CF carrier testing: Experience of relatives |
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Authors: | Nancy P. Callanan Diane Bloom James R. Sorenson Brenda M. DeVellis Brian Cheuvront |
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Affiliation: | (1) Department of Pediatrics, School of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina;(2) Bloom Research, Chapel Hill, North Carolina;(3) Department of Health Behavior and Health Education, School of Public Health, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina;(4) Division of Genetics and Metabolism, BSRC, UNC-Chapel Hill, CB # 7250, 27599 Chapel Hill, North Carolina |
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Abstract: | Consensus exists that genetic counseling and CF carrier testing should be offered to individuals with a positive family history of CF. To learn more about their experience with genetic counseling and testing we conducted a series of structured telephone interviews and focus group discussions with individuals and couples who had undergone genetic counseling and carrier testing because of a family history of CF. Traditional genetic counseling appears to have been effective for this population. Subjects generally report having a positive counseling experience and few difficulties upon learning their carrier status. Subjects were quite knowledgeable about CF and their carrier risk and were highly motivated to seek testing. They may not be representative of all individuals with a family history of CF however. For carriers, concerns about whether and when to have children tested, and concerns about insurance implications of carrier status may emerge sometime after the initial counseling. Strategies for addressing these concerns and for providing efficient and effective education and genetic counseling for people with a family history of CF need to be developed. |
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Keywords: | CF carrier testing |
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