Receiving inconclusive genetic test results: An interpretive description of the BRCA1/2 experience†
Article first published online: 30 APR 2008
Copyright © 2008 Wiley Periodicals, Inc.
Research in Nursing & Health
Volume 31, Issue 6, pages 553–562, December 2008
How to Cite
Maheu, C. and Thorne, S. (2008), Receiving inconclusive genetic test results: An interpretive description of the BRCA1/2 experience. Res. Nurs. Health, 31: 553–562. doi: 10.1002/nur.20286
We obtained partial funding for this study from the Quebec Health Research Fund and the Canadian Association of Nurses in Oncology.
- Issue published online: 13 NOV 2008
- Article first published online: 30 APR 2008
- Manuscript Accepted: 20 MAR 2008
- genetic testing;
- inconclusive test results;
- breast cancer;
We examined the experience of 21 women diagnosed with breast or ovarian cancer who received inconclusive BRCA1/2 genetic test results. Although these women received similar information on the technical meaning of an inconclusive result, their interpretations of personal risk for a probable, inherited cancer mutation differed. Their interpretations ranged from confidence that they probably carried an undetected gene mutation to believing that their cancer had no genetic basis. Women drew from their personal experience with genetic testing and from distinctive perceptions and beliefs in attempting to understand their test results; they variously drew upon such evidence as observations of similarities and differences within familial breast/ovarian cancer patterns to explain their ultimate conclusions as to their own genetic status. © 2008 Wiley Periodicals, Inc. Res Nurs Health 31:553–562, 2008