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
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
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
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
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
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
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
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
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
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
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
12
Q
Rx for active TB
A
- 6 month treatment course. First 2 months with RIPE
- then INH and rifampin for 4 more months