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Review

Applying an Implementation Science Approach to Genomic Medicine: Workshop Summary

Washington (DC): National Academies Press (US); 2016 Jul 6.
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Review

Applying an Implementation Science Approach to Genomic Medicine: Workshop Summary

Roundtable on Translating Genomic-Based Research for Health et al.
Free Books & Documents

Excerpt

Although it is becoming increasingly more common for clinicians to use genomic data in their practices for disease prevention, diagnosis, and treatment, the process of integrating genomic data into the practice of medicine has been a slow and challenging one. Some of the major barriers impeding the incorporation of new genomic technology into clinical practice are: the difficulty of changing routine medical practices to account for the use of genetic testing, the limited knowledge of patients and providers about genomic medicine, assessing sufficient evidence to support the use of genetic tests, privacy and data security issues, and uncertainty about reimbursement.

The field of implementation science may be able to provide insights concerning efficient ways to incorporate genomic applications into routine clinical practice. The focus of implementation science studies is to identify integration bottlenecks and optimal approaches for a given setting and ultimately to promote the up-take of research findings. To explore the potential of implementation science to improve the integration of genomics into medicine, the National Academies of Sciences, Engineering, and Medicine held a workshop in Washington, DC, in November 2015. Participants explored the challenges and opportunities of integrating genomic advances into the clinic through the lens of implementation science. This report summarizes the presentations and discussions from the workshop.

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Grants and funding

This project was supported by contracts between the National Academy of Sciences and the American Academy of Nursing (unnumbered contract); American College of Medical Genetics and Genomics (unnumbered contract); American Heart Association (unnumbered contract); American Medical Association (unnumbered contract); American Society of Human Genetics (unnumbered contract); Association for Molecular Pathology (unnumbered contract); Biogen (unnumbered contract); Blue Cross and Blue Shield Association (unnumbered contract); Centers for Disease Control and Prevention (Contract No.200-2011-38807, Order No. 0039); College of American Pathologists (unnumbered contract); Department of Veterans Affairs (Contract No. VA240-14-C-0037); Eli Lilly and Company (unnumbered contract); Health Resources and Services Administration (Contract No. HHSH250200976014I, Order No. HHSH25034017T and HHSH250201500001I, Order No. HHSH25034003T); International Society for Cardiovascular Translational Research (unnumbered contract); Janssen Research & Development, LLC (unnumbered contract); Kaiser Permanente Program Offices Community Benefit II at the East Bay Community Foundation (unnumbered contract); Merck & Co., Inc. (Contract No. CMO-140505-000393 and Contract No. CMO-150107-000659); National Cancer Institute (Contract No. HHSN263201200074I, Order Nos. HHSN26300005/0002 and HHSN26300066); National Human Genome Research Institute (Contract No. HHSN263201200074I, Order Nos. HHSN26300005/0002 and HHSN26300066); National Institute of Mental Health (Contract No. HHSN263201200074I, Order Nos. HHSN26300005/0002 and HHSN26300066); National Institute of Nursing Research (Contract No. HHSN263201200074I, Order Nos. HHSN26300005/0002 and HHSN26300066); National Institute on Aging (Contract No. HHSN263201200074I, Order Nos. HHSN26300005/0002 and HHSN26300066); National Society of Genetic Counselors (unnumbered contract); Northrop Grumman Health IT (unnumbered contract); and PhRMA (unnumbered contract). Any opinions, findings, conclusions, or recommendations expressed in this publication do not necessarily reflect the views of any organization or agency that provided support for the project.

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