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Open AccessResearch article

Reuse of single-dose nevirapine in subsequent pregnancies for the prevention of mother-to-child HIV transmission in Lusaka, Zambia: A cohort study

Jan Walter1 email, Louise Kuhn2 email, Chipepo Kankasa3 email, Katherine Semrau4 email, Moses Sinkala5 email, Donald M Thea4 email and Grace M Aldrovandi1 email

Childrens Hospital Los Angeles, University of Southern California, Los Angeles, CA, USA

Gertrude H. Sergievsky Center and Department of Epidemiology, Mailman School of Public Health, Columbia University, New York, NY, USA

University Teaching Hospital, University of Zambia, Lusaka, Zambia

Center for International Health and Development at the Boston University School of Public Health, Boston, MA, USA

Lusaka District Health Management Team, Lusaka, Zambia

author email corresponding author email

BMC Infectious Diseases 2008, 8:172doi:10.1186/1471-2334-8-172

Published: 30 December 2008

Abstract

Background

Single-dose nevirapine (SDNVP) for the prevention of mother-to-child HIV transmission (PMTCT) results in the selection of resistance mutants among HIV-infected mothers. The effects of these mutations on the efficacy of SDNVP use in a subsequent pregnancy are not well understood.

Methods

We compared risks of perinatal HIV transmission between multiparous women who had previously received a dose of SDNVP (exposed) and those that had not (unexposed) and who were given SDNVP for the index pregnancy within a PMTCT clinical study. We also compared transmission risks among exposed and unexposed women who had two consecutive pregnancies within the trial. Logistic regression modeling was used to adjust for possible confounders.

Results

Transmission risks did not differ between 59 SDNVP-exposed and 782 unexposed women in unadjusted analysis or after adjustment for viral load and disease stage (adjusted odds ratio 0.6, 95% confidence interval [CI] 0.2 to 2.0). Among 43 women who had two consecutive pregnancies during the study, transmission risks were 7% (95% CI 1% to 19%) at both the first (unexposed) and second (exposed) delivery. The results were unchanged, if infant death was included as an outcome.

Conclusion

These data suggest that the efficacy of SDNVP may not be diminished when reused in subsequent pregnancies.


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