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COHESION: a core outcome set for the treatment of neonatal encephalopathy

  • Fiona A. Quirke
  • , Shabina Ariff
  • , Malcolm R. Battin
  • , Caitlin Bernard
  • , Linda Biesty
  • , Frank H. Bloomfield
  • , Mandy Daly
  • , Elaine Finucane
  • , Patricia Healy
  • , David M. Haas
  • , Jamie J. Kirkham
  • , Vincent Kibet
  • , Sarah Koskei
  • , Shireen Meher
  • , Eleanor J. Molloy
  • , Maira Niaz
  • , Elaine Ní Bhraonáin
  • , Christabell Omukagah Okaronon
  • , Matthew J. Parkes
  • , Farhana Tabassum
  • Karen Walker, James W.H. Webbe, Declan Devane
  • Health Research Board
  • University of Galway
  • University of Limerick School of Medicine
  • Aga Khan University
  • Auckland District Health Board
  • Indiana University-Purdue University Indianapolis
  • Liggins Institute
  • Advocacy and Policymaking
  • University of Manchester
  • Moi University
  • Birmingham Women’s Hospital Healthcare NHS Trust
  • Trinity College Dublin
  • Our Ladies Hospital for Sick Children
  • Coombe Women and Infants University Hospital
  • Irish Neonatal Health Alliance
  • AMPATH
  • University of Oxford Medical Sciences Division
  • Royal Prince Alfred Hospital
  • Faculty of Medicine and Health
  • George Institute for Global Health
  • Council of International Neonatal Nurses
  • Imperial College London

Research output: Contribution to a Journal (Peer & Non Peer)Articlepeer-review

13 Citations (Scopus)

Abstract

Background: Heterogeneity in outcomes reported in trials of interventions for the treatment of neonatal encephalopathy (NE) makes evaluating the effectiveness of treatments difficult. Developing a core outcome set for NE treatment would enable researchers to measure and report the same outcomes in future trials. This would minimise waste, ensure relevant outcomes are measured and enable evidence synthesis. Therefore, we aimed to develop a core outcome set for treating NE. Methods: Outcomes identified from a systematic review of the literature and interviews with parents were prioritised by stakeholders (n = 99 parents/caregivers, n = 101 healthcare providers, and n = 22 researchers/ academics) in online Delphi surveys. Agreement on the outcomes was achieved at online consensus meetings attended by n = 10 parents, n = 18 healthcare providers, and n = 13 researchers/ academics. Results: Seven outcomes were included in the final core outcome set: survival; brain injury on imaging; neurological status at discharge; cerebral palsy; general cognitive ability; quality of life of the child, and adverse events related to treatment. Conclusion: We developed a core outcome set for the treatment of NE. This will allow future trials to measure and report the same outcomes and ensure results can be compared. Future work should identify how best to measure the COS. Impact: We have identified seven outcomes that should be measured and reported in all studies for the treatment of neonatal encephalopathy. Previously, a core outcome set for neonatal encephalopathy treatments did not exist. This will help to reduce heterogeneity in outcomes reported in clinical trials and other studies, and help researchers identify the best treatments for neonatal encephalopathy.

Original languageEnglish
Pages (from-to)922-930
Number of pages9
JournalPediatric Research
Volume95
Issue number4
DOIs
Publication statusPublished - Mar 2024

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 12 - Responsible Consumption and Production
    SDG 12 Responsible Consumption and Production

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