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凝血活酶的重新评估

Reappraisal of thromboplastin.

作者信息

Ziegler F D, Rich S A, Fasco M J, Russell C, Kelly J H

出版信息

Ann Clin Lab Sci. 1981 May-Jun;11(3):202-10.

PMID:7018366
Abstract

Proficiency testing surveys in the state of New York indicate that despite increased sophistication in instrumentation, there has been no real improvement in interlaboratory reproducibility in prothrombin-time determinations over the last 10 years. This lack of improvement most pronounced in the therapeutic range of 20 to 30 sec. One reason may be that between types produced by the same manufacturer. While it has been possible in several laboratories to synthesize experimentally a thromboplastin with known content of lipid and active protein, no efforts have been made to make such a product by the same manufactures. While it has been made to make such a product commercially available. Blood levels of of warfarin were measured but cannot be reliably used to monitor anticoagulation. In a preliminary study, factor Xa activity was measured using chromogenic substrate S2222. Factor Xa activity gave a positive correlation with prothrombin times of patients receiving warfarin therapy. Chromogenic substrate factor assays may represent a future method of choice for controlling anticoagulant therapy.

摘要

纽约州的能力验证调查表明,尽管仪器设备日益精密,但在过去10年里,凝血酶原时间测定的实验室间再现性并未得到真正改善。这种缺乏改善的情况在20至30秒的治疗范围内最为明显。一个原因可能是同一制造商生产的不同类型之间存在差异。虽然在几个实验室中已经能够通过实验合成具有已知脂质和活性蛋白含量的凝血活酶,但同一制造商并未努力生产这样的产品。虽然已经努力使这种产品商业化。测量了华法林的血药浓度,但不能可靠地用于监测抗凝作用。在一项初步研究中,使用发色底物S2222测量了因子Xa活性。因子Xa活性与接受华法林治疗患者的凝血酶原时间呈正相关。发色底物因子测定可能代表了未来控制抗凝治疗的一种选择方法。

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