Publication ethics of human studies in the light of the Declaration of Helsinki – a mini-review

N. Sawicka-Gutaj, Dawid Gruszczyński, P. Guzik, A. Mostowska, J. Walkowiak
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引用次数: 27

Abstract

The Declaration of Helsinki is a set of ethical principles to be followed by scientists involved in medical research with humans or human cells and tissues. This Declaration defines how scientific research should be planned, carried out, documented, analysed, and published. We summarise and discuss some ethical issues related to publishing original articles, including clinical trials, review papers, and case reports based on the seventh revision of the Declaration of Helsinki. The principles of the Declaration of Helsinki refer most strongly to the publication of medical research results, in particular clinical trials, as original articles. Such papers must meet several ethical requirements, especially the study protocol transparency and the presentation of the results. For case reports, the bioethical aspects related to their publication are twofold - they must include informed and voluntary consent and the confidentiality of study participants. The review papers are of the least bioethical concern. However, whether patients' agreements with specific studies are valid if the data are used in meta-analyses is uncertain. Adherence to ethical policies and standards helps to ensure the highest possible quality of scientific publications. Responsibility for compliance with the Declaration of Helsinki lies not only with the authors preparing their manuscripts but also with the editorial board and reviewers, who must evaluate the ethical soundness of the submitted papers. The additional guidelines for the different types of studies facilitate the implementation of the Declaration principles.
《赫尔辛基宣言》视野下的人类研究出版伦理——一个小回顾
《赫尔辛基宣言》是参与人体或人体细胞和组织医学研究的科学家应遵守的一套伦理原则。本宣言规定了科学研究应如何规划、开展、记录、分析和发表。我们总结和讨论了一些与发表原创文章相关的伦理问题,包括临床试验、综述论文和基于赫尔辛基宣言第七次修订的病例报告。《赫尔辛基宣言》的原则最强烈地提到将医学研究成果,特别是临床试验成果作为原创文章发表。这样的论文必须满足一些伦理要求,特别是研究方案的透明度和结果的呈现。对于病例报告,与其发表相关的生物伦理方面是双重的——它们必须包括知情和自愿同意以及研究参与者的保密。这些评论论文最不涉及生物伦理问题。然而,如果数据用于荟萃分析,患者对特定研究的同意是否有效是不确定的。遵守伦理政策和标准有助于确保科学出版物的最高质量。遵守《赫尔辛基宣言》的责任不仅在于准备稿件的作者,也在于编辑委员会和审稿人,他们必须评估所提交论文的伦理合理性。针对不同类型研究的附加准则有助于《宣言》原则的实施。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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