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目的:了解西药房日常管理工作中展开药品分级监管技术的有效性。方法:抽选2014年10月-2015年10月间进入本院西药房取药1075例患者,对派药出错情况、概率进行统计,并于2015年11月-2016年11月间展开药品分级监管技术,同时选取1100例患者展开对比研究,观察此阶段药房出错状况,并对监管前/后所选病例满意度展开评估、统计。结果:展开药品分级监管技术后,出错率从2.79%降至0.18%(P<0.05)。结论:于西药房日常管理工作中展开药品分级监管技术可行性高。
OBJECTIVE: To understand the effectiveness of the drug classification regulatory technology in the daily management of western pharmacy. Methods: A total of 1075 patients admitted to our hospital from October 2014 to October 2015 were randomly selected to investigate the error rate and probability of drug delivery, and the drug grade was carried out between November 2015 and November 2016 Supervision technology, and select 1100 patients to conduct a comparative study to observe the pharmacy error status at this stage, and to monitor the satisfaction of selected patients before / after the assessment, statistics. Results: The error rate was reduced from 2.79% to 0.18% (P <0.05). Conclusion: It is feasible to carry out drug grade supervision technology in daily management of western pharmacy.