Implementing Rapid Whole-Genome Sequencing in Critical Care: A Qualitative Study of Facilitators and Barriers to New Technology Adoption
- PMID: 34023348
- DOI: 10.1016/j.jpeds.2021.05.045
Implementing Rapid Whole-Genome Sequencing in Critical Care: A Qualitative Study of Facilitators and Barriers to New Technology Adoption
Abstract
Objective: To characterize the views of members of the multi-disciplinary team regarding the implementation of rapid whole-genome sequencing (rWGS) as a first-tier test for critically ill children in diverse children's hospital settings.
Study design: Qualitative interviews informed by implementation science theory were conducted with the multidisciplinary patient care teams and hospital leaders at each of the 5 tertiary care children's hospitals involved in a statewide rWGS implementation project.
Results: Our analysis revealed 5 key themes regarding the implementation process across the sites: the need for rWGS champions, educational needs and strategies, negotiating decision-making roles and processes, workflows and workarounds, and perceptions about rWGS. From the findings a composite clinical workflow diagram was developed to summarize all of the processes involved in the implementation of the test, and the key areas where implementation practices differed.
Conclusions: These findings provide insights for design of interventions to support adoption, scale-up, and sustainability of rWGS and other novel technologies in neonatal and pediatric critical care settings.
Keywords: implementation science; neonatal intensive care; pediatric critical care; rapid whole-genome sequencing; technology adoption.
Copyright © 2021 The Author(s). Published by Elsevier Inc. All rights reserved.
Comment in
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Sources of Unease About the Use of Genome Sequencing for Diagnosing Rare Diseases in Children.J Pediatr. 2021 Oct;237:13-15. doi: 10.1016/j.jpeds.2021.06.042. Epub 2021 Jun 21. J Pediatr. 2021. PMID: 34166672 No abstract available.
Comment on
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Sources of Unease About the Use of Genome Sequencing for Diagnosing Rare Diseases in Children.J Pediatr. 2021 Oct;237:13-15. doi: 10.1016/j.jpeds.2021.06.042. Epub 2021 Jun 21. J Pediatr. 2021. PMID: 34166672 No abstract available.
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