AMERICAN MEDICAL ASSOCIATION HOUSE OF DELEGATES Resolution: 422 (A-05) 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 Introduced by: Medical Student Section Subject: Development and Support of Prospective Personalized Health Planning Referred to: Reference Committee D (Sally J. Trippel, MD, Chair) Whereas, A Prospective Health Care (PHC) system represents a paradigm shift in health care delivery, moving away from the current fragmented methodology in favor of a system that effectively synthesizes patient education, early intervention and best practices for the prevention and management of common diseases; and Whereas, Employing advances in molecular, genetic, and other technologies in a PHC system may soon allow physicians to establish patient predisposition profiles, and thus begin focusing treatment earlier in disease processes thereby either slowing or even preventing disease progression; and Whereas, Current trends of increased health care costs, decreased services, and an aging population give physicians pause for concern, and a change-over to PHC may offer a comprehensive solution for focused lifestyle and disease management programs and play a large role in addressing patient health while reducing cost; and Whereas, Replacing the currently reactive health care system with a model grounded in PHC has the potential to lead to significant declines in many of the most common chronic diseases that reach epidemic levels in the US today and account for $1 trillion in health care costs (including heart failure, hypertension, diabetes, cancer, and respiratory diseases); therefore be it RESOLVED, That our American Medical Association continue to recognize the need for possible adaptation of the US health care system to prospectively prevent the development of disease by ethically using genomics, proteomics, metabolomics, imaging and other advanced diagnostics, along with standardized informatics tools to develop individual risk assessments and personal health plans (New HOD Policy); and be it further RESOLVED, That our AMA support studies aimed at determining the viability of prospective care models and measures that will assist in creating a stronger focus on prospective care in the US health care system (Directive to Take Action); and be it further RESOLVED, That our AMA support research and discussion regarding the multidimensional ethical issues related to prospective care models, such as genetic testing. (Directive to Take Action) Fiscal Note: Staff cost estimated at less than $500 to implement. Received: 5/8/05 Resolution: 422 (A-05) Page 2 RELEVANT AMA POLICY H-185.972 Genetic Information and Insurance Coverage AMA believes: (1) Health insurance providers should be prohibited from using genetic information, or an individual's request for genetic services, to deny or limit any health benefit coverage or establish eligibility, continuation, enrollment or contribution requirements. (2) Health insurance providers should be prohibited from establishing differential rates or premium payments based on genetic information or an individual's request for genetic services. (3) Health insurance providers should be prohibited from requesting or requiring collection or disclosure of genetic information. (4) Health insurance providers and other holders of genetic information should be prohibited from releasing genetic information without express prior written authorization of the individual. Written authorization should be required for each disclosure and include to whom the disclosure would be made. (BOT Rep. 15, I-96) E-2.135 Insurance Companies and Genetic Information Physicians should not participate in genetic testing by health insurance companies to predict a person’s predisposition for disease. As a corollary, it may be necessary for physicians to maintain separate files for genetic testing results to ensure that the results are not sent to health insurance companies when requests for copies of patient medical records are fulfilled. Physicians who withhold testing results should inform insurance companies that, when medical records are sent, genetic testing results are not included. This disclosure should occur with all patients, not just those who have undergone genetic testing. (IV) Issued June 1994 based on the report "Physician Participation in Genetic Testing by Health Insurance Companies," adopted June 1993; Updated June 1996.