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How should we deal with misattributed paternity? A survey of lay public attitudes

机译:我们应该如何应对误报的父亲? 奠定公众态度调查

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Background: Increasing use of genetic technologies in clinical and research settings increases the potential for misattributed paternity to be identified. Yet existing guidance from the President's Commission for the Study of Ethical Problems in Biomedical and Behavioral Research and the Institute of Medicine (among others) offers contradictory advice. Genetic health professionals are thus likely to vary in their practice when misattributed paternity is identified, and empirical investigation into the disclosure of misattributed paternity is scarce. Given the relevance of this ethical dilemma and its significance to users of genetic services, this study aimed to investigate the attitudes of lay people with regard to the disclosure of misattributed paternity. Methods: An online questionnaire was hosted and advertised through Amazon's Mechanical Turk to 200 United States residents aged 18 years or older. Respondents were asked to rate (via a Likert scale) the ethical permissibility of possible actions a clinician may carry out when misattributed paternity is identified. Data analysis consisted of preliminary descriptive analysis, chi-squared analysis, and Wilcoxon signed-rank tests. Results: There was no clear majority support for many of the options surveyed across different contexts, with only six out often scenarios displaying some general consensus. Men were more likely to support scenarios where the father is informed of paternity. Importantly, participants' views varied according to whether the desires of the father were previously expressed, suggesting that perceptions of the permissibility of a clinician's action will depend on the interests of all parties affected. Conclusions: This sample of the general public showed attitudes that were, at least to some degree, at variance with some professional guidelines. We give arguments for why at least some of these attitudes might be justified. We argue that case-specific judgments should be made and outline some of the relevant ethical considerations. While general guidelines ought to be considered, context-specific moral judgments cannot be avoided.
机译:背景:越来越多地利用临床和研究环境在临床和研究环境中的利用增加了要识别误诊的歧视物的可能性。然而,总统委员会在生物医学和行为研究中研究道德问题和医学研究所(等)的现有指导提供了矛盾的建议。因此,当确定误判亲子关系时,遗传卫生专业人员可能会在其实践中变化,并且对误报的歧化性披露的实证调查是稀缺的。鉴于这种道德困境的相关性及其对遗传服务用户的意义,这项研究旨在调查勒索人披露误解亲子关系的态度。方法:通过亚马逊机械土耳其托管,通过亚马逊的机械土耳其到200年龄18岁或以上的美国居民送达并宣传。受访者被要求率(通过李克特量表),可能行动的道德允许临床医生可以在识别误判亲子关系时进行。数据分析包括初步描述性分析,Chi平方分析和Wilcoxon签名级别测试。结果:对不同背景调查的许多选项没有明确的多数支持,通常只有六个方案展示了一些一般共识。男人更有可能支持父亲被告知亲子关系的情景。重要的是,参与者的观点根据父亲的愿望先前表达,表明对临床医生行动允许性的看法将取决于所有受影响的各方的利益。结论:这次普通公众的这种样本表明,至少在某种程度上以某种专业指南方差的态度表现出态度。我们为什么至少有一些这些态度提供争论可能是合理的。我们认为应符合具体情况判决并概述一些相关的道德考虑因素。虽然应该考虑一般指导方针,但无法避免具体的上下文的道德判决。

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