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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 To analyze the risk factors of clinical medication and actively explore clinical safe medication. Methods Starting with the risk factors of drugs, combined with the risks of drugs prone to occur in all aspects of clinical use, the methods were elaborated and analyzed in a targeted manner. Results The rational storage of drugs, the establishment of venous distribution center, the improvement of adverse reaction monitoring system, the establishment of medication error reporting system and the improvement of hospital information system will reduce the risk of clinical medication. Conclusion Strengthening the risk management of clinical medication is of great significance to improving the quality of medical care.