人工渗透扩张剂与药物在引产中宫颈成熟的比较:系统综述和荟萃分析。

IF 2.3
Gi Wook Ryu, Sun-Young Park
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引用次数: 0

摘要

导读:随着人工渗透扩张剂的研究越来越多,对于其与其他常用的宫颈成熟方法的比较,缺乏全面的综述。本研究旨在比较人工合成渗透扩张剂与药物(前列腺素E1、前列腺素E2、催产素)在宫颈成熟引产中的安全性和有效性。方法:通过MEDLINE、Embase、CINAHL和Cochrane图书馆数据库检索,对随机对照试验(RCTs)和队列研究进行系统评价和荟萃分析。两名审稿人独立筛选研究,并以2级偏倚风险和非随机研究的偏倚风险评估干预工具的偏倚风险。以95% ci计算相对危险度(RRs)和平均差异(MDs)。结果:11项研究(8个随机对照试验,3个队列,2355名受试者)显示,合成渗透扩张剂与药物的安全性结局无统计学差异,包括产妇感染(RR, 1.27)、产后出血(RR, 0.87)、新生儿感染(RR, 1.19)、低Apgar评分(RR, 0.74)和新生儿重症监护病房入院(RR, 1.06)(均P < 0.05)。阴道分娩率(RR, 0.98)和Bishop评分变化(MD, 0.0)的疗效结果具有可比性(P均为0.05)。合成渗透性扩张剂减少了子宫过度刺激(RR, 0.45)和消化系统症状(RR, 0.15),但需要更多的人工破膜(RR, 1.57)(均P)。讨论:合成渗透性扩张剂是一种安全、有效、可行的引产选择,可降低产妇子宫过度刺激的风险。这些发现对将人工渗透扩张剂用于宫颈成熟的临床应用纳入国际指南具有重要意义。由于有证据支持其有效性和安全性,因此需要对护士和助产士进行使用合成渗透扩张器引产的教育。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Comparison of Synthetic Osmotic Dilators and Pharmacologic Agents for Cervical Ripening in Induction of Labor: A Systematic Review and Meta-Analysis.

Introduction: Given the rising number of studies on synthetic osmotic dilators, there is a lack of comprehensive reviews for their use compared with other commonly used cervical ripening methods. This study aimed to examine the maternal and neonatal safety and efficacy in cervical ripening and labor induction using synthetic osmotic dilators compared with pharmacologic agents (prostaglandin E1, prostaglandin E2, oxytocin) for labor induction.

Methods: A systematic review and meta-analysis of randomized controlled trials (RCTs) and cohort studies was conducted, using MEDLINE, Embase, CINAHL, and Cochrane Library databases search. Two reviewers independently screened studies and assessed the risk of bias with Risk of Bias 2 and Risk Of Bias In Nonrandomized Studies - of Interventions tools. Relative risks (RRs) and mean differences (MDs) were calculated with 95% CIs.

Results: Eleven studies (8 RCTs, 3 cohort; 2355 participants) showed no statistically significant differences in safety outcomes between synthetic osmotic dilators and pharmacologic agents, including maternal infection (RR, 1.27), postpartum bleeding (RR, 0.87), neonatal infection (RR, 1.19), low Apgar scores (RR, 0.74), and admission to neonatal intensive care unit (RR, 1.06) (all P > .05). Efficacy outcomes were comparable for vaginal birth rates (RR, 0.98) and Bishop score changes (MD, 0.0) (both P > .05). Synthetic osmotic dilators reduced uterine hyperstimulation (RR, 0.45) and digestive symptoms (RR, 0.15) but required more artificial rupture of membrane (RR, 1.57) (all P < .05).

Discussion: Synthetic osmotic dilators are a safe, effective, and viable option for labor induction, reducing maternal risks of uterine hyperstimulation. These findings have implications for incorporating the clinical use of synthetic osmotic dilators for cervical ripening into international guidelines. As evidence supports their efficacy and safety, educating nurses and midwives in the use of synthetic osmotic dilators for labor induction is required.

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