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[伦理与医学研究:原则、指南和法规]

[Ethics and medical research: principles, guidelines, and regulations].

作者信息

de Castilho Euclides Ayres, Kalil Jorge

机构信息

Departamento de Medicina Preventiva, Faculdade de Medicina, Universidade de São Paulo, Av. Dr. Arnaldo 455, 01246-903 São Paulo, SP, Brazil.

出版信息

Rev Soc Bras Med Trop. 2005 Jul-Aug;38(4):344-7. doi: 10.1590/s0037-86822005000400013. Epub 2005 Aug 3.

Abstract

The issue of ethics in medical research grew in importance at the end of World War II, after the Nuremberg Code. In this period, some cases in the United States had demonstrated the need for the establishment of rules and procedures in medical research. In this article, the authors discuss some ethical concepts and their philosophical basis, stressing aspects related to research. Ethics in medical research is based upon three items: peer approaches, subject informed consent, and confidentiality of individual obtained data. The authors also summarize the Brazilian laws and directives to follow the precepts and to control the process of ethical issues in research with human participants. Finally, they approach practical questions of the Informed Consent Form as a consequence of their experiences analyzing more than one thousand research projects per year as members of the Internal Review Board of the University of São Paulo School of Medicine, São Paulo, Brazil.

摘要

第二次世界大战结束后,在《纽伦堡法典》出台之后,医学研究中的伦理问题变得越发重要。在这一时期,美国的一些案例表明,医学研究需要建立规则和程序。在本文中,作者讨论了一些伦理概念及其哲学基础,重点强调了与研究相关的方面。医学研究中的伦理基于三项内容:同行方法、受试者知情同意以及所获取个人数据的保密性。作者还总结了巴西的法律和指令,以遵循这些准则并控制涉及人类受试者的研究中的伦理问题处理流程。最后,作为巴西圣保罗大学医学院内部审查委员会的成员,作者根据每年分析一千多个研究项目的经验,探讨了知情同意书的实际问题。

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