8 Respiratory Tract Infections: Tuberculosis Flashcards

1
Q

How does TB spread?

A

Through aerosol transmission

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2
Q

Name the organism that causes the tuberculosis condition

A

Mycobacterium tuberculosis

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3
Q

Describe the mycobacterium tuberculosis bacteria (in terms of structure and staining)

A
  • It has a modified peptidoglycan layer (outmost) - primarily consisted of proteins
  • Covalently attached to arabinogalactan polymer
  • Mycolic acid waxy coat - lips rich
  • Poor gram stain (high lipid content = less permeable to gram staining)
  • Acid fast (Ziehl-Neelsen stain) - needed for staining
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4
Q

Describe the mycobacterium tuberculosis bacteria (in terms of features, transmission etc.)

A
  • Obligate aerobes (need oxygen - obligated for oxygen - TB pass into the lung via air)
  • TB causes more deaths worldwide than any other single infectious agent
  • Facultative intracellular bacteria (can be fine outside host) - usually invading macrophages, dendritic cells
  • Slow growing (generation time of 12 to 18 hours; 20-30 mins for E. coli)
  • Disease course has insidious nature
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5
Q

Describe the primary pathogenesis of TB (active)

A
  • Generally, affects upper lobes (lower upper or upper lower lobes) of lung
  • Ghon focus (caseous necrosis)
  • Ghon complex (caseous necrosis) in hilar lymph nodes

Usually resolved but can produce a calcified granuloma or area of scar tissue AND may be a nidus for a secondary TB (reactivated TB)

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6
Q

Describe the secondary pathogenesis of TB (reactivated)

A

Secondary (reactivation) TB due to reactivation of a previous primary TB site

Common in:

  • Immunocompromised patients
  • And patients receiving biological therapy (mAb)
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7
Q

Describe what is is meant by TB disease can be active or latent

A

Latent disease is defined as a state of persistent immune response to stimulation by Mycobacterium tuberculosis antigens, with no evidence of clinically active TB:
- i.e. person is asymptomatic + not infectious

There is a 5–10% risk of progression to active (symptomatic) disease:
- e.g. if the patient is immunocompromised or has intercurrent illness

Multiple longitudinal epidemiological studies indicate that majority of TB disease occurs soon after initial infections, with disease rarely occurring more than 2 years after infection

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8
Q

Describe the clinical course of TB

A

TB is an example of Type 4 HSR

  • In most individuals, cell-mediated immunity (CMI) develops 2-8 weeks after infection (associate with the development of a positive tuberculin skin test)
  • Activated T cells and macrophages form granulomas that limit further replication and spread
  • Bacterial cells remain in centre of necrotic ‘caveating’ granulomas
  • Most individuals are symptomatic (latent infection) and never develop active disease (unless a subsequent in CMI occurs) = +ve skin prick test
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9
Q

Describe some respiratory clinical findings in TB

A
  • Cough
  • Shortness of breath
  • Haemoptysis
  • Chest pain
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10
Q

Describe some general clinical findings in TB

A
  • Fever
  • Drenching night sweats
  • Weight loss
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11
Q

Explain how a diagnosis of TB can be made

A
  • Early stages of disease can be difficult to detect, leading to diagnostic delays/misdiagnosis
  • Suspect active TB in any person who:
    > is at high risk of developing TB
    AND
    > has general symptoms of weight loss, fever, night sweats, anorexia or malaise

Consider pulmonary involvement if the person has a persistent productive cough, which may be associated with breathlessness and haemoptysis - but exclude other causes also

  • Extra-pulmonary involvement - involves target organ - and gives relevant symptoms
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12
Q

List some Pulmonary TB complications

A

Post-TB bronchiectasis, COPD and aspergillosis
- (fungus ball in lung - TB made space in which they exist in - residual lung cavities)

Post-TB corpulmonale (R-sided heart failure - pulmonary hypertension - fibrosis of lung) OR
Respiratory failure (low O2 and low CO2)

DEATH
- in 2006, 5.5% people notified in England were reported to have died at the last recorded outcome, and TB is known to have contributed to 35.2% of deaths

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13
Q

Give some active extra-pulmonary complications of TB

A
  • Miliary spread in lungs - invasion into:
    > (Bronchus) > (lymphatics)
  • Miliary spread to extra-pulmonary sites (spread via pulmonary veins):
    > Lymph nodes are a common site (firm, discrete, painless lymph nodes) - kidney
    > Adrenal improvement may result in Addison disease
    > Granulomatous hepatitis
    > Spread to vertebra (Pott Disease)
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14
Q

Some some serious complications of TB

A

Most serious form is Central Nervous System disease:

  • TB meningitis (especially children < 5 and HIV+)
  • Space occupying lesions (tuberculomas)
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15
Q

Name two screening techniques done for TB

A
  • Mantoux test

- Interferon Gamma Release Assay Test (IGRA)

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16
Q

Describe the Mantoux test as a screening tool for TB

A

Mantoux test

  • Tuberculin (cell envelope protein) is injected intradermally
  • Gives a firm red bump (local skin reaction)
  • Test considered positive at induration of 5mm or more
17
Q

Describe the Interferon Gamma Release Assay (IGRA) test as a screening tool for TB

A

IGRA test

  • Blood test based on detecting the response of white blood cells to TB antigens
  • Less likely to give a false positive result compared to Mantoux test
  • Rapid result
18
Q

Describe how a chest radiograph may be used in the testing for TB

A

The chest radiograph can be suggestive of TB, but not diagnostic:

Active: consolidation = opaque (most likely upper of mid zone)
> cavitating lesions, with or without calcifications
> Latent: nodules and fibrotic changes

19
Q

Describe the steps are/management available after a test for latent TB is positive

A

If a test for latent TB infection is positive:

  • The person should be assessed for active TB,
  • and if there is no evidence of active infection on the basis of symptoms and chest X-ray,
  • the person should be treated for latent infection by the local MDT TB specialist team to prevent progression to active disease

Drug regimens are usually either:

  • 3 months of isoniazid (with pyridoxine) and rifampicin
    OR
  • 6 months of isoniazid (with pyridoxine)
20
Q

Describe what investigations can be carried out when testing for TB

A
  • Bronchoalveolar lavage best for staining and culture (tissue can be cultured, urine, CSF)
  • Sputum cultures (cat 3 pathogen must be handled in cat 3 lab)
  • Culture is slow growing (2-8 weeks)
21
Q

Describe what antibody sensitivity testing is and how it helps in testing for TB

A

Performed in reference lab

Agents include (class = antimycobacterial)

  • Rifampicin (other indications)
  • Isoniazid (just TB - on cell wall and inhibition of synthesis of mycelia acids)
  • Pyrazinamide (Just TB, mechanism N/A)
  • Ethambutamol (just TB, works on cell wall)

Important to detect resistance - especially multi-drug resistant (MDR TB)
- resistance to rifampicin and isoniazid

22
Q

Who gets the BCG vaccine?

A

Bacillus Calmette-Guerin (BCG) -
- live attenuated M. Bovis strain

  • Anyone who works or lives in an area with a high rate of TB (40/100,000 or more)
  • A baby under 12 months OR previously unvaccinated should under 5
  • Any child under 16 with specific risk factors for TB
  • Anyone who works in close contact with TB bacteria
  • Previously unvaccinated people going to live or work (in countries with high rate of TB)

Also:
- Co-morbid conditions
> HIV, diabetes M, history or organ transplant
- Immunosuppressive drugs
- Under-serves groups - more deprived etc
- History of excessive alcohol, injecting drug users and smokers

23
Q

Describe the epidemiology of TB

A
  • 1.7 billion people estimated to have latent TB in the world
    (23% of the world)