摘要
分析了人工智能(artificial intelligence,AI)辅助检测医疗器械临床使用的常见风险,提出了完善AI辅助检测医疗器械设计、确保数据安全及完善社会和法律监管等应对措施,为进一步实现临床资源与数据资源的高效整合、确保医疗器械使用安全提供了参考。
The common risks of artificial intelligence-aided medical detection devices during the clinical application were analyzed.Some measures were put forward such as improving the design of the devices,ensuring data security and enhancing social and legal supervision,and references were provided for efficiently integrating clinical and data resources and achieving safety during the clinical application of medical devices.
作者
张晓燕
刘雨田
王统彩
朱丹丹
李岳飞
ZHANG Xiao-yan;LIU Yu-tian;WANG Tong-cai;ZHU Dan-dan;LI Yue-fei(Department of Medical Engineering,Inner Mongolia People's Hospital,Hohhot 010017,China;Department of Orthopedics,Hohhot First Hospital,Hohhot 010030,China;Geriatrics Center,Inner Mongolia People's Hospital,Hohhot 010017,China)
出处
《医疗卫生装备》
CAS
2024年第11期77-82,共6页
Chinese Medical Equipment Journal
基金
内蒙古自治区科技计划项目(2021GG0135)
内蒙古自治区卫生健康委员会公立医院科研联合基金科技项目(2023GLLH0088)
内蒙古自治区卫生健康委员会公立医院科研联合基金科技项目(2023GLLH0098)。
关键词
人工智能
人工智能医疗器械
人工智能辅助检测医疗器械
临床使用
风险因素分析
artificial intelligence
artificial intelligence medical device
artificial intelligence-aided medical detection device
clinical application
risk factor analysis
