Tuberculosis Flashcards

1
Q

Inhalation of M. tuberculosis has 1 of which 4 outcomes?

What % have which outcomes?

When does reactivation TB usually occur?

A
  1. Immediate clearance
  2. Rapid progression to active TB (primary disease)
  3. Reactivation of latent TB
  4. Latent infection (with or without subsequent reactivation)

90% clear/become latent
10% develop primary disease —> more common in immuosup

Reactivation TB usually occurs within 5 years

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2
Q

Which stains detect AFBs on microscopy?

A

Ziehl-Neelsen or Kinyoun stains

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3
Q

How long may it take to cultivate a positive M. tuberculosis culture and why?

A

May take 2-6 weeks

Due to VERY slow growth rate (generation time is 20-24 hours)

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4
Q

What % of people experience reactivation of latent TB?

And what RFs increase this chance?

A

5-15% of people with latent TB experience reactivation

Risk factors:

  • Immunsup: HIV, transplant, TNF-alpha blockers
  • Diseases: silicosis, dialysis
  • Environment: close contacts
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5
Q

Common clinical features of primary tuberculosis?

A
Fever! (for weeks)
Pleuritic chest pain
Rarer sx: fatigue, cough, arthralgia, pharyngitis
Night sweats
Travel history/ contacts

Patients may also have disease at more distant sites –> cervical LNs, meningitis, pericarditis, miliary dissemination

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6
Q

Radiological findings in active pulmonary TB?

CXR and CT

A

CXR: hilar lymphadenopathy!!!/mediastinal lympadenopathy, pleural effusions, consolidation

Consolidation is usually either segmental or lobar & assoc. with ipsilateral hilar LN.

CXR changes may progress over time –> worsening appearances, cavitation

POSTPRIMARY/REACTIVATION TB USUALLY INVOVLES APICAL/POSTERIOR SEGMENTS OF UPPER LOBES >80%

CT: lymphadenopathy (commonly with caseous necrosis), usually dense & homogenous consolidation, cavities in 10%, effusions in 10%
Rarer: large masses, PTx

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7
Q

Common clinical features of reactivation TB

A

Usually insidious…

Fever
Night sweats
Fatigue 
Weight loss
Dyspnoea
Cough --> worsens as disease progresses (may develop haemoptysis)

Advanced disease… pleuritic chest pain/ dyspnoea with extensive parenchymal involvement, painful ulcers of mouth/GI tract due to swallowing secretions, anorexia/wasting/malaise
Tuberculomas (in lungs)

Exam usually normal unless advanced

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8
Q

Pulmonary complications of TB

A
Haemoptysis
Extensive pulmonary destruction 
PTx
Bronchiectasis
Fistulas
Tracheobronchial stenosis
Malignancy
Chronic aspergillosis
Respiratory failure
Septic shock

All more common after reactivation TB disease

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9
Q

Common ddx to consider for a patient presenting with TB symptoms

A
  • Other mycobacterium pneumonia
  • Lymphoma/malignancy
  • Fungal infection
  • Lung abscess
  • Septic emboli
  • Meiloidosis (burkholderia - similar sx and imaging findings)
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10
Q

Why test people for latent TB?

A

A. People at risk of new infection - HCWs, homeless shelters, other high endemic areas, close contacts
B. Risk of progression from latent to active because of comorbidities

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11
Q

Diagnosis of active TB?

A

History + radiology

PLUS (options):

  • Isolate M TB from bodily secretion (sputum MCS - takes up to 6 weeks, BAL, pleural fluid, tissue/lung biopsy)
  • Sputum AFB smears (3 x consecutive mornings)
  • Nucleic acid amplification testing (NAA) of sputum - positive NAA with or without sputum AFB is considered sufficient for TB diagnosis (should be back within a few days)… AKA TB PCR!

…. From reading it seems that more weight is given to the NAA result than the AFB smears

REPORT to public health authority

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12
Q

What if you can’t get sputum for AFB smears, NAA and MCS?

A
  • Try hypertonic saline + chest physio

- Bronchoscopy - with BAL and tissue sample

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13
Q

Requirements before starting TB treatment?

A
  • Patient weight
  • FBE, LFTs, UECs
  • Visual acuity & colour vision
  • HIV testing, HBV/HCV testing
  • Discuss contraception (COCP interaction)
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14
Q

When is a patient presumed non infectious from TB?

A

Around 2 weeks of daily rx with standard short course therapy…

LONGER if:
Extensive cavitations
Suspected drug resistant TB
Smear positive 
Who do not improve with therapy

Note that children <10 considered non infectious & extrapulmonary TB in the absence of lung disease is NOT infectious

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15
Q

What is drug resistant TB? Types and commonness

A

Standard rx not appropriate

Isoniazid-monoresistant TB in 10% of cases in Australia

Multidrug resistant RB (at least isoniazid & rifampicin) uncommon in Australia)

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16
Q

Efficacy of standard short course TB in fully susceptible cases?

A

> 98% initial cure rate

Five year relapse of <1%

17
Q

What is standard short course rx of TB?

A

2/12 of isoniazid, rifampicin, ethambutol and pyrazinamide

++ pyridoxine (prevents development of peripheral neuropathy from isoniazid - particularly use in high risk pts)

Followed by further 4/12 of just isoniazid and rifampicin

Daily for whole 6/12 if HIV, MDR or no smear conversion after 2/12

18
Q

When can and can’t you use standard short course rx for TB?

A

ONLY if:

  • Fully susceptible bacteria
  • Compliant
  • Excluded TB meningitis, CNS TB and complicated MSK TB
  • No initial extensive cavitation
19
Q

What is miliary TB?

A

Extensive haematogenous spread of M TB
Characterised by presence of small, firm white nodule
Manifestations usually acute but may be subacute/chronic

May be fatal
Multiorgan failure, septic shock and ARDS may occur

20
Q

Most common sites of miliary TB disease involvement

A

Lungs, lymphatics, bones, joints, liver, CNS and adrenal glands

21
Q

Investigations / common lab findings for miliary TB

A
  • Bloods, anaemia, raised inflammatory markers, hyponatraemia, hypercalcaemia
  • Urine: sterile pyruia
  • Consider neuroimaging/LP if suspected CNS involvement
  • Consider imaging/biopsy of any areas thought to be involved
  • CXR: classic - faint reticulonodular infiltrate uniform throughout the lungs/ May have other features of TB too. CT is better than CXR
22
Q

Treatment of miliary TB?

A

Genral approach is the same as standard short course therapy - but seek advice