摘要
目的:为有效保证患者临床诊断的有效性,减少医疗风险,构建体外诊断试剂监管与检验设备的评价体系,对于临床诊断与治疗具有重要的意义。方法:通过对影响临床诊断的相关因素进行分析,从而探讨构建体外诊断试剂成本与检验设备性能评价监管体系,为体外诊断试剂管理与检验数据精确稳定提供参考。结果:通过形成良好的运行机制,将医院的检验试剂纳入统一管理,保证了全院检验结果的准确性、统一性和可比性。结论:通过规范医院临床体外诊断试剂的管理,降低检验和管理成本,为临床提供可靠的检验结果。
Objective：in order to effectively guarantee the validity of the clinical diagnosis of patients with reduced risk for treating patients,build the evaluation regulation system of in vitro reagent and construction equipment,has the vital significance for clinical diagnosis and treatment.Methods：through analyzing the related factors influencing the clinical diagnosis,so as to explore construction of in vitro diagnostic reagent cost and inspection equipment performance evaluation regulation system,provide reference for clinical diagnostic reagents and equipment inspection.Results：the operation mechanism,form a good floor test reagents should be brought into the unified management,ensure the partial test results of accuracy,consistency and comparability.Conclusion：through regulating the administration of hospital clinical in-vitro diagnostic reagent,can reduce the test cost and management cost,and provide reliable test for clinical.
出处
《中国医学装备》
2014年第8期87-89,共3页
China Medical Equipment
关键词
临床诊断试剂
检验设备
监管体系
Clinical diagnostic reagents
Inspection equipment
The regulatory system
