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类风湿关节炎患者足部健康研究的研究伦理报告——系统评价。

Reporting of Research Ethics in Studies Focusing on Foot Health in Patients with Rheumatoid Arthritis - A Systematic Review.

机构信息

8058University of Turku, Turku (Finland).

60652Turku University Hospital, Turku (Finland).

出版信息

J Empir Res Hum Res Ethics. 2022 Feb-Apr;17(1-2):39-51. doi: 10.1177/15562646211047654. Epub 2021 Oct 14.

Abstract

Research ethics is a fundamental part of the entire research. Patients with rheumatoid arthritis are sensitive group of research participants because their long-term health problems cause significant changes in their foot health. In foot health research, data are usually collected through a clinical assessment of the foot or questionnaires. However, there is limited evidence of the reported research ethics of empirical studies on foot health in patients with rheumatoid arthritis. Therefore this review aimed to analyze the reported research ethics of peer-reviewed empirical studies focusing on foot health in patients with rheumatoid arthritis as research participants. This systematic review used the Medline/PubMed, CINAHL, and Embase databases. A total of 1,653 records were identified, and 32 articles were included in the final analysis. Reporting research ethics in studies of patients with rheumatoid arthritis is fragmented, focusing predominantly on ethical approval and informed consent and lacking a broader discussion about research ethics.

摘要

研究伦理是整个研究的一个基本组成部分。类风湿关节炎患者是研究参与者中的敏感群体,因为他们长期的健康问题导致脚部健康发生重大变化。在脚部健康研究中,数据通常通过脚部临床评估或问卷调查收集。然而,类风湿关节炎患者脚部健康的实证研究报告的研究伦理证据有限。因此,本综述旨在分析以类风湿关节炎患者为研究参与者的脚部健康实证研究报告的研究伦理。本系统综述使用了 Medline/PubMed、CINAHL 和 Embase 数据库。共确定了 1653 条记录,最终分析纳入了 32 篇文章。类风湿关节炎患者研究中报告研究伦理的情况是零散的,主要集中在伦理批准和知情同意上,缺乏对研究伦理的更广泛讨论。

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