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首页> 外文期刊>Disease markers >Ethical, Social and Economic Issues in Familial Breast Cancer: A Compilation of Views from the E.C. Biomed II Demonstration Project
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Ethical, Social and Economic Issues in Familial Breast Cancer: A Compilation of Views from the E.C. Biomed II Demonstration Project

机译:家族性乳腺癌的伦理,社会和经济问题:来自E.C. Biomed II示范项目的观点汇编

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Demand for clinical services for familial breast cancer is continuing to rise across Europe. Service provision is far from uniform and, in most centres, its evolution has been determined by local conditions, specifically by local research interests, rather than by central planning. However, in a number of countries there is evidence of progress towards co-ordinated development and audit of clinics providing risk assessment, counselling, screening and, in some cases, prophylactic intervention. Much important information should emerge from continued observation and comparative assessment of these developments.In most countries for which relevant data are available, there is a distinct bias towards higher social class among those who avail themselves of clinic facilities (in line with findings from many other health-promotion initiatives). This should be addressed when considering future organisation of clinical services.Molecular genetic studies designed to identify the underlying mutations responsible for familial breast cancer are not generally regarded as part of the clinical service and are funded through research grants (if at all). Economic considerations suggest that there is a case for keeping this policy under review.Familial cancers throw into sharp relief certain ethical and legal issues that have received much recent attention from government advisory bodies, patients’ representatives, professional commentators and the popular media. Two are of particular importance; first, the right to gain access to medical records of relatives, in order to provide accurate risk assessment for a given family member, versus the right to privacy in respect of personal medical information and, second, the obligation (or otherwise) to inform family members of their risk status if they have not actively sought that knowledge. The legal position seems to vary from country to country and, in many cases, is unclear. In view of pressures to establish uniform approaches to medical confidentiality across the EC, it is important to evaluate the experience of participants in this Demonstration Programme and to apply the principle of “non-malfeasance” in formulating regu-lations that should govern future practice in this field.Data on economic aspects of familial breast cancer are remarkably sparse and outdated. As evidence accrues on the influence of screening and intervention programmes on morbidity and mortality, there is a strong case for evaluating the cost-effectiveness of different models of service provision.
机译:在整个欧洲,对家族性乳腺癌临床服务的需求持续增长。服务提供远非统一,在大多数中心,服务的发展取决于当地条件,特别是取决于本地研究兴趣,而不是中央计划。但是,在许多国家中,有证据表明,在提供风险评估,咨询,筛查以及在某些情况下进行预防性干预的诊所的协调发展和审计方面取得了进展。通过对这些进展的持续观察和比较评估,应该会获得许多重要的信息。在可获得相关数据的大多数国家中,利用诊所设施的人中有明显的偏向于较高的社会阶层(与许多其他研究结果相一致)健康促进举措)。在考虑将来组织临床服务时应解决此问题。旨在鉴定导致家族性乳腺癌的潜在突变的分子遗传研究通常不被视为临床服务的一部分,而是由研究资助(如果有的话)资助的。经济上的考虑表明,有必要对该政策进行审查。家族性癌症使某些伦理和法律问题大为缓解,这些问题最近受到了政府咨询机构,患者代表,专业评论员和大众媒体的关注。有两个特别重要;首先,有权获得亲属的医疗记录,以便为给定的家庭成员提供准确的风险评估,而在个人医疗信息方面的隐私权,其次,是(或以其他方式)告知家庭的义务风险状态的成员,如果他们没有积极寻求知识。法律地位似乎因国家而异,在许多情况下还不清楚。鉴于在整个欧共体建立统一的医疗机密方法的压力,重要的是评估该示范计划参与者的经验,并在制定规范未来医疗实践的法规时运用“不渎职”原则。有关家族性乳腺癌的经济方面的数据非常稀少且过时。由于筛查和干预计划对发病率和死亡率的影响越来越多,因此有充分的理由来评估不同服务提供模式的成本效益。

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