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凝血酶原时间/国际标准化比值(PT/INR)标准化。

Standardization of Prothrombin Time/International Normalized Ratio (PT/INR).

机构信息

Department of Hematology and Blood Transfusion, School of Allied Medicine, Iran University of Medical Sciences, Tehran, Iran.

Department of Haematology, Sydney Centres for Thrombosis and Haemostasis, Institute of Clinical Pathology and Medical Research, NSW Health Pathology, Westmead Hospital, Westmead, NSW, Australia.

出版信息

Int J Lab Hematol. 2021 Feb;43(1):21-28. doi: 10.1111/ijlh.13349. Epub 2020 Sep 26.

Abstract

The prothrombin time (PT) represents the most commonly used coagulation test in clinical laboratories. The PT is mathematically converted to the international normalized ratio (INR) for use in monitoring anticoagulant therapy with vitamin K antagonists such as warfarin in order to provide test results that are adjusted for thromboplastin and instrument used. The INR is created using two major PT 'correction factors', namely the mean normal PT (MNPT) and the international sensitivity index (ISI). Manufacturers of reagents and coagulometers have made some efforts to harmonizing INRs, for example, by tailoring reagents to specific coagulometers and provide associated ISI values. Thus, two types of ISIs may be generated, with one being a 'general' or 'generic' ISI and others being reagent/coagulometer-specific ISI values. Although these play a crucial role in improving INR results between laboratories, these laboratories reported INR values are known to still differ, even when laboratories use the same thromboplastin reagent and coagulometer. Moreover, ISI values for a specific thromboplastin can vary among different models of coagulometers from a manufacturer using the same method for clot identification. All these factors can be sources of error for INR reporting, which in turn can significantly affect patient management. In this narrative review, we provide some guidance to appropriate ISI verification/validation, which may help decrease the variability in cross laboratory reporting of INRs.

摘要

凝血酶原时间(PT)是临床实验室最常用的凝血检测指标。PT 被数学转换为国际标准化比值(INR),用于监测华法林等维生素 K 拮抗剂的抗凝治疗,以提供针对使用的凝血活酶和仪器进行调整的检测结果。INR 使用两个主要的 PT“校正因子”创建,即平均正常 PT(MNPT)和国际敏感指数(ISI)。试剂和凝血仪制造商为了使 INR 标准化做出了一些努力,例如通过将试剂专门用于特定的凝血仪并提供相关的 ISI 值。因此,可能会生成两种类型的 ISI,一种是“通用”或“通用”ISI,另一种是试剂/凝血仪专用的 ISI 值。尽管这些在改善实验室之间的 INR 结果方面发挥了至关重要的作用,但即使实验室使用相同的凝血活酶试剂和凝血仪,这些实验室报告的 INR 值仍已知存在差异。此外,来自使用相同凝块识别方法的制造商的不同凝血仪模型的特定凝血活酶的 ISI 值可能有所不同。所有这些因素都可能成为 INR 报告的误差源,这反过来又会严重影响患者管理。在这篇叙述性综述中,我们提供了一些有关适当的 ISI 验证/确认的指导,这可能有助于减少跨实验室 INR 报告的变异性。

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