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Methods of induction of labor in women with obesity: A secondary analysis of two multicenter randomized controlled trials

Croll, Dorothée M. R.; De Vaan, Marieke D. T.; Moes, Shinta L.; Bloemenkamp, Kitty W. M.; Ten Eikelder, Mieke L. G.; De Heus, Roel; Jozwiak, Marta; Kooiman, Judith; Mol, Ben Willem; Verhoeven, Corine J. M.; De Boer, Marjon A.

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Authors

Dorothée M. R. Croll

Marieke D. T. De Vaan

Shinta L. Moes

Kitty W. M. Bloemenkamp

Mieke L. G. Ten Eikelder

Roel De Heus

Marta Jozwiak

Judith Kooiman

Ben Willem Mol

Marjon A. De Boer



Abstract

Introduction: Obesity is an increasing public health concern worldwide and can lead to more complications in pregnancy and childbirth. Women with obesity more often require induction of labor for various indications. The aim of this study is to assess which method of induction of labor is safest and most effective in women with obesity.

Material and methods: This is a secondary analysis of two randomized controlled trials about induction of labor. Women with a term singleton pregnancy in cephalic presentation, an unfavorable cervix, intact membranes and without a previous cesarean section were randomly allocated to cervical priming with a Foley catheter or vaginal prostaglandin‐E2‐gel (PROBAAT‐I) or a Foley catheter or oral misoprostol (PROBAAT‐II). The inclusion and exclusion criteria for the studies were identical. Induction methods were compared in women with obesity (body mass index ≥30.0). Main outcomes were cesarean section and postpartum hemorrhage (blood loss >1000 mL).

Results: A total of 2664 women, were included in the trials, 517 of whom were obese: 254 women with obesity received a Foley catheter, 176 oral misoprostol and 87 prostaglandin E2 (PGE2). A cesarean section was performed in 29.1% of women allocated to Foley vs 22.2% in the misoprostol and 23.0% in the PGE2 groups. Comparisons between groups revealed no statistically significant differences: the relative risk [RR] was 1.31 (95% confidence interval [CI] 0.94–1.84) in the Foley vs misoprostol group and 1.27 (95% CI 0.83–1.95) in the Foley vs PGE2 group. The rates of postpartum hemorrhage were comparable (10.6%, 11.4% and 6.9%, respectively; P = 0.512). In women with obesity, more often a switch to another method occurred in the Foley group, (20.1% vs 6.3% in misoprostol vs 1.1% in the PGE2 group; P < 0.001). The risk of a failed Foley placement was higher in women with obesity than in women without obesity (8.3% vs 3.2%; adjusted odds ratio 3.12, 95% CI 1.65–5.90).

Conclusions: In women with obesity we found a nonsignificant trend towards an increased rate of cesarean sections in the group induced with a Foley catheter compared to oral misoprostol; however, the study lacked power for this subgroup analysis. The finding of a higher risk of failed placement of a Foley catheter in women with obesity can be used in shared decision making.

Journal Article Type Article
Acceptance Date Oct 2, 2023
Online Publication Date Jan 6, 2024
Publication Date 2024-03
Deposit Date Jun 7, 2024
Publicly Available Date Jun 12, 2024
Journal Acta Obstetricia et Gynecologica Scandinavica
Print ISSN 0001-6349
Electronic ISSN 1600-0412
Publisher Wiley
Peer Reviewed Peer Reviewed
Volume 103
Issue 3
Pages 470-478
DOI https://doi.org/10.1111/aogs.14737
Keywords labor, induced, obesity, PGE2 misoprostol, PGE1, prostaglandins, cervical ripening, Foley catheter
Public URL https://nottingham-repository.worktribe.com/output/29539903
Publisher URL https://obgyn.onlinelibrary.wiley.com/doi/10.1111/aogs.14737

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https://creativecommons.org/licenses/by-nc-nd/4.0/

Copyright Statement
This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.





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