Document Type
Article
Publication Date
12-20-2011
Abstract
Survey data suggest that many people fear genetic discrimination by health insurers or employers. In fact, such discrimination has not yet been a significant problem. This article examines the fear and reality of genetic discrimination in the United States, describes how Congress sought to prohibit such discrimination by passing the Genetic Information Nondiscrimination Act of 2008 (GINA), and explores the implications of GINA for general internists and their institutions. It concludes that medical providers and health care institutions must be familiar with the general intent and specific terms of GINA, and should continue to collect genetic information that can contribute to the high quality provision of medical treatment. Not doing so violates their medical mission and diminishes the quality of care patients deserve.
Keywords
Health law and policy, genetics, law, policy, personalized medicine, discrimination, bioethics
Publication Title
Journal of General Internal Medicine
Repository Citation
Feldman, Eric A., "The Genetic Information Nondiscrimination Act (GINA): Public Policy and Medical Practice in the Age of Personalized Medicine" (2011). Faculty Scholarship at Penn Carey Law. 392.
https://scholarship.law.upenn.edu/faculty_scholarship/392
Included in
Civil Rights and Discrimination Commons, Community Health and Preventive Medicine Commons, Genetic Phenomena Commons, Health Law and Policy Commons, Insurance Commons, Insurance Law Commons, Labor and Employment Law Commons, Public Law and Legal Theory Commons
Publication Citation
Journal of General Internal Medicine (forthcoming 2012) (DOI 10.1007/s11606-012-1988-6)