Mycobacterium Tuberculosis Flashcards

1
Q

What is the most common type of infection? How is it transmitted?

A

Pulmonary TB
Highly contagious, respiratory droplet transmission

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2
Q

How to diagnose?

Test for suspected TB

A
  1. Chest X-ray
  2. Sputum sample
  3. Microscopy (acid-fast stain)
  4. Culture and molecular assays (nucleic-acid based testing)
  5. Drug susceptibility testing

Tuberculin skin test
Interferon gamma release assays (blood tests)

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3
Q

What does tuberculin skin test contain and show?

A
  • Intradermal injection of 100uL of tuberculin (PPD)
  • Small pale bump appears and needs to be examined in 72 hours
  • Raised, hard area of swelling >5mm: positive
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4
Q

What does false-positive TST result inclulde?

A
  • Received Bacillus Calmette-Guerin vaccine
  • Improper administration of test
  • Inaccurate interpretation of your test reults
  • Infection with nontuberculous mycobacteria
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5
Q

What are the advantages of interferon gamma release assay?

A
  • Single patient visit > blood sample
  • Results within 24 hours
  • No interpretation bias
  • TB specific
  • No cross-reactivity with BCG vaccine
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6
Q

What are the disadvantages of interferon gamma release assay?

A
  • Blood samples must be processed within 16 hours
  • Limited data on use of QFT-G in children, recently exposed to Tb patients and in immunocompromised patients
  • QFT-G cannto determine who is at risk for developing TB
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7
Q

What are the important biochemical assay tests that suggest active TB?

A
  • ADA in pleural fluid (T cell activation)
  • Renal TB –> Sterile pyuria
  • TB meningitis– > White cell, protein, glucose in CSF
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8
Q

What is the diagnosis of drug resistant TB based on?

A
  • Conventional culture methods: Solid agar methods, liquid broth methods (BACTEC/MGIT)
  • Molecular detection methods; molecular probes
  • Drug susceptibility testing
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9
Q

Describe TB sputum culture

A
  • Slow
  • Expensive
  • Gold standard in TB diagnostics
  • Sputum culture can take 1 to 8 weeks to provide results
  • Sputum cultures higher sensitivity - 82%
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10
Q

What is the 1st-line drug?

A

Combination of 2/3/4 drugs for 6 months
- First 2 months: Rifampicin, isoniazid, pyrazinamide, ethambutol
- Streptomycin not included but remains highly used
- Second 4 months: Isonizaid, rifampicin

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11
Q

Why and who are 2nd line drugs used for? What are they associated with?

A
  • Due to drug resistance, adverse effect/discontinuation of treatment, DDI
  • Non-responsive patients
  • Side effects/toxicity are significant
  • Often less potent drugs
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12
Q

What are the TB drug resistance types?

A
  • Mono-resistance (first-line anti-TB drug only)
  • Poly-resistance (>1 first-line anti-TB drug)
  • Multidrug (at least both isoniazid and rifampicin)
  • Extensive drug (any fluoroquinolone, at least one of three second-line injectable drugs + MDR)
  • Rifampicin-resistant (often used as surrogate marker for MDR)
  • Totally drug (XDR isolates which are additionally resistant to 4th and 5th line drugs)
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13
Q

Characteristics of Tb

A
  • Obligate aerobe
  • Acid fast
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14
Q

What is the stain used?

A

Ziehl neelsen stain

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15
Q

What is the pathological feature of small antigen load + high tissue hypersensitivity TB?

A
  • well formed granuloma containining MTB.
  • healing with fibrosis. encapsulation and scar formation
  • usually this case for immunocompetent ppl
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16
Q

What is the pathological feature of high antigen load + low tissue hypersensitivity TB?

A
  • Caseating (cheesy) granuloma due to poor organization of immune cells & incomplete necrosis
  • Tend to liquify and produce tuberculous cavity with high number of MTB, bronchogenic spread
  • usually immunocompromised ppl
17
Q

What are the common possibilities of progression following primary MTB infection?

A
  1. Lymphohematogenous dissemination may progress directly to military TB
  2. Seeding to apical-posterior areas of the lung (pulmonary TB/reactivation of TB)
  3. Large hilar or mediastinal lymph nodes
  4. Extrapulmonary TB
18
Q

What is the vaccine?

A

BCG (Bacille Calmette-Guerin)

19
Q

What are the limitations of the vaccine?

A
  • life attenuated (cannot give to HIV/immunocompromised)
  • Does NOT prevent infection, but prevents progression to clinical disease
  • prevents serious TB (like miliary or meningitis), but not pulmonary
  • does not prevent latent from reactivating
  • low efficacy in preventing adult TB in high endemicity area
20
Q

What are the clinical presentations?

A

**Pulmonary TB
Pleuritis (pleural cavity)
Lymphadenitis (cervical LN, Peyer’s patches)
**
Laryngeal infection (infectious), meningitis, brain, spinal cord, genitourinary tract TB, gastrointestinal TB, osteomyelitis, arthritis, skin infection (lupus vulgaris), disseminated TB (military TB)

21
Q

How does the chest X ray (CXR) in pulmonary TB commonly presents as?

A
  • Lobar
  • Diffused
  • Cavitation
  • Nodules
  • Lymph node enlargement
22
Q

What are the symptoms and signs of active TB?

A
  • Fever
  • Night sweats
  • Weight loss
  • Chronic cough
  • Haemoptysis
  • Lymphadenopathy
  • Malaise
  • Anorexia

Alarm bell symptoms - can affect any organ

23
Q

Where is the most common site of infection in the lungs?

A

Upper lobes