- Definitions
- Primary Tuberculosis
- 1-5% of cases
- Infection directly after inoculation by airborne particles
- Symptoms
- Fever (70%)
- Pleuritic chest pain (25%)
- 90% of immunocompetent patient enter latent state
- 10% develop TB pneumonia or progress to distant sites
- Usually those with poor immune responses (HIV, CKD, DM2, immunosuppressants)
- 10% develop TB pneumonia or progress to distant sites
- Latent TB (LTBI)
- Non-contageous, quiescent state
- Only manifestation is positive PPD or Quantiferon (IGRA – interferon gamma release assay)
- Reactivation TB
- 90% of adult cases in non-HIV patients
- Classic symptoms
- Cough, fatigue, fever, night sweats, weight loss
- Sometimes hemoptysis –> usually in the setting of cavitary disease
- Cough, fatigue, fever, night sweats, weight loss
- Primary Tuberculosis
- Risk Factors
- For exposure
- Foreign born
- Homeless
- Incarceration
- Health care workers
- For reactivation
- Immunocompromised
- HIV, malignancy, steroids, DM2
- Prior untreated or inadequately treated disease
- Lifetime risk for reactivation
- Immunocompetent -> 10% lifetime risk
- Immunocompromised -> 10% per year
- Immunocompromised
- For exposure
- Physical finding –> non-specific and usually absent in mild-moderate disease
- Labs
- Sputum samples
- AFB smear/culture
- Obtained by coughing vs induced (inhalation of hypertonic saline from nebulizer)
- 3 specimens at least 8 hours apart
- Most rapid and inexpensive test
- 45-80% sensitive
- AFB positive smear can represent non-tuberculosis mycobacteria (NTM) as well
- Must confirm with culture and nucleic acid amplification
- Nucleic acid amplification (NAA) tests
- Xpert MTB/RIF Test
- Detects MTB DNA and rifampin resistance mutations
- But cannot provide specific sequence information
- Smear positive sample –> 95% sensitive, 98% specific
- Smear negative sample –> 80% sensitive, 95% specific
- Negative Xpert cannot exclude active TB!
- Watch out for false positives from recent previously treated infection
- Detects MTB DNA and rifampin resistance mutations
- Xpert MTB/RIF Test
- Sequencing assays
- Sequencing assays provide specific sequence mutations and predicts drug resistance with greater accuracy
- Not approved by FDA; Remains investigational
- Sequencing assays provide specific sequence mutations and predicts drug resistance with greater accuracy
- AFB smear/culture
- Tuberculin Skin Test (TST) and quantiferon
- Only used to diagnose latent TB infection, not active TB!
- Positive result supports Dx; negative result cannot be used to rule out
- Sputum samples
- Imaging
- CXR
- Primary TB
- Hilar and peritracheal lymphadenopathy (65%)
- Small homogeneous lobar vs perihilar infiltrates (30%)
- Pleural effusion (30%)
- Reactivation TB
- Normal hosts
- apical-posterior infiltrates (85%)
- MTB prefers higher O2 tensions in the apical lung areas
- poor lymphatic flow in apices results in poor organism clearance
- cavitation
- apical-posterior infiltrates (85%)
- Immunocompromised (AIDS) Pts –> Atypical findings
- Diffuse disease (military)
- Mid/lower lung zones
- Hilar and mediastinal LAD
- CT
- More sensitive than plain CXR for early or subtle parenchymal and nodal disease
- Normal hosts
- Primary TB
- CXR
- Management
- General approach
- 6 months of treatment in 2 phases
- Intensive phase –> 2 months
- First line drugs –> “RIPE”
- Rifampin, INH, pyrazinamide, ethambutol
- First line drugs –> “RIPE”
- Continuation phase –> 4 months
- Rifampin
- INH
- Intensive phase –> 2 months
- 6 months of treatment in 2 phases
- Watch out for hepatotoxicity!
- Rifampin, INH, and pyrazinamide are all associated with hepatotoxicity
- All pts in INH should get vit B6
- Avoid fluoroquinolones in suspected TB cases!
- Avoid resistance from TB monotherapy
- General approach