Division of Reproductive Health, Centers for Disease Control and Prevention, Atlanta, GA 30345, USA.
J Acquir Immune Defic Syndr. 2010 Aug;54(5):515-23. doi: 10.1097/qai.0b013e3181e3a70e.
We assessed whether 7 days of zidovudine + lamivudine postpartum with single-dose nevirapine at labor decreases nevirapine resistance in HIV-infected women in Malawi.
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.
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)].
The significant decrease in nevirapine resistance conferred by 1 week of zidovudine + lamivudine should help policymakers optimize peripartum HIV prophylaxis recommendations.
我们评估了在马拉维,HIV 感染产妇分娩时单次应用奈韦拉平,随后在产后 7 天内给予齐多夫定+拉米夫定,是否会降低 HIV 感染者应用奈韦拉平后出现奈韦拉平耐药的情况。
我们对 132 名在分娩时单次应用奈韦拉平并在产后 7 天内接受齐多夫定+拉米夫定治疗的 HIV 感染孕妇和 66 名在分娩时仅单次应用奈韦拉平的孕妇进行了随访,随访时间从产前检查一直持续到产后 6 周。在产后 2 周和 6 周时,采用群体测序和敏感实时聚合酶链反应检测血浆样本中奈韦拉平的基因型耐药情况。采用泊松回归分析确定产后奈韦拉平耐药的预测因素。
两组产妇在入组时的中位 HIV RNA 水平相似(分别为 4.27 log 和 4.35 log,P=0.87),在产后 2 周时差异显著(分别为 2.67 log 和 3.58 log,P<0.0001),但在产后 6 周时无显著差异(分别为 4.49 log 和 4.40 log,P=0.79)。与仅接受奈韦拉平相比,分别接受奈韦拉平+齐多夫定+拉米夫定治疗的产妇在产后 2 周(分别为 10%[4/40]和 74%[31/42],P<0.0001)和 6 周(分别为 10%[11/115]和 64%[41/64],P<0.0001)时,奈韦拉平耐药率明显更低。奈韦拉平耐药的调整相对危险度为 0.18(95%置信区间为 0.10 至 0.34)。
1 周的齐多夫定+拉米夫定治疗使奈韦拉平耐药率显著降低,这有助于决策者优化围产期 HIV 预防治疗建议。