Lowe Georgia, Pugh Jonathan, Kahane Guy, Corben Louise, Lewis Sharon, Delatycki Martin, Savulescu Julian
a Bruce Lefroy Centre for Genetic Health Research Murdoch Children's Research Institute and Department of Paediatrics , University of Melbourne.
b Uehiro Centre for Practical Ethics , University of Oxford.
AJOB Empir Bioeth. 2017 Oct-Dec;8(4):234-242. doi: 10.1080/23294515.2017.1378751. Epub 2017 Sep 29.
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.
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.
There was no clear majority support for many of the options surveyed across different contexts, with only six out of ten 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.
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.
基因技术在临床和研究环境中的使用日益增加,使得识别错误认定的亲子关系的可能性增大。然而,总统生物医学和行为研究伦理问题研究委员会以及医学研究所(以及其他机构)给出的现有指导意见相互矛盾。因此,当识别出错误认定的亲子关系时,基因健康专业人员的做法可能会有所不同,而且关于披露错误认定亲子关系的实证研究很少。鉴于这一伦理困境的相关性及其对基因服务使用者的重要性,本研究旨在调查普通民众对披露错误认定亲子关系的态度。
通过亚马逊的土耳其机器人平台向200名18岁及以上的美国居民发放并宣传了一份在线问卷。要求受访者(通过李克特量表)对临床医生在识别出错误认定的亲子关系时可能采取的行动的道德可允许性进行评分。数据分析包括初步描述性分析、卡方分析和威尔科克森符号秩检验。
在不同背景下调查的许多选项中,没有明显的多数支持,十个情景中只有六个显示出一些普遍共识。男性更有可能支持告知父亲亲子关系的情景。重要的是,参与者的观点因父亲的意愿是否先前已表达而有所不同,这表明对临床医生行为可允许性的认知将取决于所有受影响方的利益。
这一普通公众样本显示出的态度至少在一定程度上与一些专业指南不一致。我们给出了为什么至少其中一些态度可能合理的论据。我们认为应该进行具体案例的判断,并概述一些相关的伦理考量。虽然应该考虑一般指南,但特定情境的道德判断无法避免。