中药房调剂质量监管对中药处方的合理性及其临床用药安全性的影响
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上海市科委项目(13401901400)


Effects of Quality Control of Traditional Chinese Medicine Pharmacy on Rationality of Prescription and Safety of Clinical Drugs
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    摘要:

    目的:观察分析中药房调剂质量监管对中药处方的合理性与临床用药安全性的影响。方法:选取2014年12月至2016年6月在北京医院接受中药处方治疗的患者1 230例,在实施中药房调剂质量监管后收治的615例为观察组,另615例为对照组。比较2组处方不合理情况(包括药物数量、剂量的不合理等)、不良反应情况。结果:观察组处方合理率95.12%,不合理率4.88%,饮片数量、单味药材剂量不合理率分别为1.63%、3.58%;有毒、小毒药材使用率分别4.72%、21.63%;有毒和小毒药材剂量合理率97.53%。对照组处方合理率79.67%,不合理率20.33%;饮片数量、单味药材剂量不合理分别14.41%、19.19%;大毒、有毒、小毒药材的使用率分别为12.68%、32.68%;有毒、小毒药材剂量合理率82.44%;以上指标组间比较P<0.05。观察组、对照组不良反应分别1.79%、14.47%,P<0.05。观察组不良反应原因:饮片质量不佳36.36%,患者自身耐受性差63.64%,对照组饮片质量不佳23.60%、配伍禁忌16.85%、药物使用方法不规范21.35%、患者耐受性差38.20%。结论:中药房调剂质量监管可有效提高中药处方的合理性和临床用药安全性,能够降低不良反应,适合临床推广。

    Abstract:

    To observe the effects of quality control of TCM pharmacy on the rationality of prescription and the safety of clinical drug.Methods:A total of 1 230 patients who were treated with TCM prescription in our hospital from December 2014 to June 2016 were chosen and divided into observation group and control group after the implementation of quality control,with 615 cases in each group.Unreasonable conditions (including improper number and dose of drugs),adverse reactions of 2 groups were compared.Results:In observation group,the rationality rate was 95.12%,and the irrationality rate was 4.88%.The irrationality rates of the number of herbs and the dose of the single herb were 1.63% and 3.58% respectively.The use rates of toxic and little toxic drug were 4.72% and 21.63% respectively.The rationality rate of the herbs with toxin and little toxin was 97.53%.In the control group,the rationality rate was 79.67%,and the irrationality rate was 20.33%.The irrationality rates of the number of herbs and the dose of the single herb were 14.41% and 19.19% respectively.The use rates of toxic and little toxic drug were 12.68% and 32.68% respectively.The rationality rate of the herbs with toxin and little toxin was 82.44%.The differences in the above indexes among groups were statistically significant (P<0.05).The rates of adverse effects in the observation group and the control group were 1.79% and 14.47% respectively (P<0.05).The reasons for the adverse effects in the observation group included poor quality of herbs (36.36%),poor tolerance of patients (63.64%).The reasons for the adverse effects in the control group included poor quality of herbs (23.60%),incompatibility of prescription (16.85%),lack of standardization in the use of drugs (21.35%) and poor tolerance of patients (38.20%).Conclusion:The quality control of TCM pharmacy can effectively improve the rationality of TCM prescription and the safety of clinical medicine,which can reduce the adverse reaction and be suitable for clinical promotion.

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张红梅,高素强,王志军.中药房调剂质量监管对中药处方的合理性及其临床用药安全性的影响[J].世界中医药,2017,(10).

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  • 收稿日期:2017-09-25
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  • 在线发布日期: 2017-11-08
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