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1.
J Med Ethics ; 32(9): 522-5, 2006 Sep.
Article in English | MEDLINE | ID: mdl-16943333

ABSTRACT

Privacy is a key ethical principle in occupational health services. Its importance is emphasised in several laws, in ethical codes of conduct as well as in the literature, yet there is only very limited empirical research on privacy in the occupational health context. Conceptual questions on privacy in the occupational health context are discussed. The baseline assumption is that, in this context, privacy cannot be approached and examined only from the employee's (an individual) vantage point but the employer's (a group) point of view must also be taken into account, and that the concept has several dimensions (physical, social, informational and psychological). Even though privacy is a basic human need, there is no universally accepted definition of the concept and no consensus on whether an organisation can have privacy in the same way as people do. Many of the challenges surrounding privacy in the context of occupational health seem to be associated with the dual loyalties of occupational health professionals towards the employee and employer and with their simultaneous duties of disseminating and protecting information (informational privacy). Privacy is thus not an absolute value, but more research is needed to understand its multidimensional nature in the context of occupational health.


Subject(s)
Occupational Health Services/ethics , Privacy , Attitude of Health Personnel , Confidentiality/ethics , Conflict, Psychological , Cooperative Behavior , Employment/ethics , Humans , Organizations/ethics , Physician's Role , Risk Assessment/ethics
2.
Sci Eng Ethics ; 6(3): 299-310, 2000 Jul.
Article in English | MEDLINE | ID: mdl-11273456

ABSTRACT

In the bioethical literature, discrimination in insurance on the basis of genetic risk factors detected by genetic testing has been defended and opposed on various ethical grounds. One important argument in favour of the practice is offered by those who believe that it is not possible to distinguish between genetic and non-genetic information, at least not for practical policy purposes such as insurance decision-making. According to the argument from indistinguishability, the use of genetic test information for insurance purposes should be permitted, because genetic test information is no different from non-genetic medical information in any relevant respect, therefore it would be inconsistent to prohibit the former whilst permitting the latter. This paper discusses and defends this argument and suggests a new, more tenable foundation.


Subject(s)
Genetic Privacy , Genetic Testing , Insurance, Health , Ethics, Medical , Prejudice , Risk Factors
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