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Intracervical Foley Catheter Plus Intravaginal Misoprostol vs Intravaginal Misoprostol Alone for Cervical Ripening: A Meta-Analysis

机译:插入粪便导管加上静脉内米索前列醇与宫内生索前司甾醇仅用于颈椎成熟:META分析

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摘要

Currently, there is no meta-analysis comparing intravaginal misoprostol plus intracervical Foley catheter versus intravaginal misoprostol alone for term pregnancy without identifying risk factors. Therefore, the purpose of this study is to conduct a systematic review and meta-analysis of randomized control trials (RCTs) comparing concurrent intravaginal misoprostol and intracervical Foley catheter versus intravaginal misoprostol alone for cervical ripening. We systematically searched Embase, Pubmed, and Cochrane Collaboration databases for randomized controlled trials (RCTs) comparing intracervical Foley catheter plus intravaginal misoprostol and intravaginal misoprostol alone using the search terms “Foley”, “misoprostol”, “cervical ripening”, and “induction” up to 29 January 2019. Data were extracted and analyzed by two independent reviewers including study characteristics, induction time, cesarean section (C/S), clinical suspicion of chorioamnionitis, uterine tachysystole, meconium stain, and neonatal intensive care unit (NICU) admissions. Data was pooled using random effects modeling and calculated with risk ratio (RR) and 95% confidence interval (CI). Pooled analysis from eight studies, including 1110 women, showed that labor induction using a combination of intracervical Foley catheter and intravaginal misoprostol decreased induction time by 2.71 h (95% CI −4.33 to −1.08, p = 0.001), as well as the risk of uterine tachysystole and meconium staining (RR 0.54, 95% CI 0.30−0.99 and RR 0.48, 95% CI 0.32−0.73, respectively) significantly compared to those using intravaginal misoprostol alone. However, there was no difference in C/S rate (RR 0.93, 95% CI 0.78−1.11) or clinical suspicion of chorioamnionitis rate (RR 1.22, CI 0.58−2.57) between the two groups. Labor induction with a combination of intracervical Foley catheter and intravaginal misoprostol may be a better choice based on advantages in shortening induction time and reducing the risk of uterine tachysystole and meconium staining compared to intravaginal misoprostol alone.
机译:目前,没有Meta分析比较静脉内米索前列醇和宫内杂散导管与静脉内腓母服甾醇单独进行术语妊娠期,而不识别风险因素。因此,本研究的目的是对随机对照试验(RCTS)进行系统评价和荟萃分析,比较同时静脉内偏寄生酚和颈静脉内杂散导管与单独的宫颈成熟的静脉内杂散导管。我们系统地搜索了用于随机对照试验(RCTS)的embase,PubMed和Cochrane协作数据库(RCTS),比较intracalical Foley导管加上静脉内偏索道甾醇和静脉内杂散氧棘甾醇单独使用搜索术语“Foley”,“Misoprostol”,“宫颈成熟”和“诱导” 2019年1月29日。通过两个独立审查员提取和分析,包括研究特征,诱导时间,剖宫产(C / S),肠甘液炎,子宫内肠炎,阳光和新生儿重症监护单位(NICU)录取的临床怀疑。使用随机效果建模和以风险比(RR)和95%置信区间(CI)计算数据来汇集数据。包括1110名妇女在内的八项研究的汇总分析表明,使用宫内流理导管和静脉内米索前列醇组合的劳动诱导减少2.71小时(95%CI -4.33至-1.08,P = 0.001),以及风险与使用单独使用静脉内米索前列甾醇的人显着比较,子宫气囊杆和粉末染色(RR 0.54,95%CI 0.30-0.99和RR 0.48,95%CI 0.32-0.73分别显着。然而,C / S率(RR 0.93,95%CI 0.78-1.11)的差异或两组之间的胆管炎率(RR 1.22,CI 0.58-2.57)的临床怀疑。植物诱导组合的脑内福利导管和静脉内偏索多斯醇组合可以是基于缩短诱导时间的优点,并降低与单独的静脉内米索前列蛋呤相比,减少子宫内氏术和胎膜染色的风险。

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