Lateral episiotomy versus no episiotomy to reduce obstetric anal sphincter injury in vacuum-assisted delivery in nulliparous women: study protocol on a randomised controlled trial.


Journal

BMJ open
ISSN: 2044-6055
Titre abrégé: BMJ Open
Pays: England
ID NLM: 101552874

Informations de publication

Date de publication:
13 03 2019
Historique:
entrez: 16 3 2019
pubmed: 16 3 2019
medline: 24 3 2020
Statut: epublish

Résumé

Obstetric anal sphincter injury (OASIS) occurs in 5%-7% of normal deliveries and increases with vacuum extraction (VE) to 12%-14% in nulliparous women in Sweden. Lateral/mediolateral episiotomy may reduce the prevalence of OASIS at VE in nulliparous women. The current use of episiotomy is restrictive. The protective effect and consequences are uncertain. This trial will investigate if lateral episiotomy can reduce the prevalence of OASIS and assess short-term and long-term effects. This is a multicentre randomised controlled trial of lateral episiotomy versus no episiotomy in nulliparous women with a singleton, live fetus, after gestational week 34+0 with indication for VE. A lateral episiotomy of 4 cm is cut at crowning, 1-3 cm from the midline, at a 60° angle. The primary outcome is OASIS by clinical diagnosis analysed according to intention to treat. To demonstrate a 50% reduction in OASIS prevalence (from 12.4% to 6.2%), 710 women will be randomised at a 1:1 ratio. Secondary outcomes are pain, blood loss, other perineal injuries, perineal complications, Apgar score, cord pH and neonatal complications. Web-based questionnaires at baseline, 2 months, 1 and 5 years will be used to assess pain, incontinence, prolapse, sexual function, quality of life and childbirth experience. A subset of women will receive follow-up by pelvic floor sonography and pelvic examination. Mode of delivery and recurrence of OASIS/episiotomy in subsequent pregnancies will be assessed at 5 and 10 years using register data. The trial is open for enrolment. The trial has received ethical approval from the Regional Ethical Review Board of Stockholm and full funding from the Swedish Research Council. Women are interested in participation. The predominant restrictive view on episiotomy may limit recruitment. Results are of global interest and will be disseminated in peer-reviewed journals and at international congresses. NCT02643108; Pre-results.

Identifiants

pubmed: 30872546
pii: bmjopen-2018-025050
doi: 10.1136/bmjopen-2018-025050
pmc: PMC6429882
doi:

Banques de données

ClinicalTrials.gov
['NCT02643108']

Types de publication

Clinical Trial Protocol Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e025050

Informations de copyright

© Author(s) (or their employer(s)) 2019. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: None declared.

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Auteurs

Sandra Bergendahl (S)

Department of Clinical Sciences, Karolinska Institutet, Stockholm, Sweden.

Victoria Ankarcrona (V)

Department of Clinical Sciences, Karolinska Institutet, Stockholm, Sweden.

Åsa Leijonhufvud (Å)

Department of Clinical Sciences Lund/Clinical Science Helsingborg, Lunds Universitet, Lund, Sweden.

Susanne Hesselman (S)

Department of Women's and Children's Health, Centre for Clinical Research Dalarna, Falu Hospital, Uppsala Universitet, Uppsala, Sweden.

Sofie Karlström (S)

Department of Clinical Science, Intervention and Technology, Karolinska Institutet, Stockholm, Sweden.

Helena Kopp Kallner (H)

Department of Women's and Children's Health, Karolinska Institutet, Stockholm, Sweden.

Sophia Brismar Wendel (S)

Department of Clinical Sciences, Karolinska Institutet, Stockholm, Sweden.

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