Genomic information for clinicians in the electronic health record: Lessons learned from the clinical genome resource project and the electronic medical records and genomics network

Marc S. Williams, Casey Overby Taylor, Nephi A. Walton, Scott R. Goehringer, Samuel Aronson, Robert R. Freimuth, Luke V. Rasmussen, Eric S. Hall, Cynthia A. Prows, Wendy K. Chung, Alexander Fedotov, Jordan Nestor, Chunhua Weng, Robb K. Rowley, Georgia L. Wiesner, Gail P. Jarvik, Guilherme Del Fiol

Research output: Contribution to journalArticle

Abstract

Genomic knowledge is being translated into clinical care. To fully realize the value, it is critical to place credible information in the hands of clinicians in time to support clinical decision making. The electronic health record is an essential component of clinician workflow. Utilizing the electronic health record to present information to support the use of genomic medicine in clinical care to improve outcomes represents a tremendous opportunity. However, there are numerous barriers that prevent the effective use of the electronic health record for this purpose. The electronic health record working groups of the Electronic Medical Records and Genomics (eMERGE) Network and the Clinical Genome Resource (ClinGen) project, along with other groups, have been defining these barriers, to allow the development of solutions that can be tested using implementation pilots. In this paper, we present “lessons learned” from these efforts to inform future efforts leading to the development of effective and sustainable solutions that will support the realization of genomic medicine.

Original languageEnglish (US)
Article number1059
JournalFrontiers in Genetics
Volume10
Issue numberOCT
DOIs
StatePublished - Jan 1 2019

Fingerprint

Electronic Health Records
Genomics
Genome
Workflow
Clinical Medicine
Conservation of Natural Resources
Medicine

Keywords

  • Clinical decision support
  • Education
  • Electronic health record
  • Genomics
  • Implementation
  • Infobutton
  • Interoperability
  • Knowledge synthesis

ASJC Scopus subject areas

  • Molecular Medicine
  • Genetics
  • Genetics(clinical)

Cite this

Genomic information for clinicians in the electronic health record : Lessons learned from the clinical genome resource project and the electronic medical records and genomics network. / Williams, Marc S.; Taylor, Casey Overby; Walton, Nephi A.; Goehringer, Scott R.; Aronson, Samuel; Freimuth, Robert R.; Rasmussen, Luke V.; Hall, Eric S.; Prows, Cynthia A.; Chung, Wendy K.; Fedotov, Alexander; Nestor, Jordan; Weng, Chunhua; Rowley, Robb K.; Wiesner, Georgia L.; Jarvik, Gail P.; Fiol, Guilherme Del.

In: Frontiers in Genetics, Vol. 10, No. OCT, 1059, 01.01.2019.

Research output: Contribution to journalArticle

Williams, MS, Taylor, CO, Walton, NA, Goehringer, SR, Aronson, S, Freimuth, RR, Rasmussen, LV, Hall, ES, Prows, CA, Chung, WK, Fedotov, A, Nestor, J, Weng, C, Rowley, RK, Wiesner, GL, Jarvik, GP & Fiol, GD 2019, 'Genomic information for clinicians in the electronic health record: Lessons learned from the clinical genome resource project and the electronic medical records and genomics network', Frontiers in Genetics, vol. 10, no. OCT, 1059. https://doi.org/10.3389/fgene.2019.01059
Williams, Marc S. ; Taylor, Casey Overby ; Walton, Nephi A. ; Goehringer, Scott R. ; Aronson, Samuel ; Freimuth, Robert R. ; Rasmussen, Luke V. ; Hall, Eric S. ; Prows, Cynthia A. ; Chung, Wendy K. ; Fedotov, Alexander ; Nestor, Jordan ; Weng, Chunhua ; Rowley, Robb K. ; Wiesner, Georgia L. ; Jarvik, Gail P. ; Fiol, Guilherme Del. / Genomic information for clinicians in the electronic health record : Lessons learned from the clinical genome resource project and the electronic medical records and genomics network. In: Frontiers in Genetics. 2019 ; Vol. 10, No. OCT.
@article{05213ae8818c4d269ae34b238cce2fa9,
title = "Genomic information for clinicians in the electronic health record: Lessons learned from the clinical genome resource project and the electronic medical records and genomics network",
abstract = "Genomic knowledge is being translated into clinical care. To fully realize the value, it is critical to place credible information in the hands of clinicians in time to support clinical decision making. The electronic health record is an essential component of clinician workflow. Utilizing the electronic health record to present information to support the use of genomic medicine in clinical care to improve outcomes represents a tremendous opportunity. However, there are numerous barriers that prevent the effective use of the electronic health record for this purpose. The electronic health record working groups of the Electronic Medical Records and Genomics (eMERGE) Network and the Clinical Genome Resource (ClinGen) project, along with other groups, have been defining these barriers, to allow the development of solutions that can be tested using implementation pilots. In this paper, we present “lessons learned” from these efforts to inform future efforts leading to the development of effective and sustainable solutions that will support the realization of genomic medicine.",
keywords = "Clinical decision support, Education, Electronic health record, Genomics, Implementation, Infobutton, Interoperability, Knowledge synthesis",
author = "Williams, {Marc S.} and Taylor, {Casey Overby} and Walton, {Nephi A.} and Goehringer, {Scott R.} and Samuel Aronson and Freimuth, {Robert R.} and Rasmussen, {Luke V.} and Hall, {Eric S.} and Prows, {Cynthia A.} and Chung, {Wendy K.} and Alexander Fedotov and Jordan Nestor and Chunhua Weng and Rowley, {Robb K.} and Wiesner, {Georgia L.} and Jarvik, {Gail P.} and Fiol, {Guilherme Del}",
year = "2019",
month = "1",
day = "1",
doi = "10.3389/fgene.2019.01059",
language = "English (US)",
volume = "10",
journal = "Frontiers in Genetics",
issn = "1664-8021",
publisher = "Frontiers Media S. A.",
number = "OCT",

}

TY - JOUR

T1 - Genomic information for clinicians in the electronic health record

T2 - Lessons learned from the clinical genome resource project and the electronic medical records and genomics network

AU - Williams, Marc S.

AU - Taylor, Casey Overby

AU - Walton, Nephi A.

AU - Goehringer, Scott R.

AU - Aronson, Samuel

AU - Freimuth, Robert R.

AU - Rasmussen, Luke V.

AU - Hall, Eric S.

AU - Prows, Cynthia A.

AU - Chung, Wendy K.

AU - Fedotov, Alexander

AU - Nestor, Jordan

AU - Weng, Chunhua

AU - Rowley, Robb K.

AU - Wiesner, Georgia L.

AU - Jarvik, Gail P.

AU - Fiol, Guilherme Del

PY - 2019/1/1

Y1 - 2019/1/1

N2 - Genomic knowledge is being translated into clinical care. To fully realize the value, it is critical to place credible information in the hands of clinicians in time to support clinical decision making. The electronic health record is an essential component of clinician workflow. Utilizing the electronic health record to present information to support the use of genomic medicine in clinical care to improve outcomes represents a tremendous opportunity. However, there are numerous barriers that prevent the effective use of the electronic health record for this purpose. The electronic health record working groups of the Electronic Medical Records and Genomics (eMERGE) Network and the Clinical Genome Resource (ClinGen) project, along with other groups, have been defining these barriers, to allow the development of solutions that can be tested using implementation pilots. In this paper, we present “lessons learned” from these efforts to inform future efforts leading to the development of effective and sustainable solutions that will support the realization of genomic medicine.

AB - Genomic knowledge is being translated into clinical care. To fully realize the value, it is critical to place credible information in the hands of clinicians in time to support clinical decision making. The electronic health record is an essential component of clinician workflow. Utilizing the electronic health record to present information to support the use of genomic medicine in clinical care to improve outcomes represents a tremendous opportunity. However, there are numerous barriers that prevent the effective use of the electronic health record for this purpose. The electronic health record working groups of the Electronic Medical Records and Genomics (eMERGE) Network and the Clinical Genome Resource (ClinGen) project, along with other groups, have been defining these barriers, to allow the development of solutions that can be tested using implementation pilots. In this paper, we present “lessons learned” from these efforts to inform future efforts leading to the development of effective and sustainable solutions that will support the realization of genomic medicine.

KW - Clinical decision support

KW - Education

KW - Electronic health record

KW - Genomics

KW - Implementation

KW - Infobutton

KW - Interoperability

KW - Knowledge synthesis

UR - http://www.scopus.com/inward/record.url?scp=85074748708&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=85074748708&partnerID=8YFLogxK

U2 - 10.3389/fgene.2019.01059

DO - 10.3389/fgene.2019.01059

M3 - Article

AN - SCOPUS:85074748708

VL - 10

JO - Frontiers in Genetics

JF - Frontiers in Genetics

SN - 1664-8021

IS - OCT

M1 - 1059

ER -