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欧洲地方研究伦理委员会工作中的性别平等:五个国家的实践研究

Gender equality in the work of local research ethics committees in Europe: a study of practice in five countries.

作者信息

Moerman C J, Haafkens J A, Söderström M, Rásky E, Maguire P, Maschewsky-Schneider U, Norstedt M, Hahn D, Reinerth H, McKevitt N

机构信息

Department of General Practice, Room J2-222, Academic Medical Center, University of Amsterdam, Meibergdreef 15, 1105 AZ Amsterdam, The Netherlands.

出版信息

J Med Ethics. 2007 Feb;33(2):107-12. doi: 10.1136/jme.2005.015206.

Abstract

BACKGROUND

Funding organisations and research ethics committees (RECs) should play a part in strengthening attention to gender equality in clinical research. In the research policy of European Union (EU), funding measures have been taken to realise this, but such measures are lacking in the EU policy regarding RECs.

OBJECTIVE

To explore how RECs in Austria, Germany, Ireland, The Netherlands and Sweden deal with gender equality issues by asking two questions: (1) Do existing procedures promote representation of women and gender expertise in the committee? (2) How are sex and gender issues dealt with in protocol evaluation?

METHODS

Two RECs were selected from each country. Data were obtained through interviews with key informants and content analysis of relevant documents (regulations, guidelines and review tools in use in 2003).

RESULTS

All countries have rules (mostly informal) to ensure the presence of women on RECs; gender expertise is not required. Drug study protocols are carefully evaluated, sometimes on a formal basis, as regards the inclusion of women of childbearing age. The reason for excluding either one of the sexes or including specific groups of women or making a gender-specific risk-benefit analysis are investigated by some RECs. Such measures are, however, neither defined in the regulations nor integrated in review tools.

CONCLUSIONS

The RECs investigated in five European member states are found to pay limited attention to gender equality in their working methods and, in particular in protocol evaluation. Policy and regulations of EU are needed to strengthen attention to gender equality in the work of RECs.

摘要

背景

资助机构和研究伦理委员会(RECs)应在加强临床研究中对性别平等的关注方面发挥作用。在欧盟(EU)的研究政策中,已采取资助措施来实现这一目标,但在欧盟关于研究伦理委员会的政策中却缺乏此类措施。

目的

通过提出两个问题来探究奥地利、德国、爱尔兰、荷兰和瑞典的研究伦理委员会如何处理性别平等问题:(1)现有程序是否促进了女性在委员会中的代表性以及性别专业知识的参与?(2)在方案评估中如何处理性别问题?

方法

从每个国家选取两个研究伦理委员会。通过对关键信息提供者的访谈以及对相关文件(2003年使用的法规、指南和审查工具)的内容分析来获取数据。

结果

所有国家都有规则(大多是非正式的)以确保女性在研究伦理委员会中的存在;不需要性别专业知识。对于药物研究方案,会仔细评估育龄女性的纳入情况,有时是正式评估。一些研究伦理委员会会调查排除某一性别的原因、纳入特定女性群体的原因或进行针对性别的风险效益分析。然而,这些措施在法规中既未明确规定,也未纳入审查工具。

结论

在五个欧洲成员国中接受调查的研究伦理委员会在其工作方法中,特别是在方案评估中,对性别平等的关注有限。需要欧盟的政策和法规来加强对研究伦理委员会工作中性别平等的关注。

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