首页> 外文期刊>Blood coagulation & fibrinolysis: an international journal in haemostasis and thrombosis >Evaluation of the Q analyzer, a new cap-piercing fully automated coagulometer with clotting, chromogenic, and immunoturbidometric capability
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Evaluation of the Q analyzer, a new cap-piercing fully automated coagulometer with clotting, chromogenic, and immunoturbidometric capability

机译:对Q分析仪进行评估,Q分析仪是一种具有凝结,生色和免疫浊度测定功能的新型盖帽式全自动凝血仪

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The Q analyzer is a recently launched fully automated photo-optical analyzer equipped with primary tube cap-piercing and capable of clotting, chromogenic, and immunoturbidometric tests. The purpose of the present study was to evaluate the performance characteristics of the Q analyzer with reagents from the instrument manufacturer. We assessed precision and throughput when performing coagulation screening tests, prothrombin time (PT)/international normalized ratio (INR), activated partial thromboplastin time (APTT), and fibrinogen assay by Clauss assay. We compared results with established reagent instrument combinations in widespread use. Precision of PT/INR and APTT was acceptable as indicated by total precision of around 3%. The time to first result was 3min for an INR and 5min for PT/APTT. The system produced 115 completed samples per hour when processing only INRs and 60 samples (120 results) per hour for PT/APTT combined. The sensitivity of the DG-APTT Synth/Q method to mild deficiency of factor VIII (FVIII), IX, and XI was excellent (as indicated by APTTs being prolonged above the upper limit of the reference range). The Q analyzer was associated with high precision, acceptable throughput, and good reliability. When used in combination with DG-PT reagent and manufacturer's instrument-specific international sensitivity index, the INRs obtained were accurate. The Q analyzer with DG-APTT Synth reagent demonstrated good sensitivity to isolated mild deficiency of FVIII, IX, and XI and had the advantage of relative insensitivity to mild FXII deficiency. Taken together, our data indicate that the Q hemostasis analyzer was suitable for routine use in combination with the reagents evaluated.
机译:Q分析仪是最近推出的全自动光电分析仪,配备了初级管帽穿孔功能,并且能够进行凝结,生色和免疫浊度测试。本研究的目的是使用仪器制造商的试剂评估Q分析仪的性能特征。在进行凝血筛查测试,凝血酶原时间(PT)/国际标准化比率(INR),活化的部分凝血活酶时间(APTT)以及通过Clauss分析进行的纤维蛋白原分析时,我们评估了精度和通量。我们将结果与已建立的广泛使用的试剂仪器组合进行了比较。 PT / INR和APTT的精度可以接受,总体精度约为3%。达到首次结果的时间对于INR为3分钟,对于PT / APTT为5分钟。当仅处理INR时,系统每小时产生115个完整样本,而对于PT / APTT,则每小时产生60个样本(120个结果)。 DG-APTT Synth / Q方法对因子VIII(FVIII),IX和XI轻度缺乏的敏感性极佳(如APTT延长超过参考范围的上限所示)。 Q分析仪具有高精度,可接受的通量和良好的可靠性。当与DG-PT试剂和制造商的特定仪器的国际灵敏度指数结合使用时,所获得的INR是准确的。带有DG-APTT Synth试剂的Q分析仪显示出对分离的FVIII,IX和XI轻度缺乏症的良好敏感性,并具有对FXII轻度缺乏症相对不敏感的优势。综上所述,我们的数据表明Q止血分析仪适合与所评估的试剂结合常规使用。

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