Week 4: Clinical TB Flashcards

1
Q

IGRAs: interferon gamma release assays

A
  • single blood test

- no cross reaction to BCG and most NTMs except M africanum, M bovid, M kansasii, M marine, M szulgai

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2
Q

Recognize NTM

A
  • Morphotype: middle aged white females, slender, tall, scoliosis, precuts excavate, MVP, higher % of CFTR genes, no cellular immune defects
  • MAC (mycobacterium avium complex): variable presentation, e.g. COPD, no previous lung disease, hot tub lung, HIV, Il-12 defects
  • M. marinum: water, fish
  • M. fortuitum: footbaths, nail salons, piercings
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3
Q

Risk factors for TB in the US

A
  • exposure history
  • foreign born from areas of high TB prevalence
  • HIV infection and other conditions assoc. with immunosuppression
  • Fibrotic changes on CXR assoc. with prior TB
  • homeless, IV drug users, prison, health care workers, lab ppl, elderly in nursing homes
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4
Q

History and physical: TB

A
Classic symptoms
-cough, >2 weeks
-may have hemoptysis
-low grade fever
-anorexia and weight loss
-night sweats
PE findings
-vary
-fever and respiratory rales most common
-exam often unrevealing
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5
Q

Active TB assessment

A
  • CBC and chemistry panel
  • 3 separate morning sputum: Acid fast stain
  • can do bronchoscopy
  • treat with standard TB treatment pending cultures
  • suspected TB should be put in isolation room
  • confirmatory AFB culture in special media, takes up to 4 weeks to grow
  • obtain drug susceptibility testing to rule out drug resistance
  • PCR/DNA test is faster
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6
Q

Pathogenesis of TB

A
  • inhalation of infected droplets
  • reaches lower respiratory tract
  • Type IV hypersensitivity reaction 6-8 weeks after initial infection
  • intracellular replication
  • mostly, initial infection is latent: no symptoms
  • reactivation of latent TB can occur years after in small % of people
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7
Q

Clinical manifestations of primary TB

A
  • usually children, but any age
  • usually lower and middle lungs, and heals with no clinical symptoms in 90% of cases
  • fibrosis and calcification
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8
Q

Manifestations of post primary Active TB infection (tb reactivation)

A
  • Upper lobes and apical segment of lower lobes
  • progression is variable
  • early: small granulomatous broncho-pneumonia infiltration
  • caseation can occur
  • infected sputum can be aspirated to other segments of lung
  • CXR (non HIV): posterior segments of upper lobes (apices) or super segments of lower lobes
  • CXR (HIV): can be normal CXR or with infiltrates in any lobes and any location
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9
Q

Progression of Active TB

A
  • Chronic parenchymal lesions: upper lobe destruction, fibrosis, and overdistended emphysema
  • Hemoptysis: erosion of blood vessels within the TB lesion
  • The lesions can also erode into blood vessels, leading to hematogenous dissemination can occur to one or more sites: lungs, CNS, genitourinary, skeletal, lymph nodes, etc
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10
Q

Latent TB infection assessment

A
  • PPD and TST (mantoux test)
    1. PPD>5mm
  • HIV+
  • known contact with person with active TB
  • fibrotic changes on CXR with prior TB
  • organ transplants, immunosuppressed
    2. PPD>10mm
  • high risk: silicosis, DM, chronic renal failure, etc
  • recent immigrants, IV drug users, residents employees in crowded settings
  • children over 4 yo
    3. PPD>15mm
  • person with no risk factors for TB
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11
Q

Treatment of latent TB

A
  • daily Isoniazid (INH) for 9 months
  • risk of side effects increases with age, >35. Most weigh risks when deciding to treat
  • liver fxn test to monitor high risk individuals
  • Directly observed therapy (DOT) for better compliance
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12
Q

Rx for active TB

A
  • 6 month treatment course. First 2 months with RIPE

- then INH and rifampin for 4 more months

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