Journal
PATIENT EDUCATION AND COUNSELING
Volume 90, Issue 3, Pages 372-377Publisher
ELSEVIER IRELAND LTD
DOI: 10.1016/j.pec.2011.09.002
Keywords
Familial hypercholesterolemia; Genetic testing; Patient perceptions; Inconclusive DNA results
Funding
- Chief Scientist's Office [CSO]
- Chief Scientist Office [CZH/4/559] Funding Source: researchfish
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Objective: To explore patients' interpretations of their DNA results for familial hypercholesterolemia (FH). Methods: In-depth interviews were conducted with patients from two lipid clinics in Scotland, who were offered genetic testing as part of a nationwide cascade screening service. Results: Patients were receptive to taking part in genetic screening and most expected a positive result. Receiving a molecular diagnosis of FH could provide reassurance to patients that diet and lifestyle factors were not the primary causes of their condition. Patients who received inconclusive results tended to interpret this as meaning that their high cholesterol was not genetic, which could induce feelings of uncertainty and self-blame. With the exception of newly diagnosed patients, for whom a positive result could provide a useful rationale for initiating statins, most perceived DNA screening to be of little relevance to their own medication use or their own approaches to lifestyle management. Conclusions: Index patients are likely to view DNA screening for FH as non-threatening. Receiving a positive DNA result can be reassuring for patients. Patients may not, however, interpret inconclusive DNA results correctly. Practice implications: Health professionals need to ensure FH index patients are prepared to receive, and fully understand, inconclusive DNA results. (C) 2011 Elsevier Ireland Ltd. All rights reserved.
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