Effect of nevirapine toxicity on choice of perinatal HIV prevention strategies
- PMID: 11867311
- PMCID: PMC1447080
- DOI: 10.2105/ajph.92.3.365
Effect of nevirapine toxicity on choice of perinatal HIV prevention strategies
Abstract
Objectives: This study evaluated the validity of concerns about the toxicity of nevirapine (NVP) that have delayed its implementation as a perinatal HIV prevention strategy.
Methods: A decision analysis model compared 3 strategies: single-dose NVP, short-course zidovudine (ZDV), and no intervention.
Results: NVP would prevent more deaths than ZDV and no intervention as long as the rate of NVP toxicity did not exceed, respectively, 9 times that observed in the earlier NVP clinical trial and 42 times that observed in the clinical trial. NVP would be economically preferable to ZDV as long as the rate of toxicity did not exceed 22 times that observed in the clinical trial.
Conclusions: Field implementation of NVP should not be delayed by concerns about its toxicity.
References
-
- Guay LA, Musoke P, Fleming T, et al. Intrapartum and neonatal single-dose nevirapine compared with zidovudine for prevention of mother-to-child transmission of HIV-1 in Kampala, Uganda: HIVNET 012 randomised trial. Lancet. 1999;354:795–802. - PubMed
-
- Campa AM, Shor-Posner G, Baum MK. HIVNET nevirapine trials [letter]. Lancet. 1999;354:1816.
-
- Marseille E, Kahn J, Mmiro F, et al. Cost effectiveness of single-dose nevirapine regimen for mothers and babies to decrease vertical HIV-1 transmission in sub-Saharan Africa. Lancet. 1999;354:803–809. - PubMed
-
- Stringer J, Rouse D, Vermund S, Goldenberg R, Sinkala M, Stinnett A. Cost-effective use of nevirapine to prevent vertical HIV transmission in sub-Saharan Africa. J AIDS. 2000;24:369–377. - PubMed
-
- Dabis F, Msellati P, Meda N, et al. Six-month efficacy, tolerance, and acceptability of a short regimen of oral zidovudine to reduce vertical transmission of HIV in breastfed children in Côte d'Ivoire and Burkina Faso: a double-blind placebo-controlled multicentre trial. Lancet. 1999;353:786–792. - PubMed
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