Cargando…
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...
Autores principales: | , , , , , , , , , , , |
---|---|
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 |
_version_ | 1783690163908509696 |
---|---|
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. |
format | Online Article Text |
id | pubmed-8108675 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT kulchakrahmalanna usertestingofadiagnosticdecisionsupportsystemwithmachineassistedchartreviewtofacilitateclinicalgenomicdiagnosis AT waltonnephia usertestingofadiagnosticdecisionsupportsystemwithmachineassistedchartreviewtofacilitateclinicalgenomicdiagnosis AT feldmanlynnk usertestingofadiagnosticdecisionsupportsystemwithmachineassistedchartreviewtofacilitateclinicalgenomicdiagnosis AT jenkinsconner usertestingofadiagnosticdecisionsupportsystemwithmachineassistedchartreviewtofacilitateclinicalgenomicdiagnosis AT jenkinstroy usertestingofadiagnosticdecisionsupportsystemwithmachineassistedchartreviewtofacilitateclinicalgenomicdiagnosis AT personthomasn usertestingofadiagnosticdecisionsupportsystemwithmachineassistedchartreviewtofacilitateclinicalgenomicdiagnosis AT petersonjoeseph usertestingofadiagnosticdecisionsupportsystemwithmachineassistedchartreviewtofacilitateclinicalgenomicdiagnosis AT reynoldsjonathonc usertestingofadiagnosticdecisionsupportsystemwithmachineassistedchartreviewtofacilitateclinicalgenomicdiagnosis AT robinsonpetern usertestingofadiagnosticdecisionsupportsystemwithmachineassistedchartreviewtofacilitateclinicalgenomicdiagnosis AT woltzmakenziea usertestingofadiagnosticdecisionsupportsystemwithmachineassistedchartreviewtofacilitateclinicalgenomicdiagnosis AT williamsmarcs usertestingofadiagnosticdecisionsupportsystemwithmachineassistedchartreviewtofacilitateclinicalgenomicdiagnosis AT segalmichaelm usertestingofadiagnosticdecisionsupportsystemwithmachineassistedchartreviewtofacilitateclinicalgenomicdiagnosis |