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1.
J Health Commun ; 16(6): 607-28, 2011 Jul.
Article in English | MEDLINE | ID: mdl-21432710

ABSTRACT

Genetic testing for the breast cancer genes 1/2 (BRCA 1/2) has helped women determine their risk of developing breast and ovarian cancer. As interest in genetic testing has grown, companies have created strategies to disseminate information about testing, including direct-to-consumer advertising (DTCA) and online genetic testing. This study examined attitudes toward DTCA and online testing for BRCA among 84 women at a high-risk clinic as well as additional factors that may be associated with these attitudes, such as personal and familial cancer history, cancer worry and risk perception, and history with genetic testing/counseling. Results showed that the majority of the women held favorable attitudes toward DTCA for BRCA testing but did not support online testing. Factors such as familial ovarian cancer, cancer worry, and satisfaction with genetic counseling/testing were associated with positive attitudes toward DTCA, whereas personal breast cancer history was related to negative attitudes. The findings suggest that women may view DTCA as informational but rely on physicians for help in their decision to undergo testing, and also suggest that cancer history may affect women's acceptance of DTCA and genetic testing.


Subject(s)
Advertising/methods , Attitude , Internet , Patient Participation/psychology , Women's Health , Adult , Aged , Aged, 80 and over , Chi-Square Distribution , Female , Genetic Testing , Health Knowledge, Attitudes, Practice , Health Surveys , Humans , Middle Aged , Neoplastic Syndromes, Hereditary/diagnosis , Neoplastic Syndromes, Hereditary/genetics , Oncology Service, Hospital , Ovarian Neoplasms/diagnosis , Ovarian Neoplasms/genetics , Patient Satisfaction , Prevalence , Risk Factors , Social Perception , Statistics, Nonparametric , Ubiquitin-Protein Ligases/genetics , Young Adult
2.
Conn Med ; 74(7): 413-23, 2010 Aug.
Article in English | MEDLINE | ID: mdl-20806621

ABSTRACT

UNLABELLED: Advances in genetics have prompted recommendations that all healthcare providers perform genetic counseling and testing. Some experts are concerned about potential negative outcomes from cancer genetic testing performed without genetic counseling by certified genetics professionals. We report a national series of cases illustrating negative outcomes of cancer genetic testing performed without counseling by a qualified provider. Three major patterns emerged from analysis of these cases: 1) Wrong genetic test ordered, 2) Genetic test results misinterpreted, and 3) Inadequate genetic counseling. Negative outcomes included unnecessary prophylactic surgeries, unnecessary testing, psychosocial distress, and false reassurance resulting in inappropriate medical management. CONCLUSION: With the complexities of cancer genetic counseling and testing, it may be unrealistic to expect all clinicians to provide these services. A more realistic approach is better provider education and a framework in which healthcare providers identify patients who would benefit from a referral to a certified genetic counselor or experienced cancer genetics professional.


Subject(s)
Diagnostic Errors , Genes, Neoplasm/genetics , Genetic Counseling/standards , Genetic Testing/standards , Female , Humans , Male
3.
Surg Oncol Clin N Am ; 18(1): 53-71, viii, 2009 Jan.
Article in English | MEDLINE | ID: mdl-19056042

ABSTRACT

Screening for genetic abnormalities is a relatively complex task requiring detailed training and knowledge. Analysis of a person's genetic makeup has implications not only for that individual but also for their progenitors, offspring, siblings, and spouses. There are potential insurance, employment, and other risks regarding disclosure of this information. With proper training, surgeons or nurses with advanced skills can be qualified to conduct this type of initial analysis. Geneticists may be the ideal professionals to counsel patients. In this article, we explore these and other issues. The goal is to provide the surgeon with the information needed to identify patients at risk for carrying identifiable mutations that might lead to the development of breast cancer.


Subject(s)
Breast Neoplasms/genetics , Neoplastic Syndromes, Hereditary/diagnosis , BRCA1 Protein/genetics , BRCA2 Protein/genetics , Breast Neoplasms/diagnosis , Family , Female , Genetic Counseling , Genetic Testing , Germ-Line Mutation , Humans , Insurance Coverage , Risk Factors , Spouses
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