Literature DB >> 32020508

Primary care physician experiences utilizing a family health history tool with electronic health record-integrated clinical decision support: an implementation process assessment.

Amy A Lemke1, Jennifer Thompson2, Peter J Hulick3, Annette W Sereika3, Christian Johnson2, Lauren Oshman4, Henry M Dunnenberger3.   

Abstract

Family health history (FHH) screening plays a key role in disease risk identification and tailored disease prevention strategies. Primary care physicians (PCPs) are in a frontline position to provide personalized medicine recommendations identified through FHH screening; however, adoption of FHH screening tools has been slow and inconsistent in practice. Information is also lacking on PCP facilitators and barriers of utilizing family history tools with clinical decision support (CDS) embedded in the electronic health record (EHR). This study reports on PCPs' initial experiences with the Genetic and Wellness Assessment (GWA), a patient-administered FHH screening tool utilizing the EHR and CDS. Semi-structured interviews were conducted with 24 PCPs who use the GWA in a network of community-based practices. Four main themes regarding GWA implementation emerged: benefits to clinical care, challenges in practice, CDS-specific issues, and physician-recommended improvements. Sub-themes included value in improving patient access to genetic services, inadequate time to discuss GWA recommendations, lack of patient follow-through with recommendations, and alert fatigue. While PCPs valued the GWA's clinical utility, a number of challenges were identified in the administration and use of the GWA in practice. Based on participants' recommendations, iterative changes have been made to the GWA and workflow to increase efficiency, upgrade the CDS process, and provide additional education to PCPs and patients. Future studies are needed to assess a diverse sample of physicians' and patients' perspectives on the utility of FHH screening utilizing EHR-based genomics recommendations.

Entities:  

Keywords:  Clinical decision support; Family health history; Genetic screening tool; Implementation; Precision medicine; Primary care

Year:  2020        PMID: 32020508      PMCID: PMC7295926          DOI: 10.1007/s12687-020-00454-8

Source DB:  PubMed          Journal:  J Community Genet        ISSN: 1868-310X


  3 in total

Review 1.  Strategic vision for improving human health at The Forefront of Genomics.

Authors:  Eric D Green; Chris Gunter; Leslie G Biesecker; Valentina Di Francesco; Carla L Easter; Elise A Feingold; Adam L Felsenfeld; David J Kaufman; Elaine A Ostrander; William J Pavan; Adam M Phillippy; Anastasia L Wise; Jyoti Gupta Dayal; Britny J Kish; Allison Mandich; Christopher R Wellington; Kris A Wetterstrand; Sarah A Bates; Darryl Leja; Susan Vasquez; William A Gahl; Bettie J Graham; Daniel L Kastner; Paul Liu; Laura Lyman Rodriguez; Benjamin D Solomon; Vence L Bonham; Lawrence C Brody; Carolyn M Hutter; Teri A Manolio
Journal:  Nature       Date:  2020-10-28       Impact factor: 49.962

2.  Primary Care Physician Experiences with Integrated Population-Scale Genetic Testing: A Mixed-Methods Assessment.

Authors:  Amy A Lemke; Laura M Amendola; Kristine Kuchta; Henry M Dunnenberger; Jennifer Thompson; Christian Johnson; Nadim Ilbawi; Lauren Oshman; Peter J Hulick
Journal:  J Pers Med       Date:  2020-10-13

3.  Prevalence and Correlates of Family Cancer History Knowledge and Communication Among US Adults.

Authors:  Melinda Krakow; Camella J Rising; Neha Trivedi; Dahye C Yoon; Robin C Vanderpool
Journal:  Prev Chronic Dis       Date:  2020-11-19       Impact factor: 2.830

  3 in total

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