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即时检验(POCT)PT-INR- 它是否足以满足患者护理需求?罗氏 Coaguchek XS 与 Stago Star 及西门子 BCS 在常规抗凝门诊患者中的比较。

POCT PT INR - Is it adequate for patient care? A comparison of the Roche Coaguchek XS vs. Stago Star vs. Siemens BCS in patients routinely seen in an anticoagulation clinic.

机构信息

University of Texas Medical Branch, Department of Preventive Medicine and Community Health, Galveston, TX, 77555-1150, United States.

University of Texas Medical Branch, Departments of Internal Medicine, Galveston, TX, 77555-1167, United States.

出版信息

Clin Chim Acta. 2017 Sep;472:139-145. doi: 10.1016/j.cca.2017.07.027. Epub 2017 Aug 1.

Abstract

BACKGROUND

In this study we examined the difference in patient INR values as measured by the POCT CoaguChek XS device and central laboratory Stago Evolution and Siemens BCS XP analyzers.

METHODS

This study composed of 100 warfarin therapy patients and 20 coagulation normal subjects, showed that the difference between the POCT and clinical laboratory values increased with increasing INR and was exacerbated by the use of different thromboplastin reagents by the POCT and central lab.

RESULTS

The CoaguChek XS and on-site Stago analyzers which used human recombinant (ISI=1.01) and rabbit brain thromboplastin (ISI=1.25), respectively, showed reasonable agreement for INR<3.0 (k=0.62) but significant difference for INR≥3.0 (k=0.10). In contrast, the CoaguChek XS and Siemens BCS XP, which both employed human recombinant thromboplastin (BCS ISI=1.02), showed greater agreement for the complete range INR values (INR<3.0 k=0.84; INR≥3.0 k=0.70). ECAA Poller calibrant data showed the automated instruments were performing as expected, indicating that ISI calibrations were correct but insufficient to standardize the INR values for the different thromboplastin methods across the full range of measured INRs. Central lab verification of POCT INR>5.0 with the Stago Evolution prevented adverse treatment events for the warfarin therapy patients in the six months preceding and following this investigation.

摘要

背景

在这项研究中,我们检查了 POCT CoaguChek XS 设备和中央实验室 Stago Evolution 和 Siemens BCS XP 分析仪测量的患者 INR 值的差异。

方法

这项研究由 100 名华法林治疗患者和 20 名凝血正常的受试者组成,结果表明,POCT 和临床实验室值之间的差异随着 INR 的增加而增加,并且 POCT 和中央实验室使用不同的凝血活酶试剂会加剧这种差异。

结果

使用人重组(ISI=1.01)和兔脑凝血活酶(ISI=1.25)的 CoaguChek XS 和现场 Stago 分析仪在 INR<3.0 时显示出合理的一致性(k=0.62),但在 INR≥3.0 时存在显著差异(k=0.10)。相比之下,使用人重组凝血活酶(BCS ISI=1.02)的 CoaguChek XS 和 Siemens BCS XP 在整个 INR 值范围内(INR<3.0 k=0.84;INR≥3.0 k=0.70)显示出更大的一致性。ECAA Poller 校准剂数据表明自动化仪器的性能符合预期,这表明 ISI 校准是正确的,但不足以标准化不同凝血活酶方法在整个 INR 测量范围内的 INR 值。在这项调查之前和之后的六个月内,中央实验室对 POCT INR>5.0 进行了 Stago Evolution 验证,这防止了华法林治疗患者的不良治疗事件。

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