Author:
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,
Abstract
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.
Funder
National Institutes of Health
Subject
Genetics (clinical),Genetics,Molecular Medicine
Cited by
38 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献