Tuberculosis Flashcards

1
Q

Mantoux interpretation

A

> 5 mm Positive

HIV-infected Immunosuppressed (TNFa, Tx, Close contacts of infectious TB Old TB on CXR

> 10 mm Positive

Medical risk factors (CRF, CA etc.) Foreign born endemic TB area HCW Nursing home, prisoners

> 15 mm Positive

All other persons BCG vaccinated

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2
Q

Interferon gamma release assay

A

Detects immune response to TB antigen

Cannot distinguish from active and latent TB

Once positive, always positive

Does not reflect severity or prognosis

Negative test does not always exclude TB

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3
Q

4 common extrapulmonary sites for TB

A

Lymph nodes

Bones and joints

Urine

Meninges/CNS

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4
Q

Presentation of TB meningitis

A
  • 1% of TB
  • Peak incidence children <4yrs
  • Adults with HIV/ immunosuppression
  • Subacute meningitis – 1wk-1m of fever, meningeal symptoms
  • Focal neurology, seizures
  • +/- pulmonary involvement
  • Diagnostics

– AFB smear/ TB-PCR poor sensitivity

– MRI- basal meningitis

– CSF- lymphocytic pleocytosis, low glucose

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5
Q

Treatment of TB meningitis

A

Isoniazid, Rifampicin, Pyrazinamide and moxifloxacin for 8-12 months

Dexamethazone 6-8 weeks

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6
Q

Adverse effects of TB treatment

A

• Common even with first line agents

– ~10% serious AE

– Risk factors- Age >60, female, HIV+

– Generally in first 2 months of therapy

  • Isoniazid- hepatitis, rash, neuropathy
  • Rifampicin- drug interactions, hepatitis
  • Pyrazinamide- hepatitis, skin, joint (gout)
  • Ethambutol- optic neuropathy
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7
Q

TB treatment induced hepatitis

A

Pyrazinamide most common, followed by isoniazid and rifampicin

Liver safe drugs ethambutol, moxifloxacin, amikacin

Need to cease therapy if LFT >5x baseline or >3x and acute hepatitis

If can’t stop therapy, use liver safe drugs

Otherwise wait until LFTs reach baseline and restart one at a time

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8
Q

TB drug resistance types

A

Monodrug resistance - Isoniazid resistance

Multidrug resistant TB 5% world wide- resistant to isoniazid and rifampicin and additional resistance

Extensive drug resistant TB - resistant to isoniazid, rifampicin, quinolones, and 1 injectable - amikacin, capreomycin or kanamycin

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9
Q

Risk factors for drug resistance

A

Previous TB treatment

Contact with MDR TB infected patients

HIV

No clinical pattern predicts MDR

60-70% have no prior treatment

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10
Q

Treatment for MDR TB

A

‘Bangladeshi regimen’

• 9-12 months treatment

4 Isoniazid(2x dose), FQ, Pyrazinamide, Ethambutol,, Amikacin, prothionamide, Clofazimine

• 5-8 months

Pyrazinamide, Etambutol, FQ, Clofazimine

• Treatment success 80-90%

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11
Q

Indications for moxifloxacin in TB regimen

A

MDR-TB

Ethambutol required but contraindicated

IV therapy required or hepatotoxicity

Possible role in severe isoniazid resistant disease (BIII)

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12
Q

TB presentation in HIV CD4 <200

A

Most commonly extra-pulmonary

  • Lymphadenopathy
  • Miliary TB
  • Meningitis

Pulmonary - non cavitating lesions, normally smear negative

CD4>200, will contract TB as any other non-HIV patient

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13
Q

Drug interactions NNRTI

A

– Efavirenz (EFV) 600mg (800mg if >60kg) + Rifampicin

– EFV (800mg) + Rifabutin (450mg) (Increases dose of both drugs)

– Rifabutin preferred with Etravirine/Rilpivirine/ Nevirapine

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14
Q

Drug interactions protease inhibitors

A

Rifampicin contraindicated, rifabutin at lower dose

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15
Q

Drug interactions integrase inhibitors

A

– Rifabutin preferred- usual dosing

– Double dose Raltegravir (50mg bd), Dolutegravir (800mg bd) if used with with rifampicin

– Elvitegravir (Genvoya/ Stribild) not with rifampicin

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16
Q

Risk factors for immune reconstitution syndrome in TB

A

High viral load

Low CD4

Early ART

17
Q

ART timing in TB

A

CD4 0-50 -> Commence ART in 2 weeks, except in TB meningitis, in which early ART does not improve outcomes

CD4 >50 -> commence ART 2-4 weeks if severe TB or poor performance status, otherwise 8-12wks

Addition of prednisolone improved performance score and symptom control, with the exception of TB meningitis