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未校准的凝血酶原酶诱导凝血时间试验。与 aPTT 相比,监测未分级肝素时同样方便,但更精确。

The uncalibrated prothrombinase-induced clotting time test. Equally convenient but more precise than the aPTT for monitoring of unfractionated heparin.

机构信息

Institut für Klinische Chemie und HämatologieFrohbergstr. 3, 9001 St. Gallen, Switzerland.

出版信息

Hamostaseologie. 2010 Nov;30(4):212-6.

PMID:21057708
Abstract

The activated partial thromboplastin time test (aPTT) represents one of the most commonly used diagnostic tools in order to monitor patients undergoing heparin therapy. Expression of aPTT coagulation time in seconds represents common practice in order to evaluate the integrity of the coagulation cascade. The prolongation of the aPTT thus can indicate whether or not the heparin level is likely to be within therapeutic range. Unfortunately aPTT results are highly variable depending on patient properties, manufacturer, different reagents and instruments among others but most importantly aPTT's dose response curve to heparin often lacks linearity. Furthermore, aPTT assays are insensitive to drugs such as, for example, low molecular weight heparin (LMWH) and direct factor Xa (FXa) inhibitors among others. On the other hand, the protrombinase-induced clotting time assay (PiCT®) has been show to be a reliable functional assay sensitive to all heparinoids as well as direct thrombin inhibitors (DTIs). So far, the commercially available PiCT assay (Pefakit®PiCT®, DSM Nutritional Products Ltd. Branch Pentapharm, Basel, Switzerland) is designed to express results in terms of units with the help of specific calibrators, while aPTT results are most commonly expressed as coagulation time in seconds. In this report, we describe the results of a pilot study indicating that the Pefakit PiCT UC assay is superior to the aPTT for the efficient monitoring of patients undergoing UFH therapy; it is also suitable to determine and quantitate the effect of LMWH therapy. This indicates a distinct benefit when using this new approach over the use of aPPT for heparin monitoring.

摘要

活化部分凝血活酶时间(aPTT)检测是监测肝素治疗患者的最常用诊断工具之一。以秒为单位表示的 aPTT 凝血时间的表达是评估凝血级联完整性的常用方法。因此,aPTT 的延长表明肝素水平是否可能在治疗范围内。不幸的是,aPTT 结果高度依赖于患者特征、制造商、不同试剂和仪器等因素,但最重要的是,aPTT 对肝素的剂量反应曲线往往缺乏线性。此外,aPTT 检测对药物不敏感,例如低分子量肝素(LMWH)和直接因子 Xa(FXa)抑制剂等。另一方面,凝血酶原诱导的凝血时间检测(PiCT®)已被证明是一种可靠的功能检测方法,对所有肝素类药物以及直接凝血酶抑制剂(DTIs)敏感。到目前为止,市售的 PiCT 检测(Pefakit®PiCT®,DSM Nutritional Products Ltd. Branch Pentapharm,Basel,Switzerland)旨在通过特定校准品以单位表达结果,而 aPTT 结果通常以秒为单位表示凝血时间。在本报告中,我们描述了一项初步研究结果,表明 Pefakit PiCT UC 检测在监测接受 UFH 治疗的患者方面优于 aPTT;它也适用于确定和定量 LMWH 治疗的效果。这表明在肝素监测中使用这种新方法比使用 aPPT 具有明显的优势。

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