摘要
目的:了解我院医务人员自愿呈报的药品不良反应/事件(ADR/ADE)报告的质量。方法:采取系统抽样法,分别从我院2004-2009年每年报告中抽取100份,共计600份;运用EpiData3.02软件录入数据、SPSS15.0软件统计分析数据。结果:我院ADR/ADE报告总体填报质量不高,0～4级报告分别为25.50%、3.83%、4.67%、47.67%、18.33%;问题主要表现为部分信息缺失或填写不规范,关联性评价不准确等。经我院ADR监测小组修订后报告质量有较大幅度提高。结论:临床应高度重视ADR/ADE报告质量,努力发现存在问题,适时进行干预,逐步提高ADR/ADE报告利用价值。
OBJECTIVE： To investigate the quality of adverse drug reaction （ADR） or adverse drug event （ADE） spontaneously reported by medical staff in our hospital. METHODS ： 600 reports were selected in our hospital from 2004- 2009 by means of systematic sampling method, input by EpiData 3.02 software, and analyzed by SPSS 15.0 software. RESULTS： The quality of the reports was not good, reports at 0-4 levels accounted for 25.50%, 3.83%, 4.67%, 47.67% and 18.33%, respectively. There were several problems about them, such as some information missing, nonstandard reporting and illogical causality assessment. There was a big improvement in quality of reports after modification of the experts by our ADR monitoring team. CONCLUSION： It is suggested that we should strengthen ADR/ADE monitoring, find out problems and timely disposal so as to improve the utilization value ofADR/ADE reoorts.
出处
《中国药房》
CAS
CSCD
北大核心
2011年第2期159-161,共3页
China Pharmacy
基金
安徽省2009年度软科学计划项目(09030503074)
关键词
药品不良反应
药品不良事件
报告
质量评价
Adverse drug reaction
Adverse drug event
Report
Quality evaluation
