Kirchhof B, Söntgerath D, Kirchhof U, Etscheid G
Department of Internal Medicine, St. Josef-Krankenhaus, Engelskirchen, FRG.
Thromb Res. 1990 Aug 1;59(3):541-51. doi: 10.1016/0049-3848(90)90414-8.
The kinetics of thrombin generation in various prothrombin-complex-preparations (PCC) were investigated using a chromogenic substrate assay. The rate of thrombin formation and the total activity of thrombin generated varied considerably among different preparations. The thrombin generation velocity influenced the rate of fibrinogen to fibrin conversion, measured as plasma viscosity alteration per unit of time. It also influenced thrombin induced platelet aggregation with regard to maximum aggregation and aggregation velocity. The kinetic parameters measured photometrically and coagulometrically showed reduced generation velocities and less thrombin effects with thrombin formed in PCCs than with thrombin generated in plasma. The quantitative differences between thrombin effects in various PCCs on platelet aggregation did not correlate with the data of the amidolytic and fibrinogenolytic measurements. The significance of the results is discussed with regard to the question of whether, or to what extent, PCCs could cause or accelerate a disseminated intravascular coagulation.
使用发色底物分析法研究了各种凝血酶原复合物制剂(PCC)中凝血酶生成的动力学。不同制剂之间,凝血酶形成的速率和所生成凝血酶的总活性差异很大。凝血酶生成速度影响纤维蛋白原向纤维蛋白的转化速率,该速率以单位时间内血浆粘度的变化来衡量。它还在最大聚集和聚集速度方面影响凝血酶诱导的血小板聚集。通过光度法和凝固法测量的动力学参数显示,与血浆中生成的凝血酶相比,PCC中生成的凝血酶生成速度降低且凝血酶作用较小。各种PCC对血小板聚集的凝血酶作用之间的定量差异与酰胺水解和纤维蛋白原水解测量的数据不相关。针对PCC是否会导致或加速弥散性血管内凝血的问题,对结果的意义进行了讨论。