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伐昔洛韦在预防巨细胞病毒母婴传播二级预防中的疗效新数据。

New data on efficacy of valacyclovir in secondary prevention of maternal-fetal transmission of cytomegalovirus.

作者信息

Egloff C, Sibiude J, Vauloup-Fellous C, Benachi A, Bouthry E, Biquard F, Hawkins-Villarreal A, Houhou-Fidouh N, Mandelbrot L, Vivanti A J, Picone O

机构信息

Service de Gynécologie-Obstétrique, Hôpital Louis-Mourier, AP-HP, Colombes, France.

University of Paris, Paris, France.

出版信息

Ultrasound Obstet Gynecol. 2023 Jan;61(1):59-66. doi: 10.1002/uog.26039.

Abstract

OBJECTIVE

Congenital cytomegalovirus (CMV) infection is the leading cause of non-genetic hearing and neurological deficits. The aim of our study was to evaluate the efficacy and safety of valacyclovir (VCV) treatment in preventing CMV transmission to the fetus after maternal primary infection.

METHODS

This was a retrospective, multicenter study evaluating the rate of maternal-fetal CMV transmission in pregnancies with maternal primary CMV infection treated with VCV at a dosage of 8 g per day (VCV group) compared with a control group of untreated women. Each case underwent virological testing to confirm maternal primary infection and to provide accurate dating of onset of infection. The primary outcome was the presence of congenital CMV infection at birth diagnosed based on polymerase chain reaction analysis of saliva, urine and/or blood samples. The efficacy of VCV treatment was assessed using logistic regression analysis adjusted for a propensity score.

RESULTS

In total, 143 patients were included in the final analysis, of whom 59 were in the VCV group and 84 were in the untreated control group. On propensity-score-adjusted analysis, VCV treatment was significantly associated with an overall reduction in the rate of maternal-fetal CMV transmission (odds ratio, 0.40 (95% CI, 0.18-0.90); P = 0.029). The rate of maternal-fetal CMV transmission, determined at birth, in the VCV vs control group was 7% (1/14) vs 10% (1/10) after periconceptional maternal primary infection (P = 1.00), 22% (8/36) vs 41% (19/46) after first-trimester maternal primary infection (P = 0.068) and 25% (2/8) vs 52% (14/27) after second-trimester maternal primary infection (P = 0.244). When analyzing the efficacy of VCV treatment according to maternal viremia at treatment initiation, there was a trend towards greater efficacy when patients were viremia-positive (21% vs 43%; P = 0.072) compared with when they were viremia-negative (22% vs 17%; P = 0.659). Maternal side effects associated with VCV were mild and non-specific in most cases.

CONCLUSION

Our findings indicate that VCV treatment of pregnant women with primary CMV infection reduces the risk of maternal-fetal transmission of CMV and may be effective in cases with primary infection in the first and second trimesters. © 2022 International Society of Ultrasound in Obstetrics and Gynecology.

摘要

目的

先天性巨细胞病毒(CMV)感染是导致非遗传性听力和神经功能缺损的主要原因。我们研究的目的是评估伐昔洛韦(VCV)治疗在预防孕妇初次感染后CMV传播给胎儿方面的疗效和安全性。

方法

这是一项回顾性多中心研究,评估每天服用8克剂量VCV治疗的孕妇初次CMV感染妊娠中母婴CMV传播率,并与未治疗女性的对照组进行比较。每例患者均接受病毒学检测以确认孕妇初次感染并准确确定感染发病时间。主要结局是根据唾液、尿液和/或血液样本的聚合酶链反应分析诊断出生时是否存在先天性CMV感染。使用倾向评分调整的逻辑回归分析评估VCV治疗的疗效。

结果

最终分析共纳入143例患者,其中59例在VCV组,84例在未治疗对照组。在倾向评分调整分析中,VCV治疗与母婴CMV传播率总体降低显著相关(优势比,0.40(95%CI,0.18 - 0.90);P = 0.029)。妊娠前孕妇初次感染后,VCV组与对照组出生时确定的母婴CMV传播率分别为7%(1/14)和10%(1/10)(P = 1.00),孕早期孕妇初次感染后分别为22%(8/36)和41%(19/46)(P = 0.068),孕中期孕妇初次感染后分别为25%(2/8)和52%(14/27)(P = 0.244)。根据治疗开始时孕妇病毒血症分析VCV治疗的疗效,病毒血症阳性患者(21%对43%;P = 0.072)与病毒血症阴性患者(22%对17%;P = 0.659)相比,有疗效更高的趋势。与VCV相关的孕妇副作用在大多数情况下较轻且不具特异性。

结论

我们的研究结果表明,对初次CMV感染的孕妇进行VCV治疗可降低CMV母婴传播风险,并且在孕早期和孕中期初次感染的病例中可能有效。© 2022国际妇产科超声学会。

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