Six vs 12 hours of Foley catheter balloon placement in the labor induction of multiparas with unfavorable cervixes: a randomized controlled trial

医学 引产 导尿管 气球 福利 随机对照试验 子宫颈 怀孕 毕肖普分数 妊娠期 胎龄 正式舞会 产科 阴道分娩 导管 外科 内科学 癌症 催产素 生物 遗传学
作者
Nadiah Kamarudzman,Siti Zawiah Omar,Farah GAN,Jesrine Hong,Mukhri Hamdan,Peng Chiong Tan
出处
期刊:American Journal Of Obstetrics & Gynecology Mfm [Elsevier]
卷期号:5 (11): 101142-101142
标识
DOI:10.1016/j.ajogmf.2023.101142
摘要

Planned 6- vs 12-hour placement of the double-balloon catheter for cervical ripening in labor induction hastens delivery. The Foley catheter is low-priced and typically performs at least as well as the proprietary double-balloon devices in labor induction. Maternal satisfaction with labor induction is usually inversely related to the speed of the process.This study aimed to compare Foley balloon placement for 6 vs 12 hours in the labor induction of multiparas with unfavorable cervixes.A randomized controlled trial was conducted in a university hospital in Malaysia from January to October of 2022. Eligible multiparous women admitted for induction of labor for various indications were enrolled. Participant inclusion criteria were multiparity (at least 1 previous vaginal delivery of ≥24 weeks' gestation), age ≥18 years, term pregnancy >37 weeks' gestation, singleton pregnancy, cephalic presentation, intact membranes, normal fetal heart rate tracing, no significant contractions (< 2 in 10 minutes), and unfavorable cervix (Bishop score < 6). Participants were randomized after successful Foley balloon insertion for the balloon to be left in place for 6 or 12 hours of passive ripening before removal to check cervical suitability for amniotomy. The primary outcomes were the induction-to-delivery interval and maternal satisfaction with the allocated intervention assessed using a visual numerical rating scale (0-10). Secondary outcomes were derived in part from the core outcome set for trials on induction of labor (Core Outcomes in Women's and Newborn Health [CROWN]). Maternal outcomes were change in first Bishop score after intervention, use of additional method for cervical ripening, time to delivery after balloon removal, mode of delivery, indication for cesarean delivery, duration of oxytocin infusion, blood loss during delivery, presence of third- or fourth-degree perineal tear, maternal infection, use of regional analgesia in labor, length of hospital stay, intensive care unit (ICU) admission, cardiorespiratory arrest, and need for hysterectomy. The secondary neonatal outcomes were Apgar score at 1 and 5 minutes, neonatal intensive care unit (NICU) admission, cord blood pH, neonatal sepsis, birthweight, birth trauma, hypoxic-ischemic encephalopathy, or need for therapeutic hypothermia. Analyses were conducted with the t-test, Mann-Whitney U test, chi-square test, and Fisher exact test, as appropriate.A total of 220 women were randomized (110 to each intervention). Regarding the 2 primary outcomes, the induction-to-delivery intervals were a median (interquartile range) of 15.9 (12.0-24.0) and 21.6 (17.3-26.0) hours (P<.001), and maternal satisfaction scores were 7 (6-8) and 7 (6-8) (P=.734) for 6- and 12-hour placement, respectively. The following rates were observed for 6- and 12-hour placement, respectively: sequential use of additional cervical ripening agent (Foley reinsertion)-29 per 110 (26.4%) and 13 per 110 (11.8%) (relative risk, 2.23; 95% confidence interval, 1.23-4.10; P=.006); spontaneous balloon expulsion-22 per 110 (20.0%) and 37 per 110 (33.6%) (relative risk, 0.60; 95% confidence interval, 0.38-0.94; P=.022); and recommendation of the allocated intervention to a friend-61 per 110 (73.6%) and 87 per 110 (79.1%) (relative risk, 0.90; 95% confidence interval, 0.80-1.08; P=.341). Other secondary outcomes, including cesarean delivery, were not significantly different.Foley balloon placement for 6 hours for cervical ripening in parous women hastens birth but does not increase maternal satisfaction relative to 12-hour placement. Foley reinsertion for additional ripening was more frequent in the 6-hour group.

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
寒江月发布了新的文献求助10
1秒前
1秒前
动听剑心发布了新的文献求助10
1秒前
2秒前
爱炸鸡也爱烧烤完成签到 ,获得积分10
2秒前
高高发布了新的文献求助10
2秒前
Orange应助迪克大采纳,获得10
5秒前
5秒前
老福贵儿应助枫竹采纳,获得10
5秒前
梦里的大子刊完成签到 ,获得积分10
5秒前
5秒前
毛豆爸爸发布了新的文献求助10
6秒前
6秒前
CipherSage应助无奈的炳采纳,获得10
6秒前
7秒前
科研通AI6.2应助nini采纳,获得10
7秒前
7秒前
Rainbow完成签到,获得积分10
8秒前
呆萌初南发布了新的文献求助10
8秒前
大力的灵雁应助victor采纳,获得10
8秒前
于归完成签到 ,获得积分10
9秒前
缓慢海亦完成签到,获得积分10
10秒前
Singularity应助升级小水桶采纳,获得10
10秒前
12秒前
12秒前
12秒前
JamRoss完成签到,获得积分20
12秒前
13秒前
pluto应助柯不正采纳,获得10
13秒前
13秒前
14秒前
14秒前
啊啊啊啊啊完成签到 ,获得积分10
14秒前
热情怡发布了新的文献求助10
15秒前
15秒前
笑哈哈发布了新的文献求助10
16秒前
ohu完成签到 ,获得积分10
16秒前
铃溪完成签到,获得积分10
16秒前
CipherSage应助愉快的宛海采纳,获得10
16秒前
爆米花应助qitengzhu采纳,获得10
17秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Handbook of pharmaceutical excipients, Ninth edition 5000
Aerospace Standards Index - 2026 ASIN2026 3000
Digital Twins of Advanced Materials Processing 2000
Polymorphism and polytypism in crystals 1000
Signals, Systems, and Signal Processing 610
Discrete-Time Signals and Systems 610
热门求助领域 (近24小时)
化学 材料科学 医学 生物 工程类 纳米技术 有机化学 物理 生物化学 化学工程 计算机科学 复合材料 内科学 催化作用 光电子学 物理化学 电极 冶金 遗传学 细胞生物学
热门帖子
关注 科研通微信公众号,转发送积分 6039756
求助须知:如何正确求助?哪些是违规求助? 7771167
关于积分的说明 16227940
捐赠科研通 5185772
什么是DOI,文献DOI怎么找? 2775087
邀请新用户注册赠送积分活动 1757977
关于科研通互助平台的介绍 1641955