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The human capacity to reflect and decide: Bioethics and the reconfiguration of the research subject in the British biomedical sciences

机译:人类反映和做出决定的能力:生物伦理学和英国生物医学科学领域的研究课题的重塑

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摘要

This article examines how a fundamental element of the British bioethical assemblage - the literature on informed consent published between 1980 and 2000, a period when bioethics became a powerful force in the UK - has influenced contemporary understandings of the research subject. Drawing on Foucault, the article argues that this corpus of texts has created a sphere of possibilities in which research subjects can imagine themselves as human beings who reflect and decide whether they want to participate in medical experimentation. In particular, it shows how the narratives found in these texts portray relationships between researchers and their human subjects as 'paternalistic', and calls for their replacement by new, more ethical relationships characterized by both 'dialogue' and 'respect' and articulated around subjects who can 'think and take decisions'. It also discusses the different strategies - using patient information sheets, a list of possible questions and invitations to take time to reflect - which the bioethical literature has developed in order to realise these new, ethical relationships. As the article suggests, these narratives and strategies provide researchers and research subjects with models and examples of how to interact with each other that are very different from the ones that prevailed before the emergence of bioethics.
机译:本文研究了英国生物伦理学的一个基本要素(1980年至2000年发表的有关知情同意的文献),这是生物伦理学在英国成为强大力量的时期,它如何影响了当代对研究主题的理解。文章以福柯为基础,认为这种语料库创造了一个可能性范围,研究对象可以将自己想象成反映并决定是否要参加医学实验的人类。特别是,它显示了这些文本中的叙述是如何将研究人员与人类受试者之间的关系描绘为“家长式”的,并要求将其替换为以“对话”和“尊重”为特征并围绕受试者进行阐述的新的,更道德的关系。谁可以“思考并做出决定”。它也讨论了不同的策略-使用患者信息表,可能的问题列表和需要花时间反映的邀请-生物伦理学文献为了实现这些新的伦理关系而发展起来。正如文章所暗示的那样,这些叙述和策略为研究人员和研究对象提供了如何与彼此互动的模型和示例,这些模型和示例与生物伦理学出现之前的模型和示例有很大不同。

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