9. TB Flashcards

1
Q

what is the causative organism of TB and how is it identified

A
  • Mycobacterium tuberculosis
  • identified via:
    1. sputum smear - acid-fast so stains red with Ziehl-Neelson stain
    2. culture (Lowenstein-Jensen medium) - gold standard for diagnosis (although slow growing,
    up to 6 wks though 1-3 wks with modern automated systems) and required for drug sensitivity testing
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2
Q

how is Mtb transmitted

A

person to person by infected droplets

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3
Q

what is a primary complex

A

result of immune response mounted against Mtb - includes:

  1. GHON’S FOCUS - containment of Mtb with caseating granuloma
  2. associated lymph node

Ghon focus is macroscopic feature - visible on Xrays

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4
Q

describe the process of primary infection

A
  1. Mtb inhaled and deposted in alveoli are phagocytosed by alveolar macrophages…
  2. Mtb prevents phagolysosome fusion but macrophages still initiate cell-mediated immunity…
  3. over 6 wks, Th cell response mounted against Mtb… produce IFNy… activates macrophages to become bactericidal and produce TNF… recruit monocytes…
  4. monocytes differentiate into ‘epithelioid hisitocytes’ - form caseating granulomas, i.e. GHON’S FOCUS

(in maj. of Ps, before healing occurs,

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5
Q

describe the microscopic appearance of a TB granuloma

A

caseous necrosis core surrounded by epithelioid marcophages, Langerhans giant cells and lymphocytes

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6
Q

what are the possible outcomes of primary complex formation

A
  1. progression to primary active disease (5%)
  2. healing/self-cure
    +/- latent infection: before healing occurs in many Ps, some bacilli enter blood and seed other parts of lungs or extra-pulmonary sites via haematogenous spread
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7
Q

what is a Ranke complex

A

healed Ghon focus that has calcified

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8
Q

name 3 differences between active and latent TB

A

Active
1- active, multiplying tubercle bacilli in body
2- symptomatic
3- infectious

Latent
1- inactive, contained tubercle bacilli in body
2- no symptoms
3- not infectious

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9
Q

how are active and latent TB differentiated in diagnostic tests

A
  • TST or IFNy tests: usually +ve in both
  • sputum smears and cultures: +ve in active, -ve in latent
  • CXR: abnormal in active, normal in latent
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10
Q

what are the risk factors for TB reactivation

A

immunosuppression, eg.

  • HIV
  • corticosteroids or other immunosuppressants
  • diabetes mellitus
  • extremes of age
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11
Q

why is post-primary TB often more serious than primary TB

A
  • secondary immune system activation - stronger response means more tissue damage
  • bacteria has time to mutate and adapt
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12
Q

what are the symptoms of TB

A

Pulmonary symptoms:

  • cough
  • haemoptysis occasionally
  • dyspnoea if pleural effusion

General symptoms:

  • fever and night sweats
  • weight loss and anorexia
  • tiredness and malaise
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13
Q

why does post-primary TB more commonly occur in upper lung zones

A

higher alveolar pO2 relatiev to rest of lung

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14
Q

name 4 negative pulmonary effects of TB infection

A
  1. cavity formation: softening and liquefaction of caseous material which is discharged into bronchus… cavity formation… fibrosis
  2. Haemorrhage from extension of caseous process into vessels of cavity walls… haemoptysis
  3. Spread to rest of lung: caseous and liquefied material spreads infection through bronchial tree to other lung zones
  4. Pleural effusion
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15
Q

name common sites of extra-pulmonary TB

A
  1. Cervical LNs (scrofula)
  2. GI or peritoneal (ascitic or adhesive)
  3. Genito-urinary - slow progression to renal disease and subsequent spreading to lower urinary tract
  4. Bones and joints, esp. spine (Pott’s disease)
  5. CNS (tuberculous meningitis)
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16
Q

what is miliary TB

A

haematogenous spread of Mtb causing widespread infection, either during primary active TB or during reactivations

lungs always involved as well as multiple other organs

17
Q

describe the treatment regimen for TB

A
  • Rifampicin
  • Isoniazid
  • Pyrazinamide
  • Ethambutol

All 4 for 2 mths then 1st 2 for 4 mths

18
Q

why might compliance to treatment be poor

A
  1. length of treatment - 6 mths
  2. drug side effects, e.g. hepatotoxicity

Need to do DOT/VOT

19
Q

what is the tuberculin sensitivity test and what does it show

what are the limitations

A

Tuberculin (mycobacterial protein) is injected intra-dermally. Presence of skin reaction (induration due to hypersensitivity reaction) 48-72hrs later at site indicates previous TB exposure.

limitations:

  • false positives (BCG, non-TB)
  • false negatives (immunocompromsied)
20
Q

what is the interferon gamma releasing assay

what are the limitations

A

P lymphocytes cultured with Mtb Ag… if previous exposure, T lymphocytes produce interferon gamma in response.

No cross-reaction with BCG but cannot distinguish between latent and active TB and similar probs with sensitivity and specificity