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褪黑素作为引产辅助药物的双盲、随机、安慰剂对照试验:MILO试验。

A double-blind, randomized, placebo-controlled trial of melatonin as an adjuvant agent for induction of labor: The MILO trial.

作者信息

Quach Diane, Mol Ben W, Springer Jamie, Tully Erin, Higgins Chloe, Jones Madeleine, Hennes David, Pham Yen, Swarnamani Kamala, Palmer Kirsten, Davies-Tuck Miranda

机构信息

Department of Obstetrics and Gynecology, Monash Women's, Monash Health, Clayton, Victoria, Australia.

Department of Obstetrics and Gynecology, Monash University, Clayton, Victoria, Australia.

出版信息

Acta Obstet Gynecol Scand. 2024 Dec;103(12):2442-2454. doi: 10.1111/aogs.14951. Epub 2024 Oct 24.

Abstract

INTRODUCTION

Melatonin has been suggested to have a biological role in the onset and progress of labor. We tested the hypothesis that the addition of melatonin during an induction of labor will reduce the need for a cesarean birth.

MATERIAL AND METHODS

This trial underwent protocol amendments that are detailed in the main text of the article. This trial is registered with the Australian and New Zealand Clinical Trials Registry (ACTRN12616000311459). At a multi-center health service including secondary and tertiary obstetric hospitals, we performed a randomized, double-blind, placebo-controlled trial in women with a singleton cephalic pregnancy, free of significant maternal or perinatal complications who were undergoing induction of labor (with or without cervical ripening). Women were randomized to 10 mg melatonin vs placebo, with cervical ripening as required, and then 6-h during their induction of labor to a maximum of four doses or until birth. The primary outcome was cesarean birth. Secondary outcomes included labor, maternal, and neonatal outcomes. Data were analyzed using intention to treat. Sub-group analyses based on mode of ripening and parity were also performed.

RESULTS

Between 2019 and 2021 we randomized 189 women (103 to melatonin and 86 to placebo). The study was prematurely terminated due to logistical complications resulting from the COVID-19 pandemic. Cesarean rates were 28/103 (27.2%) in the melatonin group vs 20/84 (23.3%) in the placebo group (RR 1.17 95% CI 0.71-1.92). There were no significant differences in rate of cesarean birth between the melatonin and placebo groups for failure to progress (13.4% and 9.3%, respectively, RR 1.46; 95% CI 0.64-3.32) or suspected fetal distress (10.7% and 10.5%, respectively, RR 1.02; 95% CI 0.44-2.34). The melatonin group had significantly lower rates of spontaneous vaginal birth within 24 h (35.0% vs. 50.0%; RR 0.70 95% CI 0.50-0.98). The rates of secondary outcomes such as total length of labor, rate of postpartum hemorrhage, and instrumental birth were comparable. Babies born in the melatonin group were more likely to need admission to the special care nursery, namely for hypoglycemic monitoring (18.5% vs. 8.1% RR 2.26; 95% CI 1.00-5.10).

CONCLUSIONS

In women undergoing induction of labor, melatonin does not reduce the cesarean section rate. Melatonin use intrapartum may also be associated with neonatal hypoglycemia.

摘要

引言

褪黑素被认为在分娩的发动和进展中具有生物学作用。我们检验了在引产过程中添加褪黑素会减少剖宫产需求这一假设。

材料与方法

本试验进行了方案修订,具体内容在文章正文详细说明。本试验已在澳大利亚和新西兰临床试验注册中心注册(ACTRN12616000311459)。在一家包括二级和三级产科医院的多中心医疗服务机构,我们对单胎头位妊娠、无严重母体或围产期并发症且正在接受引产(无论是否进行宫颈成熟)的女性进行了一项随机、双盲、安慰剂对照试验。女性被随机分为10毫克褪黑素组和安慰剂组,根据需要进行宫颈成熟,然后在引产期间每6小时给药一次,最多4剂或直至分娩。主要结局是剖宫产。次要结局包括分娩、母体和新生儿结局。数据采用意向性分析。还进行了基于成熟方式和产次的亚组分析。

结果

在2019年至2021年期间,我们将189名女性随机分组(103名至褪黑素组,86名至安慰剂组)。由于新冠疫情导致的后勤并发症,该研究提前终止。褪黑素组的剖宫产率为28/103(27.2%),安慰剂组为20/84(23.3%)(相对危险度1.17,95%置信区间0.71 - 1.92)。褪黑素组和安慰剂组在产程无进展(分别为13.4%和9.3%,相对危险度1.46;95%置信区间0.64 - 3.32)或疑似胎儿窘迫(分别为10.7%和10.5%,相对危险度1.02;95%置信区间0.44 - 2.34)情况下的剖宫产率无显著差异。褪黑素组在24小时内自然阴道分娩率显著较低(35.0%对50.0%;相对危险度0.70,95%置信区间0.50 - 0.98)。分娩总时长、产后出血率和器械助产等次要结局发生率相当。褪黑素组出生的婴儿更有可能需要入住特殊护理病房,即进行低血糖监测(18.5%对8.1%,相对危险度2.26;95%置信区间1.00 - 5.10)。

结论

在接受引产的女性中,褪黑素不会降低剖宫产率。产时使用褪黑素还可能与新生儿低血糖有关。

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