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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: 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: HIVNET 012 randomised trial.

机译:在乌干达坎帕拉,进行产前和新生儿单剂量奈韦拉平与齐多夫定的比较,以预防HIV-1的母婴传播:HIVNET 012随机试验。

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BACKGROUND: The AIDS Clinical Trials Group protocol 076 zidovudine prophylaxis regimen for HIV-1-infected pregnant women and their babies has been associated with a significant decrease in vertical HIV-1 transmission in non-breastfeeding women in developed countries. We compared the safety and efficacy of short-course nevirapine or zidovudine during labour and the first week of life. METHODS: From November, 1997, to April, 1999, we enrolled 626 HIV-1-infected pregnant women at Mulago Hospital in Kampala, Uganda. We randomly assigned mothers nevirapine 200 mg orally at onset of labour and 2 mg/kg to babies within 72 h of birth, or zidovudine 600 mg orally to the mother at onset of labour and 300 mg every 3 h until delivery, and 4 mg/kg orally twice daily to babies for 7 days after birth. We tested babies for HIV-1 infection at birth, 6-8 weeks, and 14-16 weeks by HIV-1 RNA PCR. We assessed HIV-1 transmission and HIV-1-free survival with Kaplan-Meier analysis. FINDINGS: Nearly all babies (98.8%) were breastfed, and 95.6% were still breastfeeding at age 14-16 weeks. The estimated risks of HIV-1 transmission in the zidovudine and nevirapine groups were: 10.4% and 8.2% at birth (p=0.354); 21.3% and 11.9% by age 6-8 weeks (p=0.0027); and 25.1% and 13.1% by age 14-16 weeks (p=0.0006). The efficacy of nevirapine compared with zidovudine was 47% (95% CI 20-64) up to age 14-16 weeks. The two regimens were well tolerated and adverse events were similar in the two groups. INTERPRETATION: Nevirapine lowered the risk of HIV-1 transmission during the first 14-16 weeks of life by nearly 50% in a breastfeeding population. This simple and inexpensive regimen could decrease mother-to-child HIV-1 transmission in less-developed countries.
机译:背景:艾滋病临床试验小组对076-1艾滋病毒感染的孕妇及其婴儿的预防方案齐多夫定的预防方案已与发达国家非母乳喂养妇女的垂直HIV-1传播显着减少相关。我们比较了短期分娩时奈韦拉平或齐多夫定的安全性和有效性。方法:从1997年11月到1999年4月,我们在乌干达坎帕拉的Mulago医院招募了626名受HIV-1感染的孕妇。我们将分娩开始时母亲口服200 mg奈韦拉平和分娩后72小时内的婴儿随机分配为2 mg / kg的母亲,或分娩时母亲将600 mg齐多夫定口服给母亲,分娩开始后每3 h 300 mg分配给母亲,和4 mg /出生后7天内每天两次给婴儿口服。我们通过HIV-1 RNA PCR测试了婴儿在出生时,6-8周和14-16周时是否感染HIV-1。我们通过Kaplan-Meier分析评估了HIV-1传播和无HIV-1生存。结果:在14-16周龄时,几乎所有婴儿(98.8%)都是母乳喂养,而95.6%的婴儿仍在母乳喂养。齐多夫定和奈韦拉平组中HIV-1传播的估计风险为:出生时分别为10.4%和8.2%(p = 0.354); 6-8周龄时分别为21.3%和11.9%(p = 0.0027);在14-16周龄时分别占25.1%和13.1%(p = 0.0006)。奈韦拉平与齐多夫定相比,在14-16周龄时的疗效为47%(95%CI 20-64)。两种方案的耐受性良好,两组的不良事件相似。解释:在母乳喂养的人群中,奈韦拉平将出生后14-16周内HIV-1传播的风险降低了近50%。这种简单且便宜的方案可以减少欠发达国家的母婴HIV-1传播。

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