Tuberculosis Flashcards

1
Q

What is TB?

A

Bacterial infection caused by Mycobacterium tuberculosis complex, infecting one in three people globally (5-15% develop into active TB).

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2
Q

Who is at risk?

A

*born in high prevalence area
*children <5 years old
*close contact with person with ACTIVE TB
*immunosuppressed i.e on immuno drugs

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3
Q

What is the pathogenesis of TB?

A

*airborne bacterial infection
*affect any part of body-mainly lungs
*transmitted via coughs,sneezes, singing
*inhalation of droplet through mouth/nasal cavity

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4
Q

How is TB transmitted?

A

Inhalation of an airborne droplet produced by an active TB patient coughing, sneezing, singing etc.

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5
Q

What are the three possible outcomes from inhaling TB droplets which have deposited in the lungs?

A

*immediate clearance via immune system
*primary active disease
*latent disease

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6
Q

What are the differences between latent and active TB?

A

*latent tb involves persistent immune response to mycobacterium tuberculosis antigens with no evidence of activity i.e no symptoms or progression
*active tb shows evidence of symptomatic or progressive disease of lungs and/or other organs
*latent tb patients not infective
*active tb patients infective
*90% of patients have latent tb
*10% of patients have active tb

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7
Q

What are factors for poor prognosis (life after disease)?

A

*multi-drug resistance
*increasing age
*HIV co-infection
*more extensive disease state

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8
Q

What are symptoms of active TB?

A

MAIN
*cough >3 weeks
*chest pain
*coughing up blood or sputum
OTHERS
*fatigue
*weight loss
*chills/fever
*children present with NON SPECIFIC symptoms

NB- 40% of patients can have extra pulmonary symptoms

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9
Q

What are the three classes of Tb?

A

*primary disease- progression of asymptomatic/few symptoms to active disease
*post primary disease- following treatment, disease can return if not all bacteria killed (few people)
*latent tb infection- thousands fewer tb bacteria than in active tb

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10
Q

What is extra-pulmonary tb?

A

Tb involving organs of the body other than the lungs

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11
Q

How is active pulmonary tb diagnosed?

A

*chest x-ray- shows infiltration of upper lobes
*three sputum sample’s microbiology tested

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12
Q

How is extra-pulmonary tb diagnosed?

A

*chest x-ray
*spontaneous sputum sample for microbiological testing
*ct scan
*ultrasound of lymph nodes/kidneys
*ecg of heart

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13
Q

Who should be screened for tb?

A

*those in close contact with patient with active tb
*immunocompromised
*people entering uk from high tb-prevelance
*new NHS employees working with patients

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14
Q

How is latent tb tested for?

A

*Mantoux test- small amount of PPD tuberculin injected into skin. Positive= small red hard bump within 2-3 days (strong skin reaction suggests active tb so needs further testing)
* interferon gamma release assay test (blood test)

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15
Q

What causes resistance in tb?

A

*poor mediation compliance
*unsuitable treatment
* lack of availability of high quality drugs
*interrupted treatment

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16
Q

How is tb (with no CNS involvement) treatment phased?

A

INITIAL PHASE
*use 4 drugs In combination
*2 months
*start immediately without confirmed tests if symptomatic of tb
*isoniazid (with pyridoxine) rifampicin, pyrazinamide and ethambutol

CONTINUOUS PHASE (active tb but no CNS involvement)
*use of 2 drugs in combination
*further 4 months
*for patients with active tb with NO CNS involvement
*isoniazid (with pyridoxine) and rifampicin

17
Q

How is tb of the CNS treatment phased?

A

INITIAL PHASE
*isoniazid (with puridoxine) rifampicin, pyrazinamide and ethambutol
*for 2 months

CONTINUOUS PHASE
*isoniazid (with pyridoxine) and rifampicin
*for 10 months
*high dose corticosteroids
*for 4-8 weeks

18
Q

What is mono-resistant tb?

A

Resistance to one anti-tb drug

19
Q

What is MDR (multi drug resistant) tb?

A

Resistance to at least isoniazid and rifampicin

20
Q

What is XDR (extensively drug resistant) tb?

A

Resistance to any fluoroquinolone and at least one other second-line injectable

21
Q

A patient with tb is resistant to isoniazid, what does their treatment plan look like?

A

Initial phase= rifampicin, pyrazinamide and ethambutol for 2 months
Continuous phase= rifampicin and ethambutol for 7 months

22
Q

A patient with tb is resistant to pyrazinamide, what does their treatment plan look like?

A

Initial phase= isoniazid, rifampicin and ethambutol for 2 months
Continuous phase= isoniazid and and rifampicin for 7 months

23
Q

A patient with tb is resistant to ethambutol, what does their treatment plan look like?

A

Initial phase= isoniazid, pyrazinamide, rifampicin for 2 months
Continuous phase= isoniazid and rifampicin for 4 months

24
Q

Before starting treatment, what baseline tests should be completed ?

A

*LFTs
*KFTs
*uric acid levels
*vitamin D levels
*full blood count and clotting screen
*HIV and hepatitis screen
*nutritional assessment

25
Q

What drugs are contra-indicated with isoniazid and what should patients avoid whilst taking?

A

*warfarin
*theophylline
*anti epilptics
- inhibits drug metabolism
*avoid tyramine containing foods-marmite

26
Q

What are side effects of taking isoniazid?

A

Peripheral neuropathy (nerve damage) -hence why given with pyridoxine as prophylaxis
(Signs of hepatic toxicity= jaundice, nausea, vomiting, malaise)

27
Q

Which class of drug does rifampicin interact with?

A

Contraceptives- decreases effectiveness

28
Q

What are the side effects of rifampicin?

A

*nausea
*vomitting
*thrombocytopenia (reduced platelet count)
*discoloured urine-orange/red

29
Q

What are the side effects of pyrazinamide?

A

*reduced appetite
*gout (swelling of joints)
*hepatic disorders

30
Q

What are the side effects of ethambutol?

A

*increased uric acid levels
*nerve disorders
*visual impairment (optic neuropathy) -related to dose and renal function

31
Q

What are 3 strategies to improve patient adherence to their tb medication?

A

*tablet diary
*patient interview
*supervision therapy

32
Q

Who should the Bacillus Calmette-Guerin (BCG) vaccine be offered to ?

A

*neonates/children born to parents/grandparents from high prevalence countries
*healthcare workers and lab staff
*individuals <16 years intending to live in high prevalence area for >3 months