Clinical Biology, Haematology Department, CHU de Charleroi, Charleroi, Belgium.
Int J Lab Hematol. 2019 Dec;41(6):731-737. doi: 10.1111/ijlh.13100. Epub 2019 Sep 5.
The STA R Max 2 is a new coagulation analyser developed by Diagnostica Stago, able to perform clotting, chromogenic and immuno-turbidimetric tests. A pre-analytical module build into the cap-piercing needle performs the sample integrity verification (sample tube filling and measurement of haemolysis, icterus, lipaemia). The STA R Max 2 analyser incorporates an accreditation program tools to assist technical validation of the analyser. We assessed the analytical performance of the STA R Max 2.
The following tests were assessed: prothrombin time, activated partial thromboplastin time, thrombin time, fibrinogen, factor V (FV), antithrombin (AT), D-dimers (DDI) and von Willebrand factor antigen. The assay precisions were assessed using fresh plasma samples or internal quality controls. An inter-analyser comparison was performed with a STA-R Evolution analyser or, for the FV, with a BCS XP System. Haemolysis and icterus detection were also verified.
For the intra-assay precision, the coefficients of variation (CV%) were all less than 5% and for DDI, the standard deviation (SD) was less than 0.1. For the inter-assay study, all CV% were less than 5%, with the exception of FV and AT (FV: 6.68% and 5.27%; AT: 7% and 12.14% for normal and pathological values, respectively). SD was less than 0.1 for DDI. The inter-analyser comparison demonstrated good results. Haemolysis and icterus were detected correctly for all our assessed samples.
According to our methods validation's recommendations, the results demonstrated a good technical and analytical performance of the STA R Max 2 analysers for the tests assessed.
STA R Max 2 是由 Diagnostica Stago 开发的新型凝血分析仪,能够进行凝血、显色和免疫比浊测定。内置在穿刺帽中的预分析模块执行样本完整性验证(样本管填充和测定溶血、黄疸、脂血)。STA R Max 2 分析仪包含一个认证程序工具,以协助分析仪的技术验证。我们评估了 STA R Max 2 的分析性能。
评估了以下测试:凝血酶原时间、活化部分凝血活酶时间、凝血酶时间、纤维蛋白原、因子 V(FV)、抗凝血酶(AT)、D-二聚体(DDI)和血管性血友病因子抗原。使用新鲜血浆样本或内部质量控制品评估检测精密度。使用 STA-R Evolution 分析仪或 BCS XP System(FV)进行分析仪间比较。还验证了溶血和黄疸的检测。
对于室内精密度,变异系数(CV%)均小于 5%,DDI 的标准偏差(SD)小于 0.1。对于室间研究,所有 CV%均小于 5%,FV 和 AT 除外(正常值:6.68%和 5.27%;病理值:7%和 12.14%)。DDI 的 SD 小于 0.1。分析仪间比较结果良好。所有评估样本的溶血和黄疸均正确检测。
根据我们的方法验证建议,结果表明评估的测试中 STA R Max 2 分析仪具有良好的技术和分析性能。