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从肝功能异常的患者中得出的国际敏感指数 (ISI) 提高了不同试剂测定的 INR 之间的一致性。

An International Sensitivity Index (ISI) derived from patients with abnormal liver function improves agreement between INRs determined with different reagents.

机构信息

Department of Coagulation, Northern General Hospital, Sheffield, UK.

出版信息

Thromb Haemost. 2010 Apr;103(4):757-65. doi: 10.1160/TH09-08-0535. Epub 2010 Feb 19.

DOI:10.1160/TH09-08-0535
PMID:20174759
Abstract

The International Normalised Ratio (INR)/International Sensitivity Index (ISI) system was developed as a way to standardise the prothrombin time during the monitoring of patients undergoing oral anti-coagulant therapy with vitamin K antagonists. The wide acceptance of the INR has led to its use as one of three parameters used in the Model for End stage Liver disease (MELD) scoring system to aid the prioritisation of patients for liver transplant. Literature published recently has highlighted the potential inadequacy of the INR system in this context. Our aim was to investigate the degree of difference between INR values calculated using an ISI derived from warfarinised patients and those calculated using an ISI derived from patients with liver disease. Prothrombin times from 60 patients with liver disease were determined using three working thromboplastin reagents; Innovin, Thromborel S and Thromboplastin C and two reference thromboplastins; rTF/95 and RBT/05. All thromboplastin reagents tested had standard international sensitivity indices (ISIs) assigned following calibration with patients on oral anticoagulant therapy (ISIvka). As a result of the new calibration each of the working thromboplastin reagents was assigned a specific "liver patient" ISI. Two INR values were calculated for each thromboplastin patient involved in the calibration. A comparison of the mean INRliver with INRvka showed a statistically significant difference between the two values (p<0.0001). A similar relationship existed for INRs on a further 20 patients with liver disease whose plasmas were not used to derive the ISIliver. This difference led to a change in the final MELD score and could therefore affect the prioritisation and management of these patients.

摘要

国际标准化比值(INR)/国际敏感指数(ISI)系统的开发是为了标准化口服抗凝治疗维生素 K 拮抗剂患者的凝血酶原时间监测。INR 的广泛接受导致其被用作终末期肝病模型(MELD)评分系统中的三个参数之一,以帮助优先考虑肝移植患者。最近发表的文献强调了 INR 系统在这种情况下可能存在的不足。我们的目的是研究使用来自华法林化患者的 ISI 计算的 INR 值与使用来自肝病患者的 ISI 计算的 INR 值之间的差异程度。使用三种工作性凝血活酶试剂(Innovin、Thromborel S 和 Thromboplastin C)和两种参考凝血活酶(rTF/95 和 RBT/05)测定了 60 例肝病患者的凝血酶原时间。所有测试的凝血活酶试剂均采用口服抗凝治疗患者(ISIvka)校准后具有标准国际敏感指数(ISIs)。由于新的校准,每个工作性凝血活酶试剂都被分配了一个特定的“肝病患者”ISI。为校准中涉及的每个凝血活酶患者计算了两个 INR 值。INRliver 与 INRvka 的平均值比较显示两者之间存在统计学差异(p<0.0001)。在另外 20 例未使用其血浆衍生 ISIliver 的肝病患者中也存在类似的关系。这种差异导致最终 MELD 评分发生变化,因此可能会影响这些患者的优先排序和管理。

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An International Sensitivity Index (ISI) derived from patients with abnormal liver function improves agreement between INRs determined with different reagents.从肝功能异常的患者中得出的国际敏感指数 (ISI) 提高了不同试剂测定的 INR 之间的一致性。
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2
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BMJ Open. 2015 Sep 21;5(9):e008032. doi: 10.1136/bmjopen-2015-008032.
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The validity of the INR system for patients with liver disease.
国际标准化比值(INR)系统在肝病患者中的有效性。
J Thromb Thrombolysis. 2011 Feb;31(2):209-10. doi: 10.1007/s11239-010-0508-y.