPOCHLORITE AS STANDARDIZING
PROTOCOL FOR ROOT CANAL PREPARATION AND DISINFECTION
12
3
GROUP 1 (CA + E) - IRRIGATION WAS DONE
WITH 10 ML OF 6 CITRIC ACID (CITOCID AMMDENT)
AND IRRIGANTS WERE SONICALLY AGITATED WITH
ENDOACTIVATOR (DENTSPLY) FOR 30 S PER CANAL USING REDBLUE
ENDOACTIVATOR TIP
GROUP 2 (CA) - 10 ML OF 6 CITRIC ACID FOR 1 MIN USING
27 GAUZE IRRIGATING NEEDLE
GROUP 3(SH + E) - 10 ML OF 1 SODIUM HYPOCHLORITE
SOLUTION AND SONIC ACTIVATION WITH ENDOACTIVATOR
GROUP 4(SH) - 10 ML OF 1 SODIUM HYPOCHLORITE
SOLUTION USING IRRIGATING NEEDLE (CONTROL GROUP)
bull TEETH UNDERGOING PULPECTOMY WERE RANDOMLY ENROLLED BY CHIT METHOD INTO THREE
STUDY AND ONE CONTROL GROUP
13
bull IN CITRIC ACID GROUPS FINAL RINSE WITH NORMAL SALINE WAS DONE TO REMOVE THE
REMAINING CRYSTALS (CHELATES)
bull FOLLOWING BIOMECHANICAL PREPARATION THE ROOT CANALS WERE DRIED WITH STERILE
ABSORBENT PAPER POINTS AND OBTURATED WITH VITAPEX USING HAND HELD
LENTULOSPIRAL FINAL RESTORATIONS WERE DONE USING COMPOSITE RESIN
14
bull CLINICAL FOLLOW UP WAS DONE AT 24 H1 WEEK 1 MONTH 6 MONTH AND 12
MONTH TO CHECK PAIN PRESENCE AND PAIN FREQUENCY (ONCEMORE THAN ONCE)
SWELLING FISTULA SENSITIVITY TO PERCUSSION
bull RADIOGRAPHIC FOLLOW UP WAS DONE AT 6 MONTH AND 12 MONTH FOR ANY
DEVIATED ERUPTION OF SUCCEDANEOUS TEETH EXCESS FILING MATERIAL AND ITS
RESORPTION EXTERNALINTERNAL ROOT RESORBTION CALCIFIC METAMORPHOSIS
PRESENCE OF FURCATION RADIOLUCENCY
CLINICAL amp RADIOGRAPHIC FOLLOW UP
15
RADIOGRAPHIC ASSESSMENT OF OBTURATION QUALITY
bull POSTOPERATIVE RADIOGRAPHS WERE VISUALLY ASSESSED FOR QUALITY OF OBTURATION BY
TWO INDEPENDENT EXAMINERS (SG AD) WHO WERE BLINDED WITH REGARD TO
IRRIGATION PROTOCOL GROUP TO ENHANCE CALIBRATION EACH EXAMINER ASSESSED THE
RADIOGRAPH INDEPENDENTLY AND LATER REVIEWED TOGETHER FOR FINAL ASSESSMENT
INDIVIDUAL ROOT WAS TAKEN AS UNIT OF ANALYSIS FOR GRADE OF OBTU- RATION AND
SCORING CRITERIA WERE AS GIVEN BY COLL JA 1996
1 UNDER FILLED - FILLING MATERIAL ENDED 1 MM OR MORE SHORT OF THE APEX
2 OPTIMAL FILLING- FILLING MATERIAL APPEARED TO END AT THE RADIOGRAPHICAL APEX
3 OVERFILLED - FILLING MATERIAL EXTRUDED PAST THE RADIOGRAPHIC APEX
4 OPTIMALLY FILLED ROOTS WERE FURTHER ASSESSED FOR THE PRESENCE OF VOIDS AND VOID
AREA (ROOT CANAL SURFACE UNTOUCHED BY THE ROOT CANAL FILLING MATERIAL) IN THREE
VISUALLY DIVIDED SECTIONS OF THE ROOT IE CORONAL MIDDLE AND APICAL 13RD
16
RESULTS
bull OVERALL CLINICAL AND RADIOGRAPHIC SUCCESS RATE OVER A PERIOD OF ONE YEAR WAS
9886 amp 977 RESPECTIVELY
bull ALL GROUPS WERE SIGNIFICANTLY (P = 001) EFFECTIVE IN ALLEVIATING PAIN WITHIN 24 H
OF PULPECTOMY
17 18
4
19
bull IMMEDIATE POST OPERATIVE RADIOGRAPHIC ASSESSMENT REVEALED 68 (102150) ROOTS
WITH OPTIMAL OBTURATION AND 32 (48150) WITH OVERFILLINGUNDERFILLING MAXIMUM
NO OF OPTIMAL FILLINGS WERE OBSERVED IN GROUP1 (CA + E) (3333) FOLLOWED BY
GROUP 2 (CA) (2549) GROUP 3(SH + E) (2549) AND GROUP 4(SH) (1568)
bull CITRIC ACID GROUPS HAD MORE NUMBER OF OPTIMALLY FILLED ROOTS 588 (60102) THAN
NON CITRIC ACID GROUPS 412 (42102)
bull ENDOACTIVATOR CONTRIBUTED TO 18 OF OPTIMAL OBTURATION IRRESPECTIVE OF
CHELATING AGENT USED
20
21
bull MAXIMUM NO OF VOIDS AND VOID AREAS WERE IN NON CITRIC ACID GROUPS
(6419 amp 5384) COMPARED TO CITRIC ACID GROUPS (3580 amp 4615)
RESPECTIVELY
bull ANALYSIS OF ROOT 13RD REVEALED MAXIMUM NO OF VOID AREA IN APICAL
13RD (4755) FOLLOWED BY MIDDLE 13RD (3846) AND CORONAL 13RD
(1398)
bull LEAST NO OF VOIDS amp VOID AREA (1111 amp 1608) WERE OBSERVED WHEN
ENDOACTIVATOR ALONG WITH CHELATING AGENT WAS USED (GROUP 1)
HOWEVER THIS WAS STATISTICALLY INSIGNIFICANT
22
DISCUSSION
bull IN THE PRESENT STUDY 1 SODIUM HYPOCHLORITE WAS USED ALONG WITH 6 CITRIC ACID
(CHELATING AGENT) WHICH IS REPORTED TO BE AS EFFECTIVE AS 17 EDTA
bull CITRIC ACID (BIOLOGICAL ACID) IS FOUND TO BE BIOCOMPATIBLE AND LEAST IRRITATING TO
PERIAPICAL TISSUES THAN OTHER CHELATING AGENTS
bull USE OF SODIUM HYPOCHLORITE SOLUTION FOLLOWING CHELATING AGENT WAS AVOIDED AS IT
RAPIDLY PRODUCES SEVERE EROSION OF ROOT CANAL WALL DENTIN
bull TRADITIONAL APPROACH OF DELIVERING IRRIGANTS INTO THE ROOT CANAL SPACE USING
SYRINGES AND METAL NEEDLES HAS BEEN FOUND TO BE INEFFECTIVE ESPECIALLY IN THE AREAS OF
ANASTOMOSES BETWEEN CANALS AND APICAL 13RD OF ROOT CANAL
23
bull THEREFORE TO ACHIEVE BETTER CLEANING EFFICIENCY IRRIGANT ACTIVATION HAS BEEN
RECOMMENDED SONIC ACTIVATION HAS BEEN REPORTED TO RESULT IN BETTER ROOT CANAL
CLEANLINESS AS COMPARED TO NO ACTIVATION OF IRRIGANT
24
5
CONCLUSION
bull USE OF 6 CITRIC ACID DEFINITELY HELPED IN RAPID ELIMINATION OF PAIN RESOLUTION OF
PERI-RADICULAR RADIOLUCENCY BETTER OBTURATION QUALITY IN TERMS OF LESS VOIDS AND
VOID AREAS ALONG WITH MAXIMUM NO OF OPTIMAL OBTURATION UP TO APICAL AREA
bull 6 CITRIC ACID AND ENDOACTIVATOR IRRIGATION PROTOCOL PROVED TO BE THE BETTER
IRRIGATION PROTOCOL WHICH MAY CONTRIBUTE TO LONG TERM SUCCESS OF PRIMARY
TOOTH AND THE HEALTH OF UNDERLYING PERMANENT TOOTH
bull 6 CITRIC ACID ALONG WITH ENDOACTIVATOR MAY BE RECOMMENDED AS IRRIGATION
ADJUNCTS IN PULPECTOMY PROCEDURE OF PRIMARY TEETH
25
PROS AND CONS
PROS
bull PROPER EXPLANATION OF THE MATERIALS
USED
CONS
bull NO PREOPERATIVE AND POSTOPERATIVE
RADIOGRAPHS
26
REFERENCES
bull RAMACHANDRA JA NIHAL NK NAGARATHNA C VORA MS ROOT CANAL IRRIGANTS IN
PRIMARY TEETH WORLD J DENT 20156(3)229-234
bull MOHAMMADI Z JAFARZADEH H SHALAVI S KINOSHITA JI UNUSUAL ROOT CANAL
IRRIGATION SOLUTIONS J CONTEMP DENT PRACT 201718(5)415-420
bull ZEHNDER M ROOT CANAL IRRIGANTS J ENDOD 2006 32389- 98
bull SMITH JJ amp WAYMAN BE AN EVALUATION OF THE ANTIMICROBIAL EFFECTIVENESS OF
CITRIC ACID AS A ROOT CANAL IRRIGANT JOURNAL OF ENDODONTICS 1986 12(2) 54-58
bull TANNURE PN AZEVEDO CP BARCELOS R GLEISER R PRIMO LG LONG-TERM OUTCOMES OF
PRIMARY TOOTH PULPECTOMY WITH AND WITHOUT SMEAR LAYER REMOVAL A RANDOMIZED
SPLIT-MOUTH CLINICAL TRIAL PEDIATR DENT 201133316E20 27
bull CARON G NHAM K BRONNEC F MACHTOU P EFFECTIVENESS OF DIFFERENT FINAL IRRIGANT
ACTIVATION PROTOCOLS ON SMEAR LAYER REMOVAL IN CURVED CANALS J ENDOD
2010361361E6
bull COLL JA SADRIAN R PREDICTING PULPECTOMY SUCCESS AND ITS RELATIONSHIP TO
EXFOLIATION AND SUCCEDANEOUS DENTITION PEDIATR DENT 19961857E63
28
1
LOCAL
ANESTHESIA
DR MITAKSHARA NIRWAN
CONTENTS
Definition
Methods of inducing local anesthesia
Desirable properties
Electrophysiology of nerve conduction
Impulse propagation and spread
Mode and site of action of local anesthesia
Classification of local anesthetic according to biological site and mode of action
Dissociation of local anaesthetics
Mechanism of action of local anaethetics
Local anaesthetic agent
2
3
DEFINITION
Local anesthesia is defined as a loss of sensation in
a circumscribed area of the body caused by depression
of excitation in nerve endings or an inhibition of the
conduction process in peripheral nerves
An important feature of local anesthesia is that it produces
LOSS OF SENSATION WITHOUT INDUCING LOSS OF
CONSCIOUSNESS
4
METHODS OF INDUCING LOCAL
ANESTHESIA
Low temperature
Mechanical trauma
Anoxia
Neurolytic agents such as alcohol amp phenol
Chemical agents such as local anesthetics
PROPERTIES OF LOCAL
ANESTHESIA
It should not be irritating to tissue to which it is applied
It should not cause any permanent alteration of nerve structure
Its systemic toxicity should be low
Time of onset of anesthesia should be short
It should be effective regardless of whether it is injected into the tissue or applied locally to mucous membranes
The duration of action should be long enough to permit the completion of procedure
5 6
It should have the potency sufficient to give complete
anesthesia with out the use of harmful concentration solutions
It should be free from producing allergic reactions
It should be free in solution and relatively undergo
biotransformation in the body
It should be either sterile or be capable of being sterilized by
heat with out deterioration
2
ELETROPHYSIOLOGY OF
NERVE CONDUCTION
There is an electrical charge across the membrane
This is the membrane potential
The resting potential (when the cell is not firing) is a negative
electrical potential of -70mv that exists across the nerve
membrane produced by different concentrations of either side of
the membrane
The interior of nerve is NEGATIVE in relation to exterior
7 8
inside
outside
Resting potential of neuron = -70mV
+
-
+
-
+
-
+
-
+
-
SLOW DEPOLARIRIZATION
9
RAPID DEPOLARIZATION
The interior of nerve is POSITIVE in relation to exterior
REPOLARIZATION
10
bull Repolarization takes 07 msec
bull Depolarization takes 03 msec
SODIUM PUMP -
energy comes from the oxidative metabolism of ATP
bull The entire process require 1 msec
IMPULSE PROPOGATION
IMPULSE SPREAD
The propagated impulse travels along the nerve
membrane towards CNS The spread of impulse differs
in myelinated and unmyelinated nerve fibers
DEPOLARIZED SEGMENT ADJACENT RESTING AREA
MODE AND SITE OF ACTION OF LOCAL
ANESTHETICS
Local anesthetic agent interferes with excitation
process in a nerve membrane in one of the
following ways
Altering the basic resting potential of nerve
membrane
Altering the threshold potential
Decreasing the rate of depolarization
Prolonging the rate of repolarization
12
3
CLASSIFICATION OF LOCAL ANESTHETIC
SUBSTANCES ACCORDING TO
BIOLOGICAL SITE AND MODE OF ACTION
CLASS A
Agents acting at receptor site on external surface of nerve membrane
Chemical substance Biotoxins (eg tetrodotoxin and saxitoxin)
CLASS B
Agents acting on receptor sites on internal surface of nerve membrane
Chemical substance Quaternary ammonium analogues of lidocaine
scorpion venom 13
CLASS C Agents acting by receptor independent of
physiochemical mechanism
Chemical substance Benzocaine
CLASS D Agents acting by combination of receptors and
receptor independent mechanisms
Chemical substance most clinically useful anesthetic agents
(eg lidocaine mepivacaine prilocaine)
14
BASED ON THE SOURCE
NATUAL
SYNTHETIC
OTHERS
BASED ON MODE OF APPLICATION
bull INJECTABLE
bull TOPICAL
BASED ON DURATION OF ACTION
bull ULTRA SHORT
bull SHORT
bull MEDIEM
bull LONG
BASED ON ONSET OF ACTION SHORT
INTERMEDIATE
LONG
15
DISSOCIATION OF LOCAL
ANESTHETICS
Local anesthetics are available as salts (usually
hydrochlorides) for clinical use
The salts both water soluble and stable is dissolved in
either sterile water or saline
In this solution it exists simultaneously as unchanged
molecule (RN) also called base and positively charged
molecules (RNH+) called cations
RNH+ ==== RN+ H
+
16
The relative concentration of each ionic form in the solution varies
in the pH of the solution or surrounding tissue
In the presence of high concentration of hydrogen ion (low pH) the
equilibrium shifts to left and most of the anesthetic solution exists
in cationic form
RNH+ gt RN
+ + H
+
As hydrogen ion concentration decreases (higher pH) the
equilibrium shifts towards the free base form
RNH+ lt RN + H
+
17
The relative proportion of ionic form also depends on pKa or DISSOCIATION CONSTANT of the specific local anesthetic
The pKa is a measure of molecules affinity for H+
ions
When the pH of the solution has the same value as pKa of the local anesthetic exactly half the drug will exists in the RNH
+ form and
exactly half in RN form
The percentage of drug existing in either form can be determined by Henderson Hasselbalch equation
Log baseacid = pH - pKa
18
4
MECHANISM OF ACTION OF LOCAL
ANESTHETICS
The following sequence is proposed mechanism of action of LA
Displacement of calcium ions from the sodium channel receptor site
Binding of local anesthetic molecule to this receptor site
Blockade of sodium channel
19
Decrease in sodium conductance
Depression of rate of electrical depolarization
Failure to achieve the threshold potential level
Lack of development of propagated action potential
Conduction blockadehellip
20
21
Na + Na +
22
LOCAL ANESTHETIC AGENT
COMERCIALLY PREPARED LOCAL ANESTHESIA
CONSISTS OF
Local anesthetic agent (xylocaine lignocaine 2)
Vasoconstrictor (adrenaline 1 80000)
Reducing agent (sodium metabisulphite)
Preservative (methylparabencapryl
hydrocuprienotoxin)
Fungicide (thymol)
Vehicle (distillde waterNaCl)
LOCAL ANESTHETIC AGENT
The local anesthetics used in dentistry are divided
into two groups
ESTER GROUP
AMIDE GROUP
23 24
ESTER GROUP It is composed of the following
An aromatic lipophilic group
An intermediate chain containing
an ester linkage
A hydrophilic secondary or tertiary
amino group
AMIDE GROUP It is composed of the following
An aromatic lipophilic group
An intermediate chain containing
amide linkage
A hydrophilic secondary or tertiary
amino group
5
25
CLASSIFICATION OF LOCAL ANESTHETICS
ESTERS
Esters of benzoic acid
Butacaine
Cocaine
Benzocaine
Hexylcaine
Piperocaine
Tetracaine
Esters of Para-amino
benzoic acid
Chloroprocain
Procaine
Propoxycaine
26
AMIDES Articaine
Bupivacaine
Dibucaine
Etidocaine
Lidocaine
Mepivacaine
Prilocaine
Ropivacaine
QUINOLINE
Centbucridine
PHARMACOKINETICS OF LOCAL
ANESTHETICS UPTAKE
When injected into soft tissue most local anesthetics produce
dilation of vascular bed
Cocaine is the only local anesthetic that produces
vasoconstriction initially it produces vasodilation which is
followed by prolonged vasoconstriction
Vasodilation is due to increase in the rate of absorption of the
local anesthetic into the blood thus decreasing the duration of
pain control while increasing the anesthetic blood level and
potential for over dose 27
AMIDE LOCAL ANESTHETICS
The metabolism of amide local anesthetics is more
complicated then esters The primary site of
biotransformation of amide drugs is liver
Entire metabolic process occurs in the liver for lidocaine
articaine etidocaine and bupivacaine
Prilocaine undergoes more rapid biotransformation then the
other amides
28
REFERENCES
Handbook of local anesthesia ndash Stanley F Malamed ndash 6th
edition
Essentials of Local Anesthetic Pharmacology Daniel E
Becker Anesth Prog 2006 Fall 53(3) 98ndash109
WIKIPEDIEA
29
THANK YOU
30
1
Pharmacological Methods of Behavior
Management
DR MITAKSHARA NIRWAN
DEFINITIONS
bull Conscious Sedation ndash A minimally depressed level of consciousness that retains
the patients ability to independently and continuously maintain an airway and respond appropriately to physical stimulation or verbal command
(American Dental Association House Of Delegates 2000)
bull Deep Sedation ndash An induced state of depressed consciousness
accompanied by partial loss of protective reflexes including the inability to continuously maintain an airway independently and or to respond purposefully to physical stimulation or verbal command
bull General Anesthesia (G A) ndash An induced state of unconsciousness or complete loss of
protective reflexes including the inability to continually maintain an airway independently and respond purposefully to physical stimulation or verbal command
Conscious sedation
ADVANTAGES
Conscious
Protective reflexes active amp intact
Stable vital signs
Operating dentist may perform sedation
Minimum amount of equipment required
Prolong detainment in recovery room not required
Risk of complication very low
Excellent choice for poor ndash risk pt in dental office
Cost effective
General anesthesia
ADVANTAGES Not absolutely
essential May be the only
method Not necessary (no
pain reaction) Amnesia always
present
Conscious sedation
DISADVANTAGES
Pt cooperation is essential
Extremely difficult or mentally handicapped pt cannot always be managed
Use of local anesthesia is a must
Amnesia may or may not be present
General anesthesia DISADVANTAGES
Pt unconscious
Protective reflexes are depressed
Depressed
Advanced training required Dentist must not act also as anesthetist
Special equipment necessary
Detainment in recovery area necessary
High IOP amp postoperative complications
Not indicated in dental office
More expensive
Fundamental Concepts
bull Techniques that utilize drugs to induce co-operative yet conscious state in an otherwise uncooperative child ndash CONSCIOUS SEDATION
2
GOALS
1 To facilitate the provision of quality care
2 To minimize the extremes of disruptive behavior
3 To promote a positive psychologic response to treatment
4 To promote patient welfare amp safety
5 To return the patient to physiologic state
OBJECTIVES
1 The pt mood must be altered
2 The pt must remain conscious at all times
3 The pt must be cooperative
4 All protective reflexes must remain intact and active
5 Vital signs must remain stable and with in normal limits
6 The ptrsquos pain threshold should be elevated
7 Amnesia may be present
Indications
1 Preschool children
2 Lack of Psychological Emotional maturity
3 Lack of Cognitive Physical Medical disability
4 Fearful amp anxious pts
5 Pt who require extensive amp complicated dental care amp would require or benefit from prolonged visits
6 Acute pain
7 Traumatic injuries
Operating Facilities amp Equipment
A positive pressure O2 delivery system capable of administering gt than 90 O2 at 10L min flow for 60 min (650L ldquoErdquo cylinder)
OR
Self inflating bag valve mask device (15L min)
A functional suction apparatus with appropriate suction catheters
Monitoring equipment - PO BPC PC or Capno
Inhalation sedation unit
100 O2 amp never less than 25
A fail safe mechanism that is checked and calibrated annually
Must have appropriate scavenging system
Emergency drugs
Techniques of sedation
Routes for drug administration
bull Oral
bull Rectal
bull Inhalational
bull Transmucosal
ndash Sublingual
ndash Intranasal
bull Parenteral
ndash IM
ndash sub mucosal
ndash IV
3
Oral Sedation
Advantages
1 Almost universally accepted and the easiest method
2 Decreased incidence and severity of adverse reaction
3 Low cost
Disadvantages
1 Absorption is variable
2 Prolonged latent period(30 min)
3 Reversal of any unwanted effect is also difficult
4 Inability to readily lighten or deepen the level of sedation
5 Prolonged duration of action
Rectal Sedation
Advantages 1 Incidence and intensity of
drug related side effects is minimized
2 Drug absorption occurs from the large intestine directly into the circulation
3 The lack of a needle syringe or other equipment
4 The ease of administration
5 The low cost
Disadvantages
1 Inconvenience to the administrator amp pt
2 The variable absorption of drugs from the large intestine
3 The slow onset of action amp the relatively long duration of action
4 Inability to titrate the drug dosage
5 The inability to reverse the action of the drug the prolonged recovery
Intranasal sedation
Advantages
Rapid onset (10 ndash 15 min)
Simple amp relatively painless
Less pt cooperation is required
Absorbed directly into the C V S
Intranasal sedation
Disadvantages
1 Dependence on nasal mucous membrane
2 Shorter duration of action(40-60min)
3 Multiple dosage may be necessary
Drugs
Midazolam ndash 02mgkg
Sufentanil ndash 15 ndash 3 mcgkg
Ketamine ndash 3-6mg kg
Sublingual sedation
Advantages
1 Pt acceptance
2 Rapid onset
3 High bioavailability
Drugs
Oral Transmucosal Fentanyl Citrate (OTFC)
Intramuscular Sedation
Advantages
1 More rapid onset of action
2 Absorbed directly into the C V system
3 More reliable absorption of drug
4 Pt cooperation is not as essential
Disadvantages
1 Time factor ndash its 15 min latent period
2 Pt may not be willing to accept the injection
3 The prolonged duration of action(2-4 hrs more)
4 Possibility of injury to the tissues at the site of injection caused by either the drug or the needle
4
Sites of I M administration
1 Gluteal area
2 Vastus lateralis
3 Mid ndash deltoid area
Drugs
Diazepam
Midazolam
Hydroxyzine
Inhalation Sedation
Advantages
1 The onset of action is more rapid
2 Peak clinical level is achieved rapidly(3-5min) - permit titration
3 Administrator has complete control over the actions of the drug - safety feature
4 No significant over dosage
5 Flexible duration of action
6 Recovery time is rapid amp most complete
7 No injection is required
8 With N2O- O2 it is safe with very few side effects
Disadvantages
1 The initial cost of the equipment is high 2 The continuing cost of the gases is high 3 The equipment occupies considerable space 4 N2O is not a potent agent 5 A degree of cooperation is required from the pt 6 Chronic exposure to N2O is deleterious to the health of
dental personnel
Contraindications
1 Nasal obstruction 2 Cyanosis at rest 3 Poor cooperation 4 1st trimester of pregnancy 5 Fear of masks
I V Sedation
Advantages
1 The onset of action is the most rapid 2 The dosage may be titrated 3 Suitable level of sedation can be provided 4 The recovery period is shorter 5 Side effects are extremely uncommon 6 Control of salivary secretions is possible 7 The gag reflex is diminished 8 Effectively diminishes motor disturbances 9 Provides immediate access to CVS in emergency
Disadvantages
1 Venipuncture is necessary
2 Complication may rise at the site of the venipuncture
3 Monitoring must be more intensive
4 Recovery is not complete at the end of the procedure
5 Reversal of sedation is difficult
5
N2O-O2 (Relative Analgesia)
colorless sweet smelling gas
Pharmacokinetics
Absorption through pulmonary epithelium
It is approx 15 times as soluble as is nitrogen It replaces nitrogen in blood
It is carried in solution in plasma of the blood
It is not metabolized by the body
Elimination ndash majorndash lungs minor --- skin
perspiration urine and intestinal gas
Pharmacodynamics
Dose related
10 ndash 25 Lightheaded
Changes in visual amp auditory sensation
Tingling of hands amp feet
Suffusing warmth
Remote from the immediate environment
Reduced anxiety
25-50 max analgesic properties and aberration of vision hearing and proprioception mild drowsiness euphoria amnesia and increased sleepiness and dreams
35 conc will achieve maximum analgesia
bull CNS
ndash Cerebrum-primarily affected
ndash Safe but weak anesthetic agent
bull RESPIRATORY SYSTEM
ndash Increased Tidal and minute volumes
bull CARDIOVASCULAR SYSTEM
ndash 2 studies ndash decreased cardiac output
bull FETAL SYSTEMS
ndash Miscarriage in humans
bull OTHER SYSTEMS
ndash Depression of spinal reflexes increase muscle tone indicates stage of delirium
ndash Muscle rigidity-narcotics + nitrous oxide
ndash Nausea and vomitting - GIT
ndash HEMATOPOIESIS ----- prolonged exposure
Adverse reactions and toxicity
EMOTIONAL REACTIONS
DREAMS HALLUCINATIONS
No acute toxicity
Chronic toxicity ndash bone marrow
depression
PROCEDURE
Diffusion Hypoxia
Sevoflurane
A fluorinated derivative of isopropyl ether ndash synthesized in 1970
Potent anaesthetic agent with rapid uptake amp speedy recovery
Day-case surgery
Problem
Attaching vaporiser to any of the currently available machine
BENZODIAZEPINES
Diazepam 1961 lipid soluble
Uses-alcoholism epilepsy labor tetanus and cerebral palsy
- sedation and amnesia
- varieties of neurosis amp anxiety states
Pharmacokinetics
Orally Rectal IMIV or SC
Well absorbed through GIT
Excretion in urine
6
bull Pharmacodynamics
ndash Depress the brain stem reticular system and the limbic system thalamus and hypothalamus
ndash It is a centrally acting muscle relaxant Has anti-convulsant properties
Adverse reaction amp toxicity
ndash Confusion nausea headache increased appetite decreased salivation and jaundice Thrombophlebitis
ndash Rebound phenomenon
ndash Toxicity drowsiness confusion sleep and coma
Dosage Oral or Rectal ndash 02-05mgkg
Maximum single dose 10mg
IV- 025mgkg
Supplied Tablets 2 5 10 mg
Suspension ndash 5mg
Midazolam Water soluble ndash non-irritant
Oral IM IV
Metabolism- liver
Onset IV 3 -5mins
oral 20 ndash 30mins
Oral administration anxious patients requiring relatively short dental procedure
No rebound phenomenon
Better anxiolysis amp amnesia (retrograde amnesia)
Adverse effects Respiratory depression
dose dependant apnea
Dosage Oral ndash 025 to 1mgkg to maximum single dose 20mg
IM ndash 01 to 015mgkg to a maximum of 10mg
IV ndash slow IV
Supplied Syrup ndash 2mgml
Injectable ndash 1mgml amp 5mgml vials
Flumazenil specific benzodiazepines antagonist
selectively inhibits CNS effects
IV administration amp not recommended below 18yrs of age
02mg over 15 seconds after 45seconds 02mg then after 60seconds to maximum of 1mg
Sedative-Hypnotics
Barbiturates First truly effective drugs for the management of anxiety Generalized CNS depressants Produce dose dependent effects
Sedation ---- sleep ---- GA ---- coma
Suppress the CNS and result in sedation and amnesia Advantages
Rapid onset and short duration Disadvantages
no analgesic effect and possible hypotension Must be used with caution in trauma patients because they may cause
apnea and hypoventilation
DOSE Pentobarbital Sodium 100mg Secobarbital Sodium 100 to 200mg Children 30 to 100mg
bull Chloral Hydrates (Mickey Finn Knock out drops ) First synthesized in 1832 first member of the hypnotic group of drugs
Widely used as conscious sedation agent
Properties
Unpleasant taste
Nausea vomiting
Quite irritating to skin and to mucous membranes
GI irritation
Dosages Individualized for each patient 25 ndash 50mgkg
maximum of 1g
Supplied oral capsule ndash 500mg
oral solution ndash 250 amp 500mg5ml
Rectal suppositories ndash 324 amp 648mg
Narcotics
Do produce sedation amp euphoria greater in children
LA is required but dose should be decreased
Meperidine Synthetic opiate agonist
Very water soluble
Orally SC IM or IV
Peak effect by oral 1 hr amp lasts upto 4 hrs
Adverse reactions
-Seizures
-Extreme caution in hepatic or renal diseases or history of seizures
7
Dosage Oral SC or IM ndash 1to 22mgkg not to exceed 100 mg
Supplied Oral Tablets ndash 50 amp 100mg
Oral Syrup ndash 50mgml
Parental solution ndash 25 50 75 amp 100mgml
Fentanyl
Synthetic opiate narcotic analgesic
Very potent 01mg = 10mg Morophine75mg Meperidine
Pharmacokinetics
IV IM SM
Metabolized in liver Excreted in urine
Fentanyl Onset ndash 7 to 15mins
Duration ndash 1 to 2 hrs
Pharmacodynamics
Respiratory depression RR but returns to normal rapidly Tidal volume amp response to co2 depressed for extended period
Apnea
Less emetic than meperidine
NOT RECOMMENDED IN CHILDREN BELOW 2yrs
Dosage 0002 to 0004mgkg
Supplied 005mgml in 2 amp 5ml ampoules
Reversal drug Naloxone
Semisynthetic opiate antagonist
No agonist activity
Onset 2 to 5mins SC or IM amp 1 to 2mins IV
Reversal 45mins
Pt should be kept under continual surveillance
Adverse reaction nausea vomiting sweating hypotension hypertension ventricular tachycardia fibrillation
Dosage IV SC IM 001mgkg then 01mgkg every 2- 3mins maximum 2mg
Supplied 002 004 1mg solutions
Antihistamines
Hydroxyzine
Oral or IM
Effect ndash 15 ndash 30mins
Half-life ndash 3 hrs
Uses
To relieve anxiety
Used as an anti-histamine
Used to control nausea and vomiting including that associated with motion sickness and pregnancy
Adverse reaction dry mouth drowsiness hypersentivity
Dosage Oral ndash 1 to 2mgkg
IM ndash 11mgkg
Promethazine Oral or IM Onset 15 to 60mins Duration 4 to 6 hrs Uses
To prevent and treat nausea and vomiting associated with motion pregnancy or surgery
Produces sedation and reduce swelling pain and trismus
Lower seizure threshold Adverse reaction dry mouth blurred vision thickening of bronchial secretions Dosage OralIM ndash 05-11mgkg
maximum 25 mg
Diphenhydramine
Oral IM IV
Onset -1hr
Duration ndash 4 to 6 hr
Metabolized in liver
Adverse reaction disturbed coordination thickening of bronchial secretions
Dosage Oral IM IV ndash 1 to 15mgkg
maximum 50mg
Tranquilizers
Major tranquilizer antipsychotic produce calmness control symptoms of psychoses cause reversible extra pyramidal symptoms and do not tend to cause habituation
Minor tranquilizer antianxiety agents also cause calmness do not cause extrapyramidal symptoms Used in conditions like nervous tension and mild depression
8
Classification
Antipsychotics
Phenothiazine derivatives
Chlorpromazine promazine
Butryophenones
Haloperidol
Rauwolfia alkaloids
Reserpine
Antianxiety drugs
Propyl alcohol derivatives
Meprobamate
Benzodiazepine derivatives
Diazepam
Miscellaneous compounds
Hydroxyzine
Meprobamate
White crystalline powder slightly bitter in taste
Only administered orally
Peak blood concentration ----1 to 3hrs
10 ---------excreted unchanged Rest --- excreted as a oxidized derivative or as a glucoronide
Uses
To relieve day time anxiety
Induce sleep in insomniacs
To reduce anxiety associated with dental treatment
Anti-convulsant ndash petit mal epilepsy
Adverse reaction leucopenia acute non-thrombocytopenic purpura ecchymoses eosinophilia edema adenopathy
Dosage Childrengt 6yrs 100 to 200mg
Not recommended for children under 6yrs
Monitoring during sedation
1 Pulse
2 Blood pressure
3 ECG
4 Respiration
5 Temperature
Pulse
Manual Electronic
bull Radial Brachial
bull Facial labial
Blood pressure
ndash Stethoscope amp sphygmomanometer
ndash Automatic devices
ndash Direct cannulation of an artery ndash very accurate
Electrocardiograph
Heart rate rhythm myocardial function
9
Respiration
ndash Monitoring respiratory rate
ndash Observing the rise amp fall of the chest wall
ndash Observing the color of mucous membrane
ndash Observing the inflation amp deflation of the reservoir bag
Devices for monitoring respiration
1 The Precordial pretracheal stethoscope
2 The esophageal stethoscope
ndash Respiratory rate
ndash Heart rate
ndash Any abnormal sounds
Pulse Oximeter
ndash Oxygen saturation
ndash Heart rate
ndash Oxisensor site
ndash Fingers
ndash Toe
ndash Ear lobe
Mechanism
Oxygenated Hb ndash red light
Deoxygenated Hb- infrared light
Tissue pressure from arterial pulse (plethysmography)
Advantages
ndash Safe amp noninvasive
ndash Simple to use
ndash Information is rapidly available for clinical decision
ndash Indirectly indicates respiratory adequacy
Disadvantages
ndash Finger probes can get dislodged
ndash Emitted light source may cause burning
ndash Non reusable probes are expensive
ndash Does not directly determine airway patency
Capnography
1 The presence absence of air flow
2 Indicates depth amp adequacy of respiration
3 Continues analysis of the co2 content of the respired air ndash indicates respiratory adequacy
Temperature
ndash Disposable nondisposable thermometer
ndash Esophageal rectal temp probe
10
Discharge criteria
Cardiovascular function is satisfactory amp stable
Airway patency is uncompromised amp satisfactory
Pt is easily arousable amp protective reflexes intact
State of hydration is adequate
Pt can talk if applicable
Pt can sit unaided if applicable
Pt can ambulate with minimal assistance if applicable
Presedation level of responsiveness achieved
Responsible individual is available
1
PULP THERAPY OF VITAL TEETH
DR MITAKSHARA NIRWAN
Contents
Indirect pulp capping
Direct pulp capping
Medications amp materials used in pulp capping
Pulpotomy
MTA
Apexogenesis
INDIRECT PULP CAPPING
Pieter Van Forest - first to speak about root canal therapy
Glove designed instruments that could prepare a canal to a certain size and taper(1910)
Indirect pulp capping is defined as a procedure where in small amount of carious dentin is retained in
deep areas of cavity to avoid exposure of pulp followed by placement of a suitable medicament and
restorative material that seals off the carious dentin and encourages pulp recovery (Ingle)
A procedure in which only the gross caries is removed from the lesion and the cavity is sealed for a
time with a biocompatible material (McDonald)
Objective of indirect pulp capping
These were given by Eidelman in 1965
bull Arresting the carious process
bull Promoting dentin sclerosis
bull Stimulating formation of tertiary dentin
bull Remineralization of carious dentin
Layers of Carious Dentin Indications of Indirect Pulp Capping
History
Mild pain associated with eating
Negative history of spontaneous extreme pain
Clinical Examination
Deep carious lesion which are close tobut not involving the pulp in vital primary or young
permanent teeth
No mobility
Nominal pulp inflammationdefinite layer of affected dentin after removal of infected dentin
Radiographic examination
Normal lamina dura amp PDL space
No radiolucency around the apices
2
Contraindications of Indirect Pulp Capping
History
Sharp penetrating pulpalgia
Prolonged spontaneous pain especially at night
Clinical examination
Mobility of tooth
Discoloration of tooth
Negative reaction of electric pulp testing
Radiographic examination
Definite pulp exposure
Break in the lamina dura
Radiolucency around the apices
Widened PDL space
Treatment procedure
Sequelae of Indirect Pulp Capping Three distinct types of new dentin formation take place
1 Cellular fibrillar dentinmdashfirst 2 months
2 Globular dentinmdash3 months
3 Tubular dentin (uniform mineralized dentin)
bull 15th of reparative dentin formation begins in less than 30 days
bull After 3 months 01 mm is formed
DIRECT PULP CAPPING Defined by Kopel (1992) as the placement of a medicament or non medicated material on a pulp that
has been exposed in course of excavating the last portions of deep dentinal caries or as a result of
trauma
Objective
To create new dentin in the area of the exposure and subsequent healing of the pulp
Rationale
achieve a biologic closure of the exposure site by deposition of hard tissue barrier (dentin bridge)
between pulp tissue and capping material thus walling off the
INDICATIONS
Small mechanical exposure
Easily controlled haemorrhage
Bright red haemorrhage
True pinpoint exposure
CONTRAINDICATIONS
Severe toothache at night
Spontaneous pain
Tooth mobility
Radiographic appearance of pulp periradicular de- generation
Excess of hemorrhage at the time of exposure Serous exudate from the exposure
Externalinternal root resorption
Swellingfistula
Histological Changes after Pulp Capping
These were illustrated be Glass and Zander in 1949
After 24 hours Necrotic zone adjacent to calcium
hydroxide paste is separated from healthy pulp
tissue by a deep staining basophilic layer
After 7 days Increase in cellular and fibroblastic
activity
After 14 days Partly calcified fibrous tissue lined by
odontoblastic cells is seen below the calcium
proteinate zone disappearance of necrotic zone
After 28 days Zone of new dentin
3
Medications and Materials Used for Pulp Capping Calcium hydroxide
Corticosteroids amp antibiotics
Inert materials
Collagen fibers
4-META adhesive
Direct bonding
Isobutyl cyanoacrylate
Denatured albumin
Mineral trioxide aggregate
Laser
Bone morphogenic protein
PULPOTOMY
Finn (1995) defined it as the complete removal of the coronal portion of the dental pulp
followed by placement of a suitable dressing or medicament that will promote healing and
preserve vitality of the tooth
American Academy of Pediatric Dentistry (1998) defined pulpotomy as the amputation of
affected infected coronal portion of the dental pulp preserving the vitality and function of the
remaining part of radicular pulp
Objectives
bull Removal of inflamed and infected coronal pulp at the site of exposure thus preserving the vitality of the
radicular pulp and allowing it to heal
bull Maintain the tooth in the dental arch
Rationale
bull Radicular pulp is healthy and capable of healing after surgical amputation of the infected coronal pulp
bull Preserves vitality of the radicular pulp
bull Maintains tooth in a physiologic condition
Indications of Pulpotomy bull Mechanical pulp exposure in primary teeth
bull Teeth showing a large carious lesion but free of radicular pulpitis
bull History of only spontaneous pain
bull Hemorrhage from exposure sites bright red and can be controlled
bull Absence of abscess or fistula
bull No interradicular bone loss
bull No interradicular radiolucency
Contraindications of Pulpotomy bull Persistent toothache
bull Tenderness on percussion
bull Root resorption more than 13rd of root length
bull Large carious lesion with nonrestorable crown
bull Highly viscous sluggish hemorrhage from canal orifice which is uncontrollable
bull Medical contradictions like heart disease immuno compromised patient
bull Swelling or fistula
bull External or internal resorption
bull Pathological mobility
bull Calcification of pulp
Classification of pulpotomy
4
Formocresol Pulpotomy
Iby BUCKLEY in 1904
Sweet (1930) Formulated multi visit technique
Doyle (1962) Advocated 2 sitting procedure (complete devitalization)
Spedding (1965) Gave 5 minute protocol (partial devitali- zation)
Venham (1967) Proposed 15 seconds procedure
Current concept uses 4 minutes of application time
Composition of formocresol Buckleyrsquos Formula
bull Cresol ndash 35 percent
bull Glycerol ndash 15 percent
bull Formaldehyde ndash 19 percent
bull Water ndash 31 percent
Mechanism of Action
It prevents tissue autolysis by bonding to the proteins Bonding is of peptide groups of side chain amino acids and is a reversible process accomplished without
changing the basic structure of protein molecules
Histological Changes
bull Demonstrated by Mass and Zilbermann11 in 1933 and also by Massler and Mansokhani in 1959
bull Immediately the pulp becomes fibrous and acidophillic
bull Seven to fourteen days Three zones appear
a broad eosinophilic zone of fixation
b broad pale-staining zone of atrophy with poorcellular definition
c broad zone of inflammation extending apically into normal pulp tissue
bull One yearndash Progressive apical movement of these zones with only acidophillic zone left at the end of 1 year
Modified Formocresol Pulpotomy
Used by TRASK(1972)
The technique is identical to that described for primary teeth except that the formocresol pellet is
sealed permanently in the tooth
Two-visit Devitalization Pulpotomy
Indications
bull There is evidence of sluggish bleeding at the amputation site that is difficult to control
bull Pus in the chamber but none at the amputation site
bull There is thickening of the PDL
bull History of pain
Contraindications
bull Nonrestorable tooth
bull Tooth with necrotic pulp
5
Glutaraldehyde Pulpotomy
It was first suggested by S Gravenmade Introduced by Kopel in 1979
Mechanism of Action
bull Glutaraldehyde produces rapid surface fixation of the underlying pulpal tissue
bull A narrow zone of eosinophilic stained and compressed fixed tissue is found directly beneath the area of application which blends into vital normal appearing tissue apically
bull With time the glutaraldehyde fixed zone is replaced by macrophagic action with dense collagenous tissue thus the entire root canal tissue is vital
Cvekrsquos Pulpotomy
bull This is also called as calcium hydroxide pulpotomy or young permanent partial pulpotomy
bull This was proposed by Mejare and Cvek16 in 1978
bull Indicated in young permanent teeth where the pulp is exposed by mechanical or bacterial means and the
remaining radicular tissue is judged vital by clinical and radiographic criteria whereas the root closure is
notcomplete
MINERAL TRIOXIDE AGGREGATE (MTA) Torabinejad described the physical and chemical properties of MTA in 1995
It is ash colored powder made primarily of fine hydrophilic particles of
1 tricalcium aluminate
2 tricalcium silicate
3 silicate oxide
4 tricalcium oxide
5 bismuth dioxide
Hydration of the powder results in a colloidal gel composed of calcium oxide crystals in an amorphous
structure This gel solidifies into a hard structure in less than three hours
PROPERTIES OF MTA
It is biocompatible material and its sealing ability is better than that of amalgam or ZOE
Initial pH is 102 and set pH is 125
The setting time of cement is 4 hours
The compressive strength is 70 MPA which is comparable with that of IRM
Low cytotoxicity ndash It presents with minimal inflammation if extended beyond the apex
Mineral trioxide aggregate (MTA) has demonstrated the ability to induce hard-tissue formation in
pulpal tissues and it promotes rapid cell growth
APEXOGENESIS
It is defined as the treatment of a vital pulp by capping or pulpotomy in order to permit continued
growth of the root and closure of the open apex
Rationale
Maintenance of integrity of the radicular pulp tissue to allow for continued root growth
Indications
bull Indicated for traumatized or pulpally involved vital permanent tooth when root apex is incompletely formed
bull No history of spontaneous pain
bull No sensitivity on percussion
bull No hemorrhage
bull Normal radiographic appearance
Contraindications
bull Evidence that radicular pulp has undergone degenerative changes
bull Purulent drainage
bull History of prolonged pain bull Necrotic debris in canal
bull Periapical radiolucency
6
1
Gupta A Dhingra R Chaudhari P Gupta A
Department of Paedodontics and Preventive Dentistry Faculty of Dental Sciences SGT University Gurgaon Haryana India
Journal of Indian Society of Pedodontics and Preventive Dentistry
Volume 35 I Issue 3 I July-September 2017
A COMPARISION OF VARIOUS MINIMALLY
INVASIVE TECHNIQUES FOR THE REMOVAL
OF DENTAL FLUOROSIS STAINS IN
CHILDREN
DR MITAKSHARA NIRWAN
CONTENTS
bull Introduction
bull Aims
bull Materials and Methods
bull Results
bull Discussion
bull Conclusion
bull Critical analysis
bull References
INTRODUCTION
bull Dental fluorosis is a developmental disturbance of dental enamel caused by
successive exposure to high concentrations of fluoride during tooth
development
bull Various methods of therapy are advocated for the treatment of fluorosis -
stained teeth which range from invasive ceramic veneer bonding restorations
to abrasive chemical treatments
bull The combination of dental bleaching techniques and microabrasion appears
as an excellent conservative solution to reestablish health in fluorosis
affected teeth
AIMS
bull The aim of the study was to evaluate and compare the effectiveness of
minimally invasive techniques for the removal of dental fluorosis
stains in children in vivo
MATERIALS AND METHODS
Patients visiting the department of Pedodontics and Preventive dentistry
Faculty of Dental Sciences SGT University Gurgaon
bull Sample size 90 patients
bull Age group 10 -17 years
bull Caries cracks or periodontal
disease on anterior teeth
bull Abscess draining sinus
cellulitis
bull Non vital teeth
hypersensitive exposed
crevices
bull Orthodontic appliance
bull Past history of bleaching
bull At least two permanent
maxillary anterior teeth
bull TSIF of score 4
bull Free of systemic diseases
Inclusion criteria Exclusion criteria
2
Groups
Group A In office bleaching with 35 hydrogen peroxide( Pola Office
Bleaching kit) activated by light emitting diode (LED) bleaching unit
(35 HP)
Group B Enamel microabrasion (EM) (PREMA Enamel Microabrasion
System) followed by in-office bleaching with 44 carbamide peroxide
gel (EM)
Group C In-office bleaching with 5 sodium hypochlorite (5
NaOCl)
A baseline colour evaluation was done by taking digital photograph of
the maxillary anterior teeth
RESULTS
Group 1
Colour stability
Group 2 Group 3
Tooth sensitivity
Tooth sensitivity values were taken before the treatment
which was compared to immediate postoperative and follow
up visits It was checked using an electric pulp tester
maximum
moderate
least
immediately
group 2
group 1
group 3
1 month
group 2
group 1
group 3
3 month
group 2
group 1
group 3
Patient satisfaction score
Satisfaction was assessed on visual analog scale
Range 1 to 5
Groups percentage of patients
who were satisfied with
the treatment
Number of patients
who reported slight
reappearance of colour
Group 1
90
7
Group 2
83
8
Group 3
73
7
3
Number of Appointments
Groups One sitting Two sittings Three
sittings
Group 1
25
4
1
group 2
26
3
1
Group 3
30
0
0
DISCUSSION
bull Hydrogen peroxide is capable of penetrating the tooth osmosis and through porosities and cracks subsequently acting directly on the pigmented molecules
bull Gurgan et al investigated 3 different light systems and found out that diode laser system with gave best tooth whitening and least tooth sensitivity
bull In the EM group the surface reflects and refracts light from the surface in such way that mild imperfections in underlying enamel are camouflaged While the highly polished surface of enamel enhances the aesthetic appearance
bull Train et al and Loguercio et al also had the similar results in their studies with EM mild fluorosis showed best results moderate showed moderate results while it had little effect on severe fluorosis
bull NaOCl was only effective on mild stains while moderate and severe
stains could only be lightened to quite an extent but could not be
completely removed
bull When NaOCl comes in contact with hypomineralized and discoloured
enamel it degrades and removes the chromogenic organic material
located on the enamel surface
CONCLUSION
bull It was concluded that esthetic appearance of teeth mild fluorosis can
be achieved by bleaching and microabrasion But in cases of
moderate fluorosis a combination of any of theses modalities can be
used
bull As no special maintenance precautions are required these maybe be
considered as an interesting alternative to conventional operative
treatment
bull Focuses on only TSIF of 4
bull Electric pulp testing is not the
right method to check for
sensitivity
bull Tooth Sensitivity changes
from person to person
bull Food habits can cause
staining of the teeth
bull Minimally invasive
bull Cheaper to veneers
bull Minimal loss of tooth structure
bull 4 parameters checked for the success of treatment
bull Inclusion of specific score of fluorosis for comparing the results
bull Maximum 3 appointments needed
CRITICAL ANALYSIS
Pros Cons
REFERENCES
bull Gurgan S Cakir FY Yazici E Different light-activated in officebleaching
systems Lasers Med Sci 201025817-22
bull Train TE McWhorter AG Seale NSWilson CF Guo IY Examination of
esthetic improvement and surface alteration following microabrasion in
fluorotic human incisors in vivoPediatr dent 199618353-62
bull Loguercio AD Correia LD Zago C Tagliari D Neumann E Gomes OM et al
Clinical effectiveness of two microabrasion materials materials for the
removal of enamel flurosis stains Oper Dent 200732531-8
4
4
DISCUSSION
Stainless steel files usually separate fracture due to the excessive amounts of torque and overuse or the
preexisting distortion of the instrument whereas in NiTi rotary files it is a combined result of torsional stress and cyclic fatigue
Therapeutic options for the management of separated endodontic instruments include no intervention nonsurgical (orthograde conservative) management surgical management and tooth extraction
Use of ultrasonic scaler Masserann technique Endo extractor and Cavi-Endo ultrasonic instruments are some of the methods popular for retrieval of a separated endodontic instrument in the permanent tooth
In case 1 a 6-mm-long manual reamer was retrieved successfully with the use of GG drill using a manual file and copious irrigation which is the most desired treatment outcome
In case 2 the retrieval of separated rotary file lodged in the middle third of the root canal was unsuccessful in spite of multiple attempts It was therefore managed with routine obturation followed by restoration to maintain the tooth in its physiological functional state It was kept under close periodic follow-up at least
every 3 months This treatment option should be encouraged where it is possible to follow up the patient clinically and radiographically at close periodic intervals as there is the possibility of instrument escaping
into bone due to physiological root resorption
In cases 3 and 4 an instrument has separated in the apical root portion
In case 3 it was within the root canal and thus an attempt was made for its retrieval which was
unsuccessful It was therefore extracted to prevent the fractured instrument from getting exposed in the bone following resorption as there is no accurate and consistent established age for initiation of resorption in primary teeth known per se
In case 4 an immediate extraction of involved tooth was carried out as the separated instrument was beyond the apex of the primary tooth root
Age of the child clinical signs and symptoms and amount of root resorption are the factors which can also influence the management of separated instrument in primary teeth
Moreover if an instrument has separated after initial cleaning and shaping of root canal maintaining a tooth is not a problem as clinical signs and symptoms are not anticipated and the good prognosis is expected
However if an instrument has separated early during the initial cleaning and shaping of the root canal clinical symptoms may compromise the prognosis
Therefore these factors should be kept in mind while planning a suitable management strategy to avoid or at least reduce the burden of extraction and wear of space maintainer for longer period
5
CONCLUSION
The management and prognosis of a primary tooth with a separated instrument is
dependent on the level of instrument fracture within the root age of the child root
resorption and clinical signs and symptoms of the involved tooth
Different management approaches can be tried depending on clinical situations keeping
in mind benefits vs risks in preserving the tooth
PROS amp CONS
PROS
The entire procedure is given
by step by step
Well descriptive xrays and
photographs
CONS
Medical history has not been
given
REFERENCES
1 TOMER ANIL K ET AL ldquoBROKEN FILE RETRIEVAL PUZZLE IN ENDODONTICSrdquo
(2016)
2 SHENOY A MANDAVA P BOLLA N ET AL A NOVEL TECHNIQUE FOR REMOVAL OF
BROKEN INSTRUMENT FROM ROOT CANAL IN MANDIBULAR SECOND MOLAR
INDIAN J DENT RES 201425(1)107ndash110
3 PATEL J MORAWALA A TALATHI R ET AL RETRIEVAL OF A BROKEN INSTRUMENT
FROM ROOT CANAL IN PRIMARY ANTERIOR TEETH UNIV RES J DENT 20155(3)203ndash
206
4 MORANKAR R GOYAL A GAUBA K ET AL MANUAL VERSUS ROTARY
INSTRUMENTATION FOR PRIMARY MOLAR PULPECTOMIES - A 24 MONTHS
RANDOMIZED CLINICAL TRIAL PEDIAT DENT J 201828(2)96ndash102
5 KASHYAP NILOTPOL (2018) RETAINING PRIMARY MOLARS WITH INSTRUMENT
SEPERATION A CASE REPORT AND CLINICAL GUIDE
6
1
IMPACT OF 6 CITRIC ACID AND ENDOACTIVATOR AS IRRIGATION ADJUNCTS ON OBTURATION QUALITY AND PULPECTOMY OUTCOME IN
PRIMARY TEETH
NEETU JAIN SHALINI GARG ABHISHEK DHINDSA SAKSHI JOSHI HARJOY
KHATRIA
PEDIATRIC DENTAL JOURNAL 2019 29
1
DR MITAKSHARA NIRWAN
CONTENTS
bull INTRODUCTION
bull AIMS amp OBJECTIVES
bull CASE REPORT
bull RESULTS
bull DISCUSSION
bull CONCLUSION
bull PROS AND CONS
bull REFERENCES
2
INTRODUCTION
bull ENDODONTIC THERAPY IN PRIMARY TEETH INVOLVES DISINFECTION OF THE ROOT CANAL
SYSTEM AND ITS OBTURATION WITH RESORBABLE PASTE
bull THE CONTENTS OF ROOT CANAL ALONG WITH SMEAR LAYER ARE EXPECTED TO BE REMOVED
DURING THE BIOMECHANICAL PREPARATION
bull IN VITRO AND CLINICAL DOCUMENTS HAVE INDICATED THAT MECHANICAL PREPARATION OF
THE CANAL LEAVES LARGE PORTIONS OF THE CANAL WALLS UNDEBRIDED AND COMPLETE
REMOVAL OF THE BACTERIA BY THIS MECHANICAL PROCEDURE ALONE IS UNLIKELY TO BE SEEN
THEREFORE SOME FORM OF DISINFECTIONIRRIGATION IS MANDATORY TO KILL THE
MICROORGANISMS AND TO REMOVE THE RESIDUAL TISSUES
3
bull THE IDEAL REQUISITES OF A ROOT CANAL IRRIGANT AS GIVEN BY ZEHNDER ARE
1 BROAD ANTIMICROBIAL SPECTRUM
2 HIGH EFFICACY AGAINST ANAEROBIC AND FACULTATIVE MICROORGANISMS ORGANIZED
IN BIOFILMS
3 ABILITY TO DISSOLVE NECROTIC PULP TISSUE REMNANTS
4 ABILITY TO INACTIVATE ENDOTOXIN
5 ABILITY TO PREVENT THE FORMATION OF A SMEAR LAYER DURING INSTRUMENTATION OR
TO DISSOLVE THE LATTER ONCE IT HAS FORMED
6 SYSTEMICALLY NONTOXIC WHEN THEY COME IN CONTACT WITH VITAL TISSUES
NONCAUSTIC TO PERIODONTAL TISSUES AND WITH LITTLE POTENTIAL TO CAUSE AN
ANAPHYLACTIC REACTION
SINCE NO SINGLE IRRIGANT HAS THESE OPTIMAL PROPERTIES STUDIES HAVE REPORTED THE USE
OF TWO OR MORE SOLUTIONS IN A SPECIFIC SEQUENCE OR IN COMBINATIONS FOR BETTER
RESULTS 4
bull SEVERAL IRRIGATING SOLUTIONS ALONG WITH CHELATING AGENTS HAVE BEEN USED
DURING BIOMECHANICAL PREPARATION OF ROOT CANAL BOTH IN PRIMARY AND
PERMANENT TEETH
bull HOWEVER NONE OF THE AVAILABLE IRRIGATING SOLUTIONS HAS BEEN REGARDED CLEARLY
AS OPTIMAL SOLUTION BECAUSE OF THEIR LIMITED EFFECTIVENESS ESPECIALLY IN APICAL
13RD OF THE ROOT CANAL SYSTEM
bull TO OVERCOME SUCH LIMITATIONS USE OF ENDOACTIVATOR HAS BEEN PROPOSED AS AN
IRRIGATION FACILITATOR THAT IS BASED ON SONIC VIBRATION (UP TO 10000 CPM) WHICH
FACILITATES THE IRRIGANT PENETRATION AND ITS RENEWAL WITHIN THE CANAL
bull ACTIVATION SYSTEMS RESULTED IN BETTER REMOVAL OF THE SMEAR LAYER IN THE APICAL
THIRD OF ROOT CANALS IN COMPARISON TO CONVENTIONAL IRRIGATION
5
CITRIC ACID
bull CITRIC ACID IS A WEAK ORGANIC ACID WITH THE APPEARANCE OF WHITE CRYSTALLINE
POWDER AT ROOM TEMPERATURE
bull IT CAN EXIST EITHER IN WATER-FREE FORM (ANHYDROUS) OR MONOHYDRATE FORM THE
WATER-FREE FORM CRYSTALLIZES FROM THE HOT WATER WHEREAS THE MONOHYDRATE
FORMS FROM THE COLD WATER THE LATTER MAY BE CONVERTED TO ANHYDROUS FORM BY
HEATING MORE THAN 78degC
bull CITRIC ACID OCCURS NATURALLY IN THE BODY IN MITOCHONDRIA AND IS USED BY BLOOD
BANKS TO PREVENT COAGULATION OF TRANSFUSED BLOOD CITRIC ACID IS ALSO ESSENTIAL
TO HUMAN METABOLISM AND IS FOUND IN MANY FOODS
6
2
bull THE BIOLOGICAL EFFECTS OF CITRIC ACID ON THE PERIODONTAL STRUCTURE HAS BEEN
EXTENSIVELY STUDIED IN PERIODONTICS
bull NEUMAN AND NEWMAN SHOWED THAT CITRIC ACID IS THE MOST EFFECTIVE ACID IN
ALTERING THE SOLUBILITY OF HYDROXYAPATITE
bull YAMAGUCHI ET AL SHOWED THAT CITRIC ACID SOLUTION HAD ANTIBACTERIAL EFFECTS ON
ALL 12 ROOT CANAL BACTERIA TESTED
bull ARIAS-MOLIZ ET AL SHOWED THAT ETHYLENEDIAMINETETRAACETIC ACID (EDTA) HAS NO
BACTERICIDAL ACTIVITY EVEN AFTER 1 HOUR CONTACT
bull THIS ACID HAS THE ABILITY OF ROOT CANAL IRRIGATION AND ALSO SMEAR LAYER REMOVAL
DIFFERENT CONCENTRATIONS (1ndash50) HAVE BEEN PROPOSED GUTMANN ET AL CONCLUDED
THAT 10 CITRIC ACID IS BETTER THAN ULTRASOUND FOR SMEAR LAYER REMOVAL FROM THE
ROOT END CAVITIES
7
bull STUDIES HAVE SHOWN IRRIGATION WITH 6 CA FOR 15 OR 30 SECONDS IS QUITE
EFFECTIVE IN REMOVING ALL THE COMPONENTS OF THE SMEAR LAYER OF THE PRIMARY
TEETH WHEREAS PERITUBULAR DENTIN DESTRUCTION WAS OBSERVED WHEN HIGHER
CONCENTRATION OF CITRIC ACID WAS USED AS AN IRRIGATING SOLUTION
8
AIMS amp OBJECTIVES
bull THIS STUDY WAS AIMED TO EVALUATE THE CLINICAL AND RADIOGRAPHIC OUTCOME OF
PULPECTOMY ALONG WITH QUALITY OF OBTURATION USING 6 CITRIC ACID AND
ENDOACTIVATOR
9
CASE REPORT
bull 350 CHILDREN (3-9 YEARS) WITH CLINICAL SIGNS AND SYMPTOMS OF CHRONIC IRREVERSIBLE
PULPITIS IN DEEPLY CARIOUS TEETH WERE SCREENED DURING SCHOOL DENTAL HEALTH
PROGRAM FROM MAY 2014-JULY 2014
bull 123 CHILDREN REPORTED TO THE DEPARTMENT AND 67 CHILDREN WERE SELECTED BASED ON
INCLUSION AND EXCLUSION CRITERIA
RECRUITMENT OF PATIENTS
10
INCLUSION CRITERIA
bull HISTORY OF SPONTANEOUS PAIN AND UNCONTROLLED BLEEDING AFTER PULP AMPUTATION
EXCLUSION CRITERIA
bull EVIDENCE OF INTERNAL OR EXTERNAL (PHYSIOLOGICPATHOLOGIC) ROOT RESORPTION OF MORE THAN A THIRD OF ITS LENGTH
bull ROOT CANAL OBLITERATION OR ANATOMIC ANOMALIES
bull INADEQUATE BONE SUPPORT OR NON RESTORABLE TOOTH
bull ONCE PATIENTS ELIGIBILITY WAS CONFIRMED THE TREATMENT PROCEDURE WAS
EXPLAINED TO THE PARENTGUARDIAN AND INFORMED WRITTEN CONSENT WAS
OBTAINED FROM PARENTSGUARDIANS SHOWING WILLINGNESS FOR THEIR
CHILDRENS TREATMENT 11
PROCEDURE
bull PULPECTOMY WAS PERFORMED BY ONE OPERATOR OF PEDIATRIC DENTISTRY DEPARTMENT
USING A STANDARDIZED TREATMENT PROTOCOL FOR ALL THE PATIENTS
bull AFTER ADMINISTRATION OF LOCAL ANESTHESIA RUBBER DAM WAS APPLIED FOR ISOLATION
bull ACCESS CAVITY WAS PREPARED USING AIR-ROTOR HAND PIECE WITH 8 ROUND BUR AND
PULP TISSUE WAS EXTIRPATED WITH THE HELP OF SPOON EXCAVATOR
bull FURTHER THE NEGOTIATION OF THE CANALS WAS DONE WITH 10 K-FILE
bull A DIAGNOSTIC RADIOGRAPH WAS TAKEN FOR ROOT LENGTH DETERMINATION AND
WORKING LENGTH WAS KEPT 1 MM SHORT OF THE RADIOGRAPHICAL APEX
bull ALL ROOT CANALS WERE INSTRUMENTED MANUALLY USING K-FILES AND WERE IRRIGATED
WITH 10 ML 09 NORMAL SALINE AND 1 SODIUM HYPOCHLORITE AS STANDARDIZING
PROTOCOL FOR ROOT CANAL PREPARATION AND DISINFECTION
12
3
GROUP 1 (CA + E) - IRRIGATION WAS DONE
WITH 10 ML OF 6 CITRIC ACID (CITOCID AMMDENT)
AND IRRIGANTS WERE SONICALLY AGITATED WITH
ENDOACTIVATOR (DENTSPLY) FOR 30 S PER CANAL USING REDBLUE
ENDOACTIVATOR TIP
GROUP 2 (CA) - 10 ML OF 6 CITRIC ACID FOR 1 MIN USING
27 GAUZE IRRIGATING NEEDLE
GROUP 3(SH + E) - 10 ML OF 1 SODIUM HYPOCHLORITE
SOLUTION AND SONIC ACTIVATION WITH ENDOACTIVATOR
GROUP 4(SH) - 10 ML OF 1 SODIUM HYPOCHLORITE
SOLUTION USING IRRIGATING NEEDLE (CONTROL GROUP)
bull TEETH UNDERGOING PULPECTOMY WERE RANDOMLY ENROLLED BY CHIT METHOD INTO THREE
STUDY AND ONE CONTROL GROUP
13
bull IN CITRIC ACID GROUPS FINAL RINSE WITH NORMAL SALINE WAS DONE TO REMOVE THE
REMAINING CRYSTALS (CHELATES)
bull FOLLOWING BIOMECHANICAL PREPARATION THE ROOT CANALS WERE DRIED WITH STERILE
ABSORBENT PAPER POINTS AND OBTURATED WITH VITAPEX USING HAND HELD
LENTULOSPIRAL FINAL RESTORATIONS WERE DONE USING COMPOSITE RESIN
14
bull CLINICAL FOLLOW UP WAS DONE AT 24 H1 WEEK 1 MONTH 6 MONTH AND 12
MONTH TO CHECK PAIN PRESENCE AND PAIN FREQUENCY (ONCEMORE THAN ONCE)
SWELLING FISTULA SENSITIVITY TO PERCUSSION
bull RADIOGRAPHIC FOLLOW UP WAS DONE AT 6 MONTH AND 12 MONTH FOR ANY
DEVIATED ERUPTION OF SUCCEDANEOUS TEETH EXCESS FILING MATERIAL AND ITS
RESORPTION EXTERNALINTERNAL ROOT RESORBTION CALCIFIC METAMORPHOSIS
PRESENCE OF FURCATION RADIOLUCENCY
CLINICAL amp RADIOGRAPHIC FOLLOW UP
15
RADIOGRAPHIC ASSESSMENT OF OBTURATION QUALITY
bull POSTOPERATIVE RADIOGRAPHS WERE VISUALLY ASSESSED FOR QUALITY OF OBTURATION BY
TWO INDEPENDENT EXAMINERS (SG AD) WHO WERE BLINDED WITH REGARD TO
IRRIGATION PROTOCOL GROUP TO ENHANCE CALIBRATION EACH EXAMINER ASSESSED THE
RADIOGRAPH INDEPENDENTLY AND LATER REVIEWED TOGETHER FOR FINAL ASSESSMENT
INDIVIDUAL ROOT WAS TAKEN AS UNIT OF ANALYSIS FOR GRADE OF OBTU- RATION AND
SCORING CRITERIA WERE AS GIVEN BY COLL JA 1996
1 UNDER FILLED - FILLING MATERIAL ENDED 1 MM OR MORE SHORT OF THE APEX
2 OPTIMAL FILLING- FILLING MATERIAL APPEARED TO END AT THE RADIOGRAPHICAL APEX
3 OVERFILLED - FILLING MATERIAL EXTRUDED PAST THE RADIOGRAPHIC APEX
4 OPTIMALLY FILLED ROOTS WERE FURTHER ASSESSED FOR THE PRESENCE OF VOIDS AND VOID
AREA (ROOT CANAL SURFACE UNTOUCHED BY THE ROOT CANAL FILLING MATERIAL) IN THREE
VISUALLY DIVIDED SECTIONS OF THE ROOT IE CORONAL MIDDLE AND APICAL 13RD
16
RESULTS
bull OVERALL CLINICAL AND RADIOGRAPHIC SUCCESS RATE OVER A PERIOD OF ONE YEAR WAS
9886 amp 977 RESPECTIVELY
bull ALL GROUPS WERE SIGNIFICANTLY (P = 001) EFFECTIVE IN ALLEVIATING PAIN WITHIN 24 H
OF PULPECTOMY
17 18
4
19
bull IMMEDIATE POST OPERATIVE RADIOGRAPHIC ASSESSMENT REVEALED 68 (102150) ROOTS
WITH OPTIMAL OBTURATION AND 32 (48150) WITH OVERFILLINGUNDERFILLING MAXIMUM
NO OF OPTIMAL FILLINGS WERE OBSERVED IN GROUP1 (CA + E) (3333) FOLLOWED BY
GROUP 2 (CA) (2549) GROUP 3(SH + E) (2549) AND GROUP 4(SH) (1568)
bull CITRIC ACID GROUPS HAD MORE NUMBER OF OPTIMALLY FILLED ROOTS 588 (60102) THAN
NON CITRIC ACID GROUPS 412 (42102)
bull ENDOACTIVATOR CONTRIBUTED TO 18 OF OPTIMAL OBTURATION IRRESPECTIVE OF
CHELATING AGENT USED
20
21
bull MAXIMUM NO OF VOIDS AND VOID AREAS WERE IN NON CITRIC ACID GROUPS
(6419 amp 5384) COMPARED TO CITRIC ACID GROUPS (3580 amp 4615)
RESPECTIVELY
bull ANALYSIS OF ROOT 13RD REVEALED MAXIMUM NO OF VOID AREA IN APICAL
13RD (4755) FOLLOWED BY MIDDLE 13RD (3846) AND CORONAL 13RD
(1398)
bull LEAST NO OF VOIDS amp VOID AREA (1111 amp 1608) WERE OBSERVED WHEN
ENDOACTIVATOR ALONG WITH CHELATING AGENT WAS USED (GROUP 1)
HOWEVER THIS WAS STATISTICALLY INSIGNIFICANT
22
DISCUSSION
bull IN THE PRESENT STUDY 1 SODIUM HYPOCHLORITE WAS USED ALONG WITH 6 CITRIC ACID
(CHELATING AGENT) WHICH IS REPORTED TO BE AS EFFECTIVE AS 17 EDTA
bull CITRIC ACID (BIOLOGICAL ACID) IS FOUND TO BE BIOCOMPATIBLE AND LEAST IRRITATING TO
PERIAPICAL TISSUES THAN OTHER CHELATING AGENTS
bull USE OF SODIUM HYPOCHLORITE SOLUTION FOLLOWING CHELATING AGENT WAS AVOIDED AS IT
RAPIDLY PRODUCES SEVERE EROSION OF ROOT CANAL WALL DENTIN
bull TRADITIONAL APPROACH OF DELIVERING IRRIGANTS INTO THE ROOT CANAL SPACE USING
SYRINGES AND METAL NEEDLES HAS BEEN FOUND TO BE INEFFECTIVE ESPECIALLY IN THE AREAS OF
ANASTOMOSES BETWEEN CANALS AND APICAL 13RD OF ROOT CANAL
23
bull THEREFORE TO ACHIEVE BETTER CLEANING EFFICIENCY IRRIGANT ACTIVATION HAS BEEN
RECOMMENDED SONIC ACTIVATION HAS BEEN REPORTED TO RESULT IN BETTER ROOT CANAL
CLEANLINESS AS COMPARED TO NO ACTIVATION OF IRRIGANT
24
5
CONCLUSION
bull USE OF 6 CITRIC ACID DEFINITELY HELPED IN RAPID ELIMINATION OF PAIN RESOLUTION OF
PERI-RADICULAR RADIOLUCENCY BETTER OBTURATION QUALITY IN TERMS OF LESS VOIDS AND
VOID AREAS ALONG WITH MAXIMUM NO OF OPTIMAL OBTURATION UP TO APICAL AREA
bull 6 CITRIC ACID AND ENDOACTIVATOR IRRIGATION PROTOCOL PROVED TO BE THE BETTER
IRRIGATION PROTOCOL WHICH MAY CONTRIBUTE TO LONG TERM SUCCESS OF PRIMARY
TOOTH AND THE HEALTH OF UNDERLYING PERMANENT TOOTH
bull 6 CITRIC ACID ALONG WITH ENDOACTIVATOR MAY BE RECOMMENDED AS IRRIGATION
ADJUNCTS IN PULPECTOMY PROCEDURE OF PRIMARY TEETH
25
PROS AND CONS
PROS
bull PROPER EXPLANATION OF THE MATERIALS
USED
CONS
bull NO PREOPERATIVE AND POSTOPERATIVE
RADIOGRAPHS
26
REFERENCES
bull RAMACHANDRA JA NIHAL NK NAGARATHNA C VORA MS ROOT CANAL IRRIGANTS IN
PRIMARY TEETH WORLD J DENT 20156(3)229-234
bull MOHAMMADI Z JAFARZADEH H SHALAVI S KINOSHITA JI UNUSUAL ROOT CANAL
IRRIGATION SOLUTIONS J CONTEMP DENT PRACT 201718(5)415-420
bull ZEHNDER M ROOT CANAL IRRIGANTS J ENDOD 2006 32389- 98
bull SMITH JJ amp WAYMAN BE AN EVALUATION OF THE ANTIMICROBIAL EFFECTIVENESS OF
CITRIC ACID AS A ROOT CANAL IRRIGANT JOURNAL OF ENDODONTICS 1986 12(2) 54-58
bull TANNURE PN AZEVEDO CP BARCELOS R GLEISER R PRIMO LG LONG-TERM OUTCOMES OF
PRIMARY TOOTH PULPECTOMY WITH AND WITHOUT SMEAR LAYER REMOVAL A RANDOMIZED
SPLIT-MOUTH CLINICAL TRIAL PEDIATR DENT 201133316E20 27
bull CARON G NHAM K BRONNEC F MACHTOU P EFFECTIVENESS OF DIFFERENT FINAL IRRIGANT
ACTIVATION PROTOCOLS ON SMEAR LAYER REMOVAL IN CURVED CANALS J ENDOD
2010361361E6
bull COLL JA SADRIAN R PREDICTING PULPECTOMY SUCCESS AND ITS RELATIONSHIP TO
EXFOLIATION AND SUCCEDANEOUS DENTITION PEDIATR DENT 19961857E63
28
1
LOCAL
ANESTHESIA
DR MITAKSHARA NIRWAN
CONTENTS
Definition
Methods of inducing local anesthesia
Desirable properties
Electrophysiology of nerve conduction
Impulse propagation and spread
Mode and site of action of local anesthesia
Classification of local anesthetic according to biological site and mode of action
Dissociation of local anaesthetics
Mechanism of action of local anaethetics
Local anaesthetic agent
2
3
DEFINITION
Local anesthesia is defined as a loss of sensation in
a circumscribed area of the body caused by depression
of excitation in nerve endings or an inhibition of the
conduction process in peripheral nerves
An important feature of local anesthesia is that it produces
LOSS OF SENSATION WITHOUT INDUCING LOSS OF
CONSCIOUSNESS
4
METHODS OF INDUCING LOCAL
ANESTHESIA
Low temperature
Mechanical trauma
Anoxia
Neurolytic agents such as alcohol amp phenol
Chemical agents such as local anesthetics
PROPERTIES OF LOCAL
ANESTHESIA
It should not be irritating to tissue to which it is applied
It should not cause any permanent alteration of nerve structure
Its systemic toxicity should be low
Time of onset of anesthesia should be short
It should be effective regardless of whether it is injected into the tissue or applied locally to mucous membranes
The duration of action should be long enough to permit the completion of procedure
5 6
It should have the potency sufficient to give complete
anesthesia with out the use of harmful concentration solutions
It should be free from producing allergic reactions
It should be free in solution and relatively undergo
biotransformation in the body
It should be either sterile or be capable of being sterilized by
heat with out deterioration
2
ELETROPHYSIOLOGY OF
NERVE CONDUCTION
There is an electrical charge across the membrane
This is the membrane potential
The resting potential (when the cell is not firing) is a negative
electrical potential of -70mv that exists across the nerve
membrane produced by different concentrations of either side of
the membrane
The interior of nerve is NEGATIVE in relation to exterior
7 8
inside
outside
Resting potential of neuron = -70mV
+
-
+
-
+
-
+
-
+
-
SLOW DEPOLARIRIZATION
9
RAPID DEPOLARIZATION
The interior of nerve is POSITIVE in relation to exterior
REPOLARIZATION
10
bull Repolarization takes 07 msec
bull Depolarization takes 03 msec
SODIUM PUMP -
energy comes from the oxidative metabolism of ATP
bull The entire process require 1 msec
IMPULSE PROPOGATION
IMPULSE SPREAD
The propagated impulse travels along the nerve
membrane towards CNS The spread of impulse differs
in myelinated and unmyelinated nerve fibers
DEPOLARIZED SEGMENT ADJACENT RESTING AREA
MODE AND SITE OF ACTION OF LOCAL
ANESTHETICS
Local anesthetic agent interferes with excitation
process in a nerve membrane in one of the
following ways
Altering the basic resting potential of nerve
membrane
Altering the threshold potential
Decreasing the rate of depolarization
Prolonging the rate of repolarization
12
3
CLASSIFICATION OF LOCAL ANESTHETIC
SUBSTANCES ACCORDING TO
BIOLOGICAL SITE AND MODE OF ACTION
CLASS A
Agents acting at receptor site on external surface of nerve membrane
Chemical substance Biotoxins (eg tetrodotoxin and saxitoxin)
CLASS B
Agents acting on receptor sites on internal surface of nerve membrane
Chemical substance Quaternary ammonium analogues of lidocaine
scorpion venom 13
CLASS C Agents acting by receptor independent of
physiochemical mechanism
Chemical substance Benzocaine
CLASS D Agents acting by combination of receptors and
receptor independent mechanisms
Chemical substance most clinically useful anesthetic agents
(eg lidocaine mepivacaine prilocaine)
14
BASED ON THE SOURCE
NATUAL
SYNTHETIC
OTHERS
BASED ON MODE OF APPLICATION
bull INJECTABLE
bull TOPICAL
BASED ON DURATION OF ACTION
bull ULTRA SHORT
bull SHORT
bull MEDIEM
bull LONG
BASED ON ONSET OF ACTION SHORT
INTERMEDIATE
LONG
15
DISSOCIATION OF LOCAL
ANESTHETICS
Local anesthetics are available as salts (usually
hydrochlorides) for clinical use
The salts both water soluble and stable is dissolved in
either sterile water or saline
In this solution it exists simultaneously as unchanged
molecule (RN) also called base and positively charged
molecules (RNH+) called cations
RNH+ ==== RN+ H
+
16
The relative concentration of each ionic form in the solution varies
in the pH of the solution or surrounding tissue
In the presence of high concentration of hydrogen ion (low pH) the
equilibrium shifts to left and most of the anesthetic solution exists
in cationic form
RNH+ gt RN
+ + H
+
As hydrogen ion concentration decreases (higher pH) the
equilibrium shifts towards the free base form
RNH+ lt RN + H
+
17
The relative proportion of ionic form also depends on pKa or DISSOCIATION CONSTANT of the specific local anesthetic
The pKa is a measure of molecules affinity for H+
ions
When the pH of the solution has the same value as pKa of the local anesthetic exactly half the drug will exists in the RNH
+ form and
exactly half in RN form
The percentage of drug existing in either form can be determined by Henderson Hasselbalch equation
Log baseacid = pH - pKa
18
4
MECHANISM OF ACTION OF LOCAL
ANESTHETICS
The following sequence is proposed mechanism of action of LA
Displacement of calcium ions from the sodium channel receptor site
Binding of local anesthetic molecule to this receptor site
Blockade of sodium channel
19
Decrease in sodium conductance
Depression of rate of electrical depolarization
Failure to achieve the threshold potential level
Lack of development of propagated action potential
Conduction blockadehellip
20
21
Na + Na +
22
LOCAL ANESTHETIC AGENT
COMERCIALLY PREPARED LOCAL ANESTHESIA
CONSISTS OF
Local anesthetic agent (xylocaine lignocaine 2)
Vasoconstrictor (adrenaline 1 80000)
Reducing agent (sodium metabisulphite)
Preservative (methylparabencapryl
hydrocuprienotoxin)
Fungicide (thymol)
Vehicle (distillde waterNaCl)
LOCAL ANESTHETIC AGENT
The local anesthetics used in dentistry are divided
into two groups
ESTER GROUP
AMIDE GROUP
23 24
ESTER GROUP It is composed of the following
An aromatic lipophilic group
An intermediate chain containing
an ester linkage
A hydrophilic secondary or tertiary
amino group
AMIDE GROUP It is composed of the following
An aromatic lipophilic group
An intermediate chain containing
amide linkage
A hydrophilic secondary or tertiary
amino group
5
25
CLASSIFICATION OF LOCAL ANESTHETICS
ESTERS
Esters of benzoic acid
Butacaine
Cocaine
Benzocaine
Hexylcaine
Piperocaine
Tetracaine
Esters of Para-amino
benzoic acid
Chloroprocain
Procaine
Propoxycaine
26
AMIDES Articaine
Bupivacaine
Dibucaine
Etidocaine
Lidocaine
Mepivacaine
Prilocaine
Ropivacaine
QUINOLINE
Centbucridine
PHARMACOKINETICS OF LOCAL
ANESTHETICS UPTAKE
When injected into soft tissue most local anesthetics produce
dilation of vascular bed
Cocaine is the only local anesthetic that produces
vasoconstriction initially it produces vasodilation which is
followed by prolonged vasoconstriction
Vasodilation is due to increase in the rate of absorption of the
local anesthetic into the blood thus decreasing the duration of
pain control while increasing the anesthetic blood level and
potential for over dose 27
AMIDE LOCAL ANESTHETICS
The metabolism of amide local anesthetics is more
complicated then esters The primary site of
biotransformation of amide drugs is liver
Entire metabolic process occurs in the liver for lidocaine
articaine etidocaine and bupivacaine
Prilocaine undergoes more rapid biotransformation then the
other amides
28
REFERENCES
Handbook of local anesthesia ndash Stanley F Malamed ndash 6th
edition
Essentials of Local Anesthetic Pharmacology Daniel E
Becker Anesth Prog 2006 Fall 53(3) 98ndash109
WIKIPEDIEA
29
THANK YOU
30
1
Pharmacological Methods of Behavior
Management
DR MITAKSHARA NIRWAN
DEFINITIONS
bull Conscious Sedation ndash A minimally depressed level of consciousness that retains
the patients ability to independently and continuously maintain an airway and respond appropriately to physical stimulation or verbal command
(American Dental Association House Of Delegates 2000)
bull Deep Sedation ndash An induced state of depressed consciousness
accompanied by partial loss of protective reflexes including the inability to continuously maintain an airway independently and or to respond purposefully to physical stimulation or verbal command
bull General Anesthesia (G A) ndash An induced state of unconsciousness or complete loss of
protective reflexes including the inability to continually maintain an airway independently and respond purposefully to physical stimulation or verbal command
Conscious sedation
ADVANTAGES
Conscious
Protective reflexes active amp intact
Stable vital signs
Operating dentist may perform sedation
Minimum amount of equipment required
Prolong detainment in recovery room not required
Risk of complication very low
Excellent choice for poor ndash risk pt in dental office
Cost effective
General anesthesia
ADVANTAGES Not absolutely
essential May be the only
method Not necessary (no
pain reaction) Amnesia always
present
Conscious sedation
DISADVANTAGES
Pt cooperation is essential
Extremely difficult or mentally handicapped pt cannot always be managed
Use of local anesthesia is a must
Amnesia may or may not be present
General anesthesia DISADVANTAGES
Pt unconscious
Protective reflexes are depressed
Depressed
Advanced training required Dentist must not act also as anesthetist
Special equipment necessary
Detainment in recovery area necessary
High IOP amp postoperative complications
Not indicated in dental office
More expensive
Fundamental Concepts
bull Techniques that utilize drugs to induce co-operative yet conscious state in an otherwise uncooperative child ndash CONSCIOUS SEDATION
2
GOALS
1 To facilitate the provision of quality care
2 To minimize the extremes of disruptive behavior
3 To promote a positive psychologic response to treatment
4 To promote patient welfare amp safety
5 To return the patient to physiologic state
OBJECTIVES
1 The pt mood must be altered
2 The pt must remain conscious at all times
3 The pt must be cooperative
4 All protective reflexes must remain intact and active
5 Vital signs must remain stable and with in normal limits
6 The ptrsquos pain threshold should be elevated
7 Amnesia may be present
Indications
1 Preschool children
2 Lack of Psychological Emotional maturity
3 Lack of Cognitive Physical Medical disability
4 Fearful amp anxious pts
5 Pt who require extensive amp complicated dental care amp would require or benefit from prolonged visits
6 Acute pain
7 Traumatic injuries
Operating Facilities amp Equipment
A positive pressure O2 delivery system capable of administering gt than 90 O2 at 10L min flow for 60 min (650L ldquoErdquo cylinder)
OR
Self inflating bag valve mask device (15L min)
A functional suction apparatus with appropriate suction catheters
Monitoring equipment - PO BPC PC or Capno
Inhalation sedation unit
100 O2 amp never less than 25
A fail safe mechanism that is checked and calibrated annually
Must have appropriate scavenging system
Emergency drugs
Techniques of sedation
Routes for drug administration
bull Oral
bull Rectal
bull Inhalational
bull Transmucosal
ndash Sublingual
ndash Intranasal
bull Parenteral
ndash IM
ndash sub mucosal
ndash IV
3
Oral Sedation
Advantages
1 Almost universally accepted and the easiest method
2 Decreased incidence and severity of adverse reaction
3 Low cost
Disadvantages
1 Absorption is variable
2 Prolonged latent period(30 min)
3 Reversal of any unwanted effect is also difficult
4 Inability to readily lighten or deepen the level of sedation
5 Prolonged duration of action
Rectal Sedation
Advantages 1 Incidence and intensity of
drug related side effects is minimized
2 Drug absorption occurs from the large intestine directly into the circulation
3 The lack of a needle syringe or other equipment
4 The ease of administration
5 The low cost
Disadvantages
1 Inconvenience to the administrator amp pt
2 The variable absorption of drugs from the large intestine
3 The slow onset of action amp the relatively long duration of action
4 Inability to titrate the drug dosage
5 The inability to reverse the action of the drug the prolonged recovery
Intranasal sedation
Advantages
Rapid onset (10 ndash 15 min)
Simple amp relatively painless
Less pt cooperation is required
Absorbed directly into the C V S
Intranasal sedation
Disadvantages
1 Dependence on nasal mucous membrane
2 Shorter duration of action(40-60min)
3 Multiple dosage may be necessary
Drugs
Midazolam ndash 02mgkg
Sufentanil ndash 15 ndash 3 mcgkg
Ketamine ndash 3-6mg kg
Sublingual sedation
Advantages
1 Pt acceptance
2 Rapid onset
3 High bioavailability
Drugs
Oral Transmucosal Fentanyl Citrate (OTFC)
Intramuscular Sedation
Advantages
1 More rapid onset of action
2 Absorbed directly into the C V system
3 More reliable absorption of drug
4 Pt cooperation is not as essential
Disadvantages
1 Time factor ndash its 15 min latent period
2 Pt may not be willing to accept the injection
3 The prolonged duration of action(2-4 hrs more)
4 Possibility of injury to the tissues at the site of injection caused by either the drug or the needle
4
Sites of I M administration
1 Gluteal area
2 Vastus lateralis
3 Mid ndash deltoid area
Drugs
Diazepam
Midazolam
Hydroxyzine
Inhalation Sedation
Advantages
1 The onset of action is more rapid
2 Peak clinical level is achieved rapidly(3-5min) - permit titration
3 Administrator has complete control over the actions of the drug - safety feature
4 No significant over dosage
5 Flexible duration of action
6 Recovery time is rapid amp most complete
7 No injection is required
8 With N2O- O2 it is safe with very few side effects
Disadvantages
1 The initial cost of the equipment is high 2 The continuing cost of the gases is high 3 The equipment occupies considerable space 4 N2O is not a potent agent 5 A degree of cooperation is required from the pt 6 Chronic exposure to N2O is deleterious to the health of
dental personnel
Contraindications
1 Nasal obstruction 2 Cyanosis at rest 3 Poor cooperation 4 1st trimester of pregnancy 5 Fear of masks
I V Sedation
Advantages
1 The onset of action is the most rapid 2 The dosage may be titrated 3 Suitable level of sedation can be provided 4 The recovery period is shorter 5 Side effects are extremely uncommon 6 Control of salivary secretions is possible 7 The gag reflex is diminished 8 Effectively diminishes motor disturbances 9 Provides immediate access to CVS in emergency
Disadvantages
1 Venipuncture is necessary
2 Complication may rise at the site of the venipuncture
3 Monitoring must be more intensive
4 Recovery is not complete at the end of the procedure
5 Reversal of sedation is difficult
5
N2O-O2 (Relative Analgesia)
colorless sweet smelling gas
Pharmacokinetics
Absorption through pulmonary epithelium
It is approx 15 times as soluble as is nitrogen It replaces nitrogen in blood
It is carried in solution in plasma of the blood
It is not metabolized by the body
Elimination ndash majorndash lungs minor --- skin
perspiration urine and intestinal gas
Pharmacodynamics
Dose related
10 ndash 25 Lightheaded
Changes in visual amp auditory sensation
Tingling of hands amp feet
Suffusing warmth
Remote from the immediate environment
Reduced anxiety
25-50 max analgesic properties and aberration of vision hearing and proprioception mild drowsiness euphoria amnesia and increased sleepiness and dreams
35 conc will achieve maximum analgesia
bull CNS
ndash Cerebrum-primarily affected
ndash Safe but weak anesthetic agent
bull RESPIRATORY SYSTEM
ndash Increased Tidal and minute volumes
bull CARDIOVASCULAR SYSTEM
ndash 2 studies ndash decreased cardiac output
bull FETAL SYSTEMS
ndash Miscarriage in humans
bull OTHER SYSTEMS
ndash Depression of spinal reflexes increase muscle tone indicates stage of delirium
ndash Muscle rigidity-narcotics + nitrous oxide
ndash Nausea and vomitting - GIT
ndash HEMATOPOIESIS ----- prolonged exposure
Adverse reactions and toxicity
EMOTIONAL REACTIONS
DREAMS HALLUCINATIONS
No acute toxicity
Chronic toxicity ndash bone marrow
depression
PROCEDURE
Diffusion Hypoxia
Sevoflurane
A fluorinated derivative of isopropyl ether ndash synthesized in 1970
Potent anaesthetic agent with rapid uptake amp speedy recovery
Day-case surgery
Problem
Attaching vaporiser to any of the currently available machine
BENZODIAZEPINES
Diazepam 1961 lipid soluble
Uses-alcoholism epilepsy labor tetanus and cerebral palsy
- sedation and amnesia
- varieties of neurosis amp anxiety states
Pharmacokinetics
Orally Rectal IMIV or SC
Well absorbed through GIT
Excretion in urine
6
bull Pharmacodynamics
ndash Depress the brain stem reticular system and the limbic system thalamus and hypothalamus
ndash It is a centrally acting muscle relaxant Has anti-convulsant properties
Adverse reaction amp toxicity
ndash Confusion nausea headache increased appetite decreased salivation and jaundice Thrombophlebitis
ndash Rebound phenomenon
ndash Toxicity drowsiness confusion sleep and coma
Dosage Oral or Rectal ndash 02-05mgkg
Maximum single dose 10mg
IV- 025mgkg
Supplied Tablets 2 5 10 mg
Suspension ndash 5mg
Midazolam Water soluble ndash non-irritant
Oral IM IV
Metabolism- liver
Onset IV 3 -5mins
oral 20 ndash 30mins
Oral administration anxious patients requiring relatively short dental procedure
No rebound phenomenon
Better anxiolysis amp amnesia (retrograde amnesia)
Adverse effects Respiratory depression
dose dependant apnea
Dosage Oral ndash 025 to 1mgkg to maximum single dose 20mg
IM ndash 01 to 015mgkg to a maximum of 10mg
IV ndash slow IV
Supplied Syrup ndash 2mgml
Injectable ndash 1mgml amp 5mgml vials
Flumazenil specific benzodiazepines antagonist
selectively inhibits CNS effects
IV administration amp not recommended below 18yrs of age
02mg over 15 seconds after 45seconds 02mg then after 60seconds to maximum of 1mg
Sedative-Hypnotics
Barbiturates First truly effective drugs for the management of anxiety Generalized CNS depressants Produce dose dependent effects
Sedation ---- sleep ---- GA ---- coma
Suppress the CNS and result in sedation and amnesia Advantages
Rapid onset and short duration Disadvantages
no analgesic effect and possible hypotension Must be used with caution in trauma patients because they may cause
apnea and hypoventilation
DOSE Pentobarbital Sodium 100mg Secobarbital Sodium 100 to 200mg Children 30 to 100mg
bull Chloral Hydrates (Mickey Finn Knock out drops ) First synthesized in 1832 first member of the hypnotic group of drugs
Widely used as conscious sedation agent
Properties
Unpleasant taste
Nausea vomiting
Quite irritating to skin and to mucous membranes
GI irritation
Dosages Individualized for each patient 25 ndash 50mgkg
maximum of 1g
Supplied oral capsule ndash 500mg
oral solution ndash 250 amp 500mg5ml
Rectal suppositories ndash 324 amp 648mg
Narcotics
Do produce sedation amp euphoria greater in children
LA is required but dose should be decreased
Meperidine Synthetic opiate agonist
Very water soluble
Orally SC IM or IV
Peak effect by oral 1 hr amp lasts upto 4 hrs
Adverse reactions
-Seizures
-Extreme caution in hepatic or renal diseases or history of seizures
7
Dosage Oral SC or IM ndash 1to 22mgkg not to exceed 100 mg
Supplied Oral Tablets ndash 50 amp 100mg
Oral Syrup ndash 50mgml
Parental solution ndash 25 50 75 amp 100mgml
Fentanyl
Synthetic opiate narcotic analgesic
Very potent 01mg = 10mg Morophine75mg Meperidine
Pharmacokinetics
IV IM SM
Metabolized in liver Excreted in urine
Fentanyl Onset ndash 7 to 15mins
Duration ndash 1 to 2 hrs
Pharmacodynamics
Respiratory depression RR but returns to normal rapidly Tidal volume amp response to co2 depressed for extended period
Apnea
Less emetic than meperidine
NOT RECOMMENDED IN CHILDREN BELOW 2yrs
Dosage 0002 to 0004mgkg
Supplied 005mgml in 2 amp 5ml ampoules
Reversal drug Naloxone
Semisynthetic opiate antagonist
No agonist activity
Onset 2 to 5mins SC or IM amp 1 to 2mins IV
Reversal 45mins
Pt should be kept under continual surveillance
Adverse reaction nausea vomiting sweating hypotension hypertension ventricular tachycardia fibrillation
Dosage IV SC IM 001mgkg then 01mgkg every 2- 3mins maximum 2mg
Supplied 002 004 1mg solutions
Antihistamines
Hydroxyzine
Oral or IM
Effect ndash 15 ndash 30mins
Half-life ndash 3 hrs
Uses
To relieve anxiety
Used as an anti-histamine
Used to control nausea and vomiting including that associated with motion sickness and pregnancy
Adverse reaction dry mouth drowsiness hypersentivity
Dosage Oral ndash 1 to 2mgkg
IM ndash 11mgkg
Promethazine Oral or IM Onset 15 to 60mins Duration 4 to 6 hrs Uses
To prevent and treat nausea and vomiting associated with motion pregnancy or surgery
Produces sedation and reduce swelling pain and trismus
Lower seizure threshold Adverse reaction dry mouth blurred vision thickening of bronchial secretions Dosage OralIM ndash 05-11mgkg
maximum 25 mg
Diphenhydramine
Oral IM IV
Onset -1hr
Duration ndash 4 to 6 hr
Metabolized in liver
Adverse reaction disturbed coordination thickening of bronchial secretions
Dosage Oral IM IV ndash 1 to 15mgkg
maximum 50mg
Tranquilizers
Major tranquilizer antipsychotic produce calmness control symptoms of psychoses cause reversible extra pyramidal symptoms and do not tend to cause habituation
Minor tranquilizer antianxiety agents also cause calmness do not cause extrapyramidal symptoms Used in conditions like nervous tension and mild depression
8
Classification
Antipsychotics
Phenothiazine derivatives
Chlorpromazine promazine
Butryophenones
Haloperidol
Rauwolfia alkaloids
Reserpine
Antianxiety drugs
Propyl alcohol derivatives
Meprobamate
Benzodiazepine derivatives
Diazepam
Miscellaneous compounds
Hydroxyzine
Meprobamate
White crystalline powder slightly bitter in taste
Only administered orally
Peak blood concentration ----1 to 3hrs
10 ---------excreted unchanged Rest --- excreted as a oxidized derivative or as a glucoronide
Uses
To relieve day time anxiety
Induce sleep in insomniacs
To reduce anxiety associated with dental treatment
Anti-convulsant ndash petit mal epilepsy
Adverse reaction leucopenia acute non-thrombocytopenic purpura ecchymoses eosinophilia edema adenopathy
Dosage Childrengt 6yrs 100 to 200mg
Not recommended for children under 6yrs
Monitoring during sedation
1 Pulse
2 Blood pressure
3 ECG
4 Respiration
5 Temperature
Pulse
Manual Electronic
bull Radial Brachial
bull Facial labial
Blood pressure
ndash Stethoscope amp sphygmomanometer
ndash Automatic devices
ndash Direct cannulation of an artery ndash very accurate
Electrocardiograph
Heart rate rhythm myocardial function
9
Respiration
ndash Monitoring respiratory rate
ndash Observing the rise amp fall of the chest wall
ndash Observing the color of mucous membrane
ndash Observing the inflation amp deflation of the reservoir bag
Devices for monitoring respiration
1 The Precordial pretracheal stethoscope
2 The esophageal stethoscope
ndash Respiratory rate
ndash Heart rate
ndash Any abnormal sounds
Pulse Oximeter
ndash Oxygen saturation
ndash Heart rate
ndash Oxisensor site
ndash Fingers
ndash Toe
ndash Ear lobe
Mechanism
Oxygenated Hb ndash red light
Deoxygenated Hb- infrared light
Tissue pressure from arterial pulse (plethysmography)
Advantages
ndash Safe amp noninvasive
ndash Simple to use
ndash Information is rapidly available for clinical decision
ndash Indirectly indicates respiratory adequacy
Disadvantages
ndash Finger probes can get dislodged
ndash Emitted light source may cause burning
ndash Non reusable probes are expensive
ndash Does not directly determine airway patency
Capnography
1 The presence absence of air flow
2 Indicates depth amp adequacy of respiration
3 Continues analysis of the co2 content of the respired air ndash indicates respiratory adequacy
Temperature
ndash Disposable nondisposable thermometer
ndash Esophageal rectal temp probe
10
Discharge criteria
Cardiovascular function is satisfactory amp stable
Airway patency is uncompromised amp satisfactory
Pt is easily arousable amp protective reflexes intact
State of hydration is adequate
Pt can talk if applicable
Pt can sit unaided if applicable
Pt can ambulate with minimal assistance if applicable
Presedation level of responsiveness achieved
Responsible individual is available
1
PULP THERAPY OF VITAL TEETH
DR MITAKSHARA NIRWAN
Contents
Indirect pulp capping
Direct pulp capping
Medications amp materials used in pulp capping
Pulpotomy
MTA
Apexogenesis
INDIRECT PULP CAPPING
Pieter Van Forest - first to speak about root canal therapy
Glove designed instruments that could prepare a canal to a certain size and taper(1910)
Indirect pulp capping is defined as a procedure where in small amount of carious dentin is retained in
deep areas of cavity to avoid exposure of pulp followed by placement of a suitable medicament and
restorative material that seals off the carious dentin and encourages pulp recovery (Ingle)
A procedure in which only the gross caries is removed from the lesion and the cavity is sealed for a
time with a biocompatible material (McDonald)
Objective of indirect pulp capping
These were given by Eidelman in 1965
bull Arresting the carious process
bull Promoting dentin sclerosis
bull Stimulating formation of tertiary dentin
bull Remineralization of carious dentin
Layers of Carious Dentin Indications of Indirect Pulp Capping
History
Mild pain associated with eating
Negative history of spontaneous extreme pain
Clinical Examination
Deep carious lesion which are close tobut not involving the pulp in vital primary or young
permanent teeth
No mobility
Nominal pulp inflammationdefinite layer of affected dentin after removal of infected dentin
Radiographic examination
Normal lamina dura amp PDL space
No radiolucency around the apices
2
Contraindications of Indirect Pulp Capping
History
Sharp penetrating pulpalgia
Prolonged spontaneous pain especially at night
Clinical examination
Mobility of tooth
Discoloration of tooth
Negative reaction of electric pulp testing
Radiographic examination
Definite pulp exposure
Break in the lamina dura
Radiolucency around the apices
Widened PDL space
Treatment procedure
Sequelae of Indirect Pulp Capping Three distinct types of new dentin formation take place
1 Cellular fibrillar dentinmdashfirst 2 months
2 Globular dentinmdash3 months
3 Tubular dentin (uniform mineralized dentin)
bull 15th of reparative dentin formation begins in less than 30 days
bull After 3 months 01 mm is formed
DIRECT PULP CAPPING Defined by Kopel (1992) as the placement of a medicament or non medicated material on a pulp that
has been exposed in course of excavating the last portions of deep dentinal caries or as a result of
trauma
Objective
To create new dentin in the area of the exposure and subsequent healing of the pulp
Rationale
achieve a biologic closure of the exposure site by deposition of hard tissue barrier (dentin bridge)
between pulp tissue and capping material thus walling off the
INDICATIONS
Small mechanical exposure
Easily controlled haemorrhage
Bright red haemorrhage
True pinpoint exposure
CONTRAINDICATIONS
Severe toothache at night
Spontaneous pain
Tooth mobility
Radiographic appearance of pulp periradicular de- generation
Excess of hemorrhage at the time of exposure Serous exudate from the exposure
Externalinternal root resorption
Swellingfistula
Histological Changes after Pulp Capping
These were illustrated be Glass and Zander in 1949
After 24 hours Necrotic zone adjacent to calcium
hydroxide paste is separated from healthy pulp
tissue by a deep staining basophilic layer
After 7 days Increase in cellular and fibroblastic
activity
After 14 days Partly calcified fibrous tissue lined by
odontoblastic cells is seen below the calcium
proteinate zone disappearance of necrotic zone
After 28 days Zone of new dentin
3
Medications and Materials Used for Pulp Capping Calcium hydroxide
Corticosteroids amp antibiotics
Inert materials
Collagen fibers
4-META adhesive
Direct bonding
Isobutyl cyanoacrylate
Denatured albumin
Mineral trioxide aggregate
Laser
Bone morphogenic protein
PULPOTOMY
Finn (1995) defined it as the complete removal of the coronal portion of the dental pulp
followed by placement of a suitable dressing or medicament that will promote healing and
preserve vitality of the tooth
American Academy of Pediatric Dentistry (1998) defined pulpotomy as the amputation of
affected infected coronal portion of the dental pulp preserving the vitality and function of the
remaining part of radicular pulp
Objectives
bull Removal of inflamed and infected coronal pulp at the site of exposure thus preserving the vitality of the
radicular pulp and allowing it to heal
bull Maintain the tooth in the dental arch
Rationale
bull Radicular pulp is healthy and capable of healing after surgical amputation of the infected coronal pulp
bull Preserves vitality of the radicular pulp
bull Maintains tooth in a physiologic condition
Indications of Pulpotomy bull Mechanical pulp exposure in primary teeth
bull Teeth showing a large carious lesion but free of radicular pulpitis
bull History of only spontaneous pain
bull Hemorrhage from exposure sites bright red and can be controlled
bull Absence of abscess or fistula
bull No interradicular bone loss
bull No interradicular radiolucency
Contraindications of Pulpotomy bull Persistent toothache
bull Tenderness on percussion
bull Root resorption more than 13rd of root length
bull Large carious lesion with nonrestorable crown
bull Highly viscous sluggish hemorrhage from canal orifice which is uncontrollable
bull Medical contradictions like heart disease immuno compromised patient
bull Swelling or fistula
bull External or internal resorption
bull Pathological mobility
bull Calcification of pulp
Classification of pulpotomy
4
Formocresol Pulpotomy
Iby BUCKLEY in 1904
Sweet (1930) Formulated multi visit technique
Doyle (1962) Advocated 2 sitting procedure (complete devitalization)
Spedding (1965) Gave 5 minute protocol (partial devitali- zation)
Venham (1967) Proposed 15 seconds procedure
Current concept uses 4 minutes of application time
Composition of formocresol Buckleyrsquos Formula
bull Cresol ndash 35 percent
bull Glycerol ndash 15 percent
bull Formaldehyde ndash 19 percent
bull Water ndash 31 percent
Mechanism of Action
It prevents tissue autolysis by bonding to the proteins Bonding is of peptide groups of side chain amino acids and is a reversible process accomplished without
changing the basic structure of protein molecules
Histological Changes
bull Demonstrated by Mass and Zilbermann11 in 1933 and also by Massler and Mansokhani in 1959
bull Immediately the pulp becomes fibrous and acidophillic
bull Seven to fourteen days Three zones appear
a broad eosinophilic zone of fixation
b broad pale-staining zone of atrophy with poorcellular definition
c broad zone of inflammation extending apically into normal pulp tissue
bull One yearndash Progressive apical movement of these zones with only acidophillic zone left at the end of 1 year
Modified Formocresol Pulpotomy
Used by TRASK(1972)
The technique is identical to that described for primary teeth except that the formocresol pellet is
sealed permanently in the tooth
Two-visit Devitalization Pulpotomy
Indications
bull There is evidence of sluggish bleeding at the amputation site that is difficult to control
bull Pus in the chamber but none at the amputation site
bull There is thickening of the PDL
bull History of pain
Contraindications
bull Nonrestorable tooth
bull Tooth with necrotic pulp
5
Glutaraldehyde Pulpotomy
It was first suggested by S Gravenmade Introduced by Kopel in 1979
Mechanism of Action
bull Glutaraldehyde produces rapid surface fixation of the underlying pulpal tissue
bull A narrow zone of eosinophilic stained and compressed fixed tissue is found directly beneath the area of application which blends into vital normal appearing tissue apically
bull With time the glutaraldehyde fixed zone is replaced by macrophagic action with dense collagenous tissue thus the entire root canal tissue is vital
Cvekrsquos Pulpotomy
bull This is also called as calcium hydroxide pulpotomy or young permanent partial pulpotomy
bull This was proposed by Mejare and Cvek16 in 1978
bull Indicated in young permanent teeth where the pulp is exposed by mechanical or bacterial means and the
remaining radicular tissue is judged vital by clinical and radiographic criteria whereas the root closure is
notcomplete
MINERAL TRIOXIDE AGGREGATE (MTA) Torabinejad described the physical and chemical properties of MTA in 1995
It is ash colored powder made primarily of fine hydrophilic particles of
1 tricalcium aluminate
2 tricalcium silicate
3 silicate oxide
4 tricalcium oxide
5 bismuth dioxide
Hydration of the powder results in a colloidal gel composed of calcium oxide crystals in an amorphous
structure This gel solidifies into a hard structure in less than three hours
PROPERTIES OF MTA
It is biocompatible material and its sealing ability is better than that of amalgam or ZOE
Initial pH is 102 and set pH is 125
The setting time of cement is 4 hours
The compressive strength is 70 MPA which is comparable with that of IRM
Low cytotoxicity ndash It presents with minimal inflammation if extended beyond the apex
Mineral trioxide aggregate (MTA) has demonstrated the ability to induce hard-tissue formation in
pulpal tissues and it promotes rapid cell growth
APEXOGENESIS
It is defined as the treatment of a vital pulp by capping or pulpotomy in order to permit continued
growth of the root and closure of the open apex
Rationale
Maintenance of integrity of the radicular pulp tissue to allow for continued root growth
Indications
bull Indicated for traumatized or pulpally involved vital permanent tooth when root apex is incompletely formed
bull No history of spontaneous pain
bull No sensitivity on percussion
bull No hemorrhage
bull Normal radiographic appearance
Contraindications
bull Evidence that radicular pulp has undergone degenerative changes
bull Purulent drainage
bull History of prolonged pain bull Necrotic debris in canal
bull Periapical radiolucency
6
1
Gupta A Dhingra R Chaudhari P Gupta A
Department of Paedodontics and Preventive Dentistry Faculty of Dental Sciences SGT University Gurgaon Haryana India
Journal of Indian Society of Pedodontics and Preventive Dentistry
Volume 35 I Issue 3 I July-September 2017
A COMPARISION OF VARIOUS MINIMALLY
INVASIVE TECHNIQUES FOR THE REMOVAL
OF DENTAL FLUOROSIS STAINS IN
CHILDREN
DR MITAKSHARA NIRWAN
CONTENTS
bull Introduction
bull Aims
bull Materials and Methods
bull Results
bull Discussion
bull Conclusion
bull Critical analysis
bull References
INTRODUCTION
bull Dental fluorosis is a developmental disturbance of dental enamel caused by
successive exposure to high concentrations of fluoride during tooth
development
bull Various methods of therapy are advocated for the treatment of fluorosis -
stained teeth which range from invasive ceramic veneer bonding restorations
to abrasive chemical treatments
bull The combination of dental bleaching techniques and microabrasion appears
as an excellent conservative solution to reestablish health in fluorosis
affected teeth
AIMS
bull The aim of the study was to evaluate and compare the effectiveness of
minimally invasive techniques for the removal of dental fluorosis
stains in children in vivo
MATERIALS AND METHODS
Patients visiting the department of Pedodontics and Preventive dentistry
Faculty of Dental Sciences SGT University Gurgaon
bull Sample size 90 patients
bull Age group 10 -17 years
bull Caries cracks or periodontal
disease on anterior teeth
bull Abscess draining sinus
cellulitis
bull Non vital teeth
hypersensitive exposed
crevices
bull Orthodontic appliance
bull Past history of bleaching
bull At least two permanent
maxillary anterior teeth
bull TSIF of score 4
bull Free of systemic diseases
Inclusion criteria Exclusion criteria
2
Groups
Group A In office bleaching with 35 hydrogen peroxide( Pola Office
Bleaching kit) activated by light emitting diode (LED) bleaching unit
(35 HP)
Group B Enamel microabrasion (EM) (PREMA Enamel Microabrasion
System) followed by in-office bleaching with 44 carbamide peroxide
gel (EM)
Group C In-office bleaching with 5 sodium hypochlorite (5
NaOCl)
A baseline colour evaluation was done by taking digital photograph of
the maxillary anterior teeth
RESULTS
Group 1
Colour stability
Group 2 Group 3
Tooth sensitivity
Tooth sensitivity values were taken before the treatment
which was compared to immediate postoperative and follow
up visits It was checked using an electric pulp tester
maximum
moderate
least
immediately
group 2
group 1
group 3
1 month
group 2
group 1
group 3
3 month
group 2
group 1
group 3
Patient satisfaction score
Satisfaction was assessed on visual analog scale
Range 1 to 5
Groups percentage of patients
who were satisfied with
the treatment
Number of patients
who reported slight
reappearance of colour
Group 1
90
7
Group 2
83
8
Group 3
73
7
3
Number of Appointments
Groups One sitting Two sittings Three
sittings
Group 1
25
4
1
group 2
26
3
1
Group 3
30
0
0
DISCUSSION
bull Hydrogen peroxide is capable of penetrating the tooth osmosis and through porosities and cracks subsequently acting directly on the pigmented molecules
bull Gurgan et al investigated 3 different light systems and found out that diode laser system with gave best tooth whitening and least tooth sensitivity
bull In the EM group the surface reflects and refracts light from the surface in such way that mild imperfections in underlying enamel are camouflaged While the highly polished surface of enamel enhances the aesthetic appearance
bull Train et al and Loguercio et al also had the similar results in their studies with EM mild fluorosis showed best results moderate showed moderate results while it had little effect on severe fluorosis
bull NaOCl was only effective on mild stains while moderate and severe
stains could only be lightened to quite an extent but could not be
completely removed
bull When NaOCl comes in contact with hypomineralized and discoloured
enamel it degrades and removes the chromogenic organic material
located on the enamel surface
CONCLUSION
bull It was concluded that esthetic appearance of teeth mild fluorosis can
be achieved by bleaching and microabrasion But in cases of
moderate fluorosis a combination of any of theses modalities can be
used
bull As no special maintenance precautions are required these maybe be
considered as an interesting alternative to conventional operative
treatment
bull Focuses on only TSIF of 4
bull Electric pulp testing is not the
right method to check for
sensitivity
bull Tooth Sensitivity changes
from person to person
bull Food habits can cause
staining of the teeth
bull Minimally invasive
bull Cheaper to veneers
bull Minimal loss of tooth structure
bull 4 parameters checked for the success of treatment
bull Inclusion of specific score of fluorosis for comparing the results
bull Maximum 3 appointments needed
CRITICAL ANALYSIS
Pros Cons
REFERENCES
bull Gurgan S Cakir FY Yazici E Different light-activated in officebleaching
systems Lasers Med Sci 201025817-22
bull Train TE McWhorter AG Seale NSWilson CF Guo IY Examination of
esthetic improvement and surface alteration following microabrasion in
fluorotic human incisors in vivoPediatr dent 199618353-62
bull Loguercio AD Correia LD Zago C Tagliari D Neumann E Gomes OM et al
Clinical effectiveness of two microabrasion materials materials for the
removal of enamel flurosis stains Oper Dent 200732531-8
4
5
CONCLUSION
The management and prognosis of a primary tooth with a separated instrument is
dependent on the level of instrument fracture within the root age of the child root
resorption and clinical signs and symptoms of the involved tooth
Different management approaches can be tried depending on clinical situations keeping
in mind benefits vs risks in preserving the tooth
PROS amp CONS
PROS
The entire procedure is given
by step by step
Well descriptive xrays and
photographs
CONS
Medical history has not been
given
REFERENCES
1 TOMER ANIL K ET AL ldquoBROKEN FILE RETRIEVAL PUZZLE IN ENDODONTICSrdquo
(2016)
2 SHENOY A MANDAVA P BOLLA N ET AL A NOVEL TECHNIQUE FOR REMOVAL OF
BROKEN INSTRUMENT FROM ROOT CANAL IN MANDIBULAR SECOND MOLAR
INDIAN J DENT RES 201425(1)107ndash110
3 PATEL J MORAWALA A TALATHI R ET AL RETRIEVAL OF A BROKEN INSTRUMENT
FROM ROOT CANAL IN PRIMARY ANTERIOR TEETH UNIV RES J DENT 20155(3)203ndash
206
4 MORANKAR R GOYAL A GAUBA K ET AL MANUAL VERSUS ROTARY
INSTRUMENTATION FOR PRIMARY MOLAR PULPECTOMIES - A 24 MONTHS
RANDOMIZED CLINICAL TRIAL PEDIAT DENT J 201828(2)96ndash102
5 KASHYAP NILOTPOL (2018) RETAINING PRIMARY MOLARS WITH INSTRUMENT
SEPERATION A CASE REPORT AND CLINICAL GUIDE
6
1
IMPACT OF 6 CITRIC ACID AND ENDOACTIVATOR AS IRRIGATION ADJUNCTS ON OBTURATION QUALITY AND PULPECTOMY OUTCOME IN
PRIMARY TEETH
NEETU JAIN SHALINI GARG ABHISHEK DHINDSA SAKSHI JOSHI HARJOY
KHATRIA
PEDIATRIC DENTAL JOURNAL 2019 29
1
DR MITAKSHARA NIRWAN
CONTENTS
bull INTRODUCTION
bull AIMS amp OBJECTIVES
bull CASE REPORT
bull RESULTS
bull DISCUSSION
bull CONCLUSION
bull PROS AND CONS
bull REFERENCES
2
INTRODUCTION
bull ENDODONTIC THERAPY IN PRIMARY TEETH INVOLVES DISINFECTION OF THE ROOT CANAL
SYSTEM AND ITS OBTURATION WITH RESORBABLE PASTE
bull THE CONTENTS OF ROOT CANAL ALONG WITH SMEAR LAYER ARE EXPECTED TO BE REMOVED
DURING THE BIOMECHANICAL PREPARATION
bull IN VITRO AND CLINICAL DOCUMENTS HAVE INDICATED THAT MECHANICAL PREPARATION OF
THE CANAL LEAVES LARGE PORTIONS OF THE CANAL WALLS UNDEBRIDED AND COMPLETE
REMOVAL OF THE BACTERIA BY THIS MECHANICAL PROCEDURE ALONE IS UNLIKELY TO BE SEEN
THEREFORE SOME FORM OF DISINFECTIONIRRIGATION IS MANDATORY TO KILL THE
MICROORGANISMS AND TO REMOVE THE RESIDUAL TISSUES
3
bull THE IDEAL REQUISITES OF A ROOT CANAL IRRIGANT AS GIVEN BY ZEHNDER ARE
1 BROAD ANTIMICROBIAL SPECTRUM
2 HIGH EFFICACY AGAINST ANAEROBIC AND FACULTATIVE MICROORGANISMS ORGANIZED
IN BIOFILMS
3 ABILITY TO DISSOLVE NECROTIC PULP TISSUE REMNANTS
4 ABILITY TO INACTIVATE ENDOTOXIN
5 ABILITY TO PREVENT THE FORMATION OF A SMEAR LAYER DURING INSTRUMENTATION OR
TO DISSOLVE THE LATTER ONCE IT HAS FORMED
6 SYSTEMICALLY NONTOXIC WHEN THEY COME IN CONTACT WITH VITAL TISSUES
NONCAUSTIC TO PERIODONTAL TISSUES AND WITH LITTLE POTENTIAL TO CAUSE AN
ANAPHYLACTIC REACTION
SINCE NO SINGLE IRRIGANT HAS THESE OPTIMAL PROPERTIES STUDIES HAVE REPORTED THE USE
OF TWO OR MORE SOLUTIONS IN A SPECIFIC SEQUENCE OR IN COMBINATIONS FOR BETTER
RESULTS 4
bull SEVERAL IRRIGATING SOLUTIONS ALONG WITH CHELATING AGENTS HAVE BEEN USED
DURING BIOMECHANICAL PREPARATION OF ROOT CANAL BOTH IN PRIMARY AND
PERMANENT TEETH
bull HOWEVER NONE OF THE AVAILABLE IRRIGATING SOLUTIONS HAS BEEN REGARDED CLEARLY
AS OPTIMAL SOLUTION BECAUSE OF THEIR LIMITED EFFECTIVENESS ESPECIALLY IN APICAL
13RD OF THE ROOT CANAL SYSTEM
bull TO OVERCOME SUCH LIMITATIONS USE OF ENDOACTIVATOR HAS BEEN PROPOSED AS AN
IRRIGATION FACILITATOR THAT IS BASED ON SONIC VIBRATION (UP TO 10000 CPM) WHICH
FACILITATES THE IRRIGANT PENETRATION AND ITS RENEWAL WITHIN THE CANAL
bull ACTIVATION SYSTEMS RESULTED IN BETTER REMOVAL OF THE SMEAR LAYER IN THE APICAL
THIRD OF ROOT CANALS IN COMPARISON TO CONVENTIONAL IRRIGATION
5
CITRIC ACID
bull CITRIC ACID IS A WEAK ORGANIC ACID WITH THE APPEARANCE OF WHITE CRYSTALLINE
POWDER AT ROOM TEMPERATURE
bull IT CAN EXIST EITHER IN WATER-FREE FORM (ANHYDROUS) OR MONOHYDRATE FORM THE
WATER-FREE FORM CRYSTALLIZES FROM THE HOT WATER WHEREAS THE MONOHYDRATE
FORMS FROM THE COLD WATER THE LATTER MAY BE CONVERTED TO ANHYDROUS FORM BY
HEATING MORE THAN 78degC
bull CITRIC ACID OCCURS NATURALLY IN THE BODY IN MITOCHONDRIA AND IS USED BY BLOOD
BANKS TO PREVENT COAGULATION OF TRANSFUSED BLOOD CITRIC ACID IS ALSO ESSENTIAL
TO HUMAN METABOLISM AND IS FOUND IN MANY FOODS
6
2
bull THE BIOLOGICAL EFFECTS OF CITRIC ACID ON THE PERIODONTAL STRUCTURE HAS BEEN
EXTENSIVELY STUDIED IN PERIODONTICS
bull NEUMAN AND NEWMAN SHOWED THAT CITRIC ACID IS THE MOST EFFECTIVE ACID IN
ALTERING THE SOLUBILITY OF HYDROXYAPATITE
bull YAMAGUCHI ET AL SHOWED THAT CITRIC ACID SOLUTION HAD ANTIBACTERIAL EFFECTS ON
ALL 12 ROOT CANAL BACTERIA TESTED
bull ARIAS-MOLIZ ET AL SHOWED THAT ETHYLENEDIAMINETETRAACETIC ACID (EDTA) HAS NO
BACTERICIDAL ACTIVITY EVEN AFTER 1 HOUR CONTACT
bull THIS ACID HAS THE ABILITY OF ROOT CANAL IRRIGATION AND ALSO SMEAR LAYER REMOVAL
DIFFERENT CONCENTRATIONS (1ndash50) HAVE BEEN PROPOSED GUTMANN ET AL CONCLUDED
THAT 10 CITRIC ACID IS BETTER THAN ULTRASOUND FOR SMEAR LAYER REMOVAL FROM THE
ROOT END CAVITIES
7
bull STUDIES HAVE SHOWN IRRIGATION WITH 6 CA FOR 15 OR 30 SECONDS IS QUITE
EFFECTIVE IN REMOVING ALL THE COMPONENTS OF THE SMEAR LAYER OF THE PRIMARY
TEETH WHEREAS PERITUBULAR DENTIN DESTRUCTION WAS OBSERVED WHEN HIGHER
CONCENTRATION OF CITRIC ACID WAS USED AS AN IRRIGATING SOLUTION
8
AIMS amp OBJECTIVES
bull THIS STUDY WAS AIMED TO EVALUATE THE CLINICAL AND RADIOGRAPHIC OUTCOME OF
PULPECTOMY ALONG WITH QUALITY OF OBTURATION USING 6 CITRIC ACID AND
ENDOACTIVATOR
9
CASE REPORT
bull 350 CHILDREN (3-9 YEARS) WITH CLINICAL SIGNS AND SYMPTOMS OF CHRONIC IRREVERSIBLE
PULPITIS IN DEEPLY CARIOUS TEETH WERE SCREENED DURING SCHOOL DENTAL HEALTH
PROGRAM FROM MAY 2014-JULY 2014
bull 123 CHILDREN REPORTED TO THE DEPARTMENT AND 67 CHILDREN WERE SELECTED BASED ON
INCLUSION AND EXCLUSION CRITERIA
RECRUITMENT OF PATIENTS
10
INCLUSION CRITERIA
bull HISTORY OF SPONTANEOUS PAIN AND UNCONTROLLED BLEEDING AFTER PULP AMPUTATION
EXCLUSION CRITERIA
bull EVIDENCE OF INTERNAL OR EXTERNAL (PHYSIOLOGICPATHOLOGIC) ROOT RESORPTION OF MORE THAN A THIRD OF ITS LENGTH
bull ROOT CANAL OBLITERATION OR ANATOMIC ANOMALIES
bull INADEQUATE BONE SUPPORT OR NON RESTORABLE TOOTH
bull ONCE PATIENTS ELIGIBILITY WAS CONFIRMED THE TREATMENT PROCEDURE WAS
EXPLAINED TO THE PARENTGUARDIAN AND INFORMED WRITTEN CONSENT WAS
OBTAINED FROM PARENTSGUARDIANS SHOWING WILLINGNESS FOR THEIR
CHILDRENS TREATMENT 11
PROCEDURE
bull PULPECTOMY WAS PERFORMED BY ONE OPERATOR OF PEDIATRIC DENTISTRY DEPARTMENT
USING A STANDARDIZED TREATMENT PROTOCOL FOR ALL THE PATIENTS
bull AFTER ADMINISTRATION OF LOCAL ANESTHESIA RUBBER DAM WAS APPLIED FOR ISOLATION
bull ACCESS CAVITY WAS PREPARED USING AIR-ROTOR HAND PIECE WITH 8 ROUND BUR AND
PULP TISSUE WAS EXTIRPATED WITH THE HELP OF SPOON EXCAVATOR
bull FURTHER THE NEGOTIATION OF THE CANALS WAS DONE WITH 10 K-FILE
bull A DIAGNOSTIC RADIOGRAPH WAS TAKEN FOR ROOT LENGTH DETERMINATION AND
WORKING LENGTH WAS KEPT 1 MM SHORT OF THE RADIOGRAPHICAL APEX
bull ALL ROOT CANALS WERE INSTRUMENTED MANUALLY USING K-FILES AND WERE IRRIGATED
WITH 10 ML 09 NORMAL SALINE AND 1 SODIUM HYPOCHLORITE AS STANDARDIZING
PROTOCOL FOR ROOT CANAL PREPARATION AND DISINFECTION
12
3
GROUP 1 (CA + E) - IRRIGATION WAS DONE
WITH 10 ML OF 6 CITRIC ACID (CITOCID AMMDENT)
AND IRRIGANTS WERE SONICALLY AGITATED WITH
ENDOACTIVATOR (DENTSPLY) FOR 30 S PER CANAL USING REDBLUE
ENDOACTIVATOR TIP
GROUP 2 (CA) - 10 ML OF 6 CITRIC ACID FOR 1 MIN USING
27 GAUZE IRRIGATING NEEDLE
GROUP 3(SH + E) - 10 ML OF 1 SODIUM HYPOCHLORITE
SOLUTION AND SONIC ACTIVATION WITH ENDOACTIVATOR
GROUP 4(SH) - 10 ML OF 1 SODIUM HYPOCHLORITE
SOLUTION USING IRRIGATING NEEDLE (CONTROL GROUP)
bull TEETH UNDERGOING PULPECTOMY WERE RANDOMLY ENROLLED BY CHIT METHOD INTO THREE
STUDY AND ONE CONTROL GROUP
13
bull IN CITRIC ACID GROUPS FINAL RINSE WITH NORMAL SALINE WAS DONE TO REMOVE THE
REMAINING CRYSTALS (CHELATES)
bull FOLLOWING BIOMECHANICAL PREPARATION THE ROOT CANALS WERE DRIED WITH STERILE
ABSORBENT PAPER POINTS AND OBTURATED WITH VITAPEX USING HAND HELD
LENTULOSPIRAL FINAL RESTORATIONS WERE DONE USING COMPOSITE RESIN
14
bull CLINICAL FOLLOW UP WAS DONE AT 24 H1 WEEK 1 MONTH 6 MONTH AND 12
MONTH TO CHECK PAIN PRESENCE AND PAIN FREQUENCY (ONCEMORE THAN ONCE)
SWELLING FISTULA SENSITIVITY TO PERCUSSION
bull RADIOGRAPHIC FOLLOW UP WAS DONE AT 6 MONTH AND 12 MONTH FOR ANY
DEVIATED ERUPTION OF SUCCEDANEOUS TEETH EXCESS FILING MATERIAL AND ITS
RESORPTION EXTERNALINTERNAL ROOT RESORBTION CALCIFIC METAMORPHOSIS
PRESENCE OF FURCATION RADIOLUCENCY
CLINICAL amp RADIOGRAPHIC FOLLOW UP
15
RADIOGRAPHIC ASSESSMENT OF OBTURATION QUALITY
bull POSTOPERATIVE RADIOGRAPHS WERE VISUALLY ASSESSED FOR QUALITY OF OBTURATION BY
TWO INDEPENDENT EXAMINERS (SG AD) WHO WERE BLINDED WITH REGARD TO
IRRIGATION PROTOCOL GROUP TO ENHANCE CALIBRATION EACH EXAMINER ASSESSED THE
RADIOGRAPH INDEPENDENTLY AND LATER REVIEWED TOGETHER FOR FINAL ASSESSMENT
INDIVIDUAL ROOT WAS TAKEN AS UNIT OF ANALYSIS FOR GRADE OF OBTU- RATION AND
SCORING CRITERIA WERE AS GIVEN BY COLL JA 1996
1 UNDER FILLED - FILLING MATERIAL ENDED 1 MM OR MORE SHORT OF THE APEX
2 OPTIMAL FILLING- FILLING MATERIAL APPEARED TO END AT THE RADIOGRAPHICAL APEX
3 OVERFILLED - FILLING MATERIAL EXTRUDED PAST THE RADIOGRAPHIC APEX
4 OPTIMALLY FILLED ROOTS WERE FURTHER ASSESSED FOR THE PRESENCE OF VOIDS AND VOID
AREA (ROOT CANAL SURFACE UNTOUCHED BY THE ROOT CANAL FILLING MATERIAL) IN THREE
VISUALLY DIVIDED SECTIONS OF THE ROOT IE CORONAL MIDDLE AND APICAL 13RD
16
RESULTS
bull OVERALL CLINICAL AND RADIOGRAPHIC SUCCESS RATE OVER A PERIOD OF ONE YEAR WAS
9886 amp 977 RESPECTIVELY
bull ALL GROUPS WERE SIGNIFICANTLY (P = 001) EFFECTIVE IN ALLEVIATING PAIN WITHIN 24 H
OF PULPECTOMY
17 18
4
19
bull IMMEDIATE POST OPERATIVE RADIOGRAPHIC ASSESSMENT REVEALED 68 (102150) ROOTS
WITH OPTIMAL OBTURATION AND 32 (48150) WITH OVERFILLINGUNDERFILLING MAXIMUM
NO OF OPTIMAL FILLINGS WERE OBSERVED IN GROUP1 (CA + E) (3333) FOLLOWED BY
GROUP 2 (CA) (2549) GROUP 3(SH + E) (2549) AND GROUP 4(SH) (1568)
bull CITRIC ACID GROUPS HAD MORE NUMBER OF OPTIMALLY FILLED ROOTS 588 (60102) THAN
NON CITRIC ACID GROUPS 412 (42102)
bull ENDOACTIVATOR CONTRIBUTED TO 18 OF OPTIMAL OBTURATION IRRESPECTIVE OF
CHELATING AGENT USED
20
21
bull MAXIMUM NO OF VOIDS AND VOID AREAS WERE IN NON CITRIC ACID GROUPS
(6419 amp 5384) COMPARED TO CITRIC ACID GROUPS (3580 amp 4615)
RESPECTIVELY
bull ANALYSIS OF ROOT 13RD REVEALED MAXIMUM NO OF VOID AREA IN APICAL
13RD (4755) FOLLOWED BY MIDDLE 13RD (3846) AND CORONAL 13RD
(1398)
bull LEAST NO OF VOIDS amp VOID AREA (1111 amp 1608) WERE OBSERVED WHEN
ENDOACTIVATOR ALONG WITH CHELATING AGENT WAS USED (GROUP 1)
HOWEVER THIS WAS STATISTICALLY INSIGNIFICANT
22
DISCUSSION
bull IN THE PRESENT STUDY 1 SODIUM HYPOCHLORITE WAS USED ALONG WITH 6 CITRIC ACID
(CHELATING AGENT) WHICH IS REPORTED TO BE AS EFFECTIVE AS 17 EDTA
bull CITRIC ACID (BIOLOGICAL ACID) IS FOUND TO BE BIOCOMPATIBLE AND LEAST IRRITATING TO
PERIAPICAL TISSUES THAN OTHER CHELATING AGENTS
bull USE OF SODIUM HYPOCHLORITE SOLUTION FOLLOWING CHELATING AGENT WAS AVOIDED AS IT
RAPIDLY PRODUCES SEVERE EROSION OF ROOT CANAL WALL DENTIN
bull TRADITIONAL APPROACH OF DELIVERING IRRIGANTS INTO THE ROOT CANAL SPACE USING
SYRINGES AND METAL NEEDLES HAS BEEN FOUND TO BE INEFFECTIVE ESPECIALLY IN THE AREAS OF
ANASTOMOSES BETWEEN CANALS AND APICAL 13RD OF ROOT CANAL
23
bull THEREFORE TO ACHIEVE BETTER CLEANING EFFICIENCY IRRIGANT ACTIVATION HAS BEEN
RECOMMENDED SONIC ACTIVATION HAS BEEN REPORTED TO RESULT IN BETTER ROOT CANAL
CLEANLINESS AS COMPARED TO NO ACTIVATION OF IRRIGANT
24
5
CONCLUSION
bull USE OF 6 CITRIC ACID DEFINITELY HELPED IN RAPID ELIMINATION OF PAIN RESOLUTION OF
PERI-RADICULAR RADIOLUCENCY BETTER OBTURATION QUALITY IN TERMS OF LESS VOIDS AND
VOID AREAS ALONG WITH MAXIMUM NO OF OPTIMAL OBTURATION UP TO APICAL AREA
bull 6 CITRIC ACID AND ENDOACTIVATOR IRRIGATION PROTOCOL PROVED TO BE THE BETTER
IRRIGATION PROTOCOL WHICH MAY CONTRIBUTE TO LONG TERM SUCCESS OF PRIMARY
TOOTH AND THE HEALTH OF UNDERLYING PERMANENT TOOTH
bull 6 CITRIC ACID ALONG WITH ENDOACTIVATOR MAY BE RECOMMENDED AS IRRIGATION
ADJUNCTS IN PULPECTOMY PROCEDURE OF PRIMARY TEETH
25
PROS AND CONS
PROS
bull PROPER EXPLANATION OF THE MATERIALS
USED
CONS
bull NO PREOPERATIVE AND POSTOPERATIVE
RADIOGRAPHS
26
REFERENCES
bull RAMACHANDRA JA NIHAL NK NAGARATHNA C VORA MS ROOT CANAL IRRIGANTS IN
PRIMARY TEETH WORLD J DENT 20156(3)229-234
bull MOHAMMADI Z JAFARZADEH H SHALAVI S KINOSHITA JI UNUSUAL ROOT CANAL
IRRIGATION SOLUTIONS J CONTEMP DENT PRACT 201718(5)415-420
bull ZEHNDER M ROOT CANAL IRRIGANTS J ENDOD 2006 32389- 98
bull SMITH JJ amp WAYMAN BE AN EVALUATION OF THE ANTIMICROBIAL EFFECTIVENESS OF
CITRIC ACID AS A ROOT CANAL IRRIGANT JOURNAL OF ENDODONTICS 1986 12(2) 54-58
bull TANNURE PN AZEVEDO CP BARCELOS R GLEISER R PRIMO LG LONG-TERM OUTCOMES OF
PRIMARY TOOTH PULPECTOMY WITH AND WITHOUT SMEAR LAYER REMOVAL A RANDOMIZED
SPLIT-MOUTH CLINICAL TRIAL PEDIATR DENT 201133316E20 27
bull CARON G NHAM K BRONNEC F MACHTOU P EFFECTIVENESS OF DIFFERENT FINAL IRRIGANT
ACTIVATION PROTOCOLS ON SMEAR LAYER REMOVAL IN CURVED CANALS J ENDOD
2010361361E6
bull COLL JA SADRIAN R PREDICTING PULPECTOMY SUCCESS AND ITS RELATIONSHIP TO
EXFOLIATION AND SUCCEDANEOUS DENTITION PEDIATR DENT 19961857E63
28
1
LOCAL
ANESTHESIA
DR MITAKSHARA NIRWAN
CONTENTS
Definition
Methods of inducing local anesthesia
Desirable properties
Electrophysiology of nerve conduction
Impulse propagation and spread
Mode and site of action of local anesthesia
Classification of local anesthetic according to biological site and mode of action
Dissociation of local anaesthetics
Mechanism of action of local anaethetics
Local anaesthetic agent
2
3
DEFINITION
Local anesthesia is defined as a loss of sensation in
a circumscribed area of the body caused by depression
of excitation in nerve endings or an inhibition of the
conduction process in peripheral nerves
An important feature of local anesthesia is that it produces
LOSS OF SENSATION WITHOUT INDUCING LOSS OF
CONSCIOUSNESS
4
METHODS OF INDUCING LOCAL
ANESTHESIA
Low temperature
Mechanical trauma
Anoxia
Neurolytic agents such as alcohol amp phenol
Chemical agents such as local anesthetics
PROPERTIES OF LOCAL
ANESTHESIA
It should not be irritating to tissue to which it is applied
It should not cause any permanent alteration of nerve structure
Its systemic toxicity should be low
Time of onset of anesthesia should be short
It should be effective regardless of whether it is injected into the tissue or applied locally to mucous membranes
The duration of action should be long enough to permit the completion of procedure
5 6
It should have the potency sufficient to give complete
anesthesia with out the use of harmful concentration solutions
It should be free from producing allergic reactions
It should be free in solution and relatively undergo
biotransformation in the body
It should be either sterile or be capable of being sterilized by
heat with out deterioration
2
ELETROPHYSIOLOGY OF
NERVE CONDUCTION
There is an electrical charge across the membrane
This is the membrane potential
The resting potential (when the cell is not firing) is a negative
electrical potential of -70mv that exists across the nerve
membrane produced by different concentrations of either side of
the membrane
The interior of nerve is NEGATIVE in relation to exterior
7 8
inside
outside
Resting potential of neuron = -70mV
+
-
+
-
+
-
+
-
+
-
SLOW DEPOLARIRIZATION
9
RAPID DEPOLARIZATION
The interior of nerve is POSITIVE in relation to exterior
REPOLARIZATION
10
bull Repolarization takes 07 msec
bull Depolarization takes 03 msec
SODIUM PUMP -
energy comes from the oxidative metabolism of ATP
bull The entire process require 1 msec
IMPULSE PROPOGATION
IMPULSE SPREAD
The propagated impulse travels along the nerve
membrane towards CNS The spread of impulse differs
in myelinated and unmyelinated nerve fibers
DEPOLARIZED SEGMENT ADJACENT RESTING AREA
MODE AND SITE OF ACTION OF LOCAL
ANESTHETICS
Local anesthetic agent interferes with excitation
process in a nerve membrane in one of the
following ways
Altering the basic resting potential of nerve
membrane
Altering the threshold potential
Decreasing the rate of depolarization
Prolonging the rate of repolarization
12
3
CLASSIFICATION OF LOCAL ANESTHETIC
SUBSTANCES ACCORDING TO
BIOLOGICAL SITE AND MODE OF ACTION
CLASS A
Agents acting at receptor site on external surface of nerve membrane
Chemical substance Biotoxins (eg tetrodotoxin and saxitoxin)
CLASS B
Agents acting on receptor sites on internal surface of nerve membrane
Chemical substance Quaternary ammonium analogues of lidocaine
scorpion venom 13
CLASS C Agents acting by receptor independent of
physiochemical mechanism
Chemical substance Benzocaine
CLASS D Agents acting by combination of receptors and
receptor independent mechanisms
Chemical substance most clinically useful anesthetic agents
(eg lidocaine mepivacaine prilocaine)
14
BASED ON THE SOURCE
NATUAL
SYNTHETIC
OTHERS
BASED ON MODE OF APPLICATION
bull INJECTABLE
bull TOPICAL
BASED ON DURATION OF ACTION
bull ULTRA SHORT
bull SHORT
bull MEDIEM
bull LONG
BASED ON ONSET OF ACTION SHORT
INTERMEDIATE
LONG
15
DISSOCIATION OF LOCAL
ANESTHETICS
Local anesthetics are available as salts (usually
hydrochlorides) for clinical use
The salts both water soluble and stable is dissolved in
either sterile water or saline
In this solution it exists simultaneously as unchanged
molecule (RN) also called base and positively charged
molecules (RNH+) called cations
RNH+ ==== RN+ H
+
16
The relative concentration of each ionic form in the solution varies
in the pH of the solution or surrounding tissue
In the presence of high concentration of hydrogen ion (low pH) the
equilibrium shifts to left and most of the anesthetic solution exists
in cationic form
RNH+ gt RN
+ + H
+
As hydrogen ion concentration decreases (higher pH) the
equilibrium shifts towards the free base form
RNH+ lt RN + H
+
17
The relative proportion of ionic form also depends on pKa or DISSOCIATION CONSTANT of the specific local anesthetic
The pKa is a measure of molecules affinity for H+
ions
When the pH of the solution has the same value as pKa of the local anesthetic exactly half the drug will exists in the RNH
+ form and
exactly half in RN form
The percentage of drug existing in either form can be determined by Henderson Hasselbalch equation
Log baseacid = pH - pKa
18
4
MECHANISM OF ACTION OF LOCAL
ANESTHETICS
The following sequence is proposed mechanism of action of LA
Displacement of calcium ions from the sodium channel receptor site
Binding of local anesthetic molecule to this receptor site
Blockade of sodium channel
19
Decrease in sodium conductance
Depression of rate of electrical depolarization
Failure to achieve the threshold potential level
Lack of development of propagated action potential
Conduction blockadehellip
20
21
Na + Na +
22
LOCAL ANESTHETIC AGENT
COMERCIALLY PREPARED LOCAL ANESTHESIA
CONSISTS OF
Local anesthetic agent (xylocaine lignocaine 2)
Vasoconstrictor (adrenaline 1 80000)
Reducing agent (sodium metabisulphite)
Preservative (methylparabencapryl
hydrocuprienotoxin)
Fungicide (thymol)
Vehicle (distillde waterNaCl)
LOCAL ANESTHETIC AGENT
The local anesthetics used in dentistry are divided
into two groups
ESTER GROUP
AMIDE GROUP
23 24
ESTER GROUP It is composed of the following
An aromatic lipophilic group
An intermediate chain containing
an ester linkage
A hydrophilic secondary or tertiary
amino group
AMIDE GROUP It is composed of the following
An aromatic lipophilic group
An intermediate chain containing
amide linkage
A hydrophilic secondary or tertiary
amino group
5
25
CLASSIFICATION OF LOCAL ANESTHETICS
ESTERS
Esters of benzoic acid
Butacaine
Cocaine
Benzocaine
Hexylcaine
Piperocaine
Tetracaine
Esters of Para-amino
benzoic acid
Chloroprocain
Procaine
Propoxycaine
26
AMIDES Articaine
Bupivacaine
Dibucaine
Etidocaine
Lidocaine
Mepivacaine
Prilocaine
Ropivacaine
QUINOLINE
Centbucridine
PHARMACOKINETICS OF LOCAL
ANESTHETICS UPTAKE
When injected into soft tissue most local anesthetics produce
dilation of vascular bed
Cocaine is the only local anesthetic that produces
vasoconstriction initially it produces vasodilation which is
followed by prolonged vasoconstriction
Vasodilation is due to increase in the rate of absorption of the
local anesthetic into the blood thus decreasing the duration of
pain control while increasing the anesthetic blood level and
potential for over dose 27
AMIDE LOCAL ANESTHETICS
The metabolism of amide local anesthetics is more
complicated then esters The primary site of
biotransformation of amide drugs is liver
Entire metabolic process occurs in the liver for lidocaine
articaine etidocaine and bupivacaine
Prilocaine undergoes more rapid biotransformation then the
other amides
28
REFERENCES
Handbook of local anesthesia ndash Stanley F Malamed ndash 6th
edition
Essentials of Local Anesthetic Pharmacology Daniel E
Becker Anesth Prog 2006 Fall 53(3) 98ndash109
WIKIPEDIEA
29
THANK YOU
30
1
Pharmacological Methods of Behavior
Management
DR MITAKSHARA NIRWAN
DEFINITIONS
bull Conscious Sedation ndash A minimally depressed level of consciousness that retains
the patients ability to independently and continuously maintain an airway and respond appropriately to physical stimulation or verbal command
(American Dental Association House Of Delegates 2000)
bull Deep Sedation ndash An induced state of depressed consciousness
accompanied by partial loss of protective reflexes including the inability to continuously maintain an airway independently and or to respond purposefully to physical stimulation or verbal command
bull General Anesthesia (G A) ndash An induced state of unconsciousness or complete loss of
protective reflexes including the inability to continually maintain an airway independently and respond purposefully to physical stimulation or verbal command
Conscious sedation
ADVANTAGES
Conscious
Protective reflexes active amp intact
Stable vital signs
Operating dentist may perform sedation
Minimum amount of equipment required
Prolong detainment in recovery room not required
Risk of complication very low
Excellent choice for poor ndash risk pt in dental office
Cost effective
General anesthesia
ADVANTAGES Not absolutely
essential May be the only
method Not necessary (no
pain reaction) Amnesia always
present
Conscious sedation
DISADVANTAGES
Pt cooperation is essential
Extremely difficult or mentally handicapped pt cannot always be managed
Use of local anesthesia is a must
Amnesia may or may not be present
General anesthesia DISADVANTAGES
Pt unconscious
Protective reflexes are depressed
Depressed
Advanced training required Dentist must not act also as anesthetist
Special equipment necessary
Detainment in recovery area necessary
High IOP amp postoperative complications
Not indicated in dental office
More expensive
Fundamental Concepts
bull Techniques that utilize drugs to induce co-operative yet conscious state in an otherwise uncooperative child ndash CONSCIOUS SEDATION
2
GOALS
1 To facilitate the provision of quality care
2 To minimize the extremes of disruptive behavior
3 To promote a positive psychologic response to treatment
4 To promote patient welfare amp safety
5 To return the patient to physiologic state
OBJECTIVES
1 The pt mood must be altered
2 The pt must remain conscious at all times
3 The pt must be cooperative
4 All protective reflexes must remain intact and active
5 Vital signs must remain stable and with in normal limits
6 The ptrsquos pain threshold should be elevated
7 Amnesia may be present
Indications
1 Preschool children
2 Lack of Psychological Emotional maturity
3 Lack of Cognitive Physical Medical disability
4 Fearful amp anxious pts
5 Pt who require extensive amp complicated dental care amp would require or benefit from prolonged visits
6 Acute pain
7 Traumatic injuries
Operating Facilities amp Equipment
A positive pressure O2 delivery system capable of administering gt than 90 O2 at 10L min flow for 60 min (650L ldquoErdquo cylinder)
OR
Self inflating bag valve mask device (15L min)
A functional suction apparatus with appropriate suction catheters
Monitoring equipment - PO BPC PC or Capno
Inhalation sedation unit
100 O2 amp never less than 25
A fail safe mechanism that is checked and calibrated annually
Must have appropriate scavenging system
Emergency drugs
Techniques of sedation
Routes for drug administration
bull Oral
bull Rectal
bull Inhalational
bull Transmucosal
ndash Sublingual
ndash Intranasal
bull Parenteral
ndash IM
ndash sub mucosal
ndash IV
3
Oral Sedation
Advantages
1 Almost universally accepted and the easiest method
2 Decreased incidence and severity of adverse reaction
3 Low cost
Disadvantages
1 Absorption is variable
2 Prolonged latent period(30 min)
3 Reversal of any unwanted effect is also difficult
4 Inability to readily lighten or deepen the level of sedation
5 Prolonged duration of action
Rectal Sedation
Advantages 1 Incidence and intensity of
drug related side effects is minimized
2 Drug absorption occurs from the large intestine directly into the circulation
3 The lack of a needle syringe or other equipment
4 The ease of administration
5 The low cost
Disadvantages
1 Inconvenience to the administrator amp pt
2 The variable absorption of drugs from the large intestine
3 The slow onset of action amp the relatively long duration of action
4 Inability to titrate the drug dosage
5 The inability to reverse the action of the drug the prolonged recovery
Intranasal sedation
Advantages
Rapid onset (10 ndash 15 min)
Simple amp relatively painless
Less pt cooperation is required
Absorbed directly into the C V S
Intranasal sedation
Disadvantages
1 Dependence on nasal mucous membrane
2 Shorter duration of action(40-60min)
3 Multiple dosage may be necessary
Drugs
Midazolam ndash 02mgkg
Sufentanil ndash 15 ndash 3 mcgkg
Ketamine ndash 3-6mg kg
Sublingual sedation
Advantages
1 Pt acceptance
2 Rapid onset
3 High bioavailability
Drugs
Oral Transmucosal Fentanyl Citrate (OTFC)
Intramuscular Sedation
Advantages
1 More rapid onset of action
2 Absorbed directly into the C V system
3 More reliable absorption of drug
4 Pt cooperation is not as essential
Disadvantages
1 Time factor ndash its 15 min latent period
2 Pt may not be willing to accept the injection
3 The prolonged duration of action(2-4 hrs more)
4 Possibility of injury to the tissues at the site of injection caused by either the drug or the needle
4
Sites of I M administration
1 Gluteal area
2 Vastus lateralis
3 Mid ndash deltoid area
Drugs
Diazepam
Midazolam
Hydroxyzine
Inhalation Sedation
Advantages
1 The onset of action is more rapid
2 Peak clinical level is achieved rapidly(3-5min) - permit titration
3 Administrator has complete control over the actions of the drug - safety feature
4 No significant over dosage
5 Flexible duration of action
6 Recovery time is rapid amp most complete
7 No injection is required
8 With N2O- O2 it is safe with very few side effects
Disadvantages
1 The initial cost of the equipment is high 2 The continuing cost of the gases is high 3 The equipment occupies considerable space 4 N2O is not a potent agent 5 A degree of cooperation is required from the pt 6 Chronic exposure to N2O is deleterious to the health of
dental personnel
Contraindications
1 Nasal obstruction 2 Cyanosis at rest 3 Poor cooperation 4 1st trimester of pregnancy 5 Fear of masks
I V Sedation
Advantages
1 The onset of action is the most rapid 2 The dosage may be titrated 3 Suitable level of sedation can be provided 4 The recovery period is shorter 5 Side effects are extremely uncommon 6 Control of salivary secretions is possible 7 The gag reflex is diminished 8 Effectively diminishes motor disturbances 9 Provides immediate access to CVS in emergency
Disadvantages
1 Venipuncture is necessary
2 Complication may rise at the site of the venipuncture
3 Monitoring must be more intensive
4 Recovery is not complete at the end of the procedure
5 Reversal of sedation is difficult
5
N2O-O2 (Relative Analgesia)
colorless sweet smelling gas
Pharmacokinetics
Absorption through pulmonary epithelium
It is approx 15 times as soluble as is nitrogen It replaces nitrogen in blood
It is carried in solution in plasma of the blood
It is not metabolized by the body
Elimination ndash majorndash lungs minor --- skin
perspiration urine and intestinal gas
Pharmacodynamics
Dose related
10 ndash 25 Lightheaded
Changes in visual amp auditory sensation
Tingling of hands amp feet
Suffusing warmth
Remote from the immediate environment
Reduced anxiety
25-50 max analgesic properties and aberration of vision hearing and proprioception mild drowsiness euphoria amnesia and increased sleepiness and dreams
35 conc will achieve maximum analgesia
bull CNS
ndash Cerebrum-primarily affected
ndash Safe but weak anesthetic agent
bull RESPIRATORY SYSTEM
ndash Increased Tidal and minute volumes
bull CARDIOVASCULAR SYSTEM
ndash 2 studies ndash decreased cardiac output
bull FETAL SYSTEMS
ndash Miscarriage in humans
bull OTHER SYSTEMS
ndash Depression of spinal reflexes increase muscle tone indicates stage of delirium
ndash Muscle rigidity-narcotics + nitrous oxide
ndash Nausea and vomitting - GIT
ndash HEMATOPOIESIS ----- prolonged exposure
Adverse reactions and toxicity
EMOTIONAL REACTIONS
DREAMS HALLUCINATIONS
No acute toxicity
Chronic toxicity ndash bone marrow
depression
PROCEDURE
Diffusion Hypoxia
Sevoflurane
A fluorinated derivative of isopropyl ether ndash synthesized in 1970
Potent anaesthetic agent with rapid uptake amp speedy recovery
Day-case surgery
Problem
Attaching vaporiser to any of the currently available machine
BENZODIAZEPINES
Diazepam 1961 lipid soluble
Uses-alcoholism epilepsy labor tetanus and cerebral palsy
- sedation and amnesia
- varieties of neurosis amp anxiety states
Pharmacokinetics
Orally Rectal IMIV or SC
Well absorbed through GIT
Excretion in urine
6
bull Pharmacodynamics
ndash Depress the brain stem reticular system and the limbic system thalamus and hypothalamus
ndash It is a centrally acting muscle relaxant Has anti-convulsant properties
Adverse reaction amp toxicity
ndash Confusion nausea headache increased appetite decreased salivation and jaundice Thrombophlebitis
ndash Rebound phenomenon
ndash Toxicity drowsiness confusion sleep and coma
Dosage Oral or Rectal ndash 02-05mgkg
Maximum single dose 10mg
IV- 025mgkg
Supplied Tablets 2 5 10 mg
Suspension ndash 5mg
Midazolam Water soluble ndash non-irritant
Oral IM IV
Metabolism- liver
Onset IV 3 -5mins
oral 20 ndash 30mins
Oral administration anxious patients requiring relatively short dental procedure
No rebound phenomenon
Better anxiolysis amp amnesia (retrograde amnesia)
Adverse effects Respiratory depression
dose dependant apnea
Dosage Oral ndash 025 to 1mgkg to maximum single dose 20mg
IM ndash 01 to 015mgkg to a maximum of 10mg
IV ndash slow IV
Supplied Syrup ndash 2mgml
Injectable ndash 1mgml amp 5mgml vials
Flumazenil specific benzodiazepines antagonist
selectively inhibits CNS effects
IV administration amp not recommended below 18yrs of age
02mg over 15 seconds after 45seconds 02mg then after 60seconds to maximum of 1mg
Sedative-Hypnotics
Barbiturates First truly effective drugs for the management of anxiety Generalized CNS depressants Produce dose dependent effects
Sedation ---- sleep ---- GA ---- coma
Suppress the CNS and result in sedation and amnesia Advantages
Rapid onset and short duration Disadvantages
no analgesic effect and possible hypotension Must be used with caution in trauma patients because they may cause
apnea and hypoventilation
DOSE Pentobarbital Sodium 100mg Secobarbital Sodium 100 to 200mg Children 30 to 100mg
bull Chloral Hydrates (Mickey Finn Knock out drops ) First synthesized in 1832 first member of the hypnotic group of drugs
Widely used as conscious sedation agent
Properties
Unpleasant taste
Nausea vomiting
Quite irritating to skin and to mucous membranes
GI irritation
Dosages Individualized for each patient 25 ndash 50mgkg
maximum of 1g
Supplied oral capsule ndash 500mg
oral solution ndash 250 amp 500mg5ml
Rectal suppositories ndash 324 amp 648mg
Narcotics
Do produce sedation amp euphoria greater in children
LA is required but dose should be decreased
Meperidine Synthetic opiate agonist
Very water soluble
Orally SC IM or IV
Peak effect by oral 1 hr amp lasts upto 4 hrs
Adverse reactions
-Seizures
-Extreme caution in hepatic or renal diseases or history of seizures
7
Dosage Oral SC or IM ndash 1to 22mgkg not to exceed 100 mg
Supplied Oral Tablets ndash 50 amp 100mg
Oral Syrup ndash 50mgml
Parental solution ndash 25 50 75 amp 100mgml
Fentanyl
Synthetic opiate narcotic analgesic
Very potent 01mg = 10mg Morophine75mg Meperidine
Pharmacokinetics
IV IM SM
Metabolized in liver Excreted in urine
Fentanyl Onset ndash 7 to 15mins
Duration ndash 1 to 2 hrs
Pharmacodynamics
Respiratory depression RR but returns to normal rapidly Tidal volume amp response to co2 depressed for extended period
Apnea
Less emetic than meperidine
NOT RECOMMENDED IN CHILDREN BELOW 2yrs
Dosage 0002 to 0004mgkg
Supplied 005mgml in 2 amp 5ml ampoules
Reversal drug Naloxone
Semisynthetic opiate antagonist
No agonist activity
Onset 2 to 5mins SC or IM amp 1 to 2mins IV
Reversal 45mins
Pt should be kept under continual surveillance
Adverse reaction nausea vomiting sweating hypotension hypertension ventricular tachycardia fibrillation
Dosage IV SC IM 001mgkg then 01mgkg every 2- 3mins maximum 2mg
Supplied 002 004 1mg solutions
Antihistamines
Hydroxyzine
Oral or IM
Effect ndash 15 ndash 30mins
Half-life ndash 3 hrs
Uses
To relieve anxiety
Used as an anti-histamine
Used to control nausea and vomiting including that associated with motion sickness and pregnancy
Adverse reaction dry mouth drowsiness hypersentivity
Dosage Oral ndash 1 to 2mgkg
IM ndash 11mgkg
Promethazine Oral or IM Onset 15 to 60mins Duration 4 to 6 hrs Uses
To prevent and treat nausea and vomiting associated with motion pregnancy or surgery
Produces sedation and reduce swelling pain and trismus
Lower seizure threshold Adverse reaction dry mouth blurred vision thickening of bronchial secretions Dosage OralIM ndash 05-11mgkg
maximum 25 mg
Diphenhydramine
Oral IM IV
Onset -1hr
Duration ndash 4 to 6 hr
Metabolized in liver
Adverse reaction disturbed coordination thickening of bronchial secretions
Dosage Oral IM IV ndash 1 to 15mgkg
maximum 50mg
Tranquilizers
Major tranquilizer antipsychotic produce calmness control symptoms of psychoses cause reversible extra pyramidal symptoms and do not tend to cause habituation
Minor tranquilizer antianxiety agents also cause calmness do not cause extrapyramidal symptoms Used in conditions like nervous tension and mild depression
8
Classification
Antipsychotics
Phenothiazine derivatives
Chlorpromazine promazine
Butryophenones
Haloperidol
Rauwolfia alkaloids
Reserpine
Antianxiety drugs
Propyl alcohol derivatives
Meprobamate
Benzodiazepine derivatives
Diazepam
Miscellaneous compounds
Hydroxyzine
Meprobamate
White crystalline powder slightly bitter in taste
Only administered orally
Peak blood concentration ----1 to 3hrs
10 ---------excreted unchanged Rest --- excreted as a oxidized derivative or as a glucoronide
Uses
To relieve day time anxiety
Induce sleep in insomniacs
To reduce anxiety associated with dental treatment
Anti-convulsant ndash petit mal epilepsy
Adverse reaction leucopenia acute non-thrombocytopenic purpura ecchymoses eosinophilia edema adenopathy
Dosage Childrengt 6yrs 100 to 200mg
Not recommended for children under 6yrs
Monitoring during sedation
1 Pulse
2 Blood pressure
3 ECG
4 Respiration
5 Temperature
Pulse
Manual Electronic
bull Radial Brachial
bull Facial labial
Blood pressure
ndash Stethoscope amp sphygmomanometer
ndash Automatic devices
ndash Direct cannulation of an artery ndash very accurate
Electrocardiograph
Heart rate rhythm myocardial function
9
Respiration
ndash Monitoring respiratory rate
ndash Observing the rise amp fall of the chest wall
ndash Observing the color of mucous membrane
ndash Observing the inflation amp deflation of the reservoir bag
Devices for monitoring respiration
1 The Precordial pretracheal stethoscope
2 The esophageal stethoscope
ndash Respiratory rate
ndash Heart rate
ndash Any abnormal sounds
Pulse Oximeter
ndash Oxygen saturation
ndash Heart rate
ndash Oxisensor site
ndash Fingers
ndash Toe
ndash Ear lobe
Mechanism
Oxygenated Hb ndash red light
Deoxygenated Hb- infrared light
Tissue pressure from arterial pulse (plethysmography)
Advantages
ndash Safe amp noninvasive
ndash Simple to use
ndash Information is rapidly available for clinical decision
ndash Indirectly indicates respiratory adequacy
Disadvantages
ndash Finger probes can get dislodged
ndash Emitted light source may cause burning
ndash Non reusable probes are expensive
ndash Does not directly determine airway patency
Capnography
1 The presence absence of air flow
2 Indicates depth amp adequacy of respiration
3 Continues analysis of the co2 content of the respired air ndash indicates respiratory adequacy
Temperature
ndash Disposable nondisposable thermometer
ndash Esophageal rectal temp probe
10
Discharge criteria
Cardiovascular function is satisfactory amp stable
Airway patency is uncompromised amp satisfactory
Pt is easily arousable amp protective reflexes intact
State of hydration is adequate
Pt can talk if applicable
Pt can sit unaided if applicable
Pt can ambulate with minimal assistance if applicable
Presedation level of responsiveness achieved
Responsible individual is available
1
PULP THERAPY OF VITAL TEETH
DR MITAKSHARA NIRWAN
Contents
Indirect pulp capping
Direct pulp capping
Medications amp materials used in pulp capping
Pulpotomy
MTA
Apexogenesis
INDIRECT PULP CAPPING
Pieter Van Forest - first to speak about root canal therapy
Glove designed instruments that could prepare a canal to a certain size and taper(1910)
Indirect pulp capping is defined as a procedure where in small amount of carious dentin is retained in
deep areas of cavity to avoid exposure of pulp followed by placement of a suitable medicament and
restorative material that seals off the carious dentin and encourages pulp recovery (Ingle)
A procedure in which only the gross caries is removed from the lesion and the cavity is sealed for a
time with a biocompatible material (McDonald)
Objective of indirect pulp capping
These were given by Eidelman in 1965
bull Arresting the carious process
bull Promoting dentin sclerosis
bull Stimulating formation of tertiary dentin
bull Remineralization of carious dentin
Layers of Carious Dentin Indications of Indirect Pulp Capping
History
Mild pain associated with eating
Negative history of spontaneous extreme pain
Clinical Examination
Deep carious lesion which are close tobut not involving the pulp in vital primary or young
permanent teeth
No mobility
Nominal pulp inflammationdefinite layer of affected dentin after removal of infected dentin
Radiographic examination
Normal lamina dura amp PDL space
No radiolucency around the apices
2
Contraindications of Indirect Pulp Capping
History
Sharp penetrating pulpalgia
Prolonged spontaneous pain especially at night
Clinical examination
Mobility of tooth
Discoloration of tooth
Negative reaction of electric pulp testing
Radiographic examination
Definite pulp exposure
Break in the lamina dura
Radiolucency around the apices
Widened PDL space
Treatment procedure
Sequelae of Indirect Pulp Capping Three distinct types of new dentin formation take place
1 Cellular fibrillar dentinmdashfirst 2 months
2 Globular dentinmdash3 months
3 Tubular dentin (uniform mineralized dentin)
bull 15th of reparative dentin formation begins in less than 30 days
bull After 3 months 01 mm is formed
DIRECT PULP CAPPING Defined by Kopel (1992) as the placement of a medicament or non medicated material on a pulp that
has been exposed in course of excavating the last portions of deep dentinal caries or as a result of
trauma
Objective
To create new dentin in the area of the exposure and subsequent healing of the pulp
Rationale
achieve a biologic closure of the exposure site by deposition of hard tissue barrier (dentin bridge)
between pulp tissue and capping material thus walling off the
INDICATIONS
Small mechanical exposure
Easily controlled haemorrhage
Bright red haemorrhage
True pinpoint exposure
CONTRAINDICATIONS
Severe toothache at night
Spontaneous pain
Tooth mobility
Radiographic appearance of pulp periradicular de- generation
Excess of hemorrhage at the time of exposure Serous exudate from the exposure
Externalinternal root resorption
Swellingfistula
Histological Changes after Pulp Capping
These were illustrated be Glass and Zander in 1949
After 24 hours Necrotic zone adjacent to calcium
hydroxide paste is separated from healthy pulp
tissue by a deep staining basophilic layer
After 7 days Increase in cellular and fibroblastic
activity
After 14 days Partly calcified fibrous tissue lined by
odontoblastic cells is seen below the calcium
proteinate zone disappearance of necrotic zone
After 28 days Zone of new dentin
3
Medications and Materials Used for Pulp Capping Calcium hydroxide
Corticosteroids amp antibiotics
Inert materials
Collagen fibers
4-META adhesive
Direct bonding
Isobutyl cyanoacrylate
Denatured albumin
Mineral trioxide aggregate
Laser
Bone morphogenic protein
PULPOTOMY
Finn (1995) defined it as the complete removal of the coronal portion of the dental pulp
followed by placement of a suitable dressing or medicament that will promote healing and
preserve vitality of the tooth
American Academy of Pediatric Dentistry (1998) defined pulpotomy as the amputation of
affected infected coronal portion of the dental pulp preserving the vitality and function of the
remaining part of radicular pulp
Objectives
bull Removal of inflamed and infected coronal pulp at the site of exposure thus preserving the vitality of the
radicular pulp and allowing it to heal
bull Maintain the tooth in the dental arch
Rationale
bull Radicular pulp is healthy and capable of healing after surgical amputation of the infected coronal pulp
bull Preserves vitality of the radicular pulp
bull Maintains tooth in a physiologic condition
Indications of Pulpotomy bull Mechanical pulp exposure in primary teeth
bull Teeth showing a large carious lesion but free of radicular pulpitis
bull History of only spontaneous pain
bull Hemorrhage from exposure sites bright red and can be controlled
bull Absence of abscess or fistula
bull No interradicular bone loss
bull No interradicular radiolucency
Contraindications of Pulpotomy bull Persistent toothache
bull Tenderness on percussion
bull Root resorption more than 13rd of root length
bull Large carious lesion with nonrestorable crown
bull Highly viscous sluggish hemorrhage from canal orifice which is uncontrollable
bull Medical contradictions like heart disease immuno compromised patient
bull Swelling or fistula
bull External or internal resorption
bull Pathological mobility
bull Calcification of pulp
Classification of pulpotomy
4
Formocresol Pulpotomy
Iby BUCKLEY in 1904
Sweet (1930) Formulated multi visit technique
Doyle (1962) Advocated 2 sitting procedure (complete devitalization)
Spedding (1965) Gave 5 minute protocol (partial devitali- zation)
Venham (1967) Proposed 15 seconds procedure
Current concept uses 4 minutes of application time
Composition of formocresol Buckleyrsquos Formula
bull Cresol ndash 35 percent
bull Glycerol ndash 15 percent
bull Formaldehyde ndash 19 percent
bull Water ndash 31 percent
Mechanism of Action
It prevents tissue autolysis by bonding to the proteins Bonding is of peptide groups of side chain amino acids and is a reversible process accomplished without
changing the basic structure of protein molecules
Histological Changes
bull Demonstrated by Mass and Zilbermann11 in 1933 and also by Massler and Mansokhani in 1959
bull Immediately the pulp becomes fibrous and acidophillic
bull Seven to fourteen days Three zones appear
a broad eosinophilic zone of fixation
b broad pale-staining zone of atrophy with poorcellular definition
c broad zone of inflammation extending apically into normal pulp tissue
bull One yearndash Progressive apical movement of these zones with only acidophillic zone left at the end of 1 year
Modified Formocresol Pulpotomy
Used by TRASK(1972)
The technique is identical to that described for primary teeth except that the formocresol pellet is
sealed permanently in the tooth
Two-visit Devitalization Pulpotomy
Indications
bull There is evidence of sluggish bleeding at the amputation site that is difficult to control
bull Pus in the chamber but none at the amputation site
bull There is thickening of the PDL
bull History of pain
Contraindications
bull Nonrestorable tooth
bull Tooth with necrotic pulp
5
Glutaraldehyde Pulpotomy
It was first suggested by S Gravenmade Introduced by Kopel in 1979
Mechanism of Action
bull Glutaraldehyde produces rapid surface fixation of the underlying pulpal tissue
bull A narrow zone of eosinophilic stained and compressed fixed tissue is found directly beneath the area of application which blends into vital normal appearing tissue apically
bull With time the glutaraldehyde fixed zone is replaced by macrophagic action with dense collagenous tissue thus the entire root canal tissue is vital
Cvekrsquos Pulpotomy
bull This is also called as calcium hydroxide pulpotomy or young permanent partial pulpotomy
bull This was proposed by Mejare and Cvek16 in 1978
bull Indicated in young permanent teeth where the pulp is exposed by mechanical or bacterial means and the
remaining radicular tissue is judged vital by clinical and radiographic criteria whereas the root closure is
notcomplete
MINERAL TRIOXIDE AGGREGATE (MTA) Torabinejad described the physical and chemical properties of MTA in 1995
It is ash colored powder made primarily of fine hydrophilic particles of
1 tricalcium aluminate
2 tricalcium silicate
3 silicate oxide
4 tricalcium oxide
5 bismuth dioxide
Hydration of the powder results in a colloidal gel composed of calcium oxide crystals in an amorphous
structure This gel solidifies into a hard structure in less than three hours
PROPERTIES OF MTA
It is biocompatible material and its sealing ability is better than that of amalgam or ZOE
Initial pH is 102 and set pH is 125
The setting time of cement is 4 hours
The compressive strength is 70 MPA which is comparable with that of IRM
Low cytotoxicity ndash It presents with minimal inflammation if extended beyond the apex
Mineral trioxide aggregate (MTA) has demonstrated the ability to induce hard-tissue formation in
pulpal tissues and it promotes rapid cell growth
APEXOGENESIS
It is defined as the treatment of a vital pulp by capping or pulpotomy in order to permit continued
growth of the root and closure of the open apex
Rationale
Maintenance of integrity of the radicular pulp tissue to allow for continued root growth
Indications
bull Indicated for traumatized or pulpally involved vital permanent tooth when root apex is incompletely formed
bull No history of spontaneous pain
bull No sensitivity on percussion
bull No hemorrhage
bull Normal radiographic appearance
Contraindications
bull Evidence that radicular pulp has undergone degenerative changes
bull Purulent drainage
bull History of prolonged pain bull Necrotic debris in canal
bull Periapical radiolucency
6
1
Gupta A Dhingra R Chaudhari P Gupta A
Department of Paedodontics and Preventive Dentistry Faculty of Dental Sciences SGT University Gurgaon Haryana India
Journal of Indian Society of Pedodontics and Preventive Dentistry
Volume 35 I Issue 3 I July-September 2017
A COMPARISION OF VARIOUS MINIMALLY
INVASIVE TECHNIQUES FOR THE REMOVAL
OF DENTAL FLUOROSIS STAINS IN
CHILDREN
DR MITAKSHARA NIRWAN
CONTENTS
bull Introduction
bull Aims
bull Materials and Methods
bull Results
bull Discussion
bull Conclusion
bull Critical analysis
bull References
INTRODUCTION
bull Dental fluorosis is a developmental disturbance of dental enamel caused by
successive exposure to high concentrations of fluoride during tooth
development
bull Various methods of therapy are advocated for the treatment of fluorosis -
stained teeth which range from invasive ceramic veneer bonding restorations
to abrasive chemical treatments
bull The combination of dental bleaching techniques and microabrasion appears
as an excellent conservative solution to reestablish health in fluorosis
affected teeth
AIMS
bull The aim of the study was to evaluate and compare the effectiveness of
minimally invasive techniques for the removal of dental fluorosis
stains in children in vivo
MATERIALS AND METHODS
Patients visiting the department of Pedodontics and Preventive dentistry
Faculty of Dental Sciences SGT University Gurgaon
bull Sample size 90 patients
bull Age group 10 -17 years
bull Caries cracks or periodontal
disease on anterior teeth
bull Abscess draining sinus
cellulitis
bull Non vital teeth
hypersensitive exposed
crevices
bull Orthodontic appliance
bull Past history of bleaching
bull At least two permanent
maxillary anterior teeth
bull TSIF of score 4
bull Free of systemic diseases
Inclusion criteria Exclusion criteria
2
Groups
Group A In office bleaching with 35 hydrogen peroxide( Pola Office
Bleaching kit) activated by light emitting diode (LED) bleaching unit
(35 HP)
Group B Enamel microabrasion (EM) (PREMA Enamel Microabrasion
System) followed by in-office bleaching with 44 carbamide peroxide
gel (EM)
Group C In-office bleaching with 5 sodium hypochlorite (5
NaOCl)
A baseline colour evaluation was done by taking digital photograph of
the maxillary anterior teeth
RESULTS
Group 1
Colour stability
Group 2 Group 3
Tooth sensitivity
Tooth sensitivity values were taken before the treatment
which was compared to immediate postoperative and follow
up visits It was checked using an electric pulp tester
maximum
moderate
least
immediately
group 2
group 1
group 3
1 month
group 2
group 1
group 3
3 month
group 2
group 1
group 3
Patient satisfaction score
Satisfaction was assessed on visual analog scale
Range 1 to 5
Groups percentage of patients
who were satisfied with
the treatment
Number of patients
who reported slight
reappearance of colour
Group 1
90
7
Group 2
83
8
Group 3
73
7
3
Number of Appointments
Groups One sitting Two sittings Three
sittings
Group 1
25
4
1
group 2
26
3
1
Group 3
30
0
0
DISCUSSION
bull Hydrogen peroxide is capable of penetrating the tooth osmosis and through porosities and cracks subsequently acting directly on the pigmented molecules
bull Gurgan et al investigated 3 different light systems and found out that diode laser system with gave best tooth whitening and least tooth sensitivity
bull In the EM group the surface reflects and refracts light from the surface in such way that mild imperfections in underlying enamel are camouflaged While the highly polished surface of enamel enhances the aesthetic appearance
bull Train et al and Loguercio et al also had the similar results in their studies with EM mild fluorosis showed best results moderate showed moderate results while it had little effect on severe fluorosis
bull NaOCl was only effective on mild stains while moderate and severe
stains could only be lightened to quite an extent but could not be
completely removed
bull When NaOCl comes in contact with hypomineralized and discoloured
enamel it degrades and removes the chromogenic organic material
located on the enamel surface
CONCLUSION
bull It was concluded that esthetic appearance of teeth mild fluorosis can
be achieved by bleaching and microabrasion But in cases of
moderate fluorosis a combination of any of theses modalities can be
used
bull As no special maintenance precautions are required these maybe be
considered as an interesting alternative to conventional operative
treatment
bull Focuses on only TSIF of 4
bull Electric pulp testing is not the
right method to check for
sensitivity
bull Tooth Sensitivity changes
from person to person
bull Food habits can cause
staining of the teeth
bull Minimally invasive
bull Cheaper to veneers
bull Minimal loss of tooth structure
bull 4 parameters checked for the success of treatment
bull Inclusion of specific score of fluorosis for comparing the results
bull Maximum 3 appointments needed
CRITICAL ANALYSIS
Pros Cons
REFERENCES
bull Gurgan S Cakir FY Yazici E Different light-activated in officebleaching
systems Lasers Med Sci 201025817-22
bull Train TE McWhorter AG Seale NSWilson CF Guo IY Examination of
esthetic improvement and surface alteration following microabrasion in
fluorotic human incisors in vivoPediatr dent 199618353-62
bull Loguercio AD Correia LD Zago C Tagliari D Neumann E Gomes OM et al
Clinical effectiveness of two microabrasion materials materials for the
removal of enamel flurosis stains Oper Dent 200732531-8
4
6
1
IMPACT OF 6 CITRIC ACID AND ENDOACTIVATOR AS IRRIGATION ADJUNCTS ON OBTURATION QUALITY AND PULPECTOMY OUTCOME IN
PRIMARY TEETH
NEETU JAIN SHALINI GARG ABHISHEK DHINDSA SAKSHI JOSHI HARJOY
KHATRIA
PEDIATRIC DENTAL JOURNAL 2019 29
1
DR MITAKSHARA NIRWAN
CONTENTS
bull INTRODUCTION
bull AIMS amp OBJECTIVES
bull CASE REPORT
bull RESULTS
bull DISCUSSION
bull CONCLUSION
bull PROS AND CONS
bull REFERENCES
2
INTRODUCTION
bull ENDODONTIC THERAPY IN PRIMARY TEETH INVOLVES DISINFECTION OF THE ROOT CANAL
SYSTEM AND ITS OBTURATION WITH RESORBABLE PASTE
bull THE CONTENTS OF ROOT CANAL ALONG WITH SMEAR LAYER ARE EXPECTED TO BE REMOVED
DURING THE BIOMECHANICAL PREPARATION
bull IN VITRO AND CLINICAL DOCUMENTS HAVE INDICATED THAT MECHANICAL PREPARATION OF
THE CANAL LEAVES LARGE PORTIONS OF THE CANAL WALLS UNDEBRIDED AND COMPLETE
REMOVAL OF THE BACTERIA BY THIS MECHANICAL PROCEDURE ALONE IS UNLIKELY TO BE SEEN
THEREFORE SOME FORM OF DISINFECTIONIRRIGATION IS MANDATORY TO KILL THE
MICROORGANISMS AND TO REMOVE THE RESIDUAL TISSUES
3
bull THE IDEAL REQUISITES OF A ROOT CANAL IRRIGANT AS GIVEN BY ZEHNDER ARE
1 BROAD ANTIMICROBIAL SPECTRUM
2 HIGH EFFICACY AGAINST ANAEROBIC AND FACULTATIVE MICROORGANISMS ORGANIZED
IN BIOFILMS
3 ABILITY TO DISSOLVE NECROTIC PULP TISSUE REMNANTS
4 ABILITY TO INACTIVATE ENDOTOXIN
5 ABILITY TO PREVENT THE FORMATION OF A SMEAR LAYER DURING INSTRUMENTATION OR
TO DISSOLVE THE LATTER ONCE IT HAS FORMED
6 SYSTEMICALLY NONTOXIC WHEN THEY COME IN CONTACT WITH VITAL TISSUES
NONCAUSTIC TO PERIODONTAL TISSUES AND WITH LITTLE POTENTIAL TO CAUSE AN
ANAPHYLACTIC REACTION
SINCE NO SINGLE IRRIGANT HAS THESE OPTIMAL PROPERTIES STUDIES HAVE REPORTED THE USE
OF TWO OR MORE SOLUTIONS IN A SPECIFIC SEQUENCE OR IN COMBINATIONS FOR BETTER
RESULTS 4
bull SEVERAL IRRIGATING SOLUTIONS ALONG WITH CHELATING AGENTS HAVE BEEN USED
DURING BIOMECHANICAL PREPARATION OF ROOT CANAL BOTH IN PRIMARY AND
PERMANENT TEETH
bull HOWEVER NONE OF THE AVAILABLE IRRIGATING SOLUTIONS HAS BEEN REGARDED CLEARLY
AS OPTIMAL SOLUTION BECAUSE OF THEIR LIMITED EFFECTIVENESS ESPECIALLY IN APICAL
13RD OF THE ROOT CANAL SYSTEM
bull TO OVERCOME SUCH LIMITATIONS USE OF ENDOACTIVATOR HAS BEEN PROPOSED AS AN
IRRIGATION FACILITATOR THAT IS BASED ON SONIC VIBRATION (UP TO 10000 CPM) WHICH
FACILITATES THE IRRIGANT PENETRATION AND ITS RENEWAL WITHIN THE CANAL
bull ACTIVATION SYSTEMS RESULTED IN BETTER REMOVAL OF THE SMEAR LAYER IN THE APICAL
THIRD OF ROOT CANALS IN COMPARISON TO CONVENTIONAL IRRIGATION
5
CITRIC ACID
bull CITRIC ACID IS A WEAK ORGANIC ACID WITH THE APPEARANCE OF WHITE CRYSTALLINE
POWDER AT ROOM TEMPERATURE
bull IT CAN EXIST EITHER IN WATER-FREE FORM (ANHYDROUS) OR MONOHYDRATE FORM THE
WATER-FREE FORM CRYSTALLIZES FROM THE HOT WATER WHEREAS THE MONOHYDRATE
FORMS FROM THE COLD WATER THE LATTER MAY BE CONVERTED TO ANHYDROUS FORM BY
HEATING MORE THAN 78degC
bull CITRIC ACID OCCURS NATURALLY IN THE BODY IN MITOCHONDRIA AND IS USED BY BLOOD
BANKS TO PREVENT COAGULATION OF TRANSFUSED BLOOD CITRIC ACID IS ALSO ESSENTIAL
TO HUMAN METABOLISM AND IS FOUND IN MANY FOODS
6
2
bull THE BIOLOGICAL EFFECTS OF CITRIC ACID ON THE PERIODONTAL STRUCTURE HAS BEEN
EXTENSIVELY STUDIED IN PERIODONTICS
bull NEUMAN AND NEWMAN SHOWED THAT CITRIC ACID IS THE MOST EFFECTIVE ACID IN
ALTERING THE SOLUBILITY OF HYDROXYAPATITE
bull YAMAGUCHI ET AL SHOWED THAT CITRIC ACID SOLUTION HAD ANTIBACTERIAL EFFECTS ON
ALL 12 ROOT CANAL BACTERIA TESTED
bull ARIAS-MOLIZ ET AL SHOWED THAT ETHYLENEDIAMINETETRAACETIC ACID (EDTA) HAS NO
BACTERICIDAL ACTIVITY EVEN AFTER 1 HOUR CONTACT
bull THIS ACID HAS THE ABILITY OF ROOT CANAL IRRIGATION AND ALSO SMEAR LAYER REMOVAL
DIFFERENT CONCENTRATIONS (1ndash50) HAVE BEEN PROPOSED GUTMANN ET AL CONCLUDED
THAT 10 CITRIC ACID IS BETTER THAN ULTRASOUND FOR SMEAR LAYER REMOVAL FROM THE
ROOT END CAVITIES
7
bull STUDIES HAVE SHOWN IRRIGATION WITH 6 CA FOR 15 OR 30 SECONDS IS QUITE
EFFECTIVE IN REMOVING ALL THE COMPONENTS OF THE SMEAR LAYER OF THE PRIMARY
TEETH WHEREAS PERITUBULAR DENTIN DESTRUCTION WAS OBSERVED WHEN HIGHER
CONCENTRATION OF CITRIC ACID WAS USED AS AN IRRIGATING SOLUTION
8
AIMS amp OBJECTIVES
bull THIS STUDY WAS AIMED TO EVALUATE THE CLINICAL AND RADIOGRAPHIC OUTCOME OF
PULPECTOMY ALONG WITH QUALITY OF OBTURATION USING 6 CITRIC ACID AND
ENDOACTIVATOR
9
CASE REPORT
bull 350 CHILDREN (3-9 YEARS) WITH CLINICAL SIGNS AND SYMPTOMS OF CHRONIC IRREVERSIBLE
PULPITIS IN DEEPLY CARIOUS TEETH WERE SCREENED DURING SCHOOL DENTAL HEALTH
PROGRAM FROM MAY 2014-JULY 2014
bull 123 CHILDREN REPORTED TO THE DEPARTMENT AND 67 CHILDREN WERE SELECTED BASED ON
INCLUSION AND EXCLUSION CRITERIA
RECRUITMENT OF PATIENTS
10
INCLUSION CRITERIA
bull HISTORY OF SPONTANEOUS PAIN AND UNCONTROLLED BLEEDING AFTER PULP AMPUTATION
EXCLUSION CRITERIA
bull EVIDENCE OF INTERNAL OR EXTERNAL (PHYSIOLOGICPATHOLOGIC) ROOT RESORPTION OF MORE THAN A THIRD OF ITS LENGTH
bull ROOT CANAL OBLITERATION OR ANATOMIC ANOMALIES
bull INADEQUATE BONE SUPPORT OR NON RESTORABLE TOOTH
bull ONCE PATIENTS ELIGIBILITY WAS CONFIRMED THE TREATMENT PROCEDURE WAS
EXPLAINED TO THE PARENTGUARDIAN AND INFORMED WRITTEN CONSENT WAS
OBTAINED FROM PARENTSGUARDIANS SHOWING WILLINGNESS FOR THEIR
CHILDRENS TREATMENT 11
PROCEDURE
bull PULPECTOMY WAS PERFORMED BY ONE OPERATOR OF PEDIATRIC DENTISTRY DEPARTMENT
USING A STANDARDIZED TREATMENT PROTOCOL FOR ALL THE PATIENTS
bull AFTER ADMINISTRATION OF LOCAL ANESTHESIA RUBBER DAM WAS APPLIED FOR ISOLATION
bull ACCESS CAVITY WAS PREPARED USING AIR-ROTOR HAND PIECE WITH 8 ROUND BUR AND
PULP TISSUE WAS EXTIRPATED WITH THE HELP OF SPOON EXCAVATOR
bull FURTHER THE NEGOTIATION OF THE CANALS WAS DONE WITH 10 K-FILE
bull A DIAGNOSTIC RADIOGRAPH WAS TAKEN FOR ROOT LENGTH DETERMINATION AND
WORKING LENGTH WAS KEPT 1 MM SHORT OF THE RADIOGRAPHICAL APEX
bull ALL ROOT CANALS WERE INSTRUMENTED MANUALLY USING K-FILES AND WERE IRRIGATED
WITH 10 ML 09 NORMAL SALINE AND 1 SODIUM HYPOCHLORITE AS STANDARDIZING
PROTOCOL FOR ROOT CANAL PREPARATION AND DISINFECTION
12
3
GROUP 1 (CA + E) - IRRIGATION WAS DONE
WITH 10 ML OF 6 CITRIC ACID (CITOCID AMMDENT)
AND IRRIGANTS WERE SONICALLY AGITATED WITH
ENDOACTIVATOR (DENTSPLY) FOR 30 S PER CANAL USING REDBLUE
ENDOACTIVATOR TIP
GROUP 2 (CA) - 10 ML OF 6 CITRIC ACID FOR 1 MIN USING
27 GAUZE IRRIGATING NEEDLE
GROUP 3(SH + E) - 10 ML OF 1 SODIUM HYPOCHLORITE
SOLUTION AND SONIC ACTIVATION WITH ENDOACTIVATOR
GROUP 4(SH) - 10 ML OF 1 SODIUM HYPOCHLORITE
SOLUTION USING IRRIGATING NEEDLE (CONTROL GROUP)
bull TEETH UNDERGOING PULPECTOMY WERE RANDOMLY ENROLLED BY CHIT METHOD INTO THREE
STUDY AND ONE CONTROL GROUP
13
bull IN CITRIC ACID GROUPS FINAL RINSE WITH NORMAL SALINE WAS DONE TO REMOVE THE
REMAINING CRYSTALS (CHELATES)
bull FOLLOWING BIOMECHANICAL PREPARATION THE ROOT CANALS WERE DRIED WITH STERILE
ABSORBENT PAPER POINTS AND OBTURATED WITH VITAPEX USING HAND HELD
LENTULOSPIRAL FINAL RESTORATIONS WERE DONE USING COMPOSITE RESIN
14
bull CLINICAL FOLLOW UP WAS DONE AT 24 H1 WEEK 1 MONTH 6 MONTH AND 12
MONTH TO CHECK PAIN PRESENCE AND PAIN FREQUENCY (ONCEMORE THAN ONCE)
SWELLING FISTULA SENSITIVITY TO PERCUSSION
bull RADIOGRAPHIC FOLLOW UP WAS DONE AT 6 MONTH AND 12 MONTH FOR ANY
DEVIATED ERUPTION OF SUCCEDANEOUS TEETH EXCESS FILING MATERIAL AND ITS
RESORPTION EXTERNALINTERNAL ROOT RESORBTION CALCIFIC METAMORPHOSIS
PRESENCE OF FURCATION RADIOLUCENCY
CLINICAL amp RADIOGRAPHIC FOLLOW UP
15
RADIOGRAPHIC ASSESSMENT OF OBTURATION QUALITY
bull POSTOPERATIVE RADIOGRAPHS WERE VISUALLY ASSESSED FOR QUALITY OF OBTURATION BY
TWO INDEPENDENT EXAMINERS (SG AD) WHO WERE BLINDED WITH REGARD TO
IRRIGATION PROTOCOL GROUP TO ENHANCE CALIBRATION EACH EXAMINER ASSESSED THE
RADIOGRAPH INDEPENDENTLY AND LATER REVIEWED TOGETHER FOR FINAL ASSESSMENT
INDIVIDUAL ROOT WAS TAKEN AS UNIT OF ANALYSIS FOR GRADE OF OBTU- RATION AND
SCORING CRITERIA WERE AS GIVEN BY COLL JA 1996
1 UNDER FILLED - FILLING MATERIAL ENDED 1 MM OR MORE SHORT OF THE APEX
2 OPTIMAL FILLING- FILLING MATERIAL APPEARED TO END AT THE RADIOGRAPHICAL APEX
3 OVERFILLED - FILLING MATERIAL EXTRUDED PAST THE RADIOGRAPHIC APEX
4 OPTIMALLY FILLED ROOTS WERE FURTHER ASSESSED FOR THE PRESENCE OF VOIDS AND VOID
AREA (ROOT CANAL SURFACE UNTOUCHED BY THE ROOT CANAL FILLING MATERIAL) IN THREE
VISUALLY DIVIDED SECTIONS OF THE ROOT IE CORONAL MIDDLE AND APICAL 13RD
16
RESULTS
bull OVERALL CLINICAL AND RADIOGRAPHIC SUCCESS RATE OVER A PERIOD OF ONE YEAR WAS
9886 amp 977 RESPECTIVELY
bull ALL GROUPS WERE SIGNIFICANTLY (P = 001) EFFECTIVE IN ALLEVIATING PAIN WITHIN 24 H
OF PULPECTOMY
17 18
4
19
bull IMMEDIATE POST OPERATIVE RADIOGRAPHIC ASSESSMENT REVEALED 68 (102150) ROOTS
WITH OPTIMAL OBTURATION AND 32 (48150) WITH OVERFILLINGUNDERFILLING MAXIMUM
NO OF OPTIMAL FILLINGS WERE OBSERVED IN GROUP1 (CA + E) (3333) FOLLOWED BY
GROUP 2 (CA) (2549) GROUP 3(SH + E) (2549) AND GROUP 4(SH) (1568)
bull CITRIC ACID GROUPS HAD MORE NUMBER OF OPTIMALLY FILLED ROOTS 588 (60102) THAN
NON CITRIC ACID GROUPS 412 (42102)
bull ENDOACTIVATOR CONTRIBUTED TO 18 OF OPTIMAL OBTURATION IRRESPECTIVE OF
CHELATING AGENT USED
20
21
bull MAXIMUM NO OF VOIDS AND VOID AREAS WERE IN NON CITRIC ACID GROUPS
(6419 amp 5384) COMPARED TO CITRIC ACID GROUPS (3580 amp 4615)
RESPECTIVELY
bull ANALYSIS OF ROOT 13RD REVEALED MAXIMUM NO OF VOID AREA IN APICAL
13RD (4755) FOLLOWED BY MIDDLE 13RD (3846) AND CORONAL 13RD
(1398)
bull LEAST NO OF VOIDS amp VOID AREA (1111 amp 1608) WERE OBSERVED WHEN
ENDOACTIVATOR ALONG WITH CHELATING AGENT WAS USED (GROUP 1)
HOWEVER THIS WAS STATISTICALLY INSIGNIFICANT
22
DISCUSSION
bull IN THE PRESENT STUDY 1 SODIUM HYPOCHLORITE WAS USED ALONG WITH 6 CITRIC ACID
(CHELATING AGENT) WHICH IS REPORTED TO BE AS EFFECTIVE AS 17 EDTA
bull CITRIC ACID (BIOLOGICAL ACID) IS FOUND TO BE BIOCOMPATIBLE AND LEAST IRRITATING TO
PERIAPICAL TISSUES THAN OTHER CHELATING AGENTS
bull USE OF SODIUM HYPOCHLORITE SOLUTION FOLLOWING CHELATING AGENT WAS AVOIDED AS IT
RAPIDLY PRODUCES SEVERE EROSION OF ROOT CANAL WALL DENTIN
bull TRADITIONAL APPROACH OF DELIVERING IRRIGANTS INTO THE ROOT CANAL SPACE USING
SYRINGES AND METAL NEEDLES HAS BEEN FOUND TO BE INEFFECTIVE ESPECIALLY IN THE AREAS OF
ANASTOMOSES BETWEEN CANALS AND APICAL 13RD OF ROOT CANAL
23
bull THEREFORE TO ACHIEVE BETTER CLEANING EFFICIENCY IRRIGANT ACTIVATION HAS BEEN
RECOMMENDED SONIC ACTIVATION HAS BEEN REPORTED TO RESULT IN BETTER ROOT CANAL
CLEANLINESS AS COMPARED TO NO ACTIVATION OF IRRIGANT
24
5
CONCLUSION
bull USE OF 6 CITRIC ACID DEFINITELY HELPED IN RAPID ELIMINATION OF PAIN RESOLUTION OF
PERI-RADICULAR RADIOLUCENCY BETTER OBTURATION QUALITY IN TERMS OF LESS VOIDS AND
VOID AREAS ALONG WITH MAXIMUM NO OF OPTIMAL OBTURATION UP TO APICAL AREA
bull 6 CITRIC ACID AND ENDOACTIVATOR IRRIGATION PROTOCOL PROVED TO BE THE BETTER
IRRIGATION PROTOCOL WHICH MAY CONTRIBUTE TO LONG TERM SUCCESS OF PRIMARY
TOOTH AND THE HEALTH OF UNDERLYING PERMANENT TOOTH
bull 6 CITRIC ACID ALONG WITH ENDOACTIVATOR MAY BE RECOMMENDED AS IRRIGATION
ADJUNCTS IN PULPECTOMY PROCEDURE OF PRIMARY TEETH
25
PROS AND CONS
PROS
bull PROPER EXPLANATION OF THE MATERIALS
USED
CONS
bull NO PREOPERATIVE AND POSTOPERATIVE
RADIOGRAPHS
26
REFERENCES
bull RAMACHANDRA JA NIHAL NK NAGARATHNA C VORA MS ROOT CANAL IRRIGANTS IN
PRIMARY TEETH WORLD J DENT 20156(3)229-234
bull MOHAMMADI Z JAFARZADEH H SHALAVI S KINOSHITA JI UNUSUAL ROOT CANAL
IRRIGATION SOLUTIONS J CONTEMP DENT PRACT 201718(5)415-420
bull ZEHNDER M ROOT CANAL IRRIGANTS J ENDOD 2006 32389- 98
bull SMITH JJ amp WAYMAN BE AN EVALUATION OF THE ANTIMICROBIAL EFFECTIVENESS OF
CITRIC ACID AS A ROOT CANAL IRRIGANT JOURNAL OF ENDODONTICS 1986 12(2) 54-58
bull TANNURE PN AZEVEDO CP BARCELOS R GLEISER R PRIMO LG LONG-TERM OUTCOMES OF
PRIMARY TOOTH PULPECTOMY WITH AND WITHOUT SMEAR LAYER REMOVAL A RANDOMIZED
SPLIT-MOUTH CLINICAL TRIAL PEDIATR DENT 201133316E20 27
bull CARON G NHAM K BRONNEC F MACHTOU P EFFECTIVENESS OF DIFFERENT FINAL IRRIGANT
ACTIVATION PROTOCOLS ON SMEAR LAYER REMOVAL IN CURVED CANALS J ENDOD
2010361361E6
bull COLL JA SADRIAN R PREDICTING PULPECTOMY SUCCESS AND ITS RELATIONSHIP TO
EXFOLIATION AND SUCCEDANEOUS DENTITION PEDIATR DENT 19961857E63
28
1
LOCAL
ANESTHESIA
DR MITAKSHARA NIRWAN
CONTENTS
Definition
Methods of inducing local anesthesia
Desirable properties
Electrophysiology of nerve conduction
Impulse propagation and spread
Mode and site of action of local anesthesia
Classification of local anesthetic according to biological site and mode of action
Dissociation of local anaesthetics
Mechanism of action of local anaethetics
Local anaesthetic agent
2
3
DEFINITION
Local anesthesia is defined as a loss of sensation in
a circumscribed area of the body caused by depression
of excitation in nerve endings or an inhibition of the
conduction process in peripheral nerves
An important feature of local anesthesia is that it produces
LOSS OF SENSATION WITHOUT INDUCING LOSS OF
CONSCIOUSNESS
4
METHODS OF INDUCING LOCAL
ANESTHESIA
Low temperature
Mechanical trauma
Anoxia
Neurolytic agents such as alcohol amp phenol
Chemical agents such as local anesthetics
PROPERTIES OF LOCAL
ANESTHESIA
It should not be irritating to tissue to which it is applied
It should not cause any permanent alteration of nerve structure
Its systemic toxicity should be low
Time of onset of anesthesia should be short
It should be effective regardless of whether it is injected into the tissue or applied locally to mucous membranes
The duration of action should be long enough to permit the completion of procedure
5 6
It should have the potency sufficient to give complete
anesthesia with out the use of harmful concentration solutions
It should be free from producing allergic reactions
It should be free in solution and relatively undergo
biotransformation in the body
It should be either sterile or be capable of being sterilized by
heat with out deterioration
2
ELETROPHYSIOLOGY OF
NERVE CONDUCTION
There is an electrical charge across the membrane
This is the membrane potential
The resting potential (when the cell is not firing) is a negative
electrical potential of -70mv that exists across the nerve
membrane produced by different concentrations of either side of
the membrane
The interior of nerve is NEGATIVE in relation to exterior
7 8
inside
outside
Resting potential of neuron = -70mV
+
-
+
-
+
-
+
-
+
-
SLOW DEPOLARIRIZATION
9
RAPID DEPOLARIZATION
The interior of nerve is POSITIVE in relation to exterior
REPOLARIZATION
10
bull Repolarization takes 07 msec
bull Depolarization takes 03 msec
SODIUM PUMP -
energy comes from the oxidative metabolism of ATP
bull The entire process require 1 msec
IMPULSE PROPOGATION
IMPULSE SPREAD
The propagated impulse travels along the nerve
membrane towards CNS The spread of impulse differs
in myelinated and unmyelinated nerve fibers
DEPOLARIZED SEGMENT ADJACENT RESTING AREA
MODE AND SITE OF ACTION OF LOCAL
ANESTHETICS
Local anesthetic agent interferes with excitation
process in a nerve membrane in one of the
following ways
Altering the basic resting potential of nerve
membrane
Altering the threshold potential
Decreasing the rate of depolarization
Prolonging the rate of repolarization
12
3
CLASSIFICATION OF LOCAL ANESTHETIC
SUBSTANCES ACCORDING TO
BIOLOGICAL SITE AND MODE OF ACTION
CLASS A
Agents acting at receptor site on external surface of nerve membrane
Chemical substance Biotoxins (eg tetrodotoxin and saxitoxin)
CLASS B
Agents acting on receptor sites on internal surface of nerve membrane
Chemical substance Quaternary ammonium analogues of lidocaine
scorpion venom 13
CLASS C Agents acting by receptor independent of
physiochemical mechanism
Chemical substance Benzocaine
CLASS D Agents acting by combination of receptors and
receptor independent mechanisms
Chemical substance most clinically useful anesthetic agents
(eg lidocaine mepivacaine prilocaine)
14
BASED ON THE SOURCE
NATUAL
SYNTHETIC
OTHERS
BASED ON MODE OF APPLICATION
bull INJECTABLE
bull TOPICAL
BASED ON DURATION OF ACTION
bull ULTRA SHORT
bull SHORT
bull MEDIEM
bull LONG
BASED ON ONSET OF ACTION SHORT
INTERMEDIATE
LONG
15
DISSOCIATION OF LOCAL
ANESTHETICS
Local anesthetics are available as salts (usually
hydrochlorides) for clinical use
The salts both water soluble and stable is dissolved in
either sterile water or saline
In this solution it exists simultaneously as unchanged
molecule (RN) also called base and positively charged
molecules (RNH+) called cations
RNH+ ==== RN+ H
+
16
The relative concentration of each ionic form in the solution varies
in the pH of the solution or surrounding tissue
In the presence of high concentration of hydrogen ion (low pH) the
equilibrium shifts to left and most of the anesthetic solution exists
in cationic form
RNH+ gt RN
+ + H
+
As hydrogen ion concentration decreases (higher pH) the
equilibrium shifts towards the free base form
RNH+ lt RN + H
+
17
The relative proportion of ionic form also depends on pKa or DISSOCIATION CONSTANT of the specific local anesthetic
The pKa is a measure of molecules affinity for H+
ions
When the pH of the solution has the same value as pKa of the local anesthetic exactly half the drug will exists in the RNH
+ form and
exactly half in RN form
The percentage of drug existing in either form can be determined by Henderson Hasselbalch equation
Log baseacid = pH - pKa
18
4
MECHANISM OF ACTION OF LOCAL
ANESTHETICS
The following sequence is proposed mechanism of action of LA
Displacement of calcium ions from the sodium channel receptor site
Binding of local anesthetic molecule to this receptor site
Blockade of sodium channel
19
Decrease in sodium conductance
Depression of rate of electrical depolarization
Failure to achieve the threshold potential level
Lack of development of propagated action potential
Conduction blockadehellip
20
21
Na + Na +
22
LOCAL ANESTHETIC AGENT
COMERCIALLY PREPARED LOCAL ANESTHESIA
CONSISTS OF
Local anesthetic agent (xylocaine lignocaine 2)
Vasoconstrictor (adrenaline 1 80000)
Reducing agent (sodium metabisulphite)
Preservative (methylparabencapryl
hydrocuprienotoxin)
Fungicide (thymol)
Vehicle (distillde waterNaCl)
LOCAL ANESTHETIC AGENT
The local anesthetics used in dentistry are divided
into two groups
ESTER GROUP
AMIDE GROUP
23 24
ESTER GROUP It is composed of the following
An aromatic lipophilic group
An intermediate chain containing
an ester linkage
A hydrophilic secondary or tertiary
amino group
AMIDE GROUP It is composed of the following
An aromatic lipophilic group
An intermediate chain containing
amide linkage
A hydrophilic secondary or tertiary
amino group
5
25
CLASSIFICATION OF LOCAL ANESTHETICS
ESTERS
Esters of benzoic acid
Butacaine
Cocaine
Benzocaine
Hexylcaine
Piperocaine
Tetracaine
Esters of Para-amino
benzoic acid
Chloroprocain
Procaine
Propoxycaine
26
AMIDES Articaine
Bupivacaine
Dibucaine
Etidocaine
Lidocaine
Mepivacaine
Prilocaine
Ropivacaine
QUINOLINE
Centbucridine
PHARMACOKINETICS OF LOCAL
ANESTHETICS UPTAKE
When injected into soft tissue most local anesthetics produce
dilation of vascular bed
Cocaine is the only local anesthetic that produces
vasoconstriction initially it produces vasodilation which is
followed by prolonged vasoconstriction
Vasodilation is due to increase in the rate of absorption of the
local anesthetic into the blood thus decreasing the duration of
pain control while increasing the anesthetic blood level and
potential for over dose 27
AMIDE LOCAL ANESTHETICS
The metabolism of amide local anesthetics is more
complicated then esters The primary site of
biotransformation of amide drugs is liver
Entire metabolic process occurs in the liver for lidocaine
articaine etidocaine and bupivacaine
Prilocaine undergoes more rapid biotransformation then the
other amides
28
REFERENCES
Handbook of local anesthesia ndash Stanley F Malamed ndash 6th
edition
Essentials of Local Anesthetic Pharmacology Daniel E
Becker Anesth Prog 2006 Fall 53(3) 98ndash109
WIKIPEDIEA
29
THANK YOU
30
1
Pharmacological Methods of Behavior
Management
DR MITAKSHARA NIRWAN
DEFINITIONS
bull Conscious Sedation ndash A minimally depressed level of consciousness that retains
the patients ability to independently and continuously maintain an airway and respond appropriately to physical stimulation or verbal command
(American Dental Association House Of Delegates 2000)
bull Deep Sedation ndash An induced state of depressed consciousness
accompanied by partial loss of protective reflexes including the inability to continuously maintain an airway independently and or to respond purposefully to physical stimulation or verbal command
bull General Anesthesia (G A) ndash An induced state of unconsciousness or complete loss of
protective reflexes including the inability to continually maintain an airway independently and respond purposefully to physical stimulation or verbal command
Conscious sedation
ADVANTAGES
Conscious
Protective reflexes active amp intact
Stable vital signs
Operating dentist may perform sedation
Minimum amount of equipment required
Prolong detainment in recovery room not required
Risk of complication very low
Excellent choice for poor ndash risk pt in dental office
Cost effective
General anesthesia
ADVANTAGES Not absolutely
essential May be the only
method Not necessary (no
pain reaction) Amnesia always
present
Conscious sedation
DISADVANTAGES
Pt cooperation is essential
Extremely difficult or mentally handicapped pt cannot always be managed
Use of local anesthesia is a must
Amnesia may or may not be present
General anesthesia DISADVANTAGES
Pt unconscious
Protective reflexes are depressed
Depressed
Advanced training required Dentist must not act also as anesthetist
Special equipment necessary
Detainment in recovery area necessary
High IOP amp postoperative complications
Not indicated in dental office
More expensive
Fundamental Concepts
bull Techniques that utilize drugs to induce co-operative yet conscious state in an otherwise uncooperative child ndash CONSCIOUS SEDATION
2
GOALS
1 To facilitate the provision of quality care
2 To minimize the extremes of disruptive behavior
3 To promote a positive psychologic response to treatment
4 To promote patient welfare amp safety
5 To return the patient to physiologic state
OBJECTIVES
1 The pt mood must be altered
2 The pt must remain conscious at all times
3 The pt must be cooperative
4 All protective reflexes must remain intact and active
5 Vital signs must remain stable and with in normal limits
6 The ptrsquos pain threshold should be elevated
7 Amnesia may be present
Indications
1 Preschool children
2 Lack of Psychological Emotional maturity
3 Lack of Cognitive Physical Medical disability
4 Fearful amp anxious pts
5 Pt who require extensive amp complicated dental care amp would require or benefit from prolonged visits
6 Acute pain
7 Traumatic injuries
Operating Facilities amp Equipment
A positive pressure O2 delivery system capable of administering gt than 90 O2 at 10L min flow for 60 min (650L ldquoErdquo cylinder)
OR
Self inflating bag valve mask device (15L min)
A functional suction apparatus with appropriate suction catheters
Monitoring equipment - PO BPC PC or Capno
Inhalation sedation unit
100 O2 amp never less than 25
A fail safe mechanism that is checked and calibrated annually
Must have appropriate scavenging system
Emergency drugs
Techniques of sedation
Routes for drug administration
bull Oral
bull Rectal
bull Inhalational
bull Transmucosal
ndash Sublingual
ndash Intranasal
bull Parenteral
ndash IM
ndash sub mucosal
ndash IV
3
Oral Sedation
Advantages
1 Almost universally accepted and the easiest method
2 Decreased incidence and severity of adverse reaction
3 Low cost
Disadvantages
1 Absorption is variable
2 Prolonged latent period(30 min)
3 Reversal of any unwanted effect is also difficult
4 Inability to readily lighten or deepen the level of sedation
5 Prolonged duration of action
Rectal Sedation
Advantages 1 Incidence and intensity of
drug related side effects is minimized
2 Drug absorption occurs from the large intestine directly into the circulation
3 The lack of a needle syringe or other equipment
4 The ease of administration
5 The low cost
Disadvantages
1 Inconvenience to the administrator amp pt
2 The variable absorption of drugs from the large intestine
3 The slow onset of action amp the relatively long duration of action
4 Inability to titrate the drug dosage
5 The inability to reverse the action of the drug the prolonged recovery
Intranasal sedation
Advantages
Rapid onset (10 ndash 15 min)
Simple amp relatively painless
Less pt cooperation is required
Absorbed directly into the C V S
Intranasal sedation
Disadvantages
1 Dependence on nasal mucous membrane
2 Shorter duration of action(40-60min)
3 Multiple dosage may be necessary
Drugs
Midazolam ndash 02mgkg
Sufentanil ndash 15 ndash 3 mcgkg
Ketamine ndash 3-6mg kg
Sublingual sedation
Advantages
1 Pt acceptance
2 Rapid onset
3 High bioavailability
Drugs
Oral Transmucosal Fentanyl Citrate (OTFC)
Intramuscular Sedation
Advantages
1 More rapid onset of action
2 Absorbed directly into the C V system
3 More reliable absorption of drug
4 Pt cooperation is not as essential
Disadvantages
1 Time factor ndash its 15 min latent period
2 Pt may not be willing to accept the injection
3 The prolonged duration of action(2-4 hrs more)
4 Possibility of injury to the tissues at the site of injection caused by either the drug or the needle
4
Sites of I M administration
1 Gluteal area
2 Vastus lateralis
3 Mid ndash deltoid area
Drugs
Diazepam
Midazolam
Hydroxyzine
Inhalation Sedation
Advantages
1 The onset of action is more rapid
2 Peak clinical level is achieved rapidly(3-5min) - permit titration
3 Administrator has complete control over the actions of the drug - safety feature
4 No significant over dosage
5 Flexible duration of action
6 Recovery time is rapid amp most complete
7 No injection is required
8 With N2O- O2 it is safe with very few side effects
Disadvantages
1 The initial cost of the equipment is high 2 The continuing cost of the gases is high 3 The equipment occupies considerable space 4 N2O is not a potent agent 5 A degree of cooperation is required from the pt 6 Chronic exposure to N2O is deleterious to the health of
dental personnel
Contraindications
1 Nasal obstruction 2 Cyanosis at rest 3 Poor cooperation 4 1st trimester of pregnancy 5 Fear of masks
I V Sedation
Advantages
1 The onset of action is the most rapid 2 The dosage may be titrated 3 Suitable level of sedation can be provided 4 The recovery period is shorter 5 Side effects are extremely uncommon 6 Control of salivary secretions is possible 7 The gag reflex is diminished 8 Effectively diminishes motor disturbances 9 Provides immediate access to CVS in emergency
Disadvantages
1 Venipuncture is necessary
2 Complication may rise at the site of the venipuncture
3 Monitoring must be more intensive
4 Recovery is not complete at the end of the procedure
5 Reversal of sedation is difficult
5
N2O-O2 (Relative Analgesia)
colorless sweet smelling gas
Pharmacokinetics
Absorption through pulmonary epithelium
It is approx 15 times as soluble as is nitrogen It replaces nitrogen in blood
It is carried in solution in plasma of the blood
It is not metabolized by the body
Elimination ndash majorndash lungs minor --- skin
perspiration urine and intestinal gas
Pharmacodynamics
Dose related
10 ndash 25 Lightheaded
Changes in visual amp auditory sensation
Tingling of hands amp feet
Suffusing warmth
Remote from the immediate environment
Reduced anxiety
25-50 max analgesic properties and aberration of vision hearing and proprioception mild drowsiness euphoria amnesia and increased sleepiness and dreams
35 conc will achieve maximum analgesia
bull CNS
ndash Cerebrum-primarily affected
ndash Safe but weak anesthetic agent
bull RESPIRATORY SYSTEM
ndash Increased Tidal and minute volumes
bull CARDIOVASCULAR SYSTEM
ndash 2 studies ndash decreased cardiac output
bull FETAL SYSTEMS
ndash Miscarriage in humans
bull OTHER SYSTEMS
ndash Depression of spinal reflexes increase muscle tone indicates stage of delirium
ndash Muscle rigidity-narcotics + nitrous oxide
ndash Nausea and vomitting - GIT
ndash HEMATOPOIESIS ----- prolonged exposure
Adverse reactions and toxicity
EMOTIONAL REACTIONS
DREAMS HALLUCINATIONS
No acute toxicity
Chronic toxicity ndash bone marrow
depression
PROCEDURE
Diffusion Hypoxia
Sevoflurane
A fluorinated derivative of isopropyl ether ndash synthesized in 1970
Potent anaesthetic agent with rapid uptake amp speedy recovery
Day-case surgery
Problem
Attaching vaporiser to any of the currently available machine
BENZODIAZEPINES
Diazepam 1961 lipid soluble
Uses-alcoholism epilepsy labor tetanus and cerebral palsy
- sedation and amnesia
- varieties of neurosis amp anxiety states
Pharmacokinetics
Orally Rectal IMIV or SC
Well absorbed through GIT
Excretion in urine
6
bull Pharmacodynamics
ndash Depress the brain stem reticular system and the limbic system thalamus and hypothalamus
ndash It is a centrally acting muscle relaxant Has anti-convulsant properties
Adverse reaction amp toxicity
ndash Confusion nausea headache increased appetite decreased salivation and jaundice Thrombophlebitis
ndash Rebound phenomenon
ndash Toxicity drowsiness confusion sleep and coma
Dosage Oral or Rectal ndash 02-05mgkg
Maximum single dose 10mg
IV- 025mgkg
Supplied Tablets 2 5 10 mg
Suspension ndash 5mg
Midazolam Water soluble ndash non-irritant
Oral IM IV
Metabolism- liver
Onset IV 3 -5mins
oral 20 ndash 30mins
Oral administration anxious patients requiring relatively short dental procedure
No rebound phenomenon
Better anxiolysis amp amnesia (retrograde amnesia)
Adverse effects Respiratory depression
dose dependant apnea
Dosage Oral ndash 025 to 1mgkg to maximum single dose 20mg
IM ndash 01 to 015mgkg to a maximum of 10mg
IV ndash slow IV
Supplied Syrup ndash 2mgml
Injectable ndash 1mgml amp 5mgml vials
Flumazenil specific benzodiazepines antagonist
selectively inhibits CNS effects
IV administration amp not recommended below 18yrs of age
02mg over 15 seconds after 45seconds 02mg then after 60seconds to maximum of 1mg
Sedative-Hypnotics
Barbiturates First truly effective drugs for the management of anxiety Generalized CNS depressants Produce dose dependent effects
Sedation ---- sleep ---- GA ---- coma
Suppress the CNS and result in sedation and amnesia Advantages
Rapid onset and short duration Disadvantages
no analgesic effect and possible hypotension Must be used with caution in trauma patients because they may cause
apnea and hypoventilation
DOSE Pentobarbital Sodium 100mg Secobarbital Sodium 100 to 200mg Children 30 to 100mg
bull Chloral Hydrates (Mickey Finn Knock out drops ) First synthesized in 1832 first member of the hypnotic group of drugs
Widely used as conscious sedation agent
Properties
Unpleasant taste
Nausea vomiting
Quite irritating to skin and to mucous membranes
GI irritation
Dosages Individualized for each patient 25 ndash 50mgkg
maximum of 1g
Supplied oral capsule ndash 500mg
oral solution ndash 250 amp 500mg5ml
Rectal suppositories ndash 324 amp 648mg
Narcotics
Do produce sedation amp euphoria greater in children
LA is required but dose should be decreased
Meperidine Synthetic opiate agonist
Very water soluble
Orally SC IM or IV
Peak effect by oral 1 hr amp lasts upto 4 hrs
Adverse reactions
-Seizures
-Extreme caution in hepatic or renal diseases or history of seizures
7
Dosage Oral SC or IM ndash 1to 22mgkg not to exceed 100 mg
Supplied Oral Tablets ndash 50 amp 100mg
Oral Syrup ndash 50mgml
Parental solution ndash 25 50 75 amp 100mgml
Fentanyl
Synthetic opiate narcotic analgesic
Very potent 01mg = 10mg Morophine75mg Meperidine
Pharmacokinetics
IV IM SM
Metabolized in liver Excreted in urine
Fentanyl Onset ndash 7 to 15mins
Duration ndash 1 to 2 hrs
Pharmacodynamics
Respiratory depression RR but returns to normal rapidly Tidal volume amp response to co2 depressed for extended period
Apnea
Less emetic than meperidine
NOT RECOMMENDED IN CHILDREN BELOW 2yrs
Dosage 0002 to 0004mgkg
Supplied 005mgml in 2 amp 5ml ampoules
Reversal drug Naloxone
Semisynthetic opiate antagonist
No agonist activity
Onset 2 to 5mins SC or IM amp 1 to 2mins IV
Reversal 45mins
Pt should be kept under continual surveillance
Adverse reaction nausea vomiting sweating hypotension hypertension ventricular tachycardia fibrillation
Dosage IV SC IM 001mgkg then 01mgkg every 2- 3mins maximum 2mg
Supplied 002 004 1mg solutions
Antihistamines
Hydroxyzine
Oral or IM
Effect ndash 15 ndash 30mins
Half-life ndash 3 hrs
Uses
To relieve anxiety
Used as an anti-histamine
Used to control nausea and vomiting including that associated with motion sickness and pregnancy
Adverse reaction dry mouth drowsiness hypersentivity
Dosage Oral ndash 1 to 2mgkg
IM ndash 11mgkg
Promethazine Oral or IM Onset 15 to 60mins Duration 4 to 6 hrs Uses
To prevent and treat nausea and vomiting associated with motion pregnancy or surgery
Produces sedation and reduce swelling pain and trismus
Lower seizure threshold Adverse reaction dry mouth blurred vision thickening of bronchial secretions Dosage OralIM ndash 05-11mgkg
maximum 25 mg
Diphenhydramine
Oral IM IV
Onset -1hr
Duration ndash 4 to 6 hr
Metabolized in liver
Adverse reaction disturbed coordination thickening of bronchial secretions
Dosage Oral IM IV ndash 1 to 15mgkg
maximum 50mg
Tranquilizers
Major tranquilizer antipsychotic produce calmness control symptoms of psychoses cause reversible extra pyramidal symptoms and do not tend to cause habituation
Minor tranquilizer antianxiety agents also cause calmness do not cause extrapyramidal symptoms Used in conditions like nervous tension and mild depression
8
Classification
Antipsychotics
Phenothiazine derivatives
Chlorpromazine promazine
Butryophenones
Haloperidol
Rauwolfia alkaloids
Reserpine
Antianxiety drugs
Propyl alcohol derivatives
Meprobamate
Benzodiazepine derivatives
Diazepam
Miscellaneous compounds
Hydroxyzine
Meprobamate
White crystalline powder slightly bitter in taste
Only administered orally
Peak blood concentration ----1 to 3hrs
10 ---------excreted unchanged Rest --- excreted as a oxidized derivative or as a glucoronide
Uses
To relieve day time anxiety
Induce sleep in insomniacs
To reduce anxiety associated with dental treatment
Anti-convulsant ndash petit mal epilepsy
Adverse reaction leucopenia acute non-thrombocytopenic purpura ecchymoses eosinophilia edema adenopathy
Dosage Childrengt 6yrs 100 to 200mg
Not recommended for children under 6yrs
Monitoring during sedation
1 Pulse
2 Blood pressure
3 ECG
4 Respiration
5 Temperature
Pulse
Manual Electronic
bull Radial Brachial
bull Facial labial
Blood pressure
ndash Stethoscope amp sphygmomanometer
ndash Automatic devices
ndash Direct cannulation of an artery ndash very accurate
Electrocardiograph
Heart rate rhythm myocardial function
9
Respiration
ndash Monitoring respiratory rate
ndash Observing the rise amp fall of the chest wall
ndash Observing the color of mucous membrane
ndash Observing the inflation amp deflation of the reservoir bag
Devices for monitoring respiration
1 The Precordial pretracheal stethoscope
2 The esophageal stethoscope
ndash Respiratory rate
ndash Heart rate
ndash Any abnormal sounds
Pulse Oximeter
ndash Oxygen saturation
ndash Heart rate
ndash Oxisensor site
ndash Fingers
ndash Toe
ndash Ear lobe
Mechanism
Oxygenated Hb ndash red light
Deoxygenated Hb- infrared light
Tissue pressure from arterial pulse (plethysmography)
Advantages
ndash Safe amp noninvasive
ndash Simple to use
ndash Information is rapidly available for clinical decision
ndash Indirectly indicates respiratory adequacy
Disadvantages
ndash Finger probes can get dislodged
ndash Emitted light source may cause burning
ndash Non reusable probes are expensive
ndash Does not directly determine airway patency
Capnography
1 The presence absence of air flow
2 Indicates depth amp adequacy of respiration
3 Continues analysis of the co2 content of the respired air ndash indicates respiratory adequacy
Temperature
ndash Disposable nondisposable thermometer
ndash Esophageal rectal temp probe
10
Discharge criteria
Cardiovascular function is satisfactory amp stable
Airway patency is uncompromised amp satisfactory
Pt is easily arousable amp protective reflexes intact
State of hydration is adequate
Pt can talk if applicable
Pt can sit unaided if applicable
Pt can ambulate with minimal assistance if applicable
Presedation level of responsiveness achieved
Responsible individual is available
1
PULP THERAPY OF VITAL TEETH
DR MITAKSHARA NIRWAN
Contents
Indirect pulp capping
Direct pulp capping
Medications amp materials used in pulp capping
Pulpotomy
MTA
Apexogenesis
INDIRECT PULP CAPPING
Pieter Van Forest - first to speak about root canal therapy
Glove designed instruments that could prepare a canal to a certain size and taper(1910)
Indirect pulp capping is defined as a procedure where in small amount of carious dentin is retained in
deep areas of cavity to avoid exposure of pulp followed by placement of a suitable medicament and
restorative material that seals off the carious dentin and encourages pulp recovery (Ingle)
A procedure in which only the gross caries is removed from the lesion and the cavity is sealed for a
time with a biocompatible material (McDonald)
Objective of indirect pulp capping
These were given by Eidelman in 1965
bull Arresting the carious process
bull Promoting dentin sclerosis
bull Stimulating formation of tertiary dentin
bull Remineralization of carious dentin
Layers of Carious Dentin Indications of Indirect Pulp Capping
History
Mild pain associated with eating
Negative history of spontaneous extreme pain
Clinical Examination
Deep carious lesion which are close tobut not involving the pulp in vital primary or young
permanent teeth
No mobility
Nominal pulp inflammationdefinite layer of affected dentin after removal of infected dentin
Radiographic examination
Normal lamina dura amp PDL space
No radiolucency around the apices
2
Contraindications of Indirect Pulp Capping
History
Sharp penetrating pulpalgia
Prolonged spontaneous pain especially at night
Clinical examination
Mobility of tooth
Discoloration of tooth
Negative reaction of electric pulp testing
Radiographic examination
Definite pulp exposure
Break in the lamina dura
Radiolucency around the apices
Widened PDL space
Treatment procedure
Sequelae of Indirect Pulp Capping Three distinct types of new dentin formation take place
1 Cellular fibrillar dentinmdashfirst 2 months
2 Globular dentinmdash3 months
3 Tubular dentin (uniform mineralized dentin)
bull 15th of reparative dentin formation begins in less than 30 days
bull After 3 months 01 mm is formed
DIRECT PULP CAPPING Defined by Kopel (1992) as the placement of a medicament or non medicated material on a pulp that
has been exposed in course of excavating the last portions of deep dentinal caries or as a result of
trauma
Objective
To create new dentin in the area of the exposure and subsequent healing of the pulp
Rationale
achieve a biologic closure of the exposure site by deposition of hard tissue barrier (dentin bridge)
between pulp tissue and capping material thus walling off the
INDICATIONS
Small mechanical exposure
Easily controlled haemorrhage
Bright red haemorrhage
True pinpoint exposure
CONTRAINDICATIONS
Severe toothache at night
Spontaneous pain
Tooth mobility
Radiographic appearance of pulp periradicular de- generation
Excess of hemorrhage at the time of exposure Serous exudate from the exposure
Externalinternal root resorption
Swellingfistula
Histological Changes after Pulp Capping
These were illustrated be Glass and Zander in 1949
After 24 hours Necrotic zone adjacent to calcium
hydroxide paste is separated from healthy pulp
tissue by a deep staining basophilic layer
After 7 days Increase in cellular and fibroblastic
activity
After 14 days Partly calcified fibrous tissue lined by
odontoblastic cells is seen below the calcium
proteinate zone disappearance of necrotic zone
After 28 days Zone of new dentin
3
Medications and Materials Used for Pulp Capping Calcium hydroxide
Corticosteroids amp antibiotics
Inert materials
Collagen fibers
4-META adhesive
Direct bonding
Isobutyl cyanoacrylate
Denatured albumin
Mineral trioxide aggregate
Laser
Bone morphogenic protein
PULPOTOMY
Finn (1995) defined it as the complete removal of the coronal portion of the dental pulp
followed by placement of a suitable dressing or medicament that will promote healing and
preserve vitality of the tooth
American Academy of Pediatric Dentistry (1998) defined pulpotomy as the amputation of
affected infected coronal portion of the dental pulp preserving the vitality and function of the
remaining part of radicular pulp
Objectives
bull Removal of inflamed and infected coronal pulp at the site of exposure thus preserving the vitality of the
radicular pulp and allowing it to heal
bull Maintain the tooth in the dental arch
Rationale
bull Radicular pulp is healthy and capable of healing after surgical amputation of the infected coronal pulp
bull Preserves vitality of the radicular pulp
bull Maintains tooth in a physiologic condition
Indications of Pulpotomy bull Mechanical pulp exposure in primary teeth
bull Teeth showing a large carious lesion but free of radicular pulpitis
bull History of only spontaneous pain
bull Hemorrhage from exposure sites bright red and can be controlled
bull Absence of abscess or fistula
bull No interradicular bone loss
bull No interradicular radiolucency
Contraindications of Pulpotomy bull Persistent toothache
bull Tenderness on percussion
bull Root resorption more than 13rd of root length
bull Large carious lesion with nonrestorable crown
bull Highly viscous sluggish hemorrhage from canal orifice which is uncontrollable
bull Medical contradictions like heart disease immuno compromised patient
bull Swelling or fistula
bull External or internal resorption
bull Pathological mobility
bull Calcification of pulp
Classification of pulpotomy
4
Formocresol Pulpotomy
Iby BUCKLEY in 1904
Sweet (1930) Formulated multi visit technique
Doyle (1962) Advocated 2 sitting procedure (complete devitalization)
Spedding (1965) Gave 5 minute protocol (partial devitali- zation)
Venham (1967) Proposed 15 seconds procedure
Current concept uses 4 minutes of application time
Composition of formocresol Buckleyrsquos Formula
bull Cresol ndash 35 percent
bull Glycerol ndash 15 percent
bull Formaldehyde ndash 19 percent
bull Water ndash 31 percent
Mechanism of Action
It prevents tissue autolysis by bonding to the proteins Bonding is of peptide groups of side chain amino acids and is a reversible process accomplished without
changing the basic structure of protein molecules
Histological Changes
bull Demonstrated by Mass and Zilbermann11 in 1933 and also by Massler and Mansokhani in 1959
bull Immediately the pulp becomes fibrous and acidophillic
bull Seven to fourteen days Three zones appear
a broad eosinophilic zone of fixation
b broad pale-staining zone of atrophy with poorcellular definition
c broad zone of inflammation extending apically into normal pulp tissue
bull One yearndash Progressive apical movement of these zones with only acidophillic zone left at the end of 1 year
Modified Formocresol Pulpotomy
Used by TRASK(1972)
The technique is identical to that described for primary teeth except that the formocresol pellet is
sealed permanently in the tooth
Two-visit Devitalization Pulpotomy
Indications
bull There is evidence of sluggish bleeding at the amputation site that is difficult to control
bull Pus in the chamber but none at the amputation site
bull There is thickening of the PDL
bull History of pain
Contraindications
bull Nonrestorable tooth
bull Tooth with necrotic pulp
5
Glutaraldehyde Pulpotomy
It was first suggested by S Gravenmade Introduced by Kopel in 1979
Mechanism of Action
bull Glutaraldehyde produces rapid surface fixation of the underlying pulpal tissue
bull A narrow zone of eosinophilic stained and compressed fixed tissue is found directly beneath the area of application which blends into vital normal appearing tissue apically
bull With time the glutaraldehyde fixed zone is replaced by macrophagic action with dense collagenous tissue thus the entire root canal tissue is vital
Cvekrsquos Pulpotomy
bull This is also called as calcium hydroxide pulpotomy or young permanent partial pulpotomy
bull This was proposed by Mejare and Cvek16 in 1978
bull Indicated in young permanent teeth where the pulp is exposed by mechanical or bacterial means and the
remaining radicular tissue is judged vital by clinical and radiographic criteria whereas the root closure is
notcomplete
MINERAL TRIOXIDE AGGREGATE (MTA) Torabinejad described the physical and chemical properties of MTA in 1995
It is ash colored powder made primarily of fine hydrophilic particles of
1 tricalcium aluminate
2 tricalcium silicate
3 silicate oxide
4 tricalcium oxide
5 bismuth dioxide
Hydration of the powder results in a colloidal gel composed of calcium oxide crystals in an amorphous
structure This gel solidifies into a hard structure in less than three hours
PROPERTIES OF MTA
It is biocompatible material and its sealing ability is better than that of amalgam or ZOE
Initial pH is 102 and set pH is 125
The setting time of cement is 4 hours
The compressive strength is 70 MPA which is comparable with that of IRM
Low cytotoxicity ndash It presents with minimal inflammation if extended beyond the apex
Mineral trioxide aggregate (MTA) has demonstrated the ability to induce hard-tissue formation in
pulpal tissues and it promotes rapid cell growth
APEXOGENESIS
It is defined as the treatment of a vital pulp by capping or pulpotomy in order to permit continued
growth of the root and closure of the open apex
Rationale
Maintenance of integrity of the radicular pulp tissue to allow for continued root growth
Indications
bull Indicated for traumatized or pulpally involved vital permanent tooth when root apex is incompletely formed
bull No history of spontaneous pain
bull No sensitivity on percussion
bull No hemorrhage
bull Normal radiographic appearance
Contraindications
bull Evidence that radicular pulp has undergone degenerative changes
bull Purulent drainage
bull History of prolonged pain bull Necrotic debris in canal
bull Periapical radiolucency
6
1
Gupta A Dhingra R Chaudhari P Gupta A
Department of Paedodontics and Preventive Dentistry Faculty of Dental Sciences SGT University Gurgaon Haryana India
Journal of Indian Society of Pedodontics and Preventive Dentistry
Volume 35 I Issue 3 I July-September 2017
A COMPARISION OF VARIOUS MINIMALLY
INVASIVE TECHNIQUES FOR THE REMOVAL
OF DENTAL FLUOROSIS STAINS IN
CHILDREN
DR MITAKSHARA NIRWAN
CONTENTS
bull Introduction
bull Aims
bull Materials and Methods
bull Results
bull Discussion
bull Conclusion
bull Critical analysis
bull References
INTRODUCTION
bull Dental fluorosis is a developmental disturbance of dental enamel caused by
successive exposure to high concentrations of fluoride during tooth
development
bull Various methods of therapy are advocated for the treatment of fluorosis -
stained teeth which range from invasive ceramic veneer bonding restorations
to abrasive chemical treatments
bull The combination of dental bleaching techniques and microabrasion appears
as an excellent conservative solution to reestablish health in fluorosis
affected teeth
AIMS
bull The aim of the study was to evaluate and compare the effectiveness of
minimally invasive techniques for the removal of dental fluorosis
stains in children in vivo
MATERIALS AND METHODS
Patients visiting the department of Pedodontics and Preventive dentistry
Faculty of Dental Sciences SGT University Gurgaon
bull Sample size 90 patients
bull Age group 10 -17 years
bull Caries cracks or periodontal
disease on anterior teeth
bull Abscess draining sinus
cellulitis
bull Non vital teeth
hypersensitive exposed
crevices
bull Orthodontic appliance
bull Past history of bleaching
bull At least two permanent
maxillary anterior teeth
bull TSIF of score 4
bull Free of systemic diseases
Inclusion criteria Exclusion criteria
2
Groups
Group A In office bleaching with 35 hydrogen peroxide( Pola Office
Bleaching kit) activated by light emitting diode (LED) bleaching unit
(35 HP)
Group B Enamel microabrasion (EM) (PREMA Enamel Microabrasion
System) followed by in-office bleaching with 44 carbamide peroxide
gel (EM)
Group C In-office bleaching with 5 sodium hypochlorite (5
NaOCl)
A baseline colour evaluation was done by taking digital photograph of
the maxillary anterior teeth
RESULTS
Group 1
Colour stability
Group 2 Group 3
Tooth sensitivity
Tooth sensitivity values were taken before the treatment
which was compared to immediate postoperative and follow
up visits It was checked using an electric pulp tester
maximum
moderate
least
immediately
group 2
group 1
group 3
1 month
group 2
group 1
group 3
3 month
group 2
group 1
group 3
Patient satisfaction score
Satisfaction was assessed on visual analog scale
Range 1 to 5
Groups percentage of patients
who were satisfied with
the treatment
Number of patients
who reported slight
reappearance of colour
Group 1
90
7
Group 2
83
8
Group 3
73
7
3
Number of Appointments
Groups One sitting Two sittings Three
sittings
Group 1
25
4
1
group 2
26
3
1
Group 3
30
0
0
DISCUSSION
bull Hydrogen peroxide is capable of penetrating the tooth osmosis and through porosities and cracks subsequently acting directly on the pigmented molecules
bull Gurgan et al investigated 3 different light systems and found out that diode laser system with gave best tooth whitening and least tooth sensitivity
bull In the EM group the surface reflects and refracts light from the surface in such way that mild imperfections in underlying enamel are camouflaged While the highly polished surface of enamel enhances the aesthetic appearance
bull Train et al and Loguercio et al also had the similar results in their studies with EM mild fluorosis showed best results moderate showed moderate results while it had little effect on severe fluorosis
bull NaOCl was only effective on mild stains while moderate and severe
stains could only be lightened to quite an extent but could not be
completely removed
bull When NaOCl comes in contact with hypomineralized and discoloured
enamel it degrades and removes the chromogenic organic material
located on the enamel surface
CONCLUSION
bull It was concluded that esthetic appearance of teeth mild fluorosis can
be achieved by bleaching and microabrasion But in cases of
moderate fluorosis a combination of any of theses modalities can be
used
bull As no special maintenance precautions are required these maybe be
considered as an interesting alternative to conventional operative
treatment
bull Focuses on only TSIF of 4
bull Electric pulp testing is not the
right method to check for
sensitivity
bull Tooth Sensitivity changes
from person to person
bull Food habits can cause
staining of the teeth
bull Minimally invasive
bull Cheaper to veneers
bull Minimal loss of tooth structure
bull 4 parameters checked for the success of treatment
bull Inclusion of specific score of fluorosis for comparing the results
bull Maximum 3 appointments needed
CRITICAL ANALYSIS
Pros Cons
REFERENCES
bull Gurgan S Cakir FY Yazici E Different light-activated in officebleaching
systems Lasers Med Sci 201025817-22
bull Train TE McWhorter AG Seale NSWilson CF Guo IY Examination of
esthetic improvement and surface alteration following microabrasion in
fluorotic human incisors in vivoPediatr dent 199618353-62
bull Loguercio AD Correia LD Zago C Tagliari D Neumann E Gomes OM et al
Clinical effectiveness of two microabrasion materials materials for the
removal of enamel flurosis stains Oper Dent 200732531-8
4
1
IMPACT OF 6 CITRIC ACID AND ENDOACTIVATOR AS IRRIGATION ADJUNCTS ON OBTURATION QUALITY AND PULPECTOMY OUTCOME IN
PRIMARY TEETH
NEETU JAIN SHALINI GARG ABHISHEK DHINDSA SAKSHI JOSHI HARJOY
KHATRIA
PEDIATRIC DENTAL JOURNAL 2019 29
1
DR MITAKSHARA NIRWAN
CONTENTS
bull INTRODUCTION
bull AIMS amp OBJECTIVES
bull CASE REPORT
bull RESULTS
bull DISCUSSION
bull CONCLUSION
bull PROS AND CONS
bull REFERENCES
2
INTRODUCTION
bull ENDODONTIC THERAPY IN PRIMARY TEETH INVOLVES DISINFECTION OF THE ROOT CANAL
SYSTEM AND ITS OBTURATION WITH RESORBABLE PASTE
bull THE CONTENTS OF ROOT CANAL ALONG WITH SMEAR LAYER ARE EXPECTED TO BE REMOVED
DURING THE BIOMECHANICAL PREPARATION
bull IN VITRO AND CLINICAL DOCUMENTS HAVE INDICATED THAT MECHANICAL PREPARATION OF
THE CANAL LEAVES LARGE PORTIONS OF THE CANAL WALLS UNDEBRIDED AND COMPLETE
REMOVAL OF THE BACTERIA BY THIS MECHANICAL PROCEDURE ALONE IS UNLIKELY TO BE SEEN
THEREFORE SOME FORM OF DISINFECTIONIRRIGATION IS MANDATORY TO KILL THE
MICROORGANISMS AND TO REMOVE THE RESIDUAL TISSUES
3
bull THE IDEAL REQUISITES OF A ROOT CANAL IRRIGANT AS GIVEN BY ZEHNDER ARE
1 BROAD ANTIMICROBIAL SPECTRUM
2 HIGH EFFICACY AGAINST ANAEROBIC AND FACULTATIVE MICROORGANISMS ORGANIZED
IN BIOFILMS
3 ABILITY TO DISSOLVE NECROTIC PULP TISSUE REMNANTS
4 ABILITY TO INACTIVATE ENDOTOXIN
5 ABILITY TO PREVENT THE FORMATION OF A SMEAR LAYER DURING INSTRUMENTATION OR
TO DISSOLVE THE LATTER ONCE IT HAS FORMED
6 SYSTEMICALLY NONTOXIC WHEN THEY COME IN CONTACT WITH VITAL TISSUES
NONCAUSTIC TO PERIODONTAL TISSUES AND WITH LITTLE POTENTIAL TO CAUSE AN
ANAPHYLACTIC REACTION
SINCE NO SINGLE IRRIGANT HAS THESE OPTIMAL PROPERTIES STUDIES HAVE REPORTED THE USE
OF TWO OR MORE SOLUTIONS IN A SPECIFIC SEQUENCE OR IN COMBINATIONS FOR BETTER
RESULTS 4
bull SEVERAL IRRIGATING SOLUTIONS ALONG WITH CHELATING AGENTS HAVE BEEN USED
DURING BIOMECHANICAL PREPARATION OF ROOT CANAL BOTH IN PRIMARY AND
PERMANENT TEETH
bull HOWEVER NONE OF THE AVAILABLE IRRIGATING SOLUTIONS HAS BEEN REGARDED CLEARLY
AS OPTIMAL SOLUTION BECAUSE OF THEIR LIMITED EFFECTIVENESS ESPECIALLY IN APICAL
13RD OF THE ROOT CANAL SYSTEM
bull TO OVERCOME SUCH LIMITATIONS USE OF ENDOACTIVATOR HAS BEEN PROPOSED AS AN
IRRIGATION FACILITATOR THAT IS BASED ON SONIC VIBRATION (UP TO 10000 CPM) WHICH
FACILITATES THE IRRIGANT PENETRATION AND ITS RENEWAL WITHIN THE CANAL
bull ACTIVATION SYSTEMS RESULTED IN BETTER REMOVAL OF THE SMEAR LAYER IN THE APICAL
THIRD OF ROOT CANALS IN COMPARISON TO CONVENTIONAL IRRIGATION
5
CITRIC ACID
bull CITRIC ACID IS A WEAK ORGANIC ACID WITH THE APPEARANCE OF WHITE CRYSTALLINE
POWDER AT ROOM TEMPERATURE
bull IT CAN EXIST EITHER IN WATER-FREE FORM (ANHYDROUS) OR MONOHYDRATE FORM THE
WATER-FREE FORM CRYSTALLIZES FROM THE HOT WATER WHEREAS THE MONOHYDRATE
FORMS FROM THE COLD WATER THE LATTER MAY BE CONVERTED TO ANHYDROUS FORM BY
HEATING MORE THAN 78degC
bull CITRIC ACID OCCURS NATURALLY IN THE BODY IN MITOCHONDRIA AND IS USED BY BLOOD
BANKS TO PREVENT COAGULATION OF TRANSFUSED BLOOD CITRIC ACID IS ALSO ESSENTIAL
TO HUMAN METABOLISM AND IS FOUND IN MANY FOODS
6
2
bull THE BIOLOGICAL EFFECTS OF CITRIC ACID ON THE PERIODONTAL STRUCTURE HAS BEEN
EXTENSIVELY STUDIED IN PERIODONTICS
bull NEUMAN AND NEWMAN SHOWED THAT CITRIC ACID IS THE MOST EFFECTIVE ACID IN
ALTERING THE SOLUBILITY OF HYDROXYAPATITE
bull YAMAGUCHI ET AL SHOWED THAT CITRIC ACID SOLUTION HAD ANTIBACTERIAL EFFECTS ON
ALL 12 ROOT CANAL BACTERIA TESTED
bull ARIAS-MOLIZ ET AL SHOWED THAT ETHYLENEDIAMINETETRAACETIC ACID (EDTA) HAS NO
BACTERICIDAL ACTIVITY EVEN AFTER 1 HOUR CONTACT
bull THIS ACID HAS THE ABILITY OF ROOT CANAL IRRIGATION AND ALSO SMEAR LAYER REMOVAL
DIFFERENT CONCENTRATIONS (1ndash50) HAVE BEEN PROPOSED GUTMANN ET AL CONCLUDED
THAT 10 CITRIC ACID IS BETTER THAN ULTRASOUND FOR SMEAR LAYER REMOVAL FROM THE
ROOT END CAVITIES
7
bull STUDIES HAVE SHOWN IRRIGATION WITH 6 CA FOR 15 OR 30 SECONDS IS QUITE
EFFECTIVE IN REMOVING ALL THE COMPONENTS OF THE SMEAR LAYER OF THE PRIMARY
TEETH WHEREAS PERITUBULAR DENTIN DESTRUCTION WAS OBSERVED WHEN HIGHER
CONCENTRATION OF CITRIC ACID WAS USED AS AN IRRIGATING SOLUTION
8
AIMS amp OBJECTIVES
bull THIS STUDY WAS AIMED TO EVALUATE THE CLINICAL AND RADIOGRAPHIC OUTCOME OF
PULPECTOMY ALONG WITH QUALITY OF OBTURATION USING 6 CITRIC ACID AND
ENDOACTIVATOR
9
CASE REPORT
bull 350 CHILDREN (3-9 YEARS) WITH CLINICAL SIGNS AND SYMPTOMS OF CHRONIC IRREVERSIBLE
PULPITIS IN DEEPLY CARIOUS TEETH WERE SCREENED DURING SCHOOL DENTAL HEALTH
PROGRAM FROM MAY 2014-JULY 2014
bull 123 CHILDREN REPORTED TO THE DEPARTMENT AND 67 CHILDREN WERE SELECTED BASED ON
INCLUSION AND EXCLUSION CRITERIA
RECRUITMENT OF PATIENTS
10
INCLUSION CRITERIA
bull HISTORY OF SPONTANEOUS PAIN AND UNCONTROLLED BLEEDING AFTER PULP AMPUTATION
EXCLUSION CRITERIA
bull EVIDENCE OF INTERNAL OR EXTERNAL (PHYSIOLOGICPATHOLOGIC) ROOT RESORPTION OF MORE THAN A THIRD OF ITS LENGTH
bull ROOT CANAL OBLITERATION OR ANATOMIC ANOMALIES
bull INADEQUATE BONE SUPPORT OR NON RESTORABLE TOOTH
bull ONCE PATIENTS ELIGIBILITY WAS CONFIRMED THE TREATMENT PROCEDURE WAS
EXPLAINED TO THE PARENTGUARDIAN AND INFORMED WRITTEN CONSENT WAS
OBTAINED FROM PARENTSGUARDIANS SHOWING WILLINGNESS FOR THEIR
CHILDRENS TREATMENT 11
PROCEDURE
bull PULPECTOMY WAS PERFORMED BY ONE OPERATOR OF PEDIATRIC DENTISTRY DEPARTMENT
USING A STANDARDIZED TREATMENT PROTOCOL FOR ALL THE PATIENTS
bull AFTER ADMINISTRATION OF LOCAL ANESTHESIA RUBBER DAM WAS APPLIED FOR ISOLATION
bull ACCESS CAVITY WAS PREPARED USING AIR-ROTOR HAND PIECE WITH 8 ROUND BUR AND
PULP TISSUE WAS EXTIRPATED WITH THE HELP OF SPOON EXCAVATOR
bull FURTHER THE NEGOTIATION OF THE CANALS WAS DONE WITH 10 K-FILE
bull A DIAGNOSTIC RADIOGRAPH WAS TAKEN FOR ROOT LENGTH DETERMINATION AND
WORKING LENGTH WAS KEPT 1 MM SHORT OF THE RADIOGRAPHICAL APEX
bull ALL ROOT CANALS WERE INSTRUMENTED MANUALLY USING K-FILES AND WERE IRRIGATED
WITH 10 ML 09 NORMAL SALINE AND 1 SODIUM HYPOCHLORITE AS STANDARDIZING
PROTOCOL FOR ROOT CANAL PREPARATION AND DISINFECTION
12
3
GROUP 1 (CA + E) - IRRIGATION WAS DONE
WITH 10 ML OF 6 CITRIC ACID (CITOCID AMMDENT)
AND IRRIGANTS WERE SONICALLY AGITATED WITH
ENDOACTIVATOR (DENTSPLY) FOR 30 S PER CANAL USING REDBLUE
ENDOACTIVATOR TIP
GROUP 2 (CA) - 10 ML OF 6 CITRIC ACID FOR 1 MIN USING
27 GAUZE IRRIGATING NEEDLE
GROUP 3(SH + E) - 10 ML OF 1 SODIUM HYPOCHLORITE
SOLUTION AND SONIC ACTIVATION WITH ENDOACTIVATOR
GROUP 4(SH) - 10 ML OF 1 SODIUM HYPOCHLORITE
SOLUTION USING IRRIGATING NEEDLE (CONTROL GROUP)
bull TEETH UNDERGOING PULPECTOMY WERE RANDOMLY ENROLLED BY CHIT METHOD INTO THREE
STUDY AND ONE CONTROL GROUP
13
bull IN CITRIC ACID GROUPS FINAL RINSE WITH NORMAL SALINE WAS DONE TO REMOVE THE
REMAINING CRYSTALS (CHELATES)
bull FOLLOWING BIOMECHANICAL PREPARATION THE ROOT CANALS WERE DRIED WITH STERILE
ABSORBENT PAPER POINTS AND OBTURATED WITH VITAPEX USING HAND HELD
LENTULOSPIRAL FINAL RESTORATIONS WERE DONE USING COMPOSITE RESIN
14
bull CLINICAL FOLLOW UP WAS DONE AT 24 H1 WEEK 1 MONTH 6 MONTH AND 12
MONTH TO CHECK PAIN PRESENCE AND PAIN FREQUENCY (ONCEMORE THAN ONCE)
SWELLING FISTULA SENSITIVITY TO PERCUSSION
bull RADIOGRAPHIC FOLLOW UP WAS DONE AT 6 MONTH AND 12 MONTH FOR ANY
DEVIATED ERUPTION OF SUCCEDANEOUS TEETH EXCESS FILING MATERIAL AND ITS
RESORPTION EXTERNALINTERNAL ROOT RESORBTION CALCIFIC METAMORPHOSIS
PRESENCE OF FURCATION RADIOLUCENCY
CLINICAL amp RADIOGRAPHIC FOLLOW UP
15
RADIOGRAPHIC ASSESSMENT OF OBTURATION QUALITY
bull POSTOPERATIVE RADIOGRAPHS WERE VISUALLY ASSESSED FOR QUALITY OF OBTURATION BY
TWO INDEPENDENT EXAMINERS (SG AD) WHO WERE BLINDED WITH REGARD TO
IRRIGATION PROTOCOL GROUP TO ENHANCE CALIBRATION EACH EXAMINER ASSESSED THE
RADIOGRAPH INDEPENDENTLY AND LATER REVIEWED TOGETHER FOR FINAL ASSESSMENT
INDIVIDUAL ROOT WAS TAKEN AS UNIT OF ANALYSIS FOR GRADE OF OBTU- RATION AND
SCORING CRITERIA WERE AS GIVEN BY COLL JA 1996
1 UNDER FILLED - FILLING MATERIAL ENDED 1 MM OR MORE SHORT OF THE APEX
2 OPTIMAL FILLING- FILLING MATERIAL APPEARED TO END AT THE RADIOGRAPHICAL APEX
3 OVERFILLED - FILLING MATERIAL EXTRUDED PAST THE RADIOGRAPHIC APEX
4 OPTIMALLY FILLED ROOTS WERE FURTHER ASSESSED FOR THE PRESENCE OF VOIDS AND VOID
AREA (ROOT CANAL SURFACE UNTOUCHED BY THE ROOT CANAL FILLING MATERIAL) IN THREE
VISUALLY DIVIDED SECTIONS OF THE ROOT IE CORONAL MIDDLE AND APICAL 13RD
16
RESULTS
bull OVERALL CLINICAL AND RADIOGRAPHIC SUCCESS RATE OVER A PERIOD OF ONE YEAR WAS
9886 amp 977 RESPECTIVELY
bull ALL GROUPS WERE SIGNIFICANTLY (P = 001) EFFECTIVE IN ALLEVIATING PAIN WITHIN 24 H
OF PULPECTOMY
17 18
4
19
bull IMMEDIATE POST OPERATIVE RADIOGRAPHIC ASSESSMENT REVEALED 68 (102150) ROOTS
WITH OPTIMAL OBTURATION AND 32 (48150) WITH OVERFILLINGUNDERFILLING MAXIMUM
NO OF OPTIMAL FILLINGS WERE OBSERVED IN GROUP1 (CA + E) (3333) FOLLOWED BY
GROUP 2 (CA) (2549) GROUP 3(SH + E) (2549) AND GROUP 4(SH) (1568)
bull CITRIC ACID GROUPS HAD MORE NUMBER OF OPTIMALLY FILLED ROOTS 588 (60102) THAN
NON CITRIC ACID GROUPS 412 (42102)
bull ENDOACTIVATOR CONTRIBUTED TO 18 OF OPTIMAL OBTURATION IRRESPECTIVE OF
CHELATING AGENT USED
20
21
bull MAXIMUM NO OF VOIDS AND VOID AREAS WERE IN NON CITRIC ACID GROUPS
(6419 amp 5384) COMPARED TO CITRIC ACID GROUPS (3580 amp 4615)
RESPECTIVELY
bull ANALYSIS OF ROOT 13RD REVEALED MAXIMUM NO OF VOID AREA IN APICAL
13RD (4755) FOLLOWED BY MIDDLE 13RD (3846) AND CORONAL 13RD
(1398)
bull LEAST NO OF VOIDS amp VOID AREA (1111 amp 1608) WERE OBSERVED WHEN
ENDOACTIVATOR ALONG WITH CHELATING AGENT WAS USED (GROUP 1)
HOWEVER THIS WAS STATISTICALLY INSIGNIFICANT
22
DISCUSSION
bull IN THE PRESENT STUDY 1 SODIUM HYPOCHLORITE WAS USED ALONG WITH 6 CITRIC ACID
(CHELATING AGENT) WHICH IS REPORTED TO BE AS EFFECTIVE AS 17 EDTA
bull CITRIC ACID (BIOLOGICAL ACID) IS FOUND TO BE BIOCOMPATIBLE AND LEAST IRRITATING TO
PERIAPICAL TISSUES THAN OTHER CHELATING AGENTS
bull USE OF SODIUM HYPOCHLORITE SOLUTION FOLLOWING CHELATING AGENT WAS AVOIDED AS IT
RAPIDLY PRODUCES SEVERE EROSION OF ROOT CANAL WALL DENTIN
bull TRADITIONAL APPROACH OF DELIVERING IRRIGANTS INTO THE ROOT CANAL SPACE USING
SYRINGES AND METAL NEEDLES HAS BEEN FOUND TO BE INEFFECTIVE ESPECIALLY IN THE AREAS OF
ANASTOMOSES BETWEEN CANALS AND APICAL 13RD OF ROOT CANAL
23
bull THEREFORE TO ACHIEVE BETTER CLEANING EFFICIENCY IRRIGANT ACTIVATION HAS BEEN
RECOMMENDED SONIC ACTIVATION HAS BEEN REPORTED TO RESULT IN BETTER ROOT CANAL
CLEANLINESS AS COMPARED TO NO ACTIVATION OF IRRIGANT
24
5
CONCLUSION
bull USE OF 6 CITRIC ACID DEFINITELY HELPED IN RAPID ELIMINATION OF PAIN RESOLUTION OF
PERI-RADICULAR RADIOLUCENCY BETTER OBTURATION QUALITY IN TERMS OF LESS VOIDS AND
VOID AREAS ALONG WITH MAXIMUM NO OF OPTIMAL OBTURATION UP TO APICAL AREA
bull 6 CITRIC ACID AND ENDOACTIVATOR IRRIGATION PROTOCOL PROVED TO BE THE BETTER
IRRIGATION PROTOCOL WHICH MAY CONTRIBUTE TO LONG TERM SUCCESS OF PRIMARY
TOOTH AND THE HEALTH OF UNDERLYING PERMANENT TOOTH
bull 6 CITRIC ACID ALONG WITH ENDOACTIVATOR MAY BE RECOMMENDED AS IRRIGATION
ADJUNCTS IN PULPECTOMY PROCEDURE OF PRIMARY TEETH
25
PROS AND CONS
PROS
bull PROPER EXPLANATION OF THE MATERIALS
USED
CONS
bull NO PREOPERATIVE AND POSTOPERATIVE
RADIOGRAPHS
26
REFERENCES
bull RAMACHANDRA JA NIHAL NK NAGARATHNA C VORA MS ROOT CANAL IRRIGANTS IN
PRIMARY TEETH WORLD J DENT 20156(3)229-234
bull MOHAMMADI Z JAFARZADEH H SHALAVI S KINOSHITA JI UNUSUAL ROOT CANAL
IRRIGATION SOLUTIONS J CONTEMP DENT PRACT 201718(5)415-420
bull ZEHNDER M ROOT CANAL IRRIGANTS J ENDOD 2006 32389- 98
bull SMITH JJ amp WAYMAN BE AN EVALUATION OF THE ANTIMICROBIAL EFFECTIVENESS OF
CITRIC ACID AS A ROOT CANAL IRRIGANT JOURNAL OF ENDODONTICS 1986 12(2) 54-58
bull TANNURE PN AZEVEDO CP BARCELOS R GLEISER R PRIMO LG LONG-TERM OUTCOMES OF
PRIMARY TOOTH PULPECTOMY WITH AND WITHOUT SMEAR LAYER REMOVAL A RANDOMIZED
SPLIT-MOUTH CLINICAL TRIAL PEDIATR DENT 201133316E20 27
bull CARON G NHAM K BRONNEC F MACHTOU P EFFECTIVENESS OF DIFFERENT FINAL IRRIGANT
ACTIVATION PROTOCOLS ON SMEAR LAYER REMOVAL IN CURVED CANALS J ENDOD
2010361361E6
bull COLL JA SADRIAN R PREDICTING PULPECTOMY SUCCESS AND ITS RELATIONSHIP TO
EXFOLIATION AND SUCCEDANEOUS DENTITION PEDIATR DENT 19961857E63
28
1
LOCAL
ANESTHESIA
DR MITAKSHARA NIRWAN
CONTENTS
Definition
Methods of inducing local anesthesia
Desirable properties
Electrophysiology of nerve conduction
Impulse propagation and spread
Mode and site of action of local anesthesia
Classification of local anesthetic according to biological site and mode of action
Dissociation of local anaesthetics
Mechanism of action of local anaethetics
Local anaesthetic agent
2
3
DEFINITION
Local anesthesia is defined as a loss of sensation in
a circumscribed area of the body caused by depression
of excitation in nerve endings or an inhibition of the
conduction process in peripheral nerves
An important feature of local anesthesia is that it produces
LOSS OF SENSATION WITHOUT INDUCING LOSS OF
CONSCIOUSNESS
4
METHODS OF INDUCING LOCAL
ANESTHESIA
Low temperature
Mechanical trauma
Anoxia
Neurolytic agents such as alcohol amp phenol
Chemical agents such as local anesthetics
PROPERTIES OF LOCAL
ANESTHESIA
It should not be irritating to tissue to which it is applied
It should not cause any permanent alteration of nerve structure
Its systemic toxicity should be low
Time of onset of anesthesia should be short
It should be effective regardless of whether it is injected into the tissue or applied locally to mucous membranes
The duration of action should be long enough to permit the completion of procedure
5 6
It should have the potency sufficient to give complete
anesthesia with out the use of harmful concentration solutions
It should be free from producing allergic reactions
It should be free in solution and relatively undergo
biotransformation in the body
It should be either sterile or be capable of being sterilized by
heat with out deterioration
2
ELETROPHYSIOLOGY OF
NERVE CONDUCTION
There is an electrical charge across the membrane
This is the membrane potential
The resting potential (when the cell is not firing) is a negative
electrical potential of -70mv that exists across the nerve
membrane produced by different concentrations of either side of
the membrane
The interior of nerve is NEGATIVE in relation to exterior
7 8
inside
outside
Resting potential of neuron = -70mV
+
-
+
-
+
-
+
-
+
-
SLOW DEPOLARIRIZATION
9
RAPID DEPOLARIZATION
The interior of nerve is POSITIVE in relation to exterior
REPOLARIZATION
10
bull Repolarization takes 07 msec
bull Depolarization takes 03 msec
SODIUM PUMP -
energy comes from the oxidative metabolism of ATP
bull The entire process require 1 msec
IMPULSE PROPOGATION
IMPULSE SPREAD
The propagated impulse travels along the nerve
membrane towards CNS The spread of impulse differs
in myelinated and unmyelinated nerve fibers
DEPOLARIZED SEGMENT ADJACENT RESTING AREA
MODE AND SITE OF ACTION OF LOCAL
ANESTHETICS
Local anesthetic agent interferes with excitation
process in a nerve membrane in one of the
following ways
Altering the basic resting potential of nerve
membrane
Altering the threshold potential
Decreasing the rate of depolarization
Prolonging the rate of repolarization
12
3
CLASSIFICATION OF LOCAL ANESTHETIC
SUBSTANCES ACCORDING TO
BIOLOGICAL SITE AND MODE OF ACTION
CLASS A
Agents acting at receptor site on external surface of nerve membrane
Chemical substance Biotoxins (eg tetrodotoxin and saxitoxin)
CLASS B
Agents acting on receptor sites on internal surface of nerve membrane
Chemical substance Quaternary ammonium analogues of lidocaine
scorpion venom 13
CLASS C Agents acting by receptor independent of
physiochemical mechanism
Chemical substance Benzocaine
CLASS D Agents acting by combination of receptors and
receptor independent mechanisms
Chemical substance most clinically useful anesthetic agents
(eg lidocaine mepivacaine prilocaine)
14
BASED ON THE SOURCE
NATUAL
SYNTHETIC
OTHERS
BASED ON MODE OF APPLICATION
bull INJECTABLE
bull TOPICAL
BASED ON DURATION OF ACTION
bull ULTRA SHORT
bull SHORT
bull MEDIEM
bull LONG
BASED ON ONSET OF ACTION SHORT
INTERMEDIATE
LONG
15
DISSOCIATION OF LOCAL
ANESTHETICS
Local anesthetics are available as salts (usually
hydrochlorides) for clinical use
The salts both water soluble and stable is dissolved in
either sterile water or saline
In this solution it exists simultaneously as unchanged
molecule (RN) also called base and positively charged
molecules (RNH+) called cations
RNH+ ==== RN+ H
+
16
The relative concentration of each ionic form in the solution varies
in the pH of the solution or surrounding tissue
In the presence of high concentration of hydrogen ion (low pH) the
equilibrium shifts to left and most of the anesthetic solution exists
in cationic form
RNH+ gt RN
+ + H
+
As hydrogen ion concentration decreases (higher pH) the
equilibrium shifts towards the free base form
RNH+ lt RN + H
+
17
The relative proportion of ionic form also depends on pKa or DISSOCIATION CONSTANT of the specific local anesthetic
The pKa is a measure of molecules affinity for H+
ions
When the pH of the solution has the same value as pKa of the local anesthetic exactly half the drug will exists in the RNH
+ form and
exactly half in RN form
The percentage of drug existing in either form can be determined by Henderson Hasselbalch equation
Log baseacid = pH - pKa
18
4
MECHANISM OF ACTION OF LOCAL
ANESTHETICS
The following sequence is proposed mechanism of action of LA
Displacement of calcium ions from the sodium channel receptor site
Binding of local anesthetic molecule to this receptor site
Blockade of sodium channel
19
Decrease in sodium conductance
Depression of rate of electrical depolarization
Failure to achieve the threshold potential level
Lack of development of propagated action potential
Conduction blockadehellip
20
21
Na + Na +
22
LOCAL ANESTHETIC AGENT
COMERCIALLY PREPARED LOCAL ANESTHESIA
CONSISTS OF
Local anesthetic agent (xylocaine lignocaine 2)
Vasoconstrictor (adrenaline 1 80000)
Reducing agent (sodium metabisulphite)
Preservative (methylparabencapryl
hydrocuprienotoxin)
Fungicide (thymol)
Vehicle (distillde waterNaCl)
LOCAL ANESTHETIC AGENT
The local anesthetics used in dentistry are divided
into two groups
ESTER GROUP
AMIDE GROUP
23 24
ESTER GROUP It is composed of the following
An aromatic lipophilic group
An intermediate chain containing
an ester linkage
A hydrophilic secondary or tertiary
amino group
AMIDE GROUP It is composed of the following
An aromatic lipophilic group
An intermediate chain containing
amide linkage
A hydrophilic secondary or tertiary
amino group
5
25
CLASSIFICATION OF LOCAL ANESTHETICS
ESTERS
Esters of benzoic acid
Butacaine
Cocaine
Benzocaine
Hexylcaine
Piperocaine
Tetracaine
Esters of Para-amino
benzoic acid
Chloroprocain
Procaine
Propoxycaine
26
AMIDES Articaine
Bupivacaine
Dibucaine
Etidocaine
Lidocaine
Mepivacaine
Prilocaine
Ropivacaine
QUINOLINE
Centbucridine
PHARMACOKINETICS OF LOCAL
ANESTHETICS UPTAKE
When injected into soft tissue most local anesthetics produce
dilation of vascular bed
Cocaine is the only local anesthetic that produces
vasoconstriction initially it produces vasodilation which is
followed by prolonged vasoconstriction
Vasodilation is due to increase in the rate of absorption of the
local anesthetic into the blood thus decreasing the duration of
pain control while increasing the anesthetic blood level and
potential for over dose 27
AMIDE LOCAL ANESTHETICS
The metabolism of amide local anesthetics is more
complicated then esters The primary site of
biotransformation of amide drugs is liver
Entire metabolic process occurs in the liver for lidocaine
articaine etidocaine and bupivacaine
Prilocaine undergoes more rapid biotransformation then the
other amides
28
REFERENCES
Handbook of local anesthesia ndash Stanley F Malamed ndash 6th
edition
Essentials of Local Anesthetic Pharmacology Daniel E
Becker Anesth Prog 2006 Fall 53(3) 98ndash109
WIKIPEDIEA
29
THANK YOU
30
1
Pharmacological Methods of Behavior
Management
DR MITAKSHARA NIRWAN
DEFINITIONS
bull Conscious Sedation ndash A minimally depressed level of consciousness that retains
the patients ability to independently and continuously maintain an airway and respond appropriately to physical stimulation or verbal command
(American Dental Association House Of Delegates 2000)
bull Deep Sedation ndash An induced state of depressed consciousness
accompanied by partial loss of protective reflexes including the inability to continuously maintain an airway independently and or to respond purposefully to physical stimulation or verbal command
bull General Anesthesia (G A) ndash An induced state of unconsciousness or complete loss of
protective reflexes including the inability to continually maintain an airway independently and respond purposefully to physical stimulation or verbal command
Conscious sedation
ADVANTAGES
Conscious
Protective reflexes active amp intact
Stable vital signs
Operating dentist may perform sedation
Minimum amount of equipment required
Prolong detainment in recovery room not required
Risk of complication very low
Excellent choice for poor ndash risk pt in dental office
Cost effective
General anesthesia
ADVANTAGES Not absolutely
essential May be the only
method Not necessary (no
pain reaction) Amnesia always
present
Conscious sedation
DISADVANTAGES
Pt cooperation is essential
Extremely difficult or mentally handicapped pt cannot always be managed
Use of local anesthesia is a must
Amnesia may or may not be present
General anesthesia DISADVANTAGES
Pt unconscious
Protective reflexes are depressed
Depressed
Advanced training required Dentist must not act also as anesthetist
Special equipment necessary
Detainment in recovery area necessary
High IOP amp postoperative complications
Not indicated in dental office
More expensive
Fundamental Concepts
bull Techniques that utilize drugs to induce co-operative yet conscious state in an otherwise uncooperative child ndash CONSCIOUS SEDATION
2
GOALS
1 To facilitate the provision of quality care
2 To minimize the extremes of disruptive behavior
3 To promote a positive psychologic response to treatment
4 To promote patient welfare amp safety
5 To return the patient to physiologic state
OBJECTIVES
1 The pt mood must be altered
2 The pt must remain conscious at all times
3 The pt must be cooperative
4 All protective reflexes must remain intact and active
5 Vital signs must remain stable and with in normal limits
6 The ptrsquos pain threshold should be elevated
7 Amnesia may be present
Indications
1 Preschool children
2 Lack of Psychological Emotional maturity
3 Lack of Cognitive Physical Medical disability
4 Fearful amp anxious pts
5 Pt who require extensive amp complicated dental care amp would require or benefit from prolonged visits
6 Acute pain
7 Traumatic injuries
Operating Facilities amp Equipment
A positive pressure O2 delivery system capable of administering gt than 90 O2 at 10L min flow for 60 min (650L ldquoErdquo cylinder)
OR
Self inflating bag valve mask device (15L min)
A functional suction apparatus with appropriate suction catheters
Monitoring equipment - PO BPC PC or Capno
Inhalation sedation unit
100 O2 amp never less than 25
A fail safe mechanism that is checked and calibrated annually
Must have appropriate scavenging system
Emergency drugs
Techniques of sedation
Routes for drug administration
bull Oral
bull Rectal
bull Inhalational
bull Transmucosal
ndash Sublingual
ndash Intranasal
bull Parenteral
ndash IM
ndash sub mucosal
ndash IV
3
Oral Sedation
Advantages
1 Almost universally accepted and the easiest method
2 Decreased incidence and severity of adverse reaction
3 Low cost
Disadvantages
1 Absorption is variable
2 Prolonged latent period(30 min)
3 Reversal of any unwanted effect is also difficult
4 Inability to readily lighten or deepen the level of sedation
5 Prolonged duration of action
Rectal Sedation
Advantages 1 Incidence and intensity of
drug related side effects is minimized
2 Drug absorption occurs from the large intestine directly into the circulation
3 The lack of a needle syringe or other equipment
4 The ease of administration
5 The low cost
Disadvantages
1 Inconvenience to the administrator amp pt
2 The variable absorption of drugs from the large intestine
3 The slow onset of action amp the relatively long duration of action
4 Inability to titrate the drug dosage
5 The inability to reverse the action of the drug the prolonged recovery
Intranasal sedation
Advantages
Rapid onset (10 ndash 15 min)
Simple amp relatively painless
Less pt cooperation is required
Absorbed directly into the C V S
Intranasal sedation
Disadvantages
1 Dependence on nasal mucous membrane
2 Shorter duration of action(40-60min)
3 Multiple dosage may be necessary
Drugs
Midazolam ndash 02mgkg
Sufentanil ndash 15 ndash 3 mcgkg
Ketamine ndash 3-6mg kg
Sublingual sedation
Advantages
1 Pt acceptance
2 Rapid onset
3 High bioavailability
Drugs
Oral Transmucosal Fentanyl Citrate (OTFC)
Intramuscular Sedation
Advantages
1 More rapid onset of action
2 Absorbed directly into the C V system
3 More reliable absorption of drug
4 Pt cooperation is not as essential
Disadvantages
1 Time factor ndash its 15 min latent period
2 Pt may not be willing to accept the injection
3 The prolonged duration of action(2-4 hrs more)
4 Possibility of injury to the tissues at the site of injection caused by either the drug or the needle
4
Sites of I M administration
1 Gluteal area
2 Vastus lateralis
3 Mid ndash deltoid area
Drugs
Diazepam
Midazolam
Hydroxyzine
Inhalation Sedation
Advantages
1 The onset of action is more rapid
2 Peak clinical level is achieved rapidly(3-5min) - permit titration
3 Administrator has complete control over the actions of the drug - safety feature
4 No significant over dosage
5 Flexible duration of action
6 Recovery time is rapid amp most complete
7 No injection is required
8 With N2O- O2 it is safe with very few side effects
Disadvantages
1 The initial cost of the equipment is high 2 The continuing cost of the gases is high 3 The equipment occupies considerable space 4 N2O is not a potent agent 5 A degree of cooperation is required from the pt 6 Chronic exposure to N2O is deleterious to the health of
dental personnel
Contraindications
1 Nasal obstruction 2 Cyanosis at rest 3 Poor cooperation 4 1st trimester of pregnancy 5 Fear of masks
I V Sedation
Advantages
1 The onset of action is the most rapid 2 The dosage may be titrated 3 Suitable level of sedation can be provided 4 The recovery period is shorter 5 Side effects are extremely uncommon 6 Control of salivary secretions is possible 7 The gag reflex is diminished 8 Effectively diminishes motor disturbances 9 Provides immediate access to CVS in emergency
Disadvantages
1 Venipuncture is necessary
2 Complication may rise at the site of the venipuncture
3 Monitoring must be more intensive
4 Recovery is not complete at the end of the procedure
5 Reversal of sedation is difficult
5
N2O-O2 (Relative Analgesia)
colorless sweet smelling gas
Pharmacokinetics
Absorption through pulmonary epithelium
It is approx 15 times as soluble as is nitrogen It replaces nitrogen in blood
It is carried in solution in plasma of the blood
It is not metabolized by the body
Elimination ndash majorndash lungs minor --- skin
perspiration urine and intestinal gas
Pharmacodynamics
Dose related
10 ndash 25 Lightheaded
Changes in visual amp auditory sensation
Tingling of hands amp feet
Suffusing warmth
Remote from the immediate environment
Reduced anxiety
25-50 max analgesic properties and aberration of vision hearing and proprioception mild drowsiness euphoria amnesia and increased sleepiness and dreams
35 conc will achieve maximum analgesia
bull CNS
ndash Cerebrum-primarily affected
ndash Safe but weak anesthetic agent
bull RESPIRATORY SYSTEM
ndash Increased Tidal and minute volumes
bull CARDIOVASCULAR SYSTEM
ndash 2 studies ndash decreased cardiac output
bull FETAL SYSTEMS
ndash Miscarriage in humans
bull OTHER SYSTEMS
ndash Depression of spinal reflexes increase muscle tone indicates stage of delirium
ndash Muscle rigidity-narcotics + nitrous oxide
ndash Nausea and vomitting - GIT
ndash HEMATOPOIESIS ----- prolonged exposure
Adverse reactions and toxicity
EMOTIONAL REACTIONS
DREAMS HALLUCINATIONS
No acute toxicity
Chronic toxicity ndash bone marrow
depression
PROCEDURE
Diffusion Hypoxia
Sevoflurane
A fluorinated derivative of isopropyl ether ndash synthesized in 1970
Potent anaesthetic agent with rapid uptake amp speedy recovery
Day-case surgery
Problem
Attaching vaporiser to any of the currently available machine
BENZODIAZEPINES
Diazepam 1961 lipid soluble
Uses-alcoholism epilepsy labor tetanus and cerebral palsy
- sedation and amnesia
- varieties of neurosis amp anxiety states
Pharmacokinetics
Orally Rectal IMIV or SC
Well absorbed through GIT
Excretion in urine
6
bull Pharmacodynamics
ndash Depress the brain stem reticular system and the limbic system thalamus and hypothalamus
ndash It is a centrally acting muscle relaxant Has anti-convulsant properties
Adverse reaction amp toxicity
ndash Confusion nausea headache increased appetite decreased salivation and jaundice Thrombophlebitis
ndash Rebound phenomenon
ndash Toxicity drowsiness confusion sleep and coma
Dosage Oral or Rectal ndash 02-05mgkg
Maximum single dose 10mg
IV- 025mgkg
Supplied Tablets 2 5 10 mg
Suspension ndash 5mg
Midazolam Water soluble ndash non-irritant
Oral IM IV
Metabolism- liver
Onset IV 3 -5mins
oral 20 ndash 30mins
Oral administration anxious patients requiring relatively short dental procedure
No rebound phenomenon
Better anxiolysis amp amnesia (retrograde amnesia)
Adverse effects Respiratory depression
dose dependant apnea
Dosage Oral ndash 025 to 1mgkg to maximum single dose 20mg
IM ndash 01 to 015mgkg to a maximum of 10mg
IV ndash slow IV
Supplied Syrup ndash 2mgml
Injectable ndash 1mgml amp 5mgml vials
Flumazenil specific benzodiazepines antagonist
selectively inhibits CNS effects
IV administration amp not recommended below 18yrs of age
02mg over 15 seconds after 45seconds 02mg then after 60seconds to maximum of 1mg
Sedative-Hypnotics
Barbiturates First truly effective drugs for the management of anxiety Generalized CNS depressants Produce dose dependent effects
Sedation ---- sleep ---- GA ---- coma
Suppress the CNS and result in sedation and amnesia Advantages
Rapid onset and short duration Disadvantages
no analgesic effect and possible hypotension Must be used with caution in trauma patients because they may cause
apnea and hypoventilation
DOSE Pentobarbital Sodium 100mg Secobarbital Sodium 100 to 200mg Children 30 to 100mg
bull Chloral Hydrates (Mickey Finn Knock out drops ) First synthesized in 1832 first member of the hypnotic group of drugs
Widely used as conscious sedation agent
Properties
Unpleasant taste
Nausea vomiting
Quite irritating to skin and to mucous membranes
GI irritation
Dosages Individualized for each patient 25 ndash 50mgkg
maximum of 1g
Supplied oral capsule ndash 500mg
oral solution ndash 250 amp 500mg5ml
Rectal suppositories ndash 324 amp 648mg
Narcotics
Do produce sedation amp euphoria greater in children
LA is required but dose should be decreased
Meperidine Synthetic opiate agonist
Very water soluble
Orally SC IM or IV
Peak effect by oral 1 hr amp lasts upto 4 hrs
Adverse reactions
-Seizures
-Extreme caution in hepatic or renal diseases or history of seizures
7
Dosage Oral SC or IM ndash 1to 22mgkg not to exceed 100 mg
Supplied Oral Tablets ndash 50 amp 100mg
Oral Syrup ndash 50mgml
Parental solution ndash 25 50 75 amp 100mgml
Fentanyl
Synthetic opiate narcotic analgesic
Very potent 01mg = 10mg Morophine75mg Meperidine
Pharmacokinetics
IV IM SM
Metabolized in liver Excreted in urine
Fentanyl Onset ndash 7 to 15mins
Duration ndash 1 to 2 hrs
Pharmacodynamics
Respiratory depression RR but returns to normal rapidly Tidal volume amp response to co2 depressed for extended period
Apnea
Less emetic than meperidine
NOT RECOMMENDED IN CHILDREN BELOW 2yrs
Dosage 0002 to 0004mgkg
Supplied 005mgml in 2 amp 5ml ampoules
Reversal drug Naloxone
Semisynthetic opiate antagonist
No agonist activity
Onset 2 to 5mins SC or IM amp 1 to 2mins IV
Reversal 45mins
Pt should be kept under continual surveillance
Adverse reaction nausea vomiting sweating hypotension hypertension ventricular tachycardia fibrillation
Dosage IV SC IM 001mgkg then 01mgkg every 2- 3mins maximum 2mg
Supplied 002 004 1mg solutions
Antihistamines
Hydroxyzine
Oral or IM
Effect ndash 15 ndash 30mins
Half-life ndash 3 hrs
Uses
To relieve anxiety
Used as an anti-histamine
Used to control nausea and vomiting including that associated with motion sickness and pregnancy
Adverse reaction dry mouth drowsiness hypersentivity
Dosage Oral ndash 1 to 2mgkg
IM ndash 11mgkg
Promethazine Oral or IM Onset 15 to 60mins Duration 4 to 6 hrs Uses
To prevent and treat nausea and vomiting associated with motion pregnancy or surgery
Produces sedation and reduce swelling pain and trismus
Lower seizure threshold Adverse reaction dry mouth blurred vision thickening of bronchial secretions Dosage OralIM ndash 05-11mgkg
maximum 25 mg
Diphenhydramine
Oral IM IV
Onset -1hr
Duration ndash 4 to 6 hr
Metabolized in liver
Adverse reaction disturbed coordination thickening of bronchial secretions
Dosage Oral IM IV ndash 1 to 15mgkg
maximum 50mg
Tranquilizers
Major tranquilizer antipsychotic produce calmness control symptoms of psychoses cause reversible extra pyramidal symptoms and do not tend to cause habituation
Minor tranquilizer antianxiety agents also cause calmness do not cause extrapyramidal symptoms Used in conditions like nervous tension and mild depression
8
Classification
Antipsychotics
Phenothiazine derivatives
Chlorpromazine promazine
Butryophenones
Haloperidol
Rauwolfia alkaloids
Reserpine
Antianxiety drugs
Propyl alcohol derivatives
Meprobamate
Benzodiazepine derivatives
Diazepam
Miscellaneous compounds
Hydroxyzine
Meprobamate
White crystalline powder slightly bitter in taste
Only administered orally
Peak blood concentration ----1 to 3hrs
10 ---------excreted unchanged Rest --- excreted as a oxidized derivative or as a glucoronide
Uses
To relieve day time anxiety
Induce sleep in insomniacs
To reduce anxiety associated with dental treatment
Anti-convulsant ndash petit mal epilepsy
Adverse reaction leucopenia acute non-thrombocytopenic purpura ecchymoses eosinophilia edema adenopathy
Dosage Childrengt 6yrs 100 to 200mg
Not recommended for children under 6yrs
Monitoring during sedation
1 Pulse
2 Blood pressure
3 ECG
4 Respiration
5 Temperature
Pulse
Manual Electronic
bull Radial Brachial
bull Facial labial
Blood pressure
ndash Stethoscope amp sphygmomanometer
ndash Automatic devices
ndash Direct cannulation of an artery ndash very accurate
Electrocardiograph
Heart rate rhythm myocardial function
9
Respiration
ndash Monitoring respiratory rate
ndash Observing the rise amp fall of the chest wall
ndash Observing the color of mucous membrane
ndash Observing the inflation amp deflation of the reservoir bag
Devices for monitoring respiration
1 The Precordial pretracheal stethoscope
2 The esophageal stethoscope
ndash Respiratory rate
ndash Heart rate
ndash Any abnormal sounds
Pulse Oximeter
ndash Oxygen saturation
ndash Heart rate
ndash Oxisensor site
ndash Fingers
ndash Toe
ndash Ear lobe
Mechanism
Oxygenated Hb ndash red light
Deoxygenated Hb- infrared light
Tissue pressure from arterial pulse (plethysmography)
Advantages
ndash Safe amp noninvasive
ndash Simple to use
ndash Information is rapidly available for clinical decision
ndash Indirectly indicates respiratory adequacy
Disadvantages
ndash Finger probes can get dislodged
ndash Emitted light source may cause burning
ndash Non reusable probes are expensive
ndash Does not directly determine airway patency
Capnography
1 The presence absence of air flow
2 Indicates depth amp adequacy of respiration
3 Continues analysis of the co2 content of the respired air ndash indicates respiratory adequacy
Temperature
ndash Disposable nondisposable thermometer
ndash Esophageal rectal temp probe
10
Discharge criteria
Cardiovascular function is satisfactory amp stable
Airway patency is uncompromised amp satisfactory
Pt is easily arousable amp protective reflexes intact
State of hydration is adequate
Pt can talk if applicable
Pt can sit unaided if applicable
Pt can ambulate with minimal assistance if applicable
Presedation level of responsiveness achieved
Responsible individual is available
1
PULP THERAPY OF VITAL TEETH
DR MITAKSHARA NIRWAN
Contents
Indirect pulp capping
Direct pulp capping
Medications amp materials used in pulp capping
Pulpotomy
MTA
Apexogenesis
INDIRECT PULP CAPPING
Pieter Van Forest - first to speak about root canal therapy
Glove designed instruments that could prepare a canal to a certain size and taper(1910)
Indirect pulp capping is defined as a procedure where in small amount of carious dentin is retained in
deep areas of cavity to avoid exposure of pulp followed by placement of a suitable medicament and
restorative material that seals off the carious dentin and encourages pulp recovery (Ingle)
A procedure in which only the gross caries is removed from the lesion and the cavity is sealed for a
time with a biocompatible material (McDonald)
Objective of indirect pulp capping
These were given by Eidelman in 1965
bull Arresting the carious process
bull Promoting dentin sclerosis
bull Stimulating formation of tertiary dentin
bull Remineralization of carious dentin
Layers of Carious Dentin Indications of Indirect Pulp Capping
History
Mild pain associated with eating
Negative history of spontaneous extreme pain
Clinical Examination
Deep carious lesion which are close tobut not involving the pulp in vital primary or young
permanent teeth
No mobility
Nominal pulp inflammationdefinite layer of affected dentin after removal of infected dentin
Radiographic examination
Normal lamina dura amp PDL space
No radiolucency around the apices
2
Contraindications of Indirect Pulp Capping
History
Sharp penetrating pulpalgia
Prolonged spontaneous pain especially at night
Clinical examination
Mobility of tooth
Discoloration of tooth
Negative reaction of electric pulp testing
Radiographic examination
Definite pulp exposure
Break in the lamina dura
Radiolucency around the apices
Widened PDL space
Treatment procedure
Sequelae of Indirect Pulp Capping Three distinct types of new dentin formation take place
1 Cellular fibrillar dentinmdashfirst 2 months
2 Globular dentinmdash3 months
3 Tubular dentin (uniform mineralized dentin)
bull 15th of reparative dentin formation begins in less than 30 days
bull After 3 months 01 mm is formed
DIRECT PULP CAPPING Defined by Kopel (1992) as the placement of a medicament or non medicated material on a pulp that
has been exposed in course of excavating the last portions of deep dentinal caries or as a result of
trauma
Objective
To create new dentin in the area of the exposure and subsequent healing of the pulp
Rationale
achieve a biologic closure of the exposure site by deposition of hard tissue barrier (dentin bridge)
between pulp tissue and capping material thus walling off the
INDICATIONS
Small mechanical exposure
Easily controlled haemorrhage
Bright red haemorrhage
True pinpoint exposure
CONTRAINDICATIONS
Severe toothache at night
Spontaneous pain
Tooth mobility
Radiographic appearance of pulp periradicular de- generation
Excess of hemorrhage at the time of exposure Serous exudate from the exposure
Externalinternal root resorption
Swellingfistula
Histological Changes after Pulp Capping
These were illustrated be Glass and Zander in 1949
After 24 hours Necrotic zone adjacent to calcium
hydroxide paste is separated from healthy pulp
tissue by a deep staining basophilic layer
After 7 days Increase in cellular and fibroblastic
activity
After 14 days Partly calcified fibrous tissue lined by
odontoblastic cells is seen below the calcium
proteinate zone disappearance of necrotic zone
After 28 days Zone of new dentin
3
Medications and Materials Used for Pulp Capping Calcium hydroxide
Corticosteroids amp antibiotics
Inert materials
Collagen fibers
4-META adhesive
Direct bonding
Isobutyl cyanoacrylate
Denatured albumin
Mineral trioxide aggregate
Laser
Bone morphogenic protein
PULPOTOMY
Finn (1995) defined it as the complete removal of the coronal portion of the dental pulp
followed by placement of a suitable dressing or medicament that will promote healing and
preserve vitality of the tooth
American Academy of Pediatric Dentistry (1998) defined pulpotomy as the amputation of
affected infected coronal portion of the dental pulp preserving the vitality and function of the
remaining part of radicular pulp
Objectives
bull Removal of inflamed and infected coronal pulp at the site of exposure thus preserving the vitality of the
radicular pulp and allowing it to heal
bull Maintain the tooth in the dental arch
Rationale
bull Radicular pulp is healthy and capable of healing after surgical amputation of the infected coronal pulp
bull Preserves vitality of the radicular pulp
bull Maintains tooth in a physiologic condition
Indications of Pulpotomy bull Mechanical pulp exposure in primary teeth
bull Teeth showing a large carious lesion but free of radicular pulpitis
bull History of only spontaneous pain
bull Hemorrhage from exposure sites bright red and can be controlled
bull Absence of abscess or fistula
bull No interradicular bone loss
bull No interradicular radiolucency
Contraindications of Pulpotomy bull Persistent toothache
bull Tenderness on percussion
bull Root resorption more than 13rd of root length
bull Large carious lesion with nonrestorable crown
bull Highly viscous sluggish hemorrhage from canal orifice which is uncontrollable
bull Medical contradictions like heart disease immuno compromised patient
bull Swelling or fistula
bull External or internal resorption
bull Pathological mobility
bull Calcification of pulp
Classification of pulpotomy
4
Formocresol Pulpotomy
Iby BUCKLEY in 1904
Sweet (1930) Formulated multi visit technique
Doyle (1962) Advocated 2 sitting procedure (complete devitalization)
Spedding (1965) Gave 5 minute protocol (partial devitali- zation)
Venham (1967) Proposed 15 seconds procedure
Current concept uses 4 minutes of application time
Composition of formocresol Buckleyrsquos Formula
bull Cresol ndash 35 percent
bull Glycerol ndash 15 percent
bull Formaldehyde ndash 19 percent
bull Water ndash 31 percent
Mechanism of Action
It prevents tissue autolysis by bonding to the proteins Bonding is of peptide groups of side chain amino acids and is a reversible process accomplished without
changing the basic structure of protein molecules
Histological Changes
bull Demonstrated by Mass and Zilbermann11 in 1933 and also by Massler and Mansokhani in 1959
bull Immediately the pulp becomes fibrous and acidophillic
bull Seven to fourteen days Three zones appear
a broad eosinophilic zone of fixation
b broad pale-staining zone of atrophy with poorcellular definition
c broad zone of inflammation extending apically into normal pulp tissue
bull One yearndash Progressive apical movement of these zones with only acidophillic zone left at the end of 1 year
Modified Formocresol Pulpotomy
Used by TRASK(1972)
The technique is identical to that described for primary teeth except that the formocresol pellet is
sealed permanently in the tooth
Two-visit Devitalization Pulpotomy
Indications
bull There is evidence of sluggish bleeding at the amputation site that is difficult to control
bull Pus in the chamber but none at the amputation site
bull There is thickening of the PDL
bull History of pain
Contraindications
bull Nonrestorable tooth
bull Tooth with necrotic pulp
5
Glutaraldehyde Pulpotomy
It was first suggested by S Gravenmade Introduced by Kopel in 1979
Mechanism of Action
bull Glutaraldehyde produces rapid surface fixation of the underlying pulpal tissue
bull A narrow zone of eosinophilic stained and compressed fixed tissue is found directly beneath the area of application which blends into vital normal appearing tissue apically
bull With time the glutaraldehyde fixed zone is replaced by macrophagic action with dense collagenous tissue thus the entire root canal tissue is vital
Cvekrsquos Pulpotomy
bull This is also called as calcium hydroxide pulpotomy or young permanent partial pulpotomy
bull This was proposed by Mejare and Cvek16 in 1978
bull Indicated in young permanent teeth where the pulp is exposed by mechanical or bacterial means and the
remaining radicular tissue is judged vital by clinical and radiographic criteria whereas the root closure is
notcomplete
MINERAL TRIOXIDE AGGREGATE (MTA) Torabinejad described the physical and chemical properties of MTA in 1995
It is ash colored powder made primarily of fine hydrophilic particles of
1 tricalcium aluminate
2 tricalcium silicate
3 silicate oxide
4 tricalcium oxide
5 bismuth dioxide
Hydration of the powder results in a colloidal gel composed of calcium oxide crystals in an amorphous
structure This gel solidifies into a hard structure in less than three hours
PROPERTIES OF MTA
It is biocompatible material and its sealing ability is better than that of amalgam or ZOE
Initial pH is 102 and set pH is 125
The setting time of cement is 4 hours
The compressive strength is 70 MPA which is comparable with that of IRM
Low cytotoxicity ndash It presents with minimal inflammation if extended beyond the apex
Mineral trioxide aggregate (MTA) has demonstrated the ability to induce hard-tissue formation in
pulpal tissues and it promotes rapid cell growth
APEXOGENESIS
It is defined as the treatment of a vital pulp by capping or pulpotomy in order to permit continued
growth of the root and closure of the open apex
Rationale
Maintenance of integrity of the radicular pulp tissue to allow for continued root growth
Indications
bull Indicated for traumatized or pulpally involved vital permanent tooth when root apex is incompletely formed
bull No history of spontaneous pain
bull No sensitivity on percussion
bull No hemorrhage
bull Normal radiographic appearance
Contraindications
bull Evidence that radicular pulp has undergone degenerative changes
bull Purulent drainage
bull History of prolonged pain bull Necrotic debris in canal
bull Periapical radiolucency
6
1
Gupta A Dhingra R Chaudhari P Gupta A
Department of Paedodontics and Preventive Dentistry Faculty of Dental Sciences SGT University Gurgaon Haryana India
Journal of Indian Society of Pedodontics and Preventive Dentistry
Volume 35 I Issue 3 I July-September 2017
A COMPARISION OF VARIOUS MINIMALLY
INVASIVE TECHNIQUES FOR THE REMOVAL
OF DENTAL FLUOROSIS STAINS IN
CHILDREN
DR MITAKSHARA NIRWAN
CONTENTS
bull Introduction
bull Aims
bull Materials and Methods
bull Results
bull Discussion
bull Conclusion
bull Critical analysis
bull References
INTRODUCTION
bull Dental fluorosis is a developmental disturbance of dental enamel caused by
successive exposure to high concentrations of fluoride during tooth
development
bull Various methods of therapy are advocated for the treatment of fluorosis -
stained teeth which range from invasive ceramic veneer bonding restorations
to abrasive chemical treatments
bull The combination of dental bleaching techniques and microabrasion appears
as an excellent conservative solution to reestablish health in fluorosis
affected teeth
AIMS
bull The aim of the study was to evaluate and compare the effectiveness of
minimally invasive techniques for the removal of dental fluorosis
stains in children in vivo
MATERIALS AND METHODS
Patients visiting the department of Pedodontics and Preventive dentistry
Faculty of Dental Sciences SGT University Gurgaon
bull Sample size 90 patients
bull Age group 10 -17 years
bull Caries cracks or periodontal
disease on anterior teeth
bull Abscess draining sinus
cellulitis
bull Non vital teeth
hypersensitive exposed
crevices
bull Orthodontic appliance
bull Past history of bleaching
bull At least two permanent
maxillary anterior teeth
bull TSIF of score 4
bull Free of systemic diseases
Inclusion criteria Exclusion criteria
2
Groups
Group A In office bleaching with 35 hydrogen peroxide( Pola Office
Bleaching kit) activated by light emitting diode (LED) bleaching unit
(35 HP)
Group B Enamel microabrasion (EM) (PREMA Enamel Microabrasion
System) followed by in-office bleaching with 44 carbamide peroxide
gel (EM)
Group C In-office bleaching with 5 sodium hypochlorite (5
NaOCl)
A baseline colour evaluation was done by taking digital photograph of
the maxillary anterior teeth
RESULTS
Group 1
Colour stability
Group 2 Group 3
Tooth sensitivity
Tooth sensitivity values were taken before the treatment
which was compared to immediate postoperative and follow
up visits It was checked using an electric pulp tester
maximum
moderate
least
immediately
group 2
group 1
group 3
1 month
group 2
group 1
group 3
3 month
group 2
group 1
group 3
Patient satisfaction score
Satisfaction was assessed on visual analog scale
Range 1 to 5
Groups percentage of patients
who were satisfied with
the treatment
Number of patients
who reported slight
reappearance of colour
Group 1
90
7
Group 2
83
8
Group 3
73
7
3
Number of Appointments
Groups One sitting Two sittings Three
sittings
Group 1
25
4
1
group 2
26
3
1
Group 3
30
0
0
DISCUSSION
bull Hydrogen peroxide is capable of penetrating the tooth osmosis and through porosities and cracks subsequently acting directly on the pigmented molecules
bull Gurgan et al investigated 3 different light systems and found out that diode laser system with gave best tooth whitening and least tooth sensitivity
bull In the EM group the surface reflects and refracts light from the surface in such way that mild imperfections in underlying enamel are camouflaged While the highly polished surface of enamel enhances the aesthetic appearance
bull Train et al and Loguercio et al also had the similar results in their studies with EM mild fluorosis showed best results moderate showed moderate results while it had little effect on severe fluorosis
bull NaOCl was only effective on mild stains while moderate and severe
stains could only be lightened to quite an extent but could not be
completely removed
bull When NaOCl comes in contact with hypomineralized and discoloured
enamel it degrades and removes the chromogenic organic material
located on the enamel surface
CONCLUSION
bull It was concluded that esthetic appearance of teeth mild fluorosis can
be achieved by bleaching and microabrasion But in cases of
moderate fluorosis a combination of any of theses modalities can be
used
bull As no special maintenance precautions are required these maybe be
considered as an interesting alternative to conventional operative
treatment
bull Focuses on only TSIF of 4
bull Electric pulp testing is not the
right method to check for
sensitivity
bull Tooth Sensitivity changes
from person to person
bull Food habits can cause
staining of the teeth
bull Minimally invasive
bull Cheaper to veneers
bull Minimal loss of tooth structure
bull 4 parameters checked for the success of treatment
bull Inclusion of specific score of fluorosis for comparing the results
bull Maximum 3 appointments needed
CRITICAL ANALYSIS
Pros Cons
REFERENCES
bull Gurgan S Cakir FY Yazici E Different light-activated in officebleaching
systems Lasers Med Sci 201025817-22
bull Train TE McWhorter AG Seale NSWilson CF Guo IY Examination of
esthetic improvement and surface alteration following microabrasion in
fluorotic human incisors in vivoPediatr dent 199618353-62
bull Loguercio AD Correia LD Zago C Tagliari D Neumann E Gomes OM et al
Clinical effectiveness of two microabrasion materials materials for the
removal of enamel flurosis stains Oper Dent 200732531-8
4
2
bull THE BIOLOGICAL EFFECTS OF CITRIC ACID ON THE PERIODONTAL STRUCTURE HAS BEEN
EXTENSIVELY STUDIED IN PERIODONTICS
bull NEUMAN AND NEWMAN SHOWED THAT CITRIC ACID IS THE MOST EFFECTIVE ACID IN
ALTERING THE SOLUBILITY OF HYDROXYAPATITE
bull YAMAGUCHI ET AL SHOWED THAT CITRIC ACID SOLUTION HAD ANTIBACTERIAL EFFECTS ON
ALL 12 ROOT CANAL BACTERIA TESTED
bull ARIAS-MOLIZ ET AL SHOWED THAT ETHYLENEDIAMINETETRAACETIC ACID (EDTA) HAS NO
BACTERICIDAL ACTIVITY EVEN AFTER 1 HOUR CONTACT
bull THIS ACID HAS THE ABILITY OF ROOT CANAL IRRIGATION AND ALSO SMEAR LAYER REMOVAL
DIFFERENT CONCENTRATIONS (1ndash50) HAVE BEEN PROPOSED GUTMANN ET AL CONCLUDED
THAT 10 CITRIC ACID IS BETTER THAN ULTRASOUND FOR SMEAR LAYER REMOVAL FROM THE
ROOT END CAVITIES
7
bull STUDIES HAVE SHOWN IRRIGATION WITH 6 CA FOR 15 OR 30 SECONDS IS QUITE
EFFECTIVE IN REMOVING ALL THE COMPONENTS OF THE SMEAR LAYER OF THE PRIMARY
TEETH WHEREAS PERITUBULAR DENTIN DESTRUCTION WAS OBSERVED WHEN HIGHER
CONCENTRATION OF CITRIC ACID WAS USED AS AN IRRIGATING SOLUTION
8
AIMS amp OBJECTIVES
bull THIS STUDY WAS AIMED TO EVALUATE THE CLINICAL AND RADIOGRAPHIC OUTCOME OF
PULPECTOMY ALONG WITH QUALITY OF OBTURATION USING 6 CITRIC ACID AND
ENDOACTIVATOR
9
CASE REPORT
bull 350 CHILDREN (3-9 YEARS) WITH CLINICAL SIGNS AND SYMPTOMS OF CHRONIC IRREVERSIBLE
PULPITIS IN DEEPLY CARIOUS TEETH WERE SCREENED DURING SCHOOL DENTAL HEALTH
PROGRAM FROM MAY 2014-JULY 2014
bull 123 CHILDREN REPORTED TO THE DEPARTMENT AND 67 CHILDREN WERE SELECTED BASED ON
INCLUSION AND EXCLUSION CRITERIA
RECRUITMENT OF PATIENTS
10
INCLUSION CRITERIA
bull HISTORY OF SPONTANEOUS PAIN AND UNCONTROLLED BLEEDING AFTER PULP AMPUTATION
EXCLUSION CRITERIA
bull EVIDENCE OF INTERNAL OR EXTERNAL (PHYSIOLOGICPATHOLOGIC) ROOT RESORPTION OF MORE THAN A THIRD OF ITS LENGTH
bull ROOT CANAL OBLITERATION OR ANATOMIC ANOMALIES
bull INADEQUATE BONE SUPPORT OR NON RESTORABLE TOOTH
bull ONCE PATIENTS ELIGIBILITY WAS CONFIRMED THE TREATMENT PROCEDURE WAS
EXPLAINED TO THE PARENTGUARDIAN AND INFORMED WRITTEN CONSENT WAS
OBTAINED FROM PARENTSGUARDIANS SHOWING WILLINGNESS FOR THEIR
CHILDRENS TREATMENT 11
PROCEDURE
bull PULPECTOMY WAS PERFORMED BY ONE OPERATOR OF PEDIATRIC DENTISTRY DEPARTMENT
USING A STANDARDIZED TREATMENT PROTOCOL FOR ALL THE PATIENTS
bull AFTER ADMINISTRATION OF LOCAL ANESTHESIA RUBBER DAM WAS APPLIED FOR ISOLATION
bull ACCESS CAVITY WAS PREPARED USING AIR-ROTOR HAND PIECE WITH 8 ROUND BUR AND
PULP TISSUE WAS EXTIRPATED WITH THE HELP OF SPOON EXCAVATOR
bull FURTHER THE NEGOTIATION OF THE CANALS WAS DONE WITH 10 K-FILE
bull A DIAGNOSTIC RADIOGRAPH WAS TAKEN FOR ROOT LENGTH DETERMINATION AND
WORKING LENGTH WAS KEPT 1 MM SHORT OF THE RADIOGRAPHICAL APEX
bull ALL ROOT CANALS WERE INSTRUMENTED MANUALLY USING K-FILES AND WERE IRRIGATED
WITH 10 ML 09 NORMAL SALINE AND 1 SODIUM HYPOCHLORITE AS STANDARDIZING
PROTOCOL FOR ROOT CANAL PREPARATION AND DISINFECTION
12
3
GROUP 1 (CA + E) - IRRIGATION WAS DONE
WITH 10 ML OF 6 CITRIC ACID (CITOCID AMMDENT)
AND IRRIGANTS WERE SONICALLY AGITATED WITH
ENDOACTIVATOR (DENTSPLY) FOR 30 S PER CANAL USING REDBLUE
ENDOACTIVATOR TIP
GROUP 2 (CA) - 10 ML OF 6 CITRIC ACID FOR 1 MIN USING
27 GAUZE IRRIGATING NEEDLE
GROUP 3(SH + E) - 10 ML OF 1 SODIUM HYPOCHLORITE
SOLUTION AND SONIC ACTIVATION WITH ENDOACTIVATOR
GROUP 4(SH) - 10 ML OF 1 SODIUM HYPOCHLORITE
SOLUTION USING IRRIGATING NEEDLE (CONTROL GROUP)
bull TEETH UNDERGOING PULPECTOMY WERE RANDOMLY ENROLLED BY CHIT METHOD INTO THREE
STUDY AND ONE CONTROL GROUP
13
bull IN CITRIC ACID GROUPS FINAL RINSE WITH NORMAL SALINE WAS DONE TO REMOVE THE
REMAINING CRYSTALS (CHELATES)
bull FOLLOWING BIOMECHANICAL PREPARATION THE ROOT CANALS WERE DRIED WITH STERILE
ABSORBENT PAPER POINTS AND OBTURATED WITH VITAPEX USING HAND HELD
LENTULOSPIRAL FINAL RESTORATIONS WERE DONE USING COMPOSITE RESIN
14
bull CLINICAL FOLLOW UP WAS DONE AT 24 H1 WEEK 1 MONTH 6 MONTH AND 12
MONTH TO CHECK PAIN PRESENCE AND PAIN FREQUENCY (ONCEMORE THAN ONCE)
SWELLING FISTULA SENSITIVITY TO PERCUSSION
bull RADIOGRAPHIC FOLLOW UP WAS DONE AT 6 MONTH AND 12 MONTH FOR ANY
DEVIATED ERUPTION OF SUCCEDANEOUS TEETH EXCESS FILING MATERIAL AND ITS
RESORPTION EXTERNALINTERNAL ROOT RESORBTION CALCIFIC METAMORPHOSIS
PRESENCE OF FURCATION RADIOLUCENCY
CLINICAL amp RADIOGRAPHIC FOLLOW UP
15
RADIOGRAPHIC ASSESSMENT OF OBTURATION QUALITY
bull POSTOPERATIVE RADIOGRAPHS WERE VISUALLY ASSESSED FOR QUALITY OF OBTURATION BY
TWO INDEPENDENT EXAMINERS (SG AD) WHO WERE BLINDED WITH REGARD TO
IRRIGATION PROTOCOL GROUP TO ENHANCE CALIBRATION EACH EXAMINER ASSESSED THE
RADIOGRAPH INDEPENDENTLY AND LATER REVIEWED TOGETHER FOR FINAL ASSESSMENT
INDIVIDUAL ROOT WAS TAKEN AS UNIT OF ANALYSIS FOR GRADE OF OBTU- RATION AND
SCORING CRITERIA WERE AS GIVEN BY COLL JA 1996
1 UNDER FILLED - FILLING MATERIAL ENDED 1 MM OR MORE SHORT OF THE APEX
2 OPTIMAL FILLING- FILLING MATERIAL APPEARED TO END AT THE RADIOGRAPHICAL APEX
3 OVERFILLED - FILLING MATERIAL EXTRUDED PAST THE RADIOGRAPHIC APEX
4 OPTIMALLY FILLED ROOTS WERE FURTHER ASSESSED FOR THE PRESENCE OF VOIDS AND VOID
AREA (ROOT CANAL SURFACE UNTOUCHED BY THE ROOT CANAL FILLING MATERIAL) IN THREE
VISUALLY DIVIDED SECTIONS OF THE ROOT IE CORONAL MIDDLE AND APICAL 13RD
16
RESULTS
bull OVERALL CLINICAL AND RADIOGRAPHIC SUCCESS RATE OVER A PERIOD OF ONE YEAR WAS
9886 amp 977 RESPECTIVELY
bull ALL GROUPS WERE SIGNIFICANTLY (P = 001) EFFECTIVE IN ALLEVIATING PAIN WITHIN 24 H
OF PULPECTOMY
17 18
4
19
bull IMMEDIATE POST OPERATIVE RADIOGRAPHIC ASSESSMENT REVEALED 68 (102150) ROOTS
WITH OPTIMAL OBTURATION AND 32 (48150) WITH OVERFILLINGUNDERFILLING MAXIMUM
NO OF OPTIMAL FILLINGS WERE OBSERVED IN GROUP1 (CA + E) (3333) FOLLOWED BY
GROUP 2 (CA) (2549) GROUP 3(SH + E) (2549) AND GROUP 4(SH) (1568)
bull CITRIC ACID GROUPS HAD MORE NUMBER OF OPTIMALLY FILLED ROOTS 588 (60102) THAN
NON CITRIC ACID GROUPS 412 (42102)
bull ENDOACTIVATOR CONTRIBUTED TO 18 OF OPTIMAL OBTURATION IRRESPECTIVE OF
CHELATING AGENT USED
20
21
bull MAXIMUM NO OF VOIDS AND VOID AREAS WERE IN NON CITRIC ACID GROUPS
(6419 amp 5384) COMPARED TO CITRIC ACID GROUPS (3580 amp 4615)
RESPECTIVELY
bull ANALYSIS OF ROOT 13RD REVEALED MAXIMUM NO OF VOID AREA IN APICAL
13RD (4755) FOLLOWED BY MIDDLE 13RD (3846) AND CORONAL 13RD
(1398)
bull LEAST NO OF VOIDS amp VOID AREA (1111 amp 1608) WERE OBSERVED WHEN
ENDOACTIVATOR ALONG WITH CHELATING AGENT WAS USED (GROUP 1)
HOWEVER THIS WAS STATISTICALLY INSIGNIFICANT
22
DISCUSSION
bull IN THE PRESENT STUDY 1 SODIUM HYPOCHLORITE WAS USED ALONG WITH 6 CITRIC ACID
(CHELATING AGENT) WHICH IS REPORTED TO BE AS EFFECTIVE AS 17 EDTA
bull CITRIC ACID (BIOLOGICAL ACID) IS FOUND TO BE BIOCOMPATIBLE AND LEAST IRRITATING TO
PERIAPICAL TISSUES THAN OTHER CHELATING AGENTS
bull USE OF SODIUM HYPOCHLORITE SOLUTION FOLLOWING CHELATING AGENT WAS AVOIDED AS IT
RAPIDLY PRODUCES SEVERE EROSION OF ROOT CANAL WALL DENTIN
bull TRADITIONAL APPROACH OF DELIVERING IRRIGANTS INTO THE ROOT CANAL SPACE USING
SYRINGES AND METAL NEEDLES HAS BEEN FOUND TO BE INEFFECTIVE ESPECIALLY IN THE AREAS OF
ANASTOMOSES BETWEEN CANALS AND APICAL 13RD OF ROOT CANAL
23
bull THEREFORE TO ACHIEVE BETTER CLEANING EFFICIENCY IRRIGANT ACTIVATION HAS BEEN
RECOMMENDED SONIC ACTIVATION HAS BEEN REPORTED TO RESULT IN BETTER ROOT CANAL
CLEANLINESS AS COMPARED TO NO ACTIVATION OF IRRIGANT
24
5
CONCLUSION
bull USE OF 6 CITRIC ACID DEFINITELY HELPED IN RAPID ELIMINATION OF PAIN RESOLUTION OF
PERI-RADICULAR RADIOLUCENCY BETTER OBTURATION QUALITY IN TERMS OF LESS VOIDS AND
VOID AREAS ALONG WITH MAXIMUM NO OF OPTIMAL OBTURATION UP TO APICAL AREA
bull 6 CITRIC ACID AND ENDOACTIVATOR IRRIGATION PROTOCOL PROVED TO BE THE BETTER
IRRIGATION PROTOCOL WHICH MAY CONTRIBUTE TO LONG TERM SUCCESS OF PRIMARY
TOOTH AND THE HEALTH OF UNDERLYING PERMANENT TOOTH
bull 6 CITRIC ACID ALONG WITH ENDOACTIVATOR MAY BE RECOMMENDED AS IRRIGATION
ADJUNCTS IN PULPECTOMY PROCEDURE OF PRIMARY TEETH
25
PROS AND CONS
PROS
bull PROPER EXPLANATION OF THE MATERIALS
USED
CONS
bull NO PREOPERATIVE AND POSTOPERATIVE
RADIOGRAPHS
26
REFERENCES
bull RAMACHANDRA JA NIHAL NK NAGARATHNA C VORA MS ROOT CANAL IRRIGANTS IN
PRIMARY TEETH WORLD J DENT 20156(3)229-234
bull MOHAMMADI Z JAFARZADEH H SHALAVI S KINOSHITA JI UNUSUAL ROOT CANAL
IRRIGATION SOLUTIONS J CONTEMP DENT PRACT 201718(5)415-420
bull ZEHNDER M ROOT CANAL IRRIGANTS J ENDOD 2006 32389- 98
bull SMITH JJ amp WAYMAN BE AN EVALUATION OF THE ANTIMICROBIAL EFFECTIVENESS OF
CITRIC ACID AS A ROOT CANAL IRRIGANT JOURNAL OF ENDODONTICS 1986 12(2) 54-58
bull TANNURE PN AZEVEDO CP BARCELOS R GLEISER R PRIMO LG LONG-TERM OUTCOMES OF
PRIMARY TOOTH PULPECTOMY WITH AND WITHOUT SMEAR LAYER REMOVAL A RANDOMIZED
SPLIT-MOUTH CLINICAL TRIAL PEDIATR DENT 201133316E20 27
bull CARON G NHAM K BRONNEC F MACHTOU P EFFECTIVENESS OF DIFFERENT FINAL IRRIGANT
ACTIVATION PROTOCOLS ON SMEAR LAYER REMOVAL IN CURVED CANALS J ENDOD
2010361361E6
bull COLL JA SADRIAN R PREDICTING PULPECTOMY SUCCESS AND ITS RELATIONSHIP TO
EXFOLIATION AND SUCCEDANEOUS DENTITION PEDIATR DENT 19961857E63
28
1
LOCAL
ANESTHESIA
DR MITAKSHARA NIRWAN
CONTENTS
Definition
Methods of inducing local anesthesia
Desirable properties
Electrophysiology of nerve conduction
Impulse propagation and spread
Mode and site of action of local anesthesia
Classification of local anesthetic according to biological site and mode of action
Dissociation of local anaesthetics
Mechanism of action of local anaethetics
Local anaesthetic agent
2
3
DEFINITION
Local anesthesia is defined as a loss of sensation in
a circumscribed area of the body caused by depression
of excitation in nerve endings or an inhibition of the
conduction process in peripheral nerves
An important feature of local anesthesia is that it produces
LOSS OF SENSATION WITHOUT INDUCING LOSS OF
CONSCIOUSNESS
4
METHODS OF INDUCING LOCAL
ANESTHESIA
Low temperature
Mechanical trauma
Anoxia
Neurolytic agents such as alcohol amp phenol
Chemical agents such as local anesthetics
PROPERTIES OF LOCAL
ANESTHESIA
It should not be irritating to tissue to which it is applied
It should not cause any permanent alteration of nerve structure
Its systemic toxicity should be low
Time of onset of anesthesia should be short
It should be effective regardless of whether it is injected into the tissue or applied locally to mucous membranes
The duration of action should be long enough to permit the completion of procedure
5 6
It should have the potency sufficient to give complete
anesthesia with out the use of harmful concentration solutions
It should be free from producing allergic reactions
It should be free in solution and relatively undergo
biotransformation in the body
It should be either sterile or be capable of being sterilized by
heat with out deterioration
2
ELETROPHYSIOLOGY OF
NERVE CONDUCTION
There is an electrical charge across the membrane
This is the membrane potential
The resting potential (when the cell is not firing) is a negative
electrical potential of -70mv that exists across the nerve
membrane produced by different concentrations of either side of
the membrane
The interior of nerve is NEGATIVE in relation to exterior
7 8
inside
outside
Resting potential of neuron = -70mV
+
-
+
-
+
-
+
-
+
-
SLOW DEPOLARIRIZATION
9
RAPID DEPOLARIZATION
The interior of nerve is POSITIVE in relation to exterior
REPOLARIZATION
10
bull Repolarization takes 07 msec
bull Depolarization takes 03 msec
SODIUM PUMP -
energy comes from the oxidative metabolism of ATP
bull The entire process require 1 msec
IMPULSE PROPOGATION
IMPULSE SPREAD
The propagated impulse travels along the nerve
membrane towards CNS The spread of impulse differs
in myelinated and unmyelinated nerve fibers
DEPOLARIZED SEGMENT ADJACENT RESTING AREA
MODE AND SITE OF ACTION OF LOCAL
ANESTHETICS
Local anesthetic agent interferes with excitation
process in a nerve membrane in one of the
following ways
Altering the basic resting potential of nerve
membrane
Altering the threshold potential
Decreasing the rate of depolarization
Prolonging the rate of repolarization
12
3
CLASSIFICATION OF LOCAL ANESTHETIC
SUBSTANCES ACCORDING TO
BIOLOGICAL SITE AND MODE OF ACTION
CLASS A
Agents acting at receptor site on external surface of nerve membrane
Chemical substance Biotoxins (eg tetrodotoxin and saxitoxin)
CLASS B
Agents acting on receptor sites on internal surface of nerve membrane
Chemical substance Quaternary ammonium analogues of lidocaine
scorpion venom 13
CLASS C Agents acting by receptor independent of
physiochemical mechanism
Chemical substance Benzocaine
CLASS D Agents acting by combination of receptors and
receptor independent mechanisms
Chemical substance most clinically useful anesthetic agents
(eg lidocaine mepivacaine prilocaine)
14
BASED ON THE SOURCE
NATUAL
SYNTHETIC
OTHERS
BASED ON MODE OF APPLICATION
bull INJECTABLE
bull TOPICAL
BASED ON DURATION OF ACTION
bull ULTRA SHORT
bull SHORT
bull MEDIEM
bull LONG
BASED ON ONSET OF ACTION SHORT
INTERMEDIATE
LONG
15
DISSOCIATION OF LOCAL
ANESTHETICS
Local anesthetics are available as salts (usually
hydrochlorides) for clinical use
The salts both water soluble and stable is dissolved in
either sterile water or saline
In this solution it exists simultaneously as unchanged
molecule (RN) also called base and positively charged
molecules (RNH+) called cations
RNH+ ==== RN+ H
+
16
The relative concentration of each ionic form in the solution varies
in the pH of the solution or surrounding tissue
In the presence of high concentration of hydrogen ion (low pH) the
equilibrium shifts to left and most of the anesthetic solution exists
in cationic form
RNH+ gt RN
+ + H
+
As hydrogen ion concentration decreases (higher pH) the
equilibrium shifts towards the free base form
RNH+ lt RN + H
+
17
The relative proportion of ionic form also depends on pKa or DISSOCIATION CONSTANT of the specific local anesthetic
The pKa is a measure of molecules affinity for H+
ions
When the pH of the solution has the same value as pKa of the local anesthetic exactly half the drug will exists in the RNH
+ form and
exactly half in RN form
The percentage of drug existing in either form can be determined by Henderson Hasselbalch equation
Log baseacid = pH - pKa
18
4
MECHANISM OF ACTION OF LOCAL
ANESTHETICS
The following sequence is proposed mechanism of action of LA
Displacement of calcium ions from the sodium channel receptor site
Binding of local anesthetic molecule to this receptor site
Blockade of sodium channel
19
Decrease in sodium conductance
Depression of rate of electrical depolarization
Failure to achieve the threshold potential level
Lack of development of propagated action potential
Conduction blockadehellip
20
21
Na + Na +
22
LOCAL ANESTHETIC AGENT
COMERCIALLY PREPARED LOCAL ANESTHESIA
CONSISTS OF
Local anesthetic agent (xylocaine lignocaine 2)
Vasoconstrictor (adrenaline 1 80000)
Reducing agent (sodium metabisulphite)
Preservative (methylparabencapryl
hydrocuprienotoxin)
Fungicide (thymol)
Vehicle (distillde waterNaCl)
LOCAL ANESTHETIC AGENT
The local anesthetics used in dentistry are divided
into two groups
ESTER GROUP
AMIDE GROUP
23 24
ESTER GROUP It is composed of the following
An aromatic lipophilic group
An intermediate chain containing
an ester linkage
A hydrophilic secondary or tertiary
amino group
AMIDE GROUP It is composed of the following
An aromatic lipophilic group
An intermediate chain containing
amide linkage
A hydrophilic secondary or tertiary
amino group
5
25
CLASSIFICATION OF LOCAL ANESTHETICS
ESTERS
Esters of benzoic acid
Butacaine
Cocaine
Benzocaine
Hexylcaine
Piperocaine
Tetracaine
Esters of Para-amino
benzoic acid
Chloroprocain
Procaine
Propoxycaine
26
AMIDES Articaine
Bupivacaine
Dibucaine
Etidocaine
Lidocaine
Mepivacaine
Prilocaine
Ropivacaine
QUINOLINE
Centbucridine
PHARMACOKINETICS OF LOCAL
ANESTHETICS UPTAKE
When injected into soft tissue most local anesthetics produce
dilation of vascular bed
Cocaine is the only local anesthetic that produces
vasoconstriction initially it produces vasodilation which is
followed by prolonged vasoconstriction
Vasodilation is due to increase in the rate of absorption of the
local anesthetic into the blood thus decreasing the duration of
pain control while increasing the anesthetic blood level and
potential for over dose 27
AMIDE LOCAL ANESTHETICS
The metabolism of amide local anesthetics is more
complicated then esters The primary site of
biotransformation of amide drugs is liver
Entire metabolic process occurs in the liver for lidocaine
articaine etidocaine and bupivacaine
Prilocaine undergoes more rapid biotransformation then the
other amides
28
REFERENCES
Handbook of local anesthesia ndash Stanley F Malamed ndash 6th
edition
Essentials of Local Anesthetic Pharmacology Daniel E
Becker Anesth Prog 2006 Fall 53(3) 98ndash109
WIKIPEDIEA
29
THANK YOU
30
1
Pharmacological Methods of Behavior
Management
DR MITAKSHARA NIRWAN
DEFINITIONS
bull Conscious Sedation ndash A minimally depressed level of consciousness that retains
the patients ability to independently and continuously maintain an airway and respond appropriately to physical stimulation or verbal command
(American Dental Association House Of Delegates 2000)
bull Deep Sedation ndash An induced state of depressed consciousness
accompanied by partial loss of protective reflexes including the inability to continuously maintain an airway independently and or to respond purposefully to physical stimulation or verbal command
bull General Anesthesia (G A) ndash An induced state of unconsciousness or complete loss of
protective reflexes including the inability to continually maintain an airway independently and respond purposefully to physical stimulation or verbal command
Conscious sedation
ADVANTAGES
Conscious
Protective reflexes active amp intact
Stable vital signs
Operating dentist may perform sedation
Minimum amount of equipment required
Prolong detainment in recovery room not required
Risk of complication very low
Excellent choice for poor ndash risk pt in dental office
Cost effective
General anesthesia
ADVANTAGES Not absolutely
essential May be the only
method Not necessary (no
pain reaction) Amnesia always
present
Conscious sedation
DISADVANTAGES
Pt cooperation is essential
Extremely difficult or mentally handicapped pt cannot always be managed
Use of local anesthesia is a must
Amnesia may or may not be present
General anesthesia DISADVANTAGES
Pt unconscious
Protective reflexes are depressed
Depressed
Advanced training required Dentist must not act also as anesthetist
Special equipment necessary
Detainment in recovery area necessary
High IOP amp postoperative complications
Not indicated in dental office
More expensive
Fundamental Concepts
bull Techniques that utilize drugs to induce co-operative yet conscious state in an otherwise uncooperative child ndash CONSCIOUS SEDATION
2
GOALS
1 To facilitate the provision of quality care
2 To minimize the extremes of disruptive behavior
3 To promote a positive psychologic response to treatment
4 To promote patient welfare amp safety
5 To return the patient to physiologic state
OBJECTIVES
1 The pt mood must be altered
2 The pt must remain conscious at all times
3 The pt must be cooperative
4 All protective reflexes must remain intact and active
5 Vital signs must remain stable and with in normal limits
6 The ptrsquos pain threshold should be elevated
7 Amnesia may be present
Indications
1 Preschool children
2 Lack of Psychological Emotional maturity
3 Lack of Cognitive Physical Medical disability
4 Fearful amp anxious pts
5 Pt who require extensive amp complicated dental care amp would require or benefit from prolonged visits
6 Acute pain
7 Traumatic injuries
Operating Facilities amp Equipment
A positive pressure O2 delivery system capable of administering gt than 90 O2 at 10L min flow for 60 min (650L ldquoErdquo cylinder)
OR
Self inflating bag valve mask device (15L min)
A functional suction apparatus with appropriate suction catheters
Monitoring equipment - PO BPC PC or Capno
Inhalation sedation unit
100 O2 amp never less than 25
A fail safe mechanism that is checked and calibrated annually
Must have appropriate scavenging system
Emergency drugs
Techniques of sedation
Routes for drug administration
bull Oral
bull Rectal
bull Inhalational
bull Transmucosal
ndash Sublingual
ndash Intranasal
bull Parenteral
ndash IM
ndash sub mucosal
ndash IV
3
Oral Sedation
Advantages
1 Almost universally accepted and the easiest method
2 Decreased incidence and severity of adverse reaction
3 Low cost
Disadvantages
1 Absorption is variable
2 Prolonged latent period(30 min)
3 Reversal of any unwanted effect is also difficult
4 Inability to readily lighten or deepen the level of sedation
5 Prolonged duration of action
Rectal Sedation
Advantages 1 Incidence and intensity of
drug related side effects is minimized
2 Drug absorption occurs from the large intestine directly into the circulation
3 The lack of a needle syringe or other equipment
4 The ease of administration
5 The low cost
Disadvantages
1 Inconvenience to the administrator amp pt
2 The variable absorption of drugs from the large intestine
3 The slow onset of action amp the relatively long duration of action
4 Inability to titrate the drug dosage
5 The inability to reverse the action of the drug the prolonged recovery
Intranasal sedation
Advantages
Rapid onset (10 ndash 15 min)
Simple amp relatively painless
Less pt cooperation is required
Absorbed directly into the C V S
Intranasal sedation
Disadvantages
1 Dependence on nasal mucous membrane
2 Shorter duration of action(40-60min)
3 Multiple dosage may be necessary
Drugs
Midazolam ndash 02mgkg
Sufentanil ndash 15 ndash 3 mcgkg
Ketamine ndash 3-6mg kg
Sublingual sedation
Advantages
1 Pt acceptance
2 Rapid onset
3 High bioavailability
Drugs
Oral Transmucosal Fentanyl Citrate (OTFC)
Intramuscular Sedation
Advantages
1 More rapid onset of action
2 Absorbed directly into the C V system
3 More reliable absorption of drug
4 Pt cooperation is not as essential
Disadvantages
1 Time factor ndash its 15 min latent period
2 Pt may not be willing to accept the injection
3 The prolonged duration of action(2-4 hrs more)
4 Possibility of injury to the tissues at the site of injection caused by either the drug or the needle
4
Sites of I M administration
1 Gluteal area
2 Vastus lateralis
3 Mid ndash deltoid area
Drugs
Diazepam
Midazolam
Hydroxyzine
Inhalation Sedation
Advantages
1 The onset of action is more rapid
2 Peak clinical level is achieved rapidly(3-5min) - permit titration
3 Administrator has complete control over the actions of the drug - safety feature
4 No significant over dosage
5 Flexible duration of action
6 Recovery time is rapid amp most complete
7 No injection is required
8 With N2O- O2 it is safe with very few side effects
Disadvantages
1 The initial cost of the equipment is high 2 The continuing cost of the gases is high 3 The equipment occupies considerable space 4 N2O is not a potent agent 5 A degree of cooperation is required from the pt 6 Chronic exposure to N2O is deleterious to the health of
dental personnel
Contraindications
1 Nasal obstruction 2 Cyanosis at rest 3 Poor cooperation 4 1st trimester of pregnancy 5 Fear of masks
I V Sedation
Advantages
1 The onset of action is the most rapid 2 The dosage may be titrated 3 Suitable level of sedation can be provided 4 The recovery period is shorter 5 Side effects are extremely uncommon 6 Control of salivary secretions is possible 7 The gag reflex is diminished 8 Effectively diminishes motor disturbances 9 Provides immediate access to CVS in emergency
Disadvantages
1 Venipuncture is necessary
2 Complication may rise at the site of the venipuncture
3 Monitoring must be more intensive
4 Recovery is not complete at the end of the procedure
5 Reversal of sedation is difficult
5
N2O-O2 (Relative Analgesia)
colorless sweet smelling gas
Pharmacokinetics
Absorption through pulmonary epithelium
It is approx 15 times as soluble as is nitrogen It replaces nitrogen in blood
It is carried in solution in plasma of the blood
It is not metabolized by the body
Elimination ndash majorndash lungs minor --- skin
perspiration urine and intestinal gas
Pharmacodynamics
Dose related
10 ndash 25 Lightheaded
Changes in visual amp auditory sensation
Tingling of hands amp feet
Suffusing warmth
Remote from the immediate environment
Reduced anxiety
25-50 max analgesic properties and aberration of vision hearing and proprioception mild drowsiness euphoria amnesia and increased sleepiness and dreams
35 conc will achieve maximum analgesia
bull CNS
ndash Cerebrum-primarily affected
ndash Safe but weak anesthetic agent
bull RESPIRATORY SYSTEM
ndash Increased Tidal and minute volumes
bull CARDIOVASCULAR SYSTEM
ndash 2 studies ndash decreased cardiac output
bull FETAL SYSTEMS
ndash Miscarriage in humans
bull OTHER SYSTEMS
ndash Depression of spinal reflexes increase muscle tone indicates stage of delirium
ndash Muscle rigidity-narcotics + nitrous oxide
ndash Nausea and vomitting - GIT
ndash HEMATOPOIESIS ----- prolonged exposure
Adverse reactions and toxicity
EMOTIONAL REACTIONS
DREAMS HALLUCINATIONS
No acute toxicity
Chronic toxicity ndash bone marrow
depression
PROCEDURE
Diffusion Hypoxia
Sevoflurane
A fluorinated derivative of isopropyl ether ndash synthesized in 1970
Potent anaesthetic agent with rapid uptake amp speedy recovery
Day-case surgery
Problem
Attaching vaporiser to any of the currently available machine
BENZODIAZEPINES
Diazepam 1961 lipid soluble
Uses-alcoholism epilepsy labor tetanus and cerebral palsy
- sedation and amnesia
- varieties of neurosis amp anxiety states
Pharmacokinetics
Orally Rectal IMIV or SC
Well absorbed through GIT
Excretion in urine
6
bull Pharmacodynamics
ndash Depress the brain stem reticular system and the limbic system thalamus and hypothalamus
ndash It is a centrally acting muscle relaxant Has anti-convulsant properties
Adverse reaction amp toxicity
ndash Confusion nausea headache increased appetite decreased salivation and jaundice Thrombophlebitis
ndash Rebound phenomenon
ndash Toxicity drowsiness confusion sleep and coma
Dosage Oral or Rectal ndash 02-05mgkg
Maximum single dose 10mg
IV- 025mgkg
Supplied Tablets 2 5 10 mg
Suspension ndash 5mg
Midazolam Water soluble ndash non-irritant
Oral IM IV
Metabolism- liver
Onset IV 3 -5mins
oral 20 ndash 30mins
Oral administration anxious patients requiring relatively short dental procedure
No rebound phenomenon
Better anxiolysis amp amnesia (retrograde amnesia)
Adverse effects Respiratory depression
dose dependant apnea
Dosage Oral ndash 025 to 1mgkg to maximum single dose 20mg
IM ndash 01 to 015mgkg to a maximum of 10mg
IV ndash slow IV
Supplied Syrup ndash 2mgml
Injectable ndash 1mgml amp 5mgml vials
Flumazenil specific benzodiazepines antagonist
selectively inhibits CNS effects
IV administration amp not recommended below 18yrs of age
02mg over 15 seconds after 45seconds 02mg then after 60seconds to maximum of 1mg
Sedative-Hypnotics
Barbiturates First truly effective drugs for the management of anxiety Generalized CNS depressants Produce dose dependent effects
Sedation ---- sleep ---- GA ---- coma
Suppress the CNS and result in sedation and amnesia Advantages
Rapid onset and short duration Disadvantages
no analgesic effect and possible hypotension Must be used with caution in trauma patients because they may cause
apnea and hypoventilation
DOSE Pentobarbital Sodium 100mg Secobarbital Sodium 100 to 200mg Children 30 to 100mg
bull Chloral Hydrates (Mickey Finn Knock out drops ) First synthesized in 1832 first member of the hypnotic group of drugs
Widely used as conscious sedation agent
Properties
Unpleasant taste
Nausea vomiting
Quite irritating to skin and to mucous membranes
GI irritation
Dosages Individualized for each patient 25 ndash 50mgkg
maximum of 1g
Supplied oral capsule ndash 500mg
oral solution ndash 250 amp 500mg5ml
Rectal suppositories ndash 324 amp 648mg
Narcotics
Do produce sedation amp euphoria greater in children
LA is required but dose should be decreased
Meperidine Synthetic opiate agonist
Very water soluble
Orally SC IM or IV
Peak effect by oral 1 hr amp lasts upto 4 hrs
Adverse reactions
-Seizures
-Extreme caution in hepatic or renal diseases or history of seizures
7
Dosage Oral SC or IM ndash 1to 22mgkg not to exceed 100 mg
Supplied Oral Tablets ndash 50 amp 100mg
Oral Syrup ndash 50mgml
Parental solution ndash 25 50 75 amp 100mgml
Fentanyl
Synthetic opiate narcotic analgesic
Very potent 01mg = 10mg Morophine75mg Meperidine
Pharmacokinetics
IV IM SM
Metabolized in liver Excreted in urine
Fentanyl Onset ndash 7 to 15mins
Duration ndash 1 to 2 hrs
Pharmacodynamics
Respiratory depression RR but returns to normal rapidly Tidal volume amp response to co2 depressed for extended period
Apnea
Less emetic than meperidine
NOT RECOMMENDED IN CHILDREN BELOW 2yrs
Dosage 0002 to 0004mgkg
Supplied 005mgml in 2 amp 5ml ampoules
Reversal drug Naloxone
Semisynthetic opiate antagonist
No agonist activity
Onset 2 to 5mins SC or IM amp 1 to 2mins IV
Reversal 45mins
Pt should be kept under continual surveillance
Adverse reaction nausea vomiting sweating hypotension hypertension ventricular tachycardia fibrillation
Dosage IV SC IM 001mgkg then 01mgkg every 2- 3mins maximum 2mg
Supplied 002 004 1mg solutions
Antihistamines
Hydroxyzine
Oral or IM
Effect ndash 15 ndash 30mins
Half-life ndash 3 hrs
Uses
To relieve anxiety
Used as an anti-histamine
Used to control nausea and vomiting including that associated with motion sickness and pregnancy
Adverse reaction dry mouth drowsiness hypersentivity
Dosage Oral ndash 1 to 2mgkg
IM ndash 11mgkg
Promethazine Oral or IM Onset 15 to 60mins Duration 4 to 6 hrs Uses
To prevent and treat nausea and vomiting associated with motion pregnancy or surgery
Produces sedation and reduce swelling pain and trismus
Lower seizure threshold Adverse reaction dry mouth blurred vision thickening of bronchial secretions Dosage OralIM ndash 05-11mgkg
maximum 25 mg
Diphenhydramine
Oral IM IV
Onset -1hr
Duration ndash 4 to 6 hr
Metabolized in liver
Adverse reaction disturbed coordination thickening of bronchial secretions
Dosage Oral IM IV ndash 1 to 15mgkg
maximum 50mg
Tranquilizers
Major tranquilizer antipsychotic produce calmness control symptoms of psychoses cause reversible extra pyramidal symptoms and do not tend to cause habituation
Minor tranquilizer antianxiety agents also cause calmness do not cause extrapyramidal symptoms Used in conditions like nervous tension and mild depression
8
Classification
Antipsychotics
Phenothiazine derivatives
Chlorpromazine promazine
Butryophenones
Haloperidol
Rauwolfia alkaloids
Reserpine
Antianxiety drugs
Propyl alcohol derivatives
Meprobamate
Benzodiazepine derivatives
Diazepam
Miscellaneous compounds
Hydroxyzine
Meprobamate
White crystalline powder slightly bitter in taste
Only administered orally
Peak blood concentration ----1 to 3hrs
10 ---------excreted unchanged Rest --- excreted as a oxidized derivative or as a glucoronide
Uses
To relieve day time anxiety
Induce sleep in insomniacs
To reduce anxiety associated with dental treatment
Anti-convulsant ndash petit mal epilepsy
Adverse reaction leucopenia acute non-thrombocytopenic purpura ecchymoses eosinophilia edema adenopathy
Dosage Childrengt 6yrs 100 to 200mg
Not recommended for children under 6yrs
Monitoring during sedation
1 Pulse
2 Blood pressure
3 ECG
4 Respiration
5 Temperature
Pulse
Manual Electronic
bull Radial Brachial
bull Facial labial
Blood pressure
ndash Stethoscope amp sphygmomanometer
ndash Automatic devices
ndash Direct cannulation of an artery ndash very accurate
Electrocardiograph
Heart rate rhythm myocardial function
9
Respiration
ndash Monitoring respiratory rate
ndash Observing the rise amp fall of the chest wall
ndash Observing the color of mucous membrane
ndash Observing the inflation amp deflation of the reservoir bag
Devices for monitoring respiration
1 The Precordial pretracheal stethoscope
2 The esophageal stethoscope
ndash Respiratory rate
ndash Heart rate
ndash Any abnormal sounds
Pulse Oximeter
ndash Oxygen saturation
ndash Heart rate
ndash Oxisensor site
ndash Fingers
ndash Toe
ndash Ear lobe
Mechanism
Oxygenated Hb ndash red light
Deoxygenated Hb- infrared light
Tissue pressure from arterial pulse (plethysmography)
Advantages
ndash Safe amp noninvasive
ndash Simple to use
ndash Information is rapidly available for clinical decision
ndash Indirectly indicates respiratory adequacy
Disadvantages
ndash Finger probes can get dislodged
ndash Emitted light source may cause burning
ndash Non reusable probes are expensive
ndash Does not directly determine airway patency
Capnography
1 The presence absence of air flow
2 Indicates depth amp adequacy of respiration
3 Continues analysis of the co2 content of the respired air ndash indicates respiratory adequacy
Temperature
ndash Disposable nondisposable thermometer
ndash Esophageal rectal temp probe
10
Discharge criteria
Cardiovascular function is satisfactory amp stable
Airway patency is uncompromised amp satisfactory
Pt is easily arousable amp protective reflexes intact
State of hydration is adequate
Pt can talk if applicable
Pt can sit unaided if applicable
Pt can ambulate with minimal assistance if applicable
Presedation level of responsiveness achieved
Responsible individual is available
1
PULP THERAPY OF VITAL TEETH
DR MITAKSHARA NIRWAN
Contents
Indirect pulp capping
Direct pulp capping
Medications amp materials used in pulp capping
Pulpotomy
MTA
Apexogenesis
INDIRECT PULP CAPPING
Pieter Van Forest - first to speak about root canal therapy
Glove designed instruments that could prepare a canal to a certain size and taper(1910)
Indirect pulp capping is defined as a procedure where in small amount of carious dentin is retained in
deep areas of cavity to avoid exposure of pulp followed by placement of a suitable medicament and
restorative material that seals off the carious dentin and encourages pulp recovery (Ingle)
A procedure in which only the gross caries is removed from the lesion and the cavity is sealed for a
time with a biocompatible material (McDonald)
Objective of indirect pulp capping
These were given by Eidelman in 1965
bull Arresting the carious process
bull Promoting dentin sclerosis
bull Stimulating formation of tertiary dentin
bull Remineralization of carious dentin
Layers of Carious Dentin Indications of Indirect Pulp Capping
History
Mild pain associated with eating
Negative history of spontaneous extreme pain
Clinical Examination
Deep carious lesion which are close tobut not involving the pulp in vital primary or young
permanent teeth
No mobility
Nominal pulp inflammationdefinite layer of affected dentin after removal of infected dentin
Radiographic examination
Normal lamina dura amp PDL space
No radiolucency around the apices
2
Contraindications of Indirect Pulp Capping
History
Sharp penetrating pulpalgia
Prolonged spontaneous pain especially at night
Clinical examination
Mobility of tooth
Discoloration of tooth
Negative reaction of electric pulp testing
Radiographic examination
Definite pulp exposure
Break in the lamina dura
Radiolucency around the apices
Widened PDL space
Treatment procedure
Sequelae of Indirect Pulp Capping Three distinct types of new dentin formation take place
1 Cellular fibrillar dentinmdashfirst 2 months
2 Globular dentinmdash3 months
3 Tubular dentin (uniform mineralized dentin)
bull 15th of reparative dentin formation begins in less than 30 days
bull After 3 months 01 mm is formed
DIRECT PULP CAPPING Defined by Kopel (1992) as the placement of a medicament or non medicated material on a pulp that
has been exposed in course of excavating the last portions of deep dentinal caries or as a result of
trauma
Objective
To create new dentin in the area of the exposure and subsequent healing of the pulp
Rationale
achieve a biologic closure of the exposure site by deposition of hard tissue barrier (dentin bridge)
between pulp tissue and capping material thus walling off the
INDICATIONS
Small mechanical exposure
Easily controlled haemorrhage
Bright red haemorrhage
True pinpoint exposure
CONTRAINDICATIONS
Severe toothache at night
Spontaneous pain
Tooth mobility
Radiographic appearance of pulp periradicular de- generation
Excess of hemorrhage at the time of exposure Serous exudate from the exposure
Externalinternal root resorption
Swellingfistula
Histological Changes after Pulp Capping
These were illustrated be Glass and Zander in 1949
After 24 hours Necrotic zone adjacent to calcium
hydroxide paste is separated from healthy pulp
tissue by a deep staining basophilic layer
After 7 days Increase in cellular and fibroblastic
activity
After 14 days Partly calcified fibrous tissue lined by
odontoblastic cells is seen below the calcium
proteinate zone disappearance of necrotic zone
After 28 days Zone of new dentin
3
Medications and Materials Used for Pulp Capping Calcium hydroxide
Corticosteroids amp antibiotics
Inert materials
Collagen fibers
4-META adhesive
Direct bonding
Isobutyl cyanoacrylate
Denatured albumin
Mineral trioxide aggregate
Laser
Bone morphogenic protein
PULPOTOMY
Finn (1995) defined it as the complete removal of the coronal portion of the dental pulp
followed by placement of a suitable dressing or medicament that will promote healing and
preserve vitality of the tooth
American Academy of Pediatric Dentistry (1998) defined pulpotomy as the amputation of
affected infected coronal portion of the dental pulp preserving the vitality and function of the
remaining part of radicular pulp
Objectives
bull Removal of inflamed and infected coronal pulp at the site of exposure thus preserving the vitality of the
radicular pulp and allowing it to heal
bull Maintain the tooth in the dental arch
Rationale
bull Radicular pulp is healthy and capable of healing after surgical amputation of the infected coronal pulp
bull Preserves vitality of the radicular pulp
bull Maintains tooth in a physiologic condition
Indications of Pulpotomy bull Mechanical pulp exposure in primary teeth
bull Teeth showing a large carious lesion but free of radicular pulpitis
bull History of only spontaneous pain
bull Hemorrhage from exposure sites bright red and can be controlled
bull Absence of abscess or fistula
bull No interradicular bone loss
bull No interradicular radiolucency
Contraindications of Pulpotomy bull Persistent toothache
bull Tenderness on percussion
bull Root resorption more than 13rd of root length
bull Large carious lesion with nonrestorable crown
bull Highly viscous sluggish hemorrhage from canal orifice which is uncontrollable
bull Medical contradictions like heart disease immuno compromised patient
bull Swelling or fistula
bull External or internal resorption
bull Pathological mobility
bull Calcification of pulp
Classification of pulpotomy
4
Formocresol Pulpotomy
Iby BUCKLEY in 1904
Sweet (1930) Formulated multi visit technique
Doyle (1962) Advocated 2 sitting procedure (complete devitalization)
Spedding (1965) Gave 5 minute protocol (partial devitali- zation)
Venham (1967) Proposed 15 seconds procedure
Current concept uses 4 minutes of application time
Composition of formocresol Buckleyrsquos Formula
bull Cresol ndash 35 percent
bull Glycerol ndash 15 percent
bull Formaldehyde ndash 19 percent
bull Water ndash 31 percent
Mechanism of Action
It prevents tissue autolysis by bonding to the proteins Bonding is of peptide groups of side chain amino acids and is a reversible process accomplished without
changing the basic structure of protein molecules
Histological Changes
bull Demonstrated by Mass and Zilbermann11 in 1933 and also by Massler and Mansokhani in 1959
bull Immediately the pulp becomes fibrous and acidophillic
bull Seven to fourteen days Three zones appear
a broad eosinophilic zone of fixation
b broad pale-staining zone of atrophy with poorcellular definition
c broad zone of inflammation extending apically into normal pulp tissue
bull One yearndash Progressive apical movement of these zones with only acidophillic zone left at the end of 1 year
Modified Formocresol Pulpotomy
Used by TRASK(1972)
The technique is identical to that described for primary teeth except that the formocresol pellet is
sealed permanently in the tooth
Two-visit Devitalization Pulpotomy
Indications
bull There is evidence of sluggish bleeding at the amputation site that is difficult to control
bull Pus in the chamber but none at the amputation site
bull There is thickening of the PDL
bull History of pain
Contraindications
bull Nonrestorable tooth
bull Tooth with necrotic pulp
5
Glutaraldehyde Pulpotomy
It was first suggested by S Gravenmade Introduced by Kopel in 1979
Mechanism of Action
bull Glutaraldehyde produces rapid surface fixation of the underlying pulpal tissue
bull A narrow zone of eosinophilic stained and compressed fixed tissue is found directly beneath the area of application which blends into vital normal appearing tissue apically
bull With time the glutaraldehyde fixed zone is replaced by macrophagic action with dense collagenous tissue thus the entire root canal tissue is vital
Cvekrsquos Pulpotomy
bull This is also called as calcium hydroxide pulpotomy or young permanent partial pulpotomy
bull This was proposed by Mejare and Cvek16 in 1978
bull Indicated in young permanent teeth where the pulp is exposed by mechanical or bacterial means and the
remaining radicular tissue is judged vital by clinical and radiographic criteria whereas the root closure is
notcomplete
MINERAL TRIOXIDE AGGREGATE (MTA) Torabinejad described the physical and chemical properties of MTA in 1995
It is ash colored powder made primarily of fine hydrophilic particles of
1 tricalcium aluminate
2 tricalcium silicate
3 silicate oxide
4 tricalcium oxide
5 bismuth dioxide
Hydration of the powder results in a colloidal gel composed of calcium oxide crystals in an amorphous
structure This gel solidifies into a hard structure in less than three hours
PROPERTIES OF MTA
It is biocompatible material and its sealing ability is better than that of amalgam or ZOE
Initial pH is 102 and set pH is 125
The setting time of cement is 4 hours
The compressive strength is 70 MPA which is comparable with that of IRM
Low cytotoxicity ndash It presents with minimal inflammation if extended beyond the apex
Mineral trioxide aggregate (MTA) has demonstrated the ability to induce hard-tissue formation in
pulpal tissues and it promotes rapid cell growth
APEXOGENESIS
It is defined as the treatment of a vital pulp by capping or pulpotomy in order to permit continued
growth of the root and closure of the open apex
Rationale
Maintenance of integrity of the radicular pulp tissue to allow for continued root growth
Indications
bull Indicated for traumatized or pulpally involved vital permanent tooth when root apex is incompletely formed
bull No history of spontaneous pain
bull No sensitivity on percussion
bull No hemorrhage
bull Normal radiographic appearance
Contraindications
bull Evidence that radicular pulp has undergone degenerative changes
bull Purulent drainage
bull History of prolonged pain bull Necrotic debris in canal
bull Periapical radiolucency
6
1
Gupta A Dhingra R Chaudhari P Gupta A
Department of Paedodontics and Preventive Dentistry Faculty of Dental Sciences SGT University Gurgaon Haryana India
Journal of Indian Society of Pedodontics and Preventive Dentistry
Volume 35 I Issue 3 I July-September 2017
A COMPARISION OF VARIOUS MINIMALLY
INVASIVE TECHNIQUES FOR THE REMOVAL
OF DENTAL FLUOROSIS STAINS IN
CHILDREN
DR MITAKSHARA NIRWAN
CONTENTS
bull Introduction
bull Aims
bull Materials and Methods
bull Results
bull Discussion
bull Conclusion
bull Critical analysis
bull References
INTRODUCTION
bull Dental fluorosis is a developmental disturbance of dental enamel caused by
successive exposure to high concentrations of fluoride during tooth
development
bull Various methods of therapy are advocated for the treatment of fluorosis -
stained teeth which range from invasive ceramic veneer bonding restorations
to abrasive chemical treatments
bull The combination of dental bleaching techniques and microabrasion appears
as an excellent conservative solution to reestablish health in fluorosis
affected teeth
AIMS
bull The aim of the study was to evaluate and compare the effectiveness of
minimally invasive techniques for the removal of dental fluorosis
stains in children in vivo
MATERIALS AND METHODS
Patients visiting the department of Pedodontics and Preventive dentistry
Faculty of Dental Sciences SGT University Gurgaon
bull Sample size 90 patients
bull Age group 10 -17 years
bull Caries cracks or periodontal
disease on anterior teeth
bull Abscess draining sinus
cellulitis
bull Non vital teeth
hypersensitive exposed
crevices
bull Orthodontic appliance
bull Past history of bleaching
bull At least two permanent
maxillary anterior teeth
bull TSIF of score 4
bull Free of systemic diseases
Inclusion criteria Exclusion criteria
2
Groups
Group A In office bleaching with 35 hydrogen peroxide( Pola Office
Bleaching kit) activated by light emitting diode (LED) bleaching unit
(35 HP)
Group B Enamel microabrasion (EM) (PREMA Enamel Microabrasion
System) followed by in-office bleaching with 44 carbamide peroxide
gel (EM)
Group C In-office bleaching with 5 sodium hypochlorite (5
NaOCl)
A baseline colour evaluation was done by taking digital photograph of
the maxillary anterior teeth
RESULTS
Group 1
Colour stability
Group 2 Group 3
Tooth sensitivity
Tooth sensitivity values were taken before the treatment
which was compared to immediate postoperative and follow
up visits It was checked using an electric pulp tester
maximum
moderate
least
immediately
group 2
group 1
group 3
1 month
group 2
group 1
group 3
3 month
group 2
group 1
group 3
Patient satisfaction score
Satisfaction was assessed on visual analog scale
Range 1 to 5
Groups percentage of patients
who were satisfied with
the treatment
Number of patients
who reported slight
reappearance of colour
Group 1
90
7
Group 2
83
8
Group 3
73
7
3
Number of Appointments
Groups One sitting Two sittings Three
sittings
Group 1
25
4
1
group 2
26
3
1
Group 3
30
0
0
DISCUSSION
bull Hydrogen peroxide is capable of penetrating the tooth osmosis and through porosities and cracks subsequently acting directly on the pigmented molecules
bull Gurgan et al investigated 3 different light systems and found out that diode laser system with gave best tooth whitening and least tooth sensitivity
bull In the EM group the surface reflects and refracts light from the surface in such way that mild imperfections in underlying enamel are camouflaged While the highly polished surface of enamel enhances the aesthetic appearance
bull Train et al and Loguercio et al also had the similar results in their studies with EM mild fluorosis showed best results moderate showed moderate results while it had little effect on severe fluorosis
bull NaOCl was only effective on mild stains while moderate and severe
stains could only be lightened to quite an extent but could not be
completely removed
bull When NaOCl comes in contact with hypomineralized and discoloured
enamel it degrades and removes the chromogenic organic material
located on the enamel surface
CONCLUSION
bull It was concluded that esthetic appearance of teeth mild fluorosis can
be achieved by bleaching and microabrasion But in cases of
moderate fluorosis a combination of any of theses modalities can be
used
bull As no special maintenance precautions are required these maybe be
considered as an interesting alternative to conventional operative
treatment
bull Focuses on only TSIF of 4
bull Electric pulp testing is not the
right method to check for
sensitivity
bull Tooth Sensitivity changes
from person to person
bull Food habits can cause
staining of the teeth
bull Minimally invasive
bull Cheaper to veneers
bull Minimal loss of tooth structure
bull 4 parameters checked for the success of treatment
bull Inclusion of specific score of fluorosis for comparing the results
bull Maximum 3 appointments needed
CRITICAL ANALYSIS
Pros Cons
REFERENCES
bull Gurgan S Cakir FY Yazici E Different light-activated in officebleaching
systems Lasers Med Sci 201025817-22
bull Train TE McWhorter AG Seale NSWilson CF Guo IY Examination of
esthetic improvement and surface alteration following microabrasion in
fluorotic human incisors in vivoPediatr dent 199618353-62
bull Loguercio AD Correia LD Zago C Tagliari D Neumann E Gomes OM et al
Clinical effectiveness of two microabrasion materials materials for the
removal of enamel flurosis stains Oper Dent 200732531-8
4
3
GROUP 1 (CA + E) - IRRIGATION WAS DONE
WITH 10 ML OF 6 CITRIC ACID (CITOCID AMMDENT)
AND IRRIGANTS WERE SONICALLY AGITATED WITH
ENDOACTIVATOR (DENTSPLY) FOR 30 S PER CANAL USING REDBLUE
ENDOACTIVATOR TIP
GROUP 2 (CA) - 10 ML OF 6 CITRIC ACID FOR 1 MIN USING
27 GAUZE IRRIGATING NEEDLE
GROUP 3(SH + E) - 10 ML OF 1 SODIUM HYPOCHLORITE
SOLUTION AND SONIC ACTIVATION WITH ENDOACTIVATOR
GROUP 4(SH) - 10 ML OF 1 SODIUM HYPOCHLORITE
SOLUTION USING IRRIGATING NEEDLE (CONTROL GROUP)
bull TEETH UNDERGOING PULPECTOMY WERE RANDOMLY ENROLLED BY CHIT METHOD INTO THREE
STUDY AND ONE CONTROL GROUP
13
bull IN CITRIC ACID GROUPS FINAL RINSE WITH NORMAL SALINE WAS DONE TO REMOVE THE
REMAINING CRYSTALS (CHELATES)
bull FOLLOWING BIOMECHANICAL PREPARATION THE ROOT CANALS WERE DRIED WITH STERILE
ABSORBENT PAPER POINTS AND OBTURATED WITH VITAPEX USING HAND HELD
LENTULOSPIRAL FINAL RESTORATIONS WERE DONE USING COMPOSITE RESIN
14
bull CLINICAL FOLLOW UP WAS DONE AT 24 H1 WEEK 1 MONTH 6 MONTH AND 12
MONTH TO CHECK PAIN PRESENCE AND PAIN FREQUENCY (ONCEMORE THAN ONCE)
SWELLING FISTULA SENSITIVITY TO PERCUSSION
bull RADIOGRAPHIC FOLLOW UP WAS DONE AT 6 MONTH AND 12 MONTH FOR ANY
DEVIATED ERUPTION OF SUCCEDANEOUS TEETH EXCESS FILING MATERIAL AND ITS
RESORPTION EXTERNALINTERNAL ROOT RESORBTION CALCIFIC METAMORPHOSIS
PRESENCE OF FURCATION RADIOLUCENCY
CLINICAL amp RADIOGRAPHIC FOLLOW UP
15
RADIOGRAPHIC ASSESSMENT OF OBTURATION QUALITY
bull POSTOPERATIVE RADIOGRAPHS WERE VISUALLY ASSESSED FOR QUALITY OF OBTURATION BY
TWO INDEPENDENT EXAMINERS (SG AD) WHO WERE BLINDED WITH REGARD TO
IRRIGATION PROTOCOL GROUP TO ENHANCE CALIBRATION EACH EXAMINER ASSESSED THE
RADIOGRAPH INDEPENDENTLY AND LATER REVIEWED TOGETHER FOR FINAL ASSESSMENT
INDIVIDUAL ROOT WAS TAKEN AS UNIT OF ANALYSIS FOR GRADE OF OBTU- RATION AND
SCORING CRITERIA WERE AS GIVEN BY COLL JA 1996
1 UNDER FILLED - FILLING MATERIAL ENDED 1 MM OR MORE SHORT OF THE APEX
2 OPTIMAL FILLING- FILLING MATERIAL APPEARED TO END AT THE RADIOGRAPHICAL APEX
3 OVERFILLED - FILLING MATERIAL EXTRUDED PAST THE RADIOGRAPHIC APEX
4 OPTIMALLY FILLED ROOTS WERE FURTHER ASSESSED FOR THE PRESENCE OF VOIDS AND VOID
AREA (ROOT CANAL SURFACE UNTOUCHED BY THE ROOT CANAL FILLING MATERIAL) IN THREE
VISUALLY DIVIDED SECTIONS OF THE ROOT IE CORONAL MIDDLE AND APICAL 13RD
16
RESULTS
bull OVERALL CLINICAL AND RADIOGRAPHIC SUCCESS RATE OVER A PERIOD OF ONE YEAR WAS
9886 amp 977 RESPECTIVELY
bull ALL GROUPS WERE SIGNIFICANTLY (P = 001) EFFECTIVE IN ALLEVIATING PAIN WITHIN 24 H
OF PULPECTOMY
17 18
4
19
bull IMMEDIATE POST OPERATIVE RADIOGRAPHIC ASSESSMENT REVEALED 68 (102150) ROOTS
WITH OPTIMAL OBTURATION AND 32 (48150) WITH OVERFILLINGUNDERFILLING MAXIMUM
NO OF OPTIMAL FILLINGS WERE OBSERVED IN GROUP1 (CA + E) (3333) FOLLOWED BY
GROUP 2 (CA) (2549) GROUP 3(SH + E) (2549) AND GROUP 4(SH) (1568)
bull CITRIC ACID GROUPS HAD MORE NUMBER OF OPTIMALLY FILLED ROOTS 588 (60102) THAN
NON CITRIC ACID GROUPS 412 (42102)
bull ENDOACTIVATOR CONTRIBUTED TO 18 OF OPTIMAL OBTURATION IRRESPECTIVE OF
CHELATING AGENT USED
20
21
bull MAXIMUM NO OF VOIDS AND VOID AREAS WERE IN NON CITRIC ACID GROUPS
(6419 amp 5384) COMPARED TO CITRIC ACID GROUPS (3580 amp 4615)
RESPECTIVELY
bull ANALYSIS OF ROOT 13RD REVEALED MAXIMUM NO OF VOID AREA IN APICAL
13RD (4755) FOLLOWED BY MIDDLE 13RD (3846) AND CORONAL 13RD
(1398)
bull LEAST NO OF VOIDS amp VOID AREA (1111 amp 1608) WERE OBSERVED WHEN
ENDOACTIVATOR ALONG WITH CHELATING AGENT WAS USED (GROUP 1)
HOWEVER THIS WAS STATISTICALLY INSIGNIFICANT
22
DISCUSSION
bull IN THE PRESENT STUDY 1 SODIUM HYPOCHLORITE WAS USED ALONG WITH 6 CITRIC ACID
(CHELATING AGENT) WHICH IS REPORTED TO BE AS EFFECTIVE AS 17 EDTA
bull CITRIC ACID (BIOLOGICAL ACID) IS FOUND TO BE BIOCOMPATIBLE AND LEAST IRRITATING TO
PERIAPICAL TISSUES THAN OTHER CHELATING AGENTS
bull USE OF SODIUM HYPOCHLORITE SOLUTION FOLLOWING CHELATING AGENT WAS AVOIDED AS IT
RAPIDLY PRODUCES SEVERE EROSION OF ROOT CANAL WALL DENTIN
bull TRADITIONAL APPROACH OF DELIVERING IRRIGANTS INTO THE ROOT CANAL SPACE USING
SYRINGES AND METAL NEEDLES HAS BEEN FOUND TO BE INEFFECTIVE ESPECIALLY IN THE AREAS OF
ANASTOMOSES BETWEEN CANALS AND APICAL 13RD OF ROOT CANAL
23
bull THEREFORE TO ACHIEVE BETTER CLEANING EFFICIENCY IRRIGANT ACTIVATION HAS BEEN
RECOMMENDED SONIC ACTIVATION HAS BEEN REPORTED TO RESULT IN BETTER ROOT CANAL
CLEANLINESS AS COMPARED TO NO ACTIVATION OF IRRIGANT
24
5
CONCLUSION
bull USE OF 6 CITRIC ACID DEFINITELY HELPED IN RAPID ELIMINATION OF PAIN RESOLUTION OF
PERI-RADICULAR RADIOLUCENCY BETTER OBTURATION QUALITY IN TERMS OF LESS VOIDS AND
VOID AREAS ALONG WITH MAXIMUM NO OF OPTIMAL OBTURATION UP TO APICAL AREA
bull 6 CITRIC ACID AND ENDOACTIVATOR IRRIGATION PROTOCOL PROVED TO BE THE BETTER
IRRIGATION PROTOCOL WHICH MAY CONTRIBUTE TO LONG TERM SUCCESS OF PRIMARY
TOOTH AND THE HEALTH OF UNDERLYING PERMANENT TOOTH
bull 6 CITRIC ACID ALONG WITH ENDOACTIVATOR MAY BE RECOMMENDED AS IRRIGATION
ADJUNCTS IN PULPECTOMY PROCEDURE OF PRIMARY TEETH
25
PROS AND CONS
PROS
bull PROPER EXPLANATION OF THE MATERIALS
USED
CONS
bull NO PREOPERATIVE AND POSTOPERATIVE
RADIOGRAPHS
26
REFERENCES
bull RAMACHANDRA JA NIHAL NK NAGARATHNA C VORA MS ROOT CANAL IRRIGANTS IN
PRIMARY TEETH WORLD J DENT 20156(3)229-234
bull MOHAMMADI Z JAFARZADEH H SHALAVI S KINOSHITA JI UNUSUAL ROOT CANAL
IRRIGATION SOLUTIONS J CONTEMP DENT PRACT 201718(5)415-420
bull ZEHNDER M ROOT CANAL IRRIGANTS J ENDOD 2006 32389- 98
bull SMITH JJ amp WAYMAN BE AN EVALUATION OF THE ANTIMICROBIAL EFFECTIVENESS OF
CITRIC ACID AS A ROOT CANAL IRRIGANT JOURNAL OF ENDODONTICS 1986 12(2) 54-58
bull TANNURE PN AZEVEDO CP BARCELOS R GLEISER R PRIMO LG LONG-TERM OUTCOMES OF
PRIMARY TOOTH PULPECTOMY WITH AND WITHOUT SMEAR LAYER REMOVAL A RANDOMIZED
SPLIT-MOUTH CLINICAL TRIAL PEDIATR DENT 201133316E20 27
bull CARON G NHAM K BRONNEC F MACHTOU P EFFECTIVENESS OF DIFFERENT FINAL IRRIGANT
ACTIVATION PROTOCOLS ON SMEAR LAYER REMOVAL IN CURVED CANALS J ENDOD
2010361361E6
bull COLL JA SADRIAN R PREDICTING PULPECTOMY SUCCESS AND ITS RELATIONSHIP TO
EXFOLIATION AND SUCCEDANEOUS DENTITION PEDIATR DENT 19961857E63
28
1
LOCAL
ANESTHESIA
DR MITAKSHARA NIRWAN
CONTENTS
Definition
Methods of inducing local anesthesia
Desirable properties
Electrophysiology of nerve conduction
Impulse propagation and spread
Mode and site of action of local anesthesia
Classification of local anesthetic according to biological site and mode of action
Dissociation of local anaesthetics
Mechanism of action of local anaethetics
Local anaesthetic agent
2
3
DEFINITION
Local anesthesia is defined as a loss of sensation in
a circumscribed area of the body caused by depression
of excitation in nerve endings or an inhibition of the
conduction process in peripheral nerves
An important feature of local anesthesia is that it produces
LOSS OF SENSATION WITHOUT INDUCING LOSS OF
CONSCIOUSNESS
4
METHODS OF INDUCING LOCAL
ANESTHESIA
Low temperature
Mechanical trauma
Anoxia
Neurolytic agents such as alcohol amp phenol
Chemical agents such as local anesthetics
PROPERTIES OF LOCAL
ANESTHESIA
It should not be irritating to tissue to which it is applied
It should not cause any permanent alteration of nerve structure
Its systemic toxicity should be low
Time of onset of anesthesia should be short
It should be effective regardless of whether it is injected into the tissue or applied locally to mucous membranes
The duration of action should be long enough to permit the completion of procedure
5 6
It should have the potency sufficient to give complete
anesthesia with out the use of harmful concentration solutions
It should be free from producing allergic reactions
It should be free in solution and relatively undergo
biotransformation in the body
It should be either sterile or be capable of being sterilized by
heat with out deterioration
2
ELETROPHYSIOLOGY OF
NERVE CONDUCTION
There is an electrical charge across the membrane
This is the membrane potential
The resting potential (when the cell is not firing) is a negative
electrical potential of -70mv that exists across the nerve
membrane produced by different concentrations of either side of
the membrane
The interior of nerve is NEGATIVE in relation to exterior
7 8
inside
outside
Resting potential of neuron = -70mV
+
-
+
-
+
-
+
-
+
-
SLOW DEPOLARIRIZATION
9
RAPID DEPOLARIZATION
The interior of nerve is POSITIVE in relation to exterior
REPOLARIZATION
10
bull Repolarization takes 07 msec
bull Depolarization takes 03 msec
SODIUM PUMP -
energy comes from the oxidative metabolism of ATP
bull The entire process require 1 msec
IMPULSE PROPOGATION
IMPULSE SPREAD
The propagated impulse travels along the nerve
membrane towards CNS The spread of impulse differs
in myelinated and unmyelinated nerve fibers
DEPOLARIZED SEGMENT ADJACENT RESTING AREA
MODE AND SITE OF ACTION OF LOCAL
ANESTHETICS
Local anesthetic agent interferes with excitation
process in a nerve membrane in one of the
following ways
Altering the basic resting potential of nerve
membrane
Altering the threshold potential
Decreasing the rate of depolarization
Prolonging the rate of repolarization
12
3
CLASSIFICATION OF LOCAL ANESTHETIC
SUBSTANCES ACCORDING TO
BIOLOGICAL SITE AND MODE OF ACTION
CLASS A
Agents acting at receptor site on external surface of nerve membrane
Chemical substance Biotoxins (eg tetrodotoxin and saxitoxin)
CLASS B
Agents acting on receptor sites on internal surface of nerve membrane
Chemical substance Quaternary ammonium analogues of lidocaine
scorpion venom 13
CLASS C Agents acting by receptor independent of
physiochemical mechanism
Chemical substance Benzocaine
CLASS D Agents acting by combination of receptors and
receptor independent mechanisms
Chemical substance most clinically useful anesthetic agents
(eg lidocaine mepivacaine prilocaine)
14
BASED ON THE SOURCE
NATUAL
SYNTHETIC
OTHERS
BASED ON MODE OF APPLICATION
bull INJECTABLE
bull TOPICAL
BASED ON DURATION OF ACTION
bull ULTRA SHORT
bull SHORT
bull MEDIEM
bull LONG
BASED ON ONSET OF ACTION SHORT
INTERMEDIATE
LONG
15
DISSOCIATION OF LOCAL
ANESTHETICS
Local anesthetics are available as salts (usually
hydrochlorides) for clinical use
The salts both water soluble and stable is dissolved in
either sterile water or saline
In this solution it exists simultaneously as unchanged
molecule (RN) also called base and positively charged
molecules (RNH+) called cations
RNH+ ==== RN+ H
+
16
The relative concentration of each ionic form in the solution varies
in the pH of the solution or surrounding tissue
In the presence of high concentration of hydrogen ion (low pH) the
equilibrium shifts to left and most of the anesthetic solution exists
in cationic form
RNH+ gt RN
+ + H
+
As hydrogen ion concentration decreases (higher pH) the
equilibrium shifts towards the free base form
RNH+ lt RN + H
+
17
The relative proportion of ionic form also depends on pKa or DISSOCIATION CONSTANT of the specific local anesthetic
The pKa is a measure of molecules affinity for H+
ions
When the pH of the solution has the same value as pKa of the local anesthetic exactly half the drug will exists in the RNH
+ form and
exactly half in RN form
The percentage of drug existing in either form can be determined by Henderson Hasselbalch equation
Log baseacid = pH - pKa
18
4
MECHANISM OF ACTION OF LOCAL
ANESTHETICS
The following sequence is proposed mechanism of action of LA
Displacement of calcium ions from the sodium channel receptor site
Binding of local anesthetic molecule to this receptor site
Blockade of sodium channel
19
Decrease in sodium conductance
Depression of rate of electrical depolarization
Failure to achieve the threshold potential level
Lack of development of propagated action potential
Conduction blockadehellip
20
21
Na + Na +
22
LOCAL ANESTHETIC AGENT
COMERCIALLY PREPARED LOCAL ANESTHESIA
CONSISTS OF
Local anesthetic agent (xylocaine lignocaine 2)
Vasoconstrictor (adrenaline 1 80000)
Reducing agent (sodium metabisulphite)
Preservative (methylparabencapryl
hydrocuprienotoxin)
Fungicide (thymol)
Vehicle (distillde waterNaCl)
LOCAL ANESTHETIC AGENT
The local anesthetics used in dentistry are divided
into two groups
ESTER GROUP
AMIDE GROUP
23 24
ESTER GROUP It is composed of the following
An aromatic lipophilic group
An intermediate chain containing
an ester linkage
A hydrophilic secondary or tertiary
amino group
AMIDE GROUP It is composed of the following
An aromatic lipophilic group
An intermediate chain containing
amide linkage
A hydrophilic secondary or tertiary
amino group
5
25
CLASSIFICATION OF LOCAL ANESTHETICS
ESTERS
Esters of benzoic acid
Butacaine
Cocaine
Benzocaine
Hexylcaine
Piperocaine
Tetracaine
Esters of Para-amino
benzoic acid
Chloroprocain
Procaine
Propoxycaine
26
AMIDES Articaine
Bupivacaine
Dibucaine
Etidocaine
Lidocaine
Mepivacaine
Prilocaine
Ropivacaine
QUINOLINE
Centbucridine
PHARMACOKINETICS OF LOCAL
ANESTHETICS UPTAKE
When injected into soft tissue most local anesthetics produce
dilation of vascular bed
Cocaine is the only local anesthetic that produces
vasoconstriction initially it produces vasodilation which is
followed by prolonged vasoconstriction
Vasodilation is due to increase in the rate of absorption of the
local anesthetic into the blood thus decreasing the duration of
pain control while increasing the anesthetic blood level and
potential for over dose 27
AMIDE LOCAL ANESTHETICS
The metabolism of amide local anesthetics is more
complicated then esters The primary site of
biotransformation of amide drugs is liver
Entire metabolic process occurs in the liver for lidocaine
articaine etidocaine and bupivacaine
Prilocaine undergoes more rapid biotransformation then the
other amides
28
REFERENCES
Handbook of local anesthesia ndash Stanley F Malamed ndash 6th
edition
Essentials of Local Anesthetic Pharmacology Daniel E
Becker Anesth Prog 2006 Fall 53(3) 98ndash109
WIKIPEDIEA
29
THANK YOU
30
1
Pharmacological Methods of Behavior
Management
DR MITAKSHARA NIRWAN
DEFINITIONS
bull Conscious Sedation ndash A minimally depressed level of consciousness that retains
the patients ability to independently and continuously maintain an airway and respond appropriately to physical stimulation or verbal command
(American Dental Association House Of Delegates 2000)
bull Deep Sedation ndash An induced state of depressed consciousness
accompanied by partial loss of protective reflexes including the inability to continuously maintain an airway independently and or to respond purposefully to physical stimulation or verbal command
bull General Anesthesia (G A) ndash An induced state of unconsciousness or complete loss of
protective reflexes including the inability to continually maintain an airway independently and respond purposefully to physical stimulation or verbal command
Conscious sedation
ADVANTAGES
Conscious
Protective reflexes active amp intact
Stable vital signs
Operating dentist may perform sedation
Minimum amount of equipment required
Prolong detainment in recovery room not required
Risk of complication very low
Excellent choice for poor ndash risk pt in dental office
Cost effective
General anesthesia
ADVANTAGES Not absolutely
essential May be the only
method Not necessary (no
pain reaction) Amnesia always
present
Conscious sedation
DISADVANTAGES
Pt cooperation is essential
Extremely difficult or mentally handicapped pt cannot always be managed
Use of local anesthesia is a must
Amnesia may or may not be present
General anesthesia DISADVANTAGES
Pt unconscious
Protective reflexes are depressed
Depressed
Advanced training required Dentist must not act also as anesthetist
Special equipment necessary
Detainment in recovery area necessary
High IOP amp postoperative complications
Not indicated in dental office
More expensive
Fundamental Concepts
bull Techniques that utilize drugs to induce co-operative yet conscious state in an otherwise uncooperative child ndash CONSCIOUS SEDATION
2
GOALS
1 To facilitate the provision of quality care
2 To minimize the extremes of disruptive behavior
3 To promote a positive psychologic response to treatment
4 To promote patient welfare amp safety
5 To return the patient to physiologic state
OBJECTIVES
1 The pt mood must be altered
2 The pt must remain conscious at all times
3 The pt must be cooperative
4 All protective reflexes must remain intact and active
5 Vital signs must remain stable and with in normal limits
6 The ptrsquos pain threshold should be elevated
7 Amnesia may be present
Indications
1 Preschool children
2 Lack of Psychological Emotional maturity
3 Lack of Cognitive Physical Medical disability
4 Fearful amp anxious pts
5 Pt who require extensive amp complicated dental care amp would require or benefit from prolonged visits
6 Acute pain
7 Traumatic injuries
Operating Facilities amp Equipment
A positive pressure O2 delivery system capable of administering gt than 90 O2 at 10L min flow for 60 min (650L ldquoErdquo cylinder)
OR
Self inflating bag valve mask device (15L min)
A functional suction apparatus with appropriate suction catheters
Monitoring equipment - PO BPC PC or Capno
Inhalation sedation unit
100 O2 amp never less than 25
A fail safe mechanism that is checked and calibrated annually
Must have appropriate scavenging system
Emergency drugs
Techniques of sedation
Routes for drug administration
bull Oral
bull Rectal
bull Inhalational
bull Transmucosal
ndash Sublingual
ndash Intranasal
bull Parenteral
ndash IM
ndash sub mucosal
ndash IV
3
Oral Sedation
Advantages
1 Almost universally accepted and the easiest method
2 Decreased incidence and severity of adverse reaction
3 Low cost
Disadvantages
1 Absorption is variable
2 Prolonged latent period(30 min)
3 Reversal of any unwanted effect is also difficult
4 Inability to readily lighten or deepen the level of sedation
5 Prolonged duration of action
Rectal Sedation
Advantages 1 Incidence and intensity of
drug related side effects is minimized
2 Drug absorption occurs from the large intestine directly into the circulation
3 The lack of a needle syringe or other equipment
4 The ease of administration
5 The low cost
Disadvantages
1 Inconvenience to the administrator amp pt
2 The variable absorption of drugs from the large intestine
3 The slow onset of action amp the relatively long duration of action
4 Inability to titrate the drug dosage
5 The inability to reverse the action of the drug the prolonged recovery
Intranasal sedation
Advantages
Rapid onset (10 ndash 15 min)
Simple amp relatively painless
Less pt cooperation is required
Absorbed directly into the C V S
Intranasal sedation
Disadvantages
1 Dependence on nasal mucous membrane
2 Shorter duration of action(40-60min)
3 Multiple dosage may be necessary
Drugs
Midazolam ndash 02mgkg
Sufentanil ndash 15 ndash 3 mcgkg
Ketamine ndash 3-6mg kg
Sublingual sedation
Advantages
1 Pt acceptance
2 Rapid onset
3 High bioavailability
Drugs
Oral Transmucosal Fentanyl Citrate (OTFC)
Intramuscular Sedation
Advantages
1 More rapid onset of action
2 Absorbed directly into the C V system
3 More reliable absorption of drug
4 Pt cooperation is not as essential
Disadvantages
1 Time factor ndash its 15 min latent period
2 Pt may not be willing to accept the injection
3 The prolonged duration of action(2-4 hrs more)
4 Possibility of injury to the tissues at the site of injection caused by either the drug or the needle
4
Sites of I M administration
1 Gluteal area
2 Vastus lateralis
3 Mid ndash deltoid area
Drugs
Diazepam
Midazolam
Hydroxyzine
Inhalation Sedation
Advantages
1 The onset of action is more rapid
2 Peak clinical level is achieved rapidly(3-5min) - permit titration
3 Administrator has complete control over the actions of the drug - safety feature
4 No significant over dosage
5 Flexible duration of action
6 Recovery time is rapid amp most complete
7 No injection is required
8 With N2O- O2 it is safe with very few side effects
Disadvantages
1 The initial cost of the equipment is high 2 The continuing cost of the gases is high 3 The equipment occupies considerable space 4 N2O is not a potent agent 5 A degree of cooperation is required from the pt 6 Chronic exposure to N2O is deleterious to the health of
dental personnel
Contraindications
1 Nasal obstruction 2 Cyanosis at rest 3 Poor cooperation 4 1st trimester of pregnancy 5 Fear of masks
I V Sedation
Advantages
1 The onset of action is the most rapid 2 The dosage may be titrated 3 Suitable level of sedation can be provided 4 The recovery period is shorter 5 Side effects are extremely uncommon 6 Control of salivary secretions is possible 7 The gag reflex is diminished 8 Effectively diminishes motor disturbances 9 Provides immediate access to CVS in emergency
Disadvantages
1 Venipuncture is necessary
2 Complication may rise at the site of the venipuncture
3 Monitoring must be more intensive
4 Recovery is not complete at the end of the procedure
5 Reversal of sedation is difficult
5
N2O-O2 (Relative Analgesia)
colorless sweet smelling gas
Pharmacokinetics
Absorption through pulmonary epithelium
It is approx 15 times as soluble as is nitrogen It replaces nitrogen in blood
It is carried in solution in plasma of the blood
It is not metabolized by the body
Elimination ndash majorndash lungs minor --- skin
perspiration urine and intestinal gas
Pharmacodynamics
Dose related
10 ndash 25 Lightheaded
Changes in visual amp auditory sensation
Tingling of hands amp feet
Suffusing warmth
Remote from the immediate environment
Reduced anxiety
25-50 max analgesic properties and aberration of vision hearing and proprioception mild drowsiness euphoria amnesia and increased sleepiness and dreams
35 conc will achieve maximum analgesia
bull CNS
ndash Cerebrum-primarily affected
ndash Safe but weak anesthetic agent
bull RESPIRATORY SYSTEM
ndash Increased Tidal and minute volumes
bull CARDIOVASCULAR SYSTEM
ndash 2 studies ndash decreased cardiac output
bull FETAL SYSTEMS
ndash Miscarriage in humans
bull OTHER SYSTEMS
ndash Depression of spinal reflexes increase muscle tone indicates stage of delirium
ndash Muscle rigidity-narcotics + nitrous oxide
ndash Nausea and vomitting - GIT
ndash HEMATOPOIESIS ----- prolonged exposure
Adverse reactions and toxicity
EMOTIONAL REACTIONS
DREAMS HALLUCINATIONS
No acute toxicity
Chronic toxicity ndash bone marrow
depression
PROCEDURE
Diffusion Hypoxia
Sevoflurane
A fluorinated derivative of isopropyl ether ndash synthesized in 1970
Potent anaesthetic agent with rapid uptake amp speedy recovery
Day-case surgery
Problem
Attaching vaporiser to any of the currently available machine
BENZODIAZEPINES
Diazepam 1961 lipid soluble
Uses-alcoholism epilepsy labor tetanus and cerebral palsy
- sedation and amnesia
- varieties of neurosis amp anxiety states
Pharmacokinetics
Orally Rectal IMIV or SC
Well absorbed through GIT
Excretion in urine
6
bull Pharmacodynamics
ndash Depress the brain stem reticular system and the limbic system thalamus and hypothalamus
ndash It is a centrally acting muscle relaxant Has anti-convulsant properties
Adverse reaction amp toxicity
ndash Confusion nausea headache increased appetite decreased salivation and jaundice Thrombophlebitis
ndash Rebound phenomenon
ndash Toxicity drowsiness confusion sleep and coma
Dosage Oral or Rectal ndash 02-05mgkg
Maximum single dose 10mg
IV- 025mgkg
Supplied Tablets 2 5 10 mg
Suspension ndash 5mg
Midazolam Water soluble ndash non-irritant
Oral IM IV
Metabolism- liver
Onset IV 3 -5mins
oral 20 ndash 30mins
Oral administration anxious patients requiring relatively short dental procedure
No rebound phenomenon
Better anxiolysis amp amnesia (retrograde amnesia)
Adverse effects Respiratory depression
dose dependant apnea
Dosage Oral ndash 025 to 1mgkg to maximum single dose 20mg
IM ndash 01 to 015mgkg to a maximum of 10mg
IV ndash slow IV
Supplied Syrup ndash 2mgml
Injectable ndash 1mgml amp 5mgml vials
Flumazenil specific benzodiazepines antagonist
selectively inhibits CNS effects
IV administration amp not recommended below 18yrs of age
02mg over 15 seconds after 45seconds 02mg then after 60seconds to maximum of 1mg
Sedative-Hypnotics
Barbiturates First truly effective drugs for the management of anxiety Generalized CNS depressants Produce dose dependent effects
Sedation ---- sleep ---- GA ---- coma
Suppress the CNS and result in sedation and amnesia Advantages
Rapid onset and short duration Disadvantages
no analgesic effect and possible hypotension Must be used with caution in trauma patients because they may cause
apnea and hypoventilation
DOSE Pentobarbital Sodium 100mg Secobarbital Sodium 100 to 200mg Children 30 to 100mg
bull Chloral Hydrates (Mickey Finn Knock out drops ) First synthesized in 1832 first member of the hypnotic group of drugs
Widely used as conscious sedation agent
Properties
Unpleasant taste
Nausea vomiting
Quite irritating to skin and to mucous membranes
GI irritation
Dosages Individualized for each patient 25 ndash 50mgkg
maximum of 1g
Supplied oral capsule ndash 500mg
oral solution ndash 250 amp 500mg5ml
Rectal suppositories ndash 324 amp 648mg
Narcotics
Do produce sedation amp euphoria greater in children
LA is required but dose should be decreased
Meperidine Synthetic opiate agonist
Very water soluble
Orally SC IM or IV
Peak effect by oral 1 hr amp lasts upto 4 hrs
Adverse reactions
-Seizures
-Extreme caution in hepatic or renal diseases or history of seizures
7
Dosage Oral SC or IM ndash 1to 22mgkg not to exceed 100 mg
Supplied Oral Tablets ndash 50 amp 100mg
Oral Syrup ndash 50mgml
Parental solution ndash 25 50 75 amp 100mgml
Fentanyl
Synthetic opiate narcotic analgesic
Very potent 01mg = 10mg Morophine75mg Meperidine
Pharmacokinetics
IV IM SM
Metabolized in liver Excreted in urine
Fentanyl Onset ndash 7 to 15mins
Duration ndash 1 to 2 hrs
Pharmacodynamics
Respiratory depression RR but returns to normal rapidly Tidal volume amp response to co2 depressed for extended period
Apnea
Less emetic than meperidine
NOT RECOMMENDED IN CHILDREN BELOW 2yrs
Dosage 0002 to 0004mgkg
Supplied 005mgml in 2 amp 5ml ampoules
Reversal drug Naloxone
Semisynthetic opiate antagonist
No agonist activity
Onset 2 to 5mins SC or IM amp 1 to 2mins IV
Reversal 45mins
Pt should be kept under continual surveillance
Adverse reaction nausea vomiting sweating hypotension hypertension ventricular tachycardia fibrillation
Dosage IV SC IM 001mgkg then 01mgkg every 2- 3mins maximum 2mg
Supplied 002 004 1mg solutions
Antihistamines
Hydroxyzine
Oral or IM
Effect ndash 15 ndash 30mins
Half-life ndash 3 hrs
Uses
To relieve anxiety
Used as an anti-histamine
Used to control nausea and vomiting including that associated with motion sickness and pregnancy
Adverse reaction dry mouth drowsiness hypersentivity
Dosage Oral ndash 1 to 2mgkg
IM ndash 11mgkg
Promethazine Oral or IM Onset 15 to 60mins Duration 4 to 6 hrs Uses
To prevent and treat nausea and vomiting associated with motion pregnancy or surgery
Produces sedation and reduce swelling pain and trismus
Lower seizure threshold Adverse reaction dry mouth blurred vision thickening of bronchial secretions Dosage OralIM ndash 05-11mgkg
maximum 25 mg
Diphenhydramine
Oral IM IV
Onset -1hr
Duration ndash 4 to 6 hr
Metabolized in liver
Adverse reaction disturbed coordination thickening of bronchial secretions
Dosage Oral IM IV ndash 1 to 15mgkg
maximum 50mg
Tranquilizers
Major tranquilizer antipsychotic produce calmness control symptoms of psychoses cause reversible extra pyramidal symptoms and do not tend to cause habituation
Minor tranquilizer antianxiety agents also cause calmness do not cause extrapyramidal symptoms Used in conditions like nervous tension and mild depression
8
Classification
Antipsychotics
Phenothiazine derivatives
Chlorpromazine promazine
Butryophenones
Haloperidol
Rauwolfia alkaloids
Reserpine
Antianxiety drugs
Propyl alcohol derivatives
Meprobamate
Benzodiazepine derivatives
Diazepam
Miscellaneous compounds
Hydroxyzine
Meprobamate
White crystalline powder slightly bitter in taste
Only administered orally
Peak blood concentration ----1 to 3hrs
10 ---------excreted unchanged Rest --- excreted as a oxidized derivative or as a glucoronide
Uses
To relieve day time anxiety
Induce sleep in insomniacs
To reduce anxiety associated with dental treatment
Anti-convulsant ndash petit mal epilepsy
Adverse reaction leucopenia acute non-thrombocytopenic purpura ecchymoses eosinophilia edema adenopathy
Dosage Childrengt 6yrs 100 to 200mg
Not recommended for children under 6yrs
Monitoring during sedation
1 Pulse
2 Blood pressure
3 ECG
4 Respiration
5 Temperature
Pulse
Manual Electronic
bull Radial Brachial
bull Facial labial
Blood pressure
ndash Stethoscope amp sphygmomanometer
ndash Automatic devices
ndash Direct cannulation of an artery ndash very accurate
Electrocardiograph
Heart rate rhythm myocardial function
9
Respiration
ndash Monitoring respiratory rate
ndash Observing the rise amp fall of the chest wall
ndash Observing the color of mucous membrane
ndash Observing the inflation amp deflation of the reservoir bag
Devices for monitoring respiration
1 The Precordial pretracheal stethoscope
2 The esophageal stethoscope
ndash Respiratory rate
ndash Heart rate
ndash Any abnormal sounds
Pulse Oximeter
ndash Oxygen saturation
ndash Heart rate
ndash Oxisensor site
ndash Fingers
ndash Toe
ndash Ear lobe
Mechanism
Oxygenated Hb ndash red light
Deoxygenated Hb- infrared light
Tissue pressure from arterial pulse (plethysmography)
Advantages
ndash Safe amp noninvasive
ndash Simple to use
ndash Information is rapidly available for clinical decision
ndash Indirectly indicates respiratory adequacy
Disadvantages
ndash Finger probes can get dislodged
ndash Emitted light source may cause burning
ndash Non reusable probes are expensive
ndash Does not directly determine airway patency
Capnography
1 The presence absence of air flow
2 Indicates depth amp adequacy of respiration
3 Continues analysis of the co2 content of the respired air ndash indicates respiratory adequacy
Temperature
ndash Disposable nondisposable thermometer
ndash Esophageal rectal temp probe
10
Discharge criteria
Cardiovascular function is satisfactory amp stable
Airway patency is uncompromised amp satisfactory
Pt is easily arousable amp protective reflexes intact
State of hydration is adequate
Pt can talk if applicable
Pt can sit unaided if applicable
Pt can ambulate with minimal assistance if applicable
Presedation level of responsiveness achieved
Responsible individual is available
1
PULP THERAPY OF VITAL TEETH
DR MITAKSHARA NIRWAN
Contents
Indirect pulp capping
Direct pulp capping
Medications amp materials used in pulp capping
Pulpotomy
MTA
Apexogenesis
INDIRECT PULP CAPPING
Pieter Van Forest - first to speak about root canal therapy
Glove designed instruments that could prepare a canal to a certain size and taper(1910)
Indirect pulp capping is defined as a procedure where in small amount of carious dentin is retained in
deep areas of cavity to avoid exposure of pulp followed by placement of a suitable medicament and
restorative material that seals off the carious dentin and encourages pulp recovery (Ingle)
A procedure in which only the gross caries is removed from the lesion and the cavity is sealed for a
time with a biocompatible material (McDonald)
Objective of indirect pulp capping
These were given by Eidelman in 1965
bull Arresting the carious process
bull Promoting dentin sclerosis
bull Stimulating formation of tertiary dentin
bull Remineralization of carious dentin
Layers of Carious Dentin Indications of Indirect Pulp Capping
History
Mild pain associated with eating
Negative history of spontaneous extreme pain
Clinical Examination
Deep carious lesion which are close tobut not involving the pulp in vital primary or young
permanent teeth
No mobility
Nominal pulp inflammationdefinite layer of affected dentin after removal of infected dentin
Radiographic examination
Normal lamina dura amp PDL space
No radiolucency around the apices
2
Contraindications of Indirect Pulp Capping
History
Sharp penetrating pulpalgia
Prolonged spontaneous pain especially at night
Clinical examination
Mobility of tooth
Discoloration of tooth
Negative reaction of electric pulp testing
Radiographic examination
Definite pulp exposure
Break in the lamina dura
Radiolucency around the apices
Widened PDL space
Treatment procedure
Sequelae of Indirect Pulp Capping Three distinct types of new dentin formation take place
1 Cellular fibrillar dentinmdashfirst 2 months
2 Globular dentinmdash3 months
3 Tubular dentin (uniform mineralized dentin)
bull 15th of reparative dentin formation begins in less than 30 days
bull After 3 months 01 mm is formed
DIRECT PULP CAPPING Defined by Kopel (1992) as the placement of a medicament or non medicated material on a pulp that
has been exposed in course of excavating the last portions of deep dentinal caries or as a result of
trauma
Objective
To create new dentin in the area of the exposure and subsequent healing of the pulp
Rationale
achieve a biologic closure of the exposure site by deposition of hard tissue barrier (dentin bridge)
between pulp tissue and capping material thus walling off the
INDICATIONS
Small mechanical exposure
Easily controlled haemorrhage
Bright red haemorrhage
True pinpoint exposure
CONTRAINDICATIONS
Severe toothache at night
Spontaneous pain
Tooth mobility
Radiographic appearance of pulp periradicular de- generation
Excess of hemorrhage at the time of exposure Serous exudate from the exposure
Externalinternal root resorption
Swellingfistula
Histological Changes after Pulp Capping
These were illustrated be Glass and Zander in 1949
After 24 hours Necrotic zone adjacent to calcium
hydroxide paste is separated from healthy pulp
tissue by a deep staining basophilic layer
After 7 days Increase in cellular and fibroblastic
activity
After 14 days Partly calcified fibrous tissue lined by
odontoblastic cells is seen below the calcium
proteinate zone disappearance of necrotic zone
After 28 days Zone of new dentin
3
Medications and Materials Used for Pulp Capping Calcium hydroxide
Corticosteroids amp antibiotics
Inert materials
Collagen fibers
4-META adhesive
Direct bonding
Isobutyl cyanoacrylate
Denatured albumin
Mineral trioxide aggregate
Laser
Bone morphogenic protein
PULPOTOMY
Finn (1995) defined it as the complete removal of the coronal portion of the dental pulp
followed by placement of a suitable dressing or medicament that will promote healing and
preserve vitality of the tooth
American Academy of Pediatric Dentistry (1998) defined pulpotomy as the amputation of
affected infected coronal portion of the dental pulp preserving the vitality and function of the
remaining part of radicular pulp
Objectives
bull Removal of inflamed and infected coronal pulp at the site of exposure thus preserving the vitality of the
radicular pulp and allowing it to heal
bull Maintain the tooth in the dental arch
Rationale
bull Radicular pulp is healthy and capable of healing after surgical amputation of the infected coronal pulp
bull Preserves vitality of the radicular pulp
bull Maintains tooth in a physiologic condition
Indications of Pulpotomy bull Mechanical pulp exposure in primary teeth
bull Teeth showing a large carious lesion but free of radicular pulpitis
bull History of only spontaneous pain
bull Hemorrhage from exposure sites bright red and can be controlled
bull Absence of abscess or fistula
bull No interradicular bone loss
bull No interradicular radiolucency
Contraindications of Pulpotomy bull Persistent toothache
bull Tenderness on percussion
bull Root resorption more than 13rd of root length
bull Large carious lesion with nonrestorable crown
bull Highly viscous sluggish hemorrhage from canal orifice which is uncontrollable
bull Medical contradictions like heart disease immuno compromised patient
bull Swelling or fistula
bull External or internal resorption
bull Pathological mobility
bull Calcification of pulp
Classification of pulpotomy
4
Formocresol Pulpotomy
Iby BUCKLEY in 1904
Sweet (1930) Formulated multi visit technique
Doyle (1962) Advocated 2 sitting procedure (complete devitalization)
Spedding (1965) Gave 5 minute protocol (partial devitali- zation)
Venham (1967) Proposed 15 seconds procedure
Current concept uses 4 minutes of application time
Composition of formocresol Buckleyrsquos Formula
bull Cresol ndash 35 percent
bull Glycerol ndash 15 percent
bull Formaldehyde ndash 19 percent
bull Water ndash 31 percent
Mechanism of Action
It prevents tissue autolysis by bonding to the proteins Bonding is of peptide groups of side chain amino acids and is a reversible process accomplished without
changing the basic structure of protein molecules
Histological Changes
bull Demonstrated by Mass and Zilbermann11 in 1933 and also by Massler and Mansokhani in 1959
bull Immediately the pulp becomes fibrous and acidophillic
bull Seven to fourteen days Three zones appear
a broad eosinophilic zone of fixation
b broad pale-staining zone of atrophy with poorcellular definition
c broad zone of inflammation extending apically into normal pulp tissue
bull One yearndash Progressive apical movement of these zones with only acidophillic zone left at the end of 1 year
Modified Formocresol Pulpotomy
Used by TRASK(1972)
The technique is identical to that described for primary teeth except that the formocresol pellet is
sealed permanently in the tooth
Two-visit Devitalization Pulpotomy
Indications
bull There is evidence of sluggish bleeding at the amputation site that is difficult to control
bull Pus in the chamber but none at the amputation site
bull There is thickening of the PDL
bull History of pain
Contraindications
bull Nonrestorable tooth
bull Tooth with necrotic pulp
5
Glutaraldehyde Pulpotomy
It was first suggested by S Gravenmade Introduced by Kopel in 1979
Mechanism of Action
bull Glutaraldehyde produces rapid surface fixation of the underlying pulpal tissue
bull A narrow zone of eosinophilic stained and compressed fixed tissue is found directly beneath the area of application which blends into vital normal appearing tissue apically
bull With time the glutaraldehyde fixed zone is replaced by macrophagic action with dense collagenous tissue thus the entire root canal tissue is vital
Cvekrsquos Pulpotomy
bull This is also called as calcium hydroxide pulpotomy or young permanent partial pulpotomy
bull This was proposed by Mejare and Cvek16 in 1978
bull Indicated in young permanent teeth where the pulp is exposed by mechanical or bacterial means and the
remaining radicular tissue is judged vital by clinical and radiographic criteria whereas the root closure is
notcomplete
MINERAL TRIOXIDE AGGREGATE (MTA) Torabinejad described the physical and chemical properties of MTA in 1995
It is ash colored powder made primarily of fine hydrophilic particles of
1 tricalcium aluminate
2 tricalcium silicate
3 silicate oxide
4 tricalcium oxide
5 bismuth dioxide
Hydration of the powder results in a colloidal gel composed of calcium oxide crystals in an amorphous
structure This gel solidifies into a hard structure in less than three hours
PROPERTIES OF MTA
It is biocompatible material and its sealing ability is better than that of amalgam or ZOE
Initial pH is 102 and set pH is 125
The setting time of cement is 4 hours
The compressive strength is 70 MPA which is comparable with that of IRM
Low cytotoxicity ndash It presents with minimal inflammation if extended beyond the apex
Mineral trioxide aggregate (MTA) has demonstrated the ability to induce hard-tissue formation in
pulpal tissues and it promotes rapid cell growth
APEXOGENESIS
It is defined as the treatment of a vital pulp by capping or pulpotomy in order to permit continued
growth of the root and closure of the open apex
Rationale
Maintenance of integrity of the radicular pulp tissue to allow for continued root growth
Indications
bull Indicated for traumatized or pulpally involved vital permanent tooth when root apex is incompletely formed
bull No history of spontaneous pain
bull No sensitivity on percussion
bull No hemorrhage
bull Normal radiographic appearance
Contraindications
bull Evidence that radicular pulp has undergone degenerative changes
bull Purulent drainage
bull History of prolonged pain bull Necrotic debris in canal
bull Periapical radiolucency
6
1
Gupta A Dhingra R Chaudhari P Gupta A
Department of Paedodontics and Preventive Dentistry Faculty of Dental Sciences SGT University Gurgaon Haryana India
Journal of Indian Society of Pedodontics and Preventive Dentistry
Volume 35 I Issue 3 I July-September 2017
A COMPARISION OF VARIOUS MINIMALLY
INVASIVE TECHNIQUES FOR THE REMOVAL
OF DENTAL FLUOROSIS STAINS IN
CHILDREN
DR MITAKSHARA NIRWAN
CONTENTS
bull Introduction
bull Aims
bull Materials and Methods
bull Results
bull Discussion
bull Conclusion
bull Critical analysis
bull References
INTRODUCTION
bull Dental fluorosis is a developmental disturbance of dental enamel caused by
successive exposure to high concentrations of fluoride during tooth
development
bull Various methods of therapy are advocated for the treatment of fluorosis -
stained teeth which range from invasive ceramic veneer bonding restorations
to abrasive chemical treatments
bull The combination of dental bleaching techniques and microabrasion appears
as an excellent conservative solution to reestablish health in fluorosis
affected teeth
AIMS
bull The aim of the study was to evaluate and compare the effectiveness of
minimally invasive techniques for the removal of dental fluorosis
stains in children in vivo
MATERIALS AND METHODS
Patients visiting the department of Pedodontics and Preventive dentistry
Faculty of Dental Sciences SGT University Gurgaon
bull Sample size 90 patients
bull Age group 10 -17 years
bull Caries cracks or periodontal
disease on anterior teeth
bull Abscess draining sinus
cellulitis
bull Non vital teeth
hypersensitive exposed
crevices
bull Orthodontic appliance
bull Past history of bleaching
bull At least two permanent
maxillary anterior teeth
bull TSIF of score 4
bull Free of systemic diseases
Inclusion criteria Exclusion criteria
2
Groups
Group A In office bleaching with 35 hydrogen peroxide( Pola Office
Bleaching kit) activated by light emitting diode (LED) bleaching unit
(35 HP)
Group B Enamel microabrasion (EM) (PREMA Enamel Microabrasion
System) followed by in-office bleaching with 44 carbamide peroxide
gel (EM)
Group C In-office bleaching with 5 sodium hypochlorite (5
NaOCl)
A baseline colour evaluation was done by taking digital photograph of
the maxillary anterior teeth
RESULTS
Group 1
Colour stability
Group 2 Group 3
Tooth sensitivity
Tooth sensitivity values were taken before the treatment
which was compared to immediate postoperative and follow
up visits It was checked using an electric pulp tester
maximum
moderate
least
immediately
group 2
group 1
group 3
1 month
group 2
group 1
group 3
3 month
group 2
group 1
group 3
Patient satisfaction score
Satisfaction was assessed on visual analog scale
Range 1 to 5
Groups percentage of patients
who were satisfied with
the treatment
Number of patients
who reported slight
reappearance of colour
Group 1
90
7
Group 2
83
8
Group 3
73
7
3
Number of Appointments
Groups One sitting Two sittings Three
sittings
Group 1
25
4
1
group 2
26
3
1
Group 3
30
0
0
DISCUSSION
bull Hydrogen peroxide is capable of penetrating the tooth osmosis and through porosities and cracks subsequently acting directly on the pigmented molecules
bull Gurgan et al investigated 3 different light systems and found out that diode laser system with gave best tooth whitening and least tooth sensitivity
bull In the EM group the surface reflects and refracts light from the surface in such way that mild imperfections in underlying enamel are camouflaged While the highly polished surface of enamel enhances the aesthetic appearance
bull Train et al and Loguercio et al also had the similar results in their studies with EM mild fluorosis showed best results moderate showed moderate results while it had little effect on severe fluorosis
bull NaOCl was only effective on mild stains while moderate and severe
stains could only be lightened to quite an extent but could not be
completely removed
bull When NaOCl comes in contact with hypomineralized and discoloured
enamel it degrades and removes the chromogenic organic material
located on the enamel surface
CONCLUSION
bull It was concluded that esthetic appearance of teeth mild fluorosis can
be achieved by bleaching and microabrasion But in cases of
moderate fluorosis a combination of any of theses modalities can be
used
bull As no special maintenance precautions are required these maybe be
considered as an interesting alternative to conventional operative
treatment
bull Focuses on only TSIF of 4
bull Electric pulp testing is not the
right method to check for
sensitivity
bull Tooth Sensitivity changes
from person to person
bull Food habits can cause
staining of the teeth
bull Minimally invasive
bull Cheaper to veneers
bull Minimal loss of tooth structure
bull 4 parameters checked for the success of treatment
bull Inclusion of specific score of fluorosis for comparing the results
bull Maximum 3 appointments needed
CRITICAL ANALYSIS
Pros Cons
REFERENCES
bull Gurgan S Cakir FY Yazici E Different light-activated in officebleaching
systems Lasers Med Sci 201025817-22
bull Train TE McWhorter AG Seale NSWilson CF Guo IY Examination of
esthetic improvement and surface alteration following microabrasion in
fluorotic human incisors in vivoPediatr dent 199618353-62
bull Loguercio AD Correia LD Zago C Tagliari D Neumann E Gomes OM et al
Clinical effectiveness of two microabrasion materials materials for the
removal of enamel flurosis stains Oper Dent 200732531-8
4
4
19
bull IMMEDIATE POST OPERATIVE RADIOGRAPHIC ASSESSMENT REVEALED 68 (102150) ROOTS
WITH OPTIMAL OBTURATION AND 32 (48150) WITH OVERFILLINGUNDERFILLING MAXIMUM
NO OF OPTIMAL FILLINGS WERE OBSERVED IN GROUP1 (CA + E) (3333) FOLLOWED BY
GROUP 2 (CA) (2549) GROUP 3(SH + E) (2549) AND GROUP 4(SH) (1568)
bull CITRIC ACID GROUPS HAD MORE NUMBER OF OPTIMALLY FILLED ROOTS 588 (60102) THAN
NON CITRIC ACID GROUPS 412 (42102)
bull ENDOACTIVATOR CONTRIBUTED TO 18 OF OPTIMAL OBTURATION IRRESPECTIVE OF
CHELATING AGENT USED
20
21
bull MAXIMUM NO OF VOIDS AND VOID AREAS WERE IN NON CITRIC ACID GROUPS
(6419 amp 5384) COMPARED TO CITRIC ACID GROUPS (3580 amp 4615)
RESPECTIVELY
bull ANALYSIS OF ROOT 13RD REVEALED MAXIMUM NO OF VOID AREA IN APICAL
13RD (4755) FOLLOWED BY MIDDLE 13RD (3846) AND CORONAL 13RD
(1398)
bull LEAST NO OF VOIDS amp VOID AREA (1111 amp 1608) WERE OBSERVED WHEN
ENDOACTIVATOR ALONG WITH CHELATING AGENT WAS USED (GROUP 1)
HOWEVER THIS WAS STATISTICALLY INSIGNIFICANT
22
DISCUSSION
bull IN THE PRESENT STUDY 1 SODIUM HYPOCHLORITE WAS USED ALONG WITH 6 CITRIC ACID
(CHELATING AGENT) WHICH IS REPORTED TO BE AS EFFECTIVE AS 17 EDTA
bull CITRIC ACID (BIOLOGICAL ACID) IS FOUND TO BE BIOCOMPATIBLE AND LEAST IRRITATING TO
PERIAPICAL TISSUES THAN OTHER CHELATING AGENTS
bull USE OF SODIUM HYPOCHLORITE SOLUTION FOLLOWING CHELATING AGENT WAS AVOIDED AS IT
RAPIDLY PRODUCES SEVERE EROSION OF ROOT CANAL WALL DENTIN
bull TRADITIONAL APPROACH OF DELIVERING IRRIGANTS INTO THE ROOT CANAL SPACE USING
SYRINGES AND METAL NEEDLES HAS BEEN FOUND TO BE INEFFECTIVE ESPECIALLY IN THE AREAS OF
ANASTOMOSES BETWEEN CANALS AND APICAL 13RD OF ROOT CANAL
23
bull THEREFORE TO ACHIEVE BETTER CLEANING EFFICIENCY IRRIGANT ACTIVATION HAS BEEN
RECOMMENDED SONIC ACTIVATION HAS BEEN REPORTED TO RESULT IN BETTER ROOT CANAL
CLEANLINESS AS COMPARED TO NO ACTIVATION OF IRRIGANT
24
5
CONCLUSION
bull USE OF 6 CITRIC ACID DEFINITELY HELPED IN RAPID ELIMINATION OF PAIN RESOLUTION OF
PERI-RADICULAR RADIOLUCENCY BETTER OBTURATION QUALITY IN TERMS OF LESS VOIDS AND
VOID AREAS ALONG WITH MAXIMUM NO OF OPTIMAL OBTURATION UP TO APICAL AREA
bull 6 CITRIC ACID AND ENDOACTIVATOR IRRIGATION PROTOCOL PROVED TO BE THE BETTER
IRRIGATION PROTOCOL WHICH MAY CONTRIBUTE TO LONG TERM SUCCESS OF PRIMARY
TOOTH AND THE HEALTH OF UNDERLYING PERMANENT TOOTH
bull 6 CITRIC ACID ALONG WITH ENDOACTIVATOR MAY BE RECOMMENDED AS IRRIGATION
ADJUNCTS IN PULPECTOMY PROCEDURE OF PRIMARY TEETH
25
PROS AND CONS
PROS
bull PROPER EXPLANATION OF THE MATERIALS
USED
CONS
bull NO PREOPERATIVE AND POSTOPERATIVE
RADIOGRAPHS
26
REFERENCES
bull RAMACHANDRA JA NIHAL NK NAGARATHNA C VORA MS ROOT CANAL IRRIGANTS IN
PRIMARY TEETH WORLD J DENT 20156(3)229-234
bull MOHAMMADI Z JAFARZADEH H SHALAVI S KINOSHITA JI UNUSUAL ROOT CANAL
IRRIGATION SOLUTIONS J CONTEMP DENT PRACT 201718(5)415-420
bull ZEHNDER M ROOT CANAL IRRIGANTS J ENDOD 2006 32389- 98
bull SMITH JJ amp WAYMAN BE AN EVALUATION OF THE ANTIMICROBIAL EFFECTIVENESS OF
CITRIC ACID AS A ROOT CANAL IRRIGANT JOURNAL OF ENDODONTICS 1986 12(2) 54-58
bull TANNURE PN AZEVEDO CP BARCELOS R GLEISER R PRIMO LG LONG-TERM OUTCOMES OF
PRIMARY TOOTH PULPECTOMY WITH AND WITHOUT SMEAR LAYER REMOVAL A RANDOMIZED
SPLIT-MOUTH CLINICAL TRIAL PEDIATR DENT 201133316E20 27
bull CARON G NHAM K BRONNEC F MACHTOU P EFFECTIVENESS OF DIFFERENT FINAL IRRIGANT
ACTIVATION PROTOCOLS ON SMEAR LAYER REMOVAL IN CURVED CANALS J ENDOD
2010361361E6
bull COLL JA SADRIAN R PREDICTING PULPECTOMY SUCCESS AND ITS RELATIONSHIP TO
EXFOLIATION AND SUCCEDANEOUS DENTITION PEDIATR DENT 19961857E63
28
1
LOCAL
ANESTHESIA
DR MITAKSHARA NIRWAN
CONTENTS
Definition
Methods of inducing local anesthesia
Desirable properties
Electrophysiology of nerve conduction
Impulse propagation and spread
Mode and site of action of local anesthesia
Classification of local anesthetic according to biological site and mode of action
Dissociation of local anaesthetics
Mechanism of action of local anaethetics
Local anaesthetic agent
2
3
DEFINITION
Local anesthesia is defined as a loss of sensation in
a circumscribed area of the body caused by depression
of excitation in nerve endings or an inhibition of the
conduction process in peripheral nerves
An important feature of local anesthesia is that it produces
LOSS OF SENSATION WITHOUT INDUCING LOSS OF
CONSCIOUSNESS
4
METHODS OF INDUCING LOCAL
ANESTHESIA
Low temperature
Mechanical trauma
Anoxia
Neurolytic agents such as alcohol amp phenol
Chemical agents such as local anesthetics
PROPERTIES OF LOCAL
ANESTHESIA
It should not be irritating to tissue to which it is applied
It should not cause any permanent alteration of nerve structure
Its systemic toxicity should be low
Time of onset of anesthesia should be short
It should be effective regardless of whether it is injected into the tissue or applied locally to mucous membranes
The duration of action should be long enough to permit the completion of procedure
5 6
It should have the potency sufficient to give complete
anesthesia with out the use of harmful concentration solutions
It should be free from producing allergic reactions
It should be free in solution and relatively undergo
biotransformation in the body
It should be either sterile or be capable of being sterilized by
heat with out deterioration
2
ELETROPHYSIOLOGY OF
NERVE CONDUCTION
There is an electrical charge across the membrane
This is the membrane potential
The resting potential (when the cell is not firing) is a negative
electrical potential of -70mv that exists across the nerve
membrane produced by different concentrations of either side of
the membrane
The interior of nerve is NEGATIVE in relation to exterior
7 8
inside
outside
Resting potential of neuron = -70mV
+
-
+
-
+
-
+
-
+
-
SLOW DEPOLARIRIZATION
9
RAPID DEPOLARIZATION
The interior of nerve is POSITIVE in relation to exterior
REPOLARIZATION
10
bull Repolarization takes 07 msec
bull Depolarization takes 03 msec
SODIUM PUMP -
energy comes from the oxidative metabolism of ATP
bull The entire process require 1 msec
IMPULSE PROPOGATION
IMPULSE SPREAD
The propagated impulse travels along the nerve
membrane towards CNS The spread of impulse differs
in myelinated and unmyelinated nerve fibers
DEPOLARIZED SEGMENT ADJACENT RESTING AREA
MODE AND SITE OF ACTION OF LOCAL
ANESTHETICS
Local anesthetic agent interferes with excitation
process in a nerve membrane in one of the
following ways
Altering the basic resting potential of nerve
membrane
Altering the threshold potential
Decreasing the rate of depolarization
Prolonging the rate of repolarization
12
3
CLASSIFICATION OF LOCAL ANESTHETIC
SUBSTANCES ACCORDING TO
BIOLOGICAL SITE AND MODE OF ACTION
CLASS A
Agents acting at receptor site on external surface of nerve membrane
Chemical substance Biotoxins (eg tetrodotoxin and saxitoxin)
CLASS B
Agents acting on receptor sites on internal surface of nerve membrane
Chemical substance Quaternary ammonium analogues of lidocaine
scorpion venom 13
CLASS C Agents acting by receptor independent of
physiochemical mechanism
Chemical substance Benzocaine
CLASS D Agents acting by combination of receptors and
receptor independent mechanisms
Chemical substance most clinically useful anesthetic agents
(eg lidocaine mepivacaine prilocaine)
14
BASED ON THE SOURCE
NATUAL
SYNTHETIC
OTHERS
BASED ON MODE OF APPLICATION
bull INJECTABLE
bull TOPICAL
BASED ON DURATION OF ACTION
bull ULTRA SHORT
bull SHORT
bull MEDIEM
bull LONG
BASED ON ONSET OF ACTION SHORT
INTERMEDIATE
LONG
15
DISSOCIATION OF LOCAL
ANESTHETICS
Local anesthetics are available as salts (usually
hydrochlorides) for clinical use
The salts both water soluble and stable is dissolved in
either sterile water or saline
In this solution it exists simultaneously as unchanged
molecule (RN) also called base and positively charged
molecules (RNH+) called cations
RNH+ ==== RN+ H
+
16
The relative concentration of each ionic form in the solution varies
in the pH of the solution or surrounding tissue
In the presence of high concentration of hydrogen ion (low pH) the
equilibrium shifts to left and most of the anesthetic solution exists
in cationic form
RNH+ gt RN
+ + H
+
As hydrogen ion concentration decreases (higher pH) the
equilibrium shifts towards the free base form
RNH+ lt RN + H
+
17
The relative proportion of ionic form also depends on pKa or DISSOCIATION CONSTANT of the specific local anesthetic
The pKa is a measure of molecules affinity for H+
ions
When the pH of the solution has the same value as pKa of the local anesthetic exactly half the drug will exists in the RNH
+ form and
exactly half in RN form
The percentage of drug existing in either form can be determined by Henderson Hasselbalch equation
Log baseacid = pH - pKa
18
4
MECHANISM OF ACTION OF LOCAL
ANESTHETICS
The following sequence is proposed mechanism of action of LA
Displacement of calcium ions from the sodium channel receptor site
Binding of local anesthetic molecule to this receptor site
Blockade of sodium channel
19
Decrease in sodium conductance
Depression of rate of electrical depolarization
Failure to achieve the threshold potential level
Lack of development of propagated action potential
Conduction blockadehellip
20
21
Na + Na +
22
LOCAL ANESTHETIC AGENT
COMERCIALLY PREPARED LOCAL ANESTHESIA
CONSISTS OF
Local anesthetic agent (xylocaine lignocaine 2)
Vasoconstrictor (adrenaline 1 80000)
Reducing agent (sodium metabisulphite)
Preservative (methylparabencapryl
hydrocuprienotoxin)
Fungicide (thymol)
Vehicle (distillde waterNaCl)
LOCAL ANESTHETIC AGENT
The local anesthetics used in dentistry are divided
into two groups
ESTER GROUP
AMIDE GROUP
23 24
ESTER GROUP It is composed of the following
An aromatic lipophilic group
An intermediate chain containing
an ester linkage
A hydrophilic secondary or tertiary
amino group
AMIDE GROUP It is composed of the following
An aromatic lipophilic group
An intermediate chain containing
amide linkage
A hydrophilic secondary or tertiary
amino group
5
25
CLASSIFICATION OF LOCAL ANESTHETICS
ESTERS
Esters of benzoic acid
Butacaine
Cocaine
Benzocaine
Hexylcaine
Piperocaine
Tetracaine
Esters of Para-amino
benzoic acid
Chloroprocain
Procaine
Propoxycaine
26
AMIDES Articaine
Bupivacaine
Dibucaine
Etidocaine
Lidocaine
Mepivacaine
Prilocaine
Ropivacaine
QUINOLINE
Centbucridine
PHARMACOKINETICS OF LOCAL
ANESTHETICS UPTAKE
When injected into soft tissue most local anesthetics produce
dilation of vascular bed
Cocaine is the only local anesthetic that produces
vasoconstriction initially it produces vasodilation which is
followed by prolonged vasoconstriction
Vasodilation is due to increase in the rate of absorption of the
local anesthetic into the blood thus decreasing the duration of
pain control while increasing the anesthetic blood level and
potential for over dose 27
AMIDE LOCAL ANESTHETICS
The metabolism of amide local anesthetics is more
complicated then esters The primary site of
biotransformation of amide drugs is liver
Entire metabolic process occurs in the liver for lidocaine
articaine etidocaine and bupivacaine
Prilocaine undergoes more rapid biotransformation then the
other amides
28
REFERENCES
Handbook of local anesthesia ndash Stanley F Malamed ndash 6th
edition
Essentials of Local Anesthetic Pharmacology Daniel E
Becker Anesth Prog 2006 Fall 53(3) 98ndash109
WIKIPEDIEA
29
THANK YOU
30
1
Pharmacological Methods of Behavior
Management
DR MITAKSHARA NIRWAN
DEFINITIONS
bull Conscious Sedation ndash A minimally depressed level of consciousness that retains
the patients ability to independently and continuously maintain an airway and respond appropriately to physical stimulation or verbal command
(American Dental Association House Of Delegates 2000)
bull Deep Sedation ndash An induced state of depressed consciousness
accompanied by partial loss of protective reflexes including the inability to continuously maintain an airway independently and or to respond purposefully to physical stimulation or verbal command
bull General Anesthesia (G A) ndash An induced state of unconsciousness or complete loss of
protective reflexes including the inability to continually maintain an airway independently and respond purposefully to physical stimulation or verbal command
Conscious sedation
ADVANTAGES
Conscious
Protective reflexes active amp intact
Stable vital signs
Operating dentist may perform sedation
Minimum amount of equipment required
Prolong detainment in recovery room not required
Risk of complication very low
Excellent choice for poor ndash risk pt in dental office
Cost effective
General anesthesia
ADVANTAGES Not absolutely
essential May be the only
method Not necessary (no
pain reaction) Amnesia always
present
Conscious sedation
DISADVANTAGES
Pt cooperation is essential
Extremely difficult or mentally handicapped pt cannot always be managed
Use of local anesthesia is a must
Amnesia may or may not be present
General anesthesia DISADVANTAGES
Pt unconscious
Protective reflexes are depressed
Depressed
Advanced training required Dentist must not act also as anesthetist
Special equipment necessary
Detainment in recovery area necessary
High IOP amp postoperative complications
Not indicated in dental office
More expensive
Fundamental Concepts
bull Techniques that utilize drugs to induce co-operative yet conscious state in an otherwise uncooperative child ndash CONSCIOUS SEDATION
2
GOALS
1 To facilitate the provision of quality care
2 To minimize the extremes of disruptive behavior
3 To promote a positive psychologic response to treatment
4 To promote patient welfare amp safety
5 To return the patient to physiologic state
OBJECTIVES
1 The pt mood must be altered
2 The pt must remain conscious at all times
3 The pt must be cooperative
4 All protective reflexes must remain intact and active
5 Vital signs must remain stable and with in normal limits
6 The ptrsquos pain threshold should be elevated
7 Amnesia may be present
Indications
1 Preschool children
2 Lack of Psychological Emotional maturity
3 Lack of Cognitive Physical Medical disability
4 Fearful amp anxious pts
5 Pt who require extensive amp complicated dental care amp would require or benefit from prolonged visits
6 Acute pain
7 Traumatic injuries
Operating Facilities amp Equipment
A positive pressure O2 delivery system capable of administering gt than 90 O2 at 10L min flow for 60 min (650L ldquoErdquo cylinder)
OR
Self inflating bag valve mask device (15L min)
A functional suction apparatus with appropriate suction catheters
Monitoring equipment - PO BPC PC or Capno
Inhalation sedation unit
100 O2 amp never less than 25
A fail safe mechanism that is checked and calibrated annually
Must have appropriate scavenging system
Emergency drugs
Techniques of sedation
Routes for drug administration
bull Oral
bull Rectal
bull Inhalational
bull Transmucosal
ndash Sublingual
ndash Intranasal
bull Parenteral
ndash IM
ndash sub mucosal
ndash IV
3
Oral Sedation
Advantages
1 Almost universally accepted and the easiest method
2 Decreased incidence and severity of adverse reaction
3 Low cost
Disadvantages
1 Absorption is variable
2 Prolonged latent period(30 min)
3 Reversal of any unwanted effect is also difficult
4 Inability to readily lighten or deepen the level of sedation
5 Prolonged duration of action
Rectal Sedation
Advantages 1 Incidence and intensity of
drug related side effects is minimized
2 Drug absorption occurs from the large intestine directly into the circulation
3 The lack of a needle syringe or other equipment
4 The ease of administration
5 The low cost
Disadvantages
1 Inconvenience to the administrator amp pt
2 The variable absorption of drugs from the large intestine
3 The slow onset of action amp the relatively long duration of action
4 Inability to titrate the drug dosage
5 The inability to reverse the action of the drug the prolonged recovery
Intranasal sedation
Advantages
Rapid onset (10 ndash 15 min)
Simple amp relatively painless
Less pt cooperation is required
Absorbed directly into the C V S
Intranasal sedation
Disadvantages
1 Dependence on nasal mucous membrane
2 Shorter duration of action(40-60min)
3 Multiple dosage may be necessary
Drugs
Midazolam ndash 02mgkg
Sufentanil ndash 15 ndash 3 mcgkg
Ketamine ndash 3-6mg kg
Sublingual sedation
Advantages
1 Pt acceptance
2 Rapid onset
3 High bioavailability
Drugs
Oral Transmucosal Fentanyl Citrate (OTFC)
Intramuscular Sedation
Advantages
1 More rapid onset of action
2 Absorbed directly into the C V system
3 More reliable absorption of drug
4 Pt cooperation is not as essential
Disadvantages
1 Time factor ndash its 15 min latent period
2 Pt may not be willing to accept the injection
3 The prolonged duration of action(2-4 hrs more)
4 Possibility of injury to the tissues at the site of injection caused by either the drug or the needle
4
Sites of I M administration
1 Gluteal area
2 Vastus lateralis
3 Mid ndash deltoid area
Drugs
Diazepam
Midazolam
Hydroxyzine
Inhalation Sedation
Advantages
1 The onset of action is more rapid
2 Peak clinical level is achieved rapidly(3-5min) - permit titration
3 Administrator has complete control over the actions of the drug - safety feature
4 No significant over dosage
5 Flexible duration of action
6 Recovery time is rapid amp most complete
7 No injection is required
8 With N2O- O2 it is safe with very few side effects
Disadvantages
1 The initial cost of the equipment is high 2 The continuing cost of the gases is high 3 The equipment occupies considerable space 4 N2O is not a potent agent 5 A degree of cooperation is required from the pt 6 Chronic exposure to N2O is deleterious to the health of
dental personnel
Contraindications
1 Nasal obstruction 2 Cyanosis at rest 3 Poor cooperation 4 1st trimester of pregnancy 5 Fear of masks
I V Sedation
Advantages
1 The onset of action is the most rapid 2 The dosage may be titrated 3 Suitable level of sedation can be provided 4 The recovery period is shorter 5 Side effects are extremely uncommon 6 Control of salivary secretions is possible 7 The gag reflex is diminished 8 Effectively diminishes motor disturbances 9 Provides immediate access to CVS in emergency
Disadvantages
1 Venipuncture is necessary
2 Complication may rise at the site of the venipuncture
3 Monitoring must be more intensive
4 Recovery is not complete at the end of the procedure
5 Reversal of sedation is difficult
5
N2O-O2 (Relative Analgesia)
colorless sweet smelling gas
Pharmacokinetics
Absorption through pulmonary epithelium
It is approx 15 times as soluble as is nitrogen It replaces nitrogen in blood
It is carried in solution in plasma of the blood
It is not metabolized by the body
Elimination ndash majorndash lungs minor --- skin
perspiration urine and intestinal gas
Pharmacodynamics
Dose related
10 ndash 25 Lightheaded
Changes in visual amp auditory sensation
Tingling of hands amp feet
Suffusing warmth
Remote from the immediate environment
Reduced anxiety
25-50 max analgesic properties and aberration of vision hearing and proprioception mild drowsiness euphoria amnesia and increased sleepiness and dreams
35 conc will achieve maximum analgesia
bull CNS
ndash Cerebrum-primarily affected
ndash Safe but weak anesthetic agent
bull RESPIRATORY SYSTEM
ndash Increased Tidal and minute volumes
bull CARDIOVASCULAR SYSTEM
ndash 2 studies ndash decreased cardiac output
bull FETAL SYSTEMS
ndash Miscarriage in humans
bull OTHER SYSTEMS
ndash Depression of spinal reflexes increase muscle tone indicates stage of delirium
ndash Muscle rigidity-narcotics + nitrous oxide
ndash Nausea and vomitting - GIT
ndash HEMATOPOIESIS ----- prolonged exposure
Adverse reactions and toxicity
EMOTIONAL REACTIONS
DREAMS HALLUCINATIONS
No acute toxicity
Chronic toxicity ndash bone marrow
depression
PROCEDURE
Diffusion Hypoxia
Sevoflurane
A fluorinated derivative of isopropyl ether ndash synthesized in 1970
Potent anaesthetic agent with rapid uptake amp speedy recovery
Day-case surgery
Problem
Attaching vaporiser to any of the currently available machine
BENZODIAZEPINES
Diazepam 1961 lipid soluble
Uses-alcoholism epilepsy labor tetanus and cerebral palsy
- sedation and amnesia
- varieties of neurosis amp anxiety states
Pharmacokinetics
Orally Rectal IMIV or SC
Well absorbed through GIT
Excretion in urine
6
bull Pharmacodynamics
ndash Depress the brain stem reticular system and the limbic system thalamus and hypothalamus
ndash It is a centrally acting muscle relaxant Has anti-convulsant properties
Adverse reaction amp toxicity
ndash Confusion nausea headache increased appetite decreased salivation and jaundice Thrombophlebitis
ndash Rebound phenomenon
ndash Toxicity drowsiness confusion sleep and coma
Dosage Oral or Rectal ndash 02-05mgkg
Maximum single dose 10mg
IV- 025mgkg
Supplied Tablets 2 5 10 mg
Suspension ndash 5mg
Midazolam Water soluble ndash non-irritant
Oral IM IV
Metabolism- liver
Onset IV 3 -5mins
oral 20 ndash 30mins
Oral administration anxious patients requiring relatively short dental procedure
No rebound phenomenon
Better anxiolysis amp amnesia (retrograde amnesia)
Adverse effects Respiratory depression
dose dependant apnea
Dosage Oral ndash 025 to 1mgkg to maximum single dose 20mg
IM ndash 01 to 015mgkg to a maximum of 10mg
IV ndash slow IV
Supplied Syrup ndash 2mgml
Injectable ndash 1mgml amp 5mgml vials
Flumazenil specific benzodiazepines antagonist
selectively inhibits CNS effects
IV administration amp not recommended below 18yrs of age
02mg over 15 seconds after 45seconds 02mg then after 60seconds to maximum of 1mg
Sedative-Hypnotics
Barbiturates First truly effective drugs for the management of anxiety Generalized CNS depressants Produce dose dependent effects
Sedation ---- sleep ---- GA ---- coma
Suppress the CNS and result in sedation and amnesia Advantages
Rapid onset and short duration Disadvantages
no analgesic effect and possible hypotension Must be used with caution in trauma patients because they may cause
apnea and hypoventilation
DOSE Pentobarbital Sodium 100mg Secobarbital Sodium 100 to 200mg Children 30 to 100mg
bull Chloral Hydrates (Mickey Finn Knock out drops ) First synthesized in 1832 first member of the hypnotic group of drugs
Widely used as conscious sedation agent
Properties
Unpleasant taste
Nausea vomiting
Quite irritating to skin and to mucous membranes
GI irritation
Dosages Individualized for each patient 25 ndash 50mgkg
maximum of 1g
Supplied oral capsule ndash 500mg
oral solution ndash 250 amp 500mg5ml
Rectal suppositories ndash 324 amp 648mg
Narcotics
Do produce sedation amp euphoria greater in children
LA is required but dose should be decreased
Meperidine Synthetic opiate agonist
Very water soluble
Orally SC IM or IV
Peak effect by oral 1 hr amp lasts upto 4 hrs
Adverse reactions
-Seizures
-Extreme caution in hepatic or renal diseases or history of seizures
7
Dosage Oral SC or IM ndash 1to 22mgkg not to exceed 100 mg
Supplied Oral Tablets ndash 50 amp 100mg
Oral Syrup ndash 50mgml
Parental solution ndash 25 50 75 amp 100mgml
Fentanyl
Synthetic opiate narcotic analgesic
Very potent 01mg = 10mg Morophine75mg Meperidine
Pharmacokinetics
IV IM SM
Metabolized in liver Excreted in urine
Fentanyl Onset ndash 7 to 15mins
Duration ndash 1 to 2 hrs
Pharmacodynamics
Respiratory depression RR but returns to normal rapidly Tidal volume amp response to co2 depressed for extended period
Apnea
Less emetic than meperidine
NOT RECOMMENDED IN CHILDREN BELOW 2yrs
Dosage 0002 to 0004mgkg
Supplied 005mgml in 2 amp 5ml ampoules
Reversal drug Naloxone
Semisynthetic opiate antagonist
No agonist activity
Onset 2 to 5mins SC or IM amp 1 to 2mins IV
Reversal 45mins
Pt should be kept under continual surveillance
Adverse reaction nausea vomiting sweating hypotension hypertension ventricular tachycardia fibrillation
Dosage IV SC IM 001mgkg then 01mgkg every 2- 3mins maximum 2mg
Supplied 002 004 1mg solutions
Antihistamines
Hydroxyzine
Oral or IM
Effect ndash 15 ndash 30mins
Half-life ndash 3 hrs
Uses
To relieve anxiety
Used as an anti-histamine
Used to control nausea and vomiting including that associated with motion sickness and pregnancy
Adverse reaction dry mouth drowsiness hypersentivity
Dosage Oral ndash 1 to 2mgkg
IM ndash 11mgkg
Promethazine Oral or IM Onset 15 to 60mins Duration 4 to 6 hrs Uses
To prevent and treat nausea and vomiting associated with motion pregnancy or surgery
Produces sedation and reduce swelling pain and trismus
Lower seizure threshold Adverse reaction dry mouth blurred vision thickening of bronchial secretions Dosage OralIM ndash 05-11mgkg
maximum 25 mg
Diphenhydramine
Oral IM IV
Onset -1hr
Duration ndash 4 to 6 hr
Metabolized in liver
Adverse reaction disturbed coordination thickening of bronchial secretions
Dosage Oral IM IV ndash 1 to 15mgkg
maximum 50mg
Tranquilizers
Major tranquilizer antipsychotic produce calmness control symptoms of psychoses cause reversible extra pyramidal symptoms and do not tend to cause habituation
Minor tranquilizer antianxiety agents also cause calmness do not cause extrapyramidal symptoms Used in conditions like nervous tension and mild depression
8
Classification
Antipsychotics
Phenothiazine derivatives
Chlorpromazine promazine
Butryophenones
Haloperidol
Rauwolfia alkaloids
Reserpine
Antianxiety drugs
Propyl alcohol derivatives
Meprobamate
Benzodiazepine derivatives
Diazepam
Miscellaneous compounds
Hydroxyzine
Meprobamate
White crystalline powder slightly bitter in taste
Only administered orally
Peak blood concentration ----1 to 3hrs
10 ---------excreted unchanged Rest --- excreted as a oxidized derivative or as a glucoronide
Uses
To relieve day time anxiety
Induce sleep in insomniacs
To reduce anxiety associated with dental treatment
Anti-convulsant ndash petit mal epilepsy
Adverse reaction leucopenia acute non-thrombocytopenic purpura ecchymoses eosinophilia edema adenopathy
Dosage Childrengt 6yrs 100 to 200mg
Not recommended for children under 6yrs
Monitoring during sedation
1 Pulse
2 Blood pressure
3 ECG
4 Respiration
5 Temperature
Pulse
Manual Electronic
bull Radial Brachial
bull Facial labial
Blood pressure
ndash Stethoscope amp sphygmomanometer
ndash Automatic devices
ndash Direct cannulation of an artery ndash very accurate
Electrocardiograph
Heart rate rhythm myocardial function
9
Respiration
ndash Monitoring respiratory rate
ndash Observing the rise amp fall of the chest wall
ndash Observing the color of mucous membrane
ndash Observing the inflation amp deflation of the reservoir bag
Devices for monitoring respiration
1 The Precordial pretracheal stethoscope
2 The esophageal stethoscope
ndash Respiratory rate
ndash Heart rate
ndash Any abnormal sounds
Pulse Oximeter
ndash Oxygen saturation
ndash Heart rate
ndash Oxisensor site
ndash Fingers
ndash Toe
ndash Ear lobe
Mechanism
Oxygenated Hb ndash red light
Deoxygenated Hb- infrared light
Tissue pressure from arterial pulse (plethysmography)
Advantages
ndash Safe amp noninvasive
ndash Simple to use
ndash Information is rapidly available for clinical decision
ndash Indirectly indicates respiratory adequacy
Disadvantages
ndash Finger probes can get dislodged
ndash Emitted light source may cause burning
ndash Non reusable probes are expensive
ndash Does not directly determine airway patency
Capnography
1 The presence absence of air flow
2 Indicates depth amp adequacy of respiration
3 Continues analysis of the co2 content of the respired air ndash indicates respiratory adequacy
Temperature
ndash Disposable nondisposable thermometer
ndash Esophageal rectal temp probe
10
Discharge criteria
Cardiovascular function is satisfactory amp stable
Airway patency is uncompromised amp satisfactory
Pt is easily arousable amp protective reflexes intact
State of hydration is adequate
Pt can talk if applicable
Pt can sit unaided if applicable
Pt can ambulate with minimal assistance if applicable
Presedation level of responsiveness achieved
Responsible individual is available
1
PULP THERAPY OF VITAL TEETH
DR MITAKSHARA NIRWAN
Contents
Indirect pulp capping
Direct pulp capping
Medications amp materials used in pulp capping
Pulpotomy
MTA
Apexogenesis
INDIRECT PULP CAPPING
Pieter Van Forest - first to speak about root canal therapy
Glove designed instruments that could prepare a canal to a certain size and taper(1910)
Indirect pulp capping is defined as a procedure where in small amount of carious dentin is retained in
deep areas of cavity to avoid exposure of pulp followed by placement of a suitable medicament and
restorative material that seals off the carious dentin and encourages pulp recovery (Ingle)
A procedure in which only the gross caries is removed from the lesion and the cavity is sealed for a
time with a biocompatible material (McDonald)
Objective of indirect pulp capping
These were given by Eidelman in 1965
bull Arresting the carious process
bull Promoting dentin sclerosis
bull Stimulating formation of tertiary dentin
bull Remineralization of carious dentin
Layers of Carious Dentin Indications of Indirect Pulp Capping
History
Mild pain associated with eating
Negative history of spontaneous extreme pain
Clinical Examination
Deep carious lesion which are close tobut not involving the pulp in vital primary or young
permanent teeth
No mobility
Nominal pulp inflammationdefinite layer of affected dentin after removal of infected dentin
Radiographic examination
Normal lamina dura amp PDL space
No radiolucency around the apices
2
Contraindications of Indirect Pulp Capping
History
Sharp penetrating pulpalgia
Prolonged spontaneous pain especially at night
Clinical examination
Mobility of tooth
Discoloration of tooth
Negative reaction of electric pulp testing
Radiographic examination
Definite pulp exposure
Break in the lamina dura
Radiolucency around the apices
Widened PDL space
Treatment procedure
Sequelae of Indirect Pulp Capping Three distinct types of new dentin formation take place
1 Cellular fibrillar dentinmdashfirst 2 months
2 Globular dentinmdash3 months
3 Tubular dentin (uniform mineralized dentin)
bull 15th of reparative dentin formation begins in less than 30 days
bull After 3 months 01 mm is formed
DIRECT PULP CAPPING Defined by Kopel (1992) as the placement of a medicament or non medicated material on a pulp that
has been exposed in course of excavating the last portions of deep dentinal caries or as a result of
trauma
Objective
To create new dentin in the area of the exposure and subsequent healing of the pulp
Rationale
achieve a biologic closure of the exposure site by deposition of hard tissue barrier (dentin bridge)
between pulp tissue and capping material thus walling off the
INDICATIONS
Small mechanical exposure
Easily controlled haemorrhage
Bright red haemorrhage
True pinpoint exposure
CONTRAINDICATIONS
Severe toothache at night
Spontaneous pain
Tooth mobility
Radiographic appearance of pulp periradicular de- generation
Excess of hemorrhage at the time of exposure Serous exudate from the exposure
Externalinternal root resorption
Swellingfistula
Histological Changes after Pulp Capping
These were illustrated be Glass and Zander in 1949
After 24 hours Necrotic zone adjacent to calcium
hydroxide paste is separated from healthy pulp
tissue by a deep staining basophilic layer
After 7 days Increase in cellular and fibroblastic
activity
After 14 days Partly calcified fibrous tissue lined by
odontoblastic cells is seen below the calcium
proteinate zone disappearance of necrotic zone
After 28 days Zone of new dentin
3
Medications and Materials Used for Pulp Capping Calcium hydroxide
Corticosteroids amp antibiotics
Inert materials
Collagen fibers
4-META adhesive
Direct bonding
Isobutyl cyanoacrylate
Denatured albumin
Mineral trioxide aggregate
Laser
Bone morphogenic protein
PULPOTOMY
Finn (1995) defined it as the complete removal of the coronal portion of the dental pulp
followed by placement of a suitable dressing or medicament that will promote healing and
preserve vitality of the tooth
American Academy of Pediatric Dentistry (1998) defined pulpotomy as the amputation of
affected infected coronal portion of the dental pulp preserving the vitality and function of the
remaining part of radicular pulp
Objectives
bull Removal of inflamed and infected coronal pulp at the site of exposure thus preserving the vitality of the
radicular pulp and allowing it to heal
bull Maintain the tooth in the dental arch
Rationale
bull Radicular pulp is healthy and capable of healing after surgical amputation of the infected coronal pulp
bull Preserves vitality of the radicular pulp
bull Maintains tooth in a physiologic condition
Indications of Pulpotomy bull Mechanical pulp exposure in primary teeth
bull Teeth showing a large carious lesion but free of radicular pulpitis
bull History of only spontaneous pain
bull Hemorrhage from exposure sites bright red and can be controlled
bull Absence of abscess or fistula
bull No interradicular bone loss
bull No interradicular radiolucency
Contraindications of Pulpotomy bull Persistent toothache
bull Tenderness on percussion
bull Root resorption more than 13rd of root length
bull Large carious lesion with nonrestorable crown
bull Highly viscous sluggish hemorrhage from canal orifice which is uncontrollable
bull Medical contradictions like heart disease immuno compromised patient
bull Swelling or fistula
bull External or internal resorption
bull Pathological mobility
bull Calcification of pulp
Classification of pulpotomy
4
Formocresol Pulpotomy
Iby BUCKLEY in 1904
Sweet (1930) Formulated multi visit technique
Doyle (1962) Advocated 2 sitting procedure (complete devitalization)
Spedding (1965) Gave 5 minute protocol (partial devitali- zation)
Venham (1967) Proposed 15 seconds procedure
Current concept uses 4 minutes of application time
Composition of formocresol Buckleyrsquos Formula
bull Cresol ndash 35 percent
bull Glycerol ndash 15 percent
bull Formaldehyde ndash 19 percent
bull Water ndash 31 percent
Mechanism of Action
It prevents tissue autolysis by bonding to the proteins Bonding is of peptide groups of side chain amino acids and is a reversible process accomplished without
changing the basic structure of protein molecules
Histological Changes
bull Demonstrated by Mass and Zilbermann11 in 1933 and also by Massler and Mansokhani in 1959
bull Immediately the pulp becomes fibrous and acidophillic
bull Seven to fourteen days Three zones appear
a broad eosinophilic zone of fixation
b broad pale-staining zone of atrophy with poorcellular definition
c broad zone of inflammation extending apically into normal pulp tissue
bull One yearndash Progressive apical movement of these zones with only acidophillic zone left at the end of 1 year
Modified Formocresol Pulpotomy
Used by TRASK(1972)
The technique is identical to that described for primary teeth except that the formocresol pellet is
sealed permanently in the tooth
Two-visit Devitalization Pulpotomy
Indications
bull There is evidence of sluggish bleeding at the amputation site that is difficult to control
bull Pus in the chamber but none at the amputation site
bull There is thickening of the PDL
bull History of pain
Contraindications
bull Nonrestorable tooth
bull Tooth with necrotic pulp
5
Glutaraldehyde Pulpotomy
It was first suggested by S Gravenmade Introduced by Kopel in 1979
Mechanism of Action
bull Glutaraldehyde produces rapid surface fixation of the underlying pulpal tissue
bull A narrow zone of eosinophilic stained and compressed fixed tissue is found directly beneath the area of application which blends into vital normal appearing tissue apically
bull With time the glutaraldehyde fixed zone is replaced by macrophagic action with dense collagenous tissue thus the entire root canal tissue is vital
Cvekrsquos Pulpotomy
bull This is also called as calcium hydroxide pulpotomy or young permanent partial pulpotomy
bull This was proposed by Mejare and Cvek16 in 1978
bull Indicated in young permanent teeth where the pulp is exposed by mechanical or bacterial means and the
remaining radicular tissue is judged vital by clinical and radiographic criteria whereas the root closure is
notcomplete
MINERAL TRIOXIDE AGGREGATE (MTA) Torabinejad described the physical and chemical properties of MTA in 1995
It is ash colored powder made primarily of fine hydrophilic particles of
1 tricalcium aluminate
2 tricalcium silicate
3 silicate oxide
4 tricalcium oxide
5 bismuth dioxide
Hydration of the powder results in a colloidal gel composed of calcium oxide crystals in an amorphous
structure This gel solidifies into a hard structure in less than three hours
PROPERTIES OF MTA
It is biocompatible material and its sealing ability is better than that of amalgam or ZOE
Initial pH is 102 and set pH is 125
The setting time of cement is 4 hours
The compressive strength is 70 MPA which is comparable with that of IRM
Low cytotoxicity ndash It presents with minimal inflammation if extended beyond the apex
Mineral trioxide aggregate (MTA) has demonstrated the ability to induce hard-tissue formation in
pulpal tissues and it promotes rapid cell growth
APEXOGENESIS
It is defined as the treatment of a vital pulp by capping or pulpotomy in order to permit continued
growth of the root and closure of the open apex
Rationale
Maintenance of integrity of the radicular pulp tissue to allow for continued root growth
Indications
bull Indicated for traumatized or pulpally involved vital permanent tooth when root apex is incompletely formed
bull No history of spontaneous pain
bull No sensitivity on percussion
bull No hemorrhage
bull Normal radiographic appearance
Contraindications
bull Evidence that radicular pulp has undergone degenerative changes
bull Purulent drainage
bull History of prolonged pain bull Necrotic debris in canal
bull Periapical radiolucency
6
1
Gupta A Dhingra R Chaudhari P Gupta A
Department of Paedodontics and Preventive Dentistry Faculty of Dental Sciences SGT University Gurgaon Haryana India
Journal of Indian Society of Pedodontics and Preventive Dentistry
Volume 35 I Issue 3 I July-September 2017
A COMPARISION OF VARIOUS MINIMALLY
INVASIVE TECHNIQUES FOR THE REMOVAL
OF DENTAL FLUOROSIS STAINS IN
CHILDREN
DR MITAKSHARA NIRWAN
CONTENTS
bull Introduction
bull Aims
bull Materials and Methods
bull Results
bull Discussion
bull Conclusion
bull Critical analysis
bull References
INTRODUCTION
bull Dental fluorosis is a developmental disturbance of dental enamel caused by
successive exposure to high concentrations of fluoride during tooth
development
bull Various methods of therapy are advocated for the treatment of fluorosis -
stained teeth which range from invasive ceramic veneer bonding restorations
to abrasive chemical treatments
bull The combination of dental bleaching techniques and microabrasion appears
as an excellent conservative solution to reestablish health in fluorosis
affected teeth
AIMS
bull The aim of the study was to evaluate and compare the effectiveness of
minimally invasive techniques for the removal of dental fluorosis
stains in children in vivo
MATERIALS AND METHODS
Patients visiting the department of Pedodontics and Preventive dentistry
Faculty of Dental Sciences SGT University Gurgaon
bull Sample size 90 patients
bull Age group 10 -17 years
bull Caries cracks or periodontal
disease on anterior teeth
bull Abscess draining sinus
cellulitis
bull Non vital teeth
hypersensitive exposed
crevices
bull Orthodontic appliance
bull Past history of bleaching
bull At least two permanent
maxillary anterior teeth
bull TSIF of score 4
bull Free of systemic diseases
Inclusion criteria Exclusion criteria
2
Groups
Group A In office bleaching with 35 hydrogen peroxide( Pola Office
Bleaching kit) activated by light emitting diode (LED) bleaching unit
(35 HP)
Group B Enamel microabrasion (EM) (PREMA Enamel Microabrasion
System) followed by in-office bleaching with 44 carbamide peroxide
gel (EM)
Group C In-office bleaching with 5 sodium hypochlorite (5
NaOCl)
A baseline colour evaluation was done by taking digital photograph of
the maxillary anterior teeth
RESULTS
Group 1
Colour stability
Group 2 Group 3
Tooth sensitivity
Tooth sensitivity values were taken before the treatment
which was compared to immediate postoperative and follow
up visits It was checked using an electric pulp tester
maximum
moderate
least
immediately
group 2
group 1
group 3
1 month
group 2
group 1
group 3
3 month
group 2
group 1
group 3
Patient satisfaction score
Satisfaction was assessed on visual analog scale
Range 1 to 5
Groups percentage of patients
who were satisfied with
the treatment
Number of patients
who reported slight
reappearance of colour
Group 1
90
7
Group 2
83
8
Group 3
73
7
3
Number of Appointments
Groups One sitting Two sittings Three
sittings
Group 1
25
4
1
group 2
26
3
1
Group 3
30
0
0
DISCUSSION
bull Hydrogen peroxide is capable of penetrating the tooth osmosis and through porosities and cracks subsequently acting directly on the pigmented molecules
bull Gurgan et al investigated 3 different light systems and found out that diode laser system with gave best tooth whitening and least tooth sensitivity
bull In the EM group the surface reflects and refracts light from the surface in such way that mild imperfections in underlying enamel are camouflaged While the highly polished surface of enamel enhances the aesthetic appearance
bull Train et al and Loguercio et al also had the similar results in their studies with EM mild fluorosis showed best results moderate showed moderate results while it had little effect on severe fluorosis
bull NaOCl was only effective on mild stains while moderate and severe
stains could only be lightened to quite an extent but could not be
completely removed
bull When NaOCl comes in contact with hypomineralized and discoloured
enamel it degrades and removes the chromogenic organic material
located on the enamel surface
CONCLUSION
bull It was concluded that esthetic appearance of teeth mild fluorosis can
be achieved by bleaching and microabrasion But in cases of
moderate fluorosis a combination of any of theses modalities can be
used
bull As no special maintenance precautions are required these maybe be
considered as an interesting alternative to conventional operative
treatment
bull Focuses on only TSIF of 4
bull Electric pulp testing is not the
right method to check for
sensitivity
bull Tooth Sensitivity changes
from person to person
bull Food habits can cause
staining of the teeth
bull Minimally invasive
bull Cheaper to veneers
bull Minimal loss of tooth structure
bull 4 parameters checked for the success of treatment
bull Inclusion of specific score of fluorosis for comparing the results
bull Maximum 3 appointments needed
CRITICAL ANALYSIS
Pros Cons
REFERENCES
bull Gurgan S Cakir FY Yazici E Different light-activated in officebleaching
systems Lasers Med Sci 201025817-22
bull Train TE McWhorter AG Seale NSWilson CF Guo IY Examination of
esthetic improvement and surface alteration following microabrasion in
fluorotic human incisors in vivoPediatr dent 199618353-62
bull Loguercio AD Correia LD Zago C Tagliari D Neumann E Gomes OM et al
Clinical effectiveness of two microabrasion materials materials for the
removal of enamel flurosis stains Oper Dent 200732531-8
4
5
CONCLUSION
bull USE OF 6 CITRIC ACID DEFINITELY HELPED IN RAPID ELIMINATION OF PAIN RESOLUTION OF
PERI-RADICULAR RADIOLUCENCY BETTER OBTURATION QUALITY IN TERMS OF LESS VOIDS AND
VOID AREAS ALONG WITH MAXIMUM NO OF OPTIMAL OBTURATION UP TO APICAL AREA
bull 6 CITRIC ACID AND ENDOACTIVATOR IRRIGATION PROTOCOL PROVED TO BE THE BETTER
IRRIGATION PROTOCOL WHICH MAY CONTRIBUTE TO LONG TERM SUCCESS OF PRIMARY
TOOTH AND THE HEALTH OF UNDERLYING PERMANENT TOOTH
bull 6 CITRIC ACID ALONG WITH ENDOACTIVATOR MAY BE RECOMMENDED AS IRRIGATION
ADJUNCTS IN PULPECTOMY PROCEDURE OF PRIMARY TEETH
25
PROS AND CONS
PROS
bull PROPER EXPLANATION OF THE MATERIALS
USED
CONS
bull NO PREOPERATIVE AND POSTOPERATIVE
RADIOGRAPHS
26
REFERENCES
bull RAMACHANDRA JA NIHAL NK NAGARATHNA C VORA MS ROOT CANAL IRRIGANTS IN
PRIMARY TEETH WORLD J DENT 20156(3)229-234
bull MOHAMMADI Z JAFARZADEH H SHALAVI S KINOSHITA JI UNUSUAL ROOT CANAL
IRRIGATION SOLUTIONS J CONTEMP DENT PRACT 201718(5)415-420
bull ZEHNDER M ROOT CANAL IRRIGANTS J ENDOD 2006 32389- 98
bull SMITH JJ amp WAYMAN BE AN EVALUATION OF THE ANTIMICROBIAL EFFECTIVENESS OF
CITRIC ACID AS A ROOT CANAL IRRIGANT JOURNAL OF ENDODONTICS 1986 12(2) 54-58
bull TANNURE PN AZEVEDO CP BARCELOS R GLEISER R PRIMO LG LONG-TERM OUTCOMES OF
PRIMARY TOOTH PULPECTOMY WITH AND WITHOUT SMEAR LAYER REMOVAL A RANDOMIZED
SPLIT-MOUTH CLINICAL TRIAL PEDIATR DENT 201133316E20 27
bull CARON G NHAM K BRONNEC F MACHTOU P EFFECTIVENESS OF DIFFERENT FINAL IRRIGANT
ACTIVATION PROTOCOLS ON SMEAR LAYER REMOVAL IN CURVED CANALS J ENDOD
2010361361E6
bull COLL JA SADRIAN R PREDICTING PULPECTOMY SUCCESS AND ITS RELATIONSHIP TO
EXFOLIATION AND SUCCEDANEOUS DENTITION PEDIATR DENT 19961857E63
28
1
LOCAL
ANESTHESIA
DR MITAKSHARA NIRWAN
CONTENTS
Definition
Methods of inducing local anesthesia
Desirable properties
Electrophysiology of nerve conduction
Impulse propagation and spread
Mode and site of action of local anesthesia
Classification of local anesthetic according to biological site and mode of action
Dissociation of local anaesthetics
Mechanism of action of local anaethetics
Local anaesthetic agent
2
3
DEFINITION
Local anesthesia is defined as a loss of sensation in
a circumscribed area of the body caused by depression
of excitation in nerve endings or an inhibition of the
conduction process in peripheral nerves
An important feature of local anesthesia is that it produces
LOSS OF SENSATION WITHOUT INDUCING LOSS OF
CONSCIOUSNESS
4
METHODS OF INDUCING LOCAL
ANESTHESIA
Low temperature
Mechanical trauma
Anoxia
Neurolytic agents such as alcohol amp phenol
Chemical agents such as local anesthetics
PROPERTIES OF LOCAL
ANESTHESIA
It should not be irritating to tissue to which it is applied
It should not cause any permanent alteration of nerve structure
Its systemic toxicity should be low
Time of onset of anesthesia should be short
It should be effective regardless of whether it is injected into the tissue or applied locally to mucous membranes
The duration of action should be long enough to permit the completion of procedure
5 6
It should have the potency sufficient to give complete
anesthesia with out the use of harmful concentration solutions
It should be free from producing allergic reactions
It should be free in solution and relatively undergo
biotransformation in the body
It should be either sterile or be capable of being sterilized by
heat with out deterioration
2
ELETROPHYSIOLOGY OF
NERVE CONDUCTION
There is an electrical charge across the membrane
This is the membrane potential
The resting potential (when the cell is not firing) is a negative
electrical potential of -70mv that exists across the nerve
membrane produced by different concentrations of either side of
the membrane
The interior of nerve is NEGATIVE in relation to exterior
7 8
inside
outside
Resting potential of neuron = -70mV
+
-
+
-
+
-
+
-
+
-
SLOW DEPOLARIRIZATION
9
RAPID DEPOLARIZATION
The interior of nerve is POSITIVE in relation to exterior
REPOLARIZATION
10
bull Repolarization takes 07 msec
bull Depolarization takes 03 msec
SODIUM PUMP -
energy comes from the oxidative metabolism of ATP
bull The entire process require 1 msec
IMPULSE PROPOGATION
IMPULSE SPREAD
The propagated impulse travels along the nerve
membrane towards CNS The spread of impulse differs
in myelinated and unmyelinated nerve fibers
DEPOLARIZED SEGMENT ADJACENT RESTING AREA
MODE AND SITE OF ACTION OF LOCAL
ANESTHETICS
Local anesthetic agent interferes with excitation
process in a nerve membrane in one of the
following ways
Altering the basic resting potential of nerve
membrane
Altering the threshold potential
Decreasing the rate of depolarization
Prolonging the rate of repolarization
12
3
CLASSIFICATION OF LOCAL ANESTHETIC
SUBSTANCES ACCORDING TO
BIOLOGICAL SITE AND MODE OF ACTION
CLASS A
Agents acting at receptor site on external surface of nerve membrane
Chemical substance Biotoxins (eg tetrodotoxin and saxitoxin)
CLASS B
Agents acting on receptor sites on internal surface of nerve membrane
Chemical substance Quaternary ammonium analogues of lidocaine
scorpion venom 13
CLASS C Agents acting by receptor independent of
physiochemical mechanism
Chemical substance Benzocaine
CLASS D Agents acting by combination of receptors and
receptor independent mechanisms
Chemical substance most clinically useful anesthetic agents
(eg lidocaine mepivacaine prilocaine)
14
BASED ON THE SOURCE
NATUAL
SYNTHETIC
OTHERS
BASED ON MODE OF APPLICATION
bull INJECTABLE
bull TOPICAL
BASED ON DURATION OF ACTION
bull ULTRA SHORT
bull SHORT
bull MEDIEM
bull LONG
BASED ON ONSET OF ACTION SHORT
INTERMEDIATE
LONG
15
DISSOCIATION OF LOCAL
ANESTHETICS
Local anesthetics are available as salts (usually
hydrochlorides) for clinical use
The salts both water soluble and stable is dissolved in
either sterile water or saline
In this solution it exists simultaneously as unchanged
molecule (RN) also called base and positively charged
molecules (RNH+) called cations
RNH+ ==== RN+ H
+
16
The relative concentration of each ionic form in the solution varies
in the pH of the solution or surrounding tissue
In the presence of high concentration of hydrogen ion (low pH) the
equilibrium shifts to left and most of the anesthetic solution exists
in cationic form
RNH+ gt RN
+ + H
+
As hydrogen ion concentration decreases (higher pH) the
equilibrium shifts towards the free base form
RNH+ lt RN + H
+
17
The relative proportion of ionic form also depends on pKa or DISSOCIATION CONSTANT of the specific local anesthetic
The pKa is a measure of molecules affinity for H+
ions
When the pH of the solution has the same value as pKa of the local anesthetic exactly half the drug will exists in the RNH
+ form and
exactly half in RN form
The percentage of drug existing in either form can be determined by Henderson Hasselbalch equation
Log baseacid = pH - pKa
18
4
MECHANISM OF ACTION OF LOCAL
ANESTHETICS
The following sequence is proposed mechanism of action of LA
Displacement of calcium ions from the sodium channel receptor site
Binding of local anesthetic molecule to this receptor site
Blockade of sodium channel
19
Decrease in sodium conductance
Depression of rate of electrical depolarization
Failure to achieve the threshold potential level
Lack of development of propagated action potential
Conduction blockadehellip
20
21
Na + Na +
22
LOCAL ANESTHETIC AGENT
COMERCIALLY PREPARED LOCAL ANESTHESIA
CONSISTS OF
Local anesthetic agent (xylocaine lignocaine 2)
Vasoconstrictor (adrenaline 1 80000)
Reducing agent (sodium metabisulphite)
Preservative (methylparabencapryl
hydrocuprienotoxin)
Fungicide (thymol)
Vehicle (distillde waterNaCl)
LOCAL ANESTHETIC AGENT
The local anesthetics used in dentistry are divided
into two groups
ESTER GROUP
AMIDE GROUP
23 24
ESTER GROUP It is composed of the following
An aromatic lipophilic group
An intermediate chain containing
an ester linkage
A hydrophilic secondary or tertiary
amino group
AMIDE GROUP It is composed of the following
An aromatic lipophilic group
An intermediate chain containing
amide linkage
A hydrophilic secondary or tertiary
amino group
5
25
CLASSIFICATION OF LOCAL ANESTHETICS
ESTERS
Esters of benzoic acid
Butacaine
Cocaine
Benzocaine
Hexylcaine
Piperocaine
Tetracaine
Esters of Para-amino
benzoic acid
Chloroprocain
Procaine
Propoxycaine
26
AMIDES Articaine
Bupivacaine
Dibucaine
Etidocaine
Lidocaine
Mepivacaine
Prilocaine
Ropivacaine
QUINOLINE
Centbucridine
PHARMACOKINETICS OF LOCAL
ANESTHETICS UPTAKE
When injected into soft tissue most local anesthetics produce
dilation of vascular bed
Cocaine is the only local anesthetic that produces
vasoconstriction initially it produces vasodilation which is
followed by prolonged vasoconstriction
Vasodilation is due to increase in the rate of absorption of the
local anesthetic into the blood thus decreasing the duration of
pain control while increasing the anesthetic blood level and
potential for over dose 27
AMIDE LOCAL ANESTHETICS
The metabolism of amide local anesthetics is more
complicated then esters The primary site of
biotransformation of amide drugs is liver
Entire metabolic process occurs in the liver for lidocaine
articaine etidocaine and bupivacaine
Prilocaine undergoes more rapid biotransformation then the
other amides
28
REFERENCES
Handbook of local anesthesia ndash Stanley F Malamed ndash 6th
edition
Essentials of Local Anesthetic Pharmacology Daniel E
Becker Anesth Prog 2006 Fall 53(3) 98ndash109
WIKIPEDIEA
29
THANK YOU
30
1
Pharmacological Methods of Behavior
Management
DR MITAKSHARA NIRWAN
DEFINITIONS
bull Conscious Sedation ndash A minimally depressed level of consciousness that retains
the patients ability to independently and continuously maintain an airway and respond appropriately to physical stimulation or verbal command
(American Dental Association House Of Delegates 2000)
bull Deep Sedation ndash An induced state of depressed consciousness
accompanied by partial loss of protective reflexes including the inability to continuously maintain an airway independently and or to respond purposefully to physical stimulation or verbal command
bull General Anesthesia (G A) ndash An induced state of unconsciousness or complete loss of
protective reflexes including the inability to continually maintain an airway independently and respond purposefully to physical stimulation or verbal command
Conscious sedation
ADVANTAGES
Conscious
Protective reflexes active amp intact
Stable vital signs
Operating dentist may perform sedation
Minimum amount of equipment required
Prolong detainment in recovery room not required
Risk of complication very low
Excellent choice for poor ndash risk pt in dental office
Cost effective
General anesthesia
ADVANTAGES Not absolutely
essential May be the only
method Not necessary (no
pain reaction) Amnesia always
present
Conscious sedation
DISADVANTAGES
Pt cooperation is essential
Extremely difficult or mentally handicapped pt cannot always be managed
Use of local anesthesia is a must
Amnesia may or may not be present
General anesthesia DISADVANTAGES
Pt unconscious
Protective reflexes are depressed
Depressed
Advanced training required Dentist must not act also as anesthetist
Special equipment necessary
Detainment in recovery area necessary
High IOP amp postoperative complications
Not indicated in dental office
More expensive
Fundamental Concepts
bull Techniques that utilize drugs to induce co-operative yet conscious state in an otherwise uncooperative child ndash CONSCIOUS SEDATION
2
GOALS
1 To facilitate the provision of quality care
2 To minimize the extremes of disruptive behavior
3 To promote a positive psychologic response to treatment
4 To promote patient welfare amp safety
5 To return the patient to physiologic state
OBJECTIVES
1 The pt mood must be altered
2 The pt must remain conscious at all times
3 The pt must be cooperative
4 All protective reflexes must remain intact and active
5 Vital signs must remain stable and with in normal limits
6 The ptrsquos pain threshold should be elevated
7 Amnesia may be present
Indications
1 Preschool children
2 Lack of Psychological Emotional maturity
3 Lack of Cognitive Physical Medical disability
4 Fearful amp anxious pts
5 Pt who require extensive amp complicated dental care amp would require or benefit from prolonged visits
6 Acute pain
7 Traumatic injuries
Operating Facilities amp Equipment
A positive pressure O2 delivery system capable of administering gt than 90 O2 at 10L min flow for 60 min (650L ldquoErdquo cylinder)
OR
Self inflating bag valve mask device (15L min)
A functional suction apparatus with appropriate suction catheters
Monitoring equipment - PO BPC PC or Capno
Inhalation sedation unit
100 O2 amp never less than 25
A fail safe mechanism that is checked and calibrated annually
Must have appropriate scavenging system
Emergency drugs
Techniques of sedation
Routes for drug administration
bull Oral
bull Rectal
bull Inhalational
bull Transmucosal
ndash Sublingual
ndash Intranasal
bull Parenteral
ndash IM
ndash sub mucosal
ndash IV
3
Oral Sedation
Advantages
1 Almost universally accepted and the easiest method
2 Decreased incidence and severity of adverse reaction
3 Low cost
Disadvantages
1 Absorption is variable
2 Prolonged latent period(30 min)
3 Reversal of any unwanted effect is also difficult
4 Inability to readily lighten or deepen the level of sedation
5 Prolonged duration of action
Rectal Sedation
Advantages 1 Incidence and intensity of
drug related side effects is minimized
2 Drug absorption occurs from the large intestine directly into the circulation
3 The lack of a needle syringe or other equipment
4 The ease of administration
5 The low cost
Disadvantages
1 Inconvenience to the administrator amp pt
2 The variable absorption of drugs from the large intestine
3 The slow onset of action amp the relatively long duration of action
4 Inability to titrate the drug dosage
5 The inability to reverse the action of the drug the prolonged recovery
Intranasal sedation
Advantages
Rapid onset (10 ndash 15 min)
Simple amp relatively painless
Less pt cooperation is required
Absorbed directly into the C V S
Intranasal sedation
Disadvantages
1 Dependence on nasal mucous membrane
2 Shorter duration of action(40-60min)
3 Multiple dosage may be necessary
Drugs
Midazolam ndash 02mgkg
Sufentanil ndash 15 ndash 3 mcgkg
Ketamine ndash 3-6mg kg
Sublingual sedation
Advantages
1 Pt acceptance
2 Rapid onset
3 High bioavailability
Drugs
Oral Transmucosal Fentanyl Citrate (OTFC)
Intramuscular Sedation
Advantages
1 More rapid onset of action
2 Absorbed directly into the C V system
3 More reliable absorption of drug
4 Pt cooperation is not as essential
Disadvantages
1 Time factor ndash its 15 min latent period
2 Pt may not be willing to accept the injection
3 The prolonged duration of action(2-4 hrs more)
4 Possibility of injury to the tissues at the site of injection caused by either the drug or the needle
4
Sites of I M administration
1 Gluteal area
2 Vastus lateralis
3 Mid ndash deltoid area
Drugs
Diazepam
Midazolam
Hydroxyzine
Inhalation Sedation
Advantages
1 The onset of action is more rapid
2 Peak clinical level is achieved rapidly(3-5min) - permit titration
3 Administrator has complete control over the actions of the drug - safety feature
4 No significant over dosage
5 Flexible duration of action
6 Recovery time is rapid amp most complete
7 No injection is required
8 With N2O- O2 it is safe with very few side effects
Disadvantages
1 The initial cost of the equipment is high 2 The continuing cost of the gases is high 3 The equipment occupies considerable space 4 N2O is not a potent agent 5 A degree of cooperation is required from the pt 6 Chronic exposure to N2O is deleterious to the health of
dental personnel
Contraindications
1 Nasal obstruction 2 Cyanosis at rest 3 Poor cooperation 4 1st trimester of pregnancy 5 Fear of masks
I V Sedation
Advantages
1 The onset of action is the most rapid 2 The dosage may be titrated 3 Suitable level of sedation can be provided 4 The recovery period is shorter 5 Side effects are extremely uncommon 6 Control of salivary secretions is possible 7 The gag reflex is diminished 8 Effectively diminishes motor disturbances 9 Provides immediate access to CVS in emergency
Disadvantages
1 Venipuncture is necessary
2 Complication may rise at the site of the venipuncture
3 Monitoring must be more intensive
4 Recovery is not complete at the end of the procedure
5 Reversal of sedation is difficult
5
N2O-O2 (Relative Analgesia)
colorless sweet smelling gas
Pharmacokinetics
Absorption through pulmonary epithelium
It is approx 15 times as soluble as is nitrogen It replaces nitrogen in blood
It is carried in solution in plasma of the blood
It is not metabolized by the body
Elimination ndash majorndash lungs minor --- skin
perspiration urine and intestinal gas
Pharmacodynamics
Dose related
10 ndash 25 Lightheaded
Changes in visual amp auditory sensation
Tingling of hands amp feet
Suffusing warmth
Remote from the immediate environment
Reduced anxiety
25-50 max analgesic properties and aberration of vision hearing and proprioception mild drowsiness euphoria amnesia and increased sleepiness and dreams
35 conc will achieve maximum analgesia
bull CNS
ndash Cerebrum-primarily affected
ndash Safe but weak anesthetic agent
bull RESPIRATORY SYSTEM
ndash Increased Tidal and minute volumes
bull CARDIOVASCULAR SYSTEM
ndash 2 studies ndash decreased cardiac output
bull FETAL SYSTEMS
ndash Miscarriage in humans
bull OTHER SYSTEMS
ndash Depression of spinal reflexes increase muscle tone indicates stage of delirium
ndash Muscle rigidity-narcotics + nitrous oxide
ndash Nausea and vomitting - GIT
ndash HEMATOPOIESIS ----- prolonged exposure
Adverse reactions and toxicity
EMOTIONAL REACTIONS
DREAMS HALLUCINATIONS
No acute toxicity
Chronic toxicity ndash bone marrow
depression
PROCEDURE
Diffusion Hypoxia
Sevoflurane
A fluorinated derivative of isopropyl ether ndash synthesized in 1970
Potent anaesthetic agent with rapid uptake amp speedy recovery
Day-case surgery
Problem
Attaching vaporiser to any of the currently available machine
BENZODIAZEPINES
Diazepam 1961 lipid soluble
Uses-alcoholism epilepsy labor tetanus and cerebral palsy
- sedation and amnesia
- varieties of neurosis amp anxiety states
Pharmacokinetics
Orally Rectal IMIV or SC
Well absorbed through GIT
Excretion in urine
6
bull Pharmacodynamics
ndash Depress the brain stem reticular system and the limbic system thalamus and hypothalamus
ndash It is a centrally acting muscle relaxant Has anti-convulsant properties
Adverse reaction amp toxicity
ndash Confusion nausea headache increased appetite decreased salivation and jaundice Thrombophlebitis
ndash Rebound phenomenon
ndash Toxicity drowsiness confusion sleep and coma
Dosage Oral or Rectal ndash 02-05mgkg
Maximum single dose 10mg
IV- 025mgkg
Supplied Tablets 2 5 10 mg
Suspension ndash 5mg
Midazolam Water soluble ndash non-irritant
Oral IM IV
Metabolism- liver
Onset IV 3 -5mins
oral 20 ndash 30mins
Oral administration anxious patients requiring relatively short dental procedure
No rebound phenomenon
Better anxiolysis amp amnesia (retrograde amnesia)
Adverse effects Respiratory depression
dose dependant apnea
Dosage Oral ndash 025 to 1mgkg to maximum single dose 20mg
IM ndash 01 to 015mgkg to a maximum of 10mg
IV ndash slow IV
Supplied Syrup ndash 2mgml
Injectable ndash 1mgml amp 5mgml vials
Flumazenil specific benzodiazepines antagonist
selectively inhibits CNS effects
IV administration amp not recommended below 18yrs of age
02mg over 15 seconds after 45seconds 02mg then after 60seconds to maximum of 1mg
Sedative-Hypnotics
Barbiturates First truly effective drugs for the management of anxiety Generalized CNS depressants Produce dose dependent effects
Sedation ---- sleep ---- GA ---- coma
Suppress the CNS and result in sedation and amnesia Advantages
Rapid onset and short duration Disadvantages
no analgesic effect and possible hypotension Must be used with caution in trauma patients because they may cause
apnea and hypoventilation
DOSE Pentobarbital Sodium 100mg Secobarbital Sodium 100 to 200mg Children 30 to 100mg
bull Chloral Hydrates (Mickey Finn Knock out drops ) First synthesized in 1832 first member of the hypnotic group of drugs
Widely used as conscious sedation agent
Properties
Unpleasant taste
Nausea vomiting
Quite irritating to skin and to mucous membranes
GI irritation
Dosages Individualized for each patient 25 ndash 50mgkg
maximum of 1g
Supplied oral capsule ndash 500mg
oral solution ndash 250 amp 500mg5ml
Rectal suppositories ndash 324 amp 648mg
Narcotics
Do produce sedation amp euphoria greater in children
LA is required but dose should be decreased
Meperidine Synthetic opiate agonist
Very water soluble
Orally SC IM or IV
Peak effect by oral 1 hr amp lasts upto 4 hrs
Adverse reactions
-Seizures
-Extreme caution in hepatic or renal diseases or history of seizures
7
Dosage Oral SC or IM ndash 1to 22mgkg not to exceed 100 mg
Supplied Oral Tablets ndash 50 amp 100mg
Oral Syrup ndash 50mgml
Parental solution ndash 25 50 75 amp 100mgml
Fentanyl
Synthetic opiate narcotic analgesic
Very potent 01mg = 10mg Morophine75mg Meperidine
Pharmacokinetics
IV IM SM
Metabolized in liver Excreted in urine
Fentanyl Onset ndash 7 to 15mins
Duration ndash 1 to 2 hrs
Pharmacodynamics
Respiratory depression RR but returns to normal rapidly Tidal volume amp response to co2 depressed for extended period
Apnea
Less emetic than meperidine
NOT RECOMMENDED IN CHILDREN BELOW 2yrs
Dosage 0002 to 0004mgkg
Supplied 005mgml in 2 amp 5ml ampoules
Reversal drug Naloxone
Semisynthetic opiate antagonist
No agonist activity
Onset 2 to 5mins SC or IM amp 1 to 2mins IV
Reversal 45mins
Pt should be kept under continual surveillance
Adverse reaction nausea vomiting sweating hypotension hypertension ventricular tachycardia fibrillation
Dosage IV SC IM 001mgkg then 01mgkg every 2- 3mins maximum 2mg
Supplied 002 004 1mg solutions
Antihistamines
Hydroxyzine
Oral or IM
Effect ndash 15 ndash 30mins
Half-life ndash 3 hrs
Uses
To relieve anxiety
Used as an anti-histamine
Used to control nausea and vomiting including that associated with motion sickness and pregnancy
Adverse reaction dry mouth drowsiness hypersentivity
Dosage Oral ndash 1 to 2mgkg
IM ndash 11mgkg
Promethazine Oral or IM Onset 15 to 60mins Duration 4 to 6 hrs Uses
To prevent and treat nausea and vomiting associated with motion pregnancy or surgery
Produces sedation and reduce swelling pain and trismus
Lower seizure threshold Adverse reaction dry mouth blurred vision thickening of bronchial secretions Dosage OralIM ndash 05-11mgkg
maximum 25 mg
Diphenhydramine
Oral IM IV
Onset -1hr
Duration ndash 4 to 6 hr
Metabolized in liver
Adverse reaction disturbed coordination thickening of bronchial secretions
Dosage Oral IM IV ndash 1 to 15mgkg
maximum 50mg
Tranquilizers
Major tranquilizer antipsychotic produce calmness control symptoms of psychoses cause reversible extra pyramidal symptoms and do not tend to cause habituation
Minor tranquilizer antianxiety agents also cause calmness do not cause extrapyramidal symptoms Used in conditions like nervous tension and mild depression
8
Classification
Antipsychotics
Phenothiazine derivatives
Chlorpromazine promazine
Butryophenones
Haloperidol
Rauwolfia alkaloids
Reserpine
Antianxiety drugs
Propyl alcohol derivatives
Meprobamate
Benzodiazepine derivatives
Diazepam
Miscellaneous compounds
Hydroxyzine
Meprobamate
White crystalline powder slightly bitter in taste
Only administered orally
Peak blood concentration ----1 to 3hrs
10 ---------excreted unchanged Rest --- excreted as a oxidized derivative or as a glucoronide
Uses
To relieve day time anxiety
Induce sleep in insomniacs
To reduce anxiety associated with dental treatment
Anti-convulsant ndash petit mal epilepsy
Adverse reaction leucopenia acute non-thrombocytopenic purpura ecchymoses eosinophilia edema adenopathy
Dosage Childrengt 6yrs 100 to 200mg
Not recommended for children under 6yrs
Monitoring during sedation
1 Pulse
2 Blood pressure
3 ECG
4 Respiration
5 Temperature
Pulse
Manual Electronic
bull Radial Brachial
bull Facial labial
Blood pressure
ndash Stethoscope amp sphygmomanometer
ndash Automatic devices
ndash Direct cannulation of an artery ndash very accurate
Electrocardiograph
Heart rate rhythm myocardial function
9
Respiration
ndash Monitoring respiratory rate
ndash Observing the rise amp fall of the chest wall
ndash Observing the color of mucous membrane
ndash Observing the inflation amp deflation of the reservoir bag
Devices for monitoring respiration
1 The Precordial pretracheal stethoscope
2 The esophageal stethoscope
ndash Respiratory rate
ndash Heart rate
ndash Any abnormal sounds
Pulse Oximeter
ndash Oxygen saturation
ndash Heart rate
ndash Oxisensor site
ndash Fingers
ndash Toe
ndash Ear lobe
Mechanism
Oxygenated Hb ndash red light
Deoxygenated Hb- infrared light
Tissue pressure from arterial pulse (plethysmography)
Advantages
ndash Safe amp noninvasive
ndash Simple to use
ndash Information is rapidly available for clinical decision
ndash Indirectly indicates respiratory adequacy
Disadvantages
ndash Finger probes can get dislodged
ndash Emitted light source may cause burning
ndash Non reusable probes are expensive
ndash Does not directly determine airway patency
Capnography
1 The presence absence of air flow
2 Indicates depth amp adequacy of respiration
3 Continues analysis of the co2 content of the respired air ndash indicates respiratory adequacy
Temperature
ndash Disposable nondisposable thermometer
ndash Esophageal rectal temp probe
10
Discharge criteria
Cardiovascular function is satisfactory amp stable
Airway patency is uncompromised amp satisfactory
Pt is easily arousable amp protective reflexes intact
State of hydration is adequate
Pt can talk if applicable
Pt can sit unaided if applicable
Pt can ambulate with minimal assistance if applicable
Presedation level of responsiveness achieved
Responsible individual is available
1
PULP THERAPY OF VITAL TEETH
DR MITAKSHARA NIRWAN
Contents
Indirect pulp capping
Direct pulp capping
Medications amp materials used in pulp capping
Pulpotomy
MTA
Apexogenesis
INDIRECT PULP CAPPING
Pieter Van Forest - first to speak about root canal therapy
Glove designed instruments that could prepare a canal to a certain size and taper(1910)
Indirect pulp capping is defined as a procedure where in small amount of carious dentin is retained in
deep areas of cavity to avoid exposure of pulp followed by placement of a suitable medicament and
restorative material that seals off the carious dentin and encourages pulp recovery (Ingle)
A procedure in which only the gross caries is removed from the lesion and the cavity is sealed for a
time with a biocompatible material (McDonald)
Objective of indirect pulp capping
These were given by Eidelman in 1965
bull Arresting the carious process
bull Promoting dentin sclerosis
bull Stimulating formation of tertiary dentin
bull Remineralization of carious dentin
Layers of Carious Dentin Indications of Indirect Pulp Capping
History
Mild pain associated with eating
Negative history of spontaneous extreme pain
Clinical Examination
Deep carious lesion which are close tobut not involving the pulp in vital primary or young
permanent teeth
No mobility
Nominal pulp inflammationdefinite layer of affected dentin after removal of infected dentin
Radiographic examination
Normal lamina dura amp PDL space
No radiolucency around the apices
2
Contraindications of Indirect Pulp Capping
History
Sharp penetrating pulpalgia
Prolonged spontaneous pain especially at night
Clinical examination
Mobility of tooth
Discoloration of tooth
Negative reaction of electric pulp testing
Radiographic examination
Definite pulp exposure
Break in the lamina dura
Radiolucency around the apices
Widened PDL space
Treatment procedure
Sequelae of Indirect Pulp Capping Three distinct types of new dentin formation take place
1 Cellular fibrillar dentinmdashfirst 2 months
2 Globular dentinmdash3 months
3 Tubular dentin (uniform mineralized dentin)
bull 15th of reparative dentin formation begins in less than 30 days
bull After 3 months 01 mm is formed
DIRECT PULP CAPPING Defined by Kopel (1992) as the placement of a medicament or non medicated material on a pulp that
has been exposed in course of excavating the last portions of deep dentinal caries or as a result of
trauma
Objective
To create new dentin in the area of the exposure and subsequent healing of the pulp
Rationale
achieve a biologic closure of the exposure site by deposition of hard tissue barrier (dentin bridge)
between pulp tissue and capping material thus walling off the
INDICATIONS
Small mechanical exposure
Easily controlled haemorrhage
Bright red haemorrhage
True pinpoint exposure
CONTRAINDICATIONS
Severe toothache at night
Spontaneous pain
Tooth mobility
Radiographic appearance of pulp periradicular de- generation
Excess of hemorrhage at the time of exposure Serous exudate from the exposure
Externalinternal root resorption
Swellingfistula
Histological Changes after Pulp Capping
These were illustrated be Glass and Zander in 1949
After 24 hours Necrotic zone adjacent to calcium
hydroxide paste is separated from healthy pulp
tissue by a deep staining basophilic layer
After 7 days Increase in cellular and fibroblastic
activity
After 14 days Partly calcified fibrous tissue lined by
odontoblastic cells is seen below the calcium
proteinate zone disappearance of necrotic zone
After 28 days Zone of new dentin
3
Medications and Materials Used for Pulp Capping Calcium hydroxide
Corticosteroids amp antibiotics
Inert materials
Collagen fibers
4-META adhesive
Direct bonding
Isobutyl cyanoacrylate
Denatured albumin
Mineral trioxide aggregate
Laser
Bone morphogenic protein
PULPOTOMY
Finn (1995) defined it as the complete removal of the coronal portion of the dental pulp
followed by placement of a suitable dressing or medicament that will promote healing and
preserve vitality of the tooth
American Academy of Pediatric Dentistry (1998) defined pulpotomy as the amputation of
affected infected coronal portion of the dental pulp preserving the vitality and function of the
remaining part of radicular pulp
Objectives
bull Removal of inflamed and infected coronal pulp at the site of exposure thus preserving the vitality of the
radicular pulp and allowing it to heal
bull Maintain the tooth in the dental arch
Rationale
bull Radicular pulp is healthy and capable of healing after surgical amputation of the infected coronal pulp
bull Preserves vitality of the radicular pulp
bull Maintains tooth in a physiologic condition
Indications of Pulpotomy bull Mechanical pulp exposure in primary teeth
bull Teeth showing a large carious lesion but free of radicular pulpitis
bull History of only spontaneous pain
bull Hemorrhage from exposure sites bright red and can be controlled
bull Absence of abscess or fistula
bull No interradicular bone loss
bull No interradicular radiolucency
Contraindications of Pulpotomy bull Persistent toothache
bull Tenderness on percussion
bull Root resorption more than 13rd of root length
bull Large carious lesion with nonrestorable crown
bull Highly viscous sluggish hemorrhage from canal orifice which is uncontrollable
bull Medical contradictions like heart disease immuno compromised patient
bull Swelling or fistula
bull External or internal resorption
bull Pathological mobility
bull Calcification of pulp
Classification of pulpotomy
4
Formocresol Pulpotomy
Iby BUCKLEY in 1904
Sweet (1930) Formulated multi visit technique
Doyle (1962) Advocated 2 sitting procedure (complete devitalization)
Spedding (1965) Gave 5 minute protocol (partial devitali- zation)
Venham (1967) Proposed 15 seconds procedure
Current concept uses 4 minutes of application time
Composition of formocresol Buckleyrsquos Formula
bull Cresol ndash 35 percent
bull Glycerol ndash 15 percent
bull Formaldehyde ndash 19 percent
bull Water ndash 31 percent
Mechanism of Action
It prevents tissue autolysis by bonding to the proteins Bonding is of peptide groups of side chain amino acids and is a reversible process accomplished without
changing the basic structure of protein molecules
Histological Changes
bull Demonstrated by Mass and Zilbermann11 in 1933 and also by Massler and Mansokhani in 1959
bull Immediately the pulp becomes fibrous and acidophillic
bull Seven to fourteen days Three zones appear
a broad eosinophilic zone of fixation
b broad pale-staining zone of atrophy with poorcellular definition
c broad zone of inflammation extending apically into normal pulp tissue
bull One yearndash Progressive apical movement of these zones with only acidophillic zone left at the end of 1 year
Modified Formocresol Pulpotomy
Used by TRASK(1972)
The technique is identical to that described for primary teeth except that the formocresol pellet is
sealed permanently in the tooth
Two-visit Devitalization Pulpotomy
Indications
bull There is evidence of sluggish bleeding at the amputation site that is difficult to control
bull Pus in the chamber but none at the amputation site
bull There is thickening of the PDL
bull History of pain
Contraindications
bull Nonrestorable tooth
bull Tooth with necrotic pulp
5
Glutaraldehyde Pulpotomy
It was first suggested by S Gravenmade Introduced by Kopel in 1979
Mechanism of Action
bull Glutaraldehyde produces rapid surface fixation of the underlying pulpal tissue
bull A narrow zone of eosinophilic stained and compressed fixed tissue is found directly beneath the area of application which blends into vital normal appearing tissue apically
bull With time the glutaraldehyde fixed zone is replaced by macrophagic action with dense collagenous tissue thus the entire root canal tissue is vital
Cvekrsquos Pulpotomy
bull This is also called as calcium hydroxide pulpotomy or young permanent partial pulpotomy
bull This was proposed by Mejare and Cvek16 in 1978
bull Indicated in young permanent teeth where the pulp is exposed by mechanical or bacterial means and the
remaining radicular tissue is judged vital by clinical and radiographic criteria whereas the root closure is
notcomplete
MINERAL TRIOXIDE AGGREGATE (MTA) Torabinejad described the physical and chemical properties of MTA in 1995
It is ash colored powder made primarily of fine hydrophilic particles of
1 tricalcium aluminate
2 tricalcium silicate
3 silicate oxide
4 tricalcium oxide
5 bismuth dioxide
Hydration of the powder results in a colloidal gel composed of calcium oxide crystals in an amorphous
structure This gel solidifies into a hard structure in less than three hours
PROPERTIES OF MTA
It is biocompatible material and its sealing ability is better than that of amalgam or ZOE
Initial pH is 102 and set pH is 125
The setting time of cement is 4 hours
The compressive strength is 70 MPA which is comparable with that of IRM
Low cytotoxicity ndash It presents with minimal inflammation if extended beyond the apex
Mineral trioxide aggregate (MTA) has demonstrated the ability to induce hard-tissue formation in
pulpal tissues and it promotes rapid cell growth
APEXOGENESIS
It is defined as the treatment of a vital pulp by capping or pulpotomy in order to permit continued
growth of the root and closure of the open apex
Rationale
Maintenance of integrity of the radicular pulp tissue to allow for continued root growth
Indications
bull Indicated for traumatized or pulpally involved vital permanent tooth when root apex is incompletely formed
bull No history of spontaneous pain
bull No sensitivity on percussion
bull No hemorrhage
bull Normal radiographic appearance
Contraindications
bull Evidence that radicular pulp has undergone degenerative changes
bull Purulent drainage
bull History of prolonged pain bull Necrotic debris in canal
bull Periapical radiolucency
6
1
Gupta A Dhingra R Chaudhari P Gupta A
Department of Paedodontics and Preventive Dentistry Faculty of Dental Sciences SGT University Gurgaon Haryana India
Journal of Indian Society of Pedodontics and Preventive Dentistry
Volume 35 I Issue 3 I July-September 2017
A COMPARISION OF VARIOUS MINIMALLY
INVASIVE TECHNIQUES FOR THE REMOVAL
OF DENTAL FLUOROSIS STAINS IN
CHILDREN
DR MITAKSHARA NIRWAN
CONTENTS
bull Introduction
bull Aims
bull Materials and Methods
bull Results
bull Discussion
bull Conclusion
bull Critical analysis
bull References
INTRODUCTION
bull Dental fluorosis is a developmental disturbance of dental enamel caused by
successive exposure to high concentrations of fluoride during tooth
development
bull Various methods of therapy are advocated for the treatment of fluorosis -
stained teeth which range from invasive ceramic veneer bonding restorations
to abrasive chemical treatments
bull The combination of dental bleaching techniques and microabrasion appears
as an excellent conservative solution to reestablish health in fluorosis
affected teeth
AIMS
bull The aim of the study was to evaluate and compare the effectiveness of
minimally invasive techniques for the removal of dental fluorosis
stains in children in vivo
MATERIALS AND METHODS
Patients visiting the department of Pedodontics and Preventive dentistry
Faculty of Dental Sciences SGT University Gurgaon
bull Sample size 90 patients
bull Age group 10 -17 years
bull Caries cracks or periodontal
disease on anterior teeth
bull Abscess draining sinus
cellulitis
bull Non vital teeth
hypersensitive exposed
crevices
bull Orthodontic appliance
bull Past history of bleaching
bull At least two permanent
maxillary anterior teeth
bull TSIF of score 4
bull Free of systemic diseases
Inclusion criteria Exclusion criteria
2
Groups
Group A In office bleaching with 35 hydrogen peroxide( Pola Office
Bleaching kit) activated by light emitting diode (LED) bleaching unit
(35 HP)
Group B Enamel microabrasion (EM) (PREMA Enamel Microabrasion
System) followed by in-office bleaching with 44 carbamide peroxide
gel (EM)
Group C In-office bleaching with 5 sodium hypochlorite (5
NaOCl)
A baseline colour evaluation was done by taking digital photograph of
the maxillary anterior teeth
RESULTS
Group 1
Colour stability
Group 2 Group 3
Tooth sensitivity
Tooth sensitivity values were taken before the treatment
which was compared to immediate postoperative and follow
up visits It was checked using an electric pulp tester
maximum
moderate
least
immediately
group 2
group 1
group 3
1 month
group 2
group 1
group 3
3 month
group 2
group 1
group 3
Patient satisfaction score
Satisfaction was assessed on visual analog scale
Range 1 to 5
Groups percentage of patients
who were satisfied with
the treatment
Number of patients
who reported slight
reappearance of colour
Group 1
90
7
Group 2
83
8
Group 3
73
7
3
Number of Appointments
Groups One sitting Two sittings Three
sittings
Group 1
25
4
1
group 2
26
3
1
Group 3
30
0
0
DISCUSSION
bull Hydrogen peroxide is capable of penetrating the tooth osmosis and through porosities and cracks subsequently acting directly on the pigmented molecules
bull Gurgan et al investigated 3 different light systems and found out that diode laser system with gave best tooth whitening and least tooth sensitivity
bull In the EM group the surface reflects and refracts light from the surface in such way that mild imperfections in underlying enamel are camouflaged While the highly polished surface of enamel enhances the aesthetic appearance
bull Train et al and Loguercio et al also had the similar results in their studies with EM mild fluorosis showed best results moderate showed moderate results while it had little effect on severe fluorosis
bull NaOCl was only effective on mild stains while moderate and severe
stains could only be lightened to quite an extent but could not be
completely removed
bull When NaOCl comes in contact with hypomineralized and discoloured
enamel it degrades and removes the chromogenic organic material
located on the enamel surface
CONCLUSION
bull It was concluded that esthetic appearance of teeth mild fluorosis can
be achieved by bleaching and microabrasion But in cases of
moderate fluorosis a combination of any of theses modalities can be
used
bull As no special maintenance precautions are required these maybe be
considered as an interesting alternative to conventional operative
treatment
bull Focuses on only TSIF of 4
bull Electric pulp testing is not the
right method to check for
sensitivity
bull Tooth Sensitivity changes
from person to person
bull Food habits can cause
staining of the teeth
bull Minimally invasive
bull Cheaper to veneers
bull Minimal loss of tooth structure
bull 4 parameters checked for the success of treatment
bull Inclusion of specific score of fluorosis for comparing the results
bull Maximum 3 appointments needed
CRITICAL ANALYSIS
Pros Cons
REFERENCES
bull Gurgan S Cakir FY Yazici E Different light-activated in officebleaching
systems Lasers Med Sci 201025817-22
bull Train TE McWhorter AG Seale NSWilson CF Guo IY Examination of
esthetic improvement and surface alteration following microabrasion in
fluorotic human incisors in vivoPediatr dent 199618353-62
bull Loguercio AD Correia LD Zago C Tagliari D Neumann E Gomes OM et al
Clinical effectiveness of two microabrasion materials materials for the
removal of enamel flurosis stains Oper Dent 200732531-8
4
1
LOCAL
ANESTHESIA
DR MITAKSHARA NIRWAN
CONTENTS
Definition
Methods of inducing local anesthesia
Desirable properties
Electrophysiology of nerve conduction
Impulse propagation and spread
Mode and site of action of local anesthesia
Classification of local anesthetic according to biological site and mode of action
Dissociation of local anaesthetics
Mechanism of action of local anaethetics
Local anaesthetic agent
2
3
DEFINITION
Local anesthesia is defined as a loss of sensation in
a circumscribed area of the body caused by depression
of excitation in nerve endings or an inhibition of the
conduction process in peripheral nerves
An important feature of local anesthesia is that it produces
LOSS OF SENSATION WITHOUT INDUCING LOSS OF
CONSCIOUSNESS
4
METHODS OF INDUCING LOCAL
ANESTHESIA
Low temperature
Mechanical trauma
Anoxia
Neurolytic agents such as alcohol amp phenol
Chemical agents such as local anesthetics
PROPERTIES OF LOCAL
ANESTHESIA
It should not be irritating to tissue to which it is applied
It should not cause any permanent alteration of nerve structure
Its systemic toxicity should be low
Time of onset of anesthesia should be short
It should be effective regardless of whether it is injected into the tissue or applied locally to mucous membranes
The duration of action should be long enough to permit the completion of procedure
5 6
It should have the potency sufficient to give complete
anesthesia with out the use of harmful concentration solutions
It should be free from producing allergic reactions
It should be free in solution and relatively undergo
biotransformation in the body
It should be either sterile or be capable of being sterilized by
heat with out deterioration
2
ELETROPHYSIOLOGY OF
NERVE CONDUCTION
There is an electrical charge across the membrane
This is the membrane potential
The resting potential (when the cell is not firing) is a negative
electrical potential of -70mv that exists across the nerve
membrane produced by different concentrations of either side of
the membrane
The interior of nerve is NEGATIVE in relation to exterior
7 8
inside
outside
Resting potential of neuron = -70mV
+
-
+
-
+
-
+
-
+
-
SLOW DEPOLARIRIZATION
9
RAPID DEPOLARIZATION
The interior of nerve is POSITIVE in relation to exterior
REPOLARIZATION
10
bull Repolarization takes 07 msec
bull Depolarization takes 03 msec
SODIUM PUMP -
energy comes from the oxidative metabolism of ATP
bull The entire process require 1 msec
IMPULSE PROPOGATION
IMPULSE SPREAD
The propagated impulse travels along the nerve
membrane towards CNS The spread of impulse differs
in myelinated and unmyelinated nerve fibers
DEPOLARIZED SEGMENT ADJACENT RESTING AREA
MODE AND SITE OF ACTION OF LOCAL
ANESTHETICS
Local anesthetic agent interferes with excitation
process in a nerve membrane in one of the
following ways
Altering the basic resting potential of nerve
membrane
Altering the threshold potential
Decreasing the rate of depolarization
Prolonging the rate of repolarization
12
3
CLASSIFICATION OF LOCAL ANESTHETIC
SUBSTANCES ACCORDING TO
BIOLOGICAL SITE AND MODE OF ACTION
CLASS A
Agents acting at receptor site on external surface of nerve membrane
Chemical substance Biotoxins (eg tetrodotoxin and saxitoxin)
CLASS B
Agents acting on receptor sites on internal surface of nerve membrane
Chemical substance Quaternary ammonium analogues of lidocaine
scorpion venom 13
CLASS C Agents acting by receptor independent of
physiochemical mechanism
Chemical substance Benzocaine
CLASS D Agents acting by combination of receptors and
receptor independent mechanisms
Chemical substance most clinically useful anesthetic agents
(eg lidocaine mepivacaine prilocaine)
14
BASED ON THE SOURCE
NATUAL
SYNTHETIC
OTHERS
BASED ON MODE OF APPLICATION
bull INJECTABLE
bull TOPICAL
BASED ON DURATION OF ACTION
bull ULTRA SHORT
bull SHORT
bull MEDIEM
bull LONG
BASED ON ONSET OF ACTION SHORT
INTERMEDIATE
LONG
15
DISSOCIATION OF LOCAL
ANESTHETICS
Local anesthetics are available as salts (usually
hydrochlorides) for clinical use
The salts both water soluble and stable is dissolved in
either sterile water or saline
In this solution it exists simultaneously as unchanged
molecule (RN) also called base and positively charged
molecules (RNH+) called cations
RNH+ ==== RN+ H
+
16
The relative concentration of each ionic form in the solution varies
in the pH of the solution or surrounding tissue
In the presence of high concentration of hydrogen ion (low pH) the
equilibrium shifts to left and most of the anesthetic solution exists
in cationic form
RNH+ gt RN
+ + H
+
As hydrogen ion concentration decreases (higher pH) the
equilibrium shifts towards the free base form
RNH+ lt RN + H
+
17
The relative proportion of ionic form also depends on pKa or DISSOCIATION CONSTANT of the specific local anesthetic
The pKa is a measure of molecules affinity for H+
ions
When the pH of the solution has the same value as pKa of the local anesthetic exactly half the drug will exists in the RNH
+ form and
exactly half in RN form
The percentage of drug existing in either form can be determined by Henderson Hasselbalch equation
Log baseacid = pH - pKa
18
4
MECHANISM OF ACTION OF LOCAL
ANESTHETICS
The following sequence is proposed mechanism of action of LA
Displacement of calcium ions from the sodium channel receptor site
Binding of local anesthetic molecule to this receptor site
Blockade of sodium channel
19
Decrease in sodium conductance
Depression of rate of electrical depolarization
Failure to achieve the threshold potential level
Lack of development of propagated action potential
Conduction blockadehellip
20
21
Na + Na +
22
LOCAL ANESTHETIC AGENT
COMERCIALLY PREPARED LOCAL ANESTHESIA
CONSISTS OF
Local anesthetic agent (xylocaine lignocaine 2)
Vasoconstrictor (adrenaline 1 80000)
Reducing agent (sodium metabisulphite)
Preservative (methylparabencapryl
hydrocuprienotoxin)
Fungicide (thymol)
Vehicle (distillde waterNaCl)
LOCAL ANESTHETIC AGENT
The local anesthetics used in dentistry are divided
into two groups
ESTER GROUP
AMIDE GROUP
23 24
ESTER GROUP It is composed of the following
An aromatic lipophilic group
An intermediate chain containing
an ester linkage
A hydrophilic secondary or tertiary
amino group
AMIDE GROUP It is composed of the following
An aromatic lipophilic group
An intermediate chain containing
amide linkage
A hydrophilic secondary or tertiary
amino group
5
25
CLASSIFICATION OF LOCAL ANESTHETICS
ESTERS
Esters of benzoic acid
Butacaine
Cocaine
Benzocaine
Hexylcaine
Piperocaine
Tetracaine
Esters of Para-amino
benzoic acid
Chloroprocain
Procaine
Propoxycaine
26
AMIDES Articaine
Bupivacaine
Dibucaine
Etidocaine
Lidocaine
Mepivacaine
Prilocaine
Ropivacaine
QUINOLINE
Centbucridine
PHARMACOKINETICS OF LOCAL
ANESTHETICS UPTAKE
When injected into soft tissue most local anesthetics produce
dilation of vascular bed
Cocaine is the only local anesthetic that produces
vasoconstriction initially it produces vasodilation which is
followed by prolonged vasoconstriction
Vasodilation is due to increase in the rate of absorption of the
local anesthetic into the blood thus decreasing the duration of
pain control while increasing the anesthetic blood level and
potential for over dose 27
AMIDE LOCAL ANESTHETICS
The metabolism of amide local anesthetics is more
complicated then esters The primary site of
biotransformation of amide drugs is liver
Entire metabolic process occurs in the liver for lidocaine
articaine etidocaine and bupivacaine
Prilocaine undergoes more rapid biotransformation then the
other amides
28
REFERENCES
Handbook of local anesthesia ndash Stanley F Malamed ndash 6th
edition
Essentials of Local Anesthetic Pharmacology Daniel E
Becker Anesth Prog 2006 Fall 53(3) 98ndash109
WIKIPEDIEA
29
THANK YOU
30
1
Pharmacological Methods of Behavior
Management
DR MITAKSHARA NIRWAN
DEFINITIONS
bull Conscious Sedation ndash A minimally depressed level of consciousness that retains
the patients ability to independently and continuously maintain an airway and respond appropriately to physical stimulation or verbal command
(American Dental Association House Of Delegates 2000)
bull Deep Sedation ndash An induced state of depressed consciousness
accompanied by partial loss of protective reflexes including the inability to continuously maintain an airway independently and or to respond purposefully to physical stimulation or verbal command
bull General Anesthesia (G A) ndash An induced state of unconsciousness or complete loss of
protective reflexes including the inability to continually maintain an airway independently and respond purposefully to physical stimulation or verbal command
Conscious sedation
ADVANTAGES
Conscious
Protective reflexes active amp intact
Stable vital signs
Operating dentist may perform sedation
Minimum amount of equipment required
Prolong detainment in recovery room not required
Risk of complication very low
Excellent choice for poor ndash risk pt in dental office
Cost effective
General anesthesia
ADVANTAGES Not absolutely
essential May be the only
method Not necessary (no
pain reaction) Amnesia always
present
Conscious sedation
DISADVANTAGES
Pt cooperation is essential
Extremely difficult or mentally handicapped pt cannot always be managed
Use of local anesthesia is a must
Amnesia may or may not be present
General anesthesia DISADVANTAGES
Pt unconscious
Protective reflexes are depressed
Depressed
Advanced training required Dentist must not act also as anesthetist
Special equipment necessary
Detainment in recovery area necessary
High IOP amp postoperative complications
Not indicated in dental office
More expensive
Fundamental Concepts
bull Techniques that utilize drugs to induce co-operative yet conscious state in an otherwise uncooperative child ndash CONSCIOUS SEDATION
2
GOALS
1 To facilitate the provision of quality care
2 To minimize the extremes of disruptive behavior
3 To promote a positive psychologic response to treatment
4 To promote patient welfare amp safety
5 To return the patient to physiologic state
OBJECTIVES
1 The pt mood must be altered
2 The pt must remain conscious at all times
3 The pt must be cooperative
4 All protective reflexes must remain intact and active
5 Vital signs must remain stable and with in normal limits
6 The ptrsquos pain threshold should be elevated
7 Amnesia may be present
Indications
1 Preschool children
2 Lack of Psychological Emotional maturity
3 Lack of Cognitive Physical Medical disability
4 Fearful amp anxious pts
5 Pt who require extensive amp complicated dental care amp would require or benefit from prolonged visits
6 Acute pain
7 Traumatic injuries
Operating Facilities amp Equipment
A positive pressure O2 delivery system capable of administering gt than 90 O2 at 10L min flow for 60 min (650L ldquoErdquo cylinder)
OR
Self inflating bag valve mask device (15L min)
A functional suction apparatus with appropriate suction catheters
Monitoring equipment - PO BPC PC or Capno
Inhalation sedation unit
100 O2 amp never less than 25
A fail safe mechanism that is checked and calibrated annually
Must have appropriate scavenging system
Emergency drugs
Techniques of sedation
Routes for drug administration
bull Oral
bull Rectal
bull Inhalational
bull Transmucosal
ndash Sublingual
ndash Intranasal
bull Parenteral
ndash IM
ndash sub mucosal
ndash IV
3
Oral Sedation
Advantages
1 Almost universally accepted and the easiest method
2 Decreased incidence and severity of adverse reaction
3 Low cost
Disadvantages
1 Absorption is variable
2 Prolonged latent period(30 min)
3 Reversal of any unwanted effect is also difficult
4 Inability to readily lighten or deepen the level of sedation
5 Prolonged duration of action
Rectal Sedation
Advantages 1 Incidence and intensity of
drug related side effects is minimized
2 Drug absorption occurs from the large intestine directly into the circulation
3 The lack of a needle syringe or other equipment
4 The ease of administration
5 The low cost
Disadvantages
1 Inconvenience to the administrator amp pt
2 The variable absorption of drugs from the large intestine
3 The slow onset of action amp the relatively long duration of action
4 Inability to titrate the drug dosage
5 The inability to reverse the action of the drug the prolonged recovery
Intranasal sedation
Advantages
Rapid onset (10 ndash 15 min)
Simple amp relatively painless
Less pt cooperation is required
Absorbed directly into the C V S
Intranasal sedation
Disadvantages
1 Dependence on nasal mucous membrane
2 Shorter duration of action(40-60min)
3 Multiple dosage may be necessary
Drugs
Midazolam ndash 02mgkg
Sufentanil ndash 15 ndash 3 mcgkg
Ketamine ndash 3-6mg kg
Sublingual sedation
Advantages
1 Pt acceptance
2 Rapid onset
3 High bioavailability
Drugs
Oral Transmucosal Fentanyl Citrate (OTFC)
Intramuscular Sedation
Advantages
1 More rapid onset of action
2 Absorbed directly into the C V system
3 More reliable absorption of drug
4 Pt cooperation is not as essential
Disadvantages
1 Time factor ndash its 15 min latent period
2 Pt may not be willing to accept the injection
3 The prolonged duration of action(2-4 hrs more)
4 Possibility of injury to the tissues at the site of injection caused by either the drug or the needle
4
Sites of I M administration
1 Gluteal area
2 Vastus lateralis
3 Mid ndash deltoid area
Drugs
Diazepam
Midazolam
Hydroxyzine
Inhalation Sedation
Advantages
1 The onset of action is more rapid
2 Peak clinical level is achieved rapidly(3-5min) - permit titration
3 Administrator has complete control over the actions of the drug - safety feature
4 No significant over dosage
5 Flexible duration of action
6 Recovery time is rapid amp most complete
7 No injection is required
8 With N2O- O2 it is safe with very few side effects
Disadvantages
1 The initial cost of the equipment is high 2 The continuing cost of the gases is high 3 The equipment occupies considerable space 4 N2O is not a potent agent 5 A degree of cooperation is required from the pt 6 Chronic exposure to N2O is deleterious to the health of
dental personnel
Contraindications
1 Nasal obstruction 2 Cyanosis at rest 3 Poor cooperation 4 1st trimester of pregnancy 5 Fear of masks
I V Sedation
Advantages
1 The onset of action is the most rapid 2 The dosage may be titrated 3 Suitable level of sedation can be provided 4 The recovery period is shorter 5 Side effects are extremely uncommon 6 Control of salivary secretions is possible 7 The gag reflex is diminished 8 Effectively diminishes motor disturbances 9 Provides immediate access to CVS in emergency
Disadvantages
1 Venipuncture is necessary
2 Complication may rise at the site of the venipuncture
3 Monitoring must be more intensive
4 Recovery is not complete at the end of the procedure
5 Reversal of sedation is difficult
5
N2O-O2 (Relative Analgesia)
colorless sweet smelling gas
Pharmacokinetics
Absorption through pulmonary epithelium
It is approx 15 times as soluble as is nitrogen It replaces nitrogen in blood
It is carried in solution in plasma of the blood
It is not metabolized by the body
Elimination ndash majorndash lungs minor --- skin
perspiration urine and intestinal gas
Pharmacodynamics
Dose related
10 ndash 25 Lightheaded
Changes in visual amp auditory sensation
Tingling of hands amp feet
Suffusing warmth
Remote from the immediate environment
Reduced anxiety
25-50 max analgesic properties and aberration of vision hearing and proprioception mild drowsiness euphoria amnesia and increased sleepiness and dreams
35 conc will achieve maximum analgesia
bull CNS
ndash Cerebrum-primarily affected
ndash Safe but weak anesthetic agent
bull RESPIRATORY SYSTEM
ndash Increased Tidal and minute volumes
bull CARDIOVASCULAR SYSTEM
ndash 2 studies ndash decreased cardiac output
bull FETAL SYSTEMS
ndash Miscarriage in humans
bull OTHER SYSTEMS
ndash Depression of spinal reflexes increase muscle tone indicates stage of delirium
ndash Muscle rigidity-narcotics + nitrous oxide
ndash Nausea and vomitting - GIT
ndash HEMATOPOIESIS ----- prolonged exposure
Adverse reactions and toxicity
EMOTIONAL REACTIONS
DREAMS HALLUCINATIONS
No acute toxicity
Chronic toxicity ndash bone marrow
depression
PROCEDURE
Diffusion Hypoxia
Sevoflurane
A fluorinated derivative of isopropyl ether ndash synthesized in 1970
Potent anaesthetic agent with rapid uptake amp speedy recovery
Day-case surgery
Problem
Attaching vaporiser to any of the currently available machine
BENZODIAZEPINES
Diazepam 1961 lipid soluble
Uses-alcoholism epilepsy labor tetanus and cerebral palsy
- sedation and amnesia
- varieties of neurosis amp anxiety states
Pharmacokinetics
Orally Rectal IMIV or SC
Well absorbed through GIT
Excretion in urine
6
bull Pharmacodynamics
ndash Depress the brain stem reticular system and the limbic system thalamus and hypothalamus
ndash It is a centrally acting muscle relaxant Has anti-convulsant properties
Adverse reaction amp toxicity
ndash Confusion nausea headache increased appetite decreased salivation and jaundice Thrombophlebitis
ndash Rebound phenomenon
ndash Toxicity drowsiness confusion sleep and coma
Dosage Oral or Rectal ndash 02-05mgkg
Maximum single dose 10mg
IV- 025mgkg
Supplied Tablets 2 5 10 mg
Suspension ndash 5mg
Midazolam Water soluble ndash non-irritant
Oral IM IV
Metabolism- liver
Onset IV 3 -5mins
oral 20 ndash 30mins
Oral administration anxious patients requiring relatively short dental procedure
No rebound phenomenon
Better anxiolysis amp amnesia (retrograde amnesia)
Adverse effects Respiratory depression
dose dependant apnea
Dosage Oral ndash 025 to 1mgkg to maximum single dose 20mg
IM ndash 01 to 015mgkg to a maximum of 10mg
IV ndash slow IV
Supplied Syrup ndash 2mgml
Injectable ndash 1mgml amp 5mgml vials
Flumazenil specific benzodiazepines antagonist
selectively inhibits CNS effects
IV administration amp not recommended below 18yrs of age
02mg over 15 seconds after 45seconds 02mg then after 60seconds to maximum of 1mg
Sedative-Hypnotics
Barbiturates First truly effective drugs for the management of anxiety Generalized CNS depressants Produce dose dependent effects
Sedation ---- sleep ---- GA ---- coma
Suppress the CNS and result in sedation and amnesia Advantages
Rapid onset and short duration Disadvantages
no analgesic effect and possible hypotension Must be used with caution in trauma patients because they may cause
apnea and hypoventilation
DOSE Pentobarbital Sodium 100mg Secobarbital Sodium 100 to 200mg Children 30 to 100mg
bull Chloral Hydrates (Mickey Finn Knock out drops ) First synthesized in 1832 first member of the hypnotic group of drugs
Widely used as conscious sedation agent
Properties
Unpleasant taste
Nausea vomiting
Quite irritating to skin and to mucous membranes
GI irritation
Dosages Individualized for each patient 25 ndash 50mgkg
maximum of 1g
Supplied oral capsule ndash 500mg
oral solution ndash 250 amp 500mg5ml
Rectal suppositories ndash 324 amp 648mg
Narcotics
Do produce sedation amp euphoria greater in children
LA is required but dose should be decreased
Meperidine Synthetic opiate agonist
Very water soluble
Orally SC IM or IV
Peak effect by oral 1 hr amp lasts upto 4 hrs
Adverse reactions
-Seizures
-Extreme caution in hepatic or renal diseases or history of seizures
7
Dosage Oral SC or IM ndash 1to 22mgkg not to exceed 100 mg
Supplied Oral Tablets ndash 50 amp 100mg
Oral Syrup ndash 50mgml
Parental solution ndash 25 50 75 amp 100mgml
Fentanyl
Synthetic opiate narcotic analgesic
Very potent 01mg = 10mg Morophine75mg Meperidine
Pharmacokinetics
IV IM SM
Metabolized in liver Excreted in urine
Fentanyl Onset ndash 7 to 15mins
Duration ndash 1 to 2 hrs
Pharmacodynamics
Respiratory depression RR but returns to normal rapidly Tidal volume amp response to co2 depressed for extended period
Apnea
Less emetic than meperidine
NOT RECOMMENDED IN CHILDREN BELOW 2yrs
Dosage 0002 to 0004mgkg
Supplied 005mgml in 2 amp 5ml ampoules
Reversal drug Naloxone
Semisynthetic opiate antagonist
No agonist activity
Onset 2 to 5mins SC or IM amp 1 to 2mins IV
Reversal 45mins
Pt should be kept under continual surveillance
Adverse reaction nausea vomiting sweating hypotension hypertension ventricular tachycardia fibrillation
Dosage IV SC IM 001mgkg then 01mgkg every 2- 3mins maximum 2mg
Supplied 002 004 1mg solutions
Antihistamines
Hydroxyzine
Oral or IM
Effect ndash 15 ndash 30mins
Half-life ndash 3 hrs
Uses
To relieve anxiety
Used as an anti-histamine
Used to control nausea and vomiting including that associated with motion sickness and pregnancy
Adverse reaction dry mouth drowsiness hypersentivity
Dosage Oral ndash 1 to 2mgkg
IM ndash 11mgkg
Promethazine Oral or IM Onset 15 to 60mins Duration 4 to 6 hrs Uses
To prevent and treat nausea and vomiting associated with motion pregnancy or surgery
Produces sedation and reduce swelling pain and trismus
Lower seizure threshold Adverse reaction dry mouth blurred vision thickening of bronchial secretions Dosage OralIM ndash 05-11mgkg
maximum 25 mg
Diphenhydramine
Oral IM IV
Onset -1hr
Duration ndash 4 to 6 hr
Metabolized in liver
Adverse reaction disturbed coordination thickening of bronchial secretions
Dosage Oral IM IV ndash 1 to 15mgkg
maximum 50mg
Tranquilizers
Major tranquilizer antipsychotic produce calmness control symptoms of psychoses cause reversible extra pyramidal symptoms and do not tend to cause habituation
Minor tranquilizer antianxiety agents also cause calmness do not cause extrapyramidal symptoms Used in conditions like nervous tension and mild depression
8
Classification
Antipsychotics
Phenothiazine derivatives
Chlorpromazine promazine
Butryophenones
Haloperidol
Rauwolfia alkaloids
Reserpine
Antianxiety drugs
Propyl alcohol derivatives
Meprobamate
Benzodiazepine derivatives
Diazepam
Miscellaneous compounds
Hydroxyzine
Meprobamate
White crystalline powder slightly bitter in taste
Only administered orally
Peak blood concentration ----1 to 3hrs
10 ---------excreted unchanged Rest --- excreted as a oxidized derivative or as a glucoronide
Uses
To relieve day time anxiety
Induce sleep in insomniacs
To reduce anxiety associated with dental treatment
Anti-convulsant ndash petit mal epilepsy
Adverse reaction leucopenia acute non-thrombocytopenic purpura ecchymoses eosinophilia edema adenopathy
Dosage Childrengt 6yrs 100 to 200mg
Not recommended for children under 6yrs
Monitoring during sedation
1 Pulse
2 Blood pressure
3 ECG
4 Respiration
5 Temperature
Pulse
Manual Electronic
bull Radial Brachial
bull Facial labial
Blood pressure
ndash Stethoscope amp sphygmomanometer
ndash Automatic devices
ndash Direct cannulation of an artery ndash very accurate
Electrocardiograph
Heart rate rhythm myocardial function
9
Respiration
ndash Monitoring respiratory rate
ndash Observing the rise amp fall of the chest wall
ndash Observing the color of mucous membrane
ndash Observing the inflation amp deflation of the reservoir bag
Devices for monitoring respiration
1 The Precordial pretracheal stethoscope
2 The esophageal stethoscope
ndash Respiratory rate
ndash Heart rate
ndash Any abnormal sounds
Pulse Oximeter
ndash Oxygen saturation
ndash Heart rate
ndash Oxisensor site
ndash Fingers
ndash Toe
ndash Ear lobe
Mechanism
Oxygenated Hb ndash red light
Deoxygenated Hb- infrared light
Tissue pressure from arterial pulse (plethysmography)
Advantages
ndash Safe amp noninvasive
ndash Simple to use
ndash Information is rapidly available for clinical decision
ndash Indirectly indicates respiratory adequacy
Disadvantages
ndash Finger probes can get dislodged
ndash Emitted light source may cause burning
ndash Non reusable probes are expensive
ndash Does not directly determine airway patency
Capnography
1 The presence absence of air flow
2 Indicates depth amp adequacy of respiration
3 Continues analysis of the co2 content of the respired air ndash indicates respiratory adequacy
Temperature
ndash Disposable nondisposable thermometer
ndash Esophageal rectal temp probe
10
Discharge criteria
Cardiovascular function is satisfactory amp stable
Airway patency is uncompromised amp satisfactory
Pt is easily arousable amp protective reflexes intact
State of hydration is adequate
Pt can talk if applicable
Pt can sit unaided if applicable
Pt can ambulate with minimal assistance if applicable
Presedation level of responsiveness achieved
Responsible individual is available
1
PULP THERAPY OF VITAL TEETH
DR MITAKSHARA NIRWAN
Contents
Indirect pulp capping
Direct pulp capping
Medications amp materials used in pulp capping
Pulpotomy
MTA
Apexogenesis
INDIRECT PULP CAPPING
Pieter Van Forest - first to speak about root canal therapy
Glove designed instruments that could prepare a canal to a certain size and taper(1910)
Indirect pulp capping is defined as a procedure where in small amount of carious dentin is retained in
deep areas of cavity to avoid exposure of pulp followed by placement of a suitable medicament and
restorative material that seals off the carious dentin and encourages pulp recovery (Ingle)
A procedure in which only the gross caries is removed from the lesion and the cavity is sealed for a
time with a biocompatible material (McDonald)
Objective of indirect pulp capping
These were given by Eidelman in 1965
bull Arresting the carious process
bull Promoting dentin sclerosis
bull Stimulating formation of tertiary dentin
bull Remineralization of carious dentin
Layers of Carious Dentin Indications of Indirect Pulp Capping
History
Mild pain associated with eating
Negative history of spontaneous extreme pain
Clinical Examination
Deep carious lesion which are close tobut not involving the pulp in vital primary or young
permanent teeth
No mobility
Nominal pulp inflammationdefinite layer of affected dentin after removal of infected dentin
Radiographic examination
Normal lamina dura amp PDL space
No radiolucency around the apices
2
Contraindications of Indirect Pulp Capping
History
Sharp penetrating pulpalgia
Prolonged spontaneous pain especially at night
Clinical examination
Mobility of tooth
Discoloration of tooth
Negative reaction of electric pulp testing
Radiographic examination
Definite pulp exposure
Break in the lamina dura
Radiolucency around the apices
Widened PDL space
Treatment procedure
Sequelae of Indirect Pulp Capping Three distinct types of new dentin formation take place
1 Cellular fibrillar dentinmdashfirst 2 months
2 Globular dentinmdash3 months
3 Tubular dentin (uniform mineralized dentin)
bull 15th of reparative dentin formation begins in less than 30 days
bull After 3 months 01 mm is formed
DIRECT PULP CAPPING Defined by Kopel (1992) as the placement of a medicament or non medicated material on a pulp that
has been exposed in course of excavating the last portions of deep dentinal caries or as a result of
trauma
Objective
To create new dentin in the area of the exposure and subsequent healing of the pulp
Rationale
achieve a biologic closure of the exposure site by deposition of hard tissue barrier (dentin bridge)
between pulp tissue and capping material thus walling off the
INDICATIONS
Small mechanical exposure
Easily controlled haemorrhage
Bright red haemorrhage
True pinpoint exposure
CONTRAINDICATIONS
Severe toothache at night
Spontaneous pain
Tooth mobility
Radiographic appearance of pulp periradicular de- generation
Excess of hemorrhage at the time of exposure Serous exudate from the exposure
Externalinternal root resorption
Swellingfistula
Histological Changes after Pulp Capping
These were illustrated be Glass and Zander in 1949
After 24 hours Necrotic zone adjacent to calcium
hydroxide paste is separated from healthy pulp
tissue by a deep staining basophilic layer
After 7 days Increase in cellular and fibroblastic
activity
After 14 days Partly calcified fibrous tissue lined by
odontoblastic cells is seen below the calcium
proteinate zone disappearance of necrotic zone
After 28 days Zone of new dentin
3
Medications and Materials Used for Pulp Capping Calcium hydroxide
Corticosteroids amp antibiotics
Inert materials
Collagen fibers
4-META adhesive
Direct bonding
Isobutyl cyanoacrylate
Denatured albumin
Mineral trioxide aggregate
Laser
Bone morphogenic protein
PULPOTOMY
Finn (1995) defined it as the complete removal of the coronal portion of the dental pulp
followed by placement of a suitable dressing or medicament that will promote healing and
preserve vitality of the tooth
American Academy of Pediatric Dentistry (1998) defined pulpotomy as the amputation of
affected infected coronal portion of the dental pulp preserving the vitality and function of the
remaining part of radicular pulp
Objectives
bull Removal of inflamed and infected coronal pulp at the site of exposure thus preserving the vitality of the
radicular pulp and allowing it to heal
bull Maintain the tooth in the dental arch
Rationale
bull Radicular pulp is healthy and capable of healing after surgical amputation of the infected coronal pulp
bull Preserves vitality of the radicular pulp
bull Maintains tooth in a physiologic condition
Indications of Pulpotomy bull Mechanical pulp exposure in primary teeth
bull Teeth showing a large carious lesion but free of radicular pulpitis
bull History of only spontaneous pain
bull Hemorrhage from exposure sites bright red and can be controlled
bull Absence of abscess or fistula
bull No interradicular bone loss
bull No interradicular radiolucency
Contraindications of Pulpotomy bull Persistent toothache
bull Tenderness on percussion
bull Root resorption more than 13rd of root length
bull Large carious lesion with nonrestorable crown
bull Highly viscous sluggish hemorrhage from canal orifice which is uncontrollable
bull Medical contradictions like heart disease immuno compromised patient
bull Swelling or fistula
bull External or internal resorption
bull Pathological mobility
bull Calcification of pulp
Classification of pulpotomy
4
Formocresol Pulpotomy
Iby BUCKLEY in 1904
Sweet (1930) Formulated multi visit technique
Doyle (1962) Advocated 2 sitting procedure (complete devitalization)
Spedding (1965) Gave 5 minute protocol (partial devitali- zation)
Venham (1967) Proposed 15 seconds procedure
Current concept uses 4 minutes of application time
Composition of formocresol Buckleyrsquos Formula
bull Cresol ndash 35 percent
bull Glycerol ndash 15 percent
bull Formaldehyde ndash 19 percent
bull Water ndash 31 percent
Mechanism of Action
It prevents tissue autolysis by bonding to the proteins Bonding is of peptide groups of side chain amino acids and is a reversible process accomplished without
changing the basic structure of protein molecules
Histological Changes
bull Demonstrated by Mass and Zilbermann11 in 1933 and also by Massler and Mansokhani in 1959
bull Immediately the pulp becomes fibrous and acidophillic
bull Seven to fourteen days Three zones appear
a broad eosinophilic zone of fixation
b broad pale-staining zone of atrophy with poorcellular definition
c broad zone of inflammation extending apically into normal pulp tissue
bull One yearndash Progressive apical movement of these zones with only acidophillic zone left at the end of 1 year
Modified Formocresol Pulpotomy
Used by TRASK(1972)
The technique is identical to that described for primary teeth except that the formocresol pellet is
sealed permanently in the tooth
Two-visit Devitalization Pulpotomy
Indications
bull There is evidence of sluggish bleeding at the amputation site that is difficult to control
bull Pus in the chamber but none at the amputation site
bull There is thickening of the PDL
bull History of pain
Contraindications
bull Nonrestorable tooth
bull Tooth with necrotic pulp
5
Glutaraldehyde Pulpotomy
It was first suggested by S Gravenmade Introduced by Kopel in 1979
Mechanism of Action
bull Glutaraldehyde produces rapid surface fixation of the underlying pulpal tissue
bull A narrow zone of eosinophilic stained and compressed fixed tissue is found directly beneath the area of application which blends into vital normal appearing tissue apically
bull With time the glutaraldehyde fixed zone is replaced by macrophagic action with dense collagenous tissue thus the entire root canal tissue is vital
Cvekrsquos Pulpotomy
bull This is also called as calcium hydroxide pulpotomy or young permanent partial pulpotomy
bull This was proposed by Mejare and Cvek16 in 1978
bull Indicated in young permanent teeth where the pulp is exposed by mechanical or bacterial means and the
remaining radicular tissue is judged vital by clinical and radiographic criteria whereas the root closure is
notcomplete
MINERAL TRIOXIDE AGGREGATE (MTA) Torabinejad described the physical and chemical properties of MTA in 1995
It is ash colored powder made primarily of fine hydrophilic particles of
1 tricalcium aluminate
2 tricalcium silicate
3 silicate oxide
4 tricalcium oxide
5 bismuth dioxide
Hydration of the powder results in a colloidal gel composed of calcium oxide crystals in an amorphous
structure This gel solidifies into a hard structure in less than three hours
PROPERTIES OF MTA
It is biocompatible material and its sealing ability is better than that of amalgam or ZOE
Initial pH is 102 and set pH is 125
The setting time of cement is 4 hours
The compressive strength is 70 MPA which is comparable with that of IRM
Low cytotoxicity ndash It presents with minimal inflammation if extended beyond the apex
Mineral trioxide aggregate (MTA) has demonstrated the ability to induce hard-tissue formation in
pulpal tissues and it promotes rapid cell growth
APEXOGENESIS
It is defined as the treatment of a vital pulp by capping or pulpotomy in order to permit continued
growth of the root and closure of the open apex
Rationale
Maintenance of integrity of the radicular pulp tissue to allow for continued root growth
Indications
bull Indicated for traumatized or pulpally involved vital permanent tooth when root apex is incompletely formed
bull No history of spontaneous pain
bull No sensitivity on percussion
bull No hemorrhage
bull Normal radiographic appearance
Contraindications
bull Evidence that radicular pulp has undergone degenerative changes
bull Purulent drainage
bull History of prolonged pain bull Necrotic debris in canal
bull Periapical radiolucency
6
1
Gupta A Dhingra R Chaudhari P Gupta A
Department of Paedodontics and Preventive Dentistry Faculty of Dental Sciences SGT University Gurgaon Haryana India
Journal of Indian Society of Pedodontics and Preventive Dentistry
Volume 35 I Issue 3 I July-September 2017
A COMPARISION OF VARIOUS MINIMALLY
INVASIVE TECHNIQUES FOR THE REMOVAL
OF DENTAL FLUOROSIS STAINS IN
CHILDREN
DR MITAKSHARA NIRWAN
CONTENTS
bull Introduction
bull Aims
bull Materials and Methods
bull Results
bull Discussion
bull Conclusion
bull Critical analysis
bull References
INTRODUCTION
bull Dental fluorosis is a developmental disturbance of dental enamel caused by
successive exposure to high concentrations of fluoride during tooth
development
bull Various methods of therapy are advocated for the treatment of fluorosis -
stained teeth which range from invasive ceramic veneer bonding restorations
to abrasive chemical treatments
bull The combination of dental bleaching techniques and microabrasion appears
as an excellent conservative solution to reestablish health in fluorosis
affected teeth
AIMS
bull The aim of the study was to evaluate and compare the effectiveness of
minimally invasive techniques for the removal of dental fluorosis
stains in children in vivo
MATERIALS AND METHODS
Patients visiting the department of Pedodontics and Preventive dentistry
Faculty of Dental Sciences SGT University Gurgaon
bull Sample size 90 patients
bull Age group 10 -17 years
bull Caries cracks or periodontal
disease on anterior teeth
bull Abscess draining sinus
cellulitis
bull Non vital teeth
hypersensitive exposed
crevices
bull Orthodontic appliance
bull Past history of bleaching
bull At least two permanent
maxillary anterior teeth
bull TSIF of score 4
bull Free of systemic diseases
Inclusion criteria Exclusion criteria
2
Groups
Group A In office bleaching with 35 hydrogen peroxide( Pola Office
Bleaching kit) activated by light emitting diode (LED) bleaching unit
(35 HP)
Group B Enamel microabrasion (EM) (PREMA Enamel Microabrasion
System) followed by in-office bleaching with 44 carbamide peroxide
gel (EM)
Group C In-office bleaching with 5 sodium hypochlorite (5
NaOCl)
A baseline colour evaluation was done by taking digital photograph of
the maxillary anterior teeth
RESULTS
Group 1
Colour stability
Group 2 Group 3
Tooth sensitivity
Tooth sensitivity values were taken before the treatment
which was compared to immediate postoperative and follow
up visits It was checked using an electric pulp tester
maximum
moderate
least
immediately
group 2
group 1
group 3
1 month
group 2
group 1
group 3
3 month
group 2
group 1
group 3
Patient satisfaction score
Satisfaction was assessed on visual analog scale
Range 1 to 5
Groups percentage of patients
who were satisfied with
the treatment
Number of patients
who reported slight
reappearance of colour
Group 1
90
7
Group 2
83
8
Group 3
73
7
3
Number of Appointments
Groups One sitting Two sittings Three
sittings
Group 1
25
4
1
group 2
26
3
1
Group 3
30
0
0
DISCUSSION
bull Hydrogen peroxide is capable of penetrating the tooth osmosis and through porosities and cracks subsequently acting directly on the pigmented molecules
bull Gurgan et al investigated 3 different light systems and found out that diode laser system with gave best tooth whitening and least tooth sensitivity
bull In the EM group the surface reflects and refracts light from the surface in such way that mild imperfections in underlying enamel are camouflaged While the highly polished surface of enamel enhances the aesthetic appearance
bull Train et al and Loguercio et al also had the similar results in their studies with EM mild fluorosis showed best results moderate showed moderate results while it had little effect on severe fluorosis
bull NaOCl was only effective on mild stains while moderate and severe
stains could only be lightened to quite an extent but could not be
completely removed
bull When NaOCl comes in contact with hypomineralized and discoloured
enamel it degrades and removes the chromogenic organic material
located on the enamel surface
CONCLUSION
bull It was concluded that esthetic appearance of teeth mild fluorosis can
be achieved by bleaching and microabrasion But in cases of
moderate fluorosis a combination of any of theses modalities can be
used
bull As no special maintenance precautions are required these maybe be
considered as an interesting alternative to conventional operative
treatment
bull Focuses on only TSIF of 4
bull Electric pulp testing is not the
right method to check for
sensitivity
bull Tooth Sensitivity changes
from person to person
bull Food habits can cause
staining of the teeth
bull Minimally invasive
bull Cheaper to veneers
bull Minimal loss of tooth structure
bull 4 parameters checked for the success of treatment
bull Inclusion of specific score of fluorosis for comparing the results
bull Maximum 3 appointments needed
CRITICAL ANALYSIS
Pros Cons
REFERENCES
bull Gurgan S Cakir FY Yazici E Different light-activated in officebleaching
systems Lasers Med Sci 201025817-22
bull Train TE McWhorter AG Seale NSWilson CF Guo IY Examination of
esthetic improvement and surface alteration following microabrasion in
fluorotic human incisors in vivoPediatr dent 199618353-62
bull Loguercio AD Correia LD Zago C Tagliari D Neumann E Gomes OM et al
Clinical effectiveness of two microabrasion materials materials for the
removal of enamel flurosis stains Oper Dent 200732531-8
4
2
ELETROPHYSIOLOGY OF
NERVE CONDUCTION
There is an electrical charge across the membrane
This is the membrane potential
The resting potential (when the cell is not firing) is a negative
electrical potential of -70mv that exists across the nerve
membrane produced by different concentrations of either side of
the membrane
The interior of nerve is NEGATIVE in relation to exterior
7 8
inside
outside
Resting potential of neuron = -70mV
+
-
+
-
+
-
+
-
+
-
SLOW DEPOLARIRIZATION
9
RAPID DEPOLARIZATION
The interior of nerve is POSITIVE in relation to exterior
REPOLARIZATION
10
bull Repolarization takes 07 msec
bull Depolarization takes 03 msec
SODIUM PUMP -
energy comes from the oxidative metabolism of ATP
bull The entire process require 1 msec
IMPULSE PROPOGATION
IMPULSE SPREAD
The propagated impulse travels along the nerve
membrane towards CNS The spread of impulse differs
in myelinated and unmyelinated nerve fibers
DEPOLARIZED SEGMENT ADJACENT RESTING AREA
MODE AND SITE OF ACTION OF LOCAL
ANESTHETICS
Local anesthetic agent interferes with excitation
process in a nerve membrane in one of the
following ways
Altering the basic resting potential of nerve
membrane
Altering the threshold potential
Decreasing the rate of depolarization
Prolonging the rate of repolarization
12
3
CLASSIFICATION OF LOCAL ANESTHETIC
SUBSTANCES ACCORDING TO
BIOLOGICAL SITE AND MODE OF ACTION
CLASS A
Agents acting at receptor site on external surface of nerve membrane
Chemical substance Biotoxins (eg tetrodotoxin and saxitoxin)
CLASS B
Agents acting on receptor sites on internal surface of nerve membrane
Chemical substance Quaternary ammonium analogues of lidocaine
scorpion venom 13
CLASS C Agents acting by receptor independent of
physiochemical mechanism
Chemical substance Benzocaine
CLASS D Agents acting by combination of receptors and
receptor independent mechanisms
Chemical substance most clinically useful anesthetic agents
(eg lidocaine mepivacaine prilocaine)
14
BASED ON THE SOURCE
NATUAL
SYNTHETIC
OTHERS
BASED ON MODE OF APPLICATION
bull INJECTABLE
bull TOPICAL
BASED ON DURATION OF ACTION
bull ULTRA SHORT
bull SHORT
bull MEDIEM
bull LONG
BASED ON ONSET OF ACTION SHORT
INTERMEDIATE
LONG
15
DISSOCIATION OF LOCAL
ANESTHETICS
Local anesthetics are available as salts (usually
hydrochlorides) for clinical use
The salts both water soluble and stable is dissolved in
either sterile water or saline
In this solution it exists simultaneously as unchanged
molecule (RN) also called base and positively charged
molecules (RNH+) called cations
RNH+ ==== RN+ H
+
16
The relative concentration of each ionic form in the solution varies
in the pH of the solution or surrounding tissue
In the presence of high concentration of hydrogen ion (low pH) the
equilibrium shifts to left and most of the anesthetic solution exists
in cationic form
RNH+ gt RN
+ + H
+
As hydrogen ion concentration decreases (higher pH) the
equilibrium shifts towards the free base form
RNH+ lt RN + H
+
17
The relative proportion of ionic form also depends on pKa or DISSOCIATION CONSTANT of the specific local anesthetic
The pKa is a measure of molecules affinity for H+
ions
When the pH of the solution has the same value as pKa of the local anesthetic exactly half the drug will exists in the RNH
+ form and
exactly half in RN form
The percentage of drug existing in either form can be determined by Henderson Hasselbalch equation
Log baseacid = pH - pKa
18
4
MECHANISM OF ACTION OF LOCAL
ANESTHETICS
The following sequence is proposed mechanism of action of LA
Displacement of calcium ions from the sodium channel receptor site
Binding of local anesthetic molecule to this receptor site
Blockade of sodium channel
19
Decrease in sodium conductance
Depression of rate of electrical depolarization
Failure to achieve the threshold potential level
Lack of development of propagated action potential
Conduction blockadehellip
20
21
Na + Na +
22
LOCAL ANESTHETIC AGENT
COMERCIALLY PREPARED LOCAL ANESTHESIA
CONSISTS OF
Local anesthetic agent (xylocaine lignocaine 2)
Vasoconstrictor (adrenaline 1 80000)
Reducing agent (sodium metabisulphite)
Preservative (methylparabencapryl
hydrocuprienotoxin)
Fungicide (thymol)
Vehicle (distillde waterNaCl)
LOCAL ANESTHETIC AGENT
The local anesthetics used in dentistry are divided
into two groups
ESTER GROUP
AMIDE GROUP
23 24
ESTER GROUP It is composed of the following
An aromatic lipophilic group
An intermediate chain containing
an ester linkage
A hydrophilic secondary or tertiary
amino group
AMIDE GROUP It is composed of the following
An aromatic lipophilic group
An intermediate chain containing
amide linkage
A hydrophilic secondary or tertiary
amino group
5
25
CLASSIFICATION OF LOCAL ANESTHETICS
ESTERS
Esters of benzoic acid
Butacaine
Cocaine
Benzocaine
Hexylcaine
Piperocaine
Tetracaine
Esters of Para-amino
benzoic acid
Chloroprocain
Procaine
Propoxycaine
26
AMIDES Articaine
Bupivacaine
Dibucaine
Etidocaine
Lidocaine
Mepivacaine
Prilocaine
Ropivacaine
QUINOLINE
Centbucridine
PHARMACOKINETICS OF LOCAL
ANESTHETICS UPTAKE
When injected into soft tissue most local anesthetics produce
dilation of vascular bed
Cocaine is the only local anesthetic that produces
vasoconstriction initially it produces vasodilation which is
followed by prolonged vasoconstriction
Vasodilation is due to increase in the rate of absorption of the
local anesthetic into the blood thus decreasing the duration of
pain control while increasing the anesthetic blood level and
potential for over dose 27
AMIDE LOCAL ANESTHETICS
The metabolism of amide local anesthetics is more
complicated then esters The primary site of
biotransformation of amide drugs is liver
Entire metabolic process occurs in the liver for lidocaine
articaine etidocaine and bupivacaine
Prilocaine undergoes more rapid biotransformation then the
other amides
28
REFERENCES
Handbook of local anesthesia ndash Stanley F Malamed ndash 6th
edition
Essentials of Local Anesthetic Pharmacology Daniel E
Becker Anesth Prog 2006 Fall 53(3) 98ndash109
WIKIPEDIEA
29
THANK YOU
30
1
Pharmacological Methods of Behavior
Management
DR MITAKSHARA NIRWAN
DEFINITIONS
bull Conscious Sedation ndash A minimally depressed level of consciousness that retains
the patients ability to independently and continuously maintain an airway and respond appropriately to physical stimulation or verbal command
(American Dental Association House Of Delegates 2000)
bull Deep Sedation ndash An induced state of depressed consciousness
accompanied by partial loss of protective reflexes including the inability to continuously maintain an airway independently and or to respond purposefully to physical stimulation or verbal command
bull General Anesthesia (G A) ndash An induced state of unconsciousness or complete loss of
protective reflexes including the inability to continually maintain an airway independently and respond purposefully to physical stimulation or verbal command
Conscious sedation
ADVANTAGES
Conscious
Protective reflexes active amp intact
Stable vital signs
Operating dentist may perform sedation
Minimum amount of equipment required
Prolong detainment in recovery room not required
Risk of complication very low
Excellent choice for poor ndash risk pt in dental office
Cost effective
General anesthesia
ADVANTAGES Not absolutely
essential May be the only
method Not necessary (no
pain reaction) Amnesia always
present
Conscious sedation
DISADVANTAGES
Pt cooperation is essential
Extremely difficult or mentally handicapped pt cannot always be managed
Use of local anesthesia is a must
Amnesia may or may not be present
General anesthesia DISADVANTAGES
Pt unconscious
Protective reflexes are depressed
Depressed
Advanced training required Dentist must not act also as anesthetist
Special equipment necessary
Detainment in recovery area necessary
High IOP amp postoperative complications
Not indicated in dental office
More expensive
Fundamental Concepts
bull Techniques that utilize drugs to induce co-operative yet conscious state in an otherwise uncooperative child ndash CONSCIOUS SEDATION
2
GOALS
1 To facilitate the provision of quality care
2 To minimize the extremes of disruptive behavior
3 To promote a positive psychologic response to treatment
4 To promote patient welfare amp safety
5 To return the patient to physiologic state
OBJECTIVES
1 The pt mood must be altered
2 The pt must remain conscious at all times
3 The pt must be cooperative
4 All protective reflexes must remain intact and active
5 Vital signs must remain stable and with in normal limits
6 The ptrsquos pain threshold should be elevated
7 Amnesia may be present
Indications
1 Preschool children
2 Lack of Psychological Emotional maturity
3 Lack of Cognitive Physical Medical disability
4 Fearful amp anxious pts
5 Pt who require extensive amp complicated dental care amp would require or benefit from prolonged visits
6 Acute pain
7 Traumatic injuries
Operating Facilities amp Equipment
A positive pressure O2 delivery system capable of administering gt than 90 O2 at 10L min flow for 60 min (650L ldquoErdquo cylinder)
OR
Self inflating bag valve mask device (15L min)
A functional suction apparatus with appropriate suction catheters
Monitoring equipment - PO BPC PC or Capno
Inhalation sedation unit
100 O2 amp never less than 25
A fail safe mechanism that is checked and calibrated annually
Must have appropriate scavenging system
Emergency drugs
Techniques of sedation
Routes for drug administration
bull Oral
bull Rectal
bull Inhalational
bull Transmucosal
ndash Sublingual
ndash Intranasal
bull Parenteral
ndash IM
ndash sub mucosal
ndash IV
3
Oral Sedation
Advantages
1 Almost universally accepted and the easiest method
2 Decreased incidence and severity of adverse reaction
3 Low cost
Disadvantages
1 Absorption is variable
2 Prolonged latent period(30 min)
3 Reversal of any unwanted effect is also difficult
4 Inability to readily lighten or deepen the level of sedation
5 Prolonged duration of action
Rectal Sedation
Advantages 1 Incidence and intensity of
drug related side effects is minimized
2 Drug absorption occurs from the large intestine directly into the circulation
3 The lack of a needle syringe or other equipment
4 The ease of administration
5 The low cost
Disadvantages
1 Inconvenience to the administrator amp pt
2 The variable absorption of drugs from the large intestine
3 The slow onset of action amp the relatively long duration of action
4 Inability to titrate the drug dosage
5 The inability to reverse the action of the drug the prolonged recovery
Intranasal sedation
Advantages
Rapid onset (10 ndash 15 min)
Simple amp relatively painless
Less pt cooperation is required
Absorbed directly into the C V S
Intranasal sedation
Disadvantages
1 Dependence on nasal mucous membrane
2 Shorter duration of action(40-60min)
3 Multiple dosage may be necessary
Drugs
Midazolam ndash 02mgkg
Sufentanil ndash 15 ndash 3 mcgkg
Ketamine ndash 3-6mg kg
Sublingual sedation
Advantages
1 Pt acceptance
2 Rapid onset
3 High bioavailability
Drugs
Oral Transmucosal Fentanyl Citrate (OTFC)
Intramuscular Sedation
Advantages
1 More rapid onset of action
2 Absorbed directly into the C V system
3 More reliable absorption of drug
4 Pt cooperation is not as essential
Disadvantages
1 Time factor ndash its 15 min latent period
2 Pt may not be willing to accept the injection
3 The prolonged duration of action(2-4 hrs more)
4 Possibility of injury to the tissues at the site of injection caused by either the drug or the needle
4
Sites of I M administration
1 Gluteal area
2 Vastus lateralis
3 Mid ndash deltoid area
Drugs
Diazepam
Midazolam
Hydroxyzine
Inhalation Sedation
Advantages
1 The onset of action is more rapid
2 Peak clinical level is achieved rapidly(3-5min) - permit titration
3 Administrator has complete control over the actions of the drug - safety feature
4 No significant over dosage
5 Flexible duration of action
6 Recovery time is rapid amp most complete
7 No injection is required
8 With N2O- O2 it is safe with very few side effects
Disadvantages
1 The initial cost of the equipment is high 2 The continuing cost of the gases is high 3 The equipment occupies considerable space 4 N2O is not a potent agent 5 A degree of cooperation is required from the pt 6 Chronic exposure to N2O is deleterious to the health of
dental personnel
Contraindications
1 Nasal obstruction 2 Cyanosis at rest 3 Poor cooperation 4 1st trimester of pregnancy 5 Fear of masks
I V Sedation
Advantages
1 The onset of action is the most rapid 2 The dosage may be titrated 3 Suitable level of sedation can be provided 4 The recovery period is shorter 5 Side effects are extremely uncommon 6 Control of salivary secretions is possible 7 The gag reflex is diminished 8 Effectively diminishes motor disturbances 9 Provides immediate access to CVS in emergency
Disadvantages
1 Venipuncture is necessary
2 Complication may rise at the site of the venipuncture
3 Monitoring must be more intensive
4 Recovery is not complete at the end of the procedure
5 Reversal of sedation is difficult
5
N2O-O2 (Relative Analgesia)
colorless sweet smelling gas
Pharmacokinetics
Absorption through pulmonary epithelium
It is approx 15 times as soluble as is nitrogen It replaces nitrogen in blood
It is carried in solution in plasma of the blood
It is not metabolized by the body
Elimination ndash majorndash lungs minor --- skin
perspiration urine and intestinal gas
Pharmacodynamics
Dose related
10 ndash 25 Lightheaded
Changes in visual amp auditory sensation
Tingling of hands amp feet
Suffusing warmth
Remote from the immediate environment
Reduced anxiety
25-50 max analgesic properties and aberration of vision hearing and proprioception mild drowsiness euphoria amnesia and increased sleepiness and dreams
35 conc will achieve maximum analgesia
bull CNS
ndash Cerebrum-primarily affected
ndash Safe but weak anesthetic agent
bull RESPIRATORY SYSTEM
ndash Increased Tidal and minute volumes
bull CARDIOVASCULAR SYSTEM
ndash 2 studies ndash decreased cardiac output
bull FETAL SYSTEMS
ndash Miscarriage in humans
bull OTHER SYSTEMS
ndash Depression of spinal reflexes increase muscle tone indicates stage of delirium
ndash Muscle rigidity-narcotics + nitrous oxide
ndash Nausea and vomitting - GIT
ndash HEMATOPOIESIS ----- prolonged exposure
Adverse reactions and toxicity
EMOTIONAL REACTIONS
DREAMS HALLUCINATIONS
No acute toxicity
Chronic toxicity ndash bone marrow
depression
PROCEDURE
Diffusion Hypoxia
Sevoflurane
A fluorinated derivative of isopropyl ether ndash synthesized in 1970
Potent anaesthetic agent with rapid uptake amp speedy recovery
Day-case surgery
Problem
Attaching vaporiser to any of the currently available machine
BENZODIAZEPINES
Diazepam 1961 lipid soluble
Uses-alcoholism epilepsy labor tetanus and cerebral palsy
- sedation and amnesia
- varieties of neurosis amp anxiety states
Pharmacokinetics
Orally Rectal IMIV or SC
Well absorbed through GIT
Excretion in urine
6
bull Pharmacodynamics
ndash Depress the brain stem reticular system and the limbic system thalamus and hypothalamus
ndash It is a centrally acting muscle relaxant Has anti-convulsant properties
Adverse reaction amp toxicity
ndash Confusion nausea headache increased appetite decreased salivation and jaundice Thrombophlebitis
ndash Rebound phenomenon
ndash Toxicity drowsiness confusion sleep and coma
Dosage Oral or Rectal ndash 02-05mgkg
Maximum single dose 10mg
IV- 025mgkg
Supplied Tablets 2 5 10 mg
Suspension ndash 5mg
Midazolam Water soluble ndash non-irritant
Oral IM IV
Metabolism- liver
Onset IV 3 -5mins
oral 20 ndash 30mins
Oral administration anxious patients requiring relatively short dental procedure
No rebound phenomenon
Better anxiolysis amp amnesia (retrograde amnesia)
Adverse effects Respiratory depression
dose dependant apnea
Dosage Oral ndash 025 to 1mgkg to maximum single dose 20mg
IM ndash 01 to 015mgkg to a maximum of 10mg
IV ndash slow IV
Supplied Syrup ndash 2mgml
Injectable ndash 1mgml amp 5mgml vials
Flumazenil specific benzodiazepines antagonist
selectively inhibits CNS effects
IV administration amp not recommended below 18yrs of age
02mg over 15 seconds after 45seconds 02mg then after 60seconds to maximum of 1mg
Sedative-Hypnotics
Barbiturates First truly effective drugs for the management of anxiety Generalized CNS depressants Produce dose dependent effects
Sedation ---- sleep ---- GA ---- coma
Suppress the CNS and result in sedation and amnesia Advantages
Rapid onset and short duration Disadvantages
no analgesic effect and possible hypotension Must be used with caution in trauma patients because they may cause
apnea and hypoventilation
DOSE Pentobarbital Sodium 100mg Secobarbital Sodium 100 to 200mg Children 30 to 100mg
bull Chloral Hydrates (Mickey Finn Knock out drops ) First synthesized in 1832 first member of the hypnotic group of drugs
Widely used as conscious sedation agent
Properties
Unpleasant taste
Nausea vomiting
Quite irritating to skin and to mucous membranes
GI irritation
Dosages Individualized for each patient 25 ndash 50mgkg
maximum of 1g
Supplied oral capsule ndash 500mg
oral solution ndash 250 amp 500mg5ml
Rectal suppositories ndash 324 amp 648mg
Narcotics
Do produce sedation amp euphoria greater in children
LA is required but dose should be decreased
Meperidine Synthetic opiate agonist
Very water soluble
Orally SC IM or IV
Peak effect by oral 1 hr amp lasts upto 4 hrs
Adverse reactions
-Seizures
-Extreme caution in hepatic or renal diseases or history of seizures
7
Dosage Oral SC or IM ndash 1to 22mgkg not to exceed 100 mg
Supplied Oral Tablets ndash 50 amp 100mg
Oral Syrup ndash 50mgml
Parental solution ndash 25 50 75 amp 100mgml
Fentanyl
Synthetic opiate narcotic analgesic
Very potent 01mg = 10mg Morophine75mg Meperidine
Pharmacokinetics
IV IM SM
Metabolized in liver Excreted in urine
Fentanyl Onset ndash 7 to 15mins
Duration ndash 1 to 2 hrs
Pharmacodynamics
Respiratory depression RR but returns to normal rapidly Tidal volume amp response to co2 depressed for extended period
Apnea
Less emetic than meperidine
NOT RECOMMENDED IN CHILDREN BELOW 2yrs
Dosage 0002 to 0004mgkg
Supplied 005mgml in 2 amp 5ml ampoules
Reversal drug Naloxone
Semisynthetic opiate antagonist
No agonist activity
Onset 2 to 5mins SC or IM amp 1 to 2mins IV
Reversal 45mins
Pt should be kept under continual surveillance
Adverse reaction nausea vomiting sweating hypotension hypertension ventricular tachycardia fibrillation
Dosage IV SC IM 001mgkg then 01mgkg every 2- 3mins maximum 2mg
Supplied 002 004 1mg solutions
Antihistamines
Hydroxyzine
Oral or IM
Effect ndash 15 ndash 30mins
Half-life ndash 3 hrs
Uses
To relieve anxiety
Used as an anti-histamine
Used to control nausea and vomiting including that associated with motion sickness and pregnancy
Adverse reaction dry mouth drowsiness hypersentivity
Dosage Oral ndash 1 to 2mgkg
IM ndash 11mgkg
Promethazine Oral or IM Onset 15 to 60mins Duration 4 to 6 hrs Uses
To prevent and treat nausea and vomiting associated with motion pregnancy or surgery
Produces sedation and reduce swelling pain and trismus
Lower seizure threshold Adverse reaction dry mouth blurred vision thickening of bronchial secretions Dosage OralIM ndash 05-11mgkg
maximum 25 mg
Diphenhydramine
Oral IM IV
Onset -1hr
Duration ndash 4 to 6 hr
Metabolized in liver
Adverse reaction disturbed coordination thickening of bronchial secretions
Dosage Oral IM IV ndash 1 to 15mgkg
maximum 50mg
Tranquilizers
Major tranquilizer antipsychotic produce calmness control symptoms of psychoses cause reversible extra pyramidal symptoms and do not tend to cause habituation
Minor tranquilizer antianxiety agents also cause calmness do not cause extrapyramidal symptoms Used in conditions like nervous tension and mild depression
8
Classification
Antipsychotics
Phenothiazine derivatives
Chlorpromazine promazine
Butryophenones
Haloperidol
Rauwolfia alkaloids
Reserpine
Antianxiety drugs
Propyl alcohol derivatives
Meprobamate
Benzodiazepine derivatives
Diazepam
Miscellaneous compounds
Hydroxyzine
Meprobamate
White crystalline powder slightly bitter in taste
Only administered orally
Peak blood concentration ----1 to 3hrs
10 ---------excreted unchanged Rest --- excreted as a oxidized derivative or as a glucoronide
Uses
To relieve day time anxiety
Induce sleep in insomniacs
To reduce anxiety associated with dental treatment
Anti-convulsant ndash petit mal epilepsy
Adverse reaction leucopenia acute non-thrombocytopenic purpura ecchymoses eosinophilia edema adenopathy
Dosage Childrengt 6yrs 100 to 200mg
Not recommended for children under 6yrs
Monitoring during sedation
1 Pulse
2 Blood pressure
3 ECG
4 Respiration
5 Temperature
Pulse
Manual Electronic
bull Radial Brachial
bull Facial labial
Blood pressure
ndash Stethoscope amp sphygmomanometer
ndash Automatic devices
ndash Direct cannulation of an artery ndash very accurate
Electrocardiograph
Heart rate rhythm myocardial function
9
Respiration
ndash Monitoring respiratory rate
ndash Observing the rise amp fall of the chest wall
ndash Observing the color of mucous membrane
ndash Observing the inflation amp deflation of the reservoir bag
Devices for monitoring respiration
1 The Precordial pretracheal stethoscope
2 The esophageal stethoscope
ndash Respiratory rate
ndash Heart rate
ndash Any abnormal sounds
Pulse Oximeter
ndash Oxygen saturation
ndash Heart rate
ndash Oxisensor site
ndash Fingers
ndash Toe
ndash Ear lobe
Mechanism
Oxygenated Hb ndash red light
Deoxygenated Hb- infrared light
Tissue pressure from arterial pulse (plethysmography)
Advantages
ndash Safe amp noninvasive
ndash Simple to use
ndash Information is rapidly available for clinical decision
ndash Indirectly indicates respiratory adequacy
Disadvantages
ndash Finger probes can get dislodged
ndash Emitted light source may cause burning
ndash Non reusable probes are expensive
ndash Does not directly determine airway patency
Capnography
1 The presence absence of air flow
2 Indicates depth amp adequacy of respiration
3 Continues analysis of the co2 content of the respired air ndash indicates respiratory adequacy
Temperature
ndash Disposable nondisposable thermometer
ndash Esophageal rectal temp probe
10
Discharge criteria
Cardiovascular function is satisfactory amp stable
Airway patency is uncompromised amp satisfactory
Pt is easily arousable amp protective reflexes intact
State of hydration is adequate
Pt can talk if applicable
Pt can sit unaided if applicable
Pt can ambulate with minimal assistance if applicable
Presedation level of responsiveness achieved
Responsible individual is available
1
PULP THERAPY OF VITAL TEETH
DR MITAKSHARA NIRWAN
Contents
Indirect pulp capping
Direct pulp capping
Medications amp materials used in pulp capping
Pulpotomy
MTA
Apexogenesis
INDIRECT PULP CAPPING
Pieter Van Forest - first to speak about root canal therapy
Glove designed instruments that could prepare a canal to a certain size and taper(1910)
Indirect pulp capping is defined as a procedure where in small amount of carious dentin is retained in
deep areas of cavity to avoid exposure of pulp followed by placement of a suitable medicament and
restorative material that seals off the carious dentin and encourages pulp recovery (Ingle)
A procedure in which only the gross caries is removed from the lesion and the cavity is sealed for a
time with a biocompatible material (McDonald)
Objective of indirect pulp capping
These were given by Eidelman in 1965
bull Arresting the carious process
bull Promoting dentin sclerosis
bull Stimulating formation of tertiary dentin
bull Remineralization of carious dentin
Layers of Carious Dentin Indications of Indirect Pulp Capping
History
Mild pain associated with eating
Negative history of spontaneous extreme pain
Clinical Examination
Deep carious lesion which are close tobut not involving the pulp in vital primary or young
permanent teeth
No mobility
Nominal pulp inflammationdefinite layer of affected dentin after removal of infected dentin
Radiographic examination
Normal lamina dura amp PDL space
No radiolucency around the apices
2
Contraindications of Indirect Pulp Capping
History
Sharp penetrating pulpalgia
Prolonged spontaneous pain especially at night
Clinical examination
Mobility of tooth
Discoloration of tooth
Negative reaction of electric pulp testing
Radiographic examination
Definite pulp exposure
Break in the lamina dura
Radiolucency around the apices
Widened PDL space
Treatment procedure
Sequelae of Indirect Pulp Capping Three distinct types of new dentin formation take place
1 Cellular fibrillar dentinmdashfirst 2 months
2 Globular dentinmdash3 months
3 Tubular dentin (uniform mineralized dentin)
bull 15th of reparative dentin formation begins in less than 30 days
bull After 3 months 01 mm is formed
DIRECT PULP CAPPING Defined by Kopel (1992) as the placement of a medicament or non medicated material on a pulp that
has been exposed in course of excavating the last portions of deep dentinal caries or as a result of
trauma
Objective
To create new dentin in the area of the exposure and subsequent healing of the pulp
Rationale
achieve a biologic closure of the exposure site by deposition of hard tissue barrier (dentin bridge)
between pulp tissue and capping material thus walling off the
INDICATIONS
Small mechanical exposure
Easily controlled haemorrhage
Bright red haemorrhage
True pinpoint exposure
CONTRAINDICATIONS
Severe toothache at night
Spontaneous pain
Tooth mobility
Radiographic appearance of pulp periradicular de- generation
Excess of hemorrhage at the time of exposure Serous exudate from the exposure
Externalinternal root resorption
Swellingfistula
Histological Changes after Pulp Capping
These were illustrated be Glass and Zander in 1949
After 24 hours Necrotic zone adjacent to calcium
hydroxide paste is separated from healthy pulp
tissue by a deep staining basophilic layer
After 7 days Increase in cellular and fibroblastic
activity
After 14 days Partly calcified fibrous tissue lined by
odontoblastic cells is seen below the calcium
proteinate zone disappearance of necrotic zone
After 28 days Zone of new dentin
3
Medications and Materials Used for Pulp Capping Calcium hydroxide
Corticosteroids amp antibiotics
Inert materials
Collagen fibers
4-META adhesive
Direct bonding
Isobutyl cyanoacrylate
Denatured albumin
Mineral trioxide aggregate
Laser
Bone morphogenic protein
PULPOTOMY
Finn (1995) defined it as the complete removal of the coronal portion of the dental pulp
followed by placement of a suitable dressing or medicament that will promote healing and
preserve vitality of the tooth
American Academy of Pediatric Dentistry (1998) defined pulpotomy as the amputation of
affected infected coronal portion of the dental pulp preserving the vitality and function of the
remaining part of radicular pulp
Objectives
bull Removal of inflamed and infected coronal pulp at the site of exposure thus preserving the vitality of the
radicular pulp and allowing it to heal
bull Maintain the tooth in the dental arch
Rationale
bull Radicular pulp is healthy and capable of healing after surgical amputation of the infected coronal pulp
bull Preserves vitality of the radicular pulp
bull Maintains tooth in a physiologic condition
Indications of Pulpotomy bull Mechanical pulp exposure in primary teeth
bull Teeth showing a large carious lesion but free of radicular pulpitis
bull History of only spontaneous pain
bull Hemorrhage from exposure sites bright red and can be controlled
bull Absence of abscess or fistula
bull No interradicular bone loss
bull No interradicular radiolucency
Contraindications of Pulpotomy bull Persistent toothache
bull Tenderness on percussion
bull Root resorption more than 13rd of root length
bull Large carious lesion with nonrestorable crown
bull Highly viscous sluggish hemorrhage from canal orifice which is uncontrollable
bull Medical contradictions like heart disease immuno compromised patient
bull Swelling or fistula
bull External or internal resorption
bull Pathological mobility
bull Calcification of pulp
Classification of pulpotomy
4
Formocresol Pulpotomy
Iby BUCKLEY in 1904
Sweet (1930) Formulated multi visit technique
Doyle (1962) Advocated 2 sitting procedure (complete devitalization)
Spedding (1965) Gave 5 minute protocol (partial devitali- zation)
Venham (1967) Proposed 15 seconds procedure
Current concept uses 4 minutes of application time
Composition of formocresol Buckleyrsquos Formula
bull Cresol ndash 35 percent
bull Glycerol ndash 15 percent
bull Formaldehyde ndash 19 percent
bull Water ndash 31 percent
Mechanism of Action
It prevents tissue autolysis by bonding to the proteins Bonding is of peptide groups of side chain amino acids and is a reversible process accomplished without
changing the basic structure of protein molecules
Histological Changes
bull Demonstrated by Mass and Zilbermann11 in 1933 and also by Massler and Mansokhani in 1959
bull Immediately the pulp becomes fibrous and acidophillic
bull Seven to fourteen days Three zones appear
a broad eosinophilic zone of fixation
b broad pale-staining zone of atrophy with poorcellular definition
c broad zone of inflammation extending apically into normal pulp tissue
bull One yearndash Progressive apical movement of these zones with only acidophillic zone left at the end of 1 year
Modified Formocresol Pulpotomy
Used by TRASK(1972)
The technique is identical to that described for primary teeth except that the formocresol pellet is
sealed permanently in the tooth
Two-visit Devitalization Pulpotomy
Indications
bull There is evidence of sluggish bleeding at the amputation site that is difficult to control
bull Pus in the chamber but none at the amputation site
bull There is thickening of the PDL
bull History of pain
Contraindications
bull Nonrestorable tooth
bull Tooth with necrotic pulp
5
Glutaraldehyde Pulpotomy
It was first suggested by S Gravenmade Introduced by Kopel in 1979
Mechanism of Action
bull Glutaraldehyde produces rapid surface fixation of the underlying pulpal tissue
bull A narrow zone of eosinophilic stained and compressed fixed tissue is found directly beneath the area of application which blends into vital normal appearing tissue apically
bull With time the glutaraldehyde fixed zone is replaced by macrophagic action with dense collagenous tissue thus the entire root canal tissue is vital
Cvekrsquos Pulpotomy
bull This is also called as calcium hydroxide pulpotomy or young permanent partial pulpotomy
bull This was proposed by Mejare and Cvek16 in 1978
bull Indicated in young permanent teeth where the pulp is exposed by mechanical or bacterial means and the
remaining radicular tissue is judged vital by clinical and radiographic criteria whereas the root closure is
notcomplete
MINERAL TRIOXIDE AGGREGATE (MTA) Torabinejad described the physical and chemical properties of MTA in 1995
It is ash colored powder made primarily of fine hydrophilic particles of
1 tricalcium aluminate
2 tricalcium silicate
3 silicate oxide
4 tricalcium oxide
5 bismuth dioxide
Hydration of the powder results in a colloidal gel composed of calcium oxide crystals in an amorphous
structure This gel solidifies into a hard structure in less than three hours
PROPERTIES OF MTA
It is biocompatible material and its sealing ability is better than that of amalgam or ZOE
Initial pH is 102 and set pH is 125
The setting time of cement is 4 hours
The compressive strength is 70 MPA which is comparable with that of IRM
Low cytotoxicity ndash It presents with minimal inflammation if extended beyond the apex
Mineral trioxide aggregate (MTA) has demonstrated the ability to induce hard-tissue formation in
pulpal tissues and it promotes rapid cell growth
APEXOGENESIS
It is defined as the treatment of a vital pulp by capping or pulpotomy in order to permit continued
growth of the root and closure of the open apex
Rationale
Maintenance of integrity of the radicular pulp tissue to allow for continued root growth
Indications
bull Indicated for traumatized or pulpally involved vital permanent tooth when root apex is incompletely formed
bull No history of spontaneous pain
bull No sensitivity on percussion
bull No hemorrhage
bull Normal radiographic appearance
Contraindications
bull Evidence that radicular pulp has undergone degenerative changes
bull Purulent drainage
bull History of prolonged pain bull Necrotic debris in canal
bull Periapical radiolucency
6
1
Gupta A Dhingra R Chaudhari P Gupta A
Department of Paedodontics and Preventive Dentistry Faculty of Dental Sciences SGT University Gurgaon Haryana India
Journal of Indian Society of Pedodontics and Preventive Dentistry
Volume 35 I Issue 3 I July-September 2017
A COMPARISION OF VARIOUS MINIMALLY
INVASIVE TECHNIQUES FOR THE REMOVAL
OF DENTAL FLUOROSIS STAINS IN
CHILDREN
DR MITAKSHARA NIRWAN
CONTENTS
bull Introduction
bull Aims
bull Materials and Methods
bull Results
bull Discussion
bull Conclusion
bull Critical analysis
bull References
INTRODUCTION
bull Dental fluorosis is a developmental disturbance of dental enamel caused by
successive exposure to high concentrations of fluoride during tooth
development
bull Various methods of therapy are advocated for the treatment of fluorosis -
stained teeth which range from invasive ceramic veneer bonding restorations
to abrasive chemical treatments
bull The combination of dental bleaching techniques and microabrasion appears
as an excellent conservative solution to reestablish health in fluorosis
affected teeth
AIMS
bull The aim of the study was to evaluate and compare the effectiveness of
minimally invasive techniques for the removal of dental fluorosis
stains in children in vivo
MATERIALS AND METHODS
Patients visiting the department of Pedodontics and Preventive dentistry
Faculty of Dental Sciences SGT University Gurgaon
bull Sample size 90 patients
bull Age group 10 -17 years
bull Caries cracks or periodontal
disease on anterior teeth
bull Abscess draining sinus
cellulitis
bull Non vital teeth
hypersensitive exposed
crevices
bull Orthodontic appliance
bull Past history of bleaching
bull At least two permanent
maxillary anterior teeth
bull TSIF of score 4
bull Free of systemic diseases
Inclusion criteria Exclusion criteria
2
Groups
Group A In office bleaching with 35 hydrogen peroxide( Pola Office
Bleaching kit) activated by light emitting diode (LED) bleaching unit
(35 HP)
Group B Enamel microabrasion (EM) (PREMA Enamel Microabrasion
System) followed by in-office bleaching with 44 carbamide peroxide
gel (EM)
Group C In-office bleaching with 5 sodium hypochlorite (5
NaOCl)
A baseline colour evaluation was done by taking digital photograph of
the maxillary anterior teeth
RESULTS
Group 1
Colour stability
Group 2 Group 3
Tooth sensitivity
Tooth sensitivity values were taken before the treatment
which was compared to immediate postoperative and follow
up visits It was checked using an electric pulp tester
maximum
moderate
least
immediately
group 2
group 1
group 3
1 month
group 2
group 1
group 3
3 month
group 2
group 1
group 3
Patient satisfaction score
Satisfaction was assessed on visual analog scale
Range 1 to 5
Groups percentage of patients
who were satisfied with
the treatment
Number of patients
who reported slight
reappearance of colour
Group 1
90
7
Group 2
83
8
Group 3
73
7
3
Number of Appointments
Groups One sitting Two sittings Three
sittings
Group 1
25
4
1
group 2
26
3
1
Group 3
30
0
0
DISCUSSION
bull Hydrogen peroxide is capable of penetrating the tooth osmosis and through porosities and cracks subsequently acting directly on the pigmented molecules
bull Gurgan et al investigated 3 different light systems and found out that diode laser system with gave best tooth whitening and least tooth sensitivity
bull In the EM group the surface reflects and refracts light from the surface in such way that mild imperfections in underlying enamel are camouflaged While the highly polished surface of enamel enhances the aesthetic appearance
bull Train et al and Loguercio et al also had the similar results in their studies with EM mild fluorosis showed best results moderate showed moderate results while it had little effect on severe fluorosis
bull NaOCl was only effective on mild stains while moderate and severe
stains could only be lightened to quite an extent but could not be
completely removed
bull When NaOCl comes in contact with hypomineralized and discoloured
enamel it degrades and removes the chromogenic organic material
located on the enamel surface
CONCLUSION
bull It was concluded that esthetic appearance of teeth mild fluorosis can
be achieved by bleaching and microabrasion But in cases of
moderate fluorosis a combination of any of theses modalities can be
used
bull As no special maintenance precautions are required these maybe be
considered as an interesting alternative to conventional operative
treatment
bull Focuses on only TSIF of 4
bull Electric pulp testing is not the
right method to check for
sensitivity
bull Tooth Sensitivity changes
from person to person
bull Food habits can cause
staining of the teeth
bull Minimally invasive
bull Cheaper to veneers
bull Minimal loss of tooth structure
bull 4 parameters checked for the success of treatment
bull Inclusion of specific score of fluorosis for comparing the results
bull Maximum 3 appointments needed
CRITICAL ANALYSIS
Pros Cons
REFERENCES
bull Gurgan S Cakir FY Yazici E Different light-activated in officebleaching
systems Lasers Med Sci 201025817-22
bull Train TE McWhorter AG Seale NSWilson CF Guo IY Examination of
esthetic improvement and surface alteration following microabrasion in
fluorotic human incisors in vivoPediatr dent 199618353-62
bull Loguercio AD Correia LD Zago C Tagliari D Neumann E Gomes OM et al
Clinical effectiveness of two microabrasion materials materials for the
removal of enamel flurosis stains Oper Dent 200732531-8
4
3
CLASSIFICATION OF LOCAL ANESTHETIC
SUBSTANCES ACCORDING TO
BIOLOGICAL SITE AND MODE OF ACTION
CLASS A
Agents acting at receptor site on external surface of nerve membrane
Chemical substance Biotoxins (eg tetrodotoxin and saxitoxin)
CLASS B
Agents acting on receptor sites on internal surface of nerve membrane
Chemical substance Quaternary ammonium analogues of lidocaine
scorpion venom 13
CLASS C Agents acting by receptor independent of
physiochemical mechanism
Chemical substance Benzocaine
CLASS D Agents acting by combination of receptors and
receptor independent mechanisms
Chemical substance most clinically useful anesthetic agents
(eg lidocaine mepivacaine prilocaine)
14
BASED ON THE SOURCE
NATUAL
SYNTHETIC
OTHERS
BASED ON MODE OF APPLICATION
bull INJECTABLE
bull TOPICAL
BASED ON DURATION OF ACTION
bull ULTRA SHORT
bull SHORT
bull MEDIEM
bull LONG
BASED ON ONSET OF ACTION SHORT
INTERMEDIATE
LONG
15
DISSOCIATION OF LOCAL
ANESTHETICS
Local anesthetics are available as salts (usually
hydrochlorides) for clinical use
The salts both water soluble and stable is dissolved in
either sterile water or saline
In this solution it exists simultaneously as unchanged
molecule (RN) also called base and positively charged
molecules (RNH+) called cations
RNH+ ==== RN+ H
+
16
The relative concentration of each ionic form in the solution varies
in the pH of the solution or surrounding tissue
In the presence of high concentration of hydrogen ion (low pH) the
equilibrium shifts to left and most of the anesthetic solution exists
in cationic form
RNH+ gt RN
+ + H
+
As hydrogen ion concentration decreases (higher pH) the
equilibrium shifts towards the free base form
RNH+ lt RN + H
+
17
The relative proportion of ionic form also depends on pKa or DISSOCIATION CONSTANT of the specific local anesthetic
The pKa is a measure of molecules affinity for H+
ions
When the pH of the solution has the same value as pKa of the local anesthetic exactly half the drug will exists in the RNH
+ form and
exactly half in RN form
The percentage of drug existing in either form can be determined by Henderson Hasselbalch equation
Log baseacid = pH - pKa
18
4
MECHANISM OF ACTION OF LOCAL
ANESTHETICS
The following sequence is proposed mechanism of action of LA
Displacement of calcium ions from the sodium channel receptor site
Binding of local anesthetic molecule to this receptor site
Blockade of sodium channel
19
Decrease in sodium conductance
Depression of rate of electrical depolarization
Failure to achieve the threshold potential level
Lack of development of propagated action potential
Conduction blockadehellip
20
21
Na + Na +
22
LOCAL ANESTHETIC AGENT
COMERCIALLY PREPARED LOCAL ANESTHESIA
CONSISTS OF
Local anesthetic agent (xylocaine lignocaine 2)
Vasoconstrictor (adrenaline 1 80000)
Reducing agent (sodium metabisulphite)
Preservative (methylparabencapryl
hydrocuprienotoxin)
Fungicide (thymol)
Vehicle (distillde waterNaCl)
LOCAL ANESTHETIC AGENT
The local anesthetics used in dentistry are divided
into two groups
ESTER GROUP
AMIDE GROUP
23 24
ESTER GROUP It is composed of the following
An aromatic lipophilic group
An intermediate chain containing
an ester linkage
A hydrophilic secondary or tertiary
amino group
AMIDE GROUP It is composed of the following
An aromatic lipophilic group
An intermediate chain containing
amide linkage
A hydrophilic secondary or tertiary
amino group
5
25
CLASSIFICATION OF LOCAL ANESTHETICS
ESTERS
Esters of benzoic acid
Butacaine
Cocaine
Benzocaine
Hexylcaine
Piperocaine
Tetracaine
Esters of Para-amino
benzoic acid
Chloroprocain
Procaine
Propoxycaine
26
AMIDES Articaine
Bupivacaine
Dibucaine
Etidocaine
Lidocaine
Mepivacaine
Prilocaine
Ropivacaine
QUINOLINE
Centbucridine
PHARMACOKINETICS OF LOCAL
ANESTHETICS UPTAKE
When injected into soft tissue most local anesthetics produce
dilation of vascular bed
Cocaine is the only local anesthetic that produces
vasoconstriction initially it produces vasodilation which is
followed by prolonged vasoconstriction
Vasodilation is due to increase in the rate of absorption of the
local anesthetic into the blood thus decreasing the duration of
pain control while increasing the anesthetic blood level and
potential for over dose 27
AMIDE LOCAL ANESTHETICS
The metabolism of amide local anesthetics is more
complicated then esters The primary site of
biotransformation of amide drugs is liver
Entire metabolic process occurs in the liver for lidocaine
articaine etidocaine and bupivacaine
Prilocaine undergoes more rapid biotransformation then the
other amides
28
REFERENCES
Handbook of local anesthesia ndash Stanley F Malamed ndash 6th
edition
Essentials of Local Anesthetic Pharmacology Daniel E
Becker Anesth Prog 2006 Fall 53(3) 98ndash109
WIKIPEDIEA
29
THANK YOU
30
1
Pharmacological Methods of Behavior
Management
DR MITAKSHARA NIRWAN
DEFINITIONS
bull Conscious Sedation ndash A minimally depressed level of consciousness that retains
the patients ability to independently and continuously maintain an airway and respond appropriately to physical stimulation or verbal command
(American Dental Association House Of Delegates 2000)
bull Deep Sedation ndash An induced state of depressed consciousness
accompanied by partial loss of protective reflexes including the inability to continuously maintain an airway independently and or to respond purposefully to physical stimulation or verbal command
bull General Anesthesia (G A) ndash An induced state of unconsciousness or complete loss of
protective reflexes including the inability to continually maintain an airway independently and respond purposefully to physical stimulation or verbal command
Conscious sedation
ADVANTAGES
Conscious
Protective reflexes active amp intact
Stable vital signs
Operating dentist may perform sedation
Minimum amount of equipment required
Prolong detainment in recovery room not required
Risk of complication very low
Excellent choice for poor ndash risk pt in dental office
Cost effective
General anesthesia
ADVANTAGES Not absolutely
essential May be the only
method Not necessary (no
pain reaction) Amnesia always
present
Conscious sedation
DISADVANTAGES
Pt cooperation is essential
Extremely difficult or mentally handicapped pt cannot always be managed
Use of local anesthesia is a must
Amnesia may or may not be present
General anesthesia DISADVANTAGES
Pt unconscious
Protective reflexes are depressed
Depressed
Advanced training required Dentist must not act also as anesthetist
Special equipment necessary
Detainment in recovery area necessary
High IOP amp postoperative complications
Not indicated in dental office
More expensive
Fundamental Concepts
bull Techniques that utilize drugs to induce co-operative yet conscious state in an otherwise uncooperative child ndash CONSCIOUS SEDATION
2
GOALS
1 To facilitate the provision of quality care
2 To minimize the extremes of disruptive behavior
3 To promote a positive psychologic response to treatment
4 To promote patient welfare amp safety
5 To return the patient to physiologic state
OBJECTIVES
1 The pt mood must be altered
2 The pt must remain conscious at all times
3 The pt must be cooperative
4 All protective reflexes must remain intact and active
5 Vital signs must remain stable and with in normal limits
6 The ptrsquos pain threshold should be elevated
7 Amnesia may be present
Indications
1 Preschool children
2 Lack of Psychological Emotional maturity
3 Lack of Cognitive Physical Medical disability
4 Fearful amp anxious pts
5 Pt who require extensive amp complicated dental care amp would require or benefit from prolonged visits
6 Acute pain
7 Traumatic injuries
Operating Facilities amp Equipment
A positive pressure O2 delivery system capable of administering gt than 90 O2 at 10L min flow for 60 min (650L ldquoErdquo cylinder)
OR
Self inflating bag valve mask device (15L min)
A functional suction apparatus with appropriate suction catheters
Monitoring equipment - PO BPC PC or Capno
Inhalation sedation unit
100 O2 amp never less than 25
A fail safe mechanism that is checked and calibrated annually
Must have appropriate scavenging system
Emergency drugs
Techniques of sedation
Routes for drug administration
bull Oral
bull Rectal
bull Inhalational
bull Transmucosal
ndash Sublingual
ndash Intranasal
bull Parenteral
ndash IM
ndash sub mucosal
ndash IV
3
Oral Sedation
Advantages
1 Almost universally accepted and the easiest method
2 Decreased incidence and severity of adverse reaction
3 Low cost
Disadvantages
1 Absorption is variable
2 Prolonged latent period(30 min)
3 Reversal of any unwanted effect is also difficult
4 Inability to readily lighten or deepen the level of sedation
5 Prolonged duration of action
Rectal Sedation
Advantages 1 Incidence and intensity of
drug related side effects is minimized
2 Drug absorption occurs from the large intestine directly into the circulation
3 The lack of a needle syringe or other equipment
4 The ease of administration
5 The low cost
Disadvantages
1 Inconvenience to the administrator amp pt
2 The variable absorption of drugs from the large intestine
3 The slow onset of action amp the relatively long duration of action
4 Inability to titrate the drug dosage
5 The inability to reverse the action of the drug the prolonged recovery
Intranasal sedation
Advantages
Rapid onset (10 ndash 15 min)
Simple amp relatively painless
Less pt cooperation is required
Absorbed directly into the C V S
Intranasal sedation
Disadvantages
1 Dependence on nasal mucous membrane
2 Shorter duration of action(40-60min)
3 Multiple dosage may be necessary
Drugs
Midazolam ndash 02mgkg
Sufentanil ndash 15 ndash 3 mcgkg
Ketamine ndash 3-6mg kg
Sublingual sedation
Advantages
1 Pt acceptance
2 Rapid onset
3 High bioavailability
Drugs
Oral Transmucosal Fentanyl Citrate (OTFC)
Intramuscular Sedation
Advantages
1 More rapid onset of action
2 Absorbed directly into the C V system
3 More reliable absorption of drug
4 Pt cooperation is not as essential
Disadvantages
1 Time factor ndash its 15 min latent period
2 Pt may not be willing to accept the injection
3 The prolonged duration of action(2-4 hrs more)
4 Possibility of injury to the tissues at the site of injection caused by either the drug or the needle
4
Sites of I M administration
1 Gluteal area
2 Vastus lateralis
3 Mid ndash deltoid area
Drugs
Diazepam
Midazolam
Hydroxyzine
Inhalation Sedation
Advantages
1 The onset of action is more rapid
2 Peak clinical level is achieved rapidly(3-5min) - permit titration
3 Administrator has complete control over the actions of the drug - safety feature
4 No significant over dosage
5 Flexible duration of action
6 Recovery time is rapid amp most complete
7 No injection is required
8 With N2O- O2 it is safe with very few side effects
Disadvantages
1 The initial cost of the equipment is high 2 The continuing cost of the gases is high 3 The equipment occupies considerable space 4 N2O is not a potent agent 5 A degree of cooperation is required from the pt 6 Chronic exposure to N2O is deleterious to the health of
dental personnel
Contraindications
1 Nasal obstruction 2 Cyanosis at rest 3 Poor cooperation 4 1st trimester of pregnancy 5 Fear of masks
I V Sedation
Advantages
1 The onset of action is the most rapid 2 The dosage may be titrated 3 Suitable level of sedation can be provided 4 The recovery period is shorter 5 Side effects are extremely uncommon 6 Control of salivary secretions is possible 7 The gag reflex is diminished 8 Effectively diminishes motor disturbances 9 Provides immediate access to CVS in emergency
Disadvantages
1 Venipuncture is necessary
2 Complication may rise at the site of the venipuncture
3 Monitoring must be more intensive
4 Recovery is not complete at the end of the procedure
5 Reversal of sedation is difficult
5
N2O-O2 (Relative Analgesia)
colorless sweet smelling gas
Pharmacokinetics
Absorption through pulmonary epithelium
It is approx 15 times as soluble as is nitrogen It replaces nitrogen in blood
It is carried in solution in plasma of the blood
It is not metabolized by the body
Elimination ndash majorndash lungs minor --- skin
perspiration urine and intestinal gas
Pharmacodynamics
Dose related
10 ndash 25 Lightheaded
Changes in visual amp auditory sensation
Tingling of hands amp feet
Suffusing warmth
Remote from the immediate environment
Reduced anxiety
25-50 max analgesic properties and aberration of vision hearing and proprioception mild drowsiness euphoria amnesia and increased sleepiness and dreams
35 conc will achieve maximum analgesia
bull CNS
ndash Cerebrum-primarily affected
ndash Safe but weak anesthetic agent
bull RESPIRATORY SYSTEM
ndash Increased Tidal and minute volumes
bull CARDIOVASCULAR SYSTEM
ndash 2 studies ndash decreased cardiac output
bull FETAL SYSTEMS
ndash Miscarriage in humans
bull OTHER SYSTEMS
ndash Depression of spinal reflexes increase muscle tone indicates stage of delirium
ndash Muscle rigidity-narcotics + nitrous oxide
ndash Nausea and vomitting - GIT
ndash HEMATOPOIESIS ----- prolonged exposure
Adverse reactions and toxicity
EMOTIONAL REACTIONS
DREAMS HALLUCINATIONS
No acute toxicity
Chronic toxicity ndash bone marrow
depression
PROCEDURE
Diffusion Hypoxia
Sevoflurane
A fluorinated derivative of isopropyl ether ndash synthesized in 1970
Potent anaesthetic agent with rapid uptake amp speedy recovery
Day-case surgery
Problem
Attaching vaporiser to any of the currently available machine
BENZODIAZEPINES
Diazepam 1961 lipid soluble
Uses-alcoholism epilepsy labor tetanus and cerebral palsy
- sedation and amnesia
- varieties of neurosis amp anxiety states
Pharmacokinetics
Orally Rectal IMIV or SC
Well absorbed through GIT
Excretion in urine
6
bull Pharmacodynamics
ndash Depress the brain stem reticular system and the limbic system thalamus and hypothalamus
ndash It is a centrally acting muscle relaxant Has anti-convulsant properties
Adverse reaction amp toxicity
ndash Confusion nausea headache increased appetite decreased salivation and jaundice Thrombophlebitis
ndash Rebound phenomenon
ndash Toxicity drowsiness confusion sleep and coma
Dosage Oral or Rectal ndash 02-05mgkg
Maximum single dose 10mg
IV- 025mgkg
Supplied Tablets 2 5 10 mg
Suspension ndash 5mg
Midazolam Water soluble ndash non-irritant
Oral IM IV
Metabolism- liver
Onset IV 3 -5mins
oral 20 ndash 30mins
Oral administration anxious patients requiring relatively short dental procedure
No rebound phenomenon
Better anxiolysis amp amnesia (retrograde amnesia)
Adverse effects Respiratory depression
dose dependant apnea
Dosage Oral ndash 025 to 1mgkg to maximum single dose 20mg
IM ndash 01 to 015mgkg to a maximum of 10mg
IV ndash slow IV
Supplied Syrup ndash 2mgml
Injectable ndash 1mgml amp 5mgml vials
Flumazenil specific benzodiazepines antagonist
selectively inhibits CNS effects
IV administration amp not recommended below 18yrs of age
02mg over 15 seconds after 45seconds 02mg then after 60seconds to maximum of 1mg
Sedative-Hypnotics
Barbiturates First truly effective drugs for the management of anxiety Generalized CNS depressants Produce dose dependent effects
Sedation ---- sleep ---- GA ---- coma
Suppress the CNS and result in sedation and amnesia Advantages
Rapid onset and short duration Disadvantages
no analgesic effect and possible hypotension Must be used with caution in trauma patients because they may cause
apnea and hypoventilation
DOSE Pentobarbital Sodium 100mg Secobarbital Sodium 100 to 200mg Children 30 to 100mg
bull Chloral Hydrates (Mickey Finn Knock out drops ) First synthesized in 1832 first member of the hypnotic group of drugs
Widely used as conscious sedation agent
Properties
Unpleasant taste
Nausea vomiting
Quite irritating to skin and to mucous membranes
GI irritation
Dosages Individualized for each patient 25 ndash 50mgkg
maximum of 1g
Supplied oral capsule ndash 500mg
oral solution ndash 250 amp 500mg5ml
Rectal suppositories ndash 324 amp 648mg
Narcotics
Do produce sedation amp euphoria greater in children
LA is required but dose should be decreased
Meperidine Synthetic opiate agonist
Very water soluble
Orally SC IM or IV
Peak effect by oral 1 hr amp lasts upto 4 hrs
Adverse reactions
-Seizures
-Extreme caution in hepatic or renal diseases or history of seizures
7
Dosage Oral SC or IM ndash 1to 22mgkg not to exceed 100 mg
Supplied Oral Tablets ndash 50 amp 100mg
Oral Syrup ndash 50mgml
Parental solution ndash 25 50 75 amp 100mgml
Fentanyl
Synthetic opiate narcotic analgesic
Very potent 01mg = 10mg Morophine75mg Meperidine
Pharmacokinetics
IV IM SM
Metabolized in liver Excreted in urine
Fentanyl Onset ndash 7 to 15mins
Duration ndash 1 to 2 hrs
Pharmacodynamics
Respiratory depression RR but returns to normal rapidly Tidal volume amp response to co2 depressed for extended period
Apnea
Less emetic than meperidine
NOT RECOMMENDED IN CHILDREN BELOW 2yrs
Dosage 0002 to 0004mgkg
Supplied 005mgml in 2 amp 5ml ampoules
Reversal drug Naloxone
Semisynthetic opiate antagonist
No agonist activity
Onset 2 to 5mins SC or IM amp 1 to 2mins IV
Reversal 45mins
Pt should be kept under continual surveillance
Adverse reaction nausea vomiting sweating hypotension hypertension ventricular tachycardia fibrillation
Dosage IV SC IM 001mgkg then 01mgkg every 2- 3mins maximum 2mg
Supplied 002 004 1mg solutions
Antihistamines
Hydroxyzine
Oral or IM
Effect ndash 15 ndash 30mins
Half-life ndash 3 hrs
Uses
To relieve anxiety
Used as an anti-histamine
Used to control nausea and vomiting including that associated with motion sickness and pregnancy
Adverse reaction dry mouth drowsiness hypersentivity
Dosage Oral ndash 1 to 2mgkg
IM ndash 11mgkg
Promethazine Oral or IM Onset 15 to 60mins Duration 4 to 6 hrs Uses
To prevent and treat nausea and vomiting associated with motion pregnancy or surgery
Produces sedation and reduce swelling pain and trismus
Lower seizure threshold Adverse reaction dry mouth blurred vision thickening of bronchial secretions Dosage OralIM ndash 05-11mgkg
maximum 25 mg
Diphenhydramine
Oral IM IV
Onset -1hr
Duration ndash 4 to 6 hr
Metabolized in liver
Adverse reaction disturbed coordination thickening of bronchial secretions
Dosage Oral IM IV ndash 1 to 15mgkg
maximum 50mg
Tranquilizers
Major tranquilizer antipsychotic produce calmness control symptoms of psychoses cause reversible extra pyramidal symptoms and do not tend to cause habituation
Minor tranquilizer antianxiety agents also cause calmness do not cause extrapyramidal symptoms Used in conditions like nervous tension and mild depression
8
Classification
Antipsychotics
Phenothiazine derivatives
Chlorpromazine promazine
Butryophenones
Haloperidol
Rauwolfia alkaloids
Reserpine
Antianxiety drugs
Propyl alcohol derivatives
Meprobamate
Benzodiazepine derivatives
Diazepam
Miscellaneous compounds
Hydroxyzine
Meprobamate
White crystalline powder slightly bitter in taste
Only administered orally
Peak blood concentration ----1 to 3hrs
10 ---------excreted unchanged Rest --- excreted as a oxidized derivative or as a glucoronide
Uses
To relieve day time anxiety
Induce sleep in insomniacs
To reduce anxiety associated with dental treatment
Anti-convulsant ndash petit mal epilepsy
Adverse reaction leucopenia acute non-thrombocytopenic purpura ecchymoses eosinophilia edema adenopathy
Dosage Childrengt 6yrs 100 to 200mg
Not recommended for children under 6yrs
Monitoring during sedation
1 Pulse
2 Blood pressure
3 ECG
4 Respiration
5 Temperature
Pulse
Manual Electronic
bull Radial Brachial
bull Facial labial
Blood pressure
ndash Stethoscope amp sphygmomanometer
ndash Automatic devices
ndash Direct cannulation of an artery ndash very accurate
Electrocardiograph
Heart rate rhythm myocardial function
9
Respiration
ndash Monitoring respiratory rate
ndash Observing the rise amp fall of the chest wall
ndash Observing the color of mucous membrane
ndash Observing the inflation amp deflation of the reservoir bag
Devices for monitoring respiration
1 The Precordial pretracheal stethoscope
2 The esophageal stethoscope
ndash Respiratory rate
ndash Heart rate
ndash Any abnormal sounds
Pulse Oximeter
ndash Oxygen saturation
ndash Heart rate
ndash Oxisensor site
ndash Fingers
ndash Toe
ndash Ear lobe
Mechanism
Oxygenated Hb ndash red light
Deoxygenated Hb- infrared light
Tissue pressure from arterial pulse (plethysmography)
Advantages
ndash Safe amp noninvasive
ndash Simple to use
ndash Information is rapidly available for clinical decision
ndash Indirectly indicates respiratory adequacy
Disadvantages
ndash Finger probes can get dislodged
ndash Emitted light source may cause burning
ndash Non reusable probes are expensive
ndash Does not directly determine airway patency
Capnography
1 The presence absence of air flow
2 Indicates depth amp adequacy of respiration
3 Continues analysis of the co2 content of the respired air ndash indicates respiratory adequacy
Temperature
ndash Disposable nondisposable thermometer
ndash Esophageal rectal temp probe
10
Discharge criteria
Cardiovascular function is satisfactory amp stable
Airway patency is uncompromised amp satisfactory
Pt is easily arousable amp protective reflexes intact
State of hydration is adequate
Pt can talk if applicable
Pt can sit unaided if applicable
Pt can ambulate with minimal assistance if applicable
Presedation level of responsiveness achieved
Responsible individual is available
1
PULP THERAPY OF VITAL TEETH
DR MITAKSHARA NIRWAN
Contents
Indirect pulp capping
Direct pulp capping
Medications amp materials used in pulp capping
Pulpotomy
MTA
Apexogenesis
INDIRECT PULP CAPPING
Pieter Van Forest - first to speak about root canal therapy
Glove designed instruments that could prepare a canal to a certain size and taper(1910)
Indirect pulp capping is defined as a procedure where in small amount of carious dentin is retained in
deep areas of cavity to avoid exposure of pulp followed by placement of a suitable medicament and
restorative material that seals off the carious dentin and encourages pulp recovery (Ingle)
A procedure in which only the gross caries is removed from the lesion and the cavity is sealed for a
time with a biocompatible material (McDonald)
Objective of indirect pulp capping
These were given by Eidelman in 1965
bull Arresting the carious process
bull Promoting dentin sclerosis
bull Stimulating formation of tertiary dentin
bull Remineralization of carious dentin
Layers of Carious Dentin Indications of Indirect Pulp Capping
History
Mild pain associated with eating
Negative history of spontaneous extreme pain
Clinical Examination
Deep carious lesion which are close tobut not involving the pulp in vital primary or young
permanent teeth
No mobility
Nominal pulp inflammationdefinite layer of affected dentin after removal of infected dentin
Radiographic examination
Normal lamina dura amp PDL space
No radiolucency around the apices
2
Contraindications of Indirect Pulp Capping
History
Sharp penetrating pulpalgia
Prolonged spontaneous pain especially at night
Clinical examination
Mobility of tooth
Discoloration of tooth
Negative reaction of electric pulp testing
Radiographic examination
Definite pulp exposure
Break in the lamina dura
Radiolucency around the apices
Widened PDL space
Treatment procedure
Sequelae of Indirect Pulp Capping Three distinct types of new dentin formation take place
1 Cellular fibrillar dentinmdashfirst 2 months
2 Globular dentinmdash3 months
3 Tubular dentin (uniform mineralized dentin)
bull 15th of reparative dentin formation begins in less than 30 days
bull After 3 months 01 mm is formed
DIRECT PULP CAPPING Defined by Kopel (1992) as the placement of a medicament or non medicated material on a pulp that
has been exposed in course of excavating the last portions of deep dentinal caries or as a result of
trauma
Objective
To create new dentin in the area of the exposure and subsequent healing of the pulp
Rationale
achieve a biologic closure of the exposure site by deposition of hard tissue barrier (dentin bridge)
between pulp tissue and capping material thus walling off the
INDICATIONS
Small mechanical exposure
Easily controlled haemorrhage
Bright red haemorrhage
True pinpoint exposure
CONTRAINDICATIONS
Severe toothache at night
Spontaneous pain
Tooth mobility
Radiographic appearance of pulp periradicular de- generation
Excess of hemorrhage at the time of exposure Serous exudate from the exposure
Externalinternal root resorption
Swellingfistula
Histological Changes after Pulp Capping
These were illustrated be Glass and Zander in 1949
After 24 hours Necrotic zone adjacent to calcium
hydroxide paste is separated from healthy pulp
tissue by a deep staining basophilic layer
After 7 days Increase in cellular and fibroblastic
activity
After 14 days Partly calcified fibrous tissue lined by
odontoblastic cells is seen below the calcium
proteinate zone disappearance of necrotic zone
After 28 days Zone of new dentin
3
Medications and Materials Used for Pulp Capping Calcium hydroxide
Corticosteroids amp antibiotics
Inert materials
Collagen fibers
4-META adhesive
Direct bonding
Isobutyl cyanoacrylate
Denatured albumin
Mineral trioxide aggregate
Laser
Bone morphogenic protein
PULPOTOMY
Finn (1995) defined it as the complete removal of the coronal portion of the dental pulp
followed by placement of a suitable dressing or medicament that will promote healing and
preserve vitality of the tooth
American Academy of Pediatric Dentistry (1998) defined pulpotomy as the amputation of
affected infected coronal portion of the dental pulp preserving the vitality and function of the
remaining part of radicular pulp
Objectives
bull Removal of inflamed and infected coronal pulp at the site of exposure thus preserving the vitality of the
radicular pulp and allowing it to heal
bull Maintain the tooth in the dental arch
Rationale
bull Radicular pulp is healthy and capable of healing after surgical amputation of the infected coronal pulp
bull Preserves vitality of the radicular pulp
bull Maintains tooth in a physiologic condition
Indications of Pulpotomy bull Mechanical pulp exposure in primary teeth
bull Teeth showing a large carious lesion but free of radicular pulpitis
bull History of only spontaneous pain
bull Hemorrhage from exposure sites bright red and can be controlled
bull Absence of abscess or fistula
bull No interradicular bone loss
bull No interradicular radiolucency
Contraindications of Pulpotomy bull Persistent toothache
bull Tenderness on percussion
bull Root resorption more than 13rd of root length
bull Large carious lesion with nonrestorable crown
bull Highly viscous sluggish hemorrhage from canal orifice which is uncontrollable
bull Medical contradictions like heart disease immuno compromised patient
bull Swelling or fistula
bull External or internal resorption
bull Pathological mobility
bull Calcification of pulp
Classification of pulpotomy
4
Formocresol Pulpotomy
Iby BUCKLEY in 1904
Sweet (1930) Formulated multi visit technique
Doyle (1962) Advocated 2 sitting procedure (complete devitalization)
Spedding (1965) Gave 5 minute protocol (partial devitali- zation)
Venham (1967) Proposed 15 seconds procedure
Current concept uses 4 minutes of application time
Composition of formocresol Buckleyrsquos Formula
bull Cresol ndash 35 percent
bull Glycerol ndash 15 percent
bull Formaldehyde ndash 19 percent
bull Water ndash 31 percent
Mechanism of Action
It prevents tissue autolysis by bonding to the proteins Bonding is of peptide groups of side chain amino acids and is a reversible process accomplished without
changing the basic structure of protein molecules
Histological Changes
bull Demonstrated by Mass and Zilbermann11 in 1933 and also by Massler and Mansokhani in 1959
bull Immediately the pulp becomes fibrous and acidophillic
bull Seven to fourteen days Three zones appear
a broad eosinophilic zone of fixation
b broad pale-staining zone of atrophy with poorcellular definition
c broad zone of inflammation extending apically into normal pulp tissue
bull One yearndash Progressive apical movement of these zones with only acidophillic zone left at the end of 1 year
Modified Formocresol Pulpotomy
Used by TRASK(1972)
The technique is identical to that described for primary teeth except that the formocresol pellet is
sealed permanently in the tooth
Two-visit Devitalization Pulpotomy
Indications
bull There is evidence of sluggish bleeding at the amputation site that is difficult to control
bull Pus in the chamber but none at the amputation site
bull There is thickening of the PDL
bull History of pain
Contraindications
bull Nonrestorable tooth
bull Tooth with necrotic pulp
5
Glutaraldehyde Pulpotomy
It was first suggested by S Gravenmade Introduced by Kopel in 1979
Mechanism of Action
bull Glutaraldehyde produces rapid surface fixation of the underlying pulpal tissue
bull A narrow zone of eosinophilic stained and compressed fixed tissue is found directly beneath the area of application which blends into vital normal appearing tissue apically
bull With time the glutaraldehyde fixed zone is replaced by macrophagic action with dense collagenous tissue thus the entire root canal tissue is vital
Cvekrsquos Pulpotomy
bull This is also called as calcium hydroxide pulpotomy or young permanent partial pulpotomy
bull This was proposed by Mejare and Cvek16 in 1978
bull Indicated in young permanent teeth where the pulp is exposed by mechanical or bacterial means and the
remaining radicular tissue is judged vital by clinical and radiographic criteria whereas the root closure is
notcomplete
MINERAL TRIOXIDE AGGREGATE (MTA) Torabinejad described the physical and chemical properties of MTA in 1995
It is ash colored powder made primarily of fine hydrophilic particles of
1 tricalcium aluminate
2 tricalcium silicate
3 silicate oxide
4 tricalcium oxide
5 bismuth dioxide
Hydration of the powder results in a colloidal gel composed of calcium oxide crystals in an amorphous
structure This gel solidifies into a hard structure in less than three hours
PROPERTIES OF MTA
It is biocompatible material and its sealing ability is better than that of amalgam or ZOE
Initial pH is 102 and set pH is 125
The setting time of cement is 4 hours
The compressive strength is 70 MPA which is comparable with that of IRM
Low cytotoxicity ndash It presents with minimal inflammation if extended beyond the apex
Mineral trioxide aggregate (MTA) has demonstrated the ability to induce hard-tissue formation in
pulpal tissues and it promotes rapid cell growth
APEXOGENESIS
It is defined as the treatment of a vital pulp by capping or pulpotomy in order to permit continued
growth of the root and closure of the open apex
Rationale
Maintenance of integrity of the radicular pulp tissue to allow for continued root growth
Indications
bull Indicated for traumatized or pulpally involved vital permanent tooth when root apex is incompletely formed
bull No history of spontaneous pain
bull No sensitivity on percussion
bull No hemorrhage
bull Normal radiographic appearance
Contraindications
bull Evidence that radicular pulp has undergone degenerative changes
bull Purulent drainage
bull History of prolonged pain bull Necrotic debris in canal
bull Periapical radiolucency
6
1
Gupta A Dhingra R Chaudhari P Gupta A
Department of Paedodontics and Preventive Dentistry Faculty of Dental Sciences SGT University Gurgaon Haryana India
Journal of Indian Society of Pedodontics and Preventive Dentistry
Volume 35 I Issue 3 I July-September 2017
A COMPARISION OF VARIOUS MINIMALLY
INVASIVE TECHNIQUES FOR THE REMOVAL
OF DENTAL FLUOROSIS STAINS IN
CHILDREN
DR MITAKSHARA NIRWAN
CONTENTS
bull Introduction
bull Aims
bull Materials and Methods
bull Results
bull Discussion
bull Conclusion
bull Critical analysis
bull References
INTRODUCTION
bull Dental fluorosis is a developmental disturbance of dental enamel caused by
successive exposure to high concentrations of fluoride during tooth
development
bull Various methods of therapy are advocated for the treatment of fluorosis -
stained teeth which range from invasive ceramic veneer bonding restorations
to abrasive chemical treatments
bull The combination of dental bleaching techniques and microabrasion appears
as an excellent conservative solution to reestablish health in fluorosis
affected teeth
AIMS
bull The aim of the study was to evaluate and compare the effectiveness of
minimally invasive techniques for the removal of dental fluorosis
stains in children in vivo
MATERIALS AND METHODS
Patients visiting the department of Pedodontics and Preventive dentistry
Faculty of Dental Sciences SGT University Gurgaon
bull Sample size 90 patients
bull Age group 10 -17 years
bull Caries cracks or periodontal
disease on anterior teeth
bull Abscess draining sinus
cellulitis
bull Non vital teeth
hypersensitive exposed
crevices
bull Orthodontic appliance
bull Past history of bleaching
bull At least two permanent
maxillary anterior teeth
bull TSIF of score 4
bull Free of systemic diseases
Inclusion criteria Exclusion criteria
2
Groups
Group A In office bleaching with 35 hydrogen peroxide( Pola Office
Bleaching kit) activated by light emitting diode (LED) bleaching unit
(35 HP)
Group B Enamel microabrasion (EM) (PREMA Enamel Microabrasion
System) followed by in-office bleaching with 44 carbamide peroxide
gel (EM)
Group C In-office bleaching with 5 sodium hypochlorite (5
NaOCl)
A baseline colour evaluation was done by taking digital photograph of
the maxillary anterior teeth
RESULTS
Group 1
Colour stability
Group 2 Group 3
Tooth sensitivity
Tooth sensitivity values were taken before the treatment
which was compared to immediate postoperative and follow
up visits It was checked using an electric pulp tester
maximum
moderate
least
immediately
group 2
group 1
group 3
1 month
group 2
group 1
group 3
3 month
group 2
group 1
group 3
Patient satisfaction score
Satisfaction was assessed on visual analog scale
Range 1 to 5
Groups percentage of patients
who were satisfied with
the treatment
Number of patients
who reported slight
reappearance of colour
Group 1
90
7
Group 2
83
8
Group 3
73
7
3
Number of Appointments
Groups One sitting Two sittings Three
sittings
Group 1
25
4
1
group 2
26
3
1
Group 3
30
0
0
DISCUSSION
bull Hydrogen peroxide is capable of penetrating the tooth osmosis and through porosities and cracks subsequently acting directly on the pigmented molecules
bull Gurgan et al investigated 3 different light systems and found out that diode laser system with gave best tooth whitening and least tooth sensitivity
bull In the EM group the surface reflects and refracts light from the surface in such way that mild imperfections in underlying enamel are camouflaged While the highly polished surface of enamel enhances the aesthetic appearance
bull Train et al and Loguercio et al also had the similar results in their studies with EM mild fluorosis showed best results moderate showed moderate results while it had little effect on severe fluorosis
bull NaOCl was only effective on mild stains while moderate and severe
stains could only be lightened to quite an extent but could not be
completely removed
bull When NaOCl comes in contact with hypomineralized and discoloured
enamel it degrades and removes the chromogenic organic material
located on the enamel surface
CONCLUSION
bull It was concluded that esthetic appearance of teeth mild fluorosis can
be achieved by bleaching and microabrasion But in cases of
moderate fluorosis a combination of any of theses modalities can be
used
bull As no special maintenance precautions are required these maybe be
considered as an interesting alternative to conventional operative
treatment
bull Focuses on only TSIF of 4
bull Electric pulp testing is not the
right method to check for
sensitivity
bull Tooth Sensitivity changes
from person to person
bull Food habits can cause
staining of the teeth
bull Minimally invasive
bull Cheaper to veneers
bull Minimal loss of tooth structure
bull 4 parameters checked for the success of treatment
bull Inclusion of specific score of fluorosis for comparing the results
bull Maximum 3 appointments needed
CRITICAL ANALYSIS
Pros Cons
REFERENCES
bull Gurgan S Cakir FY Yazici E Different light-activated in officebleaching
systems Lasers Med Sci 201025817-22
bull Train TE McWhorter AG Seale NSWilson CF Guo IY Examination of
esthetic improvement and surface alteration following microabrasion in
fluorotic human incisors in vivoPediatr dent 199618353-62
bull Loguercio AD Correia LD Zago C Tagliari D Neumann E Gomes OM et al
Clinical effectiveness of two microabrasion materials materials for the
removal of enamel flurosis stains Oper Dent 200732531-8
4
4
MECHANISM OF ACTION OF LOCAL
ANESTHETICS
The following sequence is proposed mechanism of action of LA
Displacement of calcium ions from the sodium channel receptor site
Binding of local anesthetic molecule to this receptor site
Blockade of sodium channel
19
Decrease in sodium conductance
Depression of rate of electrical depolarization
Failure to achieve the threshold potential level
Lack of development of propagated action potential
Conduction blockadehellip
20
21
Na + Na +
22
LOCAL ANESTHETIC AGENT
COMERCIALLY PREPARED LOCAL ANESTHESIA
CONSISTS OF
Local anesthetic agent (xylocaine lignocaine 2)
Vasoconstrictor (adrenaline 1 80000)
Reducing agent (sodium metabisulphite)
Preservative (methylparabencapryl
hydrocuprienotoxin)
Fungicide (thymol)
Vehicle (distillde waterNaCl)
LOCAL ANESTHETIC AGENT
The local anesthetics used in dentistry are divided
into two groups
ESTER GROUP
AMIDE GROUP
23 24
ESTER GROUP It is composed of the following
An aromatic lipophilic group
An intermediate chain containing
an ester linkage
A hydrophilic secondary or tertiary
amino group
AMIDE GROUP It is composed of the following
An aromatic lipophilic group
An intermediate chain containing
amide linkage
A hydrophilic secondary or tertiary
amino group
5
25
CLASSIFICATION OF LOCAL ANESTHETICS
ESTERS
Esters of benzoic acid
Butacaine
Cocaine
Benzocaine
Hexylcaine
Piperocaine
Tetracaine
Esters of Para-amino
benzoic acid
Chloroprocain
Procaine
Propoxycaine
26
AMIDES Articaine
Bupivacaine
Dibucaine
Etidocaine
Lidocaine
Mepivacaine
Prilocaine
Ropivacaine
QUINOLINE
Centbucridine
PHARMACOKINETICS OF LOCAL
ANESTHETICS UPTAKE
When injected into soft tissue most local anesthetics produce
dilation of vascular bed
Cocaine is the only local anesthetic that produces
vasoconstriction initially it produces vasodilation which is
followed by prolonged vasoconstriction
Vasodilation is due to increase in the rate of absorption of the
local anesthetic into the blood thus decreasing the duration of
pain control while increasing the anesthetic blood level and
potential for over dose 27
AMIDE LOCAL ANESTHETICS
The metabolism of amide local anesthetics is more
complicated then esters The primary site of
biotransformation of amide drugs is liver
Entire metabolic process occurs in the liver for lidocaine
articaine etidocaine and bupivacaine
Prilocaine undergoes more rapid biotransformation then the
other amides
28
REFERENCES
Handbook of local anesthesia ndash Stanley F Malamed ndash 6th
edition
Essentials of Local Anesthetic Pharmacology Daniel E
Becker Anesth Prog 2006 Fall 53(3) 98ndash109
WIKIPEDIEA
29
THANK YOU
30
1
Pharmacological Methods of Behavior
Management
DR MITAKSHARA NIRWAN
DEFINITIONS
bull Conscious Sedation ndash A minimally depressed level of consciousness that retains
the patients ability to independently and continuously maintain an airway and respond appropriately to physical stimulation or verbal command
(American Dental Association House Of Delegates 2000)
bull Deep Sedation ndash An induced state of depressed consciousness
accompanied by partial loss of protective reflexes including the inability to continuously maintain an airway independently and or to respond purposefully to physical stimulation or verbal command
bull General Anesthesia (G A) ndash An induced state of unconsciousness or complete loss of
protective reflexes including the inability to continually maintain an airway independently and respond purposefully to physical stimulation or verbal command
Conscious sedation
ADVANTAGES
Conscious
Protective reflexes active amp intact
Stable vital signs
Operating dentist may perform sedation
Minimum amount of equipment required
Prolong detainment in recovery room not required
Risk of complication very low
Excellent choice for poor ndash risk pt in dental office
Cost effective
General anesthesia
ADVANTAGES Not absolutely
essential May be the only
method Not necessary (no
pain reaction) Amnesia always
present
Conscious sedation
DISADVANTAGES
Pt cooperation is essential
Extremely difficult or mentally handicapped pt cannot always be managed
Use of local anesthesia is a must
Amnesia may or may not be present
General anesthesia DISADVANTAGES
Pt unconscious
Protective reflexes are depressed
Depressed
Advanced training required Dentist must not act also as anesthetist
Special equipment necessary
Detainment in recovery area necessary
High IOP amp postoperative complications
Not indicated in dental office
More expensive
Fundamental Concepts
bull Techniques that utilize drugs to induce co-operative yet conscious state in an otherwise uncooperative child ndash CONSCIOUS SEDATION
2
GOALS
1 To facilitate the provision of quality care
2 To minimize the extremes of disruptive behavior
3 To promote a positive psychologic response to treatment
4 To promote patient welfare amp safety
5 To return the patient to physiologic state
OBJECTIVES
1 The pt mood must be altered
2 The pt must remain conscious at all times
3 The pt must be cooperative
4 All protective reflexes must remain intact and active
5 Vital signs must remain stable and with in normal limits
6 The ptrsquos pain threshold should be elevated
7 Amnesia may be present
Indications
1 Preschool children
2 Lack of Psychological Emotional maturity
3 Lack of Cognitive Physical Medical disability
4 Fearful amp anxious pts
5 Pt who require extensive amp complicated dental care amp would require or benefit from prolonged visits
6 Acute pain
7 Traumatic injuries
Operating Facilities amp Equipment
A positive pressure O2 delivery system capable of administering gt than 90 O2 at 10L min flow for 60 min (650L ldquoErdquo cylinder)
OR
Self inflating bag valve mask device (15L min)
A functional suction apparatus with appropriate suction catheters
Monitoring equipment - PO BPC PC or Capno
Inhalation sedation unit
100 O2 amp never less than 25
A fail safe mechanism that is checked and calibrated annually
Must have appropriate scavenging system
Emergency drugs
Techniques of sedation
Routes for drug administration
bull Oral
bull Rectal
bull Inhalational
bull Transmucosal
ndash Sublingual
ndash Intranasal
bull Parenteral
ndash IM
ndash sub mucosal
ndash IV
3
Oral Sedation
Advantages
1 Almost universally accepted and the easiest method
2 Decreased incidence and severity of adverse reaction
3 Low cost
Disadvantages
1 Absorption is variable
2 Prolonged latent period(30 min)
3 Reversal of any unwanted effect is also difficult
4 Inability to readily lighten or deepen the level of sedation
5 Prolonged duration of action
Rectal Sedation
Advantages 1 Incidence and intensity of
drug related side effects is minimized
2 Drug absorption occurs from the large intestine directly into the circulation
3 The lack of a needle syringe or other equipment
4 The ease of administration
5 The low cost
Disadvantages
1 Inconvenience to the administrator amp pt
2 The variable absorption of drugs from the large intestine
3 The slow onset of action amp the relatively long duration of action
4 Inability to titrate the drug dosage
5 The inability to reverse the action of the drug the prolonged recovery
Intranasal sedation
Advantages
Rapid onset (10 ndash 15 min)
Simple amp relatively painless
Less pt cooperation is required
Absorbed directly into the C V S
Intranasal sedation
Disadvantages
1 Dependence on nasal mucous membrane
2 Shorter duration of action(40-60min)
3 Multiple dosage may be necessary
Drugs
Midazolam ndash 02mgkg
Sufentanil ndash 15 ndash 3 mcgkg
Ketamine ndash 3-6mg kg
Sublingual sedation
Advantages
1 Pt acceptance
2 Rapid onset
3 High bioavailability
Drugs
Oral Transmucosal Fentanyl Citrate (OTFC)
Intramuscular Sedation
Advantages
1 More rapid onset of action
2 Absorbed directly into the C V system
3 More reliable absorption of drug
4 Pt cooperation is not as essential
Disadvantages
1 Time factor ndash its 15 min latent period
2 Pt may not be willing to accept the injection
3 The prolonged duration of action(2-4 hrs more)
4 Possibility of injury to the tissues at the site of injection caused by either the drug or the needle
4
Sites of I M administration
1 Gluteal area
2 Vastus lateralis
3 Mid ndash deltoid area
Drugs
Diazepam
Midazolam
Hydroxyzine
Inhalation Sedation
Advantages
1 The onset of action is more rapid
2 Peak clinical level is achieved rapidly(3-5min) - permit titration
3 Administrator has complete control over the actions of the drug - safety feature
4 No significant over dosage
5 Flexible duration of action
6 Recovery time is rapid amp most complete
7 No injection is required
8 With N2O- O2 it is safe with very few side effects
Disadvantages
1 The initial cost of the equipment is high 2 The continuing cost of the gases is high 3 The equipment occupies considerable space 4 N2O is not a potent agent 5 A degree of cooperation is required from the pt 6 Chronic exposure to N2O is deleterious to the health of
dental personnel
Contraindications
1 Nasal obstruction 2 Cyanosis at rest 3 Poor cooperation 4 1st trimester of pregnancy 5 Fear of masks
I V Sedation
Advantages
1 The onset of action is the most rapid 2 The dosage may be titrated 3 Suitable level of sedation can be provided 4 The recovery period is shorter 5 Side effects are extremely uncommon 6 Control of salivary secretions is possible 7 The gag reflex is diminished 8 Effectively diminishes motor disturbances 9 Provides immediate access to CVS in emergency
Disadvantages
1 Venipuncture is necessary
2 Complication may rise at the site of the venipuncture
3 Monitoring must be more intensive
4 Recovery is not complete at the end of the procedure
5 Reversal of sedation is difficult
5
N2O-O2 (Relative Analgesia)
colorless sweet smelling gas
Pharmacokinetics
Absorption through pulmonary epithelium
It is approx 15 times as soluble as is nitrogen It replaces nitrogen in blood
It is carried in solution in plasma of the blood
It is not metabolized by the body
Elimination ndash majorndash lungs minor --- skin
perspiration urine and intestinal gas
Pharmacodynamics
Dose related
10 ndash 25 Lightheaded
Changes in visual amp auditory sensation
Tingling of hands amp feet
Suffusing warmth
Remote from the immediate environment
Reduced anxiety
25-50 max analgesic properties and aberration of vision hearing and proprioception mild drowsiness euphoria amnesia and increased sleepiness and dreams
35 conc will achieve maximum analgesia
bull CNS
ndash Cerebrum-primarily affected
ndash Safe but weak anesthetic agent
bull RESPIRATORY SYSTEM
ndash Increased Tidal and minute volumes
bull CARDIOVASCULAR SYSTEM
ndash 2 studies ndash decreased cardiac output
bull FETAL SYSTEMS
ndash Miscarriage in humans
bull OTHER SYSTEMS
ndash Depression of spinal reflexes increase muscle tone indicates stage of delirium
ndash Muscle rigidity-narcotics + nitrous oxide
ndash Nausea and vomitting - GIT
ndash HEMATOPOIESIS ----- prolonged exposure
Adverse reactions and toxicity
EMOTIONAL REACTIONS
DREAMS HALLUCINATIONS
No acute toxicity
Chronic toxicity ndash bone marrow
depression
PROCEDURE
Diffusion Hypoxia
Sevoflurane
A fluorinated derivative of isopropyl ether ndash synthesized in 1970
Potent anaesthetic agent with rapid uptake amp speedy recovery
Day-case surgery
Problem
Attaching vaporiser to any of the currently available machine
BENZODIAZEPINES
Diazepam 1961 lipid soluble
Uses-alcoholism epilepsy labor tetanus and cerebral palsy
- sedation and amnesia
- varieties of neurosis amp anxiety states
Pharmacokinetics
Orally Rectal IMIV or SC
Well absorbed through GIT
Excretion in urine
6
bull Pharmacodynamics
ndash Depress the brain stem reticular system and the limbic system thalamus and hypothalamus
ndash It is a centrally acting muscle relaxant Has anti-convulsant properties
Adverse reaction amp toxicity
ndash Confusion nausea headache increased appetite decreased salivation and jaundice Thrombophlebitis
ndash Rebound phenomenon
ndash Toxicity drowsiness confusion sleep and coma
Dosage Oral or Rectal ndash 02-05mgkg
Maximum single dose 10mg
IV- 025mgkg
Supplied Tablets 2 5 10 mg
Suspension ndash 5mg
Midazolam Water soluble ndash non-irritant
Oral IM IV
Metabolism- liver
Onset IV 3 -5mins
oral 20 ndash 30mins
Oral administration anxious patients requiring relatively short dental procedure
No rebound phenomenon
Better anxiolysis amp amnesia (retrograde amnesia)
Adverse effects Respiratory depression
dose dependant apnea
Dosage Oral ndash 025 to 1mgkg to maximum single dose 20mg
IM ndash 01 to 015mgkg to a maximum of 10mg
IV ndash slow IV
Supplied Syrup ndash 2mgml
Injectable ndash 1mgml amp 5mgml vials
Flumazenil specific benzodiazepines antagonist
selectively inhibits CNS effects
IV administration amp not recommended below 18yrs of age
02mg over 15 seconds after 45seconds 02mg then after 60seconds to maximum of 1mg
Sedative-Hypnotics
Barbiturates First truly effective drugs for the management of anxiety Generalized CNS depressants Produce dose dependent effects
Sedation ---- sleep ---- GA ---- coma
Suppress the CNS and result in sedation and amnesia Advantages
Rapid onset and short duration Disadvantages
no analgesic effect and possible hypotension Must be used with caution in trauma patients because they may cause
apnea and hypoventilation
DOSE Pentobarbital Sodium 100mg Secobarbital Sodium 100 to 200mg Children 30 to 100mg
bull Chloral Hydrates (Mickey Finn Knock out drops ) First synthesized in 1832 first member of the hypnotic group of drugs
Widely used as conscious sedation agent
Properties
Unpleasant taste
Nausea vomiting
Quite irritating to skin and to mucous membranes
GI irritation
Dosages Individualized for each patient 25 ndash 50mgkg
maximum of 1g
Supplied oral capsule ndash 500mg
oral solution ndash 250 amp 500mg5ml
Rectal suppositories ndash 324 amp 648mg
Narcotics
Do produce sedation amp euphoria greater in children
LA is required but dose should be decreased
Meperidine Synthetic opiate agonist
Very water soluble
Orally SC IM or IV
Peak effect by oral 1 hr amp lasts upto 4 hrs
Adverse reactions
-Seizures
-Extreme caution in hepatic or renal diseases or history of seizures
7
Dosage Oral SC or IM ndash 1to 22mgkg not to exceed 100 mg
Supplied Oral Tablets ndash 50 amp 100mg
Oral Syrup ndash 50mgml
Parental solution ndash 25 50 75 amp 100mgml
Fentanyl
Synthetic opiate narcotic analgesic
Very potent 01mg = 10mg Morophine75mg Meperidine
Pharmacokinetics
IV IM SM
Metabolized in liver Excreted in urine
Fentanyl Onset ndash 7 to 15mins
Duration ndash 1 to 2 hrs
Pharmacodynamics
Respiratory depression RR but returns to normal rapidly Tidal volume amp response to co2 depressed for extended period
Apnea
Less emetic than meperidine
NOT RECOMMENDED IN CHILDREN BELOW 2yrs
Dosage 0002 to 0004mgkg
Supplied 005mgml in 2 amp 5ml ampoules
Reversal drug Naloxone
Semisynthetic opiate antagonist
No agonist activity
Onset 2 to 5mins SC or IM amp 1 to 2mins IV
Reversal 45mins
Pt should be kept under continual surveillance
Adverse reaction nausea vomiting sweating hypotension hypertension ventricular tachycardia fibrillation
Dosage IV SC IM 001mgkg then 01mgkg every 2- 3mins maximum 2mg
Supplied 002 004 1mg solutions
Antihistamines
Hydroxyzine
Oral or IM
Effect ndash 15 ndash 30mins
Half-life ndash 3 hrs
Uses
To relieve anxiety
Used as an anti-histamine
Used to control nausea and vomiting including that associated with motion sickness and pregnancy
Adverse reaction dry mouth drowsiness hypersentivity
Dosage Oral ndash 1 to 2mgkg
IM ndash 11mgkg
Promethazine Oral or IM Onset 15 to 60mins Duration 4 to 6 hrs Uses
To prevent and treat nausea and vomiting associated with motion pregnancy or surgery
Produces sedation and reduce swelling pain and trismus
Lower seizure threshold Adverse reaction dry mouth blurred vision thickening of bronchial secretions Dosage OralIM ndash 05-11mgkg
maximum 25 mg
Diphenhydramine
Oral IM IV
Onset -1hr
Duration ndash 4 to 6 hr
Metabolized in liver
Adverse reaction disturbed coordination thickening of bronchial secretions
Dosage Oral IM IV ndash 1 to 15mgkg
maximum 50mg
Tranquilizers
Major tranquilizer antipsychotic produce calmness control symptoms of psychoses cause reversible extra pyramidal symptoms and do not tend to cause habituation
Minor tranquilizer antianxiety agents also cause calmness do not cause extrapyramidal symptoms Used in conditions like nervous tension and mild depression
8
Classification
Antipsychotics
Phenothiazine derivatives
Chlorpromazine promazine
Butryophenones
Haloperidol
Rauwolfia alkaloids
Reserpine
Antianxiety drugs
Propyl alcohol derivatives
Meprobamate
Benzodiazepine derivatives
Diazepam
Miscellaneous compounds
Hydroxyzine
Meprobamate
White crystalline powder slightly bitter in taste
Only administered orally
Peak blood concentration ----1 to 3hrs
10 ---------excreted unchanged Rest --- excreted as a oxidized derivative or as a glucoronide
Uses
To relieve day time anxiety
Induce sleep in insomniacs
To reduce anxiety associated with dental treatment
Anti-convulsant ndash petit mal epilepsy
Adverse reaction leucopenia acute non-thrombocytopenic purpura ecchymoses eosinophilia edema adenopathy
Dosage Childrengt 6yrs 100 to 200mg
Not recommended for children under 6yrs
Monitoring during sedation
1 Pulse
2 Blood pressure
3 ECG
4 Respiration
5 Temperature
Pulse
Manual Electronic
bull Radial Brachial
bull Facial labial
Blood pressure
ndash Stethoscope amp sphygmomanometer
ndash Automatic devices
ndash Direct cannulation of an artery ndash very accurate
Electrocardiograph
Heart rate rhythm myocardial function
9
Respiration
ndash Monitoring respiratory rate
ndash Observing the rise amp fall of the chest wall
ndash Observing the color of mucous membrane
ndash Observing the inflation amp deflation of the reservoir bag
Devices for monitoring respiration
1 The Precordial pretracheal stethoscope
2 The esophageal stethoscope
ndash Respiratory rate
ndash Heart rate
ndash Any abnormal sounds
Pulse Oximeter
ndash Oxygen saturation
ndash Heart rate
ndash Oxisensor site
ndash Fingers
ndash Toe
ndash Ear lobe
Mechanism
Oxygenated Hb ndash red light
Deoxygenated Hb- infrared light
Tissue pressure from arterial pulse (plethysmography)
Advantages
ndash Safe amp noninvasive
ndash Simple to use
ndash Information is rapidly available for clinical decision
ndash Indirectly indicates respiratory adequacy
Disadvantages
ndash Finger probes can get dislodged
ndash Emitted light source may cause burning
ndash Non reusable probes are expensive
ndash Does not directly determine airway patency
Capnography
1 The presence absence of air flow
2 Indicates depth amp adequacy of respiration
3 Continues analysis of the co2 content of the respired air ndash indicates respiratory adequacy
Temperature
ndash Disposable nondisposable thermometer
ndash Esophageal rectal temp probe
10
Discharge criteria
Cardiovascular function is satisfactory amp stable
Airway patency is uncompromised amp satisfactory
Pt is easily arousable amp protective reflexes intact
State of hydration is adequate
Pt can talk if applicable
Pt can sit unaided if applicable
Pt can ambulate with minimal assistance if applicable
Presedation level of responsiveness achieved
Responsible individual is available
1
PULP THERAPY OF VITAL TEETH
DR MITAKSHARA NIRWAN
Contents
Indirect pulp capping
Direct pulp capping
Medications amp materials used in pulp capping
Pulpotomy
MTA
Apexogenesis
INDIRECT PULP CAPPING
Pieter Van Forest - first to speak about root canal therapy
Glove designed instruments that could prepare a canal to a certain size and taper(1910)
Indirect pulp capping is defined as a procedure where in small amount of carious dentin is retained in
deep areas of cavity to avoid exposure of pulp followed by placement of a suitable medicament and
restorative material that seals off the carious dentin and encourages pulp recovery (Ingle)
A procedure in which only the gross caries is removed from the lesion and the cavity is sealed for a
time with a biocompatible material (McDonald)
Objective of indirect pulp capping
These were given by Eidelman in 1965
bull Arresting the carious process
bull Promoting dentin sclerosis
bull Stimulating formation of tertiary dentin
bull Remineralization of carious dentin
Layers of Carious Dentin Indications of Indirect Pulp Capping
History
Mild pain associated with eating
Negative history of spontaneous extreme pain
Clinical Examination
Deep carious lesion which are close tobut not involving the pulp in vital primary or young
permanent teeth
No mobility
Nominal pulp inflammationdefinite layer of affected dentin after removal of infected dentin
Radiographic examination
Normal lamina dura amp PDL space
No radiolucency around the apices
2
Contraindications of Indirect Pulp Capping
History
Sharp penetrating pulpalgia
Prolonged spontaneous pain especially at night
Clinical examination
Mobility of tooth
Discoloration of tooth
Negative reaction of electric pulp testing
Radiographic examination
Definite pulp exposure
Break in the lamina dura
Radiolucency around the apices
Widened PDL space
Treatment procedure
Sequelae of Indirect Pulp Capping Three distinct types of new dentin formation take place
1 Cellular fibrillar dentinmdashfirst 2 months
2 Globular dentinmdash3 months
3 Tubular dentin (uniform mineralized dentin)
bull 15th of reparative dentin formation begins in less than 30 days
bull After 3 months 01 mm is formed
DIRECT PULP CAPPING Defined by Kopel (1992) as the placement of a medicament or non medicated material on a pulp that
has been exposed in course of excavating the last portions of deep dentinal caries or as a result of
trauma
Objective
To create new dentin in the area of the exposure and subsequent healing of the pulp
Rationale
achieve a biologic closure of the exposure site by deposition of hard tissue barrier (dentin bridge)
between pulp tissue and capping material thus walling off the
INDICATIONS
Small mechanical exposure
Easily controlled haemorrhage
Bright red haemorrhage
True pinpoint exposure
CONTRAINDICATIONS
Severe toothache at night
Spontaneous pain
Tooth mobility
Radiographic appearance of pulp periradicular de- generation
Excess of hemorrhage at the time of exposure Serous exudate from the exposure
Externalinternal root resorption
Swellingfistula
Histological Changes after Pulp Capping
These were illustrated be Glass and Zander in 1949
After 24 hours Necrotic zone adjacent to calcium
hydroxide paste is separated from healthy pulp
tissue by a deep staining basophilic layer
After 7 days Increase in cellular and fibroblastic
activity
After 14 days Partly calcified fibrous tissue lined by
odontoblastic cells is seen below the calcium
proteinate zone disappearance of necrotic zone
After 28 days Zone of new dentin
3
Medications and Materials Used for Pulp Capping Calcium hydroxide
Corticosteroids amp antibiotics
Inert materials
Collagen fibers
4-META adhesive
Direct bonding
Isobutyl cyanoacrylate
Denatured albumin
Mineral trioxide aggregate
Laser
Bone morphogenic protein
PULPOTOMY
Finn (1995) defined it as the complete removal of the coronal portion of the dental pulp
followed by placement of a suitable dressing or medicament that will promote healing and
preserve vitality of the tooth
American Academy of Pediatric Dentistry (1998) defined pulpotomy as the amputation of
affected infected coronal portion of the dental pulp preserving the vitality and function of the
remaining part of radicular pulp
Objectives
bull Removal of inflamed and infected coronal pulp at the site of exposure thus preserving the vitality of the
radicular pulp and allowing it to heal
bull Maintain the tooth in the dental arch
Rationale
bull Radicular pulp is healthy and capable of healing after surgical amputation of the infected coronal pulp
bull Preserves vitality of the radicular pulp
bull Maintains tooth in a physiologic condition
Indications of Pulpotomy bull Mechanical pulp exposure in primary teeth
bull Teeth showing a large carious lesion but free of radicular pulpitis
bull History of only spontaneous pain
bull Hemorrhage from exposure sites bright red and can be controlled
bull Absence of abscess or fistula
bull No interradicular bone loss
bull No interradicular radiolucency
Contraindications of Pulpotomy bull Persistent toothache
bull Tenderness on percussion
bull Root resorption more than 13rd of root length
bull Large carious lesion with nonrestorable crown
bull Highly viscous sluggish hemorrhage from canal orifice which is uncontrollable
bull Medical contradictions like heart disease immuno compromised patient
bull Swelling or fistula
bull External or internal resorption
bull Pathological mobility
bull Calcification of pulp
Classification of pulpotomy
4
Formocresol Pulpotomy
Iby BUCKLEY in 1904
Sweet (1930) Formulated multi visit technique
Doyle (1962) Advocated 2 sitting procedure (complete devitalization)
Spedding (1965) Gave 5 minute protocol (partial devitali- zation)
Venham (1967) Proposed 15 seconds procedure
Current concept uses 4 minutes of application time
Composition of formocresol Buckleyrsquos Formula
bull Cresol ndash 35 percent
bull Glycerol ndash 15 percent
bull Formaldehyde ndash 19 percent
bull Water ndash 31 percent
Mechanism of Action
It prevents tissue autolysis by bonding to the proteins Bonding is of peptide groups of side chain amino acids and is a reversible process accomplished without
changing the basic structure of protein molecules
Histological Changes
bull Demonstrated by Mass and Zilbermann11 in 1933 and also by Massler and Mansokhani in 1959
bull Immediately the pulp becomes fibrous and acidophillic
bull Seven to fourteen days Three zones appear
a broad eosinophilic zone of fixation
b broad pale-staining zone of atrophy with poorcellular definition
c broad zone of inflammation extending apically into normal pulp tissue
bull One yearndash Progressive apical movement of these zones with only acidophillic zone left at the end of 1 year
Modified Formocresol Pulpotomy
Used by TRASK(1972)
The technique is identical to that described for primary teeth except that the formocresol pellet is
sealed permanently in the tooth
Two-visit Devitalization Pulpotomy
Indications
bull There is evidence of sluggish bleeding at the amputation site that is difficult to control
bull Pus in the chamber but none at the amputation site
bull There is thickening of the PDL
bull History of pain
Contraindications
bull Nonrestorable tooth
bull Tooth with necrotic pulp
5
Glutaraldehyde Pulpotomy
It was first suggested by S Gravenmade Introduced by Kopel in 1979
Mechanism of Action
bull Glutaraldehyde produces rapid surface fixation of the underlying pulpal tissue
bull A narrow zone of eosinophilic stained and compressed fixed tissue is found directly beneath the area of application which blends into vital normal appearing tissue apically
bull With time the glutaraldehyde fixed zone is replaced by macrophagic action with dense collagenous tissue thus the entire root canal tissue is vital
Cvekrsquos Pulpotomy
bull This is also called as calcium hydroxide pulpotomy or young permanent partial pulpotomy
bull This was proposed by Mejare and Cvek16 in 1978
bull Indicated in young permanent teeth where the pulp is exposed by mechanical or bacterial means and the
remaining radicular tissue is judged vital by clinical and radiographic criteria whereas the root closure is
notcomplete
MINERAL TRIOXIDE AGGREGATE (MTA) Torabinejad described the physical and chemical properties of MTA in 1995
It is ash colored powder made primarily of fine hydrophilic particles of
1 tricalcium aluminate
2 tricalcium silicate
3 silicate oxide
4 tricalcium oxide
5 bismuth dioxide
Hydration of the powder results in a colloidal gel composed of calcium oxide crystals in an amorphous
structure This gel solidifies into a hard structure in less than three hours
PROPERTIES OF MTA
It is biocompatible material and its sealing ability is better than that of amalgam or ZOE
Initial pH is 102 and set pH is 125
The setting time of cement is 4 hours
The compressive strength is 70 MPA which is comparable with that of IRM
Low cytotoxicity ndash It presents with minimal inflammation if extended beyond the apex
Mineral trioxide aggregate (MTA) has demonstrated the ability to induce hard-tissue formation in
pulpal tissues and it promotes rapid cell growth
APEXOGENESIS
It is defined as the treatment of a vital pulp by capping or pulpotomy in order to permit continued
growth of the root and closure of the open apex
Rationale
Maintenance of integrity of the radicular pulp tissue to allow for continued root growth
Indications
bull Indicated for traumatized or pulpally involved vital permanent tooth when root apex is incompletely formed
bull No history of spontaneous pain
bull No sensitivity on percussion
bull No hemorrhage
bull Normal radiographic appearance
Contraindications
bull Evidence that radicular pulp has undergone degenerative changes
bull Purulent drainage
bull History of prolonged pain bull Necrotic debris in canal
bull Periapical radiolucency
6
1
Gupta A Dhingra R Chaudhari P Gupta A
Department of Paedodontics and Preventive Dentistry Faculty of Dental Sciences SGT University Gurgaon Haryana India
Journal of Indian Society of Pedodontics and Preventive Dentistry
Volume 35 I Issue 3 I July-September 2017
A COMPARISION OF VARIOUS MINIMALLY
INVASIVE TECHNIQUES FOR THE REMOVAL
OF DENTAL FLUOROSIS STAINS IN
CHILDREN
DR MITAKSHARA NIRWAN
CONTENTS
bull Introduction
bull Aims
bull Materials and Methods
bull Results
bull Discussion
bull Conclusion
bull Critical analysis
bull References
INTRODUCTION
bull Dental fluorosis is a developmental disturbance of dental enamel caused by
successive exposure to high concentrations of fluoride during tooth
development
bull Various methods of therapy are advocated for the treatment of fluorosis -
stained teeth which range from invasive ceramic veneer bonding restorations
to abrasive chemical treatments
bull The combination of dental bleaching techniques and microabrasion appears
as an excellent conservative solution to reestablish health in fluorosis
affected teeth
AIMS
bull The aim of the study was to evaluate and compare the effectiveness of
minimally invasive techniques for the removal of dental fluorosis
stains in children in vivo
MATERIALS AND METHODS
Patients visiting the department of Pedodontics and Preventive dentistry
Faculty of Dental Sciences SGT University Gurgaon
bull Sample size 90 patients
bull Age group 10 -17 years
bull Caries cracks or periodontal
disease on anterior teeth
bull Abscess draining sinus
cellulitis
bull Non vital teeth
hypersensitive exposed
crevices
bull Orthodontic appliance
bull Past history of bleaching
bull At least two permanent
maxillary anterior teeth
bull TSIF of score 4
bull Free of systemic diseases
Inclusion criteria Exclusion criteria
2
Groups
Group A In office bleaching with 35 hydrogen peroxide( Pola Office
Bleaching kit) activated by light emitting diode (LED) bleaching unit
(35 HP)
Group B Enamel microabrasion (EM) (PREMA Enamel Microabrasion
System) followed by in-office bleaching with 44 carbamide peroxide
gel (EM)
Group C In-office bleaching with 5 sodium hypochlorite (5
NaOCl)
A baseline colour evaluation was done by taking digital photograph of
the maxillary anterior teeth
RESULTS
Group 1
Colour stability
Group 2 Group 3
Tooth sensitivity
Tooth sensitivity values were taken before the treatment
which was compared to immediate postoperative and follow
up visits It was checked using an electric pulp tester
maximum
moderate
least
immediately
group 2
group 1
group 3
1 month
group 2
group 1
group 3
3 month
group 2
group 1
group 3
Patient satisfaction score
Satisfaction was assessed on visual analog scale
Range 1 to 5
Groups percentage of patients
who were satisfied with
the treatment
Number of patients
who reported slight
reappearance of colour
Group 1
90
7
Group 2
83
8
Group 3
73
7
3
Number of Appointments
Groups One sitting Two sittings Three
sittings
Group 1
25
4
1
group 2
26
3
1
Group 3
30
0
0
DISCUSSION
bull Hydrogen peroxide is capable of penetrating the tooth osmosis and through porosities and cracks subsequently acting directly on the pigmented molecules
bull Gurgan et al investigated 3 different light systems and found out that diode laser system with gave best tooth whitening and least tooth sensitivity
bull In the EM group the surface reflects and refracts light from the surface in such way that mild imperfections in underlying enamel are camouflaged While the highly polished surface of enamel enhances the aesthetic appearance
bull Train et al and Loguercio et al also had the similar results in their studies with EM mild fluorosis showed best results moderate showed moderate results while it had little effect on severe fluorosis
bull NaOCl was only effective on mild stains while moderate and severe
stains could only be lightened to quite an extent but could not be
completely removed
bull When NaOCl comes in contact with hypomineralized and discoloured
enamel it degrades and removes the chromogenic organic material
located on the enamel surface
CONCLUSION
bull It was concluded that esthetic appearance of teeth mild fluorosis can
be achieved by bleaching and microabrasion But in cases of
moderate fluorosis a combination of any of theses modalities can be
used
bull As no special maintenance precautions are required these maybe be
considered as an interesting alternative to conventional operative
treatment
bull Focuses on only TSIF of 4
bull Electric pulp testing is not the
right method to check for
sensitivity
bull Tooth Sensitivity changes
from person to person
bull Food habits can cause
staining of the teeth
bull Minimally invasive
bull Cheaper to veneers
bull Minimal loss of tooth structure
bull 4 parameters checked for the success of treatment
bull Inclusion of specific score of fluorosis for comparing the results
bull Maximum 3 appointments needed
CRITICAL ANALYSIS
Pros Cons
REFERENCES
bull Gurgan S Cakir FY Yazici E Different light-activated in officebleaching
systems Lasers Med Sci 201025817-22
bull Train TE McWhorter AG Seale NSWilson CF Guo IY Examination of
esthetic improvement and surface alteration following microabrasion in
fluorotic human incisors in vivoPediatr dent 199618353-62
bull Loguercio AD Correia LD Zago C Tagliari D Neumann E Gomes OM et al
Clinical effectiveness of two microabrasion materials materials for the
removal of enamel flurosis stains Oper Dent 200732531-8
4
5
25
CLASSIFICATION OF LOCAL ANESTHETICS
ESTERS
Esters of benzoic acid
Butacaine
Cocaine
Benzocaine
Hexylcaine
Piperocaine
Tetracaine
Esters of Para-amino
benzoic acid
Chloroprocain
Procaine
Propoxycaine
26
AMIDES Articaine
Bupivacaine
Dibucaine
Etidocaine
Lidocaine
Mepivacaine
Prilocaine
Ropivacaine
QUINOLINE
Centbucridine
PHARMACOKINETICS OF LOCAL
ANESTHETICS UPTAKE
When injected into soft tissue most local anesthetics produce
dilation of vascular bed
Cocaine is the only local anesthetic that produces
vasoconstriction initially it produces vasodilation which is
followed by prolonged vasoconstriction
Vasodilation is due to increase in the rate of absorption of the
local anesthetic into the blood thus decreasing the duration of
pain control while increasing the anesthetic blood level and
potential for over dose 27
AMIDE LOCAL ANESTHETICS
The metabolism of amide local anesthetics is more
complicated then esters The primary site of
biotransformation of amide drugs is liver
Entire metabolic process occurs in the liver for lidocaine
articaine etidocaine and bupivacaine
Prilocaine undergoes more rapid biotransformation then the
other amides
28
REFERENCES
Handbook of local anesthesia ndash Stanley F Malamed ndash 6th
edition
Essentials of Local Anesthetic Pharmacology Daniel E
Becker Anesth Prog 2006 Fall 53(3) 98ndash109
WIKIPEDIEA
29
THANK YOU
30
1
Pharmacological Methods of Behavior
Management
DR MITAKSHARA NIRWAN
DEFINITIONS
bull Conscious Sedation ndash A minimally depressed level of consciousness that retains
the patients ability to independently and continuously maintain an airway and respond appropriately to physical stimulation or verbal command
(American Dental Association House Of Delegates 2000)
bull Deep Sedation ndash An induced state of depressed consciousness
accompanied by partial loss of protective reflexes including the inability to continuously maintain an airway independently and or to respond purposefully to physical stimulation or verbal command
bull General Anesthesia (G A) ndash An induced state of unconsciousness or complete loss of
protective reflexes including the inability to continually maintain an airway independently and respond purposefully to physical stimulation or verbal command
Conscious sedation
ADVANTAGES
Conscious
Protective reflexes active amp intact
Stable vital signs
Operating dentist may perform sedation
Minimum amount of equipment required
Prolong detainment in recovery room not required
Risk of complication very low
Excellent choice for poor ndash risk pt in dental office
Cost effective
General anesthesia
ADVANTAGES Not absolutely
essential May be the only
method Not necessary (no
pain reaction) Amnesia always
present
Conscious sedation
DISADVANTAGES
Pt cooperation is essential
Extremely difficult or mentally handicapped pt cannot always be managed
Use of local anesthesia is a must
Amnesia may or may not be present
General anesthesia DISADVANTAGES
Pt unconscious
Protective reflexes are depressed
Depressed
Advanced training required Dentist must not act also as anesthetist
Special equipment necessary
Detainment in recovery area necessary
High IOP amp postoperative complications
Not indicated in dental office
More expensive
Fundamental Concepts
bull Techniques that utilize drugs to induce co-operative yet conscious state in an otherwise uncooperative child ndash CONSCIOUS SEDATION
2
GOALS
1 To facilitate the provision of quality care
2 To minimize the extremes of disruptive behavior
3 To promote a positive psychologic response to treatment
4 To promote patient welfare amp safety
5 To return the patient to physiologic state
OBJECTIVES
1 The pt mood must be altered
2 The pt must remain conscious at all times
3 The pt must be cooperative
4 All protective reflexes must remain intact and active
5 Vital signs must remain stable and with in normal limits
6 The ptrsquos pain threshold should be elevated
7 Amnesia may be present
Indications
1 Preschool children
2 Lack of Psychological Emotional maturity
3 Lack of Cognitive Physical Medical disability
4 Fearful amp anxious pts
5 Pt who require extensive amp complicated dental care amp would require or benefit from prolonged visits
6 Acute pain
7 Traumatic injuries
Operating Facilities amp Equipment
A positive pressure O2 delivery system capable of administering gt than 90 O2 at 10L min flow for 60 min (650L ldquoErdquo cylinder)
OR
Self inflating bag valve mask device (15L min)
A functional suction apparatus with appropriate suction catheters
Monitoring equipment - PO BPC PC or Capno
Inhalation sedation unit
100 O2 amp never less than 25
A fail safe mechanism that is checked and calibrated annually
Must have appropriate scavenging system
Emergency drugs
Techniques of sedation
Routes for drug administration
bull Oral
bull Rectal
bull Inhalational
bull Transmucosal
ndash Sublingual
ndash Intranasal
bull Parenteral
ndash IM
ndash sub mucosal
ndash IV
3
Oral Sedation
Advantages
1 Almost universally accepted and the easiest method
2 Decreased incidence and severity of adverse reaction
3 Low cost
Disadvantages
1 Absorption is variable
2 Prolonged latent period(30 min)
3 Reversal of any unwanted effect is also difficult
4 Inability to readily lighten or deepen the level of sedation
5 Prolonged duration of action
Rectal Sedation
Advantages 1 Incidence and intensity of
drug related side effects is minimized
2 Drug absorption occurs from the large intestine directly into the circulation
3 The lack of a needle syringe or other equipment
4 The ease of administration
5 The low cost
Disadvantages
1 Inconvenience to the administrator amp pt
2 The variable absorption of drugs from the large intestine
3 The slow onset of action amp the relatively long duration of action
4 Inability to titrate the drug dosage
5 The inability to reverse the action of the drug the prolonged recovery
Intranasal sedation
Advantages
Rapid onset (10 ndash 15 min)
Simple amp relatively painless
Less pt cooperation is required
Absorbed directly into the C V S
Intranasal sedation
Disadvantages
1 Dependence on nasal mucous membrane
2 Shorter duration of action(40-60min)
3 Multiple dosage may be necessary
Drugs
Midazolam ndash 02mgkg
Sufentanil ndash 15 ndash 3 mcgkg
Ketamine ndash 3-6mg kg
Sublingual sedation
Advantages
1 Pt acceptance
2 Rapid onset
3 High bioavailability
Drugs
Oral Transmucosal Fentanyl Citrate (OTFC)
Intramuscular Sedation
Advantages
1 More rapid onset of action
2 Absorbed directly into the C V system
3 More reliable absorption of drug
4 Pt cooperation is not as essential
Disadvantages
1 Time factor ndash its 15 min latent period
2 Pt may not be willing to accept the injection
3 The prolonged duration of action(2-4 hrs more)
4 Possibility of injury to the tissues at the site of injection caused by either the drug or the needle
4
Sites of I M administration
1 Gluteal area
2 Vastus lateralis
3 Mid ndash deltoid area
Drugs
Diazepam
Midazolam
Hydroxyzine
Inhalation Sedation
Advantages
1 The onset of action is more rapid
2 Peak clinical level is achieved rapidly(3-5min) - permit titration
3 Administrator has complete control over the actions of the drug - safety feature
4 No significant over dosage
5 Flexible duration of action
6 Recovery time is rapid amp most complete
7 No injection is required
8 With N2O- O2 it is safe with very few side effects
Disadvantages
1 The initial cost of the equipment is high 2 The continuing cost of the gases is high 3 The equipment occupies considerable space 4 N2O is not a potent agent 5 A degree of cooperation is required from the pt 6 Chronic exposure to N2O is deleterious to the health of
dental personnel
Contraindications
1 Nasal obstruction 2 Cyanosis at rest 3 Poor cooperation 4 1st trimester of pregnancy 5 Fear of masks
I V Sedation
Advantages
1 The onset of action is the most rapid 2 The dosage may be titrated 3 Suitable level of sedation can be provided 4 The recovery period is shorter 5 Side effects are extremely uncommon 6 Control of salivary secretions is possible 7 The gag reflex is diminished 8 Effectively diminishes motor disturbances 9 Provides immediate access to CVS in emergency
Disadvantages
1 Venipuncture is necessary
2 Complication may rise at the site of the venipuncture
3 Monitoring must be more intensive
4 Recovery is not complete at the end of the procedure
5 Reversal of sedation is difficult
5
N2O-O2 (Relative Analgesia)
colorless sweet smelling gas
Pharmacokinetics
Absorption through pulmonary epithelium
It is approx 15 times as soluble as is nitrogen It replaces nitrogen in blood
It is carried in solution in plasma of the blood
It is not metabolized by the body
Elimination ndash majorndash lungs minor --- skin
perspiration urine and intestinal gas
Pharmacodynamics
Dose related
10 ndash 25 Lightheaded
Changes in visual amp auditory sensation
Tingling of hands amp feet
Suffusing warmth
Remote from the immediate environment
Reduced anxiety
25-50 max analgesic properties and aberration of vision hearing and proprioception mild drowsiness euphoria amnesia and increased sleepiness and dreams
35 conc will achieve maximum analgesia
bull CNS
ndash Cerebrum-primarily affected
ndash Safe but weak anesthetic agent
bull RESPIRATORY SYSTEM
ndash Increased Tidal and minute volumes
bull CARDIOVASCULAR SYSTEM
ndash 2 studies ndash decreased cardiac output
bull FETAL SYSTEMS
ndash Miscarriage in humans
bull OTHER SYSTEMS
ndash Depression of spinal reflexes increase muscle tone indicates stage of delirium
ndash Muscle rigidity-narcotics + nitrous oxide
ndash Nausea and vomitting - GIT
ndash HEMATOPOIESIS ----- prolonged exposure
Adverse reactions and toxicity
EMOTIONAL REACTIONS
DREAMS HALLUCINATIONS
No acute toxicity
Chronic toxicity ndash bone marrow
depression
PROCEDURE
Diffusion Hypoxia
Sevoflurane
A fluorinated derivative of isopropyl ether ndash synthesized in 1970
Potent anaesthetic agent with rapid uptake amp speedy recovery
Day-case surgery
Problem
Attaching vaporiser to any of the currently available machine
BENZODIAZEPINES
Diazepam 1961 lipid soluble
Uses-alcoholism epilepsy labor tetanus and cerebral palsy
- sedation and amnesia
- varieties of neurosis amp anxiety states
Pharmacokinetics
Orally Rectal IMIV or SC
Well absorbed through GIT
Excretion in urine
6
bull Pharmacodynamics
ndash Depress the brain stem reticular system and the limbic system thalamus and hypothalamus
ndash It is a centrally acting muscle relaxant Has anti-convulsant properties
Adverse reaction amp toxicity
ndash Confusion nausea headache increased appetite decreased salivation and jaundice Thrombophlebitis
ndash Rebound phenomenon
ndash Toxicity drowsiness confusion sleep and coma
Dosage Oral or Rectal ndash 02-05mgkg
Maximum single dose 10mg
IV- 025mgkg
Supplied Tablets 2 5 10 mg
Suspension ndash 5mg
Midazolam Water soluble ndash non-irritant
Oral IM IV
Metabolism- liver
Onset IV 3 -5mins
oral 20 ndash 30mins
Oral administration anxious patients requiring relatively short dental procedure
No rebound phenomenon
Better anxiolysis amp amnesia (retrograde amnesia)
Adverse effects Respiratory depression
dose dependant apnea
Dosage Oral ndash 025 to 1mgkg to maximum single dose 20mg
IM ndash 01 to 015mgkg to a maximum of 10mg
IV ndash slow IV
Supplied Syrup ndash 2mgml
Injectable ndash 1mgml amp 5mgml vials
Flumazenil specific benzodiazepines antagonist
selectively inhibits CNS effects
IV administration amp not recommended below 18yrs of age
02mg over 15 seconds after 45seconds 02mg then after 60seconds to maximum of 1mg
Sedative-Hypnotics
Barbiturates First truly effective drugs for the management of anxiety Generalized CNS depressants Produce dose dependent effects
Sedation ---- sleep ---- GA ---- coma
Suppress the CNS and result in sedation and amnesia Advantages
Rapid onset and short duration Disadvantages
no analgesic effect and possible hypotension Must be used with caution in trauma patients because they may cause
apnea and hypoventilation
DOSE Pentobarbital Sodium 100mg Secobarbital Sodium 100 to 200mg Children 30 to 100mg
bull Chloral Hydrates (Mickey Finn Knock out drops ) First synthesized in 1832 first member of the hypnotic group of drugs
Widely used as conscious sedation agent
Properties
Unpleasant taste
Nausea vomiting
Quite irritating to skin and to mucous membranes
GI irritation
Dosages Individualized for each patient 25 ndash 50mgkg
maximum of 1g
Supplied oral capsule ndash 500mg
oral solution ndash 250 amp 500mg5ml
Rectal suppositories ndash 324 amp 648mg
Narcotics
Do produce sedation amp euphoria greater in children
LA is required but dose should be decreased
Meperidine Synthetic opiate agonist
Very water soluble
Orally SC IM or IV
Peak effect by oral 1 hr amp lasts upto 4 hrs
Adverse reactions
-Seizures
-Extreme caution in hepatic or renal diseases or history of seizures
7
Dosage Oral SC or IM ndash 1to 22mgkg not to exceed 100 mg
Supplied Oral Tablets ndash 50 amp 100mg
Oral Syrup ndash 50mgml
Parental solution ndash 25 50 75 amp 100mgml
Fentanyl
Synthetic opiate narcotic analgesic
Very potent 01mg = 10mg Morophine75mg Meperidine
Pharmacokinetics
IV IM SM
Metabolized in liver Excreted in urine
Fentanyl Onset ndash 7 to 15mins
Duration ndash 1 to 2 hrs
Pharmacodynamics
Respiratory depression RR but returns to normal rapidly Tidal volume amp response to co2 depressed for extended period
Apnea
Less emetic than meperidine
NOT RECOMMENDED IN CHILDREN BELOW 2yrs
Dosage 0002 to 0004mgkg
Supplied 005mgml in 2 amp 5ml ampoules
Reversal drug Naloxone
Semisynthetic opiate antagonist
No agonist activity
Onset 2 to 5mins SC or IM amp 1 to 2mins IV
Reversal 45mins
Pt should be kept under continual surveillance
Adverse reaction nausea vomiting sweating hypotension hypertension ventricular tachycardia fibrillation
Dosage IV SC IM 001mgkg then 01mgkg every 2- 3mins maximum 2mg
Supplied 002 004 1mg solutions
Antihistamines
Hydroxyzine
Oral or IM
Effect ndash 15 ndash 30mins
Half-life ndash 3 hrs
Uses
To relieve anxiety
Used as an anti-histamine
Used to control nausea and vomiting including that associated with motion sickness and pregnancy
Adverse reaction dry mouth drowsiness hypersentivity
Dosage Oral ndash 1 to 2mgkg
IM ndash 11mgkg
Promethazine Oral or IM Onset 15 to 60mins Duration 4 to 6 hrs Uses
To prevent and treat nausea and vomiting associated with motion pregnancy or surgery
Produces sedation and reduce swelling pain and trismus
Lower seizure threshold Adverse reaction dry mouth blurred vision thickening of bronchial secretions Dosage OralIM ndash 05-11mgkg
maximum 25 mg
Diphenhydramine
Oral IM IV
Onset -1hr
Duration ndash 4 to 6 hr
Metabolized in liver
Adverse reaction disturbed coordination thickening of bronchial secretions
Dosage Oral IM IV ndash 1 to 15mgkg
maximum 50mg
Tranquilizers
Major tranquilizer antipsychotic produce calmness control symptoms of psychoses cause reversible extra pyramidal symptoms and do not tend to cause habituation
Minor tranquilizer antianxiety agents also cause calmness do not cause extrapyramidal symptoms Used in conditions like nervous tension and mild depression
8
Classification
Antipsychotics
Phenothiazine derivatives
Chlorpromazine promazine
Butryophenones
Haloperidol
Rauwolfia alkaloids
Reserpine
Antianxiety drugs
Propyl alcohol derivatives
Meprobamate
Benzodiazepine derivatives
Diazepam
Miscellaneous compounds
Hydroxyzine
Meprobamate
White crystalline powder slightly bitter in taste
Only administered orally
Peak blood concentration ----1 to 3hrs
10 ---------excreted unchanged Rest --- excreted as a oxidized derivative or as a glucoronide
Uses
To relieve day time anxiety
Induce sleep in insomniacs
To reduce anxiety associated with dental treatment
Anti-convulsant ndash petit mal epilepsy
Adverse reaction leucopenia acute non-thrombocytopenic purpura ecchymoses eosinophilia edema adenopathy
Dosage Childrengt 6yrs 100 to 200mg
Not recommended for children under 6yrs
Monitoring during sedation
1 Pulse
2 Blood pressure
3 ECG
4 Respiration
5 Temperature
Pulse
Manual Electronic
bull Radial Brachial
bull Facial labial
Blood pressure
ndash Stethoscope amp sphygmomanometer
ndash Automatic devices
ndash Direct cannulation of an artery ndash very accurate
Electrocardiograph
Heart rate rhythm myocardial function
9
Respiration
ndash Monitoring respiratory rate
ndash Observing the rise amp fall of the chest wall
ndash Observing the color of mucous membrane
ndash Observing the inflation amp deflation of the reservoir bag
Devices for monitoring respiration
1 The Precordial pretracheal stethoscope
2 The esophageal stethoscope
ndash Respiratory rate
ndash Heart rate
ndash Any abnormal sounds
Pulse Oximeter
ndash Oxygen saturation
ndash Heart rate
ndash Oxisensor site
ndash Fingers
ndash Toe
ndash Ear lobe
Mechanism
Oxygenated Hb ndash red light
Deoxygenated Hb- infrared light
Tissue pressure from arterial pulse (plethysmography)
Advantages
ndash Safe amp noninvasive
ndash Simple to use
ndash Information is rapidly available for clinical decision
ndash Indirectly indicates respiratory adequacy
Disadvantages
ndash Finger probes can get dislodged
ndash Emitted light source may cause burning
ndash Non reusable probes are expensive
ndash Does not directly determine airway patency
Capnography
1 The presence absence of air flow
2 Indicates depth amp adequacy of respiration
3 Continues analysis of the co2 content of the respired air ndash indicates respiratory adequacy
Temperature
ndash Disposable nondisposable thermometer
ndash Esophageal rectal temp probe
10
Discharge criteria
Cardiovascular function is satisfactory amp stable
Airway patency is uncompromised amp satisfactory
Pt is easily arousable amp protective reflexes intact
State of hydration is adequate
Pt can talk if applicable
Pt can sit unaided if applicable
Pt can ambulate with minimal assistance if applicable
Presedation level of responsiveness achieved
Responsible individual is available
1
PULP THERAPY OF VITAL TEETH
DR MITAKSHARA NIRWAN
Contents
Indirect pulp capping
Direct pulp capping
Medications amp materials used in pulp capping
Pulpotomy
MTA
Apexogenesis
INDIRECT PULP CAPPING
Pieter Van Forest - first to speak about root canal therapy
Glove designed instruments that could prepare a canal to a certain size and taper(1910)
Indirect pulp capping is defined as a procedure where in small amount of carious dentin is retained in
deep areas of cavity to avoid exposure of pulp followed by placement of a suitable medicament and
restorative material that seals off the carious dentin and encourages pulp recovery (Ingle)
A procedure in which only the gross caries is removed from the lesion and the cavity is sealed for a
time with a biocompatible material (McDonald)
Objective of indirect pulp capping
These were given by Eidelman in 1965
bull Arresting the carious process
bull Promoting dentin sclerosis
bull Stimulating formation of tertiary dentin
bull Remineralization of carious dentin
Layers of Carious Dentin Indications of Indirect Pulp Capping
History
Mild pain associated with eating
Negative history of spontaneous extreme pain
Clinical Examination
Deep carious lesion which are close tobut not involving the pulp in vital primary or young
permanent teeth
No mobility
Nominal pulp inflammationdefinite layer of affected dentin after removal of infected dentin
Radiographic examination
Normal lamina dura amp PDL space
No radiolucency around the apices
2
Contraindications of Indirect Pulp Capping
History
Sharp penetrating pulpalgia
Prolonged spontaneous pain especially at night
Clinical examination
Mobility of tooth
Discoloration of tooth
Negative reaction of electric pulp testing
Radiographic examination
Definite pulp exposure
Break in the lamina dura
Radiolucency around the apices
Widened PDL space
Treatment procedure
Sequelae of Indirect Pulp Capping Three distinct types of new dentin formation take place
1 Cellular fibrillar dentinmdashfirst 2 months
2 Globular dentinmdash3 months
3 Tubular dentin (uniform mineralized dentin)
bull 15th of reparative dentin formation begins in less than 30 days
bull After 3 months 01 mm is formed
DIRECT PULP CAPPING Defined by Kopel (1992) as the placement of a medicament or non medicated material on a pulp that
has been exposed in course of excavating the last portions of deep dentinal caries or as a result of
trauma
Objective
To create new dentin in the area of the exposure and subsequent healing of the pulp
Rationale
achieve a biologic closure of the exposure site by deposition of hard tissue barrier (dentin bridge)
between pulp tissue and capping material thus walling off the
INDICATIONS
Small mechanical exposure
Easily controlled haemorrhage
Bright red haemorrhage
True pinpoint exposure
CONTRAINDICATIONS
Severe toothache at night
Spontaneous pain
Tooth mobility
Radiographic appearance of pulp periradicular de- generation
Excess of hemorrhage at the time of exposure Serous exudate from the exposure
Externalinternal root resorption
Swellingfistula
Histological Changes after Pulp Capping
These were illustrated be Glass and Zander in 1949
After 24 hours Necrotic zone adjacent to calcium
hydroxide paste is separated from healthy pulp
tissue by a deep staining basophilic layer
After 7 days Increase in cellular and fibroblastic
activity
After 14 days Partly calcified fibrous tissue lined by
odontoblastic cells is seen below the calcium
proteinate zone disappearance of necrotic zone
After 28 days Zone of new dentin
3
Medications and Materials Used for Pulp Capping Calcium hydroxide
Corticosteroids amp antibiotics
Inert materials
Collagen fibers
4-META adhesive
Direct bonding
Isobutyl cyanoacrylate
Denatured albumin
Mineral trioxide aggregate
Laser
Bone morphogenic protein
PULPOTOMY
Finn (1995) defined it as the complete removal of the coronal portion of the dental pulp
followed by placement of a suitable dressing or medicament that will promote healing and
preserve vitality of the tooth
American Academy of Pediatric Dentistry (1998) defined pulpotomy as the amputation of
affected infected coronal portion of the dental pulp preserving the vitality and function of the
remaining part of radicular pulp
Objectives
bull Removal of inflamed and infected coronal pulp at the site of exposure thus preserving the vitality of the
radicular pulp and allowing it to heal
bull Maintain the tooth in the dental arch
Rationale
bull Radicular pulp is healthy and capable of healing after surgical amputation of the infected coronal pulp
bull Preserves vitality of the radicular pulp
bull Maintains tooth in a physiologic condition
Indications of Pulpotomy bull Mechanical pulp exposure in primary teeth
bull Teeth showing a large carious lesion but free of radicular pulpitis
bull History of only spontaneous pain
bull Hemorrhage from exposure sites bright red and can be controlled
bull Absence of abscess or fistula
bull No interradicular bone loss
bull No interradicular radiolucency
Contraindications of Pulpotomy bull Persistent toothache
bull Tenderness on percussion
bull Root resorption more than 13rd of root length
bull Large carious lesion with nonrestorable crown
bull Highly viscous sluggish hemorrhage from canal orifice which is uncontrollable
bull Medical contradictions like heart disease immuno compromised patient
bull Swelling or fistula
bull External or internal resorption
bull Pathological mobility
bull Calcification of pulp
Classification of pulpotomy
4
Formocresol Pulpotomy
Iby BUCKLEY in 1904
Sweet (1930) Formulated multi visit technique
Doyle (1962) Advocated 2 sitting procedure (complete devitalization)
Spedding (1965) Gave 5 minute protocol (partial devitali- zation)
Venham (1967) Proposed 15 seconds procedure
Current concept uses 4 minutes of application time
Composition of formocresol Buckleyrsquos Formula
bull Cresol ndash 35 percent
bull Glycerol ndash 15 percent
bull Formaldehyde ndash 19 percent
bull Water ndash 31 percent
Mechanism of Action
It prevents tissue autolysis by bonding to the proteins Bonding is of peptide groups of side chain amino acids and is a reversible process accomplished without
changing the basic structure of protein molecules
Histological Changes
bull Demonstrated by Mass and Zilbermann11 in 1933 and also by Massler and Mansokhani in 1959
bull Immediately the pulp becomes fibrous and acidophillic
bull Seven to fourteen days Three zones appear
a broad eosinophilic zone of fixation
b broad pale-staining zone of atrophy with poorcellular definition
c broad zone of inflammation extending apically into normal pulp tissue
bull One yearndash Progressive apical movement of these zones with only acidophillic zone left at the end of 1 year
Modified Formocresol Pulpotomy
Used by TRASK(1972)
The technique is identical to that described for primary teeth except that the formocresol pellet is
sealed permanently in the tooth
Two-visit Devitalization Pulpotomy
Indications
bull There is evidence of sluggish bleeding at the amputation site that is difficult to control
bull Pus in the chamber but none at the amputation site
bull There is thickening of the PDL
bull History of pain
Contraindications
bull Nonrestorable tooth
bull Tooth with necrotic pulp
5
Glutaraldehyde Pulpotomy
It was first suggested by S Gravenmade Introduced by Kopel in 1979
Mechanism of Action
bull Glutaraldehyde produces rapid surface fixation of the underlying pulpal tissue
bull A narrow zone of eosinophilic stained and compressed fixed tissue is found directly beneath the area of application which blends into vital normal appearing tissue apically
bull With time the glutaraldehyde fixed zone is replaced by macrophagic action with dense collagenous tissue thus the entire root canal tissue is vital
Cvekrsquos Pulpotomy
bull This is also called as calcium hydroxide pulpotomy or young permanent partial pulpotomy
bull This was proposed by Mejare and Cvek16 in 1978
bull Indicated in young permanent teeth where the pulp is exposed by mechanical or bacterial means and the
remaining radicular tissue is judged vital by clinical and radiographic criteria whereas the root closure is
notcomplete
MINERAL TRIOXIDE AGGREGATE (MTA) Torabinejad described the physical and chemical properties of MTA in 1995
It is ash colored powder made primarily of fine hydrophilic particles of
1 tricalcium aluminate
2 tricalcium silicate
3 silicate oxide
4 tricalcium oxide
5 bismuth dioxide
Hydration of the powder results in a colloidal gel composed of calcium oxide crystals in an amorphous
structure This gel solidifies into a hard structure in less than three hours
PROPERTIES OF MTA
It is biocompatible material and its sealing ability is better than that of amalgam or ZOE
Initial pH is 102 and set pH is 125
The setting time of cement is 4 hours
The compressive strength is 70 MPA which is comparable with that of IRM
Low cytotoxicity ndash It presents with minimal inflammation if extended beyond the apex
Mineral trioxide aggregate (MTA) has demonstrated the ability to induce hard-tissue formation in
pulpal tissues and it promotes rapid cell growth
APEXOGENESIS
It is defined as the treatment of a vital pulp by capping or pulpotomy in order to permit continued
growth of the root and closure of the open apex
Rationale
Maintenance of integrity of the radicular pulp tissue to allow for continued root growth
Indications
bull Indicated for traumatized or pulpally involved vital permanent tooth when root apex is incompletely formed
bull No history of spontaneous pain
bull No sensitivity on percussion
bull No hemorrhage
bull Normal radiographic appearance
Contraindications
bull Evidence that radicular pulp has undergone degenerative changes
bull Purulent drainage
bull History of prolonged pain bull Necrotic debris in canal
bull Periapical radiolucency
6
1
Gupta A Dhingra R Chaudhari P Gupta A
Department of Paedodontics and Preventive Dentistry Faculty of Dental Sciences SGT University Gurgaon Haryana India
Journal of Indian Society of Pedodontics and Preventive Dentistry
Volume 35 I Issue 3 I July-September 2017
A COMPARISION OF VARIOUS MINIMALLY
INVASIVE TECHNIQUES FOR THE REMOVAL
OF DENTAL FLUOROSIS STAINS IN
CHILDREN
DR MITAKSHARA NIRWAN
CONTENTS
bull Introduction
bull Aims
bull Materials and Methods
bull Results
bull Discussion
bull Conclusion
bull Critical analysis
bull References
INTRODUCTION
bull Dental fluorosis is a developmental disturbance of dental enamel caused by
successive exposure to high concentrations of fluoride during tooth
development
bull Various methods of therapy are advocated for the treatment of fluorosis -
stained teeth which range from invasive ceramic veneer bonding restorations
to abrasive chemical treatments
bull The combination of dental bleaching techniques and microabrasion appears
as an excellent conservative solution to reestablish health in fluorosis
affected teeth
AIMS
bull The aim of the study was to evaluate and compare the effectiveness of
minimally invasive techniques for the removal of dental fluorosis
stains in children in vivo
MATERIALS AND METHODS
Patients visiting the department of Pedodontics and Preventive dentistry
Faculty of Dental Sciences SGT University Gurgaon
bull Sample size 90 patients
bull Age group 10 -17 years
bull Caries cracks or periodontal
disease on anterior teeth
bull Abscess draining sinus
cellulitis
bull Non vital teeth
hypersensitive exposed
crevices
bull Orthodontic appliance
bull Past history of bleaching
bull At least two permanent
maxillary anterior teeth
bull TSIF of score 4
bull Free of systemic diseases
Inclusion criteria Exclusion criteria
2
Groups
Group A In office bleaching with 35 hydrogen peroxide( Pola Office
Bleaching kit) activated by light emitting diode (LED) bleaching unit
(35 HP)
Group B Enamel microabrasion (EM) (PREMA Enamel Microabrasion
System) followed by in-office bleaching with 44 carbamide peroxide
gel (EM)
Group C In-office bleaching with 5 sodium hypochlorite (5
NaOCl)
A baseline colour evaluation was done by taking digital photograph of
the maxillary anterior teeth
RESULTS
Group 1
Colour stability
Group 2 Group 3
Tooth sensitivity
Tooth sensitivity values were taken before the treatment
which was compared to immediate postoperative and follow
up visits It was checked using an electric pulp tester
maximum
moderate
least
immediately
group 2
group 1
group 3
1 month
group 2
group 1
group 3
3 month
group 2
group 1
group 3
Patient satisfaction score
Satisfaction was assessed on visual analog scale
Range 1 to 5
Groups percentage of patients
who were satisfied with
the treatment
Number of patients
who reported slight
reappearance of colour
Group 1
90
7
Group 2
83
8
Group 3
73
7
3
Number of Appointments
Groups One sitting Two sittings Three
sittings
Group 1
25
4
1
group 2
26
3
1
Group 3
30
0
0
DISCUSSION
bull Hydrogen peroxide is capable of penetrating the tooth osmosis and through porosities and cracks subsequently acting directly on the pigmented molecules
bull Gurgan et al investigated 3 different light systems and found out that diode laser system with gave best tooth whitening and least tooth sensitivity
bull In the EM group the surface reflects and refracts light from the surface in such way that mild imperfections in underlying enamel are camouflaged While the highly polished surface of enamel enhances the aesthetic appearance
bull Train et al and Loguercio et al also had the similar results in their studies with EM mild fluorosis showed best results moderate showed moderate results while it had little effect on severe fluorosis
bull NaOCl was only effective on mild stains while moderate and severe
stains could only be lightened to quite an extent but could not be
completely removed
bull When NaOCl comes in contact with hypomineralized and discoloured
enamel it degrades and removes the chromogenic organic material
located on the enamel surface
CONCLUSION
bull It was concluded that esthetic appearance of teeth mild fluorosis can
be achieved by bleaching and microabrasion But in cases of
moderate fluorosis a combination of any of theses modalities can be
used
bull As no special maintenance precautions are required these maybe be
considered as an interesting alternative to conventional operative
treatment
bull Focuses on only TSIF of 4
bull Electric pulp testing is not the
right method to check for
sensitivity
bull Tooth Sensitivity changes
from person to person
bull Food habits can cause
staining of the teeth
bull Minimally invasive
bull Cheaper to veneers
bull Minimal loss of tooth structure
bull 4 parameters checked for the success of treatment
bull Inclusion of specific score of fluorosis for comparing the results
bull Maximum 3 appointments needed
CRITICAL ANALYSIS
Pros Cons
REFERENCES
bull Gurgan S Cakir FY Yazici E Different light-activated in officebleaching
systems Lasers Med Sci 201025817-22
bull Train TE McWhorter AG Seale NSWilson CF Guo IY Examination of
esthetic improvement and surface alteration following microabrasion in
fluorotic human incisors in vivoPediatr dent 199618353-62
bull Loguercio AD Correia LD Zago C Tagliari D Neumann E Gomes OM et al
Clinical effectiveness of two microabrasion materials materials for the
removal of enamel flurosis stains Oper Dent 200732531-8
4
1
Pharmacological Methods of Behavior
Management
DR MITAKSHARA NIRWAN
DEFINITIONS
bull Conscious Sedation ndash A minimally depressed level of consciousness that retains
the patients ability to independently and continuously maintain an airway and respond appropriately to physical stimulation or verbal command
(American Dental Association House Of Delegates 2000)
bull Deep Sedation ndash An induced state of depressed consciousness
accompanied by partial loss of protective reflexes including the inability to continuously maintain an airway independently and or to respond purposefully to physical stimulation or verbal command
bull General Anesthesia (G A) ndash An induced state of unconsciousness or complete loss of
protective reflexes including the inability to continually maintain an airway independently and respond purposefully to physical stimulation or verbal command
Conscious sedation
ADVANTAGES
Conscious
Protective reflexes active amp intact
Stable vital signs
Operating dentist may perform sedation
Minimum amount of equipment required
Prolong detainment in recovery room not required
Risk of complication very low
Excellent choice for poor ndash risk pt in dental office
Cost effective
General anesthesia
ADVANTAGES Not absolutely
essential May be the only
method Not necessary (no
pain reaction) Amnesia always
present
Conscious sedation
DISADVANTAGES
Pt cooperation is essential
Extremely difficult or mentally handicapped pt cannot always be managed
Use of local anesthesia is a must
Amnesia may or may not be present
General anesthesia DISADVANTAGES
Pt unconscious
Protective reflexes are depressed
Depressed
Advanced training required Dentist must not act also as anesthetist
Special equipment necessary
Detainment in recovery area necessary
High IOP amp postoperative complications
Not indicated in dental office
More expensive
Fundamental Concepts
bull Techniques that utilize drugs to induce co-operative yet conscious state in an otherwise uncooperative child ndash CONSCIOUS SEDATION
2
GOALS
1 To facilitate the provision of quality care
2 To minimize the extremes of disruptive behavior
3 To promote a positive psychologic response to treatment
4 To promote patient welfare amp safety
5 To return the patient to physiologic state
OBJECTIVES
1 The pt mood must be altered
2 The pt must remain conscious at all times
3 The pt must be cooperative
4 All protective reflexes must remain intact and active
5 Vital signs must remain stable and with in normal limits
6 The ptrsquos pain threshold should be elevated
7 Amnesia may be present
Indications
1 Preschool children
2 Lack of Psychological Emotional maturity
3 Lack of Cognitive Physical Medical disability
4 Fearful amp anxious pts
5 Pt who require extensive amp complicated dental care amp would require or benefit from prolonged visits
6 Acute pain
7 Traumatic injuries
Operating Facilities amp Equipment
A positive pressure O2 delivery system capable of administering gt than 90 O2 at 10L min flow for 60 min (650L ldquoErdquo cylinder)
OR
Self inflating bag valve mask device (15L min)
A functional suction apparatus with appropriate suction catheters
Monitoring equipment - PO BPC PC or Capno
Inhalation sedation unit
100 O2 amp never less than 25
A fail safe mechanism that is checked and calibrated annually
Must have appropriate scavenging system
Emergency drugs
Techniques of sedation
Routes for drug administration
bull Oral
bull Rectal
bull Inhalational
bull Transmucosal
ndash Sublingual
ndash Intranasal
bull Parenteral
ndash IM
ndash sub mucosal
ndash IV
3
Oral Sedation
Advantages
1 Almost universally accepted and the easiest method
2 Decreased incidence and severity of adverse reaction
3 Low cost
Disadvantages
1 Absorption is variable
2 Prolonged latent period(30 min)
3 Reversal of any unwanted effect is also difficult
4 Inability to readily lighten or deepen the level of sedation
5 Prolonged duration of action
Rectal Sedation
Advantages 1 Incidence and intensity of
drug related side effects is minimized
2 Drug absorption occurs from the large intestine directly into the circulation
3 The lack of a needle syringe or other equipment
4 The ease of administration
5 The low cost
Disadvantages
1 Inconvenience to the administrator amp pt
2 The variable absorption of drugs from the large intestine
3 The slow onset of action amp the relatively long duration of action
4 Inability to titrate the drug dosage
5 The inability to reverse the action of the drug the prolonged recovery
Intranasal sedation
Advantages
Rapid onset (10 ndash 15 min)
Simple amp relatively painless
Less pt cooperation is required
Absorbed directly into the C V S
Intranasal sedation
Disadvantages
1 Dependence on nasal mucous membrane
2 Shorter duration of action(40-60min)
3 Multiple dosage may be necessary
Drugs
Midazolam ndash 02mgkg
Sufentanil ndash 15 ndash 3 mcgkg
Ketamine ndash 3-6mg kg
Sublingual sedation
Advantages
1 Pt acceptance
2 Rapid onset
3 High bioavailability
Drugs
Oral Transmucosal Fentanyl Citrate (OTFC)
Intramuscular Sedation
Advantages
1 More rapid onset of action
2 Absorbed directly into the C V system
3 More reliable absorption of drug
4 Pt cooperation is not as essential
Disadvantages
1 Time factor ndash its 15 min latent period
2 Pt may not be willing to accept the injection
3 The prolonged duration of action(2-4 hrs more)
4 Possibility of injury to the tissues at the site of injection caused by either the drug or the needle
4
Sites of I M administration
1 Gluteal area
2 Vastus lateralis
3 Mid ndash deltoid area
Drugs
Diazepam
Midazolam
Hydroxyzine
Inhalation Sedation
Advantages
1 The onset of action is more rapid
2 Peak clinical level is achieved rapidly(3-5min) - permit titration
3 Administrator has complete control over the actions of the drug - safety feature
4 No significant over dosage
5 Flexible duration of action
6 Recovery time is rapid amp most complete
7 No injection is required
8 With N2O- O2 it is safe with very few side effects
Disadvantages
1 The initial cost of the equipment is high 2 The continuing cost of the gases is high 3 The equipment occupies considerable space 4 N2O is not a potent agent 5 A degree of cooperation is required from the pt 6 Chronic exposure to N2O is deleterious to the health of
dental personnel
Contraindications
1 Nasal obstruction 2 Cyanosis at rest 3 Poor cooperation 4 1st trimester of pregnancy 5 Fear of masks
I V Sedation
Advantages
1 The onset of action is the most rapid 2 The dosage may be titrated 3 Suitable level of sedation can be provided 4 The recovery period is shorter 5 Side effects are extremely uncommon 6 Control of salivary secretions is possible 7 The gag reflex is diminished 8 Effectively diminishes motor disturbances 9 Provides immediate access to CVS in emergency
Disadvantages
1 Venipuncture is necessary
2 Complication may rise at the site of the venipuncture
3 Monitoring must be more intensive
4 Recovery is not complete at the end of the procedure
5 Reversal of sedation is difficult
5
N2O-O2 (Relative Analgesia)
colorless sweet smelling gas
Pharmacokinetics
Absorption through pulmonary epithelium
It is approx 15 times as soluble as is nitrogen It replaces nitrogen in blood
It is carried in solution in plasma of the blood
It is not metabolized by the body
Elimination ndash majorndash lungs minor --- skin
perspiration urine and intestinal gas
Pharmacodynamics
Dose related
10 ndash 25 Lightheaded
Changes in visual amp auditory sensation
Tingling of hands amp feet
Suffusing warmth
Remote from the immediate environment
Reduced anxiety
25-50 max analgesic properties and aberration of vision hearing and proprioception mild drowsiness euphoria amnesia and increased sleepiness and dreams
35 conc will achieve maximum analgesia
bull CNS
ndash Cerebrum-primarily affected
ndash Safe but weak anesthetic agent
bull RESPIRATORY SYSTEM
ndash Increased Tidal and minute volumes
bull CARDIOVASCULAR SYSTEM
ndash 2 studies ndash decreased cardiac output
bull FETAL SYSTEMS
ndash Miscarriage in humans
bull OTHER SYSTEMS
ndash Depression of spinal reflexes increase muscle tone indicates stage of delirium
ndash Muscle rigidity-narcotics + nitrous oxide
ndash Nausea and vomitting - GIT
ndash HEMATOPOIESIS ----- prolonged exposure
Adverse reactions and toxicity
EMOTIONAL REACTIONS
DREAMS HALLUCINATIONS
No acute toxicity
Chronic toxicity ndash bone marrow
depression
PROCEDURE
Diffusion Hypoxia
Sevoflurane
A fluorinated derivative of isopropyl ether ndash synthesized in 1970
Potent anaesthetic agent with rapid uptake amp speedy recovery
Day-case surgery
Problem
Attaching vaporiser to any of the currently available machine
BENZODIAZEPINES
Diazepam 1961 lipid soluble
Uses-alcoholism epilepsy labor tetanus and cerebral palsy
- sedation and amnesia
- varieties of neurosis amp anxiety states
Pharmacokinetics
Orally Rectal IMIV or SC
Well absorbed through GIT
Excretion in urine
6
bull Pharmacodynamics
ndash Depress the brain stem reticular system and the limbic system thalamus and hypothalamus
ndash It is a centrally acting muscle relaxant Has anti-convulsant properties
Adverse reaction amp toxicity
ndash Confusion nausea headache increased appetite decreased salivation and jaundice Thrombophlebitis
ndash Rebound phenomenon
ndash Toxicity drowsiness confusion sleep and coma
Dosage Oral or Rectal ndash 02-05mgkg
Maximum single dose 10mg
IV- 025mgkg
Supplied Tablets 2 5 10 mg
Suspension ndash 5mg
Midazolam Water soluble ndash non-irritant
Oral IM IV
Metabolism- liver
Onset IV 3 -5mins
oral 20 ndash 30mins
Oral administration anxious patients requiring relatively short dental procedure
No rebound phenomenon
Better anxiolysis amp amnesia (retrograde amnesia)
Adverse effects Respiratory depression
dose dependant apnea
Dosage Oral ndash 025 to 1mgkg to maximum single dose 20mg
IM ndash 01 to 015mgkg to a maximum of 10mg
IV ndash slow IV
Supplied Syrup ndash 2mgml
Injectable ndash 1mgml amp 5mgml vials
Flumazenil specific benzodiazepines antagonist
selectively inhibits CNS effects
IV administration amp not recommended below 18yrs of age
02mg over 15 seconds after 45seconds 02mg then after 60seconds to maximum of 1mg
Sedative-Hypnotics
Barbiturates First truly effective drugs for the management of anxiety Generalized CNS depressants Produce dose dependent effects
Sedation ---- sleep ---- GA ---- coma
Suppress the CNS and result in sedation and amnesia Advantages
Rapid onset and short duration Disadvantages
no analgesic effect and possible hypotension Must be used with caution in trauma patients because they may cause
apnea and hypoventilation
DOSE Pentobarbital Sodium 100mg Secobarbital Sodium 100 to 200mg Children 30 to 100mg
bull Chloral Hydrates (Mickey Finn Knock out drops ) First synthesized in 1832 first member of the hypnotic group of drugs
Widely used as conscious sedation agent
Properties
Unpleasant taste
Nausea vomiting
Quite irritating to skin and to mucous membranes
GI irritation
Dosages Individualized for each patient 25 ndash 50mgkg
maximum of 1g
Supplied oral capsule ndash 500mg
oral solution ndash 250 amp 500mg5ml
Rectal suppositories ndash 324 amp 648mg
Narcotics
Do produce sedation amp euphoria greater in children
LA is required but dose should be decreased
Meperidine Synthetic opiate agonist
Very water soluble
Orally SC IM or IV
Peak effect by oral 1 hr amp lasts upto 4 hrs
Adverse reactions
-Seizures
-Extreme caution in hepatic or renal diseases or history of seizures
7
Dosage Oral SC or IM ndash 1to 22mgkg not to exceed 100 mg
Supplied Oral Tablets ndash 50 amp 100mg
Oral Syrup ndash 50mgml
Parental solution ndash 25 50 75 amp 100mgml
Fentanyl
Synthetic opiate narcotic analgesic
Very potent 01mg = 10mg Morophine75mg Meperidine
Pharmacokinetics
IV IM SM
Metabolized in liver Excreted in urine
Fentanyl Onset ndash 7 to 15mins
Duration ndash 1 to 2 hrs
Pharmacodynamics
Respiratory depression RR but returns to normal rapidly Tidal volume amp response to co2 depressed for extended period
Apnea
Less emetic than meperidine
NOT RECOMMENDED IN CHILDREN BELOW 2yrs
Dosage 0002 to 0004mgkg
Supplied 005mgml in 2 amp 5ml ampoules
Reversal drug Naloxone
Semisynthetic opiate antagonist
No agonist activity
Onset 2 to 5mins SC or IM amp 1 to 2mins IV
Reversal 45mins
Pt should be kept under continual surveillance
Adverse reaction nausea vomiting sweating hypotension hypertension ventricular tachycardia fibrillation
Dosage IV SC IM 001mgkg then 01mgkg every 2- 3mins maximum 2mg
Supplied 002 004 1mg solutions
Antihistamines
Hydroxyzine
Oral or IM
Effect ndash 15 ndash 30mins
Half-life ndash 3 hrs
Uses
To relieve anxiety
Used as an anti-histamine
Used to control nausea and vomiting including that associated with motion sickness and pregnancy
Adverse reaction dry mouth drowsiness hypersentivity
Dosage Oral ndash 1 to 2mgkg
IM ndash 11mgkg
Promethazine Oral or IM Onset 15 to 60mins Duration 4 to 6 hrs Uses
To prevent and treat nausea and vomiting associated with motion pregnancy or surgery
Produces sedation and reduce swelling pain and trismus
Lower seizure threshold Adverse reaction dry mouth blurred vision thickening of bronchial secretions Dosage OralIM ndash 05-11mgkg
maximum 25 mg
Diphenhydramine
Oral IM IV
Onset -1hr
Duration ndash 4 to 6 hr
Metabolized in liver
Adverse reaction disturbed coordination thickening of bronchial secretions
Dosage Oral IM IV ndash 1 to 15mgkg
maximum 50mg
Tranquilizers
Major tranquilizer antipsychotic produce calmness control symptoms of psychoses cause reversible extra pyramidal symptoms and do not tend to cause habituation
Minor tranquilizer antianxiety agents also cause calmness do not cause extrapyramidal symptoms Used in conditions like nervous tension and mild depression
8
Classification
Antipsychotics
Phenothiazine derivatives
Chlorpromazine promazine
Butryophenones
Haloperidol
Rauwolfia alkaloids
Reserpine
Antianxiety drugs
Propyl alcohol derivatives
Meprobamate
Benzodiazepine derivatives
Diazepam
Miscellaneous compounds
Hydroxyzine
Meprobamate
White crystalline powder slightly bitter in taste
Only administered orally
Peak blood concentration ----1 to 3hrs
10 ---------excreted unchanged Rest --- excreted as a oxidized derivative or as a glucoronide
Uses
To relieve day time anxiety
Induce sleep in insomniacs
To reduce anxiety associated with dental treatment
Anti-convulsant ndash petit mal epilepsy
Adverse reaction leucopenia acute non-thrombocytopenic purpura ecchymoses eosinophilia edema adenopathy
Dosage Childrengt 6yrs 100 to 200mg
Not recommended for children under 6yrs
Monitoring during sedation
1 Pulse
2 Blood pressure
3 ECG
4 Respiration
5 Temperature
Pulse
Manual Electronic
bull Radial Brachial
bull Facial labial
Blood pressure
ndash Stethoscope amp sphygmomanometer
ndash Automatic devices
ndash Direct cannulation of an artery ndash very accurate
Electrocardiograph
Heart rate rhythm myocardial function
9
Respiration
ndash Monitoring respiratory rate
ndash Observing the rise amp fall of the chest wall
ndash Observing the color of mucous membrane
ndash Observing the inflation amp deflation of the reservoir bag
Devices for monitoring respiration
1 The Precordial pretracheal stethoscope
2 The esophageal stethoscope
ndash Respiratory rate
ndash Heart rate
ndash Any abnormal sounds
Pulse Oximeter
ndash Oxygen saturation
ndash Heart rate
ndash Oxisensor site
ndash Fingers
ndash Toe
ndash Ear lobe
Mechanism
Oxygenated Hb ndash red light
Deoxygenated Hb- infrared light
Tissue pressure from arterial pulse (plethysmography)
Advantages
ndash Safe amp noninvasive
ndash Simple to use
ndash Information is rapidly available for clinical decision
ndash Indirectly indicates respiratory adequacy
Disadvantages
ndash Finger probes can get dislodged
ndash Emitted light source may cause burning
ndash Non reusable probes are expensive
ndash Does not directly determine airway patency
Capnography
1 The presence absence of air flow
2 Indicates depth amp adequacy of respiration
3 Continues analysis of the co2 content of the respired air ndash indicates respiratory adequacy
Temperature
ndash Disposable nondisposable thermometer
ndash Esophageal rectal temp probe
10
Discharge criteria
Cardiovascular function is satisfactory amp stable
Airway patency is uncompromised amp satisfactory
Pt is easily arousable amp protective reflexes intact
State of hydration is adequate
Pt can talk if applicable
Pt can sit unaided if applicable
Pt can ambulate with minimal assistance if applicable
Presedation level of responsiveness achieved
Responsible individual is available
1
PULP THERAPY OF VITAL TEETH
DR MITAKSHARA NIRWAN
Contents
Indirect pulp capping
Direct pulp capping
Medications amp materials used in pulp capping
Pulpotomy
MTA
Apexogenesis
INDIRECT PULP CAPPING
Pieter Van Forest - first to speak about root canal therapy
Glove designed instruments that could prepare a canal to a certain size and taper(1910)
Indirect pulp capping is defined as a procedure where in small amount of carious dentin is retained in
deep areas of cavity to avoid exposure of pulp followed by placement of a suitable medicament and
restorative material that seals off the carious dentin and encourages pulp recovery (Ingle)
A procedure in which only the gross caries is removed from the lesion and the cavity is sealed for a
time with a biocompatible material (McDonald)
Objective of indirect pulp capping
These were given by Eidelman in 1965
bull Arresting the carious process
bull Promoting dentin sclerosis
bull Stimulating formation of tertiary dentin
bull Remineralization of carious dentin
Layers of Carious Dentin Indications of Indirect Pulp Capping
History
Mild pain associated with eating
Negative history of spontaneous extreme pain
Clinical Examination
Deep carious lesion which are close tobut not involving the pulp in vital primary or young
permanent teeth
No mobility
Nominal pulp inflammationdefinite layer of affected dentin after removal of infected dentin
Radiographic examination
Normal lamina dura amp PDL space
No radiolucency around the apices
2
Contraindications of Indirect Pulp Capping
History
Sharp penetrating pulpalgia
Prolonged spontaneous pain especially at night
Clinical examination
Mobility of tooth
Discoloration of tooth
Negative reaction of electric pulp testing
Radiographic examination
Definite pulp exposure
Break in the lamina dura
Radiolucency around the apices
Widened PDL space
Treatment procedure
Sequelae of Indirect Pulp Capping Three distinct types of new dentin formation take place
1 Cellular fibrillar dentinmdashfirst 2 months
2 Globular dentinmdash3 months
3 Tubular dentin (uniform mineralized dentin)
bull 15th of reparative dentin formation begins in less than 30 days
bull After 3 months 01 mm is formed
DIRECT PULP CAPPING Defined by Kopel (1992) as the placement of a medicament or non medicated material on a pulp that
has been exposed in course of excavating the last portions of deep dentinal caries or as a result of
trauma
Objective
To create new dentin in the area of the exposure and subsequent healing of the pulp
Rationale
achieve a biologic closure of the exposure site by deposition of hard tissue barrier (dentin bridge)
between pulp tissue and capping material thus walling off the
INDICATIONS
Small mechanical exposure
Easily controlled haemorrhage
Bright red haemorrhage
True pinpoint exposure
CONTRAINDICATIONS
Severe toothache at night
Spontaneous pain
Tooth mobility
Radiographic appearance of pulp periradicular de- generation
Excess of hemorrhage at the time of exposure Serous exudate from the exposure
Externalinternal root resorption
Swellingfistula
Histological Changes after Pulp Capping
These were illustrated be Glass and Zander in 1949
After 24 hours Necrotic zone adjacent to calcium
hydroxide paste is separated from healthy pulp
tissue by a deep staining basophilic layer
After 7 days Increase in cellular and fibroblastic
activity
After 14 days Partly calcified fibrous tissue lined by
odontoblastic cells is seen below the calcium
proteinate zone disappearance of necrotic zone
After 28 days Zone of new dentin
3
Medications and Materials Used for Pulp Capping Calcium hydroxide
Corticosteroids amp antibiotics
Inert materials
Collagen fibers
4-META adhesive
Direct bonding
Isobutyl cyanoacrylate
Denatured albumin
Mineral trioxide aggregate
Laser
Bone morphogenic protein
PULPOTOMY
Finn (1995) defined it as the complete removal of the coronal portion of the dental pulp
followed by placement of a suitable dressing or medicament that will promote healing and
preserve vitality of the tooth
American Academy of Pediatric Dentistry (1998) defined pulpotomy as the amputation of
affected infected coronal portion of the dental pulp preserving the vitality and function of the
remaining part of radicular pulp
Objectives
bull Removal of inflamed and infected coronal pulp at the site of exposure thus preserving the vitality of the
radicular pulp and allowing it to heal
bull Maintain the tooth in the dental arch
Rationale
bull Radicular pulp is healthy and capable of healing after surgical amputation of the infected coronal pulp
bull Preserves vitality of the radicular pulp
bull Maintains tooth in a physiologic condition
Indications of Pulpotomy bull Mechanical pulp exposure in primary teeth
bull Teeth showing a large carious lesion but free of radicular pulpitis
bull History of only spontaneous pain
bull Hemorrhage from exposure sites bright red and can be controlled
bull Absence of abscess or fistula
bull No interradicular bone loss
bull No interradicular radiolucency
Contraindications of Pulpotomy bull Persistent toothache
bull Tenderness on percussion
bull Root resorption more than 13rd of root length
bull Large carious lesion with nonrestorable crown
bull Highly viscous sluggish hemorrhage from canal orifice which is uncontrollable
bull Medical contradictions like heart disease immuno compromised patient
bull Swelling or fistula
bull External or internal resorption
bull Pathological mobility
bull Calcification of pulp
Classification of pulpotomy
4
Formocresol Pulpotomy
Iby BUCKLEY in 1904
Sweet (1930) Formulated multi visit technique
Doyle (1962) Advocated 2 sitting procedure (complete devitalization)
Spedding (1965) Gave 5 minute protocol (partial devitali- zation)
Venham (1967) Proposed 15 seconds procedure
Current concept uses 4 minutes of application time
Composition of formocresol Buckleyrsquos Formula
bull Cresol ndash 35 percent
bull Glycerol ndash 15 percent
bull Formaldehyde ndash 19 percent
bull Water ndash 31 percent
Mechanism of Action
It prevents tissue autolysis by bonding to the proteins Bonding is of peptide groups of side chain amino acids and is a reversible process accomplished without
changing the basic structure of protein molecules
Histological Changes
bull Demonstrated by Mass and Zilbermann11 in 1933 and also by Massler and Mansokhani in 1959
bull Immediately the pulp becomes fibrous and acidophillic
bull Seven to fourteen days Three zones appear
a broad eosinophilic zone of fixation
b broad pale-staining zone of atrophy with poorcellular definition
c broad zone of inflammation extending apically into normal pulp tissue
bull One yearndash Progressive apical movement of these zones with only acidophillic zone left at the end of 1 year
Modified Formocresol Pulpotomy
Used by TRASK(1972)
The technique is identical to that described for primary teeth except that the formocresol pellet is
sealed permanently in the tooth
Two-visit Devitalization Pulpotomy
Indications
bull There is evidence of sluggish bleeding at the amputation site that is difficult to control
bull Pus in the chamber but none at the amputation site
bull There is thickening of the PDL
bull History of pain
Contraindications
bull Nonrestorable tooth
bull Tooth with necrotic pulp
5
Glutaraldehyde Pulpotomy
It was first suggested by S Gravenmade Introduced by Kopel in 1979
Mechanism of Action
bull Glutaraldehyde produces rapid surface fixation of the underlying pulpal tissue
bull A narrow zone of eosinophilic stained and compressed fixed tissue is found directly beneath the area of application which blends into vital normal appearing tissue apically
bull With time the glutaraldehyde fixed zone is replaced by macrophagic action with dense collagenous tissue thus the entire root canal tissue is vital
Cvekrsquos Pulpotomy
bull This is also called as calcium hydroxide pulpotomy or young permanent partial pulpotomy
bull This was proposed by Mejare and Cvek16 in 1978
bull Indicated in young permanent teeth where the pulp is exposed by mechanical or bacterial means and the
remaining radicular tissue is judged vital by clinical and radiographic criteria whereas the root closure is
notcomplete
MINERAL TRIOXIDE AGGREGATE (MTA) Torabinejad described the physical and chemical properties of MTA in 1995
It is ash colored powder made primarily of fine hydrophilic particles of
1 tricalcium aluminate
2 tricalcium silicate
3 silicate oxide
4 tricalcium oxide
5 bismuth dioxide
Hydration of the powder results in a colloidal gel composed of calcium oxide crystals in an amorphous
structure This gel solidifies into a hard structure in less than three hours
PROPERTIES OF MTA
It is biocompatible material and its sealing ability is better than that of amalgam or ZOE
Initial pH is 102 and set pH is 125
The setting time of cement is 4 hours
The compressive strength is 70 MPA which is comparable with that of IRM
Low cytotoxicity ndash It presents with minimal inflammation if extended beyond the apex
Mineral trioxide aggregate (MTA) has demonstrated the ability to induce hard-tissue formation in
pulpal tissues and it promotes rapid cell growth
APEXOGENESIS
It is defined as the treatment of a vital pulp by capping or pulpotomy in order to permit continued
growth of the root and closure of the open apex
Rationale
Maintenance of integrity of the radicular pulp tissue to allow for continued root growth
Indications
bull Indicated for traumatized or pulpally involved vital permanent tooth when root apex is incompletely formed
bull No history of spontaneous pain
bull No sensitivity on percussion
bull No hemorrhage
bull Normal radiographic appearance
Contraindications
bull Evidence that radicular pulp has undergone degenerative changes
bull Purulent drainage
bull History of prolonged pain bull Necrotic debris in canal
bull Periapical radiolucency
6
1
Gupta A Dhingra R Chaudhari P Gupta A
Department of Paedodontics and Preventive Dentistry Faculty of Dental Sciences SGT University Gurgaon Haryana India
Journal of Indian Society of Pedodontics and Preventive Dentistry
Volume 35 I Issue 3 I July-September 2017
A COMPARISION OF VARIOUS MINIMALLY
INVASIVE TECHNIQUES FOR THE REMOVAL
OF DENTAL FLUOROSIS STAINS IN
CHILDREN
DR MITAKSHARA NIRWAN
CONTENTS
bull Introduction
bull Aims
bull Materials and Methods
bull Results
bull Discussion
bull Conclusion
bull Critical analysis
bull References
INTRODUCTION
bull Dental fluorosis is a developmental disturbance of dental enamel caused by
successive exposure to high concentrations of fluoride during tooth
development
bull Various methods of therapy are advocated for the treatment of fluorosis -
stained teeth which range from invasive ceramic veneer bonding restorations
to abrasive chemical treatments
bull The combination of dental bleaching techniques and microabrasion appears
as an excellent conservative solution to reestablish health in fluorosis
affected teeth
AIMS
bull The aim of the study was to evaluate and compare the effectiveness of
minimally invasive techniques for the removal of dental fluorosis
stains in children in vivo
MATERIALS AND METHODS
Patients visiting the department of Pedodontics and Preventive dentistry
Faculty of Dental Sciences SGT University Gurgaon
bull Sample size 90 patients
bull Age group 10 -17 years
bull Caries cracks or periodontal
disease on anterior teeth
bull Abscess draining sinus
cellulitis
bull Non vital teeth
hypersensitive exposed
crevices
bull Orthodontic appliance
bull Past history of bleaching
bull At least two permanent
maxillary anterior teeth
bull TSIF of score 4
bull Free of systemic diseases
Inclusion criteria Exclusion criteria
2
Groups
Group A In office bleaching with 35 hydrogen peroxide( Pola Office
Bleaching kit) activated by light emitting diode (LED) bleaching unit
(35 HP)
Group B Enamel microabrasion (EM) (PREMA Enamel Microabrasion
System) followed by in-office bleaching with 44 carbamide peroxide
gel (EM)
Group C In-office bleaching with 5 sodium hypochlorite (5
NaOCl)
A baseline colour evaluation was done by taking digital photograph of
the maxillary anterior teeth
RESULTS
Group 1
Colour stability
Group 2 Group 3
Tooth sensitivity
Tooth sensitivity values were taken before the treatment
which was compared to immediate postoperative and follow
up visits It was checked using an electric pulp tester
maximum
moderate
least
immediately
group 2
group 1
group 3
1 month
group 2
group 1
group 3
3 month
group 2
group 1
group 3
Patient satisfaction score
Satisfaction was assessed on visual analog scale
Range 1 to 5
Groups percentage of patients
who were satisfied with
the treatment
Number of patients
who reported slight
reappearance of colour
Group 1
90
7
Group 2
83
8
Group 3
73
7
3
Number of Appointments
Groups One sitting Two sittings Three
sittings
Group 1
25
4
1
group 2
26
3
1
Group 3
30
0
0
DISCUSSION
bull Hydrogen peroxide is capable of penetrating the tooth osmosis and through porosities and cracks subsequently acting directly on the pigmented molecules
bull Gurgan et al investigated 3 different light systems and found out that diode laser system with gave best tooth whitening and least tooth sensitivity
bull In the EM group the surface reflects and refracts light from the surface in such way that mild imperfections in underlying enamel are camouflaged While the highly polished surface of enamel enhances the aesthetic appearance
bull Train et al and Loguercio et al also had the similar results in their studies with EM mild fluorosis showed best results moderate showed moderate results while it had little effect on severe fluorosis
bull NaOCl was only effective on mild stains while moderate and severe
stains could only be lightened to quite an extent but could not be
completely removed
bull When NaOCl comes in contact with hypomineralized and discoloured
enamel it degrades and removes the chromogenic organic material
located on the enamel surface
CONCLUSION
bull It was concluded that esthetic appearance of teeth mild fluorosis can
be achieved by bleaching and microabrasion But in cases of
moderate fluorosis a combination of any of theses modalities can be
used
bull As no special maintenance precautions are required these maybe be
considered as an interesting alternative to conventional operative
treatment
bull Focuses on only TSIF of 4
bull Electric pulp testing is not the
right method to check for
sensitivity
bull Tooth Sensitivity changes
from person to person
bull Food habits can cause
staining of the teeth
bull Minimally invasive
bull Cheaper to veneers
bull Minimal loss of tooth structure
bull 4 parameters checked for the success of treatment
bull Inclusion of specific score of fluorosis for comparing the results
bull Maximum 3 appointments needed
CRITICAL ANALYSIS
Pros Cons
REFERENCES
bull Gurgan S Cakir FY Yazici E Different light-activated in officebleaching
systems Lasers Med Sci 201025817-22
bull Train TE McWhorter AG Seale NSWilson CF Guo IY Examination of
esthetic improvement and surface alteration following microabrasion in
fluorotic human incisors in vivoPediatr dent 199618353-62
bull Loguercio AD Correia LD Zago C Tagliari D Neumann E Gomes OM et al
Clinical effectiveness of two microabrasion materials materials for the
removal of enamel flurosis stains Oper Dent 200732531-8
4
2
GOALS
1 To facilitate the provision of quality care
2 To minimize the extremes of disruptive behavior
3 To promote a positive psychologic response to treatment
4 To promote patient welfare amp safety
5 To return the patient to physiologic state
OBJECTIVES
1 The pt mood must be altered
2 The pt must remain conscious at all times
3 The pt must be cooperative
4 All protective reflexes must remain intact and active
5 Vital signs must remain stable and with in normal limits
6 The ptrsquos pain threshold should be elevated
7 Amnesia may be present
Indications
1 Preschool children
2 Lack of Psychological Emotional maturity
3 Lack of Cognitive Physical Medical disability
4 Fearful amp anxious pts
5 Pt who require extensive amp complicated dental care amp would require or benefit from prolonged visits
6 Acute pain
7 Traumatic injuries
Operating Facilities amp Equipment
A positive pressure O2 delivery system capable of administering gt than 90 O2 at 10L min flow for 60 min (650L ldquoErdquo cylinder)
OR
Self inflating bag valve mask device (15L min)
A functional suction apparatus with appropriate suction catheters
Monitoring equipment - PO BPC PC or Capno
Inhalation sedation unit
100 O2 amp never less than 25
A fail safe mechanism that is checked and calibrated annually
Must have appropriate scavenging system
Emergency drugs
Techniques of sedation
Routes for drug administration
bull Oral
bull Rectal
bull Inhalational
bull Transmucosal
ndash Sublingual
ndash Intranasal
bull Parenteral
ndash IM
ndash sub mucosal
ndash IV
3
Oral Sedation
Advantages
1 Almost universally accepted and the easiest method
2 Decreased incidence and severity of adverse reaction
3 Low cost
Disadvantages
1 Absorption is variable
2 Prolonged latent period(30 min)
3 Reversal of any unwanted effect is also difficult
4 Inability to readily lighten or deepen the level of sedation
5 Prolonged duration of action
Rectal Sedation
Advantages 1 Incidence and intensity of
drug related side effects is minimized
2 Drug absorption occurs from the large intestine directly into the circulation
3 The lack of a needle syringe or other equipment
4 The ease of administration
5 The low cost
Disadvantages
1 Inconvenience to the administrator amp pt
2 The variable absorption of drugs from the large intestine
3 The slow onset of action amp the relatively long duration of action
4 Inability to titrate the drug dosage
5 The inability to reverse the action of the drug the prolonged recovery
Intranasal sedation
Advantages
Rapid onset (10 ndash 15 min)
Simple amp relatively painless
Less pt cooperation is required
Absorbed directly into the C V S
Intranasal sedation
Disadvantages
1 Dependence on nasal mucous membrane
2 Shorter duration of action(40-60min)
3 Multiple dosage may be necessary
Drugs
Midazolam ndash 02mgkg
Sufentanil ndash 15 ndash 3 mcgkg
Ketamine ndash 3-6mg kg
Sublingual sedation
Advantages
1 Pt acceptance
2 Rapid onset
3 High bioavailability
Drugs
Oral Transmucosal Fentanyl Citrate (OTFC)
Intramuscular Sedation
Advantages
1 More rapid onset of action
2 Absorbed directly into the C V system
3 More reliable absorption of drug
4 Pt cooperation is not as essential
Disadvantages
1 Time factor ndash its 15 min latent period
2 Pt may not be willing to accept the injection
3 The prolonged duration of action(2-4 hrs more)
4 Possibility of injury to the tissues at the site of injection caused by either the drug or the needle
4
Sites of I M administration
1 Gluteal area
2 Vastus lateralis
3 Mid ndash deltoid area
Drugs
Diazepam
Midazolam
Hydroxyzine
Inhalation Sedation
Advantages
1 The onset of action is more rapid
2 Peak clinical level is achieved rapidly(3-5min) - permit titration
3 Administrator has complete control over the actions of the drug - safety feature
4 No significant over dosage
5 Flexible duration of action
6 Recovery time is rapid amp most complete
7 No injection is required
8 With N2O- O2 it is safe with very few side effects
Disadvantages
1 The initial cost of the equipment is high 2 The continuing cost of the gases is high 3 The equipment occupies considerable space 4 N2O is not a potent agent 5 A degree of cooperation is required from the pt 6 Chronic exposure to N2O is deleterious to the health of
dental personnel
Contraindications
1 Nasal obstruction 2 Cyanosis at rest 3 Poor cooperation 4 1st trimester of pregnancy 5 Fear of masks
I V Sedation
Advantages
1 The onset of action is the most rapid 2 The dosage may be titrated 3 Suitable level of sedation can be provided 4 The recovery period is shorter 5 Side effects are extremely uncommon 6 Control of salivary secretions is possible 7 The gag reflex is diminished 8 Effectively diminishes motor disturbances 9 Provides immediate access to CVS in emergency
Disadvantages
1 Venipuncture is necessary
2 Complication may rise at the site of the venipuncture
3 Monitoring must be more intensive
4 Recovery is not complete at the end of the procedure
5 Reversal of sedation is difficult
5
N2O-O2 (Relative Analgesia)
colorless sweet smelling gas
Pharmacokinetics
Absorption through pulmonary epithelium
It is approx 15 times as soluble as is nitrogen It replaces nitrogen in blood
It is carried in solution in plasma of the blood
It is not metabolized by the body
Elimination ndash majorndash lungs minor --- skin
perspiration urine and intestinal gas
Pharmacodynamics
Dose related
10 ndash 25 Lightheaded
Changes in visual amp auditory sensation
Tingling of hands amp feet
Suffusing warmth
Remote from the immediate environment
Reduced anxiety
25-50 max analgesic properties and aberration of vision hearing and proprioception mild drowsiness euphoria amnesia and increased sleepiness and dreams
35 conc will achieve maximum analgesia
bull CNS
ndash Cerebrum-primarily affected
ndash Safe but weak anesthetic agent
bull RESPIRATORY SYSTEM
ndash Increased Tidal and minute volumes
bull CARDIOVASCULAR SYSTEM
ndash 2 studies ndash decreased cardiac output
bull FETAL SYSTEMS
ndash Miscarriage in humans
bull OTHER SYSTEMS
ndash Depression of spinal reflexes increase muscle tone indicates stage of delirium
ndash Muscle rigidity-narcotics + nitrous oxide
ndash Nausea and vomitting - GIT
ndash HEMATOPOIESIS ----- prolonged exposure
Adverse reactions and toxicity
EMOTIONAL REACTIONS
DREAMS HALLUCINATIONS
No acute toxicity
Chronic toxicity ndash bone marrow
depression
PROCEDURE
Diffusion Hypoxia
Sevoflurane
A fluorinated derivative of isopropyl ether ndash synthesized in 1970
Potent anaesthetic agent with rapid uptake amp speedy recovery
Day-case surgery
Problem
Attaching vaporiser to any of the currently available machine
BENZODIAZEPINES
Diazepam 1961 lipid soluble
Uses-alcoholism epilepsy labor tetanus and cerebral palsy
- sedation and amnesia
- varieties of neurosis amp anxiety states
Pharmacokinetics
Orally Rectal IMIV or SC
Well absorbed through GIT
Excretion in urine
6
bull Pharmacodynamics
ndash Depress the brain stem reticular system and the limbic system thalamus and hypothalamus
ndash It is a centrally acting muscle relaxant Has anti-convulsant properties
Adverse reaction amp toxicity
ndash Confusion nausea headache increased appetite decreased salivation and jaundice Thrombophlebitis
ndash Rebound phenomenon
ndash Toxicity drowsiness confusion sleep and coma
Dosage Oral or Rectal ndash 02-05mgkg
Maximum single dose 10mg
IV- 025mgkg
Supplied Tablets 2 5 10 mg
Suspension ndash 5mg
Midazolam Water soluble ndash non-irritant
Oral IM IV
Metabolism- liver
Onset IV 3 -5mins
oral 20 ndash 30mins
Oral administration anxious patients requiring relatively short dental procedure
No rebound phenomenon
Better anxiolysis amp amnesia (retrograde amnesia)
Adverse effects Respiratory depression
dose dependant apnea
Dosage Oral ndash 025 to 1mgkg to maximum single dose 20mg
IM ndash 01 to 015mgkg to a maximum of 10mg
IV ndash slow IV
Supplied Syrup ndash 2mgml
Injectable ndash 1mgml amp 5mgml vials
Flumazenil specific benzodiazepines antagonist
selectively inhibits CNS effects
IV administration amp not recommended below 18yrs of age
02mg over 15 seconds after 45seconds 02mg then after 60seconds to maximum of 1mg
Sedative-Hypnotics
Barbiturates First truly effective drugs for the management of anxiety Generalized CNS depressants Produce dose dependent effects
Sedation ---- sleep ---- GA ---- coma
Suppress the CNS and result in sedation and amnesia Advantages
Rapid onset and short duration Disadvantages
no analgesic effect and possible hypotension Must be used with caution in trauma patients because they may cause
apnea and hypoventilation
DOSE Pentobarbital Sodium 100mg Secobarbital Sodium 100 to 200mg Children 30 to 100mg
bull Chloral Hydrates (Mickey Finn Knock out drops ) First synthesized in 1832 first member of the hypnotic group of drugs
Widely used as conscious sedation agent
Properties
Unpleasant taste
Nausea vomiting
Quite irritating to skin and to mucous membranes
GI irritation
Dosages Individualized for each patient 25 ndash 50mgkg
maximum of 1g
Supplied oral capsule ndash 500mg
oral solution ndash 250 amp 500mg5ml
Rectal suppositories ndash 324 amp 648mg
Narcotics
Do produce sedation amp euphoria greater in children
LA is required but dose should be decreased
Meperidine Synthetic opiate agonist
Very water soluble
Orally SC IM or IV
Peak effect by oral 1 hr amp lasts upto 4 hrs
Adverse reactions
-Seizures
-Extreme caution in hepatic or renal diseases or history of seizures
7
Dosage Oral SC or IM ndash 1to 22mgkg not to exceed 100 mg
Supplied Oral Tablets ndash 50 amp 100mg
Oral Syrup ndash 50mgml
Parental solution ndash 25 50 75 amp 100mgml
Fentanyl
Synthetic opiate narcotic analgesic
Very potent 01mg = 10mg Morophine75mg Meperidine
Pharmacokinetics
IV IM SM
Metabolized in liver Excreted in urine
Fentanyl Onset ndash 7 to 15mins
Duration ndash 1 to 2 hrs
Pharmacodynamics
Respiratory depression RR but returns to normal rapidly Tidal volume amp response to co2 depressed for extended period
Apnea
Less emetic than meperidine
NOT RECOMMENDED IN CHILDREN BELOW 2yrs
Dosage 0002 to 0004mgkg
Supplied 005mgml in 2 amp 5ml ampoules
Reversal drug Naloxone
Semisynthetic opiate antagonist
No agonist activity
Onset 2 to 5mins SC or IM amp 1 to 2mins IV
Reversal 45mins
Pt should be kept under continual surveillance
Adverse reaction nausea vomiting sweating hypotension hypertension ventricular tachycardia fibrillation
Dosage IV SC IM 001mgkg then 01mgkg every 2- 3mins maximum 2mg
Supplied 002 004 1mg solutions
Antihistamines
Hydroxyzine
Oral or IM
Effect ndash 15 ndash 30mins
Half-life ndash 3 hrs
Uses
To relieve anxiety
Used as an anti-histamine
Used to control nausea and vomiting including that associated with motion sickness and pregnancy
Adverse reaction dry mouth drowsiness hypersentivity
Dosage Oral ndash 1 to 2mgkg
IM ndash 11mgkg
Promethazine Oral or IM Onset 15 to 60mins Duration 4 to 6 hrs Uses
To prevent and treat nausea and vomiting associated with motion pregnancy or surgery
Produces sedation and reduce swelling pain and trismus
Lower seizure threshold Adverse reaction dry mouth blurred vision thickening of bronchial secretions Dosage OralIM ndash 05-11mgkg
maximum 25 mg
Diphenhydramine
Oral IM IV
Onset -1hr
Duration ndash 4 to 6 hr
Metabolized in liver
Adverse reaction disturbed coordination thickening of bronchial secretions
Dosage Oral IM IV ndash 1 to 15mgkg
maximum 50mg
Tranquilizers
Major tranquilizer antipsychotic produce calmness control symptoms of psychoses cause reversible extra pyramidal symptoms and do not tend to cause habituation
Minor tranquilizer antianxiety agents also cause calmness do not cause extrapyramidal symptoms Used in conditions like nervous tension and mild depression
8
Classification
Antipsychotics
Phenothiazine derivatives
Chlorpromazine promazine
Butryophenones
Haloperidol
Rauwolfia alkaloids
Reserpine
Antianxiety drugs
Propyl alcohol derivatives
Meprobamate
Benzodiazepine derivatives
Diazepam
Miscellaneous compounds
Hydroxyzine
Meprobamate
White crystalline powder slightly bitter in taste
Only administered orally
Peak blood concentration ----1 to 3hrs
10 ---------excreted unchanged Rest --- excreted as a oxidized derivative or as a glucoronide
Uses
To relieve day time anxiety
Induce sleep in insomniacs
To reduce anxiety associated with dental treatment
Anti-convulsant ndash petit mal epilepsy
Adverse reaction leucopenia acute non-thrombocytopenic purpura ecchymoses eosinophilia edema adenopathy
Dosage Childrengt 6yrs 100 to 200mg
Not recommended for children under 6yrs
Monitoring during sedation
1 Pulse
2 Blood pressure
3 ECG
4 Respiration
5 Temperature
Pulse
Manual Electronic
bull Radial Brachial
bull Facial labial
Blood pressure
ndash Stethoscope amp sphygmomanometer
ndash Automatic devices
ndash Direct cannulation of an artery ndash very accurate
Electrocardiograph
Heart rate rhythm myocardial function
9
Respiration
ndash Monitoring respiratory rate
ndash Observing the rise amp fall of the chest wall
ndash Observing the color of mucous membrane
ndash Observing the inflation amp deflation of the reservoir bag
Devices for monitoring respiration
1 The Precordial pretracheal stethoscope
2 The esophageal stethoscope
ndash Respiratory rate
ndash Heart rate
ndash Any abnormal sounds
Pulse Oximeter
ndash Oxygen saturation
ndash Heart rate
ndash Oxisensor site
ndash Fingers
ndash Toe
ndash Ear lobe
Mechanism
Oxygenated Hb ndash red light
Deoxygenated Hb- infrared light
Tissue pressure from arterial pulse (plethysmography)
Advantages
ndash Safe amp noninvasive
ndash Simple to use
ndash Information is rapidly available for clinical decision
ndash Indirectly indicates respiratory adequacy
Disadvantages
ndash Finger probes can get dislodged
ndash Emitted light source may cause burning
ndash Non reusable probes are expensive
ndash Does not directly determine airway patency
Capnography
1 The presence absence of air flow
2 Indicates depth amp adequacy of respiration
3 Continues analysis of the co2 content of the respired air ndash indicates respiratory adequacy
Temperature
ndash Disposable nondisposable thermometer
ndash Esophageal rectal temp probe
10
Discharge criteria
Cardiovascular function is satisfactory amp stable
Airway patency is uncompromised amp satisfactory
Pt is easily arousable amp protective reflexes intact
State of hydration is adequate
Pt can talk if applicable
Pt can sit unaided if applicable
Pt can ambulate with minimal assistance if applicable
Presedation level of responsiveness achieved
Responsible individual is available
1
PULP THERAPY OF VITAL TEETH
DR MITAKSHARA NIRWAN
Contents
Indirect pulp capping
Direct pulp capping
Medications amp materials used in pulp capping
Pulpotomy
MTA
Apexogenesis
INDIRECT PULP CAPPING
Pieter Van Forest - first to speak about root canal therapy
Glove designed instruments that could prepare a canal to a certain size and taper(1910)
Indirect pulp capping is defined as a procedure where in small amount of carious dentin is retained in
deep areas of cavity to avoid exposure of pulp followed by placement of a suitable medicament and
restorative material that seals off the carious dentin and encourages pulp recovery (Ingle)
A procedure in which only the gross caries is removed from the lesion and the cavity is sealed for a
time with a biocompatible material (McDonald)
Objective of indirect pulp capping
These were given by Eidelman in 1965
bull Arresting the carious process
bull Promoting dentin sclerosis
bull Stimulating formation of tertiary dentin
bull Remineralization of carious dentin
Layers of Carious Dentin Indications of Indirect Pulp Capping
History
Mild pain associated with eating
Negative history of spontaneous extreme pain
Clinical Examination
Deep carious lesion which are close tobut not involving the pulp in vital primary or young
permanent teeth
No mobility
Nominal pulp inflammationdefinite layer of affected dentin after removal of infected dentin
Radiographic examination
Normal lamina dura amp PDL space
No radiolucency around the apices
2
Contraindications of Indirect Pulp Capping
History
Sharp penetrating pulpalgia
Prolonged spontaneous pain especially at night
Clinical examination
Mobility of tooth
Discoloration of tooth
Negative reaction of electric pulp testing
Radiographic examination
Definite pulp exposure
Break in the lamina dura
Radiolucency around the apices
Widened PDL space
Treatment procedure
Sequelae of Indirect Pulp Capping Three distinct types of new dentin formation take place
1 Cellular fibrillar dentinmdashfirst 2 months
2 Globular dentinmdash3 months
3 Tubular dentin (uniform mineralized dentin)
bull 15th of reparative dentin formation begins in less than 30 days
bull After 3 months 01 mm is formed
DIRECT PULP CAPPING Defined by Kopel (1992) as the placement of a medicament or non medicated material on a pulp that
has been exposed in course of excavating the last portions of deep dentinal caries or as a result of
trauma
Objective
To create new dentin in the area of the exposure and subsequent healing of the pulp
Rationale
achieve a biologic closure of the exposure site by deposition of hard tissue barrier (dentin bridge)
between pulp tissue and capping material thus walling off the
INDICATIONS
Small mechanical exposure
Easily controlled haemorrhage
Bright red haemorrhage
True pinpoint exposure
CONTRAINDICATIONS
Severe toothache at night
Spontaneous pain
Tooth mobility
Radiographic appearance of pulp periradicular de- generation
Excess of hemorrhage at the time of exposure Serous exudate from the exposure
Externalinternal root resorption
Swellingfistula
Histological Changes after Pulp Capping
These were illustrated be Glass and Zander in 1949
After 24 hours Necrotic zone adjacent to calcium
hydroxide paste is separated from healthy pulp
tissue by a deep staining basophilic layer
After 7 days Increase in cellular and fibroblastic
activity
After 14 days Partly calcified fibrous tissue lined by
odontoblastic cells is seen below the calcium
proteinate zone disappearance of necrotic zone
After 28 days Zone of new dentin
3
Medications and Materials Used for Pulp Capping Calcium hydroxide
Corticosteroids amp antibiotics
Inert materials
Collagen fibers
4-META adhesive
Direct bonding
Isobutyl cyanoacrylate
Denatured albumin
Mineral trioxide aggregate
Laser
Bone morphogenic protein
PULPOTOMY
Finn (1995) defined it as the complete removal of the coronal portion of the dental pulp
followed by placement of a suitable dressing or medicament that will promote healing and
preserve vitality of the tooth
American Academy of Pediatric Dentistry (1998) defined pulpotomy as the amputation of
affected infected coronal portion of the dental pulp preserving the vitality and function of the
remaining part of radicular pulp
Objectives
bull Removal of inflamed and infected coronal pulp at the site of exposure thus preserving the vitality of the
radicular pulp and allowing it to heal
bull Maintain the tooth in the dental arch
Rationale
bull Radicular pulp is healthy and capable of healing after surgical amputation of the infected coronal pulp
bull Preserves vitality of the radicular pulp
bull Maintains tooth in a physiologic condition
Indications of Pulpotomy bull Mechanical pulp exposure in primary teeth
bull Teeth showing a large carious lesion but free of radicular pulpitis
bull History of only spontaneous pain
bull Hemorrhage from exposure sites bright red and can be controlled
bull Absence of abscess or fistula
bull No interradicular bone loss
bull No interradicular radiolucency
Contraindications of Pulpotomy bull Persistent toothache
bull Tenderness on percussion
bull Root resorption more than 13rd of root length
bull Large carious lesion with nonrestorable crown
bull Highly viscous sluggish hemorrhage from canal orifice which is uncontrollable
bull Medical contradictions like heart disease immuno compromised patient
bull Swelling or fistula
bull External or internal resorption
bull Pathological mobility
bull Calcification of pulp
Classification of pulpotomy
4
Formocresol Pulpotomy
Iby BUCKLEY in 1904
Sweet (1930) Formulated multi visit technique
Doyle (1962) Advocated 2 sitting procedure (complete devitalization)
Spedding (1965) Gave 5 minute protocol (partial devitali- zation)
Venham (1967) Proposed 15 seconds procedure
Current concept uses 4 minutes of application time
Composition of formocresol Buckleyrsquos Formula
bull Cresol ndash 35 percent
bull Glycerol ndash 15 percent
bull Formaldehyde ndash 19 percent
bull Water ndash 31 percent
Mechanism of Action
It prevents tissue autolysis by bonding to the proteins Bonding is of peptide groups of side chain amino acids and is a reversible process accomplished without
changing the basic structure of protein molecules
Histological Changes
bull Demonstrated by Mass and Zilbermann11 in 1933 and also by Massler and Mansokhani in 1959
bull Immediately the pulp becomes fibrous and acidophillic
bull Seven to fourteen days Three zones appear
a broad eosinophilic zone of fixation
b broad pale-staining zone of atrophy with poorcellular definition
c broad zone of inflammation extending apically into normal pulp tissue
bull One yearndash Progressive apical movement of these zones with only acidophillic zone left at the end of 1 year
Modified Formocresol Pulpotomy
Used by TRASK(1972)
The technique is identical to that described for primary teeth except that the formocresol pellet is
sealed permanently in the tooth
Two-visit Devitalization Pulpotomy
Indications
bull There is evidence of sluggish bleeding at the amputation site that is difficult to control
bull Pus in the chamber but none at the amputation site
bull There is thickening of the PDL
bull History of pain
Contraindications
bull Nonrestorable tooth
bull Tooth with necrotic pulp
5
Glutaraldehyde Pulpotomy
It was first suggested by S Gravenmade Introduced by Kopel in 1979
Mechanism of Action
bull Glutaraldehyde produces rapid surface fixation of the underlying pulpal tissue
bull A narrow zone of eosinophilic stained and compressed fixed tissue is found directly beneath the area of application which blends into vital normal appearing tissue apically
bull With time the glutaraldehyde fixed zone is replaced by macrophagic action with dense collagenous tissue thus the entire root canal tissue is vital
Cvekrsquos Pulpotomy
bull This is also called as calcium hydroxide pulpotomy or young permanent partial pulpotomy
bull This was proposed by Mejare and Cvek16 in 1978
bull Indicated in young permanent teeth where the pulp is exposed by mechanical or bacterial means and the
remaining radicular tissue is judged vital by clinical and radiographic criteria whereas the root closure is
notcomplete
MINERAL TRIOXIDE AGGREGATE (MTA) Torabinejad described the physical and chemical properties of MTA in 1995
It is ash colored powder made primarily of fine hydrophilic particles of
1 tricalcium aluminate
2 tricalcium silicate
3 silicate oxide
4 tricalcium oxide
5 bismuth dioxide
Hydration of the powder results in a colloidal gel composed of calcium oxide crystals in an amorphous
structure This gel solidifies into a hard structure in less than three hours
PROPERTIES OF MTA
It is biocompatible material and its sealing ability is better than that of amalgam or ZOE
Initial pH is 102 and set pH is 125
The setting time of cement is 4 hours
The compressive strength is 70 MPA which is comparable with that of IRM
Low cytotoxicity ndash It presents with minimal inflammation if extended beyond the apex
Mineral trioxide aggregate (MTA) has demonstrated the ability to induce hard-tissue formation in
pulpal tissues and it promotes rapid cell growth
APEXOGENESIS
It is defined as the treatment of a vital pulp by capping or pulpotomy in order to permit continued
growth of the root and closure of the open apex
Rationale
Maintenance of integrity of the radicular pulp tissue to allow for continued root growth
Indications
bull Indicated for traumatized or pulpally involved vital permanent tooth when root apex is incompletely formed
bull No history of spontaneous pain
bull No sensitivity on percussion
bull No hemorrhage
bull Normal radiographic appearance
Contraindications
bull Evidence that radicular pulp has undergone degenerative changes
bull Purulent drainage
bull History of prolonged pain bull Necrotic debris in canal
bull Periapical radiolucency
6
1
Gupta A Dhingra R Chaudhari P Gupta A
Department of Paedodontics and Preventive Dentistry Faculty of Dental Sciences SGT University Gurgaon Haryana India
Journal of Indian Society of Pedodontics and Preventive Dentistry
Volume 35 I Issue 3 I July-September 2017
A COMPARISION OF VARIOUS MINIMALLY
INVASIVE TECHNIQUES FOR THE REMOVAL
OF DENTAL FLUOROSIS STAINS IN
CHILDREN
DR MITAKSHARA NIRWAN
CONTENTS
bull Introduction
bull Aims
bull Materials and Methods
bull Results
bull Discussion
bull Conclusion
bull Critical analysis
bull References
INTRODUCTION
bull Dental fluorosis is a developmental disturbance of dental enamel caused by
successive exposure to high concentrations of fluoride during tooth
development
bull Various methods of therapy are advocated for the treatment of fluorosis -
stained teeth which range from invasive ceramic veneer bonding restorations
to abrasive chemical treatments
bull The combination of dental bleaching techniques and microabrasion appears
as an excellent conservative solution to reestablish health in fluorosis
affected teeth
AIMS
bull The aim of the study was to evaluate and compare the effectiveness of
minimally invasive techniques for the removal of dental fluorosis
stains in children in vivo
MATERIALS AND METHODS
Patients visiting the department of Pedodontics and Preventive dentistry
Faculty of Dental Sciences SGT University Gurgaon
bull Sample size 90 patients
bull Age group 10 -17 years
bull Caries cracks or periodontal
disease on anterior teeth
bull Abscess draining sinus
cellulitis
bull Non vital teeth
hypersensitive exposed
crevices
bull Orthodontic appliance
bull Past history of bleaching
bull At least two permanent
maxillary anterior teeth
bull TSIF of score 4
bull Free of systemic diseases
Inclusion criteria Exclusion criteria
2
Groups
Group A In office bleaching with 35 hydrogen peroxide( Pola Office
Bleaching kit) activated by light emitting diode (LED) bleaching unit
(35 HP)
Group B Enamel microabrasion (EM) (PREMA Enamel Microabrasion
System) followed by in-office bleaching with 44 carbamide peroxide
gel (EM)
Group C In-office bleaching with 5 sodium hypochlorite (5
NaOCl)
A baseline colour evaluation was done by taking digital photograph of
the maxillary anterior teeth
RESULTS
Group 1
Colour stability
Group 2 Group 3
Tooth sensitivity
Tooth sensitivity values were taken before the treatment
which was compared to immediate postoperative and follow
up visits It was checked using an electric pulp tester
maximum
moderate
least
immediately
group 2
group 1
group 3
1 month
group 2
group 1
group 3
3 month
group 2
group 1
group 3
Patient satisfaction score
Satisfaction was assessed on visual analog scale
Range 1 to 5
Groups percentage of patients
who were satisfied with
the treatment
Number of patients
who reported slight
reappearance of colour
Group 1
90
7
Group 2
83
8
Group 3
73
7
3
Number of Appointments
Groups One sitting Two sittings Three
sittings
Group 1
25
4
1
group 2
26
3
1
Group 3
30
0
0
DISCUSSION
bull Hydrogen peroxide is capable of penetrating the tooth osmosis and through porosities and cracks subsequently acting directly on the pigmented molecules
bull Gurgan et al investigated 3 different light systems and found out that diode laser system with gave best tooth whitening and least tooth sensitivity
bull In the EM group the surface reflects and refracts light from the surface in such way that mild imperfections in underlying enamel are camouflaged While the highly polished surface of enamel enhances the aesthetic appearance
bull Train et al and Loguercio et al also had the similar results in their studies with EM mild fluorosis showed best results moderate showed moderate results while it had little effect on severe fluorosis
bull NaOCl was only effective on mild stains while moderate and severe
stains could only be lightened to quite an extent but could not be
completely removed
bull When NaOCl comes in contact with hypomineralized and discoloured
enamel it degrades and removes the chromogenic organic material
located on the enamel surface
CONCLUSION
bull It was concluded that esthetic appearance of teeth mild fluorosis can
be achieved by bleaching and microabrasion But in cases of
moderate fluorosis a combination of any of theses modalities can be
used
bull As no special maintenance precautions are required these maybe be
considered as an interesting alternative to conventional operative
treatment
bull Focuses on only TSIF of 4
bull Electric pulp testing is not the
right method to check for
sensitivity
bull Tooth Sensitivity changes
from person to person
bull Food habits can cause
staining of the teeth
bull Minimally invasive
bull Cheaper to veneers
bull Minimal loss of tooth structure
bull 4 parameters checked for the success of treatment
bull Inclusion of specific score of fluorosis for comparing the results
bull Maximum 3 appointments needed
CRITICAL ANALYSIS
Pros Cons
REFERENCES
bull Gurgan S Cakir FY Yazici E Different light-activated in officebleaching
systems Lasers Med Sci 201025817-22
bull Train TE McWhorter AG Seale NSWilson CF Guo IY Examination of
esthetic improvement and surface alteration following microabrasion in
fluorotic human incisors in vivoPediatr dent 199618353-62
bull Loguercio AD Correia LD Zago C Tagliari D Neumann E Gomes OM et al
Clinical effectiveness of two microabrasion materials materials for the
removal of enamel flurosis stains Oper Dent 200732531-8
4
3
Oral Sedation
Advantages
1 Almost universally accepted and the easiest method
2 Decreased incidence and severity of adverse reaction
3 Low cost
Disadvantages
1 Absorption is variable
2 Prolonged latent period(30 min)
3 Reversal of any unwanted effect is also difficult
4 Inability to readily lighten or deepen the level of sedation
5 Prolonged duration of action
Rectal Sedation
Advantages 1 Incidence and intensity of
drug related side effects is minimized
2 Drug absorption occurs from the large intestine directly into the circulation
3 The lack of a needle syringe or other equipment
4 The ease of administration
5 The low cost
Disadvantages
1 Inconvenience to the administrator amp pt
2 The variable absorption of drugs from the large intestine
3 The slow onset of action amp the relatively long duration of action
4 Inability to titrate the drug dosage
5 The inability to reverse the action of the drug the prolonged recovery
Intranasal sedation
Advantages
Rapid onset (10 ndash 15 min)
Simple amp relatively painless
Less pt cooperation is required
Absorbed directly into the C V S
Intranasal sedation
Disadvantages
1 Dependence on nasal mucous membrane
2 Shorter duration of action(40-60min)
3 Multiple dosage may be necessary
Drugs
Midazolam ndash 02mgkg
Sufentanil ndash 15 ndash 3 mcgkg
Ketamine ndash 3-6mg kg
Sublingual sedation
Advantages
1 Pt acceptance
2 Rapid onset
3 High bioavailability
Drugs
Oral Transmucosal Fentanyl Citrate (OTFC)
Intramuscular Sedation
Advantages
1 More rapid onset of action
2 Absorbed directly into the C V system
3 More reliable absorption of drug
4 Pt cooperation is not as essential
Disadvantages
1 Time factor ndash its 15 min latent period
2 Pt may not be willing to accept the injection
3 The prolonged duration of action(2-4 hrs more)
4 Possibility of injury to the tissues at the site of injection caused by either the drug or the needle
4
Sites of I M administration
1 Gluteal area
2 Vastus lateralis
3 Mid ndash deltoid area
Drugs
Diazepam
Midazolam
Hydroxyzine
Inhalation Sedation
Advantages
1 The onset of action is more rapid
2 Peak clinical level is achieved rapidly(3-5min) - permit titration
3 Administrator has complete control over the actions of the drug - safety feature
4 No significant over dosage
5 Flexible duration of action
6 Recovery time is rapid amp most complete
7 No injection is required
8 With N2O- O2 it is safe with very few side effects
Disadvantages
1 The initial cost of the equipment is high 2 The continuing cost of the gases is high 3 The equipment occupies considerable space 4 N2O is not a potent agent 5 A degree of cooperation is required from the pt 6 Chronic exposure to N2O is deleterious to the health of
dental personnel
Contraindications
1 Nasal obstruction 2 Cyanosis at rest 3 Poor cooperation 4 1st trimester of pregnancy 5 Fear of masks
I V Sedation
Advantages
1 The onset of action is the most rapid 2 The dosage may be titrated 3 Suitable level of sedation can be provided 4 The recovery period is shorter 5 Side effects are extremely uncommon 6 Control of salivary secretions is possible 7 The gag reflex is diminished 8 Effectively diminishes motor disturbances 9 Provides immediate access to CVS in emergency
Disadvantages
1 Venipuncture is necessary
2 Complication may rise at the site of the venipuncture
3 Monitoring must be more intensive
4 Recovery is not complete at the end of the procedure
5 Reversal of sedation is difficult
5
N2O-O2 (Relative Analgesia)
colorless sweet smelling gas
Pharmacokinetics
Absorption through pulmonary epithelium
It is approx 15 times as soluble as is nitrogen It replaces nitrogen in blood
It is carried in solution in plasma of the blood
It is not metabolized by the body
Elimination ndash majorndash lungs minor --- skin
perspiration urine and intestinal gas
Pharmacodynamics
Dose related
10 ndash 25 Lightheaded
Changes in visual amp auditory sensation
Tingling of hands amp feet
Suffusing warmth
Remote from the immediate environment
Reduced anxiety
25-50 max analgesic properties and aberration of vision hearing and proprioception mild drowsiness euphoria amnesia and increased sleepiness and dreams
35 conc will achieve maximum analgesia
bull CNS
ndash Cerebrum-primarily affected
ndash Safe but weak anesthetic agent
bull RESPIRATORY SYSTEM
ndash Increased Tidal and minute volumes
bull CARDIOVASCULAR SYSTEM
ndash 2 studies ndash decreased cardiac output
bull FETAL SYSTEMS
ndash Miscarriage in humans
bull OTHER SYSTEMS
ndash Depression of spinal reflexes increase muscle tone indicates stage of delirium
ndash Muscle rigidity-narcotics + nitrous oxide
ndash Nausea and vomitting - GIT
ndash HEMATOPOIESIS ----- prolonged exposure
Adverse reactions and toxicity
EMOTIONAL REACTIONS
DREAMS HALLUCINATIONS
No acute toxicity
Chronic toxicity ndash bone marrow
depression
PROCEDURE
Diffusion Hypoxia
Sevoflurane
A fluorinated derivative of isopropyl ether ndash synthesized in 1970
Potent anaesthetic agent with rapid uptake amp speedy recovery
Day-case surgery
Problem
Attaching vaporiser to any of the currently available machine
BENZODIAZEPINES
Diazepam 1961 lipid soluble
Uses-alcoholism epilepsy labor tetanus and cerebral palsy
- sedation and amnesia
- varieties of neurosis amp anxiety states
Pharmacokinetics
Orally Rectal IMIV or SC
Well absorbed through GIT
Excretion in urine
6
bull Pharmacodynamics
ndash Depress the brain stem reticular system and the limbic system thalamus and hypothalamus
ndash It is a centrally acting muscle relaxant Has anti-convulsant properties
Adverse reaction amp toxicity
ndash Confusion nausea headache increased appetite decreased salivation and jaundice Thrombophlebitis
ndash Rebound phenomenon
ndash Toxicity drowsiness confusion sleep and coma
Dosage Oral or Rectal ndash 02-05mgkg
Maximum single dose 10mg
IV- 025mgkg
Supplied Tablets 2 5 10 mg
Suspension ndash 5mg
Midazolam Water soluble ndash non-irritant
Oral IM IV
Metabolism- liver
Onset IV 3 -5mins
oral 20 ndash 30mins
Oral administration anxious patients requiring relatively short dental procedure
No rebound phenomenon
Better anxiolysis amp amnesia (retrograde amnesia)
Adverse effects Respiratory depression
dose dependant apnea
Dosage Oral ndash 025 to 1mgkg to maximum single dose 20mg
IM ndash 01 to 015mgkg to a maximum of 10mg
IV ndash slow IV
Supplied Syrup ndash 2mgml
Injectable ndash 1mgml amp 5mgml vials
Flumazenil specific benzodiazepines antagonist
selectively inhibits CNS effects
IV administration amp not recommended below 18yrs of age
02mg over 15 seconds after 45seconds 02mg then after 60seconds to maximum of 1mg
Sedative-Hypnotics
Barbiturates First truly effective drugs for the management of anxiety Generalized CNS depressants Produce dose dependent effects
Sedation ---- sleep ---- GA ---- coma
Suppress the CNS and result in sedation and amnesia Advantages
Rapid onset and short duration Disadvantages
no analgesic effect and possible hypotension Must be used with caution in trauma patients because they may cause
apnea and hypoventilation
DOSE Pentobarbital Sodium 100mg Secobarbital Sodium 100 to 200mg Children 30 to 100mg
bull Chloral Hydrates (Mickey Finn Knock out drops ) First synthesized in 1832 first member of the hypnotic group of drugs
Widely used as conscious sedation agent
Properties
Unpleasant taste
Nausea vomiting
Quite irritating to skin and to mucous membranes
GI irritation
Dosages Individualized for each patient 25 ndash 50mgkg
maximum of 1g
Supplied oral capsule ndash 500mg
oral solution ndash 250 amp 500mg5ml
Rectal suppositories ndash 324 amp 648mg
Narcotics
Do produce sedation amp euphoria greater in children
LA is required but dose should be decreased
Meperidine Synthetic opiate agonist
Very water soluble
Orally SC IM or IV
Peak effect by oral 1 hr amp lasts upto 4 hrs
Adverse reactions
-Seizures
-Extreme caution in hepatic or renal diseases or history of seizures
7
Dosage Oral SC or IM ndash 1to 22mgkg not to exceed 100 mg
Supplied Oral Tablets ndash 50 amp 100mg
Oral Syrup ndash 50mgml
Parental solution ndash 25 50 75 amp 100mgml
Fentanyl
Synthetic opiate narcotic analgesic
Very potent 01mg = 10mg Morophine75mg Meperidine
Pharmacokinetics
IV IM SM
Metabolized in liver Excreted in urine
Fentanyl Onset ndash 7 to 15mins
Duration ndash 1 to 2 hrs
Pharmacodynamics
Respiratory depression RR but returns to normal rapidly Tidal volume amp response to co2 depressed for extended period
Apnea
Less emetic than meperidine
NOT RECOMMENDED IN CHILDREN BELOW 2yrs
Dosage 0002 to 0004mgkg
Supplied 005mgml in 2 amp 5ml ampoules
Reversal drug Naloxone
Semisynthetic opiate antagonist
No agonist activity
Onset 2 to 5mins SC or IM amp 1 to 2mins IV
Reversal 45mins
Pt should be kept under continual surveillance
Adverse reaction nausea vomiting sweating hypotension hypertension ventricular tachycardia fibrillation
Dosage IV SC IM 001mgkg then 01mgkg every 2- 3mins maximum 2mg
Supplied 002 004 1mg solutions
Antihistamines
Hydroxyzine
Oral or IM
Effect ndash 15 ndash 30mins
Half-life ndash 3 hrs
Uses
To relieve anxiety
Used as an anti-histamine
Used to control nausea and vomiting including that associated with motion sickness and pregnancy
Adverse reaction dry mouth drowsiness hypersentivity
Dosage Oral ndash 1 to 2mgkg
IM ndash 11mgkg
Promethazine Oral or IM Onset 15 to 60mins Duration 4 to 6 hrs Uses
To prevent and treat nausea and vomiting associated with motion pregnancy or surgery
Produces sedation and reduce swelling pain and trismus
Lower seizure threshold Adverse reaction dry mouth blurred vision thickening of bronchial secretions Dosage OralIM ndash 05-11mgkg
maximum 25 mg
Diphenhydramine
Oral IM IV
Onset -1hr
Duration ndash 4 to 6 hr
Metabolized in liver
Adverse reaction disturbed coordination thickening of bronchial secretions
Dosage Oral IM IV ndash 1 to 15mgkg
maximum 50mg
Tranquilizers
Major tranquilizer antipsychotic produce calmness control symptoms of psychoses cause reversible extra pyramidal symptoms and do not tend to cause habituation
Minor tranquilizer antianxiety agents also cause calmness do not cause extrapyramidal symptoms Used in conditions like nervous tension and mild depression
8
Classification
Antipsychotics
Phenothiazine derivatives
Chlorpromazine promazine
Butryophenones
Haloperidol
Rauwolfia alkaloids
Reserpine
Antianxiety drugs
Propyl alcohol derivatives
Meprobamate
Benzodiazepine derivatives
Diazepam
Miscellaneous compounds
Hydroxyzine
Meprobamate
White crystalline powder slightly bitter in taste
Only administered orally
Peak blood concentration ----1 to 3hrs
10 ---------excreted unchanged Rest --- excreted as a oxidized derivative or as a glucoronide
Uses
To relieve day time anxiety
Induce sleep in insomniacs
To reduce anxiety associated with dental treatment
Anti-convulsant ndash petit mal epilepsy
Adverse reaction leucopenia acute non-thrombocytopenic purpura ecchymoses eosinophilia edema adenopathy
Dosage Childrengt 6yrs 100 to 200mg
Not recommended for children under 6yrs
Monitoring during sedation
1 Pulse
2 Blood pressure
3 ECG
4 Respiration
5 Temperature
Pulse
Manual Electronic
bull Radial Brachial
bull Facial labial
Blood pressure
ndash Stethoscope amp sphygmomanometer
ndash Automatic devices
ndash Direct cannulation of an artery ndash very accurate
Electrocardiograph
Heart rate rhythm myocardial function
9
Respiration
ndash Monitoring respiratory rate
ndash Observing the rise amp fall of the chest wall
ndash Observing the color of mucous membrane
ndash Observing the inflation amp deflation of the reservoir bag
Devices for monitoring respiration
1 The Precordial pretracheal stethoscope
2 The esophageal stethoscope
ndash Respiratory rate
ndash Heart rate
ndash Any abnormal sounds
Pulse Oximeter
ndash Oxygen saturation
ndash Heart rate
ndash Oxisensor site
ndash Fingers
ndash Toe
ndash Ear lobe
Mechanism
Oxygenated Hb ndash red light
Deoxygenated Hb- infrared light
Tissue pressure from arterial pulse (plethysmography)
Advantages
ndash Safe amp noninvasive
ndash Simple to use
ndash Information is rapidly available for clinical decision
ndash Indirectly indicates respiratory adequacy
Disadvantages
ndash Finger probes can get dislodged
ndash Emitted light source may cause burning
ndash Non reusable probes are expensive
ndash Does not directly determine airway patency
Capnography
1 The presence absence of air flow
2 Indicates depth amp adequacy of respiration
3 Continues analysis of the co2 content of the respired air ndash indicates respiratory adequacy
Temperature
ndash Disposable nondisposable thermometer
ndash Esophageal rectal temp probe
10
Discharge criteria
Cardiovascular function is satisfactory amp stable
Airway patency is uncompromised amp satisfactory
Pt is easily arousable amp protective reflexes intact
State of hydration is adequate
Pt can talk if applicable
Pt can sit unaided if applicable
Pt can ambulate with minimal assistance if applicable
Presedation level of responsiveness achieved
Responsible individual is available
1
PULP THERAPY OF VITAL TEETH
DR MITAKSHARA NIRWAN
Contents
Indirect pulp capping
Direct pulp capping
Medications amp materials used in pulp capping
Pulpotomy
MTA
Apexogenesis
INDIRECT PULP CAPPING
Pieter Van Forest - first to speak about root canal therapy
Glove designed instruments that could prepare a canal to a certain size and taper(1910)
Indirect pulp capping is defined as a procedure where in small amount of carious dentin is retained in
deep areas of cavity to avoid exposure of pulp followed by placement of a suitable medicament and
restorative material that seals off the carious dentin and encourages pulp recovery (Ingle)
A procedure in which only the gross caries is removed from the lesion and the cavity is sealed for a
time with a biocompatible material (McDonald)
Objective of indirect pulp capping
These were given by Eidelman in 1965
bull Arresting the carious process
bull Promoting dentin sclerosis
bull Stimulating formation of tertiary dentin
bull Remineralization of carious dentin
Layers of Carious Dentin Indications of Indirect Pulp Capping
History
Mild pain associated with eating
Negative history of spontaneous extreme pain
Clinical Examination
Deep carious lesion which are close tobut not involving the pulp in vital primary or young
permanent teeth
No mobility
Nominal pulp inflammationdefinite layer of affected dentin after removal of infected dentin
Radiographic examination
Normal lamina dura amp PDL space
No radiolucency around the apices
2
Contraindications of Indirect Pulp Capping
History
Sharp penetrating pulpalgia
Prolonged spontaneous pain especially at night
Clinical examination
Mobility of tooth
Discoloration of tooth
Negative reaction of electric pulp testing
Radiographic examination
Definite pulp exposure
Break in the lamina dura
Radiolucency around the apices
Widened PDL space
Treatment procedure
Sequelae of Indirect Pulp Capping Three distinct types of new dentin formation take place
1 Cellular fibrillar dentinmdashfirst 2 months
2 Globular dentinmdash3 months
3 Tubular dentin (uniform mineralized dentin)
bull 15th of reparative dentin formation begins in less than 30 days
bull After 3 months 01 mm is formed
DIRECT PULP CAPPING Defined by Kopel (1992) as the placement of a medicament or non medicated material on a pulp that
has been exposed in course of excavating the last portions of deep dentinal caries or as a result of
trauma
Objective
To create new dentin in the area of the exposure and subsequent healing of the pulp
Rationale
achieve a biologic closure of the exposure site by deposition of hard tissue barrier (dentin bridge)
between pulp tissue and capping material thus walling off the
INDICATIONS
Small mechanical exposure
Easily controlled haemorrhage
Bright red haemorrhage
True pinpoint exposure
CONTRAINDICATIONS
Severe toothache at night
Spontaneous pain
Tooth mobility
Radiographic appearance of pulp periradicular de- generation
Excess of hemorrhage at the time of exposure Serous exudate from the exposure
Externalinternal root resorption
Swellingfistula
Histological Changes after Pulp Capping
These were illustrated be Glass and Zander in 1949
After 24 hours Necrotic zone adjacent to calcium
hydroxide paste is separated from healthy pulp
tissue by a deep staining basophilic layer
After 7 days Increase in cellular and fibroblastic
activity
After 14 days Partly calcified fibrous tissue lined by
odontoblastic cells is seen below the calcium
proteinate zone disappearance of necrotic zone
After 28 days Zone of new dentin
3
Medications and Materials Used for Pulp Capping Calcium hydroxide
Corticosteroids amp antibiotics
Inert materials
Collagen fibers
4-META adhesive
Direct bonding
Isobutyl cyanoacrylate
Denatured albumin
Mineral trioxide aggregate
Laser
Bone morphogenic protein
PULPOTOMY
Finn (1995) defined it as the complete removal of the coronal portion of the dental pulp
followed by placement of a suitable dressing or medicament that will promote healing and
preserve vitality of the tooth
American Academy of Pediatric Dentistry (1998) defined pulpotomy as the amputation of
affected infected coronal portion of the dental pulp preserving the vitality and function of the
remaining part of radicular pulp
Objectives
bull Removal of inflamed and infected coronal pulp at the site of exposure thus preserving the vitality of the
radicular pulp and allowing it to heal
bull Maintain the tooth in the dental arch
Rationale
bull Radicular pulp is healthy and capable of healing after surgical amputation of the infected coronal pulp
bull Preserves vitality of the radicular pulp
bull Maintains tooth in a physiologic condition
Indications of Pulpotomy bull Mechanical pulp exposure in primary teeth
bull Teeth showing a large carious lesion but free of radicular pulpitis
bull History of only spontaneous pain
bull Hemorrhage from exposure sites bright red and can be controlled
bull Absence of abscess or fistula
bull No interradicular bone loss
bull No interradicular radiolucency
Contraindications of Pulpotomy bull Persistent toothache
bull Tenderness on percussion
bull Root resorption more than 13rd of root length
bull Large carious lesion with nonrestorable crown
bull Highly viscous sluggish hemorrhage from canal orifice which is uncontrollable
bull Medical contradictions like heart disease immuno compromised patient
bull Swelling or fistula
bull External or internal resorption
bull Pathological mobility
bull Calcification of pulp
Classification of pulpotomy
4
Formocresol Pulpotomy
Iby BUCKLEY in 1904
Sweet (1930) Formulated multi visit technique
Doyle (1962) Advocated 2 sitting procedure (complete devitalization)
Spedding (1965) Gave 5 minute protocol (partial devitali- zation)
Venham (1967) Proposed 15 seconds procedure
Current concept uses 4 minutes of application time
Composition of formocresol Buckleyrsquos Formula
bull Cresol ndash 35 percent
bull Glycerol ndash 15 percent
bull Formaldehyde ndash 19 percent
bull Water ndash 31 percent
Mechanism of Action
It prevents tissue autolysis by bonding to the proteins Bonding is of peptide groups of side chain amino acids and is a reversible process accomplished without
changing the basic structure of protein molecules
Histological Changes
bull Demonstrated by Mass and Zilbermann11 in 1933 and also by Massler and Mansokhani in 1959
bull Immediately the pulp becomes fibrous and acidophillic
bull Seven to fourteen days Three zones appear
a broad eosinophilic zone of fixation
b broad pale-staining zone of atrophy with poorcellular definition
c broad zone of inflammation extending apically into normal pulp tissue
bull One yearndash Progressive apical movement of these zones with only acidophillic zone left at the end of 1 year
Modified Formocresol Pulpotomy
Used by TRASK(1972)
The technique is identical to that described for primary teeth except that the formocresol pellet is
sealed permanently in the tooth
Two-visit Devitalization Pulpotomy
Indications
bull There is evidence of sluggish bleeding at the amputation site that is difficult to control
bull Pus in the chamber but none at the amputation site
bull There is thickening of the PDL
bull History of pain
Contraindications
bull Nonrestorable tooth
bull Tooth with necrotic pulp
5
Glutaraldehyde Pulpotomy
It was first suggested by S Gravenmade Introduced by Kopel in 1979
Mechanism of Action
bull Glutaraldehyde produces rapid surface fixation of the underlying pulpal tissue
bull A narrow zone of eosinophilic stained and compressed fixed tissue is found directly beneath the area of application which blends into vital normal appearing tissue apically
bull With time the glutaraldehyde fixed zone is replaced by macrophagic action with dense collagenous tissue thus the entire root canal tissue is vital
Cvekrsquos Pulpotomy
bull This is also called as calcium hydroxide pulpotomy or young permanent partial pulpotomy
bull This was proposed by Mejare and Cvek16 in 1978
bull Indicated in young permanent teeth where the pulp is exposed by mechanical or bacterial means and the
remaining radicular tissue is judged vital by clinical and radiographic criteria whereas the root closure is
notcomplete
MINERAL TRIOXIDE AGGREGATE (MTA) Torabinejad described the physical and chemical properties of MTA in 1995
It is ash colored powder made primarily of fine hydrophilic particles of
1 tricalcium aluminate
2 tricalcium silicate
3 silicate oxide
4 tricalcium oxide
5 bismuth dioxide
Hydration of the powder results in a colloidal gel composed of calcium oxide crystals in an amorphous
structure This gel solidifies into a hard structure in less than three hours
PROPERTIES OF MTA
It is biocompatible material and its sealing ability is better than that of amalgam or ZOE
Initial pH is 102 and set pH is 125
The setting time of cement is 4 hours
The compressive strength is 70 MPA which is comparable with that of IRM
Low cytotoxicity ndash It presents with minimal inflammation if extended beyond the apex
Mineral trioxide aggregate (MTA) has demonstrated the ability to induce hard-tissue formation in
pulpal tissues and it promotes rapid cell growth
APEXOGENESIS
It is defined as the treatment of a vital pulp by capping or pulpotomy in order to permit continued
growth of the root and closure of the open apex
Rationale
Maintenance of integrity of the radicular pulp tissue to allow for continued root growth
Indications
bull Indicated for traumatized or pulpally involved vital permanent tooth when root apex is incompletely formed
bull No history of spontaneous pain
bull No sensitivity on percussion
bull No hemorrhage
bull Normal radiographic appearance
Contraindications
bull Evidence that radicular pulp has undergone degenerative changes
bull Purulent drainage
bull History of prolonged pain bull Necrotic debris in canal
bull Periapical radiolucency
6
1
Gupta A Dhingra R Chaudhari P Gupta A
Department of Paedodontics and Preventive Dentistry Faculty of Dental Sciences SGT University Gurgaon Haryana India
Journal of Indian Society of Pedodontics and Preventive Dentistry
Volume 35 I Issue 3 I July-September 2017
A COMPARISION OF VARIOUS MINIMALLY
INVASIVE TECHNIQUES FOR THE REMOVAL
OF DENTAL FLUOROSIS STAINS IN
CHILDREN
DR MITAKSHARA NIRWAN
CONTENTS
bull Introduction
bull Aims
bull Materials and Methods
bull Results
bull Discussion
bull Conclusion
bull Critical analysis
bull References
INTRODUCTION
bull Dental fluorosis is a developmental disturbance of dental enamel caused by
successive exposure to high concentrations of fluoride during tooth
development
bull Various methods of therapy are advocated for the treatment of fluorosis -
stained teeth which range from invasive ceramic veneer bonding restorations
to abrasive chemical treatments
bull The combination of dental bleaching techniques and microabrasion appears
as an excellent conservative solution to reestablish health in fluorosis
affected teeth
AIMS
bull The aim of the study was to evaluate and compare the effectiveness of
minimally invasive techniques for the removal of dental fluorosis
stains in children in vivo
MATERIALS AND METHODS
Patients visiting the department of Pedodontics and Preventive dentistry
Faculty of Dental Sciences SGT University Gurgaon
bull Sample size 90 patients
bull Age group 10 -17 years
bull Caries cracks or periodontal
disease on anterior teeth
bull Abscess draining sinus
cellulitis
bull Non vital teeth
hypersensitive exposed
crevices
bull Orthodontic appliance
bull Past history of bleaching
bull At least two permanent
maxillary anterior teeth
bull TSIF of score 4
bull Free of systemic diseases
Inclusion criteria Exclusion criteria
2
Groups
Group A In office bleaching with 35 hydrogen peroxide( Pola Office
Bleaching kit) activated by light emitting diode (LED) bleaching unit
(35 HP)
Group B Enamel microabrasion (EM) (PREMA Enamel Microabrasion
System) followed by in-office bleaching with 44 carbamide peroxide
gel (EM)
Group C In-office bleaching with 5 sodium hypochlorite (5
NaOCl)
A baseline colour evaluation was done by taking digital photograph of
the maxillary anterior teeth
RESULTS
Group 1
Colour stability
Group 2 Group 3
Tooth sensitivity
Tooth sensitivity values were taken before the treatment
which was compared to immediate postoperative and follow
up visits It was checked using an electric pulp tester
maximum
moderate
least
immediately
group 2
group 1
group 3
1 month
group 2
group 1
group 3
3 month
group 2
group 1
group 3
Patient satisfaction score
Satisfaction was assessed on visual analog scale
Range 1 to 5
Groups percentage of patients
who were satisfied with
the treatment
Number of patients
who reported slight
reappearance of colour
Group 1
90
7
Group 2
83
8
Group 3
73
7
3
Number of Appointments
Groups One sitting Two sittings Three
sittings
Group 1
25
4
1
group 2
26
3
1
Group 3
30
0
0
DISCUSSION
bull Hydrogen peroxide is capable of penetrating the tooth osmosis and through porosities and cracks subsequently acting directly on the pigmented molecules
bull Gurgan et al investigated 3 different light systems and found out that diode laser system with gave best tooth whitening and least tooth sensitivity
bull In the EM group the surface reflects and refracts light from the surface in such way that mild imperfections in underlying enamel are camouflaged While the highly polished surface of enamel enhances the aesthetic appearance
bull Train et al and Loguercio et al also had the similar results in their studies with EM mild fluorosis showed best results moderate showed moderate results while it had little effect on severe fluorosis
bull NaOCl was only effective on mild stains while moderate and severe
stains could only be lightened to quite an extent but could not be
completely removed
bull When NaOCl comes in contact with hypomineralized and discoloured
enamel it degrades and removes the chromogenic organic material
located on the enamel surface
CONCLUSION
bull It was concluded that esthetic appearance of teeth mild fluorosis can
be achieved by bleaching and microabrasion But in cases of
moderate fluorosis a combination of any of theses modalities can be
used
bull As no special maintenance precautions are required these maybe be
considered as an interesting alternative to conventional operative
treatment
bull Focuses on only TSIF of 4
bull Electric pulp testing is not the
right method to check for
sensitivity
bull Tooth Sensitivity changes
from person to person
bull Food habits can cause
staining of the teeth
bull Minimally invasive
bull Cheaper to veneers
bull Minimal loss of tooth structure
bull 4 parameters checked for the success of treatment
bull Inclusion of specific score of fluorosis for comparing the results
bull Maximum 3 appointments needed
CRITICAL ANALYSIS
Pros Cons
REFERENCES
bull Gurgan S Cakir FY Yazici E Different light-activated in officebleaching
systems Lasers Med Sci 201025817-22
bull Train TE McWhorter AG Seale NSWilson CF Guo IY Examination of
esthetic improvement and surface alteration following microabrasion in
fluorotic human incisors in vivoPediatr dent 199618353-62
bull Loguercio AD Correia LD Zago C Tagliari D Neumann E Gomes OM et al
Clinical effectiveness of two microabrasion materials materials for the
removal of enamel flurosis stains Oper Dent 200732531-8
4
4
Sites of I M administration
1 Gluteal area
2 Vastus lateralis
3 Mid ndash deltoid area
Drugs
Diazepam
Midazolam
Hydroxyzine
Inhalation Sedation
Advantages
1 The onset of action is more rapid
2 Peak clinical level is achieved rapidly(3-5min) - permit titration
3 Administrator has complete control over the actions of the drug - safety feature
4 No significant over dosage
5 Flexible duration of action
6 Recovery time is rapid amp most complete
7 No injection is required
8 With N2O- O2 it is safe with very few side effects
Disadvantages
1 The initial cost of the equipment is high 2 The continuing cost of the gases is high 3 The equipment occupies considerable space 4 N2O is not a potent agent 5 A degree of cooperation is required from the pt 6 Chronic exposure to N2O is deleterious to the health of
dental personnel
Contraindications
1 Nasal obstruction 2 Cyanosis at rest 3 Poor cooperation 4 1st trimester of pregnancy 5 Fear of masks
I V Sedation
Advantages
1 The onset of action is the most rapid 2 The dosage may be titrated 3 Suitable level of sedation can be provided 4 The recovery period is shorter 5 Side effects are extremely uncommon 6 Control of salivary secretions is possible 7 The gag reflex is diminished 8 Effectively diminishes motor disturbances 9 Provides immediate access to CVS in emergency
Disadvantages
1 Venipuncture is necessary
2 Complication may rise at the site of the venipuncture
3 Monitoring must be more intensive
4 Recovery is not complete at the end of the procedure
5 Reversal of sedation is difficult
5
N2O-O2 (Relative Analgesia)
colorless sweet smelling gas
Pharmacokinetics
Absorption through pulmonary epithelium
It is approx 15 times as soluble as is nitrogen It replaces nitrogen in blood
It is carried in solution in plasma of the blood
It is not metabolized by the body
Elimination ndash majorndash lungs minor --- skin
perspiration urine and intestinal gas
Pharmacodynamics
Dose related
10 ndash 25 Lightheaded
Changes in visual amp auditory sensation
Tingling of hands amp feet
Suffusing warmth
Remote from the immediate environment
Reduced anxiety
25-50 max analgesic properties and aberration of vision hearing and proprioception mild drowsiness euphoria amnesia and increased sleepiness and dreams
35 conc will achieve maximum analgesia
bull CNS
ndash Cerebrum-primarily affected
ndash Safe but weak anesthetic agent
bull RESPIRATORY SYSTEM
ndash Increased Tidal and minute volumes
bull CARDIOVASCULAR SYSTEM
ndash 2 studies ndash decreased cardiac output
bull FETAL SYSTEMS
ndash Miscarriage in humans
bull OTHER SYSTEMS
ndash Depression of spinal reflexes increase muscle tone indicates stage of delirium
ndash Muscle rigidity-narcotics + nitrous oxide
ndash Nausea and vomitting - GIT
ndash HEMATOPOIESIS ----- prolonged exposure
Adverse reactions and toxicity
EMOTIONAL REACTIONS
DREAMS HALLUCINATIONS
No acute toxicity
Chronic toxicity ndash bone marrow
depression
PROCEDURE
Diffusion Hypoxia
Sevoflurane
A fluorinated derivative of isopropyl ether ndash synthesized in 1970
Potent anaesthetic agent with rapid uptake amp speedy recovery
Day-case surgery
Problem
Attaching vaporiser to any of the currently available machine
BENZODIAZEPINES
Diazepam 1961 lipid soluble
Uses-alcoholism epilepsy labor tetanus and cerebral palsy
- sedation and amnesia
- varieties of neurosis amp anxiety states
Pharmacokinetics
Orally Rectal IMIV or SC
Well absorbed through GIT
Excretion in urine
6
bull Pharmacodynamics
ndash Depress the brain stem reticular system and the limbic system thalamus and hypothalamus
ndash It is a centrally acting muscle relaxant Has anti-convulsant properties
Adverse reaction amp toxicity
ndash Confusion nausea headache increased appetite decreased salivation and jaundice Thrombophlebitis
ndash Rebound phenomenon
ndash Toxicity drowsiness confusion sleep and coma
Dosage Oral or Rectal ndash 02-05mgkg
Maximum single dose 10mg
IV- 025mgkg
Supplied Tablets 2 5 10 mg
Suspension ndash 5mg
Midazolam Water soluble ndash non-irritant
Oral IM IV
Metabolism- liver
Onset IV 3 -5mins
oral 20 ndash 30mins
Oral administration anxious patients requiring relatively short dental procedure
No rebound phenomenon
Better anxiolysis amp amnesia (retrograde amnesia)
Adverse effects Respiratory depression
dose dependant apnea
Dosage Oral ndash 025 to 1mgkg to maximum single dose 20mg
IM ndash 01 to 015mgkg to a maximum of 10mg
IV ndash slow IV
Supplied Syrup ndash 2mgml
Injectable ndash 1mgml amp 5mgml vials
Flumazenil specific benzodiazepines antagonist
selectively inhibits CNS effects
IV administration amp not recommended below 18yrs of age
02mg over 15 seconds after 45seconds 02mg then after 60seconds to maximum of 1mg
Sedative-Hypnotics
Barbiturates First truly effective drugs for the management of anxiety Generalized CNS depressants Produce dose dependent effects
Sedation ---- sleep ---- GA ---- coma
Suppress the CNS and result in sedation and amnesia Advantages
Rapid onset and short duration Disadvantages
no analgesic effect and possible hypotension Must be used with caution in trauma patients because they may cause
apnea and hypoventilation
DOSE Pentobarbital Sodium 100mg Secobarbital Sodium 100 to 200mg Children 30 to 100mg
bull Chloral Hydrates (Mickey Finn Knock out drops ) First synthesized in 1832 first member of the hypnotic group of drugs
Widely used as conscious sedation agent
Properties
Unpleasant taste
Nausea vomiting
Quite irritating to skin and to mucous membranes
GI irritation
Dosages Individualized for each patient 25 ndash 50mgkg
maximum of 1g
Supplied oral capsule ndash 500mg
oral solution ndash 250 amp 500mg5ml
Rectal suppositories ndash 324 amp 648mg
Narcotics
Do produce sedation amp euphoria greater in children
LA is required but dose should be decreased
Meperidine Synthetic opiate agonist
Very water soluble
Orally SC IM or IV
Peak effect by oral 1 hr amp lasts upto 4 hrs
Adverse reactions
-Seizures
-Extreme caution in hepatic or renal diseases or history of seizures
7
Dosage Oral SC or IM ndash 1to 22mgkg not to exceed 100 mg
Supplied Oral Tablets ndash 50 amp 100mg
Oral Syrup ndash 50mgml
Parental solution ndash 25 50 75 amp 100mgml
Fentanyl
Synthetic opiate narcotic analgesic
Very potent 01mg = 10mg Morophine75mg Meperidine
Pharmacokinetics
IV IM SM
Metabolized in liver Excreted in urine
Fentanyl Onset ndash 7 to 15mins
Duration ndash 1 to 2 hrs
Pharmacodynamics
Respiratory depression RR but returns to normal rapidly Tidal volume amp response to co2 depressed for extended period
Apnea
Less emetic than meperidine
NOT RECOMMENDED IN CHILDREN BELOW 2yrs
Dosage 0002 to 0004mgkg
Supplied 005mgml in 2 amp 5ml ampoules
Reversal drug Naloxone
Semisynthetic opiate antagonist
No agonist activity
Onset 2 to 5mins SC or IM amp 1 to 2mins IV
Reversal 45mins
Pt should be kept under continual surveillance
Adverse reaction nausea vomiting sweating hypotension hypertension ventricular tachycardia fibrillation
Dosage IV SC IM 001mgkg then 01mgkg every 2- 3mins maximum 2mg
Supplied 002 004 1mg solutions
Antihistamines
Hydroxyzine
Oral or IM
Effect ndash 15 ndash 30mins
Half-life ndash 3 hrs
Uses
To relieve anxiety
Used as an anti-histamine
Used to control nausea and vomiting including that associated with motion sickness and pregnancy
Adverse reaction dry mouth drowsiness hypersentivity
Dosage Oral ndash 1 to 2mgkg
IM ndash 11mgkg
Promethazine Oral or IM Onset 15 to 60mins Duration 4 to 6 hrs Uses
To prevent and treat nausea and vomiting associated with motion pregnancy or surgery
Produces sedation and reduce swelling pain and trismus
Lower seizure threshold Adverse reaction dry mouth blurred vision thickening of bronchial secretions Dosage OralIM ndash 05-11mgkg
maximum 25 mg
Diphenhydramine
Oral IM IV
Onset -1hr
Duration ndash 4 to 6 hr
Metabolized in liver
Adverse reaction disturbed coordination thickening of bronchial secretions
Dosage Oral IM IV ndash 1 to 15mgkg
maximum 50mg
Tranquilizers
Major tranquilizer antipsychotic produce calmness control symptoms of psychoses cause reversible extra pyramidal symptoms and do not tend to cause habituation
Minor tranquilizer antianxiety agents also cause calmness do not cause extrapyramidal symptoms Used in conditions like nervous tension and mild depression
8
Classification
Antipsychotics
Phenothiazine derivatives
Chlorpromazine promazine
Butryophenones
Haloperidol
Rauwolfia alkaloids
Reserpine
Antianxiety drugs
Propyl alcohol derivatives
Meprobamate
Benzodiazepine derivatives
Diazepam
Miscellaneous compounds
Hydroxyzine
Meprobamate
White crystalline powder slightly bitter in taste
Only administered orally
Peak blood concentration ----1 to 3hrs
10 ---------excreted unchanged Rest --- excreted as a oxidized derivative or as a glucoronide
Uses
To relieve day time anxiety
Induce sleep in insomniacs
To reduce anxiety associated with dental treatment
Anti-convulsant ndash petit mal epilepsy
Adverse reaction leucopenia acute non-thrombocytopenic purpura ecchymoses eosinophilia edema adenopathy
Dosage Childrengt 6yrs 100 to 200mg
Not recommended for children under 6yrs
Monitoring during sedation
1 Pulse
2 Blood pressure
3 ECG
4 Respiration
5 Temperature
Pulse
Manual Electronic
bull Radial Brachial
bull Facial labial
Blood pressure
ndash Stethoscope amp sphygmomanometer
ndash Automatic devices
ndash Direct cannulation of an artery ndash very accurate
Electrocardiograph
Heart rate rhythm myocardial function
9
Respiration
ndash Monitoring respiratory rate
ndash Observing the rise amp fall of the chest wall
ndash Observing the color of mucous membrane
ndash Observing the inflation amp deflation of the reservoir bag
Devices for monitoring respiration
1 The Precordial pretracheal stethoscope
2 The esophageal stethoscope
ndash Respiratory rate
ndash Heart rate
ndash Any abnormal sounds
Pulse Oximeter
ndash Oxygen saturation
ndash Heart rate
ndash Oxisensor site
ndash Fingers
ndash Toe
ndash Ear lobe
Mechanism
Oxygenated Hb ndash red light
Deoxygenated Hb- infrared light
Tissue pressure from arterial pulse (plethysmography)
Advantages
ndash Safe amp noninvasive
ndash Simple to use
ndash Information is rapidly available for clinical decision
ndash Indirectly indicates respiratory adequacy
Disadvantages
ndash Finger probes can get dislodged
ndash Emitted light source may cause burning
ndash Non reusable probes are expensive
ndash Does not directly determine airway patency
Capnography
1 The presence absence of air flow
2 Indicates depth amp adequacy of respiration
3 Continues analysis of the co2 content of the respired air ndash indicates respiratory adequacy
Temperature
ndash Disposable nondisposable thermometer
ndash Esophageal rectal temp probe
10
Discharge criteria
Cardiovascular function is satisfactory amp stable
Airway patency is uncompromised amp satisfactory
Pt is easily arousable amp protective reflexes intact
State of hydration is adequate
Pt can talk if applicable
Pt can sit unaided if applicable
Pt can ambulate with minimal assistance if applicable
Presedation level of responsiveness achieved
Responsible individual is available
1
PULP THERAPY OF VITAL TEETH
DR MITAKSHARA NIRWAN
Contents
Indirect pulp capping
Direct pulp capping
Medications amp materials used in pulp capping
Pulpotomy
MTA
Apexogenesis
INDIRECT PULP CAPPING
Pieter Van Forest - first to speak about root canal therapy
Glove designed instruments that could prepare a canal to a certain size and taper(1910)
Indirect pulp capping is defined as a procedure where in small amount of carious dentin is retained in
deep areas of cavity to avoid exposure of pulp followed by placement of a suitable medicament and
restorative material that seals off the carious dentin and encourages pulp recovery (Ingle)
A procedure in which only the gross caries is removed from the lesion and the cavity is sealed for a
time with a biocompatible material (McDonald)
Objective of indirect pulp capping
These were given by Eidelman in 1965
bull Arresting the carious process
bull Promoting dentin sclerosis
bull Stimulating formation of tertiary dentin
bull Remineralization of carious dentin
Layers of Carious Dentin Indications of Indirect Pulp Capping
History
Mild pain associated with eating
Negative history of spontaneous extreme pain
Clinical Examination
Deep carious lesion which are close tobut not involving the pulp in vital primary or young
permanent teeth
No mobility
Nominal pulp inflammationdefinite layer of affected dentin after removal of infected dentin
Radiographic examination
Normal lamina dura amp PDL space
No radiolucency around the apices
2
Contraindications of Indirect Pulp Capping
History
Sharp penetrating pulpalgia
Prolonged spontaneous pain especially at night
Clinical examination
Mobility of tooth
Discoloration of tooth
Negative reaction of electric pulp testing
Radiographic examination
Definite pulp exposure
Break in the lamina dura
Radiolucency around the apices
Widened PDL space
Treatment procedure
Sequelae of Indirect Pulp Capping Three distinct types of new dentin formation take place
1 Cellular fibrillar dentinmdashfirst 2 months
2 Globular dentinmdash3 months
3 Tubular dentin (uniform mineralized dentin)
bull 15th of reparative dentin formation begins in less than 30 days
bull After 3 months 01 mm is formed
DIRECT PULP CAPPING Defined by Kopel (1992) as the placement of a medicament or non medicated material on a pulp that
has been exposed in course of excavating the last portions of deep dentinal caries or as a result of
trauma
Objective
To create new dentin in the area of the exposure and subsequent healing of the pulp
Rationale
achieve a biologic closure of the exposure site by deposition of hard tissue barrier (dentin bridge)
between pulp tissue and capping material thus walling off the
INDICATIONS
Small mechanical exposure
Easily controlled haemorrhage
Bright red haemorrhage
True pinpoint exposure
CONTRAINDICATIONS
Severe toothache at night
Spontaneous pain
Tooth mobility
Radiographic appearance of pulp periradicular de- generation
Excess of hemorrhage at the time of exposure Serous exudate from the exposure
Externalinternal root resorption
Swellingfistula
Histological Changes after Pulp Capping
These were illustrated be Glass and Zander in 1949
After 24 hours Necrotic zone adjacent to calcium
hydroxide paste is separated from healthy pulp
tissue by a deep staining basophilic layer
After 7 days Increase in cellular and fibroblastic
activity
After 14 days Partly calcified fibrous tissue lined by
odontoblastic cells is seen below the calcium
proteinate zone disappearance of necrotic zone
After 28 days Zone of new dentin
3
Medications and Materials Used for Pulp Capping Calcium hydroxide
Corticosteroids amp antibiotics
Inert materials
Collagen fibers
4-META adhesive
Direct bonding
Isobutyl cyanoacrylate
Denatured albumin
Mineral trioxide aggregate
Laser
Bone morphogenic protein
PULPOTOMY
Finn (1995) defined it as the complete removal of the coronal portion of the dental pulp
followed by placement of a suitable dressing or medicament that will promote healing and
preserve vitality of the tooth
American Academy of Pediatric Dentistry (1998) defined pulpotomy as the amputation of
affected infected coronal portion of the dental pulp preserving the vitality and function of the
remaining part of radicular pulp
Objectives
bull Removal of inflamed and infected coronal pulp at the site of exposure thus preserving the vitality of the
radicular pulp and allowing it to heal
bull Maintain the tooth in the dental arch
Rationale
bull Radicular pulp is healthy and capable of healing after surgical amputation of the infected coronal pulp
bull Preserves vitality of the radicular pulp
bull Maintains tooth in a physiologic condition
Indications of Pulpotomy bull Mechanical pulp exposure in primary teeth
bull Teeth showing a large carious lesion but free of radicular pulpitis
bull History of only spontaneous pain
bull Hemorrhage from exposure sites bright red and can be controlled
bull Absence of abscess or fistula
bull No interradicular bone loss
bull No interradicular radiolucency
Contraindications of Pulpotomy bull Persistent toothache
bull Tenderness on percussion
bull Root resorption more than 13rd of root length
bull Large carious lesion with nonrestorable crown
bull Highly viscous sluggish hemorrhage from canal orifice which is uncontrollable
bull Medical contradictions like heart disease immuno compromised patient
bull Swelling or fistula
bull External or internal resorption
bull Pathological mobility
bull Calcification of pulp
Classification of pulpotomy
4
Formocresol Pulpotomy
Iby BUCKLEY in 1904
Sweet (1930) Formulated multi visit technique
Doyle (1962) Advocated 2 sitting procedure (complete devitalization)
Spedding (1965) Gave 5 minute protocol (partial devitali- zation)
Venham (1967) Proposed 15 seconds procedure
Current concept uses 4 minutes of application time
Composition of formocresol Buckleyrsquos Formula
bull Cresol ndash 35 percent
bull Glycerol ndash 15 percent
bull Formaldehyde ndash 19 percent
bull Water ndash 31 percent
Mechanism of Action
It prevents tissue autolysis by bonding to the proteins Bonding is of peptide groups of side chain amino acids and is a reversible process accomplished without
changing the basic structure of protein molecules
Histological Changes
bull Demonstrated by Mass and Zilbermann11 in 1933 and also by Massler and Mansokhani in 1959
bull Immediately the pulp becomes fibrous and acidophillic
bull Seven to fourteen days Three zones appear
a broad eosinophilic zone of fixation
b broad pale-staining zone of atrophy with poorcellular definition
c broad zone of inflammation extending apically into normal pulp tissue
bull One yearndash Progressive apical movement of these zones with only acidophillic zone left at the end of 1 year
Modified Formocresol Pulpotomy
Used by TRASK(1972)
The technique is identical to that described for primary teeth except that the formocresol pellet is
sealed permanently in the tooth
Two-visit Devitalization Pulpotomy
Indications
bull There is evidence of sluggish bleeding at the amputation site that is difficult to control
bull Pus in the chamber but none at the amputation site
bull There is thickening of the PDL
bull History of pain
Contraindications
bull Nonrestorable tooth
bull Tooth with necrotic pulp
5
Glutaraldehyde Pulpotomy
It was first suggested by S Gravenmade Introduced by Kopel in 1979
Mechanism of Action
bull Glutaraldehyde produces rapid surface fixation of the underlying pulpal tissue
bull A narrow zone of eosinophilic stained and compressed fixed tissue is found directly beneath the area of application which blends into vital normal appearing tissue apically
bull With time the glutaraldehyde fixed zone is replaced by macrophagic action with dense collagenous tissue thus the entire root canal tissue is vital
Cvekrsquos Pulpotomy
bull This is also called as calcium hydroxide pulpotomy or young permanent partial pulpotomy
bull This was proposed by Mejare and Cvek16 in 1978
bull Indicated in young permanent teeth where the pulp is exposed by mechanical or bacterial means and the
remaining radicular tissue is judged vital by clinical and radiographic criteria whereas the root closure is
notcomplete
MINERAL TRIOXIDE AGGREGATE (MTA) Torabinejad described the physical and chemical properties of MTA in 1995
It is ash colored powder made primarily of fine hydrophilic particles of
1 tricalcium aluminate
2 tricalcium silicate
3 silicate oxide
4 tricalcium oxide
5 bismuth dioxide
Hydration of the powder results in a colloidal gel composed of calcium oxide crystals in an amorphous
structure This gel solidifies into a hard structure in less than three hours
PROPERTIES OF MTA
It is biocompatible material and its sealing ability is better than that of amalgam or ZOE
Initial pH is 102 and set pH is 125
The setting time of cement is 4 hours
The compressive strength is 70 MPA which is comparable with that of IRM
Low cytotoxicity ndash It presents with minimal inflammation if extended beyond the apex
Mineral trioxide aggregate (MTA) has demonstrated the ability to induce hard-tissue formation in
pulpal tissues and it promotes rapid cell growth
APEXOGENESIS
It is defined as the treatment of a vital pulp by capping or pulpotomy in order to permit continued
growth of the root and closure of the open apex
Rationale
Maintenance of integrity of the radicular pulp tissue to allow for continued root growth
Indications
bull Indicated for traumatized or pulpally involved vital permanent tooth when root apex is incompletely formed
bull No history of spontaneous pain
bull No sensitivity on percussion
bull No hemorrhage
bull Normal radiographic appearance
Contraindications
bull Evidence that radicular pulp has undergone degenerative changes
bull Purulent drainage
bull History of prolonged pain bull Necrotic debris in canal
bull Periapical radiolucency
6
1
Gupta A Dhingra R Chaudhari P Gupta A
Department of Paedodontics and Preventive Dentistry Faculty of Dental Sciences SGT University Gurgaon Haryana India
Journal of Indian Society of Pedodontics and Preventive Dentistry
Volume 35 I Issue 3 I July-September 2017
A COMPARISION OF VARIOUS MINIMALLY
INVASIVE TECHNIQUES FOR THE REMOVAL
OF DENTAL FLUOROSIS STAINS IN
CHILDREN
DR MITAKSHARA NIRWAN
CONTENTS
bull Introduction
bull Aims
bull Materials and Methods
bull Results
bull Discussion
bull Conclusion
bull Critical analysis
bull References
INTRODUCTION
bull Dental fluorosis is a developmental disturbance of dental enamel caused by
successive exposure to high concentrations of fluoride during tooth
development
bull Various methods of therapy are advocated for the treatment of fluorosis -
stained teeth which range from invasive ceramic veneer bonding restorations
to abrasive chemical treatments
bull The combination of dental bleaching techniques and microabrasion appears
as an excellent conservative solution to reestablish health in fluorosis
affected teeth
AIMS
bull The aim of the study was to evaluate and compare the effectiveness of
minimally invasive techniques for the removal of dental fluorosis
stains in children in vivo
MATERIALS AND METHODS
Patients visiting the department of Pedodontics and Preventive dentistry
Faculty of Dental Sciences SGT University Gurgaon
bull Sample size 90 patients
bull Age group 10 -17 years
bull Caries cracks or periodontal
disease on anterior teeth
bull Abscess draining sinus
cellulitis
bull Non vital teeth
hypersensitive exposed
crevices
bull Orthodontic appliance
bull Past history of bleaching
bull At least two permanent
maxillary anterior teeth
bull TSIF of score 4
bull Free of systemic diseases
Inclusion criteria Exclusion criteria
2
Groups
Group A In office bleaching with 35 hydrogen peroxide( Pola Office
Bleaching kit) activated by light emitting diode (LED) bleaching unit
(35 HP)
Group B Enamel microabrasion (EM) (PREMA Enamel Microabrasion
System) followed by in-office bleaching with 44 carbamide peroxide
gel (EM)
Group C In-office bleaching with 5 sodium hypochlorite (5
NaOCl)
A baseline colour evaluation was done by taking digital photograph of
the maxillary anterior teeth
RESULTS
Group 1
Colour stability
Group 2 Group 3
Tooth sensitivity
Tooth sensitivity values were taken before the treatment
which was compared to immediate postoperative and follow
up visits It was checked using an electric pulp tester
maximum
moderate
least
immediately
group 2
group 1
group 3
1 month
group 2
group 1
group 3
3 month
group 2
group 1
group 3
Patient satisfaction score
Satisfaction was assessed on visual analog scale
Range 1 to 5
Groups percentage of patients
who were satisfied with
the treatment
Number of patients
who reported slight
reappearance of colour
Group 1
90
7
Group 2
83
8
Group 3
73
7
3
Number of Appointments
Groups One sitting Two sittings Three
sittings
Group 1
25
4
1
group 2
26
3
1
Group 3
30
0
0
DISCUSSION
bull Hydrogen peroxide is capable of penetrating the tooth osmosis and through porosities and cracks subsequently acting directly on the pigmented molecules
bull Gurgan et al investigated 3 different light systems and found out that diode laser system with gave best tooth whitening and least tooth sensitivity
bull In the EM group the surface reflects and refracts light from the surface in such way that mild imperfections in underlying enamel are camouflaged While the highly polished surface of enamel enhances the aesthetic appearance
bull Train et al and Loguercio et al also had the similar results in their studies with EM mild fluorosis showed best results moderate showed moderate results while it had little effect on severe fluorosis
bull NaOCl was only effective on mild stains while moderate and severe
stains could only be lightened to quite an extent but could not be
completely removed
bull When NaOCl comes in contact with hypomineralized and discoloured
enamel it degrades and removes the chromogenic organic material
located on the enamel surface
CONCLUSION
bull It was concluded that esthetic appearance of teeth mild fluorosis can
be achieved by bleaching and microabrasion But in cases of
moderate fluorosis a combination of any of theses modalities can be
used
bull As no special maintenance precautions are required these maybe be
considered as an interesting alternative to conventional operative
treatment
bull Focuses on only TSIF of 4
bull Electric pulp testing is not the
right method to check for
sensitivity
bull Tooth Sensitivity changes
from person to person
bull Food habits can cause
staining of the teeth
bull Minimally invasive
bull Cheaper to veneers
bull Minimal loss of tooth structure
bull 4 parameters checked for the success of treatment
bull Inclusion of specific score of fluorosis for comparing the results
bull Maximum 3 appointments needed
CRITICAL ANALYSIS
Pros Cons
REFERENCES
bull Gurgan S Cakir FY Yazici E Different light-activated in officebleaching
systems Lasers Med Sci 201025817-22
bull Train TE McWhorter AG Seale NSWilson CF Guo IY Examination of
esthetic improvement and surface alteration following microabrasion in
fluorotic human incisors in vivoPediatr dent 199618353-62
bull Loguercio AD Correia LD Zago C Tagliari D Neumann E Gomes OM et al
Clinical effectiveness of two microabrasion materials materials for the
removal of enamel flurosis stains Oper Dent 200732531-8
4
5
N2O-O2 (Relative Analgesia)
colorless sweet smelling gas
Pharmacokinetics
Absorption through pulmonary epithelium
It is approx 15 times as soluble as is nitrogen It replaces nitrogen in blood
It is carried in solution in plasma of the blood
It is not metabolized by the body
Elimination ndash majorndash lungs minor --- skin
perspiration urine and intestinal gas
Pharmacodynamics
Dose related
10 ndash 25 Lightheaded
Changes in visual amp auditory sensation
Tingling of hands amp feet
Suffusing warmth
Remote from the immediate environment
Reduced anxiety
25-50 max analgesic properties and aberration of vision hearing and proprioception mild drowsiness euphoria amnesia and increased sleepiness and dreams
35 conc will achieve maximum analgesia
bull CNS
ndash Cerebrum-primarily affected
ndash Safe but weak anesthetic agent
bull RESPIRATORY SYSTEM
ndash Increased Tidal and minute volumes
bull CARDIOVASCULAR SYSTEM
ndash 2 studies ndash decreased cardiac output
bull FETAL SYSTEMS
ndash Miscarriage in humans
bull OTHER SYSTEMS
ndash Depression of spinal reflexes increase muscle tone indicates stage of delirium
ndash Muscle rigidity-narcotics + nitrous oxide
ndash Nausea and vomitting - GIT
ndash HEMATOPOIESIS ----- prolonged exposure
Adverse reactions and toxicity
EMOTIONAL REACTIONS
DREAMS HALLUCINATIONS
No acute toxicity
Chronic toxicity ndash bone marrow
depression
PROCEDURE
Diffusion Hypoxia
Sevoflurane
A fluorinated derivative of isopropyl ether ndash synthesized in 1970
Potent anaesthetic agent with rapid uptake amp speedy recovery
Day-case surgery
Problem
Attaching vaporiser to any of the currently available machine
BENZODIAZEPINES
Diazepam 1961 lipid soluble
Uses-alcoholism epilepsy labor tetanus and cerebral palsy
- sedation and amnesia
- varieties of neurosis amp anxiety states
Pharmacokinetics
Orally Rectal IMIV or SC
Well absorbed through GIT
Excretion in urine
6
bull Pharmacodynamics
ndash Depress the brain stem reticular system and the limbic system thalamus and hypothalamus
ndash It is a centrally acting muscle relaxant Has anti-convulsant properties
Adverse reaction amp toxicity
ndash Confusion nausea headache increased appetite decreased salivation and jaundice Thrombophlebitis
ndash Rebound phenomenon
ndash Toxicity drowsiness confusion sleep and coma
Dosage Oral or Rectal ndash 02-05mgkg
Maximum single dose 10mg
IV- 025mgkg
Supplied Tablets 2 5 10 mg
Suspension ndash 5mg
Midazolam Water soluble ndash non-irritant
Oral IM IV
Metabolism- liver
Onset IV 3 -5mins
oral 20 ndash 30mins
Oral administration anxious patients requiring relatively short dental procedure
No rebound phenomenon
Better anxiolysis amp amnesia (retrograde amnesia)
Adverse effects Respiratory depression
dose dependant apnea
Dosage Oral ndash 025 to 1mgkg to maximum single dose 20mg
IM ndash 01 to 015mgkg to a maximum of 10mg
IV ndash slow IV
Supplied Syrup ndash 2mgml
Injectable ndash 1mgml amp 5mgml vials
Flumazenil specific benzodiazepines antagonist
selectively inhibits CNS effects
IV administration amp not recommended below 18yrs of age
02mg over 15 seconds after 45seconds 02mg then after 60seconds to maximum of 1mg
Sedative-Hypnotics
Barbiturates First truly effective drugs for the management of anxiety Generalized CNS depressants Produce dose dependent effects
Sedation ---- sleep ---- GA ---- coma
Suppress the CNS and result in sedation and amnesia Advantages
Rapid onset and short duration Disadvantages
no analgesic effect and possible hypotension Must be used with caution in trauma patients because they may cause
apnea and hypoventilation
DOSE Pentobarbital Sodium 100mg Secobarbital Sodium 100 to 200mg Children 30 to 100mg
bull Chloral Hydrates (Mickey Finn Knock out drops ) First synthesized in 1832 first member of the hypnotic group of drugs
Widely used as conscious sedation agent
Properties
Unpleasant taste
Nausea vomiting
Quite irritating to skin and to mucous membranes
GI irritation
Dosages Individualized for each patient 25 ndash 50mgkg
maximum of 1g
Supplied oral capsule ndash 500mg
oral solution ndash 250 amp 500mg5ml
Rectal suppositories ndash 324 amp 648mg
Narcotics
Do produce sedation amp euphoria greater in children
LA is required but dose should be decreased
Meperidine Synthetic opiate agonist
Very water soluble
Orally SC IM or IV
Peak effect by oral 1 hr amp lasts upto 4 hrs
Adverse reactions
-Seizures
-Extreme caution in hepatic or renal diseases or history of seizures
7
Dosage Oral SC or IM ndash 1to 22mgkg not to exceed 100 mg
Supplied Oral Tablets ndash 50 amp 100mg
Oral Syrup ndash 50mgml
Parental solution ndash 25 50 75 amp 100mgml
Fentanyl
Synthetic opiate narcotic analgesic
Very potent 01mg = 10mg Morophine75mg Meperidine
Pharmacokinetics
IV IM SM
Metabolized in liver Excreted in urine
Fentanyl Onset ndash 7 to 15mins
Duration ndash 1 to 2 hrs
Pharmacodynamics
Respiratory depression RR but returns to normal rapidly Tidal volume amp response to co2 depressed for extended period
Apnea
Less emetic than meperidine
NOT RECOMMENDED IN CHILDREN BELOW 2yrs
Dosage 0002 to 0004mgkg
Supplied 005mgml in 2 amp 5ml ampoules
Reversal drug Naloxone
Semisynthetic opiate antagonist
No agonist activity
Onset 2 to 5mins SC or IM amp 1 to 2mins IV
Reversal 45mins
Pt should be kept under continual surveillance
Adverse reaction nausea vomiting sweating hypotension hypertension ventricular tachycardia fibrillation
Dosage IV SC IM 001mgkg then 01mgkg every 2- 3mins maximum 2mg
Supplied 002 004 1mg solutions
Antihistamines
Hydroxyzine
Oral or IM
Effect ndash 15 ndash 30mins
Half-life ndash 3 hrs
Uses
To relieve anxiety
Used as an anti-histamine
Used to control nausea and vomiting including that associated with motion sickness and pregnancy
Adverse reaction dry mouth drowsiness hypersentivity
Dosage Oral ndash 1 to 2mgkg
IM ndash 11mgkg
Promethazine Oral or IM Onset 15 to 60mins Duration 4 to 6 hrs Uses
To prevent and treat nausea and vomiting associated with motion pregnancy or surgery
Produces sedation and reduce swelling pain and trismus
Lower seizure threshold Adverse reaction dry mouth blurred vision thickening of bronchial secretions Dosage OralIM ndash 05-11mgkg
maximum 25 mg
Diphenhydramine
Oral IM IV
Onset -1hr
Duration ndash 4 to 6 hr
Metabolized in liver
Adverse reaction disturbed coordination thickening of bronchial secretions
Dosage Oral IM IV ndash 1 to 15mgkg
maximum 50mg
Tranquilizers
Major tranquilizer antipsychotic produce calmness control symptoms of psychoses cause reversible extra pyramidal symptoms and do not tend to cause habituation
Minor tranquilizer antianxiety agents also cause calmness do not cause extrapyramidal symptoms Used in conditions like nervous tension and mild depression
8
Classification
Antipsychotics
Phenothiazine derivatives
Chlorpromazine promazine
Butryophenones
Haloperidol
Rauwolfia alkaloids
Reserpine
Antianxiety drugs
Propyl alcohol derivatives
Meprobamate
Benzodiazepine derivatives
Diazepam
Miscellaneous compounds
Hydroxyzine
Meprobamate
White crystalline powder slightly bitter in taste
Only administered orally
Peak blood concentration ----1 to 3hrs
10 ---------excreted unchanged Rest --- excreted as a oxidized derivative or as a glucoronide
Uses
To relieve day time anxiety
Induce sleep in insomniacs
To reduce anxiety associated with dental treatment
Anti-convulsant ndash petit mal epilepsy
Adverse reaction leucopenia acute non-thrombocytopenic purpura ecchymoses eosinophilia edema adenopathy
Dosage Childrengt 6yrs 100 to 200mg
Not recommended for children under 6yrs
Monitoring during sedation
1 Pulse
2 Blood pressure
3 ECG
4 Respiration
5 Temperature
Pulse
Manual Electronic
bull Radial Brachial
bull Facial labial
Blood pressure
ndash Stethoscope amp sphygmomanometer
ndash Automatic devices
ndash Direct cannulation of an artery ndash very accurate
Electrocardiograph
Heart rate rhythm myocardial function
9
Respiration
ndash Monitoring respiratory rate
ndash Observing the rise amp fall of the chest wall
ndash Observing the color of mucous membrane
ndash Observing the inflation amp deflation of the reservoir bag
Devices for monitoring respiration
1 The Precordial pretracheal stethoscope
2 The esophageal stethoscope
ndash Respiratory rate
ndash Heart rate
ndash Any abnormal sounds
Pulse Oximeter
ndash Oxygen saturation
ndash Heart rate
ndash Oxisensor site
ndash Fingers
ndash Toe
ndash Ear lobe
Mechanism
Oxygenated Hb ndash red light
Deoxygenated Hb- infrared light
Tissue pressure from arterial pulse (plethysmography)
Advantages
ndash Safe amp noninvasive
ndash Simple to use
ndash Information is rapidly available for clinical decision
ndash Indirectly indicates respiratory adequacy
Disadvantages
ndash Finger probes can get dislodged
ndash Emitted light source may cause burning
ndash Non reusable probes are expensive
ndash Does not directly determine airway patency
Capnography
1 The presence absence of air flow
2 Indicates depth amp adequacy of respiration
3 Continues analysis of the co2 content of the respired air ndash indicates respiratory adequacy
Temperature
ndash Disposable nondisposable thermometer
ndash Esophageal rectal temp probe
10
Discharge criteria
Cardiovascular function is satisfactory amp stable
Airway patency is uncompromised amp satisfactory
Pt is easily arousable amp protective reflexes intact
State of hydration is adequate
Pt can talk if applicable
Pt can sit unaided if applicable
Pt can ambulate with minimal assistance if applicable
Presedation level of responsiveness achieved
Responsible individual is available
1
PULP THERAPY OF VITAL TEETH
DR MITAKSHARA NIRWAN
Contents
Indirect pulp capping
Direct pulp capping
Medications amp materials used in pulp capping
Pulpotomy
MTA
Apexogenesis
INDIRECT PULP CAPPING
Pieter Van Forest - first to speak about root canal therapy
Glove designed instruments that could prepare a canal to a certain size and taper(1910)
Indirect pulp capping is defined as a procedure where in small amount of carious dentin is retained in
deep areas of cavity to avoid exposure of pulp followed by placement of a suitable medicament and
restorative material that seals off the carious dentin and encourages pulp recovery (Ingle)
A procedure in which only the gross caries is removed from the lesion and the cavity is sealed for a
time with a biocompatible material (McDonald)
Objective of indirect pulp capping
These were given by Eidelman in 1965
bull Arresting the carious process
bull Promoting dentin sclerosis
bull Stimulating formation of tertiary dentin
bull Remineralization of carious dentin
Layers of Carious Dentin Indications of Indirect Pulp Capping
History
Mild pain associated with eating
Negative history of spontaneous extreme pain
Clinical Examination
Deep carious lesion which are close tobut not involving the pulp in vital primary or young
permanent teeth
No mobility
Nominal pulp inflammationdefinite layer of affected dentin after removal of infected dentin
Radiographic examination
Normal lamina dura amp PDL space
No radiolucency around the apices
2
Contraindications of Indirect Pulp Capping
History
Sharp penetrating pulpalgia
Prolonged spontaneous pain especially at night
Clinical examination
Mobility of tooth
Discoloration of tooth
Negative reaction of electric pulp testing
Radiographic examination
Definite pulp exposure
Break in the lamina dura
Radiolucency around the apices
Widened PDL space
Treatment procedure
Sequelae of Indirect Pulp Capping Three distinct types of new dentin formation take place
1 Cellular fibrillar dentinmdashfirst 2 months
2 Globular dentinmdash3 months
3 Tubular dentin (uniform mineralized dentin)
bull 15th of reparative dentin formation begins in less than 30 days
bull After 3 months 01 mm is formed
DIRECT PULP CAPPING Defined by Kopel (1992) as the placement of a medicament or non medicated material on a pulp that
has been exposed in course of excavating the last portions of deep dentinal caries or as a result of
trauma
Objective
To create new dentin in the area of the exposure and subsequent healing of the pulp
Rationale
achieve a biologic closure of the exposure site by deposition of hard tissue barrier (dentin bridge)
between pulp tissue and capping material thus walling off the
INDICATIONS
Small mechanical exposure
Easily controlled haemorrhage
Bright red haemorrhage
True pinpoint exposure
CONTRAINDICATIONS
Severe toothache at night
Spontaneous pain
Tooth mobility
Radiographic appearance of pulp periradicular de- generation
Excess of hemorrhage at the time of exposure Serous exudate from the exposure
Externalinternal root resorption
Swellingfistula
Histological Changes after Pulp Capping
These were illustrated be Glass and Zander in 1949
After 24 hours Necrotic zone adjacent to calcium
hydroxide paste is separated from healthy pulp
tissue by a deep staining basophilic layer
After 7 days Increase in cellular and fibroblastic
activity
After 14 days Partly calcified fibrous tissue lined by
odontoblastic cells is seen below the calcium
proteinate zone disappearance of necrotic zone
After 28 days Zone of new dentin
3
Medications and Materials Used for Pulp Capping Calcium hydroxide
Corticosteroids amp antibiotics
Inert materials
Collagen fibers
4-META adhesive
Direct bonding
Isobutyl cyanoacrylate
Denatured albumin
Mineral trioxide aggregate
Laser
Bone morphogenic protein
PULPOTOMY
Finn (1995) defined it as the complete removal of the coronal portion of the dental pulp
followed by placement of a suitable dressing or medicament that will promote healing and
preserve vitality of the tooth
American Academy of Pediatric Dentistry (1998) defined pulpotomy as the amputation of
affected infected coronal portion of the dental pulp preserving the vitality and function of the
remaining part of radicular pulp
Objectives
bull Removal of inflamed and infected coronal pulp at the site of exposure thus preserving the vitality of the
radicular pulp and allowing it to heal
bull Maintain the tooth in the dental arch
Rationale
bull Radicular pulp is healthy and capable of healing after surgical amputation of the infected coronal pulp
bull Preserves vitality of the radicular pulp
bull Maintains tooth in a physiologic condition
Indications of Pulpotomy bull Mechanical pulp exposure in primary teeth
bull Teeth showing a large carious lesion but free of radicular pulpitis
bull History of only spontaneous pain
bull Hemorrhage from exposure sites bright red and can be controlled
bull Absence of abscess or fistula
bull No interradicular bone loss
bull No interradicular radiolucency
Contraindications of Pulpotomy bull Persistent toothache
bull Tenderness on percussion
bull Root resorption more than 13rd of root length
bull Large carious lesion with nonrestorable crown
bull Highly viscous sluggish hemorrhage from canal orifice which is uncontrollable
bull Medical contradictions like heart disease immuno compromised patient
bull Swelling or fistula
bull External or internal resorption
bull Pathological mobility
bull Calcification of pulp
Classification of pulpotomy
4
Formocresol Pulpotomy
Iby BUCKLEY in 1904
Sweet (1930) Formulated multi visit technique
Doyle (1962) Advocated 2 sitting procedure (complete devitalization)
Spedding (1965) Gave 5 minute protocol (partial devitali- zation)
Venham (1967) Proposed 15 seconds procedure
Current concept uses 4 minutes of application time
Composition of formocresol Buckleyrsquos Formula
bull Cresol ndash 35 percent
bull Glycerol ndash 15 percent
bull Formaldehyde ndash 19 percent
bull Water ndash 31 percent
Mechanism of Action
It prevents tissue autolysis by bonding to the proteins Bonding is of peptide groups of side chain amino acids and is a reversible process accomplished without
changing the basic structure of protein molecules
Histological Changes
bull Demonstrated by Mass and Zilbermann11 in 1933 and also by Massler and Mansokhani in 1959
bull Immediately the pulp becomes fibrous and acidophillic
bull Seven to fourteen days Three zones appear
a broad eosinophilic zone of fixation
b broad pale-staining zone of atrophy with poorcellular definition
c broad zone of inflammation extending apically into normal pulp tissue
bull One yearndash Progressive apical movement of these zones with only acidophillic zone left at the end of 1 year
Modified Formocresol Pulpotomy
Used by TRASK(1972)
The technique is identical to that described for primary teeth except that the formocresol pellet is
sealed permanently in the tooth
Two-visit Devitalization Pulpotomy
Indications
bull There is evidence of sluggish bleeding at the amputation site that is difficult to control
bull Pus in the chamber but none at the amputation site
bull There is thickening of the PDL
bull History of pain
Contraindications
bull Nonrestorable tooth
bull Tooth with necrotic pulp
5
Glutaraldehyde Pulpotomy
It was first suggested by S Gravenmade Introduced by Kopel in 1979
Mechanism of Action
bull Glutaraldehyde produces rapid surface fixation of the underlying pulpal tissue
bull A narrow zone of eosinophilic stained and compressed fixed tissue is found directly beneath the area of application which blends into vital normal appearing tissue apically
bull With time the glutaraldehyde fixed zone is replaced by macrophagic action with dense collagenous tissue thus the entire root canal tissue is vital
Cvekrsquos Pulpotomy
bull This is also called as calcium hydroxide pulpotomy or young permanent partial pulpotomy
bull This was proposed by Mejare and Cvek16 in 1978
bull Indicated in young permanent teeth where the pulp is exposed by mechanical or bacterial means and the
remaining radicular tissue is judged vital by clinical and radiographic criteria whereas the root closure is
notcomplete
MINERAL TRIOXIDE AGGREGATE (MTA) Torabinejad described the physical and chemical properties of MTA in 1995
It is ash colored powder made primarily of fine hydrophilic particles of
1 tricalcium aluminate
2 tricalcium silicate
3 silicate oxide
4 tricalcium oxide
5 bismuth dioxide
Hydration of the powder results in a colloidal gel composed of calcium oxide crystals in an amorphous
structure This gel solidifies into a hard structure in less than three hours
PROPERTIES OF MTA
It is biocompatible material and its sealing ability is better than that of amalgam or ZOE
Initial pH is 102 and set pH is 125
The setting time of cement is 4 hours
The compressive strength is 70 MPA which is comparable with that of IRM
Low cytotoxicity ndash It presents with minimal inflammation if extended beyond the apex
Mineral trioxide aggregate (MTA) has demonstrated the ability to induce hard-tissue formation in
pulpal tissues and it promotes rapid cell growth
APEXOGENESIS
It is defined as the treatment of a vital pulp by capping or pulpotomy in order to permit continued
growth of the root and closure of the open apex
Rationale
Maintenance of integrity of the radicular pulp tissue to allow for continued root growth
Indications
bull Indicated for traumatized or pulpally involved vital permanent tooth when root apex is incompletely formed
bull No history of spontaneous pain
bull No sensitivity on percussion
bull No hemorrhage
bull Normal radiographic appearance
Contraindications
bull Evidence that radicular pulp has undergone degenerative changes
bull Purulent drainage
bull History of prolonged pain bull Necrotic debris in canal
bull Periapical radiolucency
6
1
Gupta A Dhingra R Chaudhari P Gupta A
Department of Paedodontics and Preventive Dentistry Faculty of Dental Sciences SGT University Gurgaon Haryana India
Journal of Indian Society of Pedodontics and Preventive Dentistry
Volume 35 I Issue 3 I July-September 2017
A COMPARISION OF VARIOUS MINIMALLY
INVASIVE TECHNIQUES FOR THE REMOVAL
OF DENTAL FLUOROSIS STAINS IN
CHILDREN
DR MITAKSHARA NIRWAN
CONTENTS
bull Introduction
bull Aims
bull Materials and Methods
bull Results
bull Discussion
bull Conclusion
bull Critical analysis
bull References
INTRODUCTION
bull Dental fluorosis is a developmental disturbance of dental enamel caused by
successive exposure to high concentrations of fluoride during tooth
development
bull Various methods of therapy are advocated for the treatment of fluorosis -
stained teeth which range from invasive ceramic veneer bonding restorations
to abrasive chemical treatments
bull The combination of dental bleaching techniques and microabrasion appears
as an excellent conservative solution to reestablish health in fluorosis
affected teeth
AIMS
bull The aim of the study was to evaluate and compare the effectiveness of
minimally invasive techniques for the removal of dental fluorosis
stains in children in vivo
MATERIALS AND METHODS
Patients visiting the department of Pedodontics and Preventive dentistry
Faculty of Dental Sciences SGT University Gurgaon
bull Sample size 90 patients
bull Age group 10 -17 years
bull Caries cracks or periodontal
disease on anterior teeth
bull Abscess draining sinus
cellulitis
bull Non vital teeth
hypersensitive exposed
crevices
bull Orthodontic appliance
bull Past history of bleaching
bull At least two permanent
maxillary anterior teeth
bull TSIF of score 4
bull Free of systemic diseases
Inclusion criteria Exclusion criteria
2
Groups
Group A In office bleaching with 35 hydrogen peroxide( Pola Office
Bleaching kit) activated by light emitting diode (LED) bleaching unit
(35 HP)
Group B Enamel microabrasion (EM) (PREMA Enamel Microabrasion
System) followed by in-office bleaching with 44 carbamide peroxide
gel (EM)
Group C In-office bleaching with 5 sodium hypochlorite (5
NaOCl)
A baseline colour evaluation was done by taking digital photograph of
the maxillary anterior teeth
RESULTS
Group 1
Colour stability
Group 2 Group 3
Tooth sensitivity
Tooth sensitivity values were taken before the treatment
which was compared to immediate postoperative and follow
up visits It was checked using an electric pulp tester
maximum
moderate
least
immediately
group 2
group 1
group 3
1 month
group 2
group 1
group 3
3 month
group 2
group 1
group 3
Patient satisfaction score
Satisfaction was assessed on visual analog scale
Range 1 to 5
Groups percentage of patients
who were satisfied with
the treatment
Number of patients
who reported slight
reappearance of colour
Group 1
90
7
Group 2
83
8
Group 3
73
7
3
Number of Appointments
Groups One sitting Two sittings Three
sittings
Group 1
25
4
1
group 2
26
3
1
Group 3
30
0
0
DISCUSSION
bull Hydrogen peroxide is capable of penetrating the tooth osmosis and through porosities and cracks subsequently acting directly on the pigmented molecules
bull Gurgan et al investigated 3 different light systems and found out that diode laser system with gave best tooth whitening and least tooth sensitivity
bull In the EM group the surface reflects and refracts light from the surface in such way that mild imperfections in underlying enamel are camouflaged While the highly polished surface of enamel enhances the aesthetic appearance
bull Train et al and Loguercio et al also had the similar results in their studies with EM mild fluorosis showed best results moderate showed moderate results while it had little effect on severe fluorosis
bull NaOCl was only effective on mild stains while moderate and severe
stains could only be lightened to quite an extent but could not be
completely removed
bull When NaOCl comes in contact with hypomineralized and discoloured
enamel it degrades and removes the chromogenic organic material
located on the enamel surface
CONCLUSION
bull It was concluded that esthetic appearance of teeth mild fluorosis can
be achieved by bleaching and microabrasion But in cases of
moderate fluorosis a combination of any of theses modalities can be
used
bull As no special maintenance precautions are required these maybe be
considered as an interesting alternative to conventional operative
treatment
bull Focuses on only TSIF of 4
bull Electric pulp testing is not the
right method to check for
sensitivity
bull Tooth Sensitivity changes
from person to person
bull Food habits can cause
staining of the teeth
bull Minimally invasive
bull Cheaper to veneers
bull Minimal loss of tooth structure
bull 4 parameters checked for the success of treatment
bull Inclusion of specific score of fluorosis for comparing the results
bull Maximum 3 appointments needed
CRITICAL ANALYSIS
Pros Cons
REFERENCES
bull Gurgan S Cakir FY Yazici E Different light-activated in officebleaching
systems Lasers Med Sci 201025817-22
bull Train TE McWhorter AG Seale NSWilson CF Guo IY Examination of
esthetic improvement and surface alteration following microabrasion in
fluorotic human incisors in vivoPediatr dent 199618353-62
bull Loguercio AD Correia LD Zago C Tagliari D Neumann E Gomes OM et al
Clinical effectiveness of two microabrasion materials materials for the
removal of enamel flurosis stains Oper Dent 200732531-8
4
6
bull Pharmacodynamics
ndash Depress the brain stem reticular system and the limbic system thalamus and hypothalamus
ndash It is a centrally acting muscle relaxant Has anti-convulsant properties
Adverse reaction amp toxicity
ndash Confusion nausea headache increased appetite decreased salivation and jaundice Thrombophlebitis
ndash Rebound phenomenon
ndash Toxicity drowsiness confusion sleep and coma
Dosage Oral or Rectal ndash 02-05mgkg
Maximum single dose 10mg
IV- 025mgkg
Supplied Tablets 2 5 10 mg
Suspension ndash 5mg
Midazolam Water soluble ndash non-irritant
Oral IM IV
Metabolism- liver
Onset IV 3 -5mins
oral 20 ndash 30mins
Oral administration anxious patients requiring relatively short dental procedure
No rebound phenomenon
Better anxiolysis amp amnesia (retrograde amnesia)
Adverse effects Respiratory depression
dose dependant apnea
Dosage Oral ndash 025 to 1mgkg to maximum single dose 20mg
IM ndash 01 to 015mgkg to a maximum of 10mg
IV ndash slow IV
Supplied Syrup ndash 2mgml
Injectable ndash 1mgml amp 5mgml vials
Flumazenil specific benzodiazepines antagonist
selectively inhibits CNS effects
IV administration amp not recommended below 18yrs of age
02mg over 15 seconds after 45seconds 02mg then after 60seconds to maximum of 1mg
Sedative-Hypnotics
Barbiturates First truly effective drugs for the management of anxiety Generalized CNS depressants Produce dose dependent effects
Sedation ---- sleep ---- GA ---- coma
Suppress the CNS and result in sedation and amnesia Advantages
Rapid onset and short duration Disadvantages
no analgesic effect and possible hypotension Must be used with caution in trauma patients because they may cause
apnea and hypoventilation
DOSE Pentobarbital Sodium 100mg Secobarbital Sodium 100 to 200mg Children 30 to 100mg
bull Chloral Hydrates (Mickey Finn Knock out drops ) First synthesized in 1832 first member of the hypnotic group of drugs
Widely used as conscious sedation agent
Properties
Unpleasant taste
Nausea vomiting
Quite irritating to skin and to mucous membranes
GI irritation
Dosages Individualized for each patient 25 ndash 50mgkg
maximum of 1g
Supplied oral capsule ndash 500mg
oral solution ndash 250 amp 500mg5ml
Rectal suppositories ndash 324 amp 648mg
Narcotics
Do produce sedation amp euphoria greater in children
LA is required but dose should be decreased
Meperidine Synthetic opiate agonist
Very water soluble
Orally SC IM or IV
Peak effect by oral 1 hr amp lasts upto 4 hrs
Adverse reactions
-Seizures
-Extreme caution in hepatic or renal diseases or history of seizures
7
Dosage Oral SC or IM ndash 1to 22mgkg not to exceed 100 mg
Supplied Oral Tablets ndash 50 amp 100mg
Oral Syrup ndash 50mgml
Parental solution ndash 25 50 75 amp 100mgml
Fentanyl
Synthetic opiate narcotic analgesic
Very potent 01mg = 10mg Morophine75mg Meperidine
Pharmacokinetics
IV IM SM
Metabolized in liver Excreted in urine
Fentanyl Onset ndash 7 to 15mins
Duration ndash 1 to 2 hrs
Pharmacodynamics
Respiratory depression RR but returns to normal rapidly Tidal volume amp response to co2 depressed for extended period
Apnea
Less emetic than meperidine
NOT RECOMMENDED IN CHILDREN BELOW 2yrs
Dosage 0002 to 0004mgkg
Supplied 005mgml in 2 amp 5ml ampoules
Reversal drug Naloxone
Semisynthetic opiate antagonist
No agonist activity
Onset 2 to 5mins SC or IM amp 1 to 2mins IV
Reversal 45mins
Pt should be kept under continual surveillance
Adverse reaction nausea vomiting sweating hypotension hypertension ventricular tachycardia fibrillation
Dosage IV SC IM 001mgkg then 01mgkg every 2- 3mins maximum 2mg
Supplied 002 004 1mg solutions
Antihistamines
Hydroxyzine
Oral or IM
Effect ndash 15 ndash 30mins
Half-life ndash 3 hrs
Uses
To relieve anxiety
Used as an anti-histamine
Used to control nausea and vomiting including that associated with motion sickness and pregnancy
Adverse reaction dry mouth drowsiness hypersentivity
Dosage Oral ndash 1 to 2mgkg
IM ndash 11mgkg
Promethazine Oral or IM Onset 15 to 60mins Duration 4 to 6 hrs Uses
To prevent and treat nausea and vomiting associated with motion pregnancy or surgery
Produces sedation and reduce swelling pain and trismus
Lower seizure threshold Adverse reaction dry mouth blurred vision thickening of bronchial secretions Dosage OralIM ndash 05-11mgkg
maximum 25 mg
Diphenhydramine
Oral IM IV
Onset -1hr
Duration ndash 4 to 6 hr
Metabolized in liver
Adverse reaction disturbed coordination thickening of bronchial secretions
Dosage Oral IM IV ndash 1 to 15mgkg
maximum 50mg
Tranquilizers
Major tranquilizer antipsychotic produce calmness control symptoms of psychoses cause reversible extra pyramidal symptoms and do not tend to cause habituation
Minor tranquilizer antianxiety agents also cause calmness do not cause extrapyramidal symptoms Used in conditions like nervous tension and mild depression
8
Classification
Antipsychotics
Phenothiazine derivatives
Chlorpromazine promazine
Butryophenones
Haloperidol
Rauwolfia alkaloids
Reserpine
Antianxiety drugs
Propyl alcohol derivatives
Meprobamate
Benzodiazepine derivatives
Diazepam
Miscellaneous compounds
Hydroxyzine
Meprobamate
White crystalline powder slightly bitter in taste
Only administered orally
Peak blood concentration ----1 to 3hrs
10 ---------excreted unchanged Rest --- excreted as a oxidized derivative or as a glucoronide
Uses
To relieve day time anxiety
Induce sleep in insomniacs
To reduce anxiety associated with dental treatment
Anti-convulsant ndash petit mal epilepsy
Adverse reaction leucopenia acute non-thrombocytopenic purpura ecchymoses eosinophilia edema adenopathy
Dosage Childrengt 6yrs 100 to 200mg
Not recommended for children under 6yrs
Monitoring during sedation
1 Pulse
2 Blood pressure
3 ECG
4 Respiration
5 Temperature
Pulse
Manual Electronic
bull Radial Brachial
bull Facial labial
Blood pressure
ndash Stethoscope amp sphygmomanometer
ndash Automatic devices
ndash Direct cannulation of an artery ndash very accurate
Electrocardiograph
Heart rate rhythm myocardial function
9
Respiration
ndash Monitoring respiratory rate
ndash Observing the rise amp fall of the chest wall
ndash Observing the color of mucous membrane
ndash Observing the inflation amp deflation of the reservoir bag
Devices for monitoring respiration
1 The Precordial pretracheal stethoscope
2 The esophageal stethoscope
ndash Respiratory rate
ndash Heart rate
ndash Any abnormal sounds
Pulse Oximeter
ndash Oxygen saturation
ndash Heart rate
ndash Oxisensor site
ndash Fingers
ndash Toe
ndash Ear lobe
Mechanism
Oxygenated Hb ndash red light
Deoxygenated Hb- infrared light
Tissue pressure from arterial pulse (plethysmography)
Advantages
ndash Safe amp noninvasive
ndash Simple to use
ndash Information is rapidly available for clinical decision
ndash Indirectly indicates respiratory adequacy
Disadvantages
ndash Finger probes can get dislodged
ndash Emitted light source may cause burning
ndash Non reusable probes are expensive
ndash Does not directly determine airway patency
Capnography
1 The presence absence of air flow
2 Indicates depth amp adequacy of respiration
3 Continues analysis of the co2 content of the respired air ndash indicates respiratory adequacy
Temperature
ndash Disposable nondisposable thermometer
ndash Esophageal rectal temp probe
10
Discharge criteria
Cardiovascular function is satisfactory amp stable
Airway patency is uncompromised amp satisfactory
Pt is easily arousable amp protective reflexes intact
State of hydration is adequate
Pt can talk if applicable
Pt can sit unaided if applicable
Pt can ambulate with minimal assistance if applicable
Presedation level of responsiveness achieved
Responsible individual is available
1
PULP THERAPY OF VITAL TEETH
DR MITAKSHARA NIRWAN
Contents
Indirect pulp capping
Direct pulp capping
Medications amp materials used in pulp capping
Pulpotomy
MTA
Apexogenesis
INDIRECT PULP CAPPING
Pieter Van Forest - first to speak about root canal therapy
Glove designed instruments that could prepare a canal to a certain size and taper(1910)
Indirect pulp capping is defined as a procedure where in small amount of carious dentin is retained in
deep areas of cavity to avoid exposure of pulp followed by placement of a suitable medicament and
restorative material that seals off the carious dentin and encourages pulp recovery (Ingle)
A procedure in which only the gross caries is removed from the lesion and the cavity is sealed for a
time with a biocompatible material (McDonald)
Objective of indirect pulp capping
These were given by Eidelman in 1965
bull Arresting the carious process
bull Promoting dentin sclerosis
bull Stimulating formation of tertiary dentin
bull Remineralization of carious dentin
Layers of Carious Dentin Indications of Indirect Pulp Capping
History
Mild pain associated with eating
Negative history of spontaneous extreme pain
Clinical Examination
Deep carious lesion which are close tobut not involving the pulp in vital primary or young
permanent teeth
No mobility
Nominal pulp inflammationdefinite layer of affected dentin after removal of infected dentin
Radiographic examination
Normal lamina dura amp PDL space
No radiolucency around the apices
2
Contraindications of Indirect Pulp Capping
History
Sharp penetrating pulpalgia
Prolonged spontaneous pain especially at night
Clinical examination
Mobility of tooth
Discoloration of tooth
Negative reaction of electric pulp testing
Radiographic examination
Definite pulp exposure
Break in the lamina dura
Radiolucency around the apices
Widened PDL space
Treatment procedure
Sequelae of Indirect Pulp Capping Three distinct types of new dentin formation take place
1 Cellular fibrillar dentinmdashfirst 2 months
2 Globular dentinmdash3 months
3 Tubular dentin (uniform mineralized dentin)
bull 15th of reparative dentin formation begins in less than 30 days
bull After 3 months 01 mm is formed
DIRECT PULP CAPPING Defined by Kopel (1992) as the placement of a medicament or non medicated material on a pulp that
has been exposed in course of excavating the last portions of deep dentinal caries or as a result of
trauma
Objective
To create new dentin in the area of the exposure and subsequent healing of the pulp
Rationale
achieve a biologic closure of the exposure site by deposition of hard tissue barrier (dentin bridge)
between pulp tissue and capping material thus walling off the
INDICATIONS
Small mechanical exposure
Easily controlled haemorrhage
Bright red haemorrhage
True pinpoint exposure
CONTRAINDICATIONS
Severe toothache at night
Spontaneous pain
Tooth mobility
Radiographic appearance of pulp periradicular de- generation
Excess of hemorrhage at the time of exposure Serous exudate from the exposure
Externalinternal root resorption
Swellingfistula
Histological Changes after Pulp Capping
These were illustrated be Glass and Zander in 1949
After 24 hours Necrotic zone adjacent to calcium
hydroxide paste is separated from healthy pulp
tissue by a deep staining basophilic layer
After 7 days Increase in cellular and fibroblastic
activity
After 14 days Partly calcified fibrous tissue lined by
odontoblastic cells is seen below the calcium
proteinate zone disappearance of necrotic zone
After 28 days Zone of new dentin
3
Medications and Materials Used for Pulp Capping Calcium hydroxide
Corticosteroids amp antibiotics
Inert materials
Collagen fibers
4-META adhesive
Direct bonding
Isobutyl cyanoacrylate
Denatured albumin
Mineral trioxide aggregate
Laser
Bone morphogenic protein
PULPOTOMY
Finn (1995) defined it as the complete removal of the coronal portion of the dental pulp
followed by placement of a suitable dressing or medicament that will promote healing and
preserve vitality of the tooth
American Academy of Pediatric Dentistry (1998) defined pulpotomy as the amputation of
affected infected coronal portion of the dental pulp preserving the vitality and function of the
remaining part of radicular pulp
Objectives
bull Removal of inflamed and infected coronal pulp at the site of exposure thus preserving the vitality of the
radicular pulp and allowing it to heal
bull Maintain the tooth in the dental arch
Rationale
bull Radicular pulp is healthy and capable of healing after surgical amputation of the infected coronal pulp
bull Preserves vitality of the radicular pulp
bull Maintains tooth in a physiologic condition
Indications of Pulpotomy bull Mechanical pulp exposure in primary teeth
bull Teeth showing a large carious lesion but free of radicular pulpitis
bull History of only spontaneous pain
bull Hemorrhage from exposure sites bright red and can be controlled
bull Absence of abscess or fistula
bull No interradicular bone loss
bull No interradicular radiolucency
Contraindications of Pulpotomy bull Persistent toothache
bull Tenderness on percussion
bull Root resorption more than 13rd of root length
bull Large carious lesion with nonrestorable crown
bull Highly viscous sluggish hemorrhage from canal orifice which is uncontrollable
bull Medical contradictions like heart disease immuno compromised patient
bull Swelling or fistula
bull External or internal resorption
bull Pathological mobility
bull Calcification of pulp
Classification of pulpotomy
4
Formocresol Pulpotomy
Iby BUCKLEY in 1904
Sweet (1930) Formulated multi visit technique
Doyle (1962) Advocated 2 sitting procedure (complete devitalization)
Spedding (1965) Gave 5 minute protocol (partial devitali- zation)
Venham (1967) Proposed 15 seconds procedure
Current concept uses 4 minutes of application time
Composition of formocresol Buckleyrsquos Formula
bull Cresol ndash 35 percent
bull Glycerol ndash 15 percent
bull Formaldehyde ndash 19 percent
bull Water ndash 31 percent
Mechanism of Action
It prevents tissue autolysis by bonding to the proteins Bonding is of peptide groups of side chain amino acids and is a reversible process accomplished without
changing the basic structure of protein molecules
Histological Changes
bull Demonstrated by Mass and Zilbermann11 in 1933 and also by Massler and Mansokhani in 1959
bull Immediately the pulp becomes fibrous and acidophillic
bull Seven to fourteen days Three zones appear
a broad eosinophilic zone of fixation
b broad pale-staining zone of atrophy with poorcellular definition
c broad zone of inflammation extending apically into normal pulp tissue
bull One yearndash Progressive apical movement of these zones with only acidophillic zone left at the end of 1 year
Modified Formocresol Pulpotomy
Used by TRASK(1972)
The technique is identical to that described for primary teeth except that the formocresol pellet is
sealed permanently in the tooth
Two-visit Devitalization Pulpotomy
Indications
bull There is evidence of sluggish bleeding at the amputation site that is difficult to control
bull Pus in the chamber but none at the amputation site
bull There is thickening of the PDL
bull History of pain
Contraindications
bull Nonrestorable tooth
bull Tooth with necrotic pulp
5
Glutaraldehyde Pulpotomy
It was first suggested by S Gravenmade Introduced by Kopel in 1979
Mechanism of Action
bull Glutaraldehyde produces rapid surface fixation of the underlying pulpal tissue
bull A narrow zone of eosinophilic stained and compressed fixed tissue is found directly beneath the area of application which blends into vital normal appearing tissue apically
bull With time the glutaraldehyde fixed zone is replaced by macrophagic action with dense collagenous tissue thus the entire root canal tissue is vital
Cvekrsquos Pulpotomy
bull This is also called as calcium hydroxide pulpotomy or young permanent partial pulpotomy
bull This was proposed by Mejare and Cvek16 in 1978
bull Indicated in young permanent teeth where the pulp is exposed by mechanical or bacterial means and the
remaining radicular tissue is judged vital by clinical and radiographic criteria whereas the root closure is
notcomplete
MINERAL TRIOXIDE AGGREGATE (MTA) Torabinejad described the physical and chemical properties of MTA in 1995
It is ash colored powder made primarily of fine hydrophilic particles of
1 tricalcium aluminate
2 tricalcium silicate
3 silicate oxide
4 tricalcium oxide
5 bismuth dioxide
Hydration of the powder results in a colloidal gel composed of calcium oxide crystals in an amorphous
structure This gel solidifies into a hard structure in less than three hours
PROPERTIES OF MTA
It is biocompatible material and its sealing ability is better than that of amalgam or ZOE
Initial pH is 102 and set pH is 125
The setting time of cement is 4 hours
The compressive strength is 70 MPA which is comparable with that of IRM
Low cytotoxicity ndash It presents with minimal inflammation if extended beyond the apex
Mineral trioxide aggregate (MTA) has demonstrated the ability to induce hard-tissue formation in
pulpal tissues and it promotes rapid cell growth
APEXOGENESIS
It is defined as the treatment of a vital pulp by capping or pulpotomy in order to permit continued
growth of the root and closure of the open apex
Rationale
Maintenance of integrity of the radicular pulp tissue to allow for continued root growth
Indications
bull Indicated for traumatized or pulpally involved vital permanent tooth when root apex is incompletely formed
bull No history of spontaneous pain
bull No sensitivity on percussion
bull No hemorrhage
bull Normal radiographic appearance
Contraindications
bull Evidence that radicular pulp has undergone degenerative changes
bull Purulent drainage
bull History of prolonged pain bull Necrotic debris in canal
bull Periapical radiolucency
6
1
Gupta A Dhingra R Chaudhari P Gupta A
Department of Paedodontics and Preventive Dentistry Faculty of Dental Sciences SGT University Gurgaon Haryana India
Journal of Indian Society of Pedodontics and Preventive Dentistry
Volume 35 I Issue 3 I July-September 2017
A COMPARISION OF VARIOUS MINIMALLY
INVASIVE TECHNIQUES FOR THE REMOVAL
OF DENTAL FLUOROSIS STAINS IN
CHILDREN
DR MITAKSHARA NIRWAN
CONTENTS
bull Introduction
bull Aims
bull Materials and Methods
bull Results
bull Discussion
bull Conclusion
bull Critical analysis
bull References
INTRODUCTION
bull Dental fluorosis is a developmental disturbance of dental enamel caused by
successive exposure to high concentrations of fluoride during tooth
development
bull Various methods of therapy are advocated for the treatment of fluorosis -
stained teeth which range from invasive ceramic veneer bonding restorations
to abrasive chemical treatments
bull The combination of dental bleaching techniques and microabrasion appears
as an excellent conservative solution to reestablish health in fluorosis
affected teeth
AIMS
bull The aim of the study was to evaluate and compare the effectiveness of
minimally invasive techniques for the removal of dental fluorosis
stains in children in vivo
MATERIALS AND METHODS
Patients visiting the department of Pedodontics and Preventive dentistry
Faculty of Dental Sciences SGT University Gurgaon
bull Sample size 90 patients
bull Age group 10 -17 years
bull Caries cracks or periodontal
disease on anterior teeth
bull Abscess draining sinus
cellulitis
bull Non vital teeth
hypersensitive exposed
crevices
bull Orthodontic appliance
bull Past history of bleaching
bull At least two permanent
maxillary anterior teeth
bull TSIF of score 4
bull Free of systemic diseases
Inclusion criteria Exclusion criteria
2
Groups
Group A In office bleaching with 35 hydrogen peroxide( Pola Office
Bleaching kit) activated by light emitting diode (LED) bleaching unit
(35 HP)
Group B Enamel microabrasion (EM) (PREMA Enamel Microabrasion
System) followed by in-office bleaching with 44 carbamide peroxide
gel (EM)
Group C In-office bleaching with 5 sodium hypochlorite (5
NaOCl)
A baseline colour evaluation was done by taking digital photograph of
the maxillary anterior teeth
RESULTS
Group 1
Colour stability
Group 2 Group 3
Tooth sensitivity
Tooth sensitivity values were taken before the treatment
which was compared to immediate postoperative and follow
up visits It was checked using an electric pulp tester
maximum
moderate
least
immediately
group 2
group 1
group 3
1 month
group 2
group 1
group 3
3 month
group 2
group 1
group 3
Patient satisfaction score
Satisfaction was assessed on visual analog scale
Range 1 to 5
Groups percentage of patients
who were satisfied with
the treatment
Number of patients
who reported slight
reappearance of colour
Group 1
90
7
Group 2
83
8
Group 3
73
7
3
Number of Appointments
Groups One sitting Two sittings Three
sittings
Group 1
25
4
1
group 2
26
3
1
Group 3
30
0
0
DISCUSSION
bull Hydrogen peroxide is capable of penetrating the tooth osmosis and through porosities and cracks subsequently acting directly on the pigmented molecules
bull Gurgan et al investigated 3 different light systems and found out that diode laser system with gave best tooth whitening and least tooth sensitivity
bull In the EM group the surface reflects and refracts light from the surface in such way that mild imperfections in underlying enamel are camouflaged While the highly polished surface of enamel enhances the aesthetic appearance
bull Train et al and Loguercio et al also had the similar results in their studies with EM mild fluorosis showed best results moderate showed moderate results while it had little effect on severe fluorosis
bull NaOCl was only effective on mild stains while moderate and severe
stains could only be lightened to quite an extent but could not be
completely removed
bull When NaOCl comes in contact with hypomineralized and discoloured
enamel it degrades and removes the chromogenic organic material
located on the enamel surface
CONCLUSION
bull It was concluded that esthetic appearance of teeth mild fluorosis can
be achieved by bleaching and microabrasion But in cases of
moderate fluorosis a combination of any of theses modalities can be
used
bull As no special maintenance precautions are required these maybe be
considered as an interesting alternative to conventional operative
treatment
bull Focuses on only TSIF of 4
bull Electric pulp testing is not the
right method to check for
sensitivity
bull Tooth Sensitivity changes
from person to person
bull Food habits can cause
staining of the teeth
bull Minimally invasive
bull Cheaper to veneers
bull Minimal loss of tooth structure
bull 4 parameters checked for the success of treatment
bull Inclusion of specific score of fluorosis for comparing the results
bull Maximum 3 appointments needed
CRITICAL ANALYSIS
Pros Cons
REFERENCES
bull Gurgan S Cakir FY Yazici E Different light-activated in officebleaching
systems Lasers Med Sci 201025817-22
bull Train TE McWhorter AG Seale NSWilson CF Guo IY Examination of
esthetic improvement and surface alteration following microabrasion in
fluorotic human incisors in vivoPediatr dent 199618353-62
bull Loguercio AD Correia LD Zago C Tagliari D Neumann E Gomes OM et al
Clinical effectiveness of two microabrasion materials materials for the
removal of enamel flurosis stains Oper Dent 200732531-8
4
7
Dosage Oral SC or IM ndash 1to 22mgkg not to exceed 100 mg
Supplied Oral Tablets ndash 50 amp 100mg
Oral Syrup ndash 50mgml
Parental solution ndash 25 50 75 amp 100mgml
Fentanyl
Synthetic opiate narcotic analgesic
Very potent 01mg = 10mg Morophine75mg Meperidine
Pharmacokinetics
IV IM SM
Metabolized in liver Excreted in urine
Fentanyl Onset ndash 7 to 15mins
Duration ndash 1 to 2 hrs
Pharmacodynamics
Respiratory depression RR but returns to normal rapidly Tidal volume amp response to co2 depressed for extended period
Apnea
Less emetic than meperidine
NOT RECOMMENDED IN CHILDREN BELOW 2yrs
Dosage 0002 to 0004mgkg
Supplied 005mgml in 2 amp 5ml ampoules
Reversal drug Naloxone
Semisynthetic opiate antagonist
No agonist activity
Onset 2 to 5mins SC or IM amp 1 to 2mins IV
Reversal 45mins
Pt should be kept under continual surveillance
Adverse reaction nausea vomiting sweating hypotension hypertension ventricular tachycardia fibrillation
Dosage IV SC IM 001mgkg then 01mgkg every 2- 3mins maximum 2mg
Supplied 002 004 1mg solutions
Antihistamines
Hydroxyzine
Oral or IM
Effect ndash 15 ndash 30mins
Half-life ndash 3 hrs
Uses
To relieve anxiety
Used as an anti-histamine
Used to control nausea and vomiting including that associated with motion sickness and pregnancy
Adverse reaction dry mouth drowsiness hypersentivity
Dosage Oral ndash 1 to 2mgkg
IM ndash 11mgkg
Promethazine Oral or IM Onset 15 to 60mins Duration 4 to 6 hrs Uses
To prevent and treat nausea and vomiting associated with motion pregnancy or surgery
Produces sedation and reduce swelling pain and trismus
Lower seizure threshold Adverse reaction dry mouth blurred vision thickening of bronchial secretions Dosage OralIM ndash 05-11mgkg
maximum 25 mg
Diphenhydramine
Oral IM IV
Onset -1hr
Duration ndash 4 to 6 hr
Metabolized in liver
Adverse reaction disturbed coordination thickening of bronchial secretions
Dosage Oral IM IV ndash 1 to 15mgkg
maximum 50mg
Tranquilizers
Major tranquilizer antipsychotic produce calmness control symptoms of psychoses cause reversible extra pyramidal symptoms and do not tend to cause habituation
Minor tranquilizer antianxiety agents also cause calmness do not cause extrapyramidal symptoms Used in conditions like nervous tension and mild depression
8
Classification
Antipsychotics
Phenothiazine derivatives
Chlorpromazine promazine
Butryophenones
Haloperidol
Rauwolfia alkaloids
Reserpine
Antianxiety drugs
Propyl alcohol derivatives
Meprobamate
Benzodiazepine derivatives
Diazepam
Miscellaneous compounds
Hydroxyzine
Meprobamate
White crystalline powder slightly bitter in taste
Only administered orally
Peak blood concentration ----1 to 3hrs
10 ---------excreted unchanged Rest --- excreted as a oxidized derivative or as a glucoronide
Uses
To relieve day time anxiety
Induce sleep in insomniacs
To reduce anxiety associated with dental treatment
Anti-convulsant ndash petit mal epilepsy
Adverse reaction leucopenia acute non-thrombocytopenic purpura ecchymoses eosinophilia edema adenopathy
Dosage Childrengt 6yrs 100 to 200mg
Not recommended for children under 6yrs
Monitoring during sedation
1 Pulse
2 Blood pressure
3 ECG
4 Respiration
5 Temperature
Pulse
Manual Electronic
bull Radial Brachial
bull Facial labial
Blood pressure
ndash Stethoscope amp sphygmomanometer
ndash Automatic devices
ndash Direct cannulation of an artery ndash very accurate
Electrocardiograph
Heart rate rhythm myocardial function
9
Respiration
ndash Monitoring respiratory rate
ndash Observing the rise amp fall of the chest wall
ndash Observing the color of mucous membrane
ndash Observing the inflation amp deflation of the reservoir bag
Devices for monitoring respiration
1 The Precordial pretracheal stethoscope
2 The esophageal stethoscope
ndash Respiratory rate
ndash Heart rate
ndash Any abnormal sounds
Pulse Oximeter
ndash Oxygen saturation
ndash Heart rate
ndash Oxisensor site
ndash Fingers
ndash Toe
ndash Ear lobe
Mechanism
Oxygenated Hb ndash red light
Deoxygenated Hb- infrared light
Tissue pressure from arterial pulse (plethysmography)
Advantages
ndash Safe amp noninvasive
ndash Simple to use
ndash Information is rapidly available for clinical decision
ndash Indirectly indicates respiratory adequacy
Disadvantages
ndash Finger probes can get dislodged
ndash Emitted light source may cause burning
ndash Non reusable probes are expensive
ndash Does not directly determine airway patency
Capnography
1 The presence absence of air flow
2 Indicates depth amp adequacy of respiration
3 Continues analysis of the co2 content of the respired air ndash indicates respiratory adequacy
Temperature
ndash Disposable nondisposable thermometer
ndash Esophageal rectal temp probe
10
Discharge criteria
Cardiovascular function is satisfactory amp stable
Airway patency is uncompromised amp satisfactory
Pt is easily arousable amp protective reflexes intact
State of hydration is adequate
Pt can talk if applicable
Pt can sit unaided if applicable
Pt can ambulate with minimal assistance if applicable
Presedation level of responsiveness achieved
Responsible individual is available
1
PULP THERAPY OF VITAL TEETH
DR MITAKSHARA NIRWAN
Contents
Indirect pulp capping
Direct pulp capping
Medications amp materials used in pulp capping
Pulpotomy
MTA
Apexogenesis
INDIRECT PULP CAPPING
Pieter Van Forest - first to speak about root canal therapy
Glove designed instruments that could prepare a canal to a certain size and taper(1910)
Indirect pulp capping is defined as a procedure where in small amount of carious dentin is retained in
deep areas of cavity to avoid exposure of pulp followed by placement of a suitable medicament and
restorative material that seals off the carious dentin and encourages pulp recovery (Ingle)
A procedure in which only the gross caries is removed from the lesion and the cavity is sealed for a
time with a biocompatible material (McDonald)
Objective of indirect pulp capping
These were given by Eidelman in 1965
bull Arresting the carious process
bull Promoting dentin sclerosis
bull Stimulating formation of tertiary dentin
bull Remineralization of carious dentin
Layers of Carious Dentin Indications of Indirect Pulp Capping
History
Mild pain associated with eating
Negative history of spontaneous extreme pain
Clinical Examination
Deep carious lesion which are close tobut not involving the pulp in vital primary or young
permanent teeth
No mobility
Nominal pulp inflammationdefinite layer of affected dentin after removal of infected dentin
Radiographic examination
Normal lamina dura amp PDL space
No radiolucency around the apices
2
Contraindications of Indirect Pulp Capping
History
Sharp penetrating pulpalgia
Prolonged spontaneous pain especially at night
Clinical examination
Mobility of tooth
Discoloration of tooth
Negative reaction of electric pulp testing
Radiographic examination
Definite pulp exposure
Break in the lamina dura
Radiolucency around the apices
Widened PDL space
Treatment procedure
Sequelae of Indirect Pulp Capping Three distinct types of new dentin formation take place
1 Cellular fibrillar dentinmdashfirst 2 months
2 Globular dentinmdash3 months
3 Tubular dentin (uniform mineralized dentin)
bull 15th of reparative dentin formation begins in less than 30 days
bull After 3 months 01 mm is formed
DIRECT PULP CAPPING Defined by Kopel (1992) as the placement of a medicament or non medicated material on a pulp that
has been exposed in course of excavating the last portions of deep dentinal caries or as a result of
trauma
Objective
To create new dentin in the area of the exposure and subsequent healing of the pulp
Rationale
achieve a biologic closure of the exposure site by deposition of hard tissue barrier (dentin bridge)
between pulp tissue and capping material thus walling off the
INDICATIONS
Small mechanical exposure
Easily controlled haemorrhage
Bright red haemorrhage
True pinpoint exposure
CONTRAINDICATIONS
Severe toothache at night
Spontaneous pain
Tooth mobility
Radiographic appearance of pulp periradicular de- generation
Excess of hemorrhage at the time of exposure Serous exudate from the exposure
Externalinternal root resorption
Swellingfistula
Histological Changes after Pulp Capping
These were illustrated be Glass and Zander in 1949
After 24 hours Necrotic zone adjacent to calcium
hydroxide paste is separated from healthy pulp
tissue by a deep staining basophilic layer
After 7 days Increase in cellular and fibroblastic
activity
After 14 days Partly calcified fibrous tissue lined by
odontoblastic cells is seen below the calcium
proteinate zone disappearance of necrotic zone
After 28 days Zone of new dentin
3
Medications and Materials Used for Pulp Capping Calcium hydroxide
Corticosteroids amp antibiotics
Inert materials
Collagen fibers
4-META adhesive
Direct bonding
Isobutyl cyanoacrylate
Denatured albumin
Mineral trioxide aggregate
Laser
Bone morphogenic protein
PULPOTOMY
Finn (1995) defined it as the complete removal of the coronal portion of the dental pulp
followed by placement of a suitable dressing or medicament that will promote healing and
preserve vitality of the tooth
American Academy of Pediatric Dentistry (1998) defined pulpotomy as the amputation of
affected infected coronal portion of the dental pulp preserving the vitality and function of the
remaining part of radicular pulp
Objectives
bull Removal of inflamed and infected coronal pulp at the site of exposure thus preserving the vitality of the
radicular pulp and allowing it to heal
bull Maintain the tooth in the dental arch
Rationale
bull Radicular pulp is healthy and capable of healing after surgical amputation of the infected coronal pulp
bull Preserves vitality of the radicular pulp
bull Maintains tooth in a physiologic condition
Indications of Pulpotomy bull Mechanical pulp exposure in primary teeth
bull Teeth showing a large carious lesion but free of radicular pulpitis
bull History of only spontaneous pain
bull Hemorrhage from exposure sites bright red and can be controlled
bull Absence of abscess or fistula
bull No interradicular bone loss
bull No interradicular radiolucency
Contraindications of Pulpotomy bull Persistent toothache
bull Tenderness on percussion
bull Root resorption more than 13rd of root length
bull Large carious lesion with nonrestorable crown
bull Highly viscous sluggish hemorrhage from canal orifice which is uncontrollable
bull Medical contradictions like heart disease immuno compromised patient
bull Swelling or fistula
bull External or internal resorption
bull Pathological mobility
bull Calcification of pulp
Classification of pulpotomy
4
Formocresol Pulpotomy
Iby BUCKLEY in 1904
Sweet (1930) Formulated multi visit technique
Doyle (1962) Advocated 2 sitting procedure (complete devitalization)
Spedding (1965) Gave 5 minute protocol (partial devitali- zation)
Venham (1967) Proposed 15 seconds procedure
Current concept uses 4 minutes of application time
Composition of formocresol Buckleyrsquos Formula
bull Cresol ndash 35 percent
bull Glycerol ndash 15 percent
bull Formaldehyde ndash 19 percent
bull Water ndash 31 percent
Mechanism of Action
It prevents tissue autolysis by bonding to the proteins Bonding is of peptide groups of side chain amino acids and is a reversible process accomplished without
changing the basic structure of protein molecules
Histological Changes
bull Demonstrated by Mass and Zilbermann11 in 1933 and also by Massler and Mansokhani in 1959
bull Immediately the pulp becomes fibrous and acidophillic
bull Seven to fourteen days Three zones appear
a broad eosinophilic zone of fixation
b broad pale-staining zone of atrophy with poorcellular definition
c broad zone of inflammation extending apically into normal pulp tissue
bull One yearndash Progressive apical movement of these zones with only acidophillic zone left at the end of 1 year
Modified Formocresol Pulpotomy
Used by TRASK(1972)
The technique is identical to that described for primary teeth except that the formocresol pellet is
sealed permanently in the tooth
Two-visit Devitalization Pulpotomy
Indications
bull There is evidence of sluggish bleeding at the amputation site that is difficult to control
bull Pus in the chamber but none at the amputation site
bull There is thickening of the PDL
bull History of pain
Contraindications
bull Nonrestorable tooth
bull Tooth with necrotic pulp
5
Glutaraldehyde Pulpotomy
It was first suggested by S Gravenmade Introduced by Kopel in 1979
Mechanism of Action
bull Glutaraldehyde produces rapid surface fixation of the underlying pulpal tissue
bull A narrow zone of eosinophilic stained and compressed fixed tissue is found directly beneath the area of application which blends into vital normal appearing tissue apically
bull With time the glutaraldehyde fixed zone is replaced by macrophagic action with dense collagenous tissue thus the entire root canal tissue is vital
Cvekrsquos Pulpotomy
bull This is also called as calcium hydroxide pulpotomy or young permanent partial pulpotomy
bull This was proposed by Mejare and Cvek16 in 1978
bull Indicated in young permanent teeth where the pulp is exposed by mechanical or bacterial means and the
remaining radicular tissue is judged vital by clinical and radiographic criteria whereas the root closure is
notcomplete
MINERAL TRIOXIDE AGGREGATE (MTA) Torabinejad described the physical and chemical properties of MTA in 1995
It is ash colored powder made primarily of fine hydrophilic particles of
1 tricalcium aluminate
2 tricalcium silicate
3 silicate oxide
4 tricalcium oxide
5 bismuth dioxide
Hydration of the powder results in a colloidal gel composed of calcium oxide crystals in an amorphous
structure This gel solidifies into a hard structure in less than three hours
PROPERTIES OF MTA
It is biocompatible material and its sealing ability is better than that of amalgam or ZOE
Initial pH is 102 and set pH is 125
The setting time of cement is 4 hours
The compressive strength is 70 MPA which is comparable with that of IRM
Low cytotoxicity ndash It presents with minimal inflammation if extended beyond the apex
Mineral trioxide aggregate (MTA) has demonstrated the ability to induce hard-tissue formation in
pulpal tissues and it promotes rapid cell growth
APEXOGENESIS
It is defined as the treatment of a vital pulp by capping or pulpotomy in order to permit continued
growth of the root and closure of the open apex
Rationale
Maintenance of integrity of the radicular pulp tissue to allow for continued root growth
Indications
bull Indicated for traumatized or pulpally involved vital permanent tooth when root apex is incompletely formed
bull No history of spontaneous pain
bull No sensitivity on percussion
bull No hemorrhage
bull Normal radiographic appearance
Contraindications
bull Evidence that radicular pulp has undergone degenerative changes
bull Purulent drainage
bull History of prolonged pain bull Necrotic debris in canal
bull Periapical radiolucency
6
1
Gupta A Dhingra R Chaudhari P Gupta A
Department of Paedodontics and Preventive Dentistry Faculty of Dental Sciences SGT University Gurgaon Haryana India
Journal of Indian Society of Pedodontics and Preventive Dentistry
Volume 35 I Issue 3 I July-September 2017
A COMPARISION OF VARIOUS MINIMALLY
INVASIVE TECHNIQUES FOR THE REMOVAL
OF DENTAL FLUOROSIS STAINS IN
CHILDREN
DR MITAKSHARA NIRWAN
CONTENTS
bull Introduction
bull Aims
bull Materials and Methods
bull Results
bull Discussion
bull Conclusion
bull Critical analysis
bull References
INTRODUCTION
bull Dental fluorosis is a developmental disturbance of dental enamel caused by
successive exposure to high concentrations of fluoride during tooth
development
bull Various methods of therapy are advocated for the treatment of fluorosis -
stained teeth which range from invasive ceramic veneer bonding restorations
to abrasive chemical treatments
bull The combination of dental bleaching techniques and microabrasion appears
as an excellent conservative solution to reestablish health in fluorosis
affected teeth
AIMS
bull The aim of the study was to evaluate and compare the effectiveness of
minimally invasive techniques for the removal of dental fluorosis
stains in children in vivo
MATERIALS AND METHODS
Patients visiting the department of Pedodontics and Preventive dentistry
Faculty of Dental Sciences SGT University Gurgaon
bull Sample size 90 patients
bull Age group 10 -17 years
bull Caries cracks or periodontal
disease on anterior teeth
bull Abscess draining sinus
cellulitis
bull Non vital teeth
hypersensitive exposed
crevices
bull Orthodontic appliance
bull Past history of bleaching
bull At least two permanent
maxillary anterior teeth
bull TSIF of score 4
bull Free of systemic diseases
Inclusion criteria Exclusion criteria
2
Groups
Group A In office bleaching with 35 hydrogen peroxide( Pola Office
Bleaching kit) activated by light emitting diode (LED) bleaching unit
(35 HP)
Group B Enamel microabrasion (EM) (PREMA Enamel Microabrasion
System) followed by in-office bleaching with 44 carbamide peroxide
gel (EM)
Group C In-office bleaching with 5 sodium hypochlorite (5
NaOCl)
A baseline colour evaluation was done by taking digital photograph of
the maxillary anterior teeth
RESULTS
Group 1
Colour stability
Group 2 Group 3
Tooth sensitivity
Tooth sensitivity values were taken before the treatment
which was compared to immediate postoperative and follow
up visits It was checked using an electric pulp tester
maximum
moderate
least
immediately
group 2
group 1
group 3
1 month
group 2
group 1
group 3
3 month
group 2
group 1
group 3
Patient satisfaction score
Satisfaction was assessed on visual analog scale
Range 1 to 5
Groups percentage of patients
who were satisfied with
the treatment
Number of patients
who reported slight
reappearance of colour
Group 1
90
7
Group 2
83
8
Group 3
73
7
3
Number of Appointments
Groups One sitting Two sittings Three
sittings
Group 1
25
4
1
group 2
26
3
1
Group 3
30
0
0
DISCUSSION
bull Hydrogen peroxide is capable of penetrating the tooth osmosis and through porosities and cracks subsequently acting directly on the pigmented molecules
bull Gurgan et al investigated 3 different light systems and found out that diode laser system with gave best tooth whitening and least tooth sensitivity
bull In the EM group the surface reflects and refracts light from the surface in such way that mild imperfections in underlying enamel are camouflaged While the highly polished surface of enamel enhances the aesthetic appearance
bull Train et al and Loguercio et al also had the similar results in their studies with EM mild fluorosis showed best results moderate showed moderate results while it had little effect on severe fluorosis
bull NaOCl was only effective on mild stains while moderate and severe
stains could only be lightened to quite an extent but could not be
completely removed
bull When NaOCl comes in contact with hypomineralized and discoloured
enamel it degrades and removes the chromogenic organic material
located on the enamel surface
CONCLUSION
bull It was concluded that esthetic appearance of teeth mild fluorosis can
be achieved by bleaching and microabrasion But in cases of
moderate fluorosis a combination of any of theses modalities can be
used
bull As no special maintenance precautions are required these maybe be
considered as an interesting alternative to conventional operative
treatment
bull Focuses on only TSIF of 4
bull Electric pulp testing is not the
right method to check for
sensitivity
bull Tooth Sensitivity changes
from person to person
bull Food habits can cause
staining of the teeth
bull Minimally invasive
bull Cheaper to veneers
bull Minimal loss of tooth structure
bull 4 parameters checked for the success of treatment
bull Inclusion of specific score of fluorosis for comparing the results
bull Maximum 3 appointments needed
CRITICAL ANALYSIS
Pros Cons
REFERENCES
bull Gurgan S Cakir FY Yazici E Different light-activated in officebleaching
systems Lasers Med Sci 201025817-22
bull Train TE McWhorter AG Seale NSWilson CF Guo IY Examination of
esthetic improvement and surface alteration following microabrasion in
fluorotic human incisors in vivoPediatr dent 199618353-62
bull Loguercio AD Correia LD Zago C Tagliari D Neumann E Gomes OM et al
Clinical effectiveness of two microabrasion materials materials for the
removal of enamel flurosis stains Oper Dent 200732531-8
4