论文部分内容阅读
目的:分析并总结加强中药房调剂质量的监管方式及其对药物临床应用的分析。方法:回顾性分析某院2013年中药房调剂质量监管体系建立和评价的方法及其注意事项,对比质量监管体系建立前后药物不良反应事件发生情况。结果:通过2012年与2013年情况对比可见,中药房调剂质量监管体系建立后,药物不良反应事件发生率明显下降(P<0.05)。结论:医院中药房应当重视规范程序操作,严格按照医用处方抓药,加强药方的审查力度,使调配剂量及临时处理准确无误,保证中药饮品质量安全,并注意脚注和发药前对患者的交代。良好的中药房调剂质量监管体系对提升药物临床应用的安全性和有效性都有非常重要的意义。
OBJECTIVE: To analyze and summarize the regulatory methods of enhancing the quality of the pharmacy and its analysis of the clinical application of the drug. Methods: A retrospective analysis of a hospital in 2013 pharmacy transfer quality supervision system establishment and evaluation methods and precautions, contrast quality control system before and after the establishment of adverse drug reactions events. Results: According to the comparison between 2012 and 2013, the incidence of ADRs in pharmacy pharmacies decreased significantly (P <0.05) after the regulation system was established. Conclusion: The pharmacy in the hospital should pay attention to the standard procedure operation, strictly follow the prescription of medical prescription, strengthen the examination of the prescription, make the dosage and temporary treatment accurate, guarantee the quality and safety of the traditional Chinese medicine drink, and pay attention to the explanation of the footnote and the patient before delivery. Good pharmacy transfer quality regulation system to improve the clinical safety of drugs and have a very important significance.