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首页> 外文期刊>Journal of clinical laboratory analysis. >Performance Evaluation of LUMIPULSE G1200 Autoimmunoanalyzer for the Detection of Serum Hepatitis B Virus Markers
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Performance Evaluation of LUMIPULSE G1200 Autoimmunoanalyzer for the Detection of Serum Hepatitis B Virus Markers

机译:LUMIPULSE G1200自身免疫分析仪检测血清乙型肝炎病毒标志物的性能评估

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We evaluated recently introduced automated immunoassay analyzer LUMIPULSE G1200 (Fujirebio, Inc., Tokyo, Japan) for detecting serologic hepatitis B virus (HBV) markers by comparison with the results by ARCHITECT i4000SR (Abbott, Abbott Park, IL).MethodsPrecision performance was evaluated over 20 days. HBV surface antigen (HBsAg), HBV e antigen (HBeAg), antibodies to HBV core antigen (anti-HBc), antibodies to HBeAg (anti-HBe), and antibodies to HBsAg (anti-HBs) in a total of 1,000 serum samples were assessed by the two analyzers. Discrepant results were retested by COBAS e411 (Roche Diagnostics, Mannheim, Germany).ResultsLUMIPULSE showed excellent precision performance of total imprecision less than 3.5% coefficient of variation. The qualitative results between the two analyzers were agreed with each other in 92.0–99.8% of the specimens according to the different HBV markers. The degrees of reactions for HBeAg were moderately correlated between the two analyzers (r = 0.60), and those of other HBV markers were well correlated (r = 0.80 or greater). However, there were 183 discrepancies among 1,000 cases, and most of them showed degree of reaction around the cutoff values.ConclusionsLUMIPULSE G1200 showed well-concordant results with ARCITHECT for hepatitis B serologic tests. However, results near the cutoff values would need to be retested with other immunoassay or molecular methods, when the serological profiles of HBV markers are unusual or are not correlated to the clinical conditions of the patient, due to discrepancies between the immunoassay analyzers.
机译:通过与ARCHITECT i4000SR(Abbott,Abbott Park,IL)的结果进行比较,我们评估了最近推出的自动免疫分析仪LUMIPULSE G1200(日本东京富士通公司)用于检测血清乙型肝炎病毒(HBV)标记的方法。超过20天。总共1,000份血清样品中的HBV表面抗原(HBsAg),HBV e抗原(HBeAg),抗HBV核心抗原的抗体(抗HBc),抗HBeAg的抗体(抗HBe)和抗HBsAg的抗体(抗HBs)由两个分析仪评估。结果不一致的结果通过COBAS e411(德国曼海姆的罗氏诊断公司(Roche Diagnostics,Mannheim,德国))进行了重新测试。结果LUMIPULSE表现出优异的总不精确度精度,变异系数小于3.5%。根据不同的HBV标记,在92.0–99.8%的样本中,两个分析仪之间的定性结果彼此一致。在两个分析仪之间,HBeAg的反应程度具有中等程度的相关性(r = 0.60),而其他HBV标记物的反应程度也具有良好的相关性(r = 0.80或更高)。然而,在1,000例患者中,有183处差异,其中大多数显示在临界值附近的反应程度。结论LUMIPULSE G1200与ARCITHECT的乙肝血清学检查结果一致。但是,由于免疫分析仪之间的差异,当HBV标记的血清学特征异常或与患者的临床状况不相关时,接近临界值的结果将需要用其他免疫分析或分子方法重新测试。

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