在Covid的同意:一个研究人员的困境
1All India Institute of Medical Sciences (AIIMS), New Delhi, India.
Trends in anaesthesia & critical care
|April 15, 2024
概括
在COVID-19大流行期间,获得医疗保健和研究的知情同意是具有挑战性的. 为了确保患者的安全,需要进行修改,包括电子工具和特定的COVID-19同意书.
科学领域:
- 医学伦理 医学伦理
- 公共卫生 公共卫生
- 临床研究 临床研究
背景情况:
- 在医疗保健和研究中,知情同意对于患者安全至关重要.
- 由于COVID-19的流行,在医院环境中获得知情同意面临着重大挑战.
- 在公共卫生危机期间,传统的同意程序可能不足.
研究的目的:
- 在COVID-19大流行期间审查知情同意的复杂性.
- 确定对研究许可程序的必要修改.
- 强调在同意过程中患者安全的重要性.
主要方法:
- 对当前实践和知情同意方面的挑战进行文献综述.
- 分析疫情期间研究协议所需的修改.
- 讨论替代沟通方法和同意类型.
主要成果:
- 现有的同意表格需要调整以应对流行病特定风险.
- 技术和电子工具是沟通和同意的可行的替代方案.
- 可能需要新的同意策略,包括推迟,先发或放弃同意.
结论:
- 研究同意程序必须针对COVID-19大流行个性化并更新.
- 采用技术和灵活的同意模式对于正在进行的研究至关重要.
- 在同意过程中,确保患者的安全和理解仍然至关重要.
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