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Respiratory System Diseases Charles Feldman Professor of Pulmonology Charlotte Maxeke Johannesburg Academic Hospital University of the Witwatersrand

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Page 1: Respiratory System Diseases - psc.gov.za · PDF fileRespiratory System Diseases Charles Feldman Professor of Pulmonology . Charlotte Maxeke Johannesburg Academic Hospital . University

Respiratory System Diseases

Charles Feldman Professor of Pulmonology

Charlotte Maxeke Johannesburg Academic Hospital University of the Witwatersrand

Page 2: Respiratory System Diseases - psc.gov.za · PDF fileRespiratory System Diseases Charles Feldman Professor of Pulmonology . Charlotte Maxeke Johannesburg Academic Hospital . University

1990 2020 Ischaemic heart disease Cerebrovascular disease Lower resp infection Diarrhoeal disease Perinatal disorders COPD Tuberculosis Measles Road Traffic Accidents Lung Cancer

Stomach Cancer HIV

Suicide

Causes of Mortality Worldwide

Source: Murray & Lopez. Lancet 1997

Page 3: Respiratory System Diseases - psc.gov.za · PDF fileRespiratory System Diseases Charles Feldman Professor of Pulmonology . Charlotte Maxeke Johannesburg Academic Hospital . University

Some Facts about Pneumonia

• Commonest reason for admission of persons to hospital after childbirth

• Together with Influenza is second commonest cause of death in South Africa and is the commonest infection cause of death

• Involves all strata of society • HIV infection is a major risk factor • Should include tuberculosis in the discussion

Page 4: Respiratory System Diseases - psc.gov.za · PDF fileRespiratory System Diseases Charles Feldman Professor of Pulmonology . Charlotte Maxeke Johannesburg Academic Hospital . University

Risk Factors for Pneumonia

• Age (young and elderly) • Socioeconomic factors • Smoking and alcohol • HIV infection • Chronic medical conditions – cardiac, lung,

liver, kidney • Occupational risk factors

Page 5: Respiratory System Diseases - psc.gov.za · PDF fileRespiratory System Diseases Charles Feldman Professor of Pulmonology . Charlotte Maxeke Johannesburg Academic Hospital . University
Presenter
Presentation Notes
Pneumococcal pneumonia
Page 6: Respiratory System Diseases - psc.gov.za · PDF fileRespiratory System Diseases Charles Feldman Professor of Pulmonology . Charlotte Maxeke Johannesburg Academic Hospital . University

Prognosis associated with Pneumonia

• Treatment with antibiotics for ~7 days • Mostly recover complete lung function

except HIV infected persons • Ongoing symptoms may be due to

underlying risk factors • Outpatients less than 1% • In-hospital patients 5-15% • ICU patients up to 50%

Page 7: Respiratory System Diseases - psc.gov.za · PDF fileRespiratory System Diseases Charles Feldman Professor of Pulmonology . Charlotte Maxeke Johannesburg Academic Hospital . University

Natural History and Prognosis of Pneumonia

• Most studies have examined short-term prognosis – in-hospital or 30-day

• Evaluation of older patients from Medicare database

• 158,960 patients • 794,333 controls

• In-patient mortality 11% versus 5.5% • 1 year mortality 40.9% versus 29.1%

Kaplan et al Arch Intern Med 2003

Page 8: Respiratory System Diseases - psc.gov.za · PDF fileRespiratory System Diseases Charles Feldman Professor of Pulmonology . Charlotte Maxeke Johannesburg Academic Hospital . University

5

0

Pat

ient

s

10

15 20

25

30 35 40

45

Hospital mortality 1 Year mortality

CAP Control

Kaplan et al Arch Intern Med 2003

Page 9: Respiratory System Diseases - psc.gov.za · PDF fileRespiratory System Diseases Charles Feldman Professor of Pulmonology . Charlotte Maxeke Johannesburg Academic Hospital . University

1.0

0.6

0.4

0.2

0.0

0.8

Pro

babi

lity

of S

urvi

val

0 50 1000 1500 2000 Time (days)

Page 10: Respiratory System Diseases - psc.gov.za · PDF fileRespiratory System Diseases Charles Feldman Professor of Pulmonology . Charlotte Maxeke Johannesburg Academic Hospital . University

1.0

0.6

0.4

0.2

0.0

0.8

0 50 1000 1500 2000 Time (days)

Pro

babi

lity

of S

urvi

val

PSI Risk Classification

Class 1 & 2 (n=617)

Class 3 (n=613)

Class 4 (n=1306)

Class 5 (n=748)

Page 11: Respiratory System Diseases - psc.gov.za · PDF fileRespiratory System Diseases Charles Feldman Professor of Pulmonology . Charlotte Maxeke Johannesburg Academic Hospital . University

Introduction to COPD The deviation of man from the state in which he was originally placed by nature seems to have provided him with a prolific source of diseases

Jenner 18th Century

• This was never more true than when applied to

the effects of cigarette smoke and chronic obstructive pulmonary disease (COPD)

Parr DG. Proc Am Thorac Soc 2011; 8: 338-349

Page 12: Respiratory System Diseases - psc.gov.za · PDF fileRespiratory System Diseases Charles Feldman Professor of Pulmonology . Charlotte Maxeke Johannesburg Academic Hospital . University

1990 2020 Ischaemic heart disease Cerebrovascular disease Lower resp infection Diarrhoeal disease Perinatal disorders COPD Tuberculosis Measles Road Traffic Accidents Lung Cancer

Stomach Cancer HIV

Suicide

6th

3rd

COPD Mortality Worldwide

Source: Murray & Lopez. Lancet 1997

Page 13: Respiratory System Diseases - psc.gov.za · PDF fileRespiratory System Diseases Charles Feldman Professor of Pulmonology . Charlotte Maxeke Johannesburg Academic Hospital . University

Overlapping disease entities included in the definition of COPD

COPD

Airflow Obstruction

Chronic Bronchitis Emphysema

Asthma

Friedlander AL et al. J COPD 2007; 4: 355-384

Page 14: Respiratory System Diseases - psc.gov.za · PDF fileRespiratory System Diseases Charles Feldman Professor of Pulmonology . Charlotte Maxeke Johannesburg Academic Hospital . University

The Definition of COPD - GOLD

COPD is a preventable and treatable disease with some significant extrapulmonary effects that may contribute to the severity in individual patients

Its pulmonary component is characterized by airflow

limitation that is not fully reversible The airflow limitation is usually progressive and

associated with an abnormal inflammatory response of the lung to noxious particles or gases

www.goldcopd.org

Page 15: Respiratory System Diseases - psc.gov.za · PDF fileRespiratory System Diseases Charles Feldman Professor of Pulmonology . Charlotte Maxeke Johannesburg Academic Hospital . University

Allergens

Presenter
Presentation Notes
Colour photos of different allergens.
Page 16: Respiratory System Diseases - psc.gov.za · PDF fileRespiratory System Diseases Charles Feldman Professor of Pulmonology . Charlotte Maxeke Johannesburg Academic Hospital . University

Risk Factors for COPD

• Smoking • Genetic • Socioeconomic • Gestational • Occupational - silicosis • Tuberculosis • HIV infection

Page 17: Respiratory System Diseases - psc.gov.za · PDF fileRespiratory System Diseases Charles Feldman Professor of Pulmonology . Charlotte Maxeke Johannesburg Academic Hospital . University

COPD and Associated Co-Morbidities

• COPD patients are at increased risk of: • Myocardial infarction, angina • Osteoporosis • Respiratory infection • Depression • Diabetes • COPD and lung cancer

Page 18: Respiratory System Diseases - psc.gov.za · PDF fileRespiratory System Diseases Charles Feldman Professor of Pulmonology . Charlotte Maxeke Johannesburg Academic Hospital . University

Sutherland ER et al. N Eng J Med 2004; 536: 2689–2697

FEV 1

(%of

pre

dict

ed)

100

50

20

Asymptomatic Lung

function normal

Lung function reduced

Axis of progression

Sym

ptom

s

Severe

Mild

When do Patients Present? • Symptoms generally develop only after a significant

drop in FEV1 (to less than 50%) has occurred

Presenter
Presentation Notes
Notes The course of COPD begins with an asymptomatic phase in which lung function deteriorates without associated symptoms.1 Substantial deterioration has already occurred by the time most patients are symptomatic; symptoms generally develop only after FEV1 has fallen below 50% predicted.1 These patients do not have mild disease when they present to their doctor, but already have moderate or severe COPD according to the GOLD Guidelines (moderate 50-80% predicted FEV1, severe 30-50% predicted FEV1).2 References 1.Sutherland ER et al. N Eng J Med 2004; 536: 2689–2697. 2.National Collaborating Centre for Chronic Conditions (NICE). Thorax 2004; 59(Suppl 1): 1–232.
Page 19: Respiratory System Diseases - psc.gov.za · PDF fileRespiratory System Diseases Charles Feldman Professor of Pulmonology . Charlotte Maxeke Johannesburg Academic Hospital . University

SYMPTOMS cough

sputum shortness of breath

EXPOSURE TO RISK FACTORS

tobacco occupation

indoor/outdoor pollution

SPIROMETRY

How do you Diagnose COPD?

Presenter
Presentation Notes
A diagnosis of COPD should be considered in any patient who has cough, sputum production, or dyspnea and/or a history of exposure to risk factors. The diagnosis is confirmed by spirometry. To help identify individuals earlier in the course of disease, spirometry should be performed for patients who have chronic cough and sputum production even if they do not have dyspnea. Spirometry is the best way to diagnose COPD and to monitor its progression and health care workers to care for COPD patients should have assess to spirometry.
Page 20: Respiratory System Diseases - psc.gov.za · PDF fileRespiratory System Diseases Charles Feldman Professor of Pulmonology . Charlotte Maxeke Johannesburg Academic Hospital . University

Pre Post

Obstructive Very severe obstruction Non reversible COPD

Page 21: Respiratory System Diseases - psc.gov.za · PDF fileRespiratory System Diseases Charles Feldman Professor of Pulmonology . Charlotte Maxeke Johannesburg Academic Hospital . University

Classification of COPD Severity by Spirometry

Stage I: Mild FEV1/FVC < 0.70 FEV1 > 80% predicted Stage II: Moderate FEV1/FVC < 0.70 50% < FEV1 < 80% predicted Stage III: Severe FEV1/FVC < 0.70 30% < FEV1 < 50% predicted Stage IV: Very Severe FEV1/FVC < 0.70 FEV1 < 30% predicted or FEV1 < 50% predicted plus chronic respiratory failure

Page 22: Respiratory System Diseases - psc.gov.za · PDF fileRespiratory System Diseases Charles Feldman Professor of Pulmonology . Charlotte Maxeke Johannesburg Academic Hospital . University

Global Strategy for Diagnosis, Management and Prevention of COPD

Combined Assessment of COPD

Ris

k

(GO

LD C

lass

ifica

tion

of A

irflo

w L

imita

tion)

Ris

k

(Exa

cerb

atio

n hi

stor

y) > 2

1

0

(C) (D)

(A) (B)

mMRC 0-1 CAT < 10

4

3

2

1

mMRC > 2 CAT > 10

Symptoms (mMRC or CAT score)

Page 23: Respiratory System Diseases - psc.gov.za · PDF fileRespiratory System Diseases Charles Feldman Professor of Pulmonology . Charlotte Maxeke Johannesburg Academic Hospital . University

A B

C D

Lower risk

Higher risk

Low symptoms High symptoms

GOLD 2013 combined assessment

More than 1 exacerbation

or 1 admission in previous

year? No

Yes

Breathless during usual daily activity on most days?

No Yes

Simplified to 2 key questions

Page 24: Respiratory System Diseases - psc.gov.za · PDF fileRespiratory System Diseases Charles Feldman Professor of Pulmonology . Charlotte Maxeke Johannesburg Academic Hospital . University

A B

C D

Lower risk

Higher risk

Low symptoms High symptoms

GOLD 2013 combined assessment

More than 1 exacerbation

or 1 admission in previous

year? No

Yes

Breathless during usual daily activity on most days?

No Yes

Simplified to 2 key questions

Page 25: Respiratory System Diseases - psc.gov.za · PDF fileRespiratory System Diseases Charles Feldman Professor of Pulmonology . Charlotte Maxeke Johannesburg Academic Hospital . University

4

5

5

3

4

4

5

34

4

Page 26: Respiratory System Diseases - psc.gov.za · PDF fileRespiratory System Diseases Charles Feldman Professor of Pulmonology . Charlotte Maxeke Johannesburg Academic Hospital . University

Global Strategy for Diagnosis, Management and Prevention of COPD

Modified MRC (mMRC) Questionnaire

Page 27: Respiratory System Diseases - psc.gov.za · PDF fileRespiratory System Diseases Charles Feldman Professor of Pulmonology . Charlotte Maxeke Johannesburg Academic Hospital . University

Definition of an Exacerbation

“an event in the natural course of the disease characterized by a change in the patient’s baseline dyspnoea, cough, and/or sputum that is beyond normal day-to-day variations, Is acute in onset, and may warrant a change in regular medication in a patient with underlying COPD”

2006 Update

Page 28: Respiratory System Diseases - psc.gov.za · PDF fileRespiratory System Diseases Charles Feldman Professor of Pulmonology . Charlotte Maxeke Johannesburg Academic Hospital . University

Sym

ptom

s Usual pattern

Time

(a)

Sym

ptom

s

Treatment failure

Time

(b)

Initial treatment

Additional treatment

Sym

ptom

s

Recurrence

Time

(c)

> 4 weeks

> 6 weeks

Soler-Cataluna JJ et al. COPD: J COPD 2010; 7: 276-284

Page 29: Respiratory System Diseases - psc.gov.za · PDF fileRespiratory System Diseases Charles Feldman Professor of Pulmonology . Charlotte Maxeke Johannesburg Academic Hospital . University

Social withdrawal

Worsening quality of life

More exacerbations

Increased risk of hospitalisation

What Does an Exacerbation Mean to a Patient?

Greater anxiety

Decline in lung function

Garcia-Aymerich J et al. 2001 Donaldson D et al. 2002

Gore JM et al. 2000 Seemungal T et al. 1998

Pauwels Pet al. 2001 Seemungal T et al. 2000

Garcia-Aymerich J et al. 2003 Anto JM et al. 2001

Increased symptoms (I.e. breathlessness)

Increased risk of mortality

Presenter
Presentation Notes
Exacerbations of COPD are a major cause of morbidity, mortality and hospital admission.1,2 Some patients are particularly susceptible to developing frequent exacerbations, an important determinant in health-related quality of life.1–3 The downward spiral of more frequent exacerbations can lead to decline in lung function; greater anxiety; worsening quality of life; social withdrawal; more exacerbations and increased risk of hospitalisation.1-9 As frequent exacerbations are associated with a faster long-term decline in lung function, it has also been suggested that prevention of exacerbations might slow disease progression.9 In addition, a reduction in the frequency or severity of exacerbations offers an obvious means of reducing demand on the healthcare system. Patients who are prone to exacerbations have been found to have higher airway cytokine levels suggesting increased airway inflammation that could increase susceptibility to exacerbation.5 These patients are also prone to larger falls in FEV1 at exacerbations, prolonged and more frequent hospital admissions, more chronic respiratory symptoms and more severe exacerbations.4 Exacerbations that require hospital admission are associated with a high risk of mortality 10. References: 1. Rodriguez-Roisin R. Towards a consensus definition for COPD exacerbations. Chest 2000; 117: 398S–401S. 2. Wedzicha JA. Mechanisms of exacerbations. Novart Found Symp 2001; 234: 84–103. 3. Seemungal TAR, Donaldson GC, Paul EA et al. Effect of exacerbation on quality of life in patients with chronic obstructive pulmonary disease. Am J Respir Crit Care Med 1998; 157: 1418–22. 4. Garcia-Aymerich J, Monso E, Marrades RM et al. Risk factors for hospitalisation for a chronic obstructive pulmonary disease excerbation - EFRAM study. Am J Respir Crit Care Med 2001; 164: 1002–07. 5. Donaldson GC, Seemungal TA, Bhowmik A, Wedzicha JA. Relationship between exacerbation frequency and lung function decline in chronic obstructive pulmonary disease. Thorax 2002; 57(10): 847–52. 6. Gore JM, Brophy CJ, Greenstone MA. How well do we care for patients with end stage chronic obstructive pulmonary disease (COPD)? A comparison of palliative care and quality of life in COPD and lung cancer. Thorax 2000; 55: 1000–6. 7. Pauwels RA, Buist AS, Calverley PM et al. Global strategy for the diagnosis, management, and prevention of chronic obstructive pulmonary disease. NHLBI/WHO Global Initiative for Chronic Obstructive Lung Disease (GOLD) Workshop summary. Am J Respir Crit Care Med 2001; 163: 1256–76. 8. Seemungal TA, Donaldson GC, Bhowmik A et al. Time course and recovery of exacerbations in patients with chronic obstructive pulmonary disease. Am J Respir Crit Care Med 2000; 161: 1608–13. 9. Garcia-Aymerich J, Farrero E, Felez MA et al. Risk factors of readmission to hospital for a COPD exacerbation: a prospective study. Thorax 2003; 58(2): 100–5. 10. Anto JM et al. Epidemiology of chronic obstructive pulmonary disease. Eur Resp J 2001;17:982-994
Page 30: Respiratory System Diseases - psc.gov.za · PDF fileRespiratory System Diseases Charles Feldman Professor of Pulmonology . Charlotte Maxeke Johannesburg Academic Hospital . University

LML. BC Medical Journal 2010; 52: April 2010 www.bmcj.org FitzGerald JM. Postgrad Med J October 2011; 87: 655-656

Page 31: Respiratory System Diseases - psc.gov.za · PDF fileRespiratory System Diseases Charles Feldman Professor of Pulmonology . Charlotte Maxeke Johannesburg Academic Hospital . University

“Lung Attacks” vs “Heart Attacks”

Lung attack

Heart attack

In-hospital mortality

Mortality within 1 year of attack

8 – 11%

8 – 9.4%

22 – 43%

25 – 38%

Chapman K and Kaplan A, with COPD Canada and Family Physician Airways Group of Canada 2011

Page 32: Respiratory System Diseases - psc.gov.za · PDF fileRespiratory System Diseases Charles Feldman Professor of Pulmonology . Charlotte Maxeke Johannesburg Academic Hospital . University

40

60

10

0

Mor

talit

y (8

%)

50

20

30

Hospital stay

60 days 180 days 1 year 2 years

Mortality after a COPD Exacerbation

Anzueto A. Eur Respir J 2010; 19: 113-118 – quoting Connors Jr., AF. SUPPORT Study

Page 33: Respiratory System Diseases - psc.gov.za · PDF fileRespiratory System Diseases Charles Feldman Professor of Pulmonology . Charlotte Maxeke Johannesburg Academic Hospital . University

Baseline Clinical Status

Criteria Risk Factors

Pathogens Treatment

Acute tracheo-bronchitis

No underlying lung disease

Usually viral Usually none

Simple chronic bronchitis

Younger patient, FEV1 > 50%,

increased sputum volume and

virulence

H influenzae M catarrhalis

S pneumoniae

Aminopenicillin, Amox-clavulanate,

Macrolide or azalide or ketolide

Feldman C et al. S Afr Med J 2007

Classification of Bronchitis

Page 34: Respiratory System Diseases - psc.gov.za · PDF fileRespiratory System Diseases Charles Feldman Professor of Pulmonology . Charlotte Maxeke Johannesburg Academic Hospital . University

Complicated chronic bronchitis

As for 2 plus elderly, FEV1 < 50%, >4 AECB

per year, with sig. morbidity

Same pathogens but increased risk of

antibiotic resistance

Amox-clavulanate 2nd or 3rd gen.

cephalosporin, or new fluoroquinolone

Chronic bronchial sepsis

As above plus continuous sputum / year or co-morbidity

Above plus Enterobacteria P aeruginosa

Fluoroquinolone, old or new, or other

agent acc to sensitivity

Baseline Clinical Status

Criteria Risk Factors

Pathogens Treatment

Feldman C et al. S Afr Med J 2007

Classification of Bronchitis

Page 35: Respiratory System Diseases - psc.gov.za · PDF fileRespiratory System Diseases Charles Feldman Professor of Pulmonology . Charlotte Maxeke Johannesburg Academic Hospital . University

1990 2020 Ischaemic heart disease Cerebrovascular disease Lower resp infection Diarrhoeal disease Perinatal disorders COPD Tuberculosis Measles Road Traffic Accidents Lung Cancer

Stomach Cancer HIV

Suicide

Causes of Mortality Worldwide

Source: Murray & Lopez. Lancet 1997

Page 36: Respiratory System Diseases - psc.gov.za · PDF fileRespiratory System Diseases Charles Feldman Professor of Pulmonology . Charlotte Maxeke Johannesburg Academic Hospital . University

Healthy Lung Tissue

Page 37: Respiratory System Diseases - psc.gov.za · PDF fileRespiratory System Diseases Charles Feldman Professor of Pulmonology . Charlotte Maxeke Johannesburg Academic Hospital . University

Diseased Lung Tissue

Page 38: Respiratory System Diseases - psc.gov.za · PDF fileRespiratory System Diseases Charles Feldman Professor of Pulmonology . Charlotte Maxeke Johannesburg Academic Hospital . University

Diagnostic Tests

• CXR • CT Scans • MRI • Sputum cytology • Fibreoptic bronchoscopy • Transthoracic fine needle aspiration

Presenter
Presentation Notes
**As a nurse working with a client, what would be some things you could tell him or her about what to expect for each test? A chest x-ray is preformed to search for: pulmonary density, a solidary peripheral nodule (coin lesion) (a mass in the lung or airway) Atelectasis (collapsed lung) Infection fluid in the lung enlarged lymph nodes in the chest “A chest x ray is a painless, noninvasive test that creates pictures of the structures inside your chest, such as your heart, lungs, and blood vessels. "Noninvasive" means that no surgery is done and no instruments are inserted into your body Your ribs and spine are bony and absorb radiation well. They normally appear light on a chest x ray. Your lungs, which are filled with air, normally appear dark. A disease in the chest that changes how radiation is absorbed also will appear on a chest x ray”. (http://www.nhlbi.nih.gov/health/health-topics/topics/cxray/) Chest x rays have few risks. The amount of radiation used in a chest x ray is very small. A lead apron may be used to protect certain parts of your body from the radiation. CT scans shows the size, shape, and position of your lungs and other structures in your chest. Follow up on abnormal findings from standard chest x rays. Find the cause of lung symptoms, such as shortness of breath or chest pain. Find out whether you have a lung problem, such as a tumor, excess fluid around the lungs, or a pulmonary embolism. Most places will provide the patient with a gown. He/she will need to undress, usually down to their underwear, and put the gown on. If the place does not provide a gown the patient should wear loose-fitting clothes. �Any woman who suspects she may be pregnant should tell her doctor beforehand. �Doctors may ask the patient to fast (eat nothing) and even refrain from consuming liquids for a specific period before the scan. �The patient will be asked to lie down on a motorized examination table, which then goes into the giant doughnut-like machine. The couch with the patient goes into the doughnut hole. � MRI is like a CT only it uses magnetism instead of xrays, remove all metallic objects, fill out a screening form, asked to lie down on a comfortably padded table that gently glides you into the scanner. ��earplugs or headphones to protect your hearing because, when certain scanners operate, they may produce loud noises. These loud noises are normal and should not worry you. ��Nurse may inject a contrast agent called "gadolinium" in vein to help obtain a clearer picture of the area being examined. A saline solution will drip through IV to prevent clotting until the contrast material is injected at some point during the exam. �The most important thing for the patient to do is to relax and lie still. Most MRI exams take between 15 to 45 minutes to complete depending on the body part imaged and how many images are needed.�You will be asked to remain perfectly still during the time the imaging takes place, but between sequences some minor movement may be allowed. You will be guided.��may breathe normally, however, for certain examinations it may be necessary for you to hold your breath for a short period of time. ��During your MRI examination, the MR system operator will be able to speak to you, hear you, and observe you at all times. Consult the scanner operator if you have any questions or feel anything unusual.��When the MRI procedure is over, you may be asked to wait until the images are examined to determine if more images are needed. After the scan, you have no restrictions and can go about your normal activities. � Sputum cytology is rarely used to make a dx of lung Ca; medical test in which a sample of sputum (mucus) is examined under a microscope to determine whether abnormal cells are present. A sample may be obtained either by the person coughing up mucus at home or in the doctor’s office or during a bronchoscopy. Remove dentures if you wear them. • Rinse your mouth with water. • Take about four deep breaths followed by a few short coughs, then inhale deeply and cough forcefully into the container. Make sure to get a sample from deep in your airway. (http://www.lung-cancer.com/sputum.html) however fibreoptic bronchoscopy is more commonly used and provides a detailed study of the tracheobronchial tree and allows for brushings, washings, and biopsies of suspicious areas. Test to see inside the airways of your lungs, or to get samples of mucus or tissue from the lungs. Bronchoscopy involves placing a thin tube-like instrument called a bronchoscope through the nose or mouth and down into the airways of the lungs. The tube has a mini-camera at its tip, and is able to carry pictures back to a video screen or camera. not to eat after midnight the night before (or about 8 hours before) the procedure. You will also receive instructions about taking your regular medicines, smoking and removing any dentures before the procedure. Before beginning the procedure, you will inhale an aerosol spray of a medicine like Novocain, which numbs the nose and throat area and helps to prevent coughing and gagging during the procedure. After that you will be given a sedative by vein. The sedative will help you to relax, and may make you feel sleepy. The sedative may also help you to forget any unpleasant sensations felt during the test. After the procedure, do not drink for 1⁄2 to 1 hour or until the numbness completely wears off. Do not drive home by yourself after the procedure; arrange for a family member or friend to take you home. Contact your doctor immediately if you have shortness of breath or chest pain, or you cough up more than a few tablespoons of blood at home. (http://patients.thoracic.org/information-series/en/resources/fiberoptic-bronchoscopy.pdf) A transthoracic fine needle aspiration A fine needle aspiration biopsy is a test done to see if a tumor is benign (non-cancerous) or malignant (cancerous.) Fine needle aspiration (FNA) is done by inserting a thin needle into a tumor and removing cells that can be evaluated under the microscope. A pathologist looks at the cells to see if the suspicious tumor is cancer, and if it is cancer, what type of cancer. With lung cancer, the needle is inserted into the chest through the skin. Doctors can make sure the needle goes to the right part of the lung by watching it through ultrasound or a CT scanner. Given cough suppressant, CT scan or help find target of biopsy, skin cleaned just above ribs, sedative and local anesthetic for area, <30mins, small incising in skin, hold breathe stay still, insert needle thru skin and chest wall, feel pressure and pain when reach surface of lung, pain when reach area for tissue extraction. CXR done to see no collapse, short recovery time and home the same day unless a complication. (http://www.youtube.com/watch?v=abvYaB2VcmI) http://lungcancer.about.com/od/glossary/g/FNA.htm
Page 39: Respiratory System Diseases - psc.gov.za · PDF fileRespiratory System Diseases Charles Feldman Professor of Pulmonology . Charlotte Maxeke Johannesburg Academic Hospital . University

Lung Biopsy

Presenter
Presentation Notes
A lung biopsy removes a small piece of lung tissue which can be analyzed at under a microscope to determine if the tumor is cancer or not to determine the type of cancer to determine the grade of cancer (slow or fast)
Page 40: Respiratory System Diseases - psc.gov.za · PDF fileRespiratory System Diseases Charles Feldman Professor of Pulmonology . Charlotte Maxeke Johannesburg Academic Hospital . University

Lung Cancer Staging

Clinical Staging Pathological

• based on findings gathered by the doctor

• used to plan the initial therapy • may be modified by additional

information found during pathological examination

• Based on the examination of the tissue samples obtained from the primary tumor, nodes or metastasis

• Helpful in planning additional treatment and follow-up

Presenter
Presentation Notes
Clinical staging is used to plan the preliminary therapy to treat the cancer. And it may be changed by additional data found during pathological examination. It is based on findings gathered by the doctor used to plan the initial therapy may be modified by additional information found during pathological examination.
Page 41: Respiratory System Diseases - psc.gov.za · PDF fileRespiratory System Diseases Charles Feldman Professor of Pulmonology . Charlotte Maxeke Johannesburg Academic Hospital . University
Presenter
Presentation Notes
Apical segment LLL pneumonia
Page 42: Respiratory System Diseases - psc.gov.za · PDF fileRespiratory System Diseases Charles Feldman Professor of Pulmonology . Charlotte Maxeke Johannesburg Academic Hospital . University
Presenter
Presentation Notes
Lung mass =- carcinoma
Page 43: Respiratory System Diseases - psc.gov.za · PDF fileRespiratory System Diseases Charles Feldman Professor of Pulmonology . Charlotte Maxeke Johannesburg Academic Hospital . University

• Under discussion today • Pneumonia • Bronchitis • COPD • Lung Cancer

• Also need to be considered? • Asthma • Tuberculosis • HIV infection

Diseases Under discussion