Genetic information: Consumers' right to privacy versus insurance companies' right to know a public opinion survey
Journal of Business Ethics 19 (4):355 - 362 (1999)
| Abstract | In this paper we present arguments for and against the disclosure of genetic information to the insurance companies. One of the main issues which emerges from these arguments is the question of who should be responsible for the health insurance costs of the individuals who are most likely to be affected by the disclosure of genetic information. The results of a resident opinion survey related to the above question are presented and public policy alternatives related to the survey findings are discussed at the end of this paper. | |||||||||
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B. M. Kious (2010). Genetic Nondiscrimination and Health Care as an Entitlement. Journal of Medicine and Philosophy 35 (2):86-100.
Felix Thiele (2003). Genetic Tests in the Insurance System: Criteria for a Moral Evaluation. Poiesis and Praxis 1 (3):185-195.
Eli Feiring (2009). Reassessing Insurers' Access to Genetic Information: Genetic Privacy, Ignorance, and Injustice. Bioethics 23 (5):300-310.
Judith Wagner DeCew (2004). Privacy and Policy for Genetic Research. Ethics and Information Technology 6 (1):5-14.
Christiaan J. Lako, Pauline Rosenau & Chris Daw (2011). Switching Health Insurance Plans: Results From a Health Survey. Health Care Analysis 19 (4):312-328.
Patrick L. Brockett & E. Susan Tankersley (1997). The Genetics Revolution, Economics, Ethics and Insurance. Journal of Business Ethics 16 (15):1661-1676.
V. Launis (2000). The Use of Genetic Test Information in Insurance: The Argument From Indistinguishability Reconsidered. Science and Engineering Ethics 6 (3).
Joseph S. Alper & Jon Beckwith (1998). Distinguishing Genetic From Nongenetic Medical Tests: Some Implications for Antidiscrimination Legislation. Science and Engineering Ethics 4 (2):141-150.
Neil A. Manson (2007). Why Shouldn't Insurance Companies Know Your Genetic Information? Journal of Philosophical Research 32:345-356.
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