Tuberculosis: Difference between revisions
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- 9 mo inh if no hiv and neg cxr. 12 mo better but less compliance and more cost | - 9 mo inh if no hiv and neg cxr. 12 mo better but less compliance and more cost | ||
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- if previously tx pt reexposed to tb, repeat tx not recommended | - if previously tx pt reexposed to tb, repeat tx not recommended | ||
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[[Category:Pulm]] |
Revision as of 05:43, 28 March 2011
Epidemilogy
- tb resurfaced due to poor public health systems, HIV, and immigration
- rate of tb now declining due to better public health and decrease xmission of tb from pt with active tb
- many people with latent tb- poses threat if turns active
- globally, 1/3 of world pop infcted
Consequences
- xmited by air particles 1-5 microns
- xmission influenced by source criteria- number of bacteria excreted and nature of encounter
- infc by 1- 5 bacteria in terminal alveolus
- primary tb usually mild and self limited- often undiagnosed- bacteria seed other organs for subsequent reactivation later
- 5% of time, infc goes from latent to active dz in 2 yrs
- most active tb is from latent reactivation buy and also be from infc by second strain of tb- esp if immune compromised or heavy exposure to new bacilli
- classic sxs- fvr, sweats, anorexia, wt loss, weakness
- organ specific sxs- pulm- cough, CP, hemoptysis
primary tb cxr shows infc in mid to lower lungs with lymphadenopathy- reactivation is upper lobe cavitations
- signs and sxs more vaied if hiv
- lung most common site, but also lymph nodes, pleura, bone, joints. also gu, cns, abd, pericardium
Treatment
- reportable in all states- even if tx'd in private sector, reporting helps with compliance, tracking contacts, emerging resis patterns, education, outbreaks
Anti TB Drugs
- 5 first line drugs
- second line drugs are less effective or more toxic- only use if pt cannot tolerate first line or resis
Adverse Effects
INH- hepatitis, neuropathy, cns effects, elevated dilantin lvl, antabuse interaction, give with vit B6
Rif- fvr, low platelets, reduces blood levels of other drugs, caused orange urine
PZA- hyperuricemia
Ethambutol- color discrimination, visual acuity, optic neuritis
Strep- auditory and renal dysfnctn
Current Recs
- always use INH for duration of tx- effective, low cost, tolerable- if not mixed with rifampin- go 18 mo
- if double with INH/ rif- 9 mo for cure
- if triple with inh/ rif/ pza (pza for first 2 mo) shorten lenght to 6 mo
- try 3-4 meds initially and then 2 drugs afterwards
- consider local patterns of resis and schedule of administration likely to ensure adherance
- direct observation helps ensure compliance
- most common regimen- ihn/rif/pza for 8 wks, inh/rif for 16 wks with freq direct observation, and add ethambutol or streptomycin until susceptibility documented
- if cx ned, stop p 2 mo of inh/rif
- noncompliance not related to race, gender, education....cdc rec direct observation, and rewards
- get cxs- helps with resis
- baseline lfts, creatinine,cbc
- if use pza- check uric acid
- if use ethambutol- check vision and red/green color perception
- baseline cxr
- if cx neg, go by sxs and cxr at 3 mo
- sputum cx going from pos to neg - objective tx success- should change in 2 mo
- if longer than 3 mo, consider nonadherence, malabsorption, resis
- can also test urine for color in rif, urate in pza
- cx sputum at end of tx to document cure
HIV Pts
- hiv pt who adhere to standard tx do not have increased tx failure
- tx 6 mo- longer if slow response
- protease inhibitors and NNRT inhibitors mixed with rif cause rif toxicity and low levels of PI and NNRTI- avoid by using rifabutin
- do not use PI ritonivir or NNRTI delavirdine with rifabutin
Extrapulm TB
- since fewer bacilli in extrapulm site and good tissue penetration of drugs, tx should be no more difficult
- use regular 6 mo regimen
- 12 mo for meningitis in kids, bone/ joint or miliary tb
Drug Resis
- inh resis tx with rif, pza, ethambutol for 6 mo
- rif resis- inh, ethm for 18 mo or inh, pza, strep for 9 mo
- mulitidrug resis- resis to inh and rif- curable even in poor countries
Management of Latent TB
- test for tb only in high risk pt and those who will benefit from tx.
- if test low risk population- will get too many false postives
- test hiv pt, immigrants, homeless, long term care residents, health workers
- those at risk for progression from latent to active dz are immune suppressed ore recently exposed to infectious tb- highest rate of progression is from pt with both hiv and tb- also dm, crf, CA, organ xplant, ivda,
- silicosis, abnormal cxr, too thin person also indication for testing
TB Skin Test
- PPD is gold standard for latent tb testing- intradermal not multipronged
- measure induration not redness 48- 72 hrs
- 5 mm- positve if pt with weak immune response- hiv, steroid use, recent exposure and body hasn't had time to mount immune response, abnormal cxr
- 15 mm- positive if low risk pt
- 10 mm- all other pts
- if long standing infc, may actually have neg test initially- if give second skin test will be positve since first test reinvigorated immune sys- so if pt needs serial testing- do second test in 2 wks- called 2 Step Testing- if second postive represents long standing infc not recent infection
- ppd will not cause 10 mm induration in uninfected pt ever
BCG
- not recommended in US but used elsewhere
- size and persistence of tb reaction p bcg vary with bcg dose and manufacturer
- CDC rec ignoring hx of bcg when giving and interpreting ppd test since bcg only givien in high risk populations in first place
- anergy testing not recommended in tb testing of hiv pt since results highly variable and not reproducible.
Latent Tx/ PPD + Tx
- 9 mo inh if no hiv and neg cxr. 12 mo better but less compliance and more cost
- 9 mo ihn if hiv + or pos cxr or age <18yr
- can also do 2 mo of rif and pza or 4 mo of rif alone
- baseline labs if hiv +, preg, etoh, liver dz
- if duration of tx interrupted, add on additional 3 mo of inh. If lapse is greater than 3 mo, restart whole tx
- if previously tx pt reexposed to tb, repeat tx not recommended