摘要
目的:探讨中药临床合理用药安全性分析。方法选取2013年9月~2014年11月36例我院给予中药临床用药的患者,随机分为实验组和对照组,实验组采用在安全管理模式下给予临床用药,对照组采用中药常规用药,观察两组患者的中药临床用药效果。结果实验组患者不良反应的发生率、用药不安全发生率优于对照组,差异有统计学意义(P〈0.05)。结论规范中药临床用药可以提高用药的安全性,降低不良反应的发生率和用药不安全率。
Objective Medication safety of traditional chinese medicine reasonable application is to be investigated. Methods We chose 36 patients who were treated with traditional chinese medication in hospital from September 2013 to November 2014 and separated them into study group and control group at random,patients in study group were given clinical medication treatment under control of safety management,while patients in control group were given conventional traditional chinese medication treatment,and then observed and compared treatment effects between two groups. Results Compared to control group,side-effect incidence and unsafe medication probability in study group were significantly lower,there was a treatment differential between two groups,and such a differential had statistic value(P〈0.05). Conclusion Standardize traditional chinese medication treatment is able to improve medication safety and reduce side-effect incidence as wel as unsafe medication probability.
出处
《中国卫生标准管理》
2015年第11期108-109,共2页
China Health Standard Management
关键词
中药
临床合理用药
安全性
Traditional chinese medicine
Clinical y reasonable medication application
Safety