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A comparison between China-made Mindray BS-2000M biochemical analyzer and Roche cobas702 automatic biochemical analyzer

机译:国产迈瑞BS-2000M生化分析仪与罗氏cobas702全自动生化分析仪的比较

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Objective: To assess the China-made equipment Mindray BS-2000M biochemical analyzer and explore the comparability between the results of the sixteen test parameters detected by Mindray BS-2000M biochemical analyzer and by imported equipment Roche cobas702 automatic biochemical analyzer. Methods: In line with the American Clinical Laboratory Standardization Committee (NCCLS) document EP9-A2, Switzerland Roche cobas702 biochemical analyzer was used as a comparison system, while the Mindray BS-2000M served as an experimental system. Sixteen biochemical parameters from forty cases at different levels were tested at the same time. The correlation coefficient(r), linearity regression equation and absolute deviation (SE) and relative deviation (SE%) of test detection system (Y) and control detection system (X) at different medical decision levels were calculated. The clinical acceptability and comparability between different detection systems were tested according to the standard of allowed total error of American Clinical Proficiency Testing Laboratory Improvement Amendments (CLIA'88). Results: The test results of the sixteen parameters between the two different biological detection systems were well-correlated (r^2 =0.95, p0.01). Linearity study showed acceptable linearity ranges for all the parameters. The relative deviation SE% of sixteen biochemical parameters at different medical decisions levels, excepting relative deviation of TP at two levels and TBIL at one level was greater than 1/2 CLIA 88 allowable total error, while the relative deviation or absolute deviation of the rest of the test parameters at their medical decision levels was less than 1/2CLIA88 predetermined allowable total error, and the total pass rate was 93%, so the China-made equipment Mindray BS-2000M biochemical analyzer may be clinically acceptable. Conclusion: Mindray BS-2000M has achieved the desirable photometry technical and analytical performance, and can therefore be used in modern clinical laboratories.
机译:目的:评估国产设备迈瑞BS-2000M生化分析仪,探讨迈瑞BS-2000M生化分析仪与进口设备Roche cobas702全自动生化分析仪检测的16个测试参数结果之间的可比性。方法:根据美国临床实验室标准化委员会(NCCLS)文件EP9-A2,将瑞士罗氏cobas702生化分析仪用作比较系统,而迈瑞BS-2000M作为实验系统。同时测试了来自40个病例的16种不同水平的生化参数。计算了不同医学决策水平下测试检测系统(Y)和控制检测系统(X)的相关系数(r),线性回归方程以及绝对偏差(SE)和相对偏差(SE%)。根据美国临床能力测试实验室改进修正案(CLIA'88)允许的总误差标准,测试了不同检测系统之间的临床可接受性和可比性。结果:两个不同的生物检测系统之间的十六个参数的测试结果具有良好的相关性(r ^ 2> = 0.95,p <0.01)。线性研究表明,所有参数的线性范围均可接受。在不同的医疗决策水平上,十六种生化参数的相对偏差SE%,除了两个水平的TP和一个水平的TBIL的相对偏差大于1/2 CLIA 88允许的总误差外,其余的相对偏差或绝对偏差在其医学决策水平上测试参数的平均值小于1 / 2CLIA88预定的允许总误差,并且总合格率为93%,因此国产迈瑞BS-2000M生化分析仪可能在临床上可以接受。结论:迈瑞BS-2000M已达到理想的测光技术和分析性能,因此可在现代临床实验室中使用。

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