Analysis of 365 Cases of Adverse Events Reported by Electronic Infusion Pump
MA Danhua1,2, NIE Shengdong1, BIAN Rongrong2, LI Yao2
1. School of Medical Equipment and Food, Shanghai University of Science and Technology, Shanghai 200093, China;
2. Jiangsu Provincial Monitoring Center for Adverse Drug Reactions, Nanjing Jiangsu 210002, China
Abstract：Objective To provide reference for rational use in the clinic via investigating characteristics and possible causes of adverse
events in electronic infusion pump. Methods Retrospective analysis method was used to statistically analyze 365 cases of adverse
events of electronic infusion pump collected from Jiangsu database from January 1, 2016 to August 31, 2018. Results Among the 365 cases
reported, the majority were reported by medical institutions (94.79%), and the majority were women, with the highest proportion of
those aged between 21 and 30 years old (28.49%). The expected therapeutic and disease effects were mainly postoperative analgesia
(79.18%), and the adverse events were mostly component faults (64.38%). Conclusion After the occurrence of adverse events,
clinical medical staff should promptly remove the failure to ensure the safety of patients. The holder of the listing license shall fully
implement the main responsibility of the enterprise, attach importance to the monitoring of adverse reactions and be responsible for
the whole life cycle of the product.
马丹华1,2，聂生东1，卞蓉蓉2，李尧2. 365例电子输注泵不良事件报告分析[J]. 中国医疗设备, 2020, 35(4): 109-112.
MA Danhua1,2, NIE Shengdong1, BIAN Rongrong2, LI Yao2. Analysis of 365 Cases of Adverse Events Reported by Electronic Infusion Pump. China Medical Devices, 2020, 35(4): 109-112.
