应用EP10-A评价自动化学发光免疫分析系统

Evaluation of automated chemiluminescence system by EP10-A

目的 评价德国Bayer ACS:180SE(简称ACS:180SE)自动化学发光免疫分析系统相关性能,了解其现状。方法 应用美国临床实验室标准化委员会(NCCLS)颁布的《定量临床实验室方法初步评价;批准指南(EP10-A)》对 ACS:180SE自动化学发光免疫分析系统进行初步评价。结果 未见交叉污染、线性漂移等因素对精密度有明显影响。结论 ACS:180SE自动发光免疫分析系统性能可靠,适合临床实验室使用。

Objective To evaluate the performance of Bayer ACS:180SE automated chemiluminescencesystem in order to know its status. Methods Using the NCCLS Document EP10-A,i.e. Preliminary Evaluationof Quantitative Clinical Laboratory Methods;Approved Guideline.Results We have not found that thefactors of carryover and drift influence the imprecision significantly. Conclusions The performanceof Bayer ACS:180SE automated chemiluminescence system is reliable and suitable for clinical laboratoryto use.