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Precision Population Medicine in Primary Care: The Sanford Chip Experience

Genetic testing has the potential to revolutionize primary care, but few health systems have developed the infrastructure to support precision population medicine applications or attempted to evaluate its impact on patient and provider outcomes. In 2018, Sanford Health, the nation’s largest rural no...

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Detalles Bibliográficos
Autores principales: Christensen, Kurt D., Bell, Megan, Zawatsky, Carrie L. B., Galbraith, Lauren N., Green, Robert C., Hutchinson, Allison M., Jamal, Leila, LeBlanc, Jessica L., Leonhard, Jennifer R., Moore, Michelle, Mullineaux, Lisa, Petry, Natasha, Platt, Dylan M., Shaaban, Sherin, Schultz, April, Tucker, Bethany D., Van Heukelom, Joel, Wheeler, Elizabeth, Zoltick, Emilie S., Hajek, Catherine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7994529/
https://www.ncbi.nlm.nih.gov/pubmed/33777099
http://dx.doi.org/10.3389/fgene.2021.626845
Descripción
Sumario:Genetic testing has the potential to revolutionize primary care, but few health systems have developed the infrastructure to support precision population medicine applications or attempted to evaluate its impact on patient and provider outcomes. In 2018, Sanford Health, the nation’s largest rural nonprofit health care system, began offering genetic testing to its primary care patients. To date, more than 11,000 patients have participated in the Sanford Chip Program, over 90% of whom have been identified with at least one informative pharmacogenomic variant, and about 1.5% of whom have been identified with a medically actionable predisposition for disease. This manuscript describes the rationale for offering the Sanford Chip, the programs and infrastructure implemented to support it, and evolving plans for research to evaluate its real-world impact.