概括
患者有权知道什么时候人工智能 (AI) 在他们的医疗保健中被使用. 这种根植于知情同意的权利,对于患者的自主性至关重要,即使尚未明确法律.
科学领域:
- 医疗保健法律 医疗保健法律
- 生物伦理学生物伦理学
- 医疗信息学 医疗信息学
背景情况:
- 人工智能 (AI) 正在迅速融入各种医疗保健领域,包括诊断,治疗和管理.
- 在临床环境中使用人工智能带来了复杂的医疗,伦理和法律挑战,需要仔细考虑.
研究的目的:
- 审查医疗保健提供者的义务,以告知患者在临床实践中使用人工智能系统的情况.
- 检查这一职责的伦理基础,重点关注患者的自主权和获得信息和解释的权利.
- 分析现有的法律环境,包括欧盟人工智能法,GDPR和相关的国家卫生法.
主要方法:
- 系统审查与患者权利和知情同意有关的伦理原则.
- 对管理医疗保健人工智能的现行和拟议法律框架的分析.
- 审查相关的判例和专业指导方针.
主要成果:
- 患者自主权和信息权的伦理原则要求披露人工智能使用情况.
- 现有的法律框架虽然没有明确要求人工智能披露,但通过知情同意提供了这一义务的基础.
- 欧盟人工智能法和GDPR是影响医疗保健人工智能透明度的关键监管工具.
结论:
- 患者在临床决策中了解和了解AI在临床决策中的作用的权利可以从知情同意原则中得出.
- 为临床实践提供了建议,以确保有关AI使用的适当信息披露.
- 可能需要采取进一步的立法行动,明确规范患者在医疗保健中获得有关AI信息的权利.
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