Lecture 12: TB Flashcards

1
Q

What is the pathogenesis of TB?

A

Airborne droplet spread

Inhaled – deposited in terminal airspaces

Macrophages ingest bacilli – replicate within endosomes

Transported to regional lymph node

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2
Q

What are the four outcomes of TB that has spread to lymph nodes?

A

Killed

Multiply → primary TB

Dormant → asymptomatic (LTBI if exposed to host immune system)

Proliferate after period of latency → reactivation disease

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3
Q

What is the % risk of developing TB over a lifetime?

A

5-10%

This is considerably increased for those with immunodeficiency

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4
Q

What do we know about the TB bacteria?

A

Aerobic bacillus

Divides every 16-20 hours (slow)

Cell wall, but lacks phospholipid outer membrane

Does not stain strongly with Gram stain (weakly positive)
Retains stains after treatment with acids

Acid fast bacillus

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5
Q

What is meant by granulomatous inflammation?

A

Rim of lymphocytes

Fibroblasts

Central infected macrophages (giant cells)

Central necrosis – caseation

Secretion of cytokines (IFNγ) – activate macrophages to kill bacteria

AFBs in granulomas

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6
Q

What can be used to visualise M.tuberculosis?

A

Ziehl-Neelsen stain - bright red bacilli on blue background

Auramine-rhodamine stain

Fluorescent microscopy

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7
Q

What may increase the risk of transmission?

A

Close contacts of infectious cases

Contact with high risk groups

Immune deficiency

Lifestyle factors

Genetic susceptibility (twin studies of gene polymorphisms)

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8
Q

What are some causes for immune deficiency?

A
HIV
Steroids
Chemotherapy and biologics
Nutritional deficiency (vit D), 
Diabetes
End stage renal failure
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9
Q

What lifestyle factors may increase the risk of getting TB?

A

Drug / alcohol misuse

Homelessness / hostels / overcrowding

Prison inmates

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10
Q

What % of cases are primary TB?

A

1-5%

Bacilli overcome immune system soon after initial infection

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11
Q

What % of cases are latent TB?

A

2-23% cases – reactivation disease

Risk of reactivation increases with immunosuppression
HIV + risk 10% per year
HIV – risk 1%

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12
Q

How can you diagnose active TB?

A

Identify the infected area

Isolate the organism

Obtain information regarding susceptibility to antibacterials

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13
Q

How can you diagnose latent TB?

A

Identify immune response to TB proteins or TB-specific antigens

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14
Q

What is the basis for the mantoux test?

A

Circulating memory T-lymphocytes ability to mount a delayed hypersensitivity reaction

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15
Q

What are the problems with the mantoux test?

A

Cross reactive with other Mycobacterial antigens so non-specific

Maybe be falsely negative in severely ill or immunosuppressed individuals

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16
Q

What can be used as an alternative to mantoux?

A

ELISPOT/ELISA: Enzyme linked immunological assay of release of interferon-gamma in whole blood following stimulation by specific tuberculosis antigen

17
Q

What are the advantages and problems with the ELISA test for TB?

A

Advantages:

  • More specific than Mantoux
  • Correlates better with degree of exposure than Mantoux

Problem:
- Does not differentiate between latent infection and disease

18
Q

What % of cases are pulmonary TB?

A

55%

19
Q

What are the clinical features of pulmonary TB?

A
Cough
Weight loss
Haemoptysis
Fever
Chest pain
Night sweats
20
Q

How can you diagnose pulmonary TB?

A

Chest imaging

Sputum/BAL

21
Q

What sites may be affected by extra pulmonary TB?

A
Lymph nodes
CNS
Bone (Pott’s disease of the spine)
Genitourinary system
GI tract
Disseminated/miliary
22
Q

What is TB lymphadenitis?

A

Infection of LN

Often get worse on treatment - paradoxical reaction

Can form sinus tracts with chronic discharge

Cold abscess formation

23
Q

What are the symptoms of miliary TB?

A

Fevers, sweats, weight loss and malaise very common

Respiratory symptoms in majority

GI or CNS symptoms in 20% (abdo pain, diarrhoea, hepatomegaly in 50%, headache or confusion - altered mental state in 20%)

24
Q

What is the standard pharmacological treatment of TB?

A

2 months (initial phase) of Isoniazid, Rifampicin, Pyrazinamide and Ethambutol

Followed by:
4 months (continuation phase) of Isoniazid and Rifampicin
25
Q

How must the standard pharmacological treatment be taken?

A

All together on an empty stomach 1 hour before breakfast; compliance is essential for cure.

26
Q

What about the treatment changes if there is CNS involvement?

A

The continuation phase of treatment is extended to 10 months making a 12 month full treatment plan

27
Q

What are the side effects of pyrazinamide?

A
Nausea
Skin rashes
Hepatoxicity
Joint pain
N&V
28
Q

What are the side effects of rifampicin?

A

Nausea
Skin rashes
Hepatoxicity
Reddish colour to urine

29
Q

What are the side effects of isoniazid?

A
Nausea
Skin rashes
Hepatoxicity
Fever 
Peripheral neuropathy 
Optic neuritis
30
Q

What are the side effects of ethambutol?

A
Nausea
Skin rashes
Peripheral neuropathy 
Optic neuropathy
Gout
31
Q

What is the order of most hepatoxicity to least?

A

Pyrazinamide
Rifampicin
Isoniazid