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Foley catheter versus vaginal prostaglandin E2 gel for induction of labour at term (PROBAAT trial): an open-label, randomised controlled trial

机译:Foley导管与阴道前列腺素E2凝胶在足月引产(PROBAAT试验):一项开放标签,随机对照试验

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摘要

Induction of labour is a common obstetric procedure. Both mechanical (eg, Foley catheters) and pharmacological methods (eg, prostaglandins) are used for induction of labour in women with an unfavourable cervix. We aimed to compare the effectiveness and safety of induction of labour with a Foley catheter with induction with vaginal prostaglandin E2 gel. We did an open-label, randomised controlled trial in 12 hospitals in the Netherlands between Feb 10, 2009, and May 17, 2010. We enrolled women with a term singleton pregnancy in cephalic presentation, intact membranes, an unfavourable cervix, an indication for induction of labour, and no prior caesarean section. Participants were randomly allocated by an online randomisation system to induction of labour with a 30 mL Foley catheter or vaginal prostaglandin E2 gel (1:1 ratio). Because of the nature of the intervention this study was not blinded. The primary outcome was caesarean section rate. Secondary outcomes were maternal and neonatal morbidity and time from intervention to birth. All analyses were done on an intention-to-treat basis. We also did a meta-analysis that included our trial. The trial was registered with the Dutch trial registry, number NTR 1646. 824 women were allocated to induction of labour with a Foley catheter (n=412) or vaginal prostaglandin E2 gel (n=412). Caesarean section rates were much the same between the two groups (23%vs 20%, risk ratio [RR] 1·13, 95% CI 0·87-1·47). A meta-analysis including our trial data confirmed that a Foley catheter did not reduce caesarean section rates. We recorded two serious maternal adverse events, both in the prostaglandin group: one uterine perforation and one uterine rupture. In women with an unfavourable cervix at term, induction of labour with a Foley catheter is similar to induction of labour with prostaglandin E2 gel, with fewer maternal and neonatal side-effects. None
机译:引产是常见的产科程序。机械(例如,Foley导管)和药理学方法(例如,前列腺素)均用于宫颈不良妇女引产。我们旨在比较用Foley导管和阴道前列腺素E2凝胶诱导引产的有效性和安全性。我们在2009年2月10日至2010年5月17日之间在荷兰的12家医院中进行了一项开放标签,随机对照试验。我们对单胎妊娠足月妊娠,膜完整,宫颈不良,适应症为女性的妇女进行了登记。引产,且无事先剖腹产。通过在线随机系统将参与者随机分配到使用30 mL Foley导管或阴道前列腺素E2凝胶(1:1比例)引产。由于干预的性质,本研究没有盲目性。主要结局是剖腹产率。次要结局是母婴发病率以及从干预到出生的时间。所有分析均按意向性进行。我们还进行了荟萃分析,包括我们的试验。该试验已在荷兰试验注册中心登记,编号NTR1646。824名妇女被分配使用Foley导管(n = 412)或阴道前列腺素E2凝胶(n = 412)引产。两组的剖腹产率几乎相同(23%vs 20%,风险比[RR] 1·13,95%CI 0·87-1·47)。包含我们的试验数据的荟萃分析证实,Foley导管不会降低剖腹产率。我们在前列腺素组中记录了两个严重的母体不良事件:一个子宫穿孔和一个子宫破裂。在足月宫颈不良的妇女中,用Foley导管引产与使用前列腺素E2凝胶引产相似,而对母婴的不良反应较少。没有

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