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Personalising Outcomes after Child Cardiac Arrest (POCCA): design and recruitment challenges of a multicentre, observational study

Authors :
Elizabeth Hunt
Neha Patel
Ericka L Fink
Robert S B Clark
Ashok Panigrahy
Rachel Berger
Jessica Wisnowski
Stefan Bluml
David Maloney
Pamela Rubin
Tamara Haller
Hulya Bayir
Sue R Beers
Patrick M Kochanek
Anthony Fabio
Patrick Kochanek
Robert Clark
Sue Beers
Tony Fabio
Karen Walson
Alexis Topjian
Christopher JL Newth
Jordan Duval-Arnould
Binod Balakrishnan
Michael T Meyer
Melissa G Chung
Anthony Willyerd
Lincoln Smith
Jesse Wenger
Stuart Friess
Jose Pineda
Ashley Siems
Jason Patregnani
John Diddle
Aline Maddux
Lesley Doughty
Juan Piantino
Beena Desai
Maureen G Richardson
Cynthia Bates
Darshana Parikh
Janice Prodell
Maddie Winters
Jeni Kwok
Adriana Cabrales
Ronke Adewale
Pam Melvin
Sadaf Shad
Katherine Siegel
Katherine Murkowski
Mary Kasch
Josey Hensley
Lisa Steele
Danielle Brown
Brian Burrows
Lauren Hlivka
Deana Rich
Amila Tutundzic
Tina Day
Lori Barganier
Ashley Wolfe
Mackenzie Little
Elyse Tomanio
Diane Hession
Yamila Sierra
Ruth Grosskreuz
BS Kevin Van
Rhonda Jones
Laura Benken
Beata Dyar
Laura Mishler
Jonathan Elmer
Subramanian Subramanian
Julia Wallace
Tami Robinson
Andrew Frank
Keri Feldman
Avinash Vemulapalli
Linda Ryan
Scott Szypulski
Christopher Keys
Source :
BMJ Open, BMJ Open, Vol 10, Iss 10 (2020)
Publication Year :
2020

Abstract

IntroductionBlood and imaging biomarkers show promise in prognosticating outcomes after paediatric cardiac arrest in pilot studies. We describe the methods and early recruitment challenges and solutions for an ongoing multicentre (n=14) observational trial, Personalising Outcomes following Child Cardiac Arrest to validate clinical, blood and imaging biomarkers individually and together in a clinically relevant panel.Methods and analysisChildren (n=164) between 48 hours and 17 years of age who receive chest compressions irrespective of provider, duration, or event location and are admitted to an intensive care unit are eligible. Blood samples will be taken on days 1–3 for the measurement of brain-focused biomarkers analysed to predict the outcome. Clinically indicated and timed brain MRI and spectroscopy biomarkers will be analysed to predict the outcome. The primary outcome for the trial is survival with favourable (Vineland Adaptive Behavioural Scale score >70) outcome at 1 year. Secondary outcomes include mortality and pre-event and postdischarge measures of emotional, cognitive, physical and family functioning and health-related quality of life. Early enrollment targets were not met due to prolonged regulatory and subcontract processes. Multiple, simultaneous interventions including modification to inclusion criteria, additional sites and site visits were implemented with successful improvement in recruitment. Study procedures including outcomes and biomarker analysis are ongoing.Ethics and disseminationTwelve of 14 sites will use the centralised Institutional Review Board (IRB) at the University of Pittsburgh (PRO14030712). Two sites will use individual IRBs: Children’s Healthcare of Atlanta Institutional Review Board and Children’s Hospital of Wisconsin IRB. Parents and/or guardians are consented and children assented (when possible) by the site Primary investigator (PI) or research coordinator for enrollment. Study findings will be disseminated through scientific conferences, peer-reviewed journal publications, public study website materials and invited lectures.Trial registration numberNCT02769026.

Details

ISSN :
20446055
Volume :
10
Issue :
10
Database :
OpenAIRE
Journal :
BMJ open
Accession number :
edsair.doi.dedup.....539b27f7c6857961fff124bcef384117