• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

大流行期间的研究伦理:IRB 如何做好准备

Research Ethics during Pandemics: How IRBs Can Prepare.

机构信息

Associate professor of psychiatry and medical education, the director of ethics education in psychiatry, and the assistant director of the Academy for Medicine & the Humanities at the Icahn School of Medicine at Mount Sinai and an attending physician at Mount Sinai Health System.

Associate professor of environmental medicine and public health and global health at the Icahn School of Medicine at Mount Sinai.

出版信息

Ethics Hum Res. 2023 Mar;45(2):26-34. doi: 10.1002/eahr.500159.

DOI:10.1002/eahr.500159
PMID:36974455
Abstract

The Covid-19 pandemic has raised a range of complex challenges for the research community in the United States. This essay uses Covid-19 as a model pandemic illness to consider two such issues that have yet to be fully explored in the ethics literature: first, whether the informed consent process should include a discussion of pandemic risks and, if so, how precisely these risks should be conveyed to potential research participants and, second, whether and under what circumstances vaccination status should be taken into consideration when enrolling subjects in non-pandemic-related studies during a pandemic.

摘要

新冠疫情给美国的研究界带来了一系列复杂的挑战。本文以新冠疫情为例,探讨了伦理学文献中尚未充分探讨的两个问题:一是知情同意过程是否应包含对大流行风险的讨论,如果需要,应如何向潜在的研究参与者准确传达这些风险;二是在大流行期间,在非大流行相关研究中招募研究对象时,是否以及在何种情况下应考虑疫苗接种状况。

相似文献

1
Research Ethics during Pandemics: How IRBs Can Prepare.大流行期间的研究伦理:IRB 如何做好准备
Ethics Hum Res. 2023 Mar;45(2):26-34. doi: 10.1002/eahr.500159.
2
Human Research During the COVID-19 Pandemic: Insights From Behind-the-Scenes.新冠疫情期间的人类研究:幕后观察。
Narrat Inq Bioeth. 2021;11(1):47-53. doi: 10.1353/nib.2021.0020.
3
A Call for Better, Not Faster, Research Ethics Committee Reviews in the Covid-19 Era.呼吁在新冠疫情时代加强而不是加速研究伦理委员会审查。
Ethics Hum Res. 2021 Sep;43(5):42-44. doi: 10.1002/eahr.500104.
4
Clinical investigation and informed consent form in times of COVID-19 pandemic. A vision from the committee ethics of research.新冠疫情期间的临床研究与知情同意书。研究伦理委员会的视角。
Med Clin (Barc). 2021 Nov 12;157(9):e307-e308. doi: 10.1016/j.medcli.2020.09.005. Epub 2020 Dec 5.
5
Challenges and proposed solutions in making clinical research on COVID-19 ethical: a status quo analysis across German research ethics committees.COVID-19临床研究伦理面临的挑战及建议解决方案:德国研究伦理委员会的现状分析
BMC Med Ethics. 2021 Jul 19;22(1):96. doi: 10.1186/s12910-021-00666-8.
6
Waivers and Alterations of Research Informed Consent During the COVID-19 Pandemic.研究知情同意在 COVID-19 大流行期间的豁免和变更。
Ann Intern Med. 2021 Mar;174(3):415-416. doi: 10.7326/M20-6993. Epub 2020 Dec 15.
7
How IRBs view and make decisions about consent forms.机构审查委员会如何看待同意书并做出相关决策。
J Empir Res Hum Res Ethics. 2013 Feb;8(1):8-19. doi: 10.1525/jer.2013.8.1.8.
8
Research on COVID-19: Stories from IRB Members, Research Administrators, & Investigators.关于新型冠状病毒肺炎的研究:来自机构审查委员会成员、研究管理人员和研究人员的故事。
Narrat Inq Bioeth. 2021;11(1):74-76. doi: 10.1353/nib.2021.0028.
9
Viewpoint: IRBs, hospital ethics committees, and the need for "translational informed consent".观点:机构审查委员会、医院伦理委员会以及“转化性知情同意”的必要性。
Acad Med. 2007 Jul;82(7):670-4. doi: 10.1097/ACM.0b013e31806743ef.
10
Government Initiatives for Research Ethics During COVID-19 Pandemic in Korea.韩国 COVID-19 大流行期间的研究伦理政府倡议。
J Korean Med Sci. 2024 Apr 1;39(12):e116. doi: 10.3346/jkms.2024.39.e116.