Issues of consent and feedback in a genetic epidemiological study of women with breast cancer

被引:42
作者
Richards, MPM
Ponder, M
Pharoah, P
Everest, S
Mackay, J
机构
[1] Univ Cambridge, Ctr Family Res, Cambridge CB2 3RF, England
[2] Univ Cambridge, Dept Oncol, Cambridge, England
[3] Univ Cambridge, Dept Med Genet, Cambridge, England
关键词
D O I
10.1136/jme.29.2.93
中图分类号
B82 [伦理学(道德学)];
学科分类号
摘要
Women (N=21) who had had breast cancer and had been enrolled in a large genetic breast cancer epidemiological study were interviewed about their experience of participation in the study, their attitudes to the confidentiality of data, and the feedback of personal and general research results. Collection of family history information seemed more salient in indicating the genetic nature of the study than the enrolment information sheet. There were no concerns about confidentiality. While participants would have welcomed general feedback about the results of the study and were critical that this had not been provided, the feedback of personal information proved complicated and, sometimes, difficult. It is suggested that individual feedback of genetic test information in epidemiological studies should be undertaken only when there are specific reasons.
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页码:93 / 96
页数:4
相关论文
共 9 条
[1]  
[Anonymous], INS INF BAL INT US P
[2]   Solidarity and equity: new ethical frameworks for genetic databases [J].
Chadwick, R ;
Berg, K .
NATURE REVIEWS GENETICS, 2001, 2 (04) :318-321
[3]   Protection of privacy by third-party encryption in genetic research in Iceland [J].
Gulcher, JR ;
Kristjánsson, K ;
Gudbjartsson, H ;
Stefánsson, K .
EUROPEAN JOURNAL OF HUMAN GENETICS, 2000, 8 (10) :739-742
[4]  
*HUM GEN COMM, 2000, WHOS HANDS YOUR GEN
[5]  
KNOPPERS B, 2000, GENETIC LAW MONI JAN, P3
[6]  
MARTIN P, 1996, USE BIOL SAMPLE COLL
[7]  
Medical Research Council (UK), 2001, HUM TISS BIOL SAMPL
[8]  
Ponder BAJ, 2000, BRIT J CANCER, V83, P1301
[9]  
*WELLC TRUST MED R, 2000, PUBL PERC COLL HUM B