摘要
目的分析临床用药风险因素,积极探索临床安全用药措施。方法从药品风险因素入手,结合药品在临床使用各个环节容易出现的风险问题,有针对性地进行阐述和分析。结果合理储存药物、静脉配置中心的建立、不良反应监测制度的完善、用药差错报告制度的建立以及医院信息系统的完善,将对降低临床用药风险产生促进作用。结论加强临床用药风险管理,对于提高医疗质量有十分重要的意义。
Objective Analyze the risk factors of clinical medicine and explore the measures of clinical medicine. Methods From the risk factors of drugs, risks that can easily arise in all aspects of clinical drug use were described and analyzed. Results Reasonable drug storage, the establishment of intravenous admixture services, the improvement of adverse reaction monitoring system, the establishment of medicine errors report and the improvement of hospital information system, will contribute stimulative effect to reducing the risk of clinical medicine. Conclusion It is important for improving the quality of medicine to strengthen clinical drug risk management.
出处
《中国现代药物应用》
2012年第9期126-129,共4页
Chinese Journal of Modern Drug Application
关键词
临床用药
风险因素
对策
Clinical medicine
Risk factor
Measures
