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目的:通过加强中药调剂监管工作,来探讨如何减少中药房不良事件和相关差错的发生。方法:选取湖州市妇幼保健院在2015年6月~2016年6月在中药房开出的28944张处方,其中处方中有13924张为质量监管工作前开出的处方,15020张为质量监管工作后开出的处方。其中,对开展前和开展后的两组处方中出现的中药房药剂不良事件和相关差错进行统计学比较。结果:在中药房调剂时开展监督管理工作后发现,调剂监管工作前开出的处方出现的不良事件数量和相关差错的发生都高于质量调剂监管工作后的处方差错数值(P<0.05)。结论:通过在中药调剂工作中开展监督管理工作能够有效减少不良事件和相关差错的发生率,提高中药调剂质量,保证临床用药安全有效。
Objective: To explore how to reduce the occurrence of adverse events and related errors in traditional Chinese medicine pharmacies by strengthening the regulation of traditional Chinese medicine. Methods: 28,944 prescriptions in the pharmacy were collected from Huzhou MCH center from June 2015 to June 2016. Of the prescriptions, 13,924 prescriptions were issued before quality control and 15,020 were quality control Post-prescription. Among them, before and after the two sets of prescriptions occurred in pharmacy pharmacy adverse events and related errors were statistically compared. Results: The supervision and management work during the transfer of pharmacy was found to be more than the number of prescription errors (P <0.05) after the adjustment of quality control. Conclusion: By carrying out supervision and management in the adjustment of traditional Chinese medicine, it can effectively reduce the incidence of adverse events and related errors, improve the quality of Chinese medicine and ensure the safety and effectiveness of clinical medication.