ALERT: This system is being upgraded on Tuesday December 12. It will not be available
for use for several hours that day while the upgrade is in progress. Deposits to DukeSpace
will be disabled on Monday December 11, so no new items are to be added to the repository
while the upgrade is in progress. Everything should be back to normal by the end of
day, December 12.
Predictors and outcomes of Mycobacterium tuberculosis bacteremia among patients with HIV and tuberculosis co-infection enrolled in the ACTG A5221 STRIDE study.
Abstract
BACKGROUND: We evaluated predictors and outcomes of Mycobacterium tuberculosis bacteremia
among participants undergoing baseline mycobacterial blood culture in the ACTG A5221
STRIDE study, a randomized clinical trial comparing earlier with later ART among HIV-infected
patients suspected of having tuberculosis with CD4-positive T-lymphocyte counts (CD4
counts) <250 cells/mm(3). We conducted a secondary analysis comparing participants
with respect to presence or absence of M. tuberculosis bacteremia. METHODS: Participants
with a baseline mycobacterial blood culture were compared with respect to the presence
or absence of M. tuberculosis bacteremia. Baseline predictors of M. tuberculosis bacteremia
were identified and participant outcomes were compared by mycobacteremia status. RESULTS:
Of 90 participants with baseline mycobacterial blood cultures, 29 (32.2%) were female,
the median (IQR) age was 37 (31-45) years, CD4 count was 81 (33-131) cells/mm(3),
HIV-1 RNA level was 5.39 (4.96-5.83) log10 copies/mL, and 18 (20.0%) had blood cultures
positive for M. tuberculosis. In multivariable analysis, lower CD4 count (OR 0.85
per 10-cell increase, p = 0.012), hemoglobin ≤8.5 g/dL (OR 5.8, p = 0.049), and confirmed
tuberculosis (OR 17.4, p = 0.001) were associated with M. tuberculosis bacteremia.
There were no significant differences in survival and AIDS-free survival, occurrence
of tuberculosis immune reconstitution inflammatory syndrome (IRIS), or treatment interruption
or discontinuation by M. tuberculosis bacteremia status. IRIS did not differ significantly
between groups despite trends toward more virologic suppression and greater CD4 count
increases at week 48 in the bacteremic group. CONCLUSIONS: Among HIV-infected tuberculosis
suspects, lower CD4 count, hemoglobin ≤8.5 g/dL, and the presence of microbiologically
confirmed pulmonary tuberculosis were associated with increased adjusted odds of mycobacteremia.
No evidence of an association between M. tuberculosis bacteremia and the increased
risk of IRIS was detected. TRIAL REGISTRATION: ClinicalTrials.gov: NCT00108862 .
Type
Journal articleSubject
AdultAge Factors
Antiretroviral Therapy, Highly Active
Bacteremia
CD4 Lymphocyte Count
Coinfection
Female
HIV Infections
HIV-1
Humans
Male
Middle Aged
Mycobacterium tuberculosis
Sex Factors
South Africa
Survival Analysis
Tuberculosis, Pulmonary
Permalink
https://hdl.handle.net/10161/13769Published Version (Please cite this version)
10.1186/s12879-014-0735-5Publication Info
Crump, John A; Wu, Xingye; Kendall, Michelle A; Ive, Prudence D; Kumwenda, Johnstone
J; Grinsztejn, Beatriz; ... Swindells, Susan (2015). Predictors and outcomes of Mycobacterium tuberculosis bacteremia among patients with
HIV and tuberculosis co-infection enrolled in the ACTG A5221 STRIDE study. BMC Infect Dis, 15. pp. 12. 10.1186/s12879-014-0735-5. Retrieved from https://hdl.handle.net/10161/13769.This is constructed from limited available data and may be imprecise. To cite this
article, please review & use the official citation provided by the journal.
Collections
More Info
Show full item recordScholars@Duke
John Andrew Crump
Adjunct Professor in the Department of Medicine
I am based in northern Tanzania where I am Site Leader for Duke University’s
collaborative research program based at Kilimanjaro Christian Medical Centre and Director
of Tanzania Operations for the Duke Global Health Institute. I oversee the design
and implementation of research studies on infectious diseases, particularly febrile
illness, invasive bacterial disease, HIV-associated opportunistic infections, clinical
trials of antiretroviral therapy and prevention of mother-to-child tr

Articles written by Duke faculty are made available through the campus open access policy. For more information see: Duke Open Access Policy
Rights for Collection: Scholarly Articles
Works are deposited here by their authors, and represent their research and opinions, not that of Duke University. Some materials and descriptions may include offensive content. More info