Miller Franklin G
Department of Bioethics, National Institutes of Health, USA.
J Law Med Ethics. 2008 Fall;36(3):560-6. doi: 10.1111/j.1748-720X.2008.304.x.
Observational research involving access to personally identifiable data in medical records has often been conducted without informed consent, owing to practical barriers to soliciting consent and concerns about selection bias. Nevertheless, medical records research without informed consent appears to conflict with basic ethical norms relating to clinical research and personal privacy. This article analyzes the scope of these norms and provides an ethical justification for research using personally identifiable medical information without consent.
由于获取知情同意存在实际障碍以及对选择偏倚的担忧,涉及获取病历中个人可识别数据的观察性研究常常在未获得知情同意的情况下进行。然而,未经知情同意的病历研究似乎与临床研究和个人隐私的基本伦理规范相冲突。本文分析了这些规范的范围,并为未经同意使用个人可识别医疗信息的研究提供了伦理依据。