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目的:探究调剂质量监管对中药房中药处方有效性及安全性的影响。方法:医院自2014年9月在中药房实施调剂质量监管模式,选取2014年1~8月收治的500例患者作为对照组,选取2014年9月~2015年4月收治的500例患者作为观察组。比较分析两组患者不良反应发生率。结果:观察组患者不良反应发生率,明显低于对照组患者(P<0.05)。结论:调剂质量监管模式,能够有效提高中药房中药处方的有效性和安全性,降低各类不良事件的发生。
Objective: To explore the effect of regulating the quality of medicines on the prescription effectiveness and safety of traditional Chinese medicine pharmacy prescriptions. Methods: Since September 2014, the hospital implemented the quality control regulation in the pharmacy. Five hundred and fifty patients admitted from January to August in 2014 were selected as the control group. 500 patients admitted from September 2014 to April 2015 were selected as the observation group group. Comparative analysis of two groups of patients with adverse reactions. Results: The incidence of adverse reactions in the observation group was significantly lower than that in the control group (P <0.05). Conclusion: The quality control mode of adjustment can effectively improve the effectiveness and safety of traditional Chinese medicine prescriptions, and reduce the incidence of various types of adverse events.