Tuberculosis
Description
- Chronic granulomatous infection caused by *Mycobacterium tuberculosis*, primarily affecting the lungs but capable of involving almost any organ (extrapulmonary TB)
Epidemiology
- Low incidence in Australia (mostly in overseas-born individuals and specific high-risk communities) but a major global cause of infectious death; risk factors - HIV, immunosuppression (including biologics - screen before starting anti-TNF therapy), diabetes, malnutrition, incarceration, homelessness, close contact with an infectious case
Aetiopathogenesis
- Inhaled droplet nuclei -> alveolar macrophage infection -> primary infection (often asymptomatic, contained by cell-mediated immunity as a granuloma - "latent TB") -> reactivation (waning immunity - ageing, immunosuppression) or, less commonly, primary progressive disease (young children, immunocompromised)
Diagnosis
- Active pulmonary TB: chronic cough (>2-3 weeks), haemoptysis, weight loss, night sweats, fever; CXR - upper lobe cavitation classic for reactivation, primary disease often shows lower/mid-zone infiltrate +/- hilar lymphadenopathy
- Sputum smear microscopy (AFB) + culture (culture is the gold standard, but slow - weeks); nucleic acid amplification testing (e.g. GeneXpert) gives rapid results and detects rifampicin resistance
- Latent TB: tuberculin skin test (TST) or interferon-gamma release assay (IGRA) - neither distinguishes latent from active disease; a positive result needs CXR + clinical assessment to exclude active disease before treating as latent
Management
- Active TB - standard regimen: 2 months of rifampicin, isoniazid, pyrazinamide, ethambutol (2HRZE), then 4 months of rifampicin + isoniazid (4HR) - directly observed therapy (DOT) considered for adherence-risk patients
- Latent TB - isoniazid monotherapy (6-9 months) or rifampicin-based shorter regimens, to prevent reactivation
- Multidrug-resistant TB (resistant to at least rifampicin and isoniazid) requires specialist management with second-line agents for a longer duration
- Notifiable disease - triggers public health contact tracing
Associations
- HIV co-infection, immunosuppressive therapy (screen before biologics), diabetes, multidrug-resistant TB, latent TB reactivation
Natural history & complications
- Without treatment, active pulmonary TB has substantial mortality; with appropriate multidrug therapy and adherence, cure rates are high - the principal driver of treatment failure is non-adherence/incomplete treatment, which also drives resistance
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