dc.date.accessioned2022-01-04T20:31:48Z
dc.date.available2022-01-04T20:31:48Z
dc.date.created2022-01-04T20:31:48Z
dc.date.issued2013
dc.identifierhttps://hdl.handle.net/20.500.12866/10673
dc.identifierhttps://doi.org/10.1371/journal.pone.0074057
dc.description.abstractBackground: Antiretroviral therapy (ART) decreases mortality risk in HIV-infected tuberculosis patients, but the effect of the duration of anti-tuberculosis therapy and timing of anti-tuberculosis therapy initiation in relation to ART initiation on mortality, is unclear. Methods: We conducted a retrospective observational multi-center cohort study among HIV-infected persons concomitantly treated with Rifamycin-based anti-tuberculosis therapy and ART in Latin America. The study population included persons for whom 6 months of anti-tuberculosis therapy is recommended. Results: Of 253 patients who met inclusion criteria, median CD4+ lymphocyte count at ART initiation was 64 cells/mm3, 171 (68%) received >180 days of anti-tuberculosis therapy, 168 (66%) initiated anti-tuberculosis therapy before ART, and 43 (17%) died. In a multivariate Cox proportional hazards model that adjusted for CD4+ lymphocytes and HIV-1 RNA, tuberculosis diagnosed after ART initiation was associated with an increased risk of death compared to tuberculosis diagnosis before ART initiation (HR 2.40; 95% CI 1.15, 5.02; P = 0.02). In a separate model among patients surviving >6 months after tuberculosis diagnosis, after adjusting for CD4+ lymphocytes, HIV-1 RNA, and timing of ART initiation relative to tuberculosis diagnosis, receipt of >6 months of anti-tuberculosis therapy was associated with a decreased risk of death (HR 0.23; 95% CI 0.08, 0.66; P=0.007). Conclusions: The increased risk of death among persons diagnosed with tuberculosis after ART initiation highlights the importance of screening for tuberculosis before ART initiation. The decreased risk of death among persons receiving > 6 months of anti-tuberculosis therapy suggests that current anti-tuberculosis treatment duration guidelines should be re-evaluated.
dc.languageeng
dc.publisherPublic Library of Science
dc.relationPLoS ONE
dc.relation1932-6203
dc.rightshttps://creativecommons.org/licenses/by-nc-nd/4.0/deed.es
dc.rightsinfo:eu-repo/semantics/restrictedAccess
dc.subjectTuberculosis
dc.subjectHumans
dc.subjectmajor clinical study
dc.subjecttuberculosis
dc.subjectrisk factor
dc.subjectAnti-HIV Agents
dc.subjectHIV Infections
dc.subjectHuman immunodeficiency virus infection
dc.subjectTime Factors
dc.subjectantiretrovirus agent
dc.subjectcohort analysis
dc.subjectCD4 lymphocyte count
dc.subjectrisk assessment
dc.subjectRetrospective Studies
dc.subjectretrospective study
dc.subjectarticle
dc.subjectHuman immunodeficiency virus 1
dc.subjectrisk reduction
dc.subjectmortality
dc.subjectobservational study
dc.subjecttreatment duration
dc.subjectvirus RNA
dc.subjectHuman immunodeficiency virus proteinase inhibitor
dc.subjectnonnucleoside reverse transcriptase inhibitor
dc.subjectRNA directed DNA polymerase inhibitor
dc.subjectefavirenz
dc.subjectnevirapine
dc.subjectrifamycin
dc.subjectsurvival time
dc.titleDuration of Anti-Tuberculosis Therapy and Timing of Antiretroviral Therapy Initiation: Association with Mortality in HIV-Related Tuberculosis
dc.typeinfo:eu-repo/semantics/article


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