A systematic scoping review of clinical indications for induction of labour.


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2020
Historique:
received: 05 06 2019
accepted: 10 01 2020
entrez: 30 1 2020
pubmed: 30 1 2020
medline: 22 4 2020
Statut: epublish

Résumé

The proportion of women undergoing induction of labour (IOL) has risen in recent decades, with significant variation within countries and between hospitals. The aim of this study was to review research supporting indications for IOL and determine which indications are supported by evidence and where knowledge gaps exist. A systematic scoping review of quantitative studies of common indications for IOL. For each indication, we included systematic reviews/meta-analyses, randomised controlled trials (RCTs), cohort studies and case control studies that compared maternal and neonatal outcomes for different modes or timing of birth. Studies were identified via the databases PubMed, Maternity and Infant Care, CINAHL, EMBASE, and ClinicalTrials.gov from between April 2008 and November 2019, and also from reference lists of included studies. We identified 2554 abstracts and reviewed 300 full text articles. The quality of included studies was assessed using the RoB 2.0, the ROBINS-I and the ROBIN tool. 68 studies were included which related to post-term pregnancy (15), hypertension/pre-eclampsia (15), diabetes (9), prelabour rupture of membranes (5), twin pregnancy (5), suspected fetal compromise (4), maternal elevated body mass index (BMI) (4), intrahepatic cholestasis of pregnancy (3), suspected macrosomia (3), fetal gastroschisis (2), maternal age (2), and maternal cardiac disease (1). Available evidence supports IOL for women with post-term pregnancy, although the evidence is weak regarding the timing (41 versus 42 weeks), and for women with hypertension/preeclampsia in terms of improved maternal outcomes. For women with preterm premature rupture of membranes (24-37 weeks), high-quality evidence supports expectant management rather than IOL/early birth. Evidence is weakly supportive for IOL in women with term rupture of membranes. For all other indications, there were conflicting findings and/or insufficient power to provide definitive evidence. While for some indications, IOL is clearly recommended, a number of common indications for IOL do not have strong supporting evidence. Overall, few RCTs have evaluated the various indications for IOL. For conditions where clinical equipoise regarding timing of birth may still exist, such as suspected macrosomia and elevated BMI, researchers and funding agencies should prioritise studies of sufficient power that can provide quality evidence to guide care in these situations.

Sections du résumé

BACKGROUND
The proportion of women undergoing induction of labour (IOL) has risen in recent decades, with significant variation within countries and between hospitals. The aim of this study was to review research supporting indications for IOL and determine which indications are supported by evidence and where knowledge gaps exist.
METHODS
A systematic scoping review of quantitative studies of common indications for IOL. For each indication, we included systematic reviews/meta-analyses, randomised controlled trials (RCTs), cohort studies and case control studies that compared maternal and neonatal outcomes for different modes or timing of birth. Studies were identified via the databases PubMed, Maternity and Infant Care, CINAHL, EMBASE, and ClinicalTrials.gov from between April 2008 and November 2019, and also from reference lists of included studies. We identified 2554 abstracts and reviewed 300 full text articles. The quality of included studies was assessed using the RoB 2.0, the ROBINS-I and the ROBIN tool.
RESULTS
68 studies were included which related to post-term pregnancy (15), hypertension/pre-eclampsia (15), diabetes (9), prelabour rupture of membranes (5), twin pregnancy (5), suspected fetal compromise (4), maternal elevated body mass index (BMI) (4), intrahepatic cholestasis of pregnancy (3), suspected macrosomia (3), fetal gastroschisis (2), maternal age (2), and maternal cardiac disease (1). Available evidence supports IOL for women with post-term pregnancy, although the evidence is weak regarding the timing (41 versus 42 weeks), and for women with hypertension/preeclampsia in terms of improved maternal outcomes. For women with preterm premature rupture of membranes (24-37 weeks), high-quality evidence supports expectant management rather than IOL/early birth. Evidence is weakly supportive for IOL in women with term rupture of membranes. For all other indications, there were conflicting findings and/or insufficient power to provide definitive evidence.
CONCLUSIONS
While for some indications, IOL is clearly recommended, a number of common indications for IOL do not have strong supporting evidence. Overall, few RCTs have evaluated the various indications for IOL. For conditions where clinical equipoise regarding timing of birth may still exist, such as suspected macrosomia and elevated BMI, researchers and funding agencies should prioritise studies of sufficient power that can provide quality evidence to guide care in these situations.

Identifiants

pubmed: 31995603
doi: 10.1371/journal.pone.0228196
pii: PONE-D-19-15778
pmc: PMC6988952
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't Systematic Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0228196

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist.

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Auteurs

Dominiek Coates (D)

Centre for Midwifery and Child and Family Health, Faculty of Health, University of Technology Sydney, Australia.

Angela Makris (A)

Department of Medicine, Western Sydney University, Sydney, Australia.
Women's Health Initiative Translational Unit (WHITU), Liverpool Hospital, Liverpool, Australia.

Christine Catling (C)

Centre for Midwifery and Child and Family Health, Faculty of Health, University of Technology Sydney, Australia.

Amanda Henry (A)

School of Women's and Children's Health, UNSW Medicine, University of New South Wales, Sydney, Australia.
Department of Women's and Children's Health, St George Hospital, Sydney, Australia.
The George Institute for Global Health, UNSW Medicine, Sydney, Australia.

Vanessa Scarf (V)

Centre for Midwifery and Child and Family Health, Faculty of Health, University of Technology Sydney, Australia.

Nicole Watts (N)

Centre for Midwifery and Child and Family Health, Faculty of Health, University of Technology Sydney, Australia.

Deborah Fox (D)

Centre for Midwifery and Child and Family Health, Faculty of Health, University of Technology Sydney, Australia.

Purshaiyna Thirukumar (P)

School of Women's and Children's Health, UNSW Medicine, University of New South Wales, Sydney, Australia.

Vincent Wong (V)

Liverpool Diabetes Collaborative Research Unit, Ingham Institute of Applied Research Science, University of New South Wales, Liverpool, Australia.

Hamish Russell (H)

South Western Sydney Local Health District, Sydney, Australia.

Caroline Homer (C)

Centre for Midwifery and Child and Family Health, Faculty of Health, University of Technology Sydney, Australia.
Maternal and Child Health Program, Burnet Institute, Victoria, Australia.

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