首页> 外文期刊>European Journal of Obstetrics, Gynecology and Reproductive Biology: An International Journal >Foley catheter or prostaglandin E2 inserts for induction of labour at term: An open-label randomized controlled trial (PROBAAT-P trial) and systematic review of literature
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Foley catheter or prostaglandin E2 inserts for induction of labour at term: An open-label randomized controlled trial (PROBAAT-P trial) and systematic review of literature

机译:足月引产的Foley导管或前列腺素E2插入物:一项开放标签的随机对照试验(PROBAAT-P试验)和系统的文献复习

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Objective To assess the safety and effectiveness of a transcervical Foley catheter compared to vaginal prostaglandin E2 inserts for term induction of labour. Study design We conducted an open-label randomized controlled trial in five hospitals in the Netherlands. Women with a singleton term pregnancy in cephalic presentation, intact membranes, unfavourable cervix, and no prior caesarean section were enrolled. Participants were randomly allocated by a web-based randomization system to induction of labour with a 30 ml Foley catheter or 10 mg slow-release vaginal prostaglandin E2 inserts in a 1:1 ratio. Due to the nature of the intervention this study was not blinded. The primary outcome was the caesarean section rate. Secondary outcomes were maternal and neonatal morbidity and time from intervention to birth. Additionally, we carried out a systematic review and meta-analysis of similar studies. Results We analyzed 226 women: 107 received a Foley catheter and 119 inserts. Caesarean section rates were comparable (20% versus 22%, RR 0.90, 95% CI 0.54-1.50). Secondary outcomes showed no differences. We observed no serious maternal or neonatal morbidity. Meta-analysis showed comparable caesarean section rates, but significantly fewer cases of hyperstimulation during the ripening phase when a Foley catheter was used. Conclusions We found, in this relatively small study, no differences in effectiveness and safety of induction of labour with a Foley catheter and 10 mg slow release vaginal prostaglandin E2 inserts. Meta-analysis confirmed a comparable caesarean section rate, and showed fewer cases of hyperstimulation when a Foley catheter was used.
机译:目的评估经阴道Foley导管与阴道前列腺素E2插入物相比的安全性和有效性。研究设计我们在荷兰的五家医院进行了开放标签的随机对照试验。头颅表现为单胎足月妊娠,胎膜完整,子宫颈不良且未进行剖腹产的妇女参加了研究。通过基于网络的随机系统将参与者随机分配为使用30 ml Foley导管或10 mg缓释阴道前列腺素E2插件以1:1的比例引产。由于干预的性质,本研究没有盲目性。主要结果是剖腹产率。次要结局为母婴发病率以及从干预到分娩的时间。此外,我们对类似研究进行了系统的回顾和荟萃分析。结果我们分析了226名女性:107名接受了Foley导管和119个插入物。剖宫产率相当(20%vs 22%,RR 0.90,95%CI 0.54-1.50)。次要结果显示无差异。我们没有观察到严重的母亲或新生儿发病率。荟萃分析显示可比的剖腹产率,但是使用Foley导管时,在成熟阶段过度刺激的病例明显减少。结论我们在这项相对较小的研究中发现,使用Foley导管和10 mg缓释阴道前列腺素E2插入物引产的有效性和安全性没有差异。荟萃分析证实了可比的剖腹产率,并且使用Foley导管时显示出较少的过度刺激病例。

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