Mm. Burgess et al., BIOETHICS FOR CLINICIAN - 14 - ETHICS AND GENETICS IN MEDICINE, CMAJ. Canadian Medical Association journal, 158(10), 1998, pp. 1309-1313
INFORMATION ABOUT A PATIENT'S INHERITED RISK of disease has important
ethical and legal implications in clinical practice. Because genetic i
nformation is by nature highly personal yet familial, issues of confid
entiality arise. Counselling and informed consent before testing are i
mportant in view of the social and psychological risks that accompany
testing, the complexity of information surrounding testing, and the fa
ct that effective interventions are often not available. Follow-up cou
nselling is also important to help patients integrate test results int
o their lives and the lives of their relatives. Genetic counselling sh
ould be provided by practitioners who have up-to-date knowledge of the
genetics of and the tests available for specific diseases, are aware
of the social and psychological risks associated with testing, and are
able to provide appropriate clinical follow-up. Some physicians may e
lect to refer patients for genetic counselling and testing. However, i
t is inevitable that all physicians will be involved in long-term foll
ow-up both by monitoring for disease and by supporting the integration
of genetic information into patients' lives.