Stief Thomas W
Department of Laboratory Medicine, University Hospital, Marburg, Germany.
Clin Appl Thromb Hemost. 2008 Oct;14(4):447-53. doi: 10.1177/1076029607309228. Epub 2007 Dec 26.
Thrombin activity generated after plasma recalcification is of analytical and clinical interest. Fifty microliters of citrated plasma was recalcified with 5 microL of 250 mM CaCl( 2). After 0 to 90 minutes (37 degrees C) 50 microl 2.5 M arginine, pH 8.6, was added. After 20 minutes, thrombin was chromogenically quantified. In normal recalcified plasma, the generated thrombin activity is about 0.1-0.2 IU/ml (37 degrees C) when fibrin generation starts. Pooling of normal plasmas increases the generated thrombin activity about 3-fold. Plasmas of patients on heparin or coumarin generate about 10-fold less thrombin activity. Freezing of pooled plasma at -20 degrees C and thawing at room temperature or 37 degrees C increases thrombin generation approximately 1.5- or 2-fold, respectively. Only thrombin activities in the ascending part of the thrombin generation curve (RECA-t(2)/RECAt( 1)>1) are valid. So a prothrombotic state in blood or plasma can be diagnosed.
血浆重新钙化后产生的凝血酶活性具有分析和临床意义。用5微升250毫摩尔/升的氯化钙对50微升枸橼酸盐血浆进行重新钙化。在0至90分钟(37摄氏度)后,加入50微升2.5摩尔/升、pH值为8.6的精氨酸。20分钟后,对凝血酶进行显色定量。在正常重新钙化的血浆中,当纤维蛋白生成开始时,产生的凝血酶活性约为0.1 - 0.2国际单位/毫升(37摄氏度)。混合正常血浆可使产生的凝血酶活性增加约3倍。使用肝素或香豆素治疗的患者血浆产生的凝血酶活性约少10倍。将混合血浆在 -20摄氏度下冷冻,并在室温或37摄氏度下解冻,可分别使凝血酶生成增加约1.5倍或2倍。只有凝血酶生成曲线上升部分(RECA - t(2)/RECAt(1)>1)的凝血酶活性才有效。因此,可以诊断出血液或血浆中的血栓前状态。