Literature DB >> 34023348

Implementing Rapid Whole Genome Sequencing in Critical Care: A Qualitative Study of Facilitators and Barriers to New Technology Adoption.

Linda S Franck1, Rebecca M Kriz2, Seema Rego3, Karen Garman3, Charlotte Hobbs4, David Dimmock4.   

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 multi-disciplinary patient care teams and hospital leaders at each of the five 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.
Copyright © 2021 The Author(s). Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Implementation Science; Neonatal Intensive Care; Pediatric Critical Care; Rapid Whole Genome Sequencing; Technology Adoption

Year:  2021        PMID: 34023348     DOI: 10.1016/j.jpeds.2021.05.045

Source DB:  PubMed          Journal:  J Pediatr        ISSN: 0022-3476            Impact factor:   4.406


  6 in total

Review 1.  Rapid genomic testing for critically ill children: time to become standard of care?

Authors:  Zornitza Stark; Sian Ellard
Journal:  Eur J Hum Genet       Date:  2021-11-08       Impact factor: 4.246

2.  How neonatologists use genetic testing: findings from a national survey.

Authors:  Katharine Press Callahan; John Flibotte; Cara Skraban; Katherine Taylor Wild; Steven Joffe; David Munson; Chris Feudtner
Journal:  J Perinatol       Date:  2021-11-30       Impact factor: 3.225

3.  Integrating rapid exome sequencing into NICU clinical care after a pilot research study.

Authors:  Monica H Wojcik; Pankaj B Agrawal; Alissa M D'Gama; Maya C Del Rosario; Mairead A Bresnahan; Timothy W Yu
Journal:  NPJ Genom Med       Date:  2022-09-05       Impact factor: 6.083

4.  Education and Training of Non-Genetics Providers on the Return of Genome Sequencing Results in a NICU Setting.

Authors:  Kelly M East; Meagan E Cochran; Whitley V Kelley; Veronica Greve; Candice R Finnila; Tanner Coleman; Mikayla Jennings; Latonya Alexander; Elizabeth J Rahn; Maria I Danila; Greg Barsh; Bruce Korf; Greg Cooper
Journal:  J Pers Med       Date:  2022-03-05

5.  Ethical Considerations for Equitable Access to Genomic Sequencing for Critically Ill Neonates in the United States.

Authors:  Kristen P Fishler; Joshua C Euteneuer; Luca Brunelli
Journal:  Int J Neonatal Screen       Date:  2022-03-21

6.  Healthcare Professionals' Attitudes toward Rapid Whole Genome Sequencing in Pediatric Acute Care.

Authors:  Linda S Franck; Andrea Scheurer-Monaghan; Caleb P Bupp; Joseph D Fakhoury; Thomas J Hoffmann; Manasi Deshpandey; Madison Arenchild; David P Dimmock
Journal:  Children (Basel)       Date:  2022-03-04
  6 in total

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