Genetic professionals' reports of nondisclosure of genetic risk information within families

被引:0
|
作者
Angus Clarke
Martin Richards
Lauren Kerzin-Storrar
Jane Halliday
Mary Anne Young
Sheila A Simpson
Katie Featherstone
Karen Forrest
Anneke Lucassen
Patrick J Morrison
Oliver W J Quarrell
Helen Stewart
机构
[1] University Hospital of Wales,Institute of Medical Genetics
[2] Free School Lane,Centre for Family Research
[3] St Mary's Hospital,Regional Genetic Service and Academic Unit of Medical Genetics
[4] Murdoch Children's Research Institute,Public Health Genetics (on behalf of Genetic Health Services Victoria)
[5] Peter MacCallum Cancer institute,Family Cancer Centre
[6] University of Aberdeen,Department of Medical Genetics
[7] School of Medicine,CESAGen, Cardiff School of Social Sciences
[8] Polwarth Building,Department of Public Health
[9] Cardiff University,Wessex Clinical Genetics Service
[10] University of Aberdeen,Department of Medical Genetics
[11] School of Medicine,North Trent Clinical Genetics Service, Blue Wing
[12] Polwarth Building,Department of Clinical Genetics
[13] The Princess Anne Hospital,undefined
[14] Belfast City Hospital Trust,undefined
[15] Sheffield Children's NHS Trust,undefined
[16] Churchill Hospital,undefined
来源
European Journal of Human Genetics | 2005年 / 13卷
关键词
confidentiality; disclosure; genetic information; genetic counselling;
D O I
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中图分类号
学科分类号
摘要
Patients attending genetic clinics are often the main gatekeepers of information for other family members. There has been much debate about the circumstances under which professionals may have an obligation, or may be permitted, to pass on personal genetic information about their clients but without their consent to other family members. We report findings from the first prospective study investigating the frequency with which genetics professionals become concerned about the failure of clients to pass on such information to their relatives. In all, 12 UK and two Australian regional genetic services reported such cases over 12 months, including details of actions taken by professionals in response to the clients' failure to disclose information. A total of 65 cases of nondisclosure were reported, representing <1% of the genetic clinic consultations in the collaborating centres during the study period. These included 39 cases of the failure of parents not passing full information to their adult offspring, 22 cases where siblings or other relatives were not given information and four cases where information was withheld from partners – including former and prospective partners. Professionals reported clients' reasons for withholding information as complex, more often citing concern and the desire to shield relatives from distress rather than poor family relationships. In most cases, the professionals took further steps to persuade their clients to make a disclosure but in no instance did the professional force a disclosure without the client's consent.
引用
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页码:556 / 562
页数:6
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