4.6 Article

Pregnancy and Virologic Response to Antiretroviral Therapy in South Africa

Journal

PLOS ONE
Volume 6, Issue 8, Pages -

Publisher

PUBLIC LIBRARY SCIENCE
DOI: 10.1371/journal.pone.0022778

Keywords

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Funding

  1. National and Gauteng Department of Health
  2. United States Agency for International Development to Right to Care and the Institution [674-A-00-08-00007-00]
  3. National Institutes of Health, Eunice Kennedy Shriver NICHD [K99-HD-06-3961, 4R00-HD-06-3961-02]
  4. National Institute of Allergy and Infectious Diseases [P30-AI-50410]
  5. University of North Carolina Center for AIDS Research
  6. University of North Carolina-GlaxoSmithKline Center for Excellence in Pharmacoepidemiology and Public Health
  7. GlaxoSmithKline for examining IV zanamavir for influenza

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Background: Although women of reproductive age are the largest group of HIV-infected individuals in sub-Saharan Africa, little is known about the impact of pregnancy on response to highly active antiretroviral therapy (HAART) in that setting. We examined the effect of incident pregnancy after HAART initiation on virologic response to HAART. Methods and Findings: We evaluated a prospective clinical cohort of adult women who initiated HAART in Johannesburg, South Africa between 1 April 2004 and 30 September 2009, and followed up until an event, death, transfer, drop-out, or administrative end of follow-up on 31 March 2010. Women over age 45 and women who were pregnant at HAART initiation were excluded from the study; final sample size for analysis was 5,494 women. Main exposure was incident pregnancy, experienced by 541 women; main outcome was virologic failure, defined as a failure to suppress virus to <= 400 copies/ml by six months or virologic rebound >400 copies/ml thereafter. We calculated adjusted hazard ratios using marginal structural Cox proportional hazards models and weighted lifetable analysis to calculate adjusted five-year risk differences. The weighted hazard ratio for the effect of pregnancy on time to virologic failure was 1.34 (95% confidence limit [CL] 1.02, 1.78). Sensitivity analyses generally confirmed these main results. Conclusions: Incident pregnancy after HAART initiation was associated with modest increases in both relative and absolute risks of virologic failure, although uncontrolled confounding cannot be ruled out. Nonetheless, these results reinforce that family planning is an essential part of care for HIV-positive women in sub-Saharan Africa. More work is needed to confirm these findings and to explore specific etiologic pathways by which such effects may operate.

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