Vaginal misoprostol versus vaginal dinoprostone for cervical ripening and induction of labour: An individual participant data meta-analysis of randomised controlled trials.

IPD dinoprostone individual participant data induction of labour meta-analysis misoprostol prostaglandin randomised trials

Journal

BJOG : an international journal of obstetrics and gynaecology
ISSN: 1471-0528
Titre abrégé: BJOG
Pays: England
ID NLM: 100935741

Informations de publication

Date de publication:
29 Feb 2024
Historique:
revised: 08 02 2024
received: 28 12 2023
accepted: 09 02 2024
medline: 1 3 2024
pubmed: 1 3 2024
entrez: 1 3 2024
Statut: aheadofprint

Résumé

Induction of labour (IOL) is common practice and different methods carry different effectiveness and safety profiles. To compare the effectiveness, and maternal and perinatal safety outcomes of IOL with vaginal misoprostol versus vaginal dinoprostone using individual participant data from randomised clinical trials. The following databases were searched from inception to March 2023: CINAHL Plus, ClinicalTrials.gov, Cochrane Pregnancy and Childbirth Group Trial Register, Ovid Embase, Ovid Emcare, Ovid MEDLINE, Scopus and the World Health Organization (WHO) International Clinical Trials Registry Platform (ICTRP). Randomised controlled trials (RCTs), with viable singleton gestation, no language restrictions, and all published and unpublished data. An individual participant data meta-analysis was carried out. Ten of 52 eligible trials provided individual participant data, of which two were excluded after checking data integrity. The remaining eight trials compared low-dose vaginal misoprostol versus dinoprostone, including 4180 women undergoing IOL, which represents 32.8% of all participants in the published RCTs. Of these, 2077 were assigned to low-dose vaginal misoprostol and 2103 were assigned to vaginal dinoprostone. Compared with vaginal dinoprostone, low-dose vaginal misoprostol had a comparable rate of vaginal birth. Composite adverse perinatal outcomes did not differ between the groups. Compared with vaginal dinoprostone, composite adverse maternal outcomes were significantly lower with low-dose vaginal misoprostol (aOR 0.80, 95% CI 0.65-0.98, P = 0.03, I Low-dose vaginal misoprostol and vaginal dinoprostone for IOL are comparable in terms of effectiveness and perinatal safety. However, low-dose vaginal misoprostol is likely to lead to a lower rate of composite adverse maternal outcomes than vaginal dinoprostone.

Sections du résumé

BACKGROUND BACKGROUND
Induction of labour (IOL) is common practice and different methods carry different effectiveness and safety profiles.
OBJECTIVES OBJECTIVE
To compare the effectiveness, and maternal and perinatal safety outcomes of IOL with vaginal misoprostol versus vaginal dinoprostone using individual participant data from randomised clinical trials.
SEARCH STRATEGY METHODS
The following databases were searched from inception to March 2023: CINAHL Plus, ClinicalTrials.gov, Cochrane Pregnancy and Childbirth Group Trial Register, Ovid Embase, Ovid Emcare, Ovid MEDLINE, Scopus and the World Health Organization (WHO) International Clinical Trials Registry Platform (ICTRP).
SELECTION CRITERIA METHODS
Randomised controlled trials (RCTs), with viable singleton gestation, no language restrictions, and all published and unpublished data.
DATA COLLECTION AND ANALYSIS METHODS
An individual participant data meta-analysis was carried out.
MAIN RESULTS RESULTS
Ten of 52 eligible trials provided individual participant data, of which two were excluded after checking data integrity. The remaining eight trials compared low-dose vaginal misoprostol versus dinoprostone, including 4180 women undergoing IOL, which represents 32.8% of all participants in the published RCTs. Of these, 2077 were assigned to low-dose vaginal misoprostol and 2103 were assigned to vaginal dinoprostone. Compared with vaginal dinoprostone, low-dose vaginal misoprostol had a comparable rate of vaginal birth. Composite adverse perinatal outcomes did not differ between the groups. Compared with vaginal dinoprostone, composite adverse maternal outcomes were significantly lower with low-dose vaginal misoprostol (aOR 0.80, 95% CI 0.65-0.98, P = 0.03, I
CONCLUSIONS CONCLUSIONS
Low-dose vaginal misoprostol and vaginal dinoprostone for IOL are comparable in terms of effectiveness and perinatal safety. However, low-dose vaginal misoprostol is likely to lead to a lower rate of composite adverse maternal outcomes than vaginal dinoprostone.

Identifiants

pubmed: 38425020
doi: 10.1111/1471-0528.17794
doi:

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : National Health and Medical Research Council, Australian Government
ID : GNT1176437
Organisme : National Health and Medical Research Council, Australian Government
ID : GNT2016729

Informations de copyright

© 2024 The Authors. BJOG: An International Journal of Obstetrics and Gynaecology published by John Wiley & Sons Ltd.

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Auteurs

Malitha Patabendige (M)

Department of Obstetrics and Gynaecology, Monash Medical Centre, Monash University, Clayton, Victoria, Australia.
Ministry of Health, Colombo, Sri Lanka.
Monash Health - Casey Hospital, Berwick, Victoria, Australia.

Fei Chan (F)

Department of Obstetrics and Gynaecology, Monash Medical Centre, Monash University, Clayton, Victoria, Australia.

Christophe Vayssiere (C)

Centre for Epidemiology and Research in Population Health (CERPOP), UMR1295, Toulouse University, Inserm, Paul Sabatier University, Toulouse, France.
Department of Obstetrics and Gynaecology, Paule de Viguier Hospital, Toulouse University Hospital, Toulouse, France.

Virginie Ehlinger (V)

Centre for Epidemiology and Research in Population Health (CERPOP), UMR1295, Toulouse University, Inserm, Paul Sabatier University, Toulouse, France.

Nicolette Van Gemund (N)

Department of Obstetrics and Gynaecology, Franciscus Gasthuis, Rotterdam, the Netherlands.

Saskia le Cessie (S)

Department of Biomedical Data Sciences, Leiden University Medical Centre, Leiden, the Netherlands.

Martina Prager (M)

Division of Obstetrics and Gynaecology, Department of Women's and Children's Health, Karolinska University Hospital, Karolinska Institutet, Stockholm, Sweden.

Lena Marions (L)

Division of Obstetrics and Gynaecology, Department of Women's and Children's Health, Karolinska University Hospital, Karolinska Institutet, Stockholm, Sweden.

Patrick Rozenberg (P)

Department of Gynaecology and Obstetrics, Poissy Hospital, University Paris V, Paris, France.

Sylvie Chevret (S)

Department of Biostatistics, Hopital Saint-Louis, University Paris VII, INSERM, Paris, France.

David C Young (DC)

Department of Obstetrics and Gynaecology, Dalhousie University, Halifax, Nova Scotia, Canada.
IWK Health Centre, Halifax, Nova Scotia, Canada.

Paul A Le Roux (PA)

Department of Obstetrics and Gynaecology, University of Cape Town, Cape Town, South Africa.

Sarah Gregson (S)

Maternity Unit, Queen Mary's Sidcup NHS Trust, Kent, UK.

Mark Waterstone (M)

Maternity Unit, Queen Mary's Sidcup NHS Trust, Kent, UK.

Daniel L Rolnik (DL)

Department of Obstetrics and Gynaecology, Monash Medical Centre, Monash University, Clayton, Victoria, Australia.

Ben W Mol (BW)

Department of Obstetrics and Gynaecology, Monash Medical Centre, Monash University, Clayton, Victoria, Australia.

Wentao Li (W)

Department of Obstetrics and Gynaecology, Monash Medical Centre, Monash University, Clayton, Victoria, Australia.
National Perinatal Epidemiology and Statistics Unit (NPESU), Centre for Big Data Research in Health, and School of Clinical Medicine, Faculty of Medicine, University of New South Wales, Sydney, Australia.

Classifications MeSH