Study protocol: a core outcome set for perinatal interventions for congenital diaphragmatic hernia

Abstract Background Congenital diaphragmatic hernia (CDH) is, depending of the severity, a birth defect associated with significant mortality and morbidity. Prenatal screening by ultrasound may detect this condition and comprehensive assessment of severity is possible, allowing for in utero referral...

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Main Authors: Simen Vergote, Felix De Bie, Jan Bosteels, Holly Hedrick, James Duffy, Beverley Power, Alexandra Benachi, Paolo De Coppi, Caraciolo Fernandes, Kevin Lally, Irwin Reiss, Jan Deprest
Format: Article
Language:English
Published: BMC 2021-02-01
Series:Trials
Subjects:
Online Access:https://doi.org/10.1186/s13063-021-05120-z
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spelling doaj-43261585d01e45b3adf5a5be06487c972021-02-23T14:57:33ZengBMCTrials1745-62152021-02-012211710.1186/s13063-021-05120-zStudy protocol: a core outcome set for perinatal interventions for congenital diaphragmatic herniaSimen Vergote0Felix De Bie1Jan Bosteels2Holly Hedrick3James Duffy4Beverley Power5Alexandra Benachi6Paolo De Coppi7Caraciolo Fernandes8Kevin Lally9Irwin Reiss10Jan Deprest11Department of Development and Regeneration cluster Woman and Child, Biomedical Sciences, KU LeuvenDepartment of Development and Regeneration cluster Woman and Child, Biomedical Sciences, KU LeuvenDepartment of Development and Regeneration cluster Woman and Child, Biomedical Sciences, KU LeuvenDepartment of Surgery, Children’s Hospital of PhiladelphiaInstitute of Women’s Health, University College of LondonCDH UK, The DenesService de Gynécologie-Obstétrique, Hôpital Antoine Béclère, AP-HPDepartment of Specialist Neonatal and Pediatric Surgery, Great Ormond Street Hospital for ChildrenTexas Children’s Fetal Center, Texas Children’s Hospital and Department of Pediatrics - Newborn Section, Baylor College of MedicineDepartment of Pediatric Surgery, McGovern Medical School at UT Health and Children’s Memorial Hermann HospitalDepartment of Pediatrics, Division of Neonatology, Erasmus MC, University Medical Center RotterdamDepartment of Development and Regeneration cluster Woman and Child, Biomedical Sciences, KU LeuvenAbstract Background Congenital diaphragmatic hernia (CDH) is, depending of the severity, a birth defect associated with significant mortality and morbidity. Prenatal screening by ultrasound may detect this condition and comprehensive assessment of severity is possible, allowing for in utero referral to an experienced centre for planned delivery. In an effort to improve outcomes, prenatal interventions to stimulate lung development were proposed. Along the same lines, new postnatal management strategies are being developed. In order to enable proper comparison of novel perinatal interventions as well as outcomes, a set of uniform and relevant outcome measures is required. Core outcome sets (COS) are agreed, clearly defined sets of outcomes to be measured in a standardised manner and reported consistently. Herein we aim to describe the methodology we will use to define a COS for perinatal and neonatal outcomes of foetuses and newborns with congenital diaphragmatic hernia and to draft a dissemination and implementation plan. Methods We will use the methodology described in the Core Outcome Measures in Effectiveness Trials (COMET) Initiative Handbook. An international steering group will be created to guide the development of the COS. We are systematically reviewing the literature to identify all potential relevant pre- and neonatal outcomes previously used in studies on perinatal interventions for CDH. We will build a consensus on these core outcomes in a stakeholder group using the Delphi method. After completion, a stakeholder meeting will decide on a final COS, using a modified Nominal Group Technique. Thereafter, we will review potential definitions and measurements of these outcomes, and again a consensus meeting will be organised, to finalise the COS before dissemination. Discussion We have started a procedure to develop a COS for studies on perinatal interventions for congenital diaphragmatic hernia, with the purpose of improving the quality of research, guide clinical practice and improve patient care and eventual use in future clinical trials, systematic reviews and clinical practice guidelines. Trial registration We prospectively registered this study in the International Prospective Register of Systematic Reviews (PROSPERO) (registration number: CRD42019124399 ) and The Core Outcome Measures in Effectiveness Trials (COMET) Initiative (registration number: 1296 ).https://doi.org/10.1186/s13063-021-05120-zCongenital diaphragmatic herniaPerinatal interventionCore outcome setDelphi method
collection DOAJ
language English
format Article
sources DOAJ
author Simen Vergote
Felix De Bie
Jan Bosteels
Holly Hedrick
James Duffy
Beverley Power
Alexandra Benachi
Paolo De Coppi
Caraciolo Fernandes
Kevin Lally
Irwin Reiss
Jan Deprest
spellingShingle Simen Vergote
Felix De Bie
Jan Bosteels
Holly Hedrick
James Duffy
Beverley Power
Alexandra Benachi
Paolo De Coppi
Caraciolo Fernandes
Kevin Lally
Irwin Reiss
Jan Deprest
Study protocol: a core outcome set for perinatal interventions for congenital diaphragmatic hernia
Trials
Congenital diaphragmatic hernia
Perinatal intervention
Core outcome set
Delphi method
author_facet Simen Vergote
Felix De Bie
Jan Bosteels
Holly Hedrick
James Duffy
Beverley Power
Alexandra Benachi
Paolo De Coppi
Caraciolo Fernandes
Kevin Lally
Irwin Reiss
Jan Deprest
author_sort Simen Vergote
title Study protocol: a core outcome set for perinatal interventions for congenital diaphragmatic hernia
title_short Study protocol: a core outcome set for perinatal interventions for congenital diaphragmatic hernia
title_full Study protocol: a core outcome set for perinatal interventions for congenital diaphragmatic hernia
title_fullStr Study protocol: a core outcome set for perinatal interventions for congenital diaphragmatic hernia
title_full_unstemmed Study protocol: a core outcome set for perinatal interventions for congenital diaphragmatic hernia
title_sort study protocol: a core outcome set for perinatal interventions for congenital diaphragmatic hernia
publisher BMC
series Trials
issn 1745-6215
publishDate 2021-02-01
description Abstract Background Congenital diaphragmatic hernia (CDH) is, depending of the severity, a birth defect associated with significant mortality and morbidity. Prenatal screening by ultrasound may detect this condition and comprehensive assessment of severity is possible, allowing for in utero referral to an experienced centre for planned delivery. In an effort to improve outcomes, prenatal interventions to stimulate lung development were proposed. Along the same lines, new postnatal management strategies are being developed. In order to enable proper comparison of novel perinatal interventions as well as outcomes, a set of uniform and relevant outcome measures is required. Core outcome sets (COS) are agreed, clearly defined sets of outcomes to be measured in a standardised manner and reported consistently. Herein we aim to describe the methodology we will use to define a COS for perinatal and neonatal outcomes of foetuses and newborns with congenital diaphragmatic hernia and to draft a dissemination and implementation plan. Methods We will use the methodology described in the Core Outcome Measures in Effectiveness Trials (COMET) Initiative Handbook. An international steering group will be created to guide the development of the COS. We are systematically reviewing the literature to identify all potential relevant pre- and neonatal outcomes previously used in studies on perinatal interventions for CDH. We will build a consensus on these core outcomes in a stakeholder group using the Delphi method. After completion, a stakeholder meeting will decide on a final COS, using a modified Nominal Group Technique. Thereafter, we will review potential definitions and measurements of these outcomes, and again a consensus meeting will be organised, to finalise the COS before dissemination. Discussion We have started a procedure to develop a COS for studies on perinatal interventions for congenital diaphragmatic hernia, with the purpose of improving the quality of research, guide clinical practice and improve patient care and eventual use in future clinical trials, systematic reviews and clinical practice guidelines. Trial registration We prospectively registered this study in the International Prospective Register of Systematic Reviews (PROSPERO) (registration number: CRD42019124399 ) and The Core Outcome Measures in Effectiveness Trials (COMET) Initiative (registration number: 1296 ).
topic Congenital diaphragmatic hernia
Perinatal intervention
Core outcome set
Delphi method
url https://doi.org/10.1186/s13063-021-05120-z
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