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Atosiban versus fenoterol as a uterine relaxant for external cephalic version: randomised controlled trial

机译:阿托西班与非诺特罗作为外用头颅型子宫松弛剂:随机对照试验

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摘要

>Objective 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. >Design Multicentre, open label, randomised controlled trial. >Setting Eight hospitals in the Netherlands, August 2009 to May 2014. >Participants 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. >Main outcome measures 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. >Results 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. >Conclusions 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. >Trial registration Dutch Trial Register, NTR 1877.
机译:>目的,比较催产素受体拮抗剂阿托西班和β模仿非诺特罗作为接受外头位(ECV)进行臀位测试的妇女的子宫松弛剂的效果。 >设计。多中心,开放标签,随机对照试验。 >设置荷兰的八家医院,2009年8月至2014年5月。>参与者我们随机分配了830名具有单胎胎儿,臀位超过34周的女性。在ECV之前,通过静脉注射以6.75 mg阿托西班(n = 416)或40μg非诺特罗(n = 414)的1:1比例进行子宫松弛。 >主要结局指标:主要结局指标是手术后30分钟胎儿处于头位状态,分娩时出现头位表现。次要结果指标是分娩方式,胎儿和产妇并发症的发生率以及与药物相关的不良事件。所有分析均按意向性进行。 >结果阿托西班组ECV发生30分钟后的头颅位置明显少于非诺特罗组(34%vs 40%,相对危险度0.73,95%置信区间0.55至0.93)。阿托西班组35%(n = 139)和非诺特罗组40%(n = 166)(0.86,0.72至1.03)出生时呈头颅表现,剖腹产的比例为60%(n = 240)。阿托西班组的女性比例和非诺特罗组的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中未发现显着差异。 >结论:在接受ECV进行臀位示威的女性中,非诺特罗使子宫松弛可增加术后30分钟的头颅示威率。分娩时头颅表现没有统计学上的显着差异。 >试用注册:荷兰试用注册,NTR 1877。

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