摘要
通过对作者所在医院2018年度临床使用过程中涉及的25例真空采血管产品可疑不良事件,结合文献资料检索、生产企业现场调研等数据的汇总分析和研究,提出涉及该产品生产企业和临床使用机构对常见可疑不良事件的应对措施和风险控制的建议。
Based on 25 cases of suspected adverse events of vacuum blood collection products involved in the clinical use process of our hospital in 2018, combined with the data collection, analysis and research of literature retrieval, field investigation of production enterprises and other data, this paper puts forward the countermeasures and risk control suggestions for the common suspected adverse events of the production enterprises and clinical use organizations involved in this product.
作者
宣建桥
尹建兵
张淑霞
张兰
XUAN Jian-qiao;YIN Jian-bing;ZAHNG Shu-xia;ZHANG Lan(Yuyao Traditional Chinese Medicine Hospital,Zhejiang Yuyao 315400;Zhejiang Medical Device Adverse Event Monitoring and Safety Research Center,Zhejiang Hangzhou 310009;Huzhou Drug Adverse Drug Reaction Monitoring Center,Zhejiang Province,Zhejiang Huzhou 313000)
出处
《中国医疗器械信息》
2020年第1期34-35,162,共3页
China Medical Device Information
关键词
医疗器械
不良事件
风险点
真空采血管
medical device
adverse events
risk point
vacuum blood collection tube
