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首页> 外文期刊>Obstetrics and Gynecology: Journal of the American College of Obstetricians and Gynecologists >Risk factors for perinatal human immunodeficiency virus transmission in patients receiving zidovudine prophylaxis. Pediatric AIDS Clinical Trials Group protocol 076 Study Group.
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Risk factors for perinatal human immunodeficiency virus transmission in patients receiving zidovudine prophylaxis. Pediatric AIDS Clinical Trials Group protocol 076 Study Group.

机译:接受齐多夫定预防的患者围产期人免疫缺陷病毒传播的危险因素。儿科艾滋病临床试验小组规程076研究组。

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OBJECTIVE: To identify modifiable obstetric factors associated with the failure of zidovudine chemoprophylaxis to prevent perinatal human immunodeficiency virus type 1 (HIV-1) transmission. METHODS: We analyzed data from Pediatric AIDS Clinical Trials Group protocol 076, a randomized, double-masked, placebo-controlled trial that demonstrated that a zidovudine regimen could prevent perinatal HIV-1 transmission. We estimated the zidovudine treatment effect using the relative reduction in transmission risk among women randomized to treatment with zidovudine compared with women randomized to receive placebo. Univariate and multivariate statistical analyses were used to assess whether the treatment effect differed in magnitude according to potential antepartum or intrapartum risk factors. RESULTS: In the univariate analysis, the zidovudine treatment effect was found to differ significantly in magnitude according to quartile of maternal weight at the time of study entry (interaction test, P = .03); among women in the heaviest-weight quartile (weight more than 82 kg), there was a 26% relative reduction in transmission risk, compared with a 79% relative reduction among the other three quartiles (interaction test, P = .05). In the zidovudine treatment group, women who transmitted HIV-1 were significantly more likely than nontransmitters to have had antepartum procedures or conditions associated with increased risk of fetal exposure to maternal blood or cervicovaginal secretions (43% compared with 19%, P = .04). In the multivariate analysis, adjustment for the plasma HIV-1 RNA level and CD4+ cell percentage did not eliminate the differential treatment effect according to these factors. CONCLUSION: High maternal weight and conditions associated with fetal exposure to maternal blood or cervicovaginal secretions may diminish the efficacy of zidovudine chemoprophylaxis.
机译:目的:确定与齐多夫定化学预防失败有关的可改变的产科因素,以防止围产期人类免疫缺陷病毒1型(HIV-1)传播。方法:我们分析了儿科艾滋病临床试验小组协议076的数据,该协议是一项随机,双掩蔽,安慰剂对照的试验,该试验证明齐多夫定方案可以预防围产期HIV-1传播。我们使用随机分组接受齐多夫定治疗的女性与随机接受安慰剂的女性相比,通过降低传播风险来估计齐多夫定的治疗效果。使用单变量和多变量统计分析来评估治疗效果是否根据潜在的产前或产时危险因素而在大小上有所不同。结果:在单变量分析中,发现齐多夫定的治疗效果随入学时母亲体重的四分位数而显着不同(交互作用测试,P = .03);在体重最重的四分位数(体重超过82公斤)的女性中,传播风险相对降低了26%,而其他三个四分位数中的相对降低了79%(互动测试,P = 0.05)。在齐多夫定治疗组中,与未传播者相比,传播HIV-1的妇女发生产前检查程序或病症的可能性更高,与胎儿暴露于母体血液或宫颈阴道分泌物的风险增加有关(43%比19%,P = .04 )。在多变量分析中,根据这些因素调整血浆HIV-1 RNA水平和CD4 +细胞百分比并不能消除差异性治疗效果。结论:高孕妇体重和胎儿暴露于孕妇血液或宫颈阴道分泌物可能会降低齐多夫定化学预防的疗效。

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