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User testing of a diagnostic decision support system with machine-assisted chart review to facilitate clinical genomic diagnosis

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 des...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8108675/
https://www.ncbi.nlm.nih.gov/pubmed/33962988
http://dx.doi.org/10.1136/bmjhci-2021-100331
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author 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
author_facet 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
author_sort Kulchak Rahm, Alanna
collection PubMed
description 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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spelling pubmed-81086752021-05-24 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 BMJ Health Care Inform Original Research 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. BMJ Publishing Group 2021-05-07 /pmc/articles/PMC8108675/ /pubmed/33962988 http://dx.doi.org/10.1136/bmjhci-2021-100331 Text en © Author(s) (or their employer(s)) 2021. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) .
spellingShingle Original Research
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
User testing of a diagnostic decision support system with machine-assisted chart review to facilitate clinical genomic diagnosis
title User testing of a diagnostic decision support system with machine-assisted chart review to facilitate clinical genomic diagnosis
title_full User testing of a diagnostic decision support system with machine-assisted chart review to facilitate clinical genomic diagnosis
title_fullStr User testing of a diagnostic decision support system with machine-assisted chart review to facilitate clinical genomic diagnosis
title_full_unstemmed User testing of a diagnostic decision support system with machine-assisted chart review to facilitate clinical genomic diagnosis
title_short User testing of a diagnostic decision support system with machine-assisted chart review to facilitate clinical genomic diagnosis
title_sort user testing of a diagnostic decision support system with machine-assisted chart review to facilitate clinical genomic diagnosis
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8108675/
https://www.ncbi.nlm.nih.gov/pubmed/33962988
http://dx.doi.org/10.1136/bmjhci-2021-100331
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