摘要
目的分析检验科质量管理中实验室信息管理系统的应用及效果。方法选取该院东西两院区检验科未更新完善实验室信息系统的时间段(2016年1—6月)与该院东西两院区检验科应用更新完善后实验室信息系统的时间段(2018年1—6月)进行对比,分析不同时间段下检验科不良事件的发生率、检验回报合格率、危急值报告及时率、危急值漏报率。结果2016年1—6月期间检验科不良事件发生率高于2018年1—6月(P<0.05);2016年1—6月检验回报合格率、危急值报告及时率低于2018年1—6月,危急值漏报率高于2018年1—6月(P<0.05)。结论与简单的收发报告的传统实验室信息系统相比较,应用完善的实验室信息管理系统对检验科质量管理具有积极意义,有利于减少检验科不良事件的发生,提高检验回报合格率、危急值报告及时率,增进检验科质量控制效果。
Objective To analyze the application and effect of laboratory information management system in quality management of laboratory.Methods Choose the things area division did not update the two perfect laboratory information system period(January-June 2016)and the things both houses the period after the completion of clinical laboratory application update laboratory information system(January-June 2018)to analysis the clinical laboratory under different time period,the incidence of adverse events,inspection qualified rate of return,the critical value and critical value report timely non-response rates.Results The incidence of adverse events in the laboratory from January to June 2016 was higher than that in January-June 2018(P<0.05);the rate of return on test returns from January to June 2016 was lower than that in January to June 2018,the rate of underreporting of critical values was higher than January-June 2018(P<0.05).Conclusion Compared with the traditional laboratory information system for sending and receiving reports,the well-equipped laboratory information management system has positive significance for the quality management of the laboratory,which is beneficial to reduce the occurrence of adverse events in the laboratory and improve the pass rate of inspection returns.The value reports the timely rate and improves the quality control effect of the laboratory.
作者
吴凌松
WU Ling-song(Department of Clinical Laboratory,Department of Plastic Surgery,Chinese Academy of Medical Sciences,Beijing,100144 China)
出处
《中国卫生产业》
2019年第33期17-18,21,共3页
China Health Industry
关键词
检验科
质量管理
实验室信息管理系统
不良事件
危急值报告
Laboratory
Quality management
Laboratory information management system
Adverse events
Critical value report
