Foley catheter compared with controlled release dinoprostone vaginal insert for labor induction after one previous cesarean delivery: A randomized trial

地诺前列酮 医学 导尿管 阴道分娩 引产 置信区间 随机对照试验 四分位间距 产科 头位 胎龄 可视模拟标度 麻醉 妊娠期 怀孕 导管 外科 前列腺素E2 催产素 内科学 生物 遗传学
作者
Sofiah Sulaiman,Sanmugam Sivaranjani,Nuguelis Razali,Boon Kiong Lim,Mukhri Hamdan,Peng Chiong Tan
出处
期刊:International journal of gynaecology and obstetrics [Wiley]
卷期号:160 (3): 814-822 被引量:5
标识
DOI:10.1002/ijgo.14364
摘要

Abstract Objective To compare Foley catheter and controlled‐release dinoprostone vaginal insert on induction‐to‐delivery interval and maternal satisfaction in women with one previous cesarean delivery. Methods This randomized controlled trial was conducted at the University Malaya Medical Center, Kuala Lumpur, Malaysia, from December 12, 2018, to May 28, 2019. A total of 78 term women scheduled for labor induction with one previous cesarean delivery who had ripe cervixes, singleton gestation, cephalic presentation, intact membranes, and reassuring cardiotocogram were randomized to Foley catheter or dinoprostone insert. The primary outcome was induction‐to‐delivery interval (in hours) and the secondary outcomes included maternal satisfaction on birth experience (assessed by 100‐mm visual analog scale). Results Induction‐to‐delivery intervals were as follows: median 33.5 h (interquartile range [IQR], 26.1–36.2 h) versus 23.5 h (IQR, 12.7–34.5 h) ( P = 0.004), and maternal satisfaction on birth process 100‐mm visual analog scale was 80 mm (IQR, 64–88 mm) versus 82 mm (IQR, 67–88 mm) ( P = 0.919) for the Foley and controlled‐release dinoprostone arms, respectively. Cesarean delivery rates were 23 of 39 (59%) versus 20 of 39 (51%) (relative risk, 1.15 [95% confidence interval, 0.77–1.72]) ( P = 0.496) and trial device insertion to removal time mean ± standard deviation was 20.1 ± 7.1 h versus 14.2 ± 7.3 h ( P = 0.001) for Foley versus controlled‐release dinoprostone, respectively. Conclusion In term women after one previous cesarean delivery with unripe cervixes, controlled‐release dinoprostone vaginal insert compared with Foley catheter shortens the induction‐to‐delivery interval but maternal satisfaction was not significantly increased. Clinical Trial Registration This study was registered with ISRCTN on November 30, 2018, with trial identification number: ISRCTN16957529 ( https://doi.org/10.1186/ISRCTN16957529 ). The first participant was recruited on December 12, 2018.
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