Tuberculosis Flashcards

(46 cards)

1
Q

What percentage of TB patients and their households face catastrophic costs?

A

Around 49%.

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2
Q

What is the End TB Strategy target for catastrophic costs?

A

Zero.

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3
Q

What socioeconomic factors are strongly associated with TB incidence?

A

Low average income levels and undernutrition.

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4
Q

What kind of organism is Mycobacterium tuberculosis?

A

An obligate intracellular bacterium.

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5
Q

Where does M. tuberculosis grow?

A

Inside macrophages.

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6
Q

How fast does M. tuberculosis grow in the lab?

A

6 weeks.

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7
Q

How is TB transmitted?

A

Via airborne droplets <5µm that reach the alveoli.

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8
Q

How many droplet nuclei can a single cough produce?

A

About 3,000.

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9
Q

Is brief exposure sufficient to cause infection?

A

No – generally requires prolonged exposure (e.g., 8+ hours in enclosed space).

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10
Q

After inhalation, what are the possible outcomes of M. tuberculosis infection?

A

Cleared from the body (90%)
Healed with scarring (Ghon focus)
Latent infection
Primary progressive disease (no latency)

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11
Q

What kind of immunity is required to control TB?

A

Strong cell-mediated immunity.

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12
Q

Which cytokines are crucial in TB immunity?

A

IFN-γ and TNF-α.

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13
Q

When is the risk of reactivation highest?

A

In the first few years after infection.

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14
Q

What is the biggest risk factor for TB reactivation?

A

Immunocompromise (up to 100x increased risk).

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15
Q

What is the current TB vaccine?

A

BCG – a modified live strain of M. bovis.

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16
Q

What is BCG best at preventing?

A

Disseminated and meningeal TB in children.

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17
Q

What other disease does BCG protect against?

A

Leprosy.

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18
Q

How does latitude affect BCG efficacy?

A

Efficacy decreases closer to the equator.

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19
Q

What are the constitutional symptoms of TB?

A

Fever, weight loss, night sweats.

20
Q

What are the two main forms of TB?

A

Pulmonary and extra-pulmonary.

21
Q

Who is more likely to get primary progressive TB?

A

Children and immunocompromised patients.

22
Q

What are features of primary progressive TB?

A

Erythema nodosum, lymphatic obstruction, abscesses, miliary disease, TB meningitis.

23
Q

When does post-primary TB typically occur?

A

Usually within 2–5 years of initial infection.

24
Q

What lung zones are most affected in post-primary TB?

25
What are key symptoms of post-primary pulmonary TB?
Chronic cough, haemoptysis, pleural effusions, constitutional symptoms.
26
What is the most common site of extra-pulmonary TB?
Lymph nodes (especially cervical).
27
What are "cold abscesses" in TB?
Painless abscesses often found in lymph node TB.
28
Which part of the spine is most commonly affected in TB?
Thoracic spine.
29
What is Gibbus deformity?
Spinal wedging caused by TB of the spine.
30
What other organs can be affected by extra-pulmonary TB?
Brain, GI tract, kidneys, bones/joints.
31
What methods are used to obtain pulmonary TB samples?
Spontaneous sputum, induced sputum, bronchoscopy.
32
What tests are performed on TB samples?
Smear microscopy, culture, and PCR (molecular detection).
33
What are the 4 first-line drugs for TB?
Isoniazid, Rifampicin, Pyrazinamide, Ethambutol.
34
What is the standard TB treatment regimen?
2 months of RIPE 4 OR 7 months of R+I
35
What is the role of Isoniazid in TB treatment?
Bactericidal – rapidly kills multiplying bacteria.
36
What is the role of Rifampicin?
Bactericidal and sterilising – kills slow-growing bacteria.
37
How quickly do Isoniazid and Rifampicin work?
90% of bacteria dead in 2 days with isoniazid 99% dead in 14 days with rifampicin added
38
What drugs were used in TB treatment in the 1950s–60s?
PAS, Streptomycin, Isoniazid.
39
What major change occurred in the 1960s–70s?
Rifampicin replaced PAS.
40
What drug was added in the 1970s?
Pyrazinamide.
41
When was Ethambutol added as the 4th drug?
In the 1980s.
42
What is the aim of latent TB treatment?
To prevent progression to active TB.
43
What are the 3 main latent TB regimens?
6 months isoniazid 4 months rifampicin 3 months of both
44
How effective is latent TB treatment?
Reduces progression risk by ~90%.
45
What are the key risk factors for MDR/XDR-TB?
Previous incomplete treatment Contact with MDR-TB Origin from high-MDR regions Former Soviet Union, South Africa Prison treatment in the Baltics
46
Why is combination therapy essential in TB?
To prevent resistance and ensure sterilization of infection.