Tuberculosis Flashcards

1
Q

Describe the global distribution of tuberculosis and its impact on tuberculosis in the UK.

A
  • The disease burden from
  • High prevalence countries (India, China, Indonesia, Philippines, Africa)
  • 70% are non UK born, aged 15-44
  • London is a risk factor (39% of TB cases in UK)

TB globally is falling.

  • TB is the number one killer of communicable diseases
  • TB is the leading killer of people with HIV
  • Kills more than HIV and malaria together.
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2
Q

Describe the histopathology of tuberculosis.

A
  • Granulomatous inflammation
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3
Q

at risk

A
  • HIV positive, immunosuppressed

- Elderly, neonates, diabetics

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4
Q

outline the pathogenesis of tuberculosis in its primary, post- primary and fibrocaseous forms in the lung.

A
  • M. tuberculosis, M.africanum, M. bovis (bovine TB, BCG strain)

“Infection - inhalation of droplet nuclei.
M. tuberculosis is deposited in alveoli & engulfed by alveolar macrophages.
Proliferating bacilli kill macrophages & are released.

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5
Q

describe mycobacteria tuberculosis.

A
  • Non-motile bacillus, very slowly growing (disease is slow, the treatment is long)
  • Aerobic (has a predilection for apices of lungs)
  • Uniquely has a very thick fatty cell wall (Resistant to acids, alkalis and detergents
    neutrophil and macrophage destruction)
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6
Q

what do Th1 cells do in response to M. Tb, and what does this cause?

A

Th1 cells & macrophages form a granuloma to prevent further growth - latent TB

-Eliminates the number of invading mycobacteria but causes tissue destruction because of the activation of macrophages

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7
Q

Describe the pathogenesis of tuberculosis in its primary, post- primary form.

A
  • No preceding exposure or immunity
  • Progressive or latent or cleared.
  • Mycobacteria is spread via lymphatics and drains to hilar lymph nodes

In the majority (>85%)
Initial lesion + local lymph node (Primary complex)
Heals with or without scar. May calcify (Ghon focus + complex)
Associated with development of immunity to tuberculoprotein

  • Primary infection progresses to Tuberculous bronchopneumonia
  • Primary focus continues to enlarge - cavitation
  • Enlarged hilar lymph compress bronchi, lobar collapse
  • Enlarged lymph node discharges into bronchus
  • Poor prognosis
  • In a small number (1-3%)
  • 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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8
Q

hypotheses behind post-primary disease

A
  • TB entering a dormant stage with low or no replication over prolonged periods of time
  • Balanced state of replication and destruction by immune mechanisms
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9
Q

Describe the common clinical presentations of tuberculosis.

A

Usually presents with no symptoms

  • Cough
  • Fever
  • Sweats (mainly at night)
  • Weight loss
  • malaise
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10
Q

Describe the public health duties of doctors managing cases of Tuberculosis.

A
  • CXR should be obtained
  • 3 sputum samples
  • nucleic acid amplification test (NAAT) should be performed on at least one respiratory specimen.
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11
Q

Define the major groups of antituberculous drugs, their pharmacological profiles and side effects, and their practical application in the management of tuberculosis.

A
  • Isoniazid (H)
  • Pyrazinamide (z)
  • Rifampicin ( R)
  • Ethambutol (E)
  • R and H for the entire 6 months
  • -E and z for the first two months
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12
Q

side effects of isoniazid

A
  • Hepatitis

- Peripheral neuropathy

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13
Q

side effects of pyrazinamide

A
  • hepatitis
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14
Q

side effects of rifampicin

A
  • orange pee

- hepatitis

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15
Q

how can active tb occur

A

-progression of primary disease or reactivation of latent disease

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16
Q

what a cxr would show

A
  • At the apices, there is soft “fluffy” upper zone
  • Cavitation in 10-30%
  • Lymphadenopathy is rare
17
Q

latent tb screening

A

normal CXR

but also positive Mantoux test, IGRA