首页> 外文期刊>The Lancet >Intrapartum and neonatal single-dose nevirapine compared with zidovudine for prevention of mother-to-child transmission of HIV-1 in Kampala, Uganda: 18-month follow-up of the HIVNET 012 randomised trial.
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Intrapartum and neonatal single-dose nevirapine compared with zidovudine for prevention of mother-to-child transmission of HIV-1 in Kampala, Uganda: 18-month follow-up of the HIVNET 012 randomised trial.

机译:在乌干达坎帕拉,比较产前和新生儿单剂量奈韦拉平与齐多夫定的预防母婴传播HIV-1的关系:HIVNET 012随机试验的18个月随访。

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BACKGROUND: In 1999, we reported safety and efficacy data for short-course nevirapine from a Ugandan perinatal HIV-1 prevention trial when 496 babies were followed up to age 14-16 weeks. Safety and efficacy data are now presented for all babies followed up to 18 months of age. METHODS: From November, 1997, to April, 1999, HIV-1 infected pregnant women in Kampala, Uganda, were randomly assigned nevirapine (200 mg at labour onset and 2mg/kg for babies within 72 h of birth; regimen A) or zidovudine (600 mg orally at labour onset and 300 mg every 3 h until delivery, and 4 mg/kg orally twice daily for babies for 7 days, regimenB). Infant HIV-1 testing was done at birth, age 6-8 and 14-16 weeks, and age 12 months by HIV-1 RNA PCR, and by HIV-1 antibody at 18 months. HIV-1 transmission and HIV-1-free survival were assessed using Kaplan-Meier analysis. We recorded adverse experiences through 6-8 weeks postpartum for mothers, and 18 months for babies. Efficacy analyses were by intention to treat. FINDINGS: We enrolled 645 mothers to the study: 313 were assigned regimen A, 313 regimen B, and 19 placebo. Eight mothers were lost to follow-up before delivery. 99% of babies were breastfed (median duration 9 months). Estimated risks of HIV-1 transmission in the zidovudine and nevirapine groups were 10.3% and 8.1% at birth (p=0.35); 20.0% and 11.8% by age 6-8 weeks (p=0.0063); 22.1% and 13.5% by age 14-16 weeks (p=0.0064); and 25.8% and 15.7% by age 18 months (p=0.0023). Nevirapine was associated with a 41% (95% CI 16-59) reduction in relative risk of transmission through to age 18 months. Both regimens were well-tolerated with few serious side-effects. INTERPRETATION: Intrapartumeonatal nevirapine significantly lowered HIV-1 transmission risk in a breastfeeding population in Uganda compared with a short intrapartumeonatal zidovudine regimen. The absolute 8.2% reduction in transmission at 6-8 weeks was sustained at age 18 months (10.1% [95% CI 3.5-16.6]). This simple, inexpensive, well-tolerated regimen has the potential to significantly decrease HIV-1 perinatal transmission in less-developed countries.
机译:背景:1999年,我们从一项乌干达围产期HIV-1预防试验中报告了短程奈韦拉平的安全性和有效性数据,该试验对496名婴儿进行了随访,年龄在14-16周之间。现在提供了所有18个月以下婴儿的安全性和有效性数据。方法:从1997年11月至1999年4月,在乌干达坎帕拉对感染HIV-1的孕妇随机分配奈韦拉平(分娩时200 mg,分娩72小时内婴儿2 mg / kg; A方案)或齐多夫定(分娩时口服600 mg,分娩前每3 h口服300 mg,婴儿每天7次,每天两次,每次4 mg / kg,方案B)。婴儿HIV-1测试是在出生时,6-8岁和14-16周以及12个月大时通过HIV-1 RNA PCR和18个月时通过HIV-1抗体进行的。使用Kaplan-Meier分析评估了HIV-1传播和无HIV-1生存。我们记录了母亲产后6-8周和婴儿18个月的不良经历。疗效分析是有意治疗的。结果:我们招募了645位母亲参加研究:313位患者被分配了A方案,313位B方案和19个安慰剂。分娩前失去了八名母亲进行随访。 99%的婴儿是母乳喂养(中位时间为9个月)。在齐多夫定和奈韦拉平组中,估计HIV-1传播的风险在出生时分别为10.3%和8.1%(p = 0.35); 6-8周龄时分别为20.0%和11.8%(p = 0.0063); 14-16周龄时分别占22.1%和13.5%(p = 0.0064); 18个月大时分别为25.8%和15.7%(p = 0.0023)。奈韦拉平与18个月大的相对传播风险降低41%(95%CI 16-59)。两种方案的耐受性都很好,几乎没有严重的副作用。解释:与短期内产/新生儿齐多夫定方案相比,乌内达产妇/新生儿奈韦拉平显着降低了乌干达母乳喂养人群的HIV-1传播风险。 18个月大时,在6-8周时的传播绝对减少了8.2%(10.1%[95%CI 3.5-16.6])。这种简单,廉价,耐受性良好的方案有可能在欠发达国家中显着减少HIV-1围产期传播。

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