Triple-antiretroviral prophylaxis to prevent mother-to-child HIV transmission through breastfeeding--the Kisumu Breastfeeding Study, Kenya: a clinical trial.

dc.contributor.authorThomas, T.K.
dc.contributor.authorMasaba, R.
dc.contributor.authorBorkowf, C.B.
dc.contributor.authorNdivo, R.
dc.contributor.authorZeh, C.
dc.contributor.authorMisore, A.
dc.contributor.authorOtieno, J.
dc.contributor.authorJamieson, D.
dc.contributor.authorThigpen, M.C.
dc.contributor.authorBulterys, M.
dc.contributor.authorSlutsker, L.
dc.contributor.authorAmornkul, P.N.
dc.contributor.authorGreenberg, A.E.
dc.contributor.authorFowler, M.G.
dc.date.accessioned2013-04-22T09:51:17Z
dc.date.available2013-04-22T09:51:17Z
dc.date.issued2011
dc.description.abstractBACKGROUND: Effective strategies are needed for the prevention of mother-to-child HIV transmission (PMTCT) in resource-limited settings. The Kisumu Breastfeeding Study was a single-arm open label trial conducted between July 2003 and February 2009. The overall aim was to investigate whether a maternal triple-antiretroviral regimen that was designed to maximally suppress viral load in late pregnancy and the first 6 mo of lactation was a safe, well-tolerated, and effective PMTCT intervention. METHODS AND FINDINGS: HIV-infected pregnant women took zidovudine, lamivudine, and either nevirapine or nelfinavir from 34-36 weeks' gestation to 6 mo post partum. Infants received single-dose nevirapine at birth. Women were advised to breastfeed exclusively and wean rapidly just before 6 mo. Using Kaplan-Meier methods we estimated HIV-transmission and death rates from delivery to 24 mo. We compared HIV-transmission rates among subgroups defined by maternal risk factors, including baseline CD4 cell count and viral load. Among 487 live-born, singleton, or first-born infants, cumulative HIV-transmission rates at birth, 6 weeks, and 6, 12, and 24 mo were 2.5%, 4.2%, 5.0%, 5.7%, and 7.0%, respectively. The 24-mo HIV-transmission rates stratified by baseline maternal CD4 cell count <500 and ≥500 cells/mm(3) were 8.4% (95% confidence interval [CI] 5.8%-12.0%) and 4.1% (1.8%-8.8%), respectively (p = 0.06); the corresponding rates stratified by baseline maternal viral load <10,000 and ≥10,000 copies/ml were 3.0% (1.1%-7.8%) and 8.7% (6.1%-12.3%), respectively (p = 0.01). None of the 12 maternal and 51 infant deaths (including two second-born infants) were attributed to antiretrovirals. The cumulative HIV-transmission or death rate at 24 mo was 15.7% (95% CI 12.7%-19.4%). CONCLUSIONS: This trial shows that a maternal triple-antiretroviral regimen from late pregnancy through 6 months of breastfeeding for PMTCT is safe and feasible in a resource-limited setting. These findings are consistent with those from other trials using maternal triple-antiretroviral regimens during breastfeeding in comparable settings.en_GB
dc.identifier.otherdoi: 10.1371/journal.pmed.1001015
dc.identifier.urihttp://hdl.handle.net/123456789/926
dc.language.isoenen_GB
dc.relation.ispartofseriesPLoS Medicine. 2011;8(3):e1001015.
dc.subjectTriple-antiretroviralen_GB
dc.subjectProphylaxisen_GB
dc.subjectBreastfeedingen_GB
dc.subjectKenyaen_GB
dc.titleTriple-antiretroviral prophylaxis to prevent mother-to-child HIV transmission through breastfeeding--the Kisumu Breastfeeding Study, Kenya: a clinical trial.en_GB
dc.typeArticleen_GB

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