Literature DB >> 24931434

Technical desiderata for the integration of genomic data with clinical decision support.

Brandon M Welch1, Karen Eilbeck2, Guilherme Del Fiol3, Laurence J Meyer4, Kensaku Kawamoto3.   

Abstract

The ease with which whole genome sequence (WGS) information can be obtained is rapidly approaching the point where it can become useful for routine clinical care. However, significant barriers will inhibit widespread adoption unless clinicians are able to effectively integrate this information into patient care and decision-making. Electronic health records (EHR) and clinical decision support (CDS) systems may play a critical role in this integration. A previously published technical desiderata focused primarily on the integration of genomic data into the EHR. This manuscript extends the previous desiderata by specifically addressing needs related to the integration of genomic information with CDS. The objective of this study is to develop and validate a guiding set of technical desiderata for supporting the clinical use of WGS through CDS. A panel of domain experts in genomics and CDS developed a proposed set of seven additional requirements. These desiderata were reviewed by 63 experts in genomics and CDS through an online survey and refined based on the experts' comments. These additional desiderata provide important guiding principles for the technical development of CDS capabilities for the clinical use of WGS information.
Copyright © 2014 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Clinical decision support systems; Electronic health records; Genomics; Health information technology; Medical genetics; Personalized medicine

Mesh:

Year:  2014        PMID: 24931434     DOI: 10.1016/j.jbi.2014.05.014

Source DB:  PubMed          Journal:  J Biomed Inform        ISSN: 1532-0464            Impact factor:   6.317


  20 in total

1.  FHIR Lab Reports: using SMART on FHIR and CDS Hooks to increase the clinical utility of pharmacogenomic laboratory test results.

Authors:  Michael Watkins; Karen Eilbeck
Journal:  AMIA Jt Summits Transl Sci Proc       Date:  2020-05-30

2.  CSER and eMERGE: current and potential state of the display of genetic information in the electronic health record.

Authors:  Brian H Shirts; Joseph S Salama; Samuel J Aronson; Wendy K Chung; Stacy W Gray; Lucia A Hindorff; Gail P Jarvik; Sharon E Plon; Elena M Stoffel; Peter Z Tarczy-Hornoch; Eliezer M Van Allen; Karen E Weck; Christopher G Chute; Robert R Freimuth; Robert W Grundmeier; Andrea L Hartzler; Rongling Li; Peggy L Peissig; Josh F Peterson; Luke V Rasmussen; Justin B Starren; Marc S Williams; Casey L Overby
Journal:  J Am Med Inform Assoc       Date:  2015-07-03       Impact factor: 4.497

3.  Leveraging Knowledge Representation to Maintain Immunization Clinical Decision Support.

Authors:  Janos L Mathe; Scott D Nelson; Stuart T Weinberg; Christoph U Lehmann; Andras Nadas; Asli O Weitkamp
Journal:  AMIA Annu Symp Proc       Date:  2018-12-05

4.  Implementing the VMC Specification to Reduce Ambiguity in Genomic Variant Representation.

Authors:  Michael Watkins; Shawn Rynearson; Alex Henrie; Karen Eilbeck
Journal:  AMIA Annu Symp Proc       Date:  2020-03-04

Review 5.  Integrating pharmacogenomics into electronic health records with clinical decision support.

Authors:  J Kevin Hicks; Henry M Dunnenberger; Karl F Gumpper; Cyrine E Haidar; James M Hoffman
Journal:  Am J Health Syst Pharm       Date:  2016-12-01       Impact factor: 2.637

6.  Clinical decision support for whole genome sequence information leveraging a service-oriented architecture: a prototype.

Authors:  Brandon M Welch; Salvador Rodriguez-Loya; Karen Eilbeck; Kensaku Kawamoto
Journal:  AMIA Annu Symp Proc       Date:  2014-11-14

7.  Merging Electronic Health Record Data and Genomics for Cardiovascular Research: A Science Advisory From the American Heart Association.

Authors:  Jennifer L Hall; John J Ryan; Bruce E Bray; Candice Brown; David Lanfear; L Kristin Newby; Mary V Relling; Neil J Risch; Dan M Roden; Stanley Y Shaw; James E Tcheng; Jessica Tenenbaum; Thomas N Wang; William S Weintraub
Journal:  Circ Cardiovasc Genet       Date:  2016-03-14

8.  The genomic CDS sandbox: An assessment among domain experts.

Authors:  Ayesha Aziz; Kensaku Kawamoto; Karen Eilbeck; Marc S Williams; Robert R Freimuth; Mark A Hoffman; Luke V Rasmussen; Casey L Overby; Brian H Shirts; James M Hoffman; Brandon M Welch
Journal:  J Biomed Inform       Date:  2016-01-15       Impact factor: 6.317

9.  Empowering genomic medicine by establishing critical sequencing result data flows: the eMERGE example.

Authors:  Samuel Aronson; Lawrence Babb; Darren Ames; Richard A Gibbs; Eric Venner; John J Connelly; Keith Marsolo; Chunhua Weng; Marc S Williams; Andrea L Hartzler; Wayne H Liang; James D Ralston; Emily Beth Devine; Shawn Murphy; Christopher G Chute; Pedro J Caraballo; Iftikhar J Kullo; Robert R Freimuth; Luke V Rasmussen; Firas H Wehbe; Josh F Peterson; Jamie R Robinson; Ken Wiley; Casey Overby Taylor
Journal:  J Am Med Inform Assoc       Date:  2018-10-01       Impact factor: 4.497

10.  Developing knowledge resources to support precision medicine: principles from the Clinical Pharmacogenetics Implementation Consortium (CPIC).

Authors:  James M Hoffman; Henry M Dunnenberger; J Kevin Hicks; Kelly E Caudle; Michelle Whirl Carrillo; Robert R Freimuth; Marc S Williams; Teri E Klein; Josh F Peterson
Journal:  J Am Med Inform Assoc       Date:  2016-03-28       Impact factor: 7.942

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.