摘要
目的形成适合大型医疗机构的系统性药品不良反应(ADR)监测工作模式。方法利用良好的医院信息系统(HIS)运行环境和临床药学工作基础展开实践。结果形成了ADR监测的3级工作团队、2项工作规章、6项操作规程、1套药品安全突发事件应急处置流程、1本刊物、1份通报,实现了ADR数据采集、评价、分析、信息预警和流转的电子化,完成了多项结合实际的药品安全性评价应用研究。结论通过规章流程建设、信息平台开发、数据利用、应急处置和宣教培训的多方位工作探索与实践,优化了医疗机构药品ADR监测模式,成为药品风险控制的坚实前哨。
Objective To form systemic adverse drug reaction monitoring mode of the large-scale medical institution. Methods Practice on the basis of good hospital information system（HIS） operation environment and clinical pharmacy developement. Results The formation of grade 3 monitoring work team, 2 work rules, 6 procedures, a set of drug safety and emergency treatment process, a house journal, a bulletin, obtains ADR data acquisition, evaluation, analysis, early warning and transmission of electronic information, and combining with actual completed a series of drug safety evaluation of applied research. Conclusion Through the rules and process electronic platform construction, development, data utilization, emergency disposal and intersectorial work missionary training to optimize the exploration and practice of medical institution, obtains the solid outpost of drug safety and risk management.
出处
《中国药物警戒》
2010年第3期164-168,共5页
Chinese Journal of Pharmacovigilance
