凝血酶原时间测定的研究进展

J. Horsti
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引用次数: 3

摘要

华法林是应用最广泛的口服抗凝治疗药物。它抑制肝脏中凝血因子II、VII、IX和X的合成,并导致这些因子的无活性或部分活性版本的产生。无活性凝血因子干扰凝血酶原时间测量(Quick和Owren PT)测量凝血活性和抑制的总和。狭窄的治疗范围涉及严重并发症的危险以及出血或血栓形成的风险。新一代PT法可分别测定凝血活性和抑制作用。这项新技术促进了患者护理和基于体内凝血活性的抗凝药物(华法林,双酚)。治疗和实验室控制都应该毫无疑问地准确,并且完全基于体内凝血活性。非活性凝血因子(抑制)提供测量、校准和协调。利用基于体内凝血活性测量的新一代PT方法,可以开发维生素K拮抗剂(VKA)治疗,使患者获益显著。
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The progress of prothrombin time measurement
Warfarin is the most widely used medicine for oral anticoagulant therapy (OAT). It inhibits the synthesis of coagulation factors II, VII, IX, and X in the liver and results in the production of inactive or partially active versions of these factors. Inactive coagulation factors interfere with prothrombin time measurement (Quick and Owren PT) measuring the sum of coagulation activity and inhibition. The narrow therapeutic range here involves a danger of serious complications and the risk of bleeding or thrombosis. The new-generation PT method can measure coagulation activity and inhibition separately. This new technique promotes patient care and anticoagulant medication (warfarin, dicoumarol) based on coagulation activity in vivo. Both therapy and laboratory controls should be unquestionably accurate and based solely on in vivo coagulation activity. Inactive coagulation factors (inhibition) render measurement, calibration, and harmonization. The use of the new-generation PT method based on measurement of coagulation activity in vivo could develop vitamin K antagonist (VKA) therapy for the marked benefit of patients.
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