Xu Wanzhou, Tong Yongqing, Li Yan
Department of Clinical Laboratory, Renmin Hospital of Wuhan University, Wuhan 430060, China.
Ann Transl Med. 2019 Jul;7(14):300. doi: 10.21037/atm.2019.05.83.
We conducted a comprehensive comparison in the sensitivity, specificity, dilution sensitivity, and precision between two immunoassay systems, Roche Elecsys Cobas e 601 and Sysmex HISCL 5000, for the detection of hepatitis B virus surface antigen (HBsAg), antibody to hepatitis C virus (anti-HCV), treponemal antibodies (anti-TP), and human immunodeficiency virus (HIV).
One thousand unselected samples and 100 reserved weak reactive samples were tested by the two systems. Sensitivity and specificity were then calculated for each system. Seroconversion panels were used to assess the sensitivity in early stage detection. Dilution sensitivity was evaluated by dilution tests of several seroconversion panel samples. Evaluation of within-run and intermediate precision was conducted following EP-15A protocol.
The consistency rates of the two systems for the detection of four pathogens were all over 99% among unselected samples. Both Elecsys and HISCL were observed to have high sensitivity and specificity in unselected samples and weak reactive samples. Seroconversion panel tests showed that Elecsys could identify positive results earlier than HISCL in HBsAg (1 out of 4), anti-TP (1 out of 2) and HIV (1 out of 12) panels. The results of the anti-HCV panels were comparable. In dilution tests, Elecsys could detect lower concentrations than HISCL in two anti-HCV samples and one anti-TP sample. The two systems had similar performance in dilution tests of HBsAg and HIV samples. Both Elecsys and HISCL had qualified intra-assay and inter-assay precision.
Both Elecsys and HISCL have good performance in the screening of four common bloodborne pathogens. The two systems are comparable and considered adequate for clinical use.
我们对罗氏 Elecsys Cobas e 601 和希森美康 HISCL 5000 这两种免疫分析系统在检测乙型肝炎病毒表面抗原(HBsAg)、丙型肝炎病毒抗体(抗-HCV)、梅毒螺旋体抗体(抗-TP)和人类免疫缺陷病毒(HIV)时的灵敏度、特异性、稀释灵敏度和精密度进行了全面比较。
用这两种系统检测 1000 份未经选择的样本和 100 份保留的弱阳性样本。然后计算每个系统的灵敏度和特异性。使用血清转换板评估早期检测的灵敏度。通过对几个血清转换板样本进行稀释试验来评估稀释灵敏度。按照 EP-15A 方案进行批内和批间精密度评估。
在未经选择的样本中,两种系统对四种病原体检测的一致性率均超过 99%。在未经选择的样本和弱阳性样本中,Elecsys 和 HISCL 均具有高灵敏度和特异性。血清转换板试验表明,在 HBsAg(4 份中的 1 份)、抗-TP(2 份中的 1 份)和 HIV(12 份中的 1 份)板中,Elecsys 比 HISCL 能更早地识别出阳性结果。抗-HCV 板的结果相当。在稀释试验中,在两份抗-HCV 样本和一份抗-TP 样本中,Elecsys 能检测到比 HISCL 更低的浓度。在 HBsAg 和 HIV 样本的稀释试验中,两种系统表现相似。Elecsys 和 HISCL 的批内和批间精密度均合格。
Elecsys 和 HISCL 在四种常见血源性病原体的筛查中均表现良好。这两种系统具有可比性,被认为适用于临床。