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dc.contributor.authorFarr, SL
dc.contributor.authorNelson, JA
dc.contributor.authorNg'ombe, TJ
dc.contributor.authorKourtis, AP
dc.contributor.authorChasela, C
dc.contributor.authorJohnson, JA
dc.contributor.authorKashuba, AD
dc.contributor.authorTegha, GL
dc.contributor.authorWiener, J
dc.contributor.authorEron, JJ
dc.contributor.authorBanda, HN
dc.contributor.authorMpaso, M
dc.contributor.authorLipscomb, J
dc.contributor.authorMatiki, C
dc.contributor.authorFiscus, SA
dc.contributor.authorJamieson, DJ
dc.contributor.authorvan der Horst, C
dc.contributor.authorBAN Study Team.
dc.contributor.authorMeme, J
dc.date.accessioned2014-04-30T08:25:40Z
dc.date.available2014-04-30T08:25:40Z
dc.date.issued2010-08
dc.identifier.citationJ Acquir Immune Defic Syndr. 2010 Aug;54(5):515-23.en_US
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/pubmed/20672451
dc.identifier.urihttp://hdl.handle.net/11295/66192
dc.description.abstractBACKGROUND: We assessed whether 7 days of zidovudine + lamivudine postpartum with single-dose nevirapine at labor decreases nevirapine resistance in HIV-infected women in Malawi. METHODS: HIV-infected pregnant women receiving intrapartum single-dose nevirapine and 7 days of zidovudine + lamivudine (n = 132) and women receiving intrapartum single-dose nevirapine alone (n = 66) were followed from an antenatal visit through 6 weeks postpartum. Plasma specimens at 2 and 6 weeks postpartum were tested for genotypic resistance to nevirapine by population sequencing and sensitive real-time polymerase chain reaction. Poisson regression was used to determine predictors of postpartum nevirapine resistance. RESULTS: Median HIV RNA was similar at entry (4.27 log vs. 4.35 log, P = 0.87), differed at 2 weeks postpartum (2.67 log vs. 3.58 log, P < 0.0001) but not at 6 weeks postpartum (4.49 log vs. 4.40 log, P = 0.79), between single-dose nevirapine/zidovudine + lamivudine and single-dose nevirapine groups, respectively. Nevirapine resistance, measured by population sequencing and sensitive real-time polymerase chain reaction, was significantly less common in those receiving single-dose nevirapine/zidovudine + lamivudine compared with single-dose nevirapine, respectively, at 2 weeks [10% (4 of 40) vs. 74% (31 of 42), P < 0.0001] and 6 weeks postpartum [10% (11 of 115) vs. 64% (41 of 64), P < 0.0001; adjusted relative risk = 0.18, 95% confidence interval (0.10 to 0.34)]. CONCLUSIONS: The significant decrease in nevirapine resistance conferred by 1 week of zidovudine + lamivudine should help policymakers optimize peripartum HIV prophylaxis recommendations.en_US
dc.language.isoenen_US
dc.publisherUniversity of Nairobien_US
dc.titleAddition of 7 days of zidovudine plus lamivudine to peripartum single-dose nevirapine effectively reduces nevirapine resistance postpartum in HIV-infected mothers in Malawi.en_US
dc.typeArticleen_US


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