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[给患有遗传性疾病风险增加的家庭成员的信息]

[Information for family members with an increased risk for a genetic disease].

作者信息

Gordijn B

机构信息

Universitätsklinikum St Radboud, Fachbereich für Ethik, Philosophie und Geschichte der Medizin, Nijmegen, Niederlande.

出版信息

Dtsch Med Wochenschr. 2006 Mar 17;131(11):573-6. doi: 10.1055/s-2006-933700.

DOI:10.1055/s-2006-933700
PMID:16538564
Abstract

After a genetic diagnosis a physician might deem it important to inform family members of his counselee who might have an increased risk of having a certain genetic predisposition. Against this background this contribution analyzes the following ethical questions: 1. To what extent is the physician ethically obligated to see to it that the family members are being informed? 2. Are there circumstances under which the physician is ethically allowed to violate his obligation of confidentiality? 3. Is it ethically allowed to refuse a genetic test when the counselee does not agree with informing family members even if this might clearly be in their interest? 4. Is it ethically allowed to inform family members about an increased risk of a genetic predisposition in the family without their explicit request?

摘要

在进行基因诊断后,医生可能会认为告知其咨询对象的家庭成员很重要,因为这些家庭成员可能有更高的风险携带某种遗传易感性。在此背景下,本文分析了以下伦理问题:1. 医生在伦理上有多大义务确保家庭成员得到通知?2. 是否存在医生在伦理上被允许违反保密义务的情况?3. 当咨询对象不同意告知家庭成员时,即使这显然符合他们的利益,拒绝进行基因检测在伦理上是否被允许?4. 在没有家庭成员明确请求的情况下,告知他们家族中遗传易感性风险增加在伦理上是否被允许?

相似文献

1
[Information for family members with an increased risk for a genetic disease].[给患有遗传性疾病风险增加的家庭成员的信息]
Dtsch Med Wochenschr. 2006 Mar 17;131(11):573-6. doi: 10.1055/s-2006-933700.
2
Duty to warn at-risk relatives for genetic disease: genetic counselors' clinical experience.向有遗传疾病风险的亲属发出警告的职责:遗传咨询师的临床经验。
Am J Med Genet C Semin Med Genet. 2003 May 15;119C(1):27-34. doi: 10.1002/ajmg.c.10005.
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Ethical issues in ocular genetics.眼科遗传学中的伦理问题。
Curr Opin Ophthalmol. 2009 Sep;20(5):382-6. doi: 10.1097/ICU.0b013e32832f7feb.
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[The origin of informed consent].[知情同意的起源]
Acta Otorhinolaryngol Ital. 2005 Oct;25(5):312-27.
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Genetic testing and primary care: a new ethic for a new setting.基因检测与初级保健:新环境下的新伦理准则。
New Genet Soc. 2003 Dec;22(3):245-56. doi: 10.1080/1463677032000147207.
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The family covenant and genetic testing.家族契约与基因检测
Am J Bioeth. 2001 Summer;1(3):3-10. doi: 10.1162/152651601750417784.
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Informing family members about a hereditary predisposition to cancer: attitudes and practices among clinical geneticists.向家庭成员告知遗传性癌症易感性:临床遗传学家的态度和实践。
J Med Ethics. 2010 Jul;36(7):391-5. doi: 10.1136/jme.2009.033324.
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[Beyond the diagnosis of a genetic disease, the question of informing the relatives].[除了对遗传病进行诊断之外,还有告知亲属的问题]
Ann Pharm Fr. 2009 Jan;67(1):20-4. doi: 10.1016/j.pharma.2008.10.011. Epub 2008 Dec 6.
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Testing for genetic traits: the need for a new legal doctrine of informed consent.基因特征检测:对知情同意新法律原则的需求
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Ethical considerations of genetic testing.基因检测的伦理考量。
J Clin Ethics. 2002 Winter;13(4):316-23.

引用本文的文献

1
Genetic diagnosis, confidentiality and counseling: an ethics committee's potential deliberations about the do's and don'ts.
HEC Forum. 2007 Dec;19(4):303-12. doi: 10.1007/s10730-007-9057-y.