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From Nuremberg to UNESCO: informed consent to medical treatment or exam

机译:从纽伦堡到联合国教科文组织:知情同意接受医疗或检查

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The informed consent to a medical treatment or participation in medical research is nowadays considered a fundamental standard of everyday practice and scientific research in medicine. However, accepting this standard, both in medical ethics and law, is not uniquely viewed upon in terms of its content or necessity. Starting from basic principles – human dignity and individual autonomy – UNESCO’s International Committee for Bioethics has offered in sketches of three bioethics declarations unique rules which must be followed in the application of this institute, and which were consequently adopted by consensus by all UNESCO state members. Following a short historical overview, this presentation examines the standards of patients’ consent to a medical measure or exam contained in UNESCO’s bioethics declarations, namely: Universal Declaration on Human Genome and Human Rights, International Declaration on Human Genetic Data and Universal Declaration on Bioethics and Human Rights. Th e presentation will show that declarations hold only minimum standards that protect patients or participants in medical exams from self-willing treatment or research and that the authors of these documents missed the opportunity to set rigorous and explicit rules for the applications of this institute. However, bearing in mind that most countries’ domestic legal regulations are not sufficiently elaborated in regards with biomedicine and that the existing domestic laws diff er in many aspects, the author shall show that the UNESCO’s bioethics declarations are a useful source and signposts for the domestic systems in defining ethical and legal regulations regarding biomedicine. Besides, even though these documents are not legally binding, one should bear in mind that declarations of this type are the first step towards the necessary protection of human rights with regards to biomedicine worldwide and they promote a new approach to solving bioethical dilemma based on the international law on human rights.
机译:如今,知情同意接受医学治疗或参与医学研究被认为是医学日常实践和科学研究的基本标准。但是,无论是从医学伦理还是从法律角度来看,接受该标准的内容或必要性都不是唯一的。联合国教科文组织国际生物伦理学委员会从基本原则(人的尊严和个人自治)开始,在三份生物伦理学宣言的草图中提出了在该研究所的应用中必须遵循的独特规则,因此,所有教科文组织会员国均以协商一致的方式通过了这些规则。在简短的历史回顾之后,本演示文稿研究了患者同意接受教科文组织生物伦理声明中所包含的医疗措施或检查的标准,这些宣言包括:《人类基因组和人权世界宣言》,《人类遗传数据国际宣言》和《世界生物伦理宣言》以及人权。演示文稿将表明,声明仅具有最低标准,可以保护患者或参加医学考试的人员免受自愿的治疗或研究,并且这些文档的作者错过了为该研究所的应用设定严格而明确的规则的机会。但是,考虑到大多数国家在生物医学方面的国内法律法规还不够完善,并且现有的国内法律在许多方面都存在差异,因此作者应表明,教科文组织的生物伦理宣言是国内生物医学的有用来源和标志。定义有关生物医学的道德和法律法规的系统。此外,尽管这些文件不具有法律约束力,但应牢记的是,此类声明是朝着在全球范围内对生物医学进行必要的保护人权的第一步,它们促进了解决生物伦理困境的新方法。国际人权法。

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