2 current treatment of dengue virus infection
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Current Treatment of Dengue
Virus Infection
Nur Farhanah
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Epidemiology
Of the 2.5 billion people in the world living in dengue
endemic area
At risk of DF/DHF 1.3 billion live in 10 dengue endemic
countries of WHO SEA Region
In ASEAN countries 51 million people are infected /year
and 20,000 people (especially children) die
WHO SEARO (South-East Asia Region) Dengue SPEED-1SEMARANG, 26-27 MEI 2012
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Source: WHO SEARO Dengue Guideline 2011
Average Annual Number of Cases of DF/DHF reported to WHO
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Indonesia
The Ministry of Indonesian Health (ASEANDengue Conference 1st :15 June 2011) reported
in 2010 Indonesia has the largest number of
dengue patients among the ASEAN
150,000 people were infected
1,400 people, mostly children, died
(Thailand 57,000 people were infected and 70
died)
ASEAN Dengue day June 15th
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http://www.pppl.depkes.go.id/_asset/_download/DBD_2011.gif
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http://www.pppl.depkes.go.id/_asset/_download/DBD_2011.gif
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IR DBD IND, JATENG & SEMARANG
Souce:P2B2 Dinkes Kota SemarangSPEED-1
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Source; P2B2 Dinkes Kota Semarang SPEED-1SEMARANG, 26-27 MEI 2012
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Dengue Virus Pathogenesis
BEE Martina, P. Koraka, OsterhausClin.Microbiol. Rev 2009, 22 (4):564
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Thrombocytopenia
Haemorrhagic
manifestationsHypotension
/shock
Platelet
aggregation
clusterin
C3a,C5a
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1997 2009 2011
WHO Dengue Guidelines
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WHO Dengue guidelines
1997 2009 2011
Title
Guideline for treatment of
DF and DHF in small
hospitals WHO Searo
1999
Dengue Guidelines for
diagnosis, treatment,
prevention and control
WHO TDR 2009
Comprehensive guideline
for prevention and
control of Dengue and
DHF WHO Searo 2011
Page
33 160 212
Content
Clinical manifestation,
diagnosis, case
management
Chapters : (6)
Epidemiology and burden of
disease, clinical
management, vectormanagement, lab
diagnostic tests,
surveillance and emergency
response, new avenues
Chapters : (15)
Epidemiology, disease
burden,clinical
manifestation anddiagnosis, lab diagnosis,
management, surveillance,
vector, vector management,
IVM, Combi, PHC
approach, case
investigation, monitoring,
strategic plan (bi-regionallan
1997 2009 2011
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WHO Dengue Guidelines
Diagnosis Classification
1997 2009 2011Dengue fever Dengue without
warning signs
Dengue fever
DHF grade I Dengue with warning
signs
DHF grade I
DHF grade II DHF grade II
DHF grade III Severe dengue
( severe plasma
leakage, severe
hemorrhage, severeorgan involvement)
DHF grade III
DHF grade IV DHF grade IV
Expanded dengue
syndrome
Adult management Adult management
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WHO Dengue Guideline 1997
Manifestation of Dengue Virus Infection
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Probable an acute febrile illness with two or more of the followingmanifestations:
Headache
Retro-orbital pain Myalgia
Arthralgia
Rash
Haemorrhagic manifestations
Leukopenia;and
Supportive serology (a reciprocal HI antibody titre 1280, acomparable IgG ELISA titre or a positive IgM antibody test ona late acute or convalescent-phase serum specimen );
or
Occurence at the same location and time as other confirmedcases of dengue fever.
Confirmed a case confirmed by laboratory criteria
Reportabl e any probable or confirmed case should be reported
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DF DHF
1. Fever 2-7 days + +
2. Bleeding tendency Positive tourniquet test or Spontaneous bleeding
+/- +
3. Thrombocytopaenia 100,000/mm +/- +
4. Plasma leakage Pleural effusion /ascites
/hypoproteinaemia 20% increase in HCT from baseline
20% decrease in HCT from baseline
after volume-replacement treatment
- +
WHO Dengue Classification 1997
WHO Dengue Classification 1997
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Grade Sign and Symptomps Laboratory
DF DHF without plasma leakage
DHF I Fever with non-specific constitutional
symptoms; the only hemorrhagic
manifestation is a positive tourniquet test
&/or easy bruisingevidence of plasma leakage
Thrombocytopenia
(platelet count
100,000/L)
II DHF grade I plus spontaneous bleeding
III Circulatory failure manifested by a rapid,
weak pulse, narrowing of pulse pressure,
or hypotension, cold & clammy skin,
restlessness
IV Profound shock with undetectable blood
pressure
WHO 1997
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WHO Dengue Guideline 2009
Suggested dengue case classification and
level of severity
Source: WHO Dengue Guideline 2009 SPEED-1SEMARANG, 26-27 MEI 2012
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Neurological
Gastrointestinal/
hepatic
Renal
Cardiac
Ecpanded dengue syndromeExpanded Dengue Syndrome or unusual manfestation
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Respiratory
Musculoskeletal
Lymphoreticular/bonemarrow
Eye
others
Expanded Dengue Syndrome or unusual manfestation
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DF/
DHFGrade Signs and Symptoms Laboratory
DF Fever with two of the following:
HeadacheRetro-orbital pain
Myalgia
Athralgia/bone pain
Rash
Haemorrhagic manifestations
No evidance of plasma leakage
Leucopenia (WBC
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The Course of Dengue Illness
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Dengue Infection : immune response
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Diagnostic Tests
EASY to USE
Confidence
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CASE MANAGEMENTWHO Guideline
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Admission criteria
1997 2009 2011
Signs of significant
dehydration (>10%
normal body weight)
-Any warning sign
-Coexisting condition :
infancy, pregnancy,oldage, obesity, DM,
renal failure,
hpertension, chronic
hemolytic disease etc
-Social circumstance :living alone, far from
health facility, without
reliable means of
transport
-Any warning signs
-sign and symptom
related to hypotension-Bleeding
-Organ impairment
-Finding through
further investigations
-Coexisting conditions
-Social economic
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Fluid Management
1997 2009 2011
DHF grade I-II Dengue with warning
signs
DHF grade I-II
6-7ml/kg/hour
5ml/kg/hour3ml/kg/hourstop after
24-48hours
start 5-7ml/kg/hour
for 1-2hours, reduceto 3-5ml/kg/hour for
2-4hours, reduce to
2-3ml/kg/hour or less
according to clinical
respons
Maintenance (for 1
day)+5% deficit (oraland i.v together) to
be administered over
48 hours
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Fluid Management
1997 2009 2011
DSS Severe Dengue-
Compensated Shock
DHF grade III
10-20ml/kgBB bolus
repeat if necessary
Isotonic crystalloid sol
5-10ml/kg/hour over
one hourreassess
10ml/kg in children or
300-500ml in adult
over one hour or by
bolus, if necessary .
Further fluid
administration should
follow the graph
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Fluid Management
2009 2011
Severe Dengue-hypotensive
shock
DHF grade IV
Initiate i.v fluid with crystalloid or
colloid (if available) at 20ml/kg as
bolus over 15 mnt
10ml/kg bolus fluid as fast as
possible, ideally within 10-1mnt.
When BP is restored, futher iv fluid
may be given as in grade 3. If
shock isnt reversible after the first
10ml/kg, repeat bolus 10 ml/kgand lab results should be pursued
and corrected as soon as possible
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Transfusion in Severe Bleeding
2009 2011
5-10ml/kg of fresh PRC
or 10-20ml/kg of freshwhole blood of an
appropriate rate and
observe clinical
response
5ml/kg of PRC or
10ml/kg of fresh wholeblood
Reassess, repeat if
necessary
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High Risk Patients (2011)
- Infants and the elderly- Obesity
- Pregnant women
- Peptic ulcer disease
- Woman who have menstruation or abnormal vaginal
bleeding- G-6PD deficiency
- Thalassemia and other haemoglobinopathies
- Congenital heart disease
- Chronic diseases (DM, hypertension, asthma, IHD)- CRF, liver cirrhosis
- Patients on steroid or NSAID treatment
Discharge criteria
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Discharge criteria
Criteria 1997 2009 2011
Absence of fever 24hours without
antipyretic
48 hours 24hours without
antipyretic
Clinical
improvement
+ +general well
being,
apetite,hemodyna
mic status, urine
output,no respdistress
+
Return of Apetite + - +
Good urine output + - +
Stable Ht + +(without iv fluid) +
Elapse from
shock recovery
Al least 2 days - 2-3 days
No resp distress + - +
Platelet count >50.000/ul Increasing trend >50.000/ul
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National Guideline
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Tatalaksana
Protokol 1 : Penanganan tersangka
(probable)DBD dewasa tanpa syok
Protokol 2 : Pemberian cairan pada tersangka
DBD dewasa di ruang rawatProtokol 3 : Penatalaksanaan DBD dengan
peningkatan Ht >20%
Protokol 4 : Penatalaksanaan Perdarahan
Spontan pada DBD dewasa
Protokol 5 : Tatalaksana SSD pada dewasa
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Protokol 2 Pemberian Cairan pada Tersangka DBD
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Protokol 2. Pemberian Cairan pada Tersangka DBD
dewasa di Ruang Rawat
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Protokol 3 PENATALAKSANAAN DBD dengan Ht >20%
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Protokol 4 Penatalaksanaan Perdarahan Spontan
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Protokol 4. Penatalaksanaan Perdarahan Spontan
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Protokol 5. Tatalaksana Syok pada Dewasa
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Protokol 5. Tatalaksana Syok pada Dewasa
Koloid maksimal
30ml/Kg
Transfusi PRC
10ml/KgBB
Inotropik:vasoaktif Koreksi as bs,elektr, glikemia,
anemiaInfx sekunder, KID
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Conclusion
The dengue pathogenesis is very multicomplex
Case management is simple and inexpensiveThe cornerstone of treatment is early management offluid, and it could save the patients life
Revised guideline (2009 and 20011) are available andcould be applied according to clinical setting
The WHO guidelines 2009 has higher sensitivity indiagnosing dengue cases (earlier hospitalization, fluidadministration and could be decrease of fatal cases)
WHO SEARO Guidelines 2011 has similar contents and
classifications as WHO Guidelines 1997Be aware to dengue diagnosis and early managemenet
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