Tuberculosis Flashcards

1
Q

What organisms cause TB?

A

Mycobacterium tuberculosis

Mycobacterium bovis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

Describe Mycobacterium tuberculosis as an organism

A

Obligate aerobe, acid fast bacillus, non motile, gram +ve, rich glycolipid cell wall, slow growing.
Resistant so can survive in aerosols over long distances
Acid fast so can survive in gastric secretions
Waxy so resistant to antibiotics

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

How is TB transmitted?

A

Person to person by infectious droplets. Needs to be a prolonged exposure - at least 8 hours a day for 6 months

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

Describe some risk factors for catching TB

A
  • Immunosuppression - HIV, diabetes, steroid treatment
  • Drug abuse
  • Alcoholism
  • Preexisting lung disease
  • Poverty
  • Residents of congregate settings eg prisons, hospitals, homeless shelters
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Describe the pathophysiology for when TB enters the lungs…

A
  1. Alveolar macrophages phagocytose the TB bacteria but cannot eliminate them
  2. Cord factor (glycolipid in cell wall) inhibits fusion of phagosome to prevent lysis
  3. TB remains in the macrophage and divides so as not to provoke humoral response
  4. Phagocytosed TB can only be destroyed by activated lymphocytes
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

What would you see on histology if a patient had TB?

A
  • Caseating granulomas

- Polynuclear Langhan’s giant cells, central necrosis, lymphocytes and epithelioid histiocytes

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

How does active infection of TB occur?

A
  • Occurs when containment by the immune system (T cells/macrophages) is inadequate
  • Arises from primary infection or reactivation of latent disease
  • 5% of cases progress to active disease from a primary infection
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

How does latent TB occur?

A
  • Granuloma formation prevents bacteria growth and spread aka the immune system contains it
  • Patient is asymptomatic and non infectious. 1/3 of the worlds population have latent TB.
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

What is post primary TB and why does it occur?

A
  • Reactivation of latent TB (5/10% lifetime risk)
    Due to: New infection, HIV, organ transplantation, immunosuppression, silicosis, IVDU, malnutrition, high risk settings, haemodialysis
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

What are the symptoms of latent TB?

A

NONE - not even on scans

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

What are symptoms of active TB?

A

Constitutional - fever, weight loss, night sweats, fatigue, lymphadenopathy
Pulmonary - dyspnoea, productive cough of over 3 weeks, haemoptysis, pleurisy, pleural effusion

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

What are some extrapulmonary symptoms of TB?

A

Tuberculosis lymphadenitis - Painless enlargement of cervical/supraclavicular lymph nodes.
GI TB - Most disease is ileocaecal. Colicky abdominal pain, bowel obstruction due to bowel wall thickening, inflammatory adhesions or strictures.
Spinal TB - Local pain and bony tenderness for weeks/months. Slow progression.
CNS TB - Meningitis, confusion
Genitourinary TB - Dysuria, frequency, loin pain, haematuria, sterile pyuria
Cardiac TB - Pericarditis, pericardial effusion, rare to get myocardial involvement
Skin - Lupus vulgaris, scrofuloderma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

What is miliary TB?

A

Haematogenous dissemination of TB.
Leads to millet appearance of the lung as discrete foci of granulomatous tissue forms.
Needs prompt treatment!!!

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

What are the diagnostic tests for latent TB?

A
  1. Tuberculin skin testing - Mantoux test. Intradermal infection of PPD tuberculin. Size of skin induration is used to determine positivity depending on vaccination history and immune status (>5mm if risk factors, >15mm if no risk factors)
  2. Interferon gamma release assays - More specific than TST if history of BCG vaccination. (blood test)
    - Neither test can diagnose or exclude active disease (false negative 25%)
    - If immunosuppressed, sensitivity of testing decreases
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

What are the diagnostic tests for active TB?

A
  1. CXR - Fibronodular/linear opacities in the upper lobe, cavitation, calcification, miliary disease, effusion, lymphadenopathy
  2. Sputum smear - Can be induced with nebulised saline. Stained f (Ziehl Neelson) or acid fast bacilli.
  3. Sputum culture - More sensitive, culture takes 1-3 weeks. Can assess drug sensitivity.
  4. Nucleic acid amplification test - Direct detection of TB in sputum by RNA/DNA amplification. Rapid diagnosis <8 hrs. Can detect pulmonary disease
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

What are the diagnostic tests for extra pulmonary TB?

A
  1. Investigate for co-existing pulmonary disease
  2. Obtain material by aspiration/biopsy to enable AFB staining, histological examination and/or culture.
  3. NAAT can be carried out on any sterile body fluid eg CSF, pericardial fluid
17
Q

What is the treatment regimen for TB?

A
R - Rifampicin
I - Isoniazid
P - Pyrazinamide
E - Ethambutol 
RIPE - 6 months in total, all four for first 2 months, then continue RI for 4 next months.
18
Q

What should you keep in mind about rifampicin?

A
  • Enzyme inducer, care with warfarin, calcineurin inhibitors, ostreogens, phenytoin
  • Body secretions stain orange/red
  • Altered liver function
19
Q

What should you keep in mind about isoniazid?

A
  • Peripheral neuropathy
  • Altered liver function
  • Consider pyridoxine as prophylaxis if they have HIV, DM, CKD, malnutrition as increased risk of pn
20
Q

What should you keep in mind about pyrazinamide?

A
  • Idiosyncratic hepatotoxicity, reduce dose if GFR<30
21
Q

What should you keep in mind about ethambutol?

A
  • Colour blindness, optic neuritis, reduced visual acuity
  • Check visual acuity at the start of treatment and monitor with monthly visual check
  • Monitor levels if GFR<30
22
Q

When should you treat latent TB?

A
  • Balance the risk of development of active disease with possible side effects of treatment
  • Treatment if increased risk of active disease eg immunosuppression
  • Treat with 3 months RI (with pyridozine) or 6 months of I (with pyridozine)
23
Q

Is active TB a notifiable disease?

A

Yes - both clinical and cultured diagnoses

24
Q

When should you use NAAT to screen for drug resistance?

A
  1. Previous TB treatment
  2. Contract with drug resistant disease
  3. From an area with >5% cases which are drug resistant
25
Q

What should you do if rifampicin resistance is detected?

A

Treat with at least 6 agents the TB is sensitive to