4.7 Review

Optimal Timing of Antiretroviral Therapy Initiation for HIV-Infected Adults With Newly Diagnosed Pulmonary Tuberculosis A Systematic Review and Meta-analysis

Journal

ANNALS OF INTERNAL MEDICINE
Volume 163, Issue 1, Pages 32-39

Publisher

AMER COLL PHYSICIANS
DOI: 10.7326/M14-2979

Keywords

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Funding

  1. Swedish Council for Working Life and Social Research Marie Curie International Postdoctoral fellowship [2012-0064]
  2. National Institute for Allergy and Infectious Disease of the National Institutes of Health
  3. AIDS Clinical Trial Group
  4. Stellenbosch University Clinical Trial Unit [2UM1AI069521-08]
  5. Medical Education Partnership Initiative through the U.S. President Emergency Plan for AIDS Relief [T84HA21652-01-00]
  6. European Developing Countries Clinical Trial Partnership Senior Fellowship Award [TA-08-40200-021]
  7. Wellcome Trust Southern Africa Consortium for Research Excellence [WT087537MA]
  8. European Commission
  9. National Institutes of Health Research Biomedical Research Centre
  10. Stellenbosch University
  11. South African Medical Research Council
  12. Department for International Development (DFID) [201400] Funding Source: researchfish

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Background: Initiation of antiretroviral therapy (ART) during tuberculosis (TB) treatment remains challenging. Purpose: To assess evidence from randomized, controlled trials of the timing of ART initiation in HIV-infected adults with newly diagnosed pulmonary TB. Data Sources: PubMed, EMBASE, Cochrane Central Register of Controlled Trials, conference abstracts, and ClinicalTrials.gov (from January 1980 to May 2015). Study Selection: Randomized, controlled trials evaluating early versus delayed ART initiation (1 to 4 weeks vs. 8 to 12 weeks after initiation of TB treatment) or deferred ART initiation (after the end of TB treatment). Data Extraction: Three reviewers independently extracted data and assessed risk of bias. The main outcome measures were all-cause mortality and the TB-associated immune reconstitution inflammatory syndrome (TB-IRIS). Data Synthesis: The 8 included trials (n = 4568) were conducted in Africa, Asia, and the United States and were generally at low risk of bias for the assessed domains. Overall, early ART reduced mortality compared with delayed ART (relative risk [RR], 0.81 [95% CL, 0.66 to 0.99]; I-2 = 0%). In a prespecified subgroup analysis, early ART reduced mortality compared with delayed ART among patients with baseline CD4(+) 1-cell counts less than 0.050 x 10(9) cells/L (RR, 0.71 [Cl, 0.54 to 0.93]; I-2 = 0%). However, a mortality benefit from early ART Was not found among those with CD4(+) T-cell counts greater than 0.050 x 10(9) cells/L (RR, 1.05 [Cl, 0.68 to 1.61]; I-2 = 56%). Early ART was associated with a higher incidence of TB-IRIS than delayed ART (RR, 2.31 [Cl, 1.87 to 2.86]; I-2 = 19%). Limitation: Few trials provided sufficient data for subgroup analysis. Conclusion: Early ART in HIV-infected adults with newly diagnosed TB improves survival in those with CD4(+) T-cell counts less than 0.050 x 10(9) cells/L, although this is associated with a 2-fold higher frequency of TB-IRIS. In patients with CD4(+) T-cell counts greater. than 0.050 x 10(9) cells/L, evidence is insufficient to support or refute a survival benefit conferred by early versus delayed ART initiation.

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