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User testing of a diagnostic decision support system with machine-assisted chart review to facilitate clinical genomic diagnosis.
Kulchak Rahm, Alanna; Walton, Nephi A; Feldman, Lynn K; Jenkins, Conner; Jenkins, Troy; Person, Thomas N; Peterson, Joeseph; Reynolds, Jonathon C; Robinson, Peter N; Woltz, Makenzie A; Williams, Marc S; Segal, Michael M.
Afiliação
  • Kulchak Rahm A; Genomic Medicine Institute, Geisinger Health System, Danville, Pennsylvania, USA akrahm@geisinger.edu.
  • Walton NA; Intermountain Precision Genomics, Intermountain Healthcare, St. George, Utah, USA.
  • Feldman LK; SimulConsult, Inc, Chestnut Hill, Massachusetts, USA.
  • Jenkins C; University of Utah, Salt Lake City, Utah, USA.
  • Jenkins T; University of Utah, Salt Lake City, Utah, USA.
  • Person TN; Genomic Medicine Institute, Geisinger Health System, Danville, Pennsylvania, USA.
  • Peterson J; University of Utah, Salt Lake City, Utah, USA.
  • Reynolds JC; Genomic Medicine Institute, Geisinger Health System, Danville, Pennsylvania, USA.
  • Robinson PN; Jackson Laboratory for Genomic Medicine, Farmington, Connecticut, USA.
  • Woltz MA; University of Connecticut, Farmington, Connecticut, USA.
  • Williams MS; Genomic Medicine Institute, Geisinger Health System, Danville, Pennsylvania, USA.
  • Segal MM; Genomic Medicine Institute, Geisinger Health System, Danville, Pennsylvania, USA.
BMJ Health Care Inform ; 28(1)2021 May.
Article em En | MEDLINE | ID: mdl-33962988
ABSTRACT

OBJECTIVES:

There is a need in clinical genomics for systems that assist in clinical diagnosis, analysis of genomic information and periodic reanalysis of results, and can use information from the electronic health record to do so. Such systems should be built using the concepts of human-centred design, fit within clinical workflows and provide solutions to priority problems.

METHODS:

We adapted a commercially available diagnostic decision support system (DDSS) to use extracted findings from a patient record and combine them with genomic variant information in the DDSS interface. Three representative patient cases were created in a simulated clinical environment for user testing. A semistructured interview guide was created to illuminate factors relevant to human factors in CDS design and organisational implementation.

RESULTS:

Six individuals completed the user testing process. Tester responses were positive and noted good fit with real-world clinical genetics workflow. Technical issues related to interface, interaction and design were minor and fixable. Testers suggested solving issues related to terminology and usability through training and infobuttons. Time savings was estimated at 30%-50% and additional uses such as in-house clinical variant analysis were suggested for increase fit with workflow and to further address priority problems.

CONCLUSION:

This study provides preliminary evidence for usability, workflow fit, acceptability and implementation potential of a modified DDSS that includes machine-assisted chart review. Continued development and testing using principles from human-centred design and implementation science are necessary to improve technical functionality and acceptability for multiple stakeholders and organisational implementation potential to improve the genomic diagnosis process.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Sistemas de Apoio a Decisões Clínicas / Genômica / Registros Eletrônicos de Saúde Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Sistemas de Apoio a Decisões Clínicas / Genômica / Registros Eletrônicos de Saúde Idioma: En Ano de publicação: 2021 Tipo de documento: Article