Comparison of oral mifepristone with intracervical foleys catheterisation for induction of labour in term pregnancy: A randomized control trial

Juhi Vipul Amin, A. Gokhale, Vidhi Hemantkumar Shah, Aayushi Jitendra Rajani
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Abstract

The purpose of this study is to compare the efficacy of oral Mifepristone with the efficacy of intracervical Foley catheterisation for induction of labour in term pregnancy. The primary outcome of this study is to compare both methods of induction of labour in terms of induction to delivery interval and the secondary outcome is to compare the two methods in terms of route of delivery, indications of caesarean section and the neonatal outcomes. This study is a randomized control trial conducted from May 2022 to December 2022 in Department of Obstetrics and Gynecology, SSG Hospital, Baroda Medical College. 180 term pregnant patients were enrolled in this study based on a pre-established criteria. Patients were randomised into group A and B. Group A included patients who were given Tablet Mifepristone 200 mg PO followed by per vaginum Tablet Misoprostol and Group B included patients who underwent intracervical Foleys catheterisation followed by placement of per vaginum Tablet Misoprostol. The study concluded that there was significantly decreased induction-delivery interval in women induced with intracervical Foleys catheterisation (Group B) as compared to those given oral Tablet Mifepristone (Group A). There was no significant difference between the two groups in terms of the route of delivery, rate of C Sections and neonatal outcomes.Mifepristone is effective for inducing indicated term pregnancies, despite no decrease in induction delivery interval. Incidence of fetal distress with oral Mifepristone is comparable to intracervical foley's catheterization. Further research is needed to assess tachysystole/hyperstimulation and fetal distress caused by Mifepristone.
口服米非司酮与宫颈内留置导产术用于足月妊娠引产的比较:一项随机对照试验
本研究的目的是比较口服米非司酮与宫颈内Foley导产术对足月妊娠引产的疗效。本研究的主要结局是比较两种引产方法在引产间隔方面的效果,次要结局是比较两种引产方法在分娩方式、剖宫产指征和新生儿结局方面的效果。本研究是一项随机对照试验,于2022年5月至2022年12月在巴罗达医学院SSG医院妇产科进行,根据预先制定的标准入组180例足月妊娠患者。患者随机分为A组和B组。A组患者给予米非司酮片剂200 mg PO,随后口服阴道片米索前列醇;B组患者接受宫颈内foley导管置入,随后口服阴道片米索前列醇。研究得出结论,与口服米非司酮片(A组)相比,宫颈内Foleys置管(B组)诱导分娩间隔明显缩短。两组在分娩途径、剖宫产率和新生儿结局方面无显著差异。米非司酮是有效的诱导足月妊娠,尽管没有减少引产间隔。口服米非司酮导致胎儿窘迫的发生率与宫颈内foley导管置入相当。需要进一步的研究来评估米非司酮引起的心动过速/过度刺激和胎儿窘迫。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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