Literature DB >> 22047175

Practical considerations to guide development of access controls and decision support for genetic information in electronic medical records.

Diana C Darcy1, Eleanor T Lewis, Kelly E Ormond, David J Clark, Jodie A Trafton.   

Abstract

BACKGROUND: Genetic testing is increasingly used as a tool throughout the health care system. In 2011 the number of clinically available genetic tests is approaching 2,000, and wide variation exists between these tests in their sensitivity, specificity, and clinical implications, as well as the potential for discrimination based on the results. DISCUSSION: As health care systems increasingly implement electronic medical record systems (EMRs) they must carefully consider how to use information from this wide spectrum of genetic tests, with whom to share information, and how to provide decision support for clinicians to properly interpret the information. Although some characteristics of genetic tests overlap with other medical test results, there are reasons to make genetic test results widely available to health care providers and counterbalancing reasons to restrict access to these test results to honor patient preferences, and avoid distracting or confusing clinicians with irrelevant but complex information. Electronic medical records can facilitate and provide reasonable restrictions on access to genetic test results and deliver education and decision support tools to guide appropriate interpretation and use.
SUMMARY: This paper will serve to review some of the key characteristics of genetic tests as they relate to design of access control and decision support of genetic test information in the EMR, emphasizing the clear need for health information technology (HIT) to be part of optimal implementation of genetic medicine, and the importance of understanding key characteristics of genetic tests when designing HIT applications.

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Year:  2011        PMID: 22047175      PMCID: PMC3229457          DOI: 10.1186/1472-6963-11-294

Source DB:  PubMed          Journal:  BMC Health Serv Res        ISSN: 1472-6963            Impact factor:   2.655


  27 in total

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3.  Key Internet genetics resources for the clinician.

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4.  Ensuring security of high-risk information in EHRs.

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Journal:  J AHIMA       Date:  2008-09

5.  Keeping pace with the times--the Genetic Information Nondiscrimination Act of 2008.

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6.  An agenda for personalized medicine.

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7.  Genetic information: Special or not? Responses from focus groups with members of a health maintenance organization.

Authors:  Brenda Diergaarde; Deborah J Bowen; Evette J Ludman; Julie O Culver; Nancy Press; Wylie Burke
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8.  Associations between anticipated reactions to genetic test results and interest in genetic testing: will self-selection reduce the potential for harm?

Authors:  Saskia C Sanderson; Jane Wardle
Journal:  Genet Test       Date:  2008-03

9.  Variability in interpreting and reporting copy number changes detected by array-based technology in clinical laboratories.

Authors:  Karen D Tsuchiya; Lisa G Shaffer; Swaroop Aradhya; Julie M Gastier-Foster; Ankita Patel; M Katharine Rudd; Julie Sanford Biggerstaff; Warren G Sanger; Stuart Schwartz; James H Tepperberg; Erik C Thorland; Beth A Torchia; Arthur R Brothman
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10.  Genomic electronic health records: opportunities and challenges.

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  3 in total

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Review 2.  Practical challenges in integrating genomic data into the electronic health record.

Authors:  Abel N Kho; Luke V Rasmussen; John J Connolly; Peggy L Peissig; Justin Starren; Hakon Hakonarson; M Geoffrey Hayes
Journal:  Genet Med       Date:  2013-09-26       Impact factor: 8.822

3.  How the electronic health record will change the future of health care.

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  3 in total

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