Tuberculosis Flashcards

1
Q

Is the disease burden from TB increasing or decreasing?

A

It is falling globally

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2
Q

How bad is the TB epidemic?

A
  • TB is the number 1 killer of communicable diseases.

- TB kills more than HIV and Malaria together.

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3
Q

What are the vulnerable groups in the UK for TB?

A
  • Those from high prevalence countries.
  • Homeless, alcoholics, IDU’s, those with mental health problems and in prison.
  • HIV positive, Immunosuppressed.
  • Elderly, neonates, diabetics.
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4
Q

Which mycobacteria can cause TB?

A
  • M. tuberculosis, M. africanum, M. bovis.
  • They are non-motile bacillus, very slow growing and aerobic.
  • Uniquely has a very thick fatty cell wall.
  • HOWEVER, not all acid and alcohol fast bacilli (AAFBs) are TB.
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5
Q

How is TB transmitted?

A
  • Airborne (pulmonary & Laryngeal TB spreads, the others not)
  • Usually requires prolonged close contact.
  • Outdoors mycobacteria is eliminated by UV radiation and dilution.
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6
Q

What is the exception to the rule about hoe TB is spread?

A
  • Exception is Mycobacterium bovis, which can be spread by consumption of unpasteurized infected cows’ milk (very uncommon in the U.K.)
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7
Q

Immunopathology (immune responses) for TB

A

Activated macrophages > Epithelioid cells > Langhan’s giant cells

Accumulation of macrophages, epithelioid & Langhan’s cells > GRANULOMA

Central caseating necrosis (may later calcify)

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8
Q

How is the Th1 cell mediated immunological response like a two edged sword?

A
  • It eliminates/ reduces number of invading mycobacteria.

- Tissue destruction is a consequence of activation of macrophages.

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9
Q

Features of primary infection of TB

A
  • No preceding exposure or immunity.
  • Mycobacteria spread via lymphatics to draining hilar lymph nodes.
  • Usually no symtoms, can be fever, malaise.
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10
Q

What does the primary infection progress to (in a small number 1%)?

A

It progresses to Tuberculous bronchopneumonia.

  • Primary focus continues to enlarge - cavitation
  • Enlarged hilar lymph compress bronchi, lobar collapse
  • Enlarged lymph node discharges into bronchus
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11
Q

What does the primary infection progress to (in a small number 1-3%)?

A
  • Miliary TB (looked like millet seeds on autopsy) develops, with hematogenous spread of bacteria to multiple organs
  • Fine mottling on X-ray, widespread small granulomata
  • CNS TB in 10-30%
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12
Q

What does the primary infection progress to (in the majority >85%)?

A
  • Initial lesion + local lymph node (Primary complex)
  • Heals with or without scar. May calcify (Ghon focus + complex)
  • Associated with development of immunity to tuberculoprotein
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13
Q

What are the two main hypothesis’ of post primary disease?

A
  1. TB bacteria entering a dormant stage with low or no replication over prolonged periods of time.
  2. Balanced state of replication and destruction by immune mechanisms.
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14
Q

What are the clinical presentations of TB?

A
  • Cough
  • Fever
  • Sweats (mainly at night)
  • Weight loss
  • All three symptoms
  • CRP normal in 15%, ESR normal in 21%.
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15
Q

What may be absent in the clinical presentations of TB?

A
  • Fever absent in 37%
  • Sweats absent in 39%
  • Weight loss absent in 38%
  • All three absent in 25%
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16
Q

When would you consider CT post-primary TB?

A
  • Normal Chest Xray but clinical suspicion
  • Miliary TB
  • Cavitation & other differential
  • Lymphadenopathy, alternative diagnosis.
  • Targets for BAL
17
Q

How would you diagnose active pulmonary TB using Chest Xray?

A

Primary TB:

  • Mediastinal lymphadenopathy (mainly unilateral, 15% bilateral)
  • Pleural effusion
  • Miliary (hematogenous spread, 1-3%)
  • Pneumonic lesion w/ enlarged hilar nodes- consider primary TB
18
Q

How would you get a bug sample for TB?

A
  • Sputum; 3 samples, 8-24hrs gap, at least 1 early morning sample
  • Induced sputum
  • Bronchoscopy with BAL
  • Endobronchial ultrasound (EBUS) with biopsy
  • Lumbar puncture in CNS TB
  • Urine in urogenital TB
  • Aspirate/biopsy from tissue ( lymph-node, bone, joint, brain, abscess …)
  • Mantoux or IGRA are NOT routinely used in diagnosing active TB
19
Q

What drugs are used to treat TB?

A
  • Streptomycin
  • Isoniazid
  • Pyrazinamide
  • Rifampicin
  • Ethambutol
20
Q

Rules for the treatment of tuberculosis

A
  • Multiple drug therapy is essential
  • Single agent treatment leads to drug resistant organisms within 14 days.
  • Therapy must continue for at least 6 months.
  • TB therapy is a job for committed specialists only.
  • Legal requirements to notify all cases.
  • Test for HIV, Hepatitis B and C.
21
Q

What is the standard treatment for TB?

A

2 Rifampicin/Isoniazid/Ethambutol + 4 Rifampicin/Isoniazid

  • Standard 70kg patient takes 12 tablets daily.
  • 6 months duration
  • Pyridoxine (Vitamin B6) with isoniazid to reduce risk of neuropathy
  • Steroids (CNS, Milliar, Pericardial)
  • Vitamin-D substitution ?
22
Q

What are side effects of Rifampicin?

A
  • Orange ‘Irn Bru’ urine/tears/lenses
    Induces liver enzymes, prednisolone, anticonvulsants
  • All hormonal contraceptive methods ineffective
  • Hepatitis
23
Q

What are the side effects of Isoniazid?

A
  • Hepatitis

- Peripheral neuropathy (pyridoxine B6)

24
Q

Who can get the BCG vaccination?

A
  • Given selectively to risk groups since 2005
  • Neonates, or unvaccinated children under 5, whose parents/grandparents were born in a country with an annual incidence of TB of 40/100,000 or greater
  • Unimmunised contacts of cases
  • Unimmunised high risk employees
25
Q

Who should get screened for latent TB (LTBI)?

A
  • Contacts of people with active pulmonary or laryngeal TB who are aged ≤65 years (hepatotoxicity increases with age)
  • New entrants from high endemic areas
  • ‘Pre-biologics’ (TNF-alpha inhibitors)
  • Outbreaks
26
Q

What is the treatment for Latent TB (LTBI)?

A
  • Rifampicin & Isoniazid for three months or
  • Isoniazid only for six months, or
  • Rifampicin only for six months, or
  • Rifapentine & Isoniazide once weekly for 12 weeks (underserved population).