摘要
目的:对静配中心出现差错的原因进行总结,为今后进一步防范差错提供思路。方法:根据2012年2月-2013年11月我院静配中心差错登记本及工作量统计表,计算和比较各个不同时期的差错率,并对各配置环节出现的各类差错分类汇总,分析比较。结果:我院静配中心2012年2月-2013年11月共配置成品输液1124074袋,发生差错141袋,差错率为0.125‰,自运行以来差错发生率呈下降趋势,在各环节的各种差错中,退药处理失误、加药错误和用错注射器占有较大比例。结论:有针对性地采取一系列的防范措施可降低静配中心差错率,静配中心对于差错的防范是一项需要持续改进,常抓不懈的重要工作。
Objective： In order to reduce the error rate in our PIVAS,the data of error were summarized and analyzed. Methods： Error rates of different stage were calculated and compared, and the various errors were classified and summarized. Results： The error rate from February 2012 to November 2013 was 0.125‰, and the error rate of different stage have been declining. The main reasons of error were improper treatment of drug repercussion, mistake of drug adding and the misusing of syringes. Conclusion：A number of precautions should be persisted in order to decline the error rate in PIVAS.
出处
《药品评价》
CAS
2014年第12期40-42,共3页
Drug Evaluation
基金
"我省静脉用药调配中心管理模式和比较研究及探索"。山西省科技厅2013软科学项目
编号:2013041079-02
关键词
静配中心
用药差错
用药差错预防
Pharmacy Intravenous Admixture Service
Analysis of Errors
Preventive Measures
