Foley Catheter for Induction of Labor at Term: An Open-Label, Randomized Controlled Trial.

This study aimed to determine the optimal Foley catheter balloon volume (30-mL vs. 80-mL) and the maximum time for cervical ripening (12 hours vs. 24 hours) to improve vaginal delivery rate within 24 hours of induction.We conducted an open-label, randomized controlled trial in a teaching hospital in...

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Main Authors: Ning Gu, Tong Ru, Zhiqun Wang, Yimin Dai, Mingming Zheng, Biyun Xu, Yali Hu
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2015-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC4556187?pdf=render
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spelling doaj-7bfba7f4240b4a6784d163e73636cf1a2020-11-25T00:57:16ZengPublic Library of Science (PLoS)PLoS ONE1932-62032015-01-01108e013685610.1371/journal.pone.0136856Foley Catheter for Induction of Labor at Term: An Open-Label, Randomized Controlled Trial.Ning GuTong RuZhiqun WangYimin DaiMingming ZhengBiyun XuYali HuThis study aimed to determine the optimal Foley catheter balloon volume (30-mL vs. 80-mL) and the maximum time for cervical ripening (12 hours vs. 24 hours) to improve vaginal delivery rate within 24 hours of induction.We conducted an open-label, randomized controlled trial in a teaching hospital in China. Women with a term singleton pregnancy, cephalic presentation, intact membrane and an unfavorable cervix (Bishop score <6) were randomly allocated, in 1:1:1:1 ratio, to receive either one of the four treatments: (1) 30-mL balloon for a maximum of 12 hours, (2) 30-mL balloon for a maximum of 24 hours, (3) 80-mL balloon for a maximum of 12 hours, and (4) 80-mL balloon for a maximum of 24 hours. The primary outcome was vaginal delivery within 24 hours. Secondary outcomes included cesarean section rate and maternal/neonatal morbidity. Data were analyzed on a per-protocol basis.Five hundred and four women were recruited and randomized (126 women in each group); nine women did not receive the assigned intervention. More women achieved vaginal delivery within 24 hours in 12-hour Foley catheter groups than in the 24-hour Foley catheter groups (30-mL/12 hours: 54.5%, 30-mL/24 hours: 33.1%, 80-mL/12 hours: 46.4%, 80-mL/24 hours: 24.0%, p < 0.001). Cesarean section rates and the incidence of chorioaminonitis were comparable among four groups. After adjustment for confounding factors, both ripening time and balloon size did not affect the proportion of women delivered vaginally within 24 hours of induction.For women with an unfavorable cervix at term, induction of labor with a Foley catheter is safe and effective. Higher balloon volume (80-mL vs. 30-mL) and longer ripening time (24 hours vs. 12 hours) would not shorten induction to delivery interval or reduce cesarean section rate.Chinese Clinical trial registry (ChiCTR-TRC-13003044).http://europepmc.org/articles/PMC4556187?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Ning Gu
Tong Ru
Zhiqun Wang
Yimin Dai
Mingming Zheng
Biyun Xu
Yali Hu
spellingShingle Ning Gu
Tong Ru
Zhiqun Wang
Yimin Dai
Mingming Zheng
Biyun Xu
Yali Hu
Foley Catheter for Induction of Labor at Term: An Open-Label, Randomized Controlled Trial.
PLoS ONE
author_facet Ning Gu
Tong Ru
Zhiqun Wang
Yimin Dai
Mingming Zheng
Biyun Xu
Yali Hu
author_sort Ning Gu
title Foley Catheter for Induction of Labor at Term: An Open-Label, Randomized Controlled Trial.
title_short Foley Catheter for Induction of Labor at Term: An Open-Label, Randomized Controlled Trial.
title_full Foley Catheter for Induction of Labor at Term: An Open-Label, Randomized Controlled Trial.
title_fullStr Foley Catheter for Induction of Labor at Term: An Open-Label, Randomized Controlled Trial.
title_full_unstemmed Foley Catheter for Induction of Labor at Term: An Open-Label, Randomized Controlled Trial.
title_sort foley catheter for induction of labor at term: an open-label, randomized controlled trial.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2015-01-01
description This study aimed to determine the optimal Foley catheter balloon volume (30-mL vs. 80-mL) and the maximum time for cervical ripening (12 hours vs. 24 hours) to improve vaginal delivery rate within 24 hours of induction.We conducted an open-label, randomized controlled trial in a teaching hospital in China. Women with a term singleton pregnancy, cephalic presentation, intact membrane and an unfavorable cervix (Bishop score <6) were randomly allocated, in 1:1:1:1 ratio, to receive either one of the four treatments: (1) 30-mL balloon for a maximum of 12 hours, (2) 30-mL balloon for a maximum of 24 hours, (3) 80-mL balloon for a maximum of 12 hours, and (4) 80-mL balloon for a maximum of 24 hours. The primary outcome was vaginal delivery within 24 hours. Secondary outcomes included cesarean section rate and maternal/neonatal morbidity. Data were analyzed on a per-protocol basis.Five hundred and four women were recruited and randomized (126 women in each group); nine women did not receive the assigned intervention. More women achieved vaginal delivery within 24 hours in 12-hour Foley catheter groups than in the 24-hour Foley catheter groups (30-mL/12 hours: 54.5%, 30-mL/24 hours: 33.1%, 80-mL/12 hours: 46.4%, 80-mL/24 hours: 24.0%, p < 0.001). Cesarean section rates and the incidence of chorioaminonitis were comparable among four groups. After adjustment for confounding factors, both ripening time and balloon size did not affect the proportion of women delivered vaginally within 24 hours of induction.For women with an unfavorable cervix at term, induction of labor with a Foley catheter is safe and effective. Higher balloon volume (80-mL vs. 30-mL) and longer ripening time (24 hours vs. 12 hours) would not shorten induction to delivery interval or reduce cesarean section rate.Chinese Clinical trial registry (ChiCTR-TRC-13003044).
url http://europepmc.org/articles/PMC4556187?pdf=render
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