Healthcare provider education to support integration of pharmacogenomics in practice: the eMERGE Network experience
- PMID: 28639489
- PMCID: PMC5941709
- DOI: 10.2217/pgs-2017-0038
Healthcare provider education to support integration of pharmacogenomics in practice: the eMERGE Network experience
Abstract
Ten organizations within the Electronic Medical Records and Genomics Network developed programs to implement pharmacogenomic sequencing and clinical decision support into clinical settings. Recognizing the importance of informed prescribers, a variety of strategies were used to incorporate provider education to support implementation. Education experiences with pharmacogenomics are described within the context of each organization's prior involvement, including the scope and scale of implementation specific to their Electronic Medical Records and Genomics projects. We describe common and distinct education strategies, provide exemplars and share challenges. Lessons learned inform future perspectives. Future pharmacogenomics clinical implementation initiatives need to include funding toward implementing provider education and evaluating outcomes.
Keywords: clinical decision support; education; pharmacogenetics; pharmacogenomics; pre-emptive testing.
Conflict of interest statement
The Electronic Medical Records and Genomics Network was initiated and funded by the National Human Genome Research Institute through the following grants: U01HG006828 (Cincinnati Children's Hospital Medical Center/Boston Children's Hospital); U01HG006830 (Children's Hospital of Philadelphia); U01HG006389 (Essentia Institute of Rural Health, Marshfield Clinic Research Foundation and Pennsylvania State University); U01HG006382 (Geisinger Clinic); U01HG006375 (Group Health Cooperative/University of Washington); U01HG006379 (Mayo Clinic); U01HG006380 (Icahn School of Medicine at Mount Sinai); U01HG006388 (Northwestern University); U01HG006378 (Vanderbilt University Medical Center); and U01HG006385 (Vanderbilt University Medical Center serving as the Coordinating Center). This work was also supported in part by Mayo Clinic Center for Individualized Medicine. The authors have no other relevant affiliations or financial involvement with any organization or entity with a financial interest in or financial conflict with the subject matter or materials discussed in the manuscript apart from those disclosed.
No writing assistance was utilized in the production of this manuscript.
References
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- National Human Genome Research Institute. Electronic medical records and genomics (eMERGE) network. https://emerge.mc.vanderbilt.edu/about-emerge/
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Grants and funding
- U01 HG006385/HG/NHGRI NIH HHS/United States
- U01 HG006375/HG/NHGRI NIH HHS/United States
- U01 HG008657/HG/NHGRI NIH HHS/United States
- U01 HG006382/HG/NHGRI NIH HHS/United States
- U01 HG006389/HG/NHGRI NIH HHS/United States
- U01 HG006828/HG/NHGRI NIH HHS/United States
- U01 HG008679/HG/NHGRI NIH HHS/United States
- U01 HG006380/HG/NHGRI NIH HHS/United States
- U01 HG008666/HG/NHGRI NIH HHS/United States
- U01 HG006379/HG/NHGRI NIH HHS/United States
- U01 HG006388/HG/NHGRI NIH HHS/United States
- U01 HG006378/HG/NHGRI NIH HHS/United States
- U01 HG008701/HG/NHGRI NIH HHS/United States
- U01 HG006830/HG/NHGRI NIH HHS/United States
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