Velzel Joost, Vlemmix Floortje, Opmeer Brent C, Molkenboer Jan F M, Verhoeven Corine J, van Pampus Mariëlle G, Papatsonis Dimitri N M, Bais Joke M J, Vollebregt Karlijn C, van der Esch Liesbeth, Van der Post Joris A M, Mol Ben Willem, Kok Marjolein
Department of Obstetrics and Gynaecology, Academic Medical Centre, Amsterdam, Netherlands
Department of Obstetrics and Gynaecology, Academic Medical Centre, Amsterdam, Netherlands.
BMJ. 2017 Jan 26;356:i6773. doi: 10.1136/bmj.i6773.
To compare the effectiveness of the oxytocin receptor antagonist atosiban with the beta mimetic fenoterol as uterine relaxants in women undergoing external cephalic version (ECV) for breech presentation.
Multicentre, open label, randomised controlled trial.
Eight hospitals in the Netherlands, August 2009 to May 2014.
830 women with a singleton fetus in breech presentation and a gestational age of more than 34 weeks were randomly allocated in a 1:1 ratio to either 6.75 mg atosiban (n=416) or 40 μg fenoterol (n=414) intravenously for uterine relaxation before ECV.
The primary outcome measures were a fetus in cephalic position 30 minutes after the procedure and cephalic presentation at delivery. Secondary outcome measures were mode of delivery, incidence of fetal and maternal complications, and drug related adverse events. All analyses were done on an intention-to-treat basis.
Cephalic position 30 minutes after ECV occurred significantly less in the atosiban group than in the fenoterol group (34% v 40%, relative risk 0.73, 95% confidence interval 0.55 to 0.93). Presentation at birth was cephalic in 35% (n=139) of the atosiban group and 40% (n=166) of the fenoterol group (0.86, 0.72 to 1.03), and caesarean delivery was performed in 60% (n=240) of women in the atosiban group and 55% (n=218) in the fenoterol group (1.09, 0.96 to 1.20). No significant differences were found in neonatal outcomes or drug related adverse events.
In women undergoing ECV for breech presentation, uterine relaxation with fenoterol increases the rate of cephalic presentation 30 minutes after the procedure. No statistically significant difference was found for cephalic presentation at delivery.
Dutch Trial Register, NTR 1877.
比较缩宫素受体拮抗剂阿托西班与β受体激动剂非诺特罗作为子宫松弛剂在臀位孕妇外倒转术(ECV)中的有效性。
多中心、开放标签、随机对照试验。
荷兰的八家医院,2009年8月至2014年5月。
830名单胎臀位妊娠且孕周超过34周的孕妇按1:1比例随机分为两组,分别静脉注射6.75毫克阿托西班(n = 416)或40微克非诺特罗(n = 414)以在ECV前松弛子宫。
主要结局指标为术后30分钟胎儿呈头位以及分娩时头先露。次要结局指标为分娩方式、胎儿和母亲并发症的发生率以及药物相关不良事件。所有分析均基于意向性治疗原则进行。
阿托西班组术后30分钟胎儿呈头位的比例显著低于非诺特罗组(34%对40%,相对风险0.73,95%置信区间0.55至0.93)。阿托西班组35%(n = 139)的产妇分娩时头先露,非诺特罗组为40%(n = 166)(0.86,0.72至1.03),阿托西班组60%(n = 240)的产妇进行了剖宫产,非诺特罗组为55%(n = 218)(1.09,0.96至1.20)。在新生儿结局或药物相关不良事件方面未发现显著差异。
在接受ECV的臀位孕妇中,使用非诺特罗松弛子宫可提高术后30分钟胎儿头先露的比例。在分娩时头先露方面未发现统计学上的显著差异。
荷兰试验注册库,NTR 1877