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Survey of European clinical geneticists on awareness, experiences and attitudes towards direct-to-consumer genetic testing

机译:欧洲临床遗传学家对直接面向消费者的基因测试的认识,经验和态度的调查

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Background The advent of direct-to-consumer (DTC) genetic testing (GT) has sparked a number of debates regarding the scientific validity of tests, their broad health and ethical implications for society as well as their legal status. To date, relatively few empirical studies have been published regarding this phenomenon. We conducted a survey of European clinical geneticists to gauge their awareness of, experiences with, and attitudes towards DTC GT. Methods We invited 300 clinical geneticists from 28 European countries to complete an online questionnaire. Statistical analyses of closed-ended questions were performed using the STATISTICA software package. Answers to open-ended questions were analysed for recurring themes. Results One hundred and thirty-one clinical geneticists answered our survey (response rate, 44%). Eighty-six percent (110/128) of respondents were aware of DTC GT, and over one-third had been contacted by at least one patient regarding these services. The majority (84%) of respondents did not agree with telephone medical supervision outside of an established doctor-patient relationship. The majority of clinical geneticists also found it unacceptable to provide non-face-to-face medical supervision for: (i) a presymptomatic test for a condition with very high penetrance; (ii) a predictive test for a condition that has a 'medium' penetrance of 50% to 60%; and (iii) carrier testing. For conditions that are neither treatable nor preventable and for disorders with serious health consequences, clinical geneticists were almost unanimous in expressing the unacceptability of offering such genetic tests outside of the traditional healthcare setting, without an established physician-patient relationship and without face-to-face medical supervision. Conclusion A high percentage of European clinical geneticists are aware of DTC GT and the majority do not agree with the model of provision used by many commercial companies for certain severe or actionable health conditions. Despite this disagreement with the DTC model of provision, >85% of respondents said that they would offer genetic counselling to patients who asked for a consultation after having undergone DTC genetic testing. The understanding of the views and opinions of this expert stakeholder group should be considered in the attempts to shape responsible policy and guidelines for these services.
机译:背景技术直接面向消费者(DTC)的基因检测(GT)的出现引发了关于检测的科学有效性,检测的广泛健康和对社会的伦理影响以及其法律地位的众多争论。迄今为止,关于这种现象的经验研究相对较少。我们对欧洲临床遗传学家进行了一项调查,以评估他们对DTC GT的认识,经历和态度。方法我们邀请了来自28个欧洲国家的300名临床遗传学家完成在线问卷。使用STATISTICA软件包对封闭式问题进行了统计分析。对开放式问题的答案进行了反复分析。结果131位临床遗传学家回答了我们的调查(答复率为44%)。百分之八十六(110/128)的被调查者知道DTC GT,并且至少三分之一的患者就这些服务与DTC取得了联系。大多数(84%)的受访者不同意在既定的医患关系之外进行电话医疗监督。大多数临床遗传学家还发现为以下情况提供非面对面的医学监督是不可接受的:(i)对渗透率很高的病症进行症状前检查; (ii)对“中度”渗透率为50%至60%的疾病的预测性测试; (iii)运营商测试。对于既无法治疗也无法预防的疾病以及对健康造成严重后果的疾病,临床遗传学家几乎一致表示无法接受传统医疗环境之外提供的此类基因检测,没有既定的医患关系,也没有面对面的面对医疗监督。结论大多数欧洲临床遗传学家都知道DTC GT,并且大多数人不认同许多商业公司针对某些严重或可采取的健康状况所采用的提供模式。尽管与DTC的提供模式存在分歧,但仍有超过85%的受访者表示,他们将为接受DTC基因测试后要求咨询的患者提供基因咨询。在试图为这些服务制定负责任的政策和指南时,应考虑对该专家利益相关者小组的观点和意见的理解。

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