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作 者:何春容[1] 黄杰[1] 黄潇苇[1] 吴晓丽[1]
机构地区:[1]成都市第三人民医院检验科,四川成都610031
出 处:《四川生理科学杂志》2012年第1期8-11,共4页Sichuan Journal of Physiological Sciences
摘 要:目的:分析本实验室两台仪器Elecsys2010和Elecsys170同时测定血清神经元特异性烯醇化酶(NSE)和细胞角蛋白片段(CFYRA21-1)的结果,探讨这两个项目的可比性,以确保不同仪器在检测相同项目时结果的准确性和一致性。方法:根据美国临床实验室标准化委员会(NCCLS)EP9-A2文件的要求,以Elecsys2010为比较方法,Elecsys170为试验方法,平行测定40例病人血清中的NSE和CYFRA21-1浓度,计算各自的相关系数、直线回归方程和临界值处的相对偏差(SE%),并评价两方法检测结果的可比性。结果:(1)NSE和CYFRA21-1在两台仪器上的检测结果均有差异,Elecsys170的检测结果都低于Elecsys2010。(2)NSE和CYFRA21-1在两台仪器上的检测结果相关性均较好,相关系数都大于97.5%。(3)临床可接受性:NSE和CYFRA21-1在各自临界值处的偏差均在临床可接受的范围内。结论:当同一实验室同一检验项目存在2个以上的检测系统时,应进行方法比对和偏差评估,以保证检验结果的可比性。Objective: To analyze the comparability of serum NSE and CYFRA21-1 to confirm the accuracy and consistency between the two instruments. Methods: According to National Committee for Clinical Laboratory Standards(NCCLS) document EP9- A2, Elecsys2010 (comparison method) and Eleesys170 (laboratory method) were used respectively to measure the serum concentrations of NSE and CYFRA21-1 of 40 patients. The correlation coefficient, the linear equation and the relative system bias (SE~) at their cutoff levels were measured subsequently to evaluate the comparability of the two instruments. Results. (1) Serum NSE and CYFRA21-1 were lower detected by Eleesysl70 than Elecsys2010. (2)Both of the two instruments had a great correlation and the correlation coefficient of each item was above 97.5%. (3) Clinical acceptability: The bias of NSE and CYFRA21--1 at their cutoff values were both acceptable in clinic. Conclusions: If the same test is determined in more than two systems, it is necessary to judge clinical acceptability by method comparison and bias estimation so as to insure the comparability.
关 键 词:NSE CYFRA21-1方法比对 偏差评估
分 类 号:R197.39[医药卫生—卫生事业管理]
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