Vaginal dinoprostone vs Foley catheter for induction of labor at term with an unfavorable cervix: an open-label randomized controlled trial

IF 3.8 2区 医学 Q1 OBSTETRICS & GYNECOLOGY American Journal of Obstetrics & Gynecology Mfm Pub Date : 2024-09-01 DOI:10.1016/j.ajogmf.2024.101436
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Abstract

Background

Induction of labor (IOL) with mechanical methods or pharmacological agents is used in about 20% to 30% of all pregnant women. We specialized in comparing the effectiveness and safety of dinoprostone vs transcervical Foley catheter for IOL in term pregnant women with an unfavorable cervix with adequate samples.

Objective

To compare the effectiveness and safety of dinoprostone vs transcervical Foley catheter for IOL in term pregnant women with an unfavorable cervix.

Study Design

This is a parallel, open-label randomized controlled trial in two maternal centers in Shanghai, China between October 2019 and July 2022. Women with a singleton pregnancy in cephalic presentation at term and an unfavorable cervix (Bishop score <6) scheduled for IOL were eligible. A total of 1860 women were randomly allocated to cervical ripening with either a dinoprostone vaginal insert (10 mg) or a 60 cc Foley catheter for up to 24 hours. The primary outcomes were vaginal delivery rate and time to vaginal delivery. Secondary outcomes included time to delivery and maternal and neonatal morbidity. Analysis was done from an intention-to-treat perspective. The trial was registered with the China trial registry (CTR2000038435).

Results

The vaginal birth rates were 72.8% (677/930) vs 69.9% (650/930) in vaginal dinoprostone and Foley catheter, respectively (aRR 1.04, 95% confidence interval [CI] 0.98-1.10, risk difference: 0.03). Time to vaginal delivery was not significantly different between the two groups (sub-distribution hazard ratio 1.11, 95% CI 0.99-1.24). Vaginal dinoprostone was more likely complicated with hyperstimulation with fetal heart rate changes (5.8% vs 2.8%, aRR 2.09, 95% CI 1.32-3.31) and placenta abruption (0.9% vs 0.1%, aRR: 8.04, 95% CI 1.01-64.15), while Foley catheter was more likely complicated with suspected intrapartum infection (5.1% vs 8.2%, aRR: 0.62, 95% CI 0.44-0.88) and postpartum infection (1.4% vs 3.7%, aRR: 0.38, 95% CI 0.20-0.72). The composite of poor neonatal outcomes was not significantly different between the two groups (4.5% vs 3.8%, aRR 1.21, 95% CI 0.78-1.88), while more neonatal asphyxia occurred in the dinoprostone group (1.2% vs 0.2%, aRR 5.39, 95% CI 1.22-23.92). In a subgroup analysis, vaginal dinoprostone decreased vaginal birth rate slightly in multiparous women (90.6% vs 97.0%, aRR 0.93, 95% CI 0.88-0.99).

Conclusions

In term pregnant women with an unfavorable cervix, IOL with vaginal dinoprostone or Foley catheter has similar effectiveness. Foley catheter leads to better safety for neonates, while it may result in a higher risk of maternal infection. Furthermore, Foley catheter should be preferred in multiparous women.

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阴道地诺前列酮与 Foley 导管用于宫颈不利的足月引产:开放标签随机对照试验。
背景:约有20%-30%的孕妇使用机械方法或药物引产。我们专门比较了地诺前列酮与经宫颈福来导管对宫颈不佳且样本充足的足月孕妇引产的有效性和安全性:比较地诺前列酮与经宫颈福来导管用于宫颈不利的足月孕妇引产的有效性和安全性:这是一项平行、开放标签的随机对照试验,于2019年10月至2022年7月期间在中国上海的两家妇产中心进行。研究对象为足月头位单胎妊娠且宫颈不良(Bishop评分小于6分)、计划引产的女性。1,860名妇女被随机分配到使用地诺前列酮阴道插入物(10毫克)或60cc Foley导尿管进行宫颈成熟,最长24小时。主要结果是阴道分娩率和阴道分娩时间。次要结果包括分娩时间、产妇和新生儿发病率。分析从意向治疗的角度进行。该试验已在中国试验注册中心注册(CTR2000038435):阴道分娩率分别为 72.8%(677/930)vs 69.9%(650/930)(aRR 1.04,95% CI 0.98 至 1.10,风险差异:0.03)。两组的阴道分娩时间无明显差异(亚分布危险比 1.11,95% CI 0.99-1.24)。阴道地诺前列酮更有可能并发胎心率改变的高刺激(5.8% vs. 2.8%,aRR 2.09,95% CI 1.32-3.31)和胎盘早剥(0.9% vs. 0.1%,aRR:8.04,95% CI 1.01-64.15),而 Foley 导管更有可能并发胎心率改变的高刺激。15),而 Foley 导管更可能并发疑似产内感染(5.1% 对 8.2%,aRR:0.62,95% CI 0.44-0.88)和产后感染(1.4% 对 3.7%,aRR:0.38,95% CI 0.20-0.72)。两组新生儿不良预后的综合结果无显著差异(4.5% 对 3.8%,aRR 1.21,95% CI 0.78 至 1.88),而地诺前列酮组新生儿窒息发生率更高(1.2% 对 0.2%,aRR 5.39,95% CI 1.22 至 23.92)。在一项亚组分析中,阴道地诺前列酮可使多产妇的阴道分娩率略有下降(90.6% 对 97.0%,aRR 0.93,95% CI 0.88 对 0.99):对于宫颈不佳的足月孕妇,使用阴道地诺前列酮或福来导管引产的效果相似。使用 Foley 导管对新生儿更安全,但可能会增加产妇感染的风险。此外,多产妇应首选 Foley 导管。
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来源期刊
CiteScore
7.40
自引率
3.20%
发文量
254
审稿时长
40 days
期刊介绍: The American Journal of Obstetrics and Gynecology (AJOG) is a highly esteemed publication with two companion titles. One of these is the American Journal of Obstetrics and Gynecology Maternal-Fetal Medicine (AJOG MFM), which is dedicated to the latest research in the field of maternal-fetal medicine, specifically concerning high-risk pregnancies. The journal encompasses a wide range of topics, including: Maternal Complications: It addresses significant studies that have the potential to change clinical practice regarding complications faced by pregnant women. Fetal Complications: The journal covers prenatal diagnosis, ultrasound, and genetic issues related to the fetus, providing insights into the management and care of fetal health. Prenatal Care: It discusses the best practices in prenatal care to ensure the health and well-being of both the mother and the unborn child. Intrapartum Care: It provides guidance on the care provided during the childbirth process, which is critical for the safety of both mother and baby. Postpartum Issues: The journal also tackles issues that arise after childbirth, focusing on the postpartum period and its implications for maternal health. AJOG MFM serves as a reliable forum for peer-reviewed research, with a preference for randomized trials and meta-analyses. The goal is to equip researchers and clinicians with the most current information and evidence-based strategies to effectively manage high-risk pregnancies and to provide the best possible care for mothers and their unborn children.
期刊最新文献
Activity restriction and risk of adverse pregnancy outcomes Oxytocin regimen used for induction of labor and pregnancy outcomes. Results of the RE-DINO multicenter randomized trial on the repeated use of vaginal dinoprostone (Propess®) for labor induction in patients at term. Corrigendum to ‘Prevention of preterm birth in twin pregnancies’ American Journal of Obstetrics & Gynecology MFM/ Volume 4 (2022) 100551 Validation of the PROMIS© Medication Adherence Scale for Pregnant Patients Taking Aspirin.
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