Abstract

BackgroundWe aimed at developing a core outcome and variables of interest set to investigate the effects of mediolateral episiotomy on Obstetric Anal Sphincter Injury (OASI) during and after operative delivery in nulliparous women in a large-scale one-year observational French study including 15,000 women (INSTRUMODA).MethodsA list of outcomes and variables of interest was suggested to obstetricians participating in the INSTRUMODA study using online questionnaires divided into 7 categories: the woman’s history and course of pregnancy, course of labor, modalities of operative delivery, episiotomy characteristics, immediate maternal morbidity, one-year maternal morbidity, immediate neonatal morbidity. We used a three-round DELPHI method to reach a consensus. In the first round, outcomes and variables considered as essential by 70% or more of obstetricians were included in the corpus whereas they were excluded when 70% rated them as “not important”. In the second round, non-consensual outcomes and variables were reassessed and excluded or definitively included if considered as “not important” or essential by 50% or more of the obstetricians. During the first round, obstetricians were invited to suggest new outcomes and/or variables that were then assessed in the second and third round. We used the same method to develop a core outcome and variables of interest set in a population of women in the community recruited via an association of patients. At the end of the procedure the core outcome and variables of interest sets were merged to provide the final core outcome set for the INSTRUMODA study.ResultsFifty-three obstetricians and 16 women filled out questionnaires. After the 3 rounds of Delphi procedure in each population, 74 outcomes and variables were consensually reported by obstetricians and 92 by women in the community. By mixing these two consensual corpora we reported a final consensual list of 114 variables of interest and outcomes for both obstetricians and women.ConclusionWe established a core outcome and variables of interest set among obstetricians and women in the community to investigate the association between mediolateral episiotomy and OASI during operative delivery.Trial registrationThe INSTRUMODA study was registered on https://clinicaltrials.gov on June 25, 2020 (NCT04446780).

Highlights

  • We aimed at developing a core outcome and variables of interest set to investigate the effects of mediolateral episiotomy on Obstetric Anal Sphincter Injury (OASI) during and after operative delivery in nulliparous women in a large-scale one-year observational French study including 15,000 women (INSTRUMODA)

  • We established a core outcome and variables of interest set among obstetricians and women in the community to investigate the association between mediolateral episiotomy and OASI during operative delivery

  • Development of a core outcome and variable of interest set in the population of obstetricians At the time of organization of the core outcome and variables of interest set process, we planned to recruit 109 centers and an invitation to participate was sent to the main investigator of each center

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Summary

Introduction

We aimed at developing a core outcome and variables of interest set to investigate the effects of mediolateral episiotomy on Obstetric Anal Sphincter Injury (OASI) during and after operative delivery in nulliparous women in a large-scale one-year observational French study including 15,000 women (INSTRUMODA). Obstetric anal sphincter injury (OASI) is a maternal delivery complication defined as a perineal tear involving at least a superficial tear of the external anal sphincter and, at worst, an opening of the rectal mucosae [1, 2] Such a perineal trauma is associated with significant alteration in women’s health: anal incontinence, perineal pain, dyspareunia, and postnatal depression [3]. While several retrospective studies have reported that mediolateral episiotomy has a protective effect against OASI, a small pilot randomized trial failed to identify a significant preventive effect [5,6,7,8, 10, 11]. There are no clear recommendations about its use during operative vaginal delivery [2, 12, 13]

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