Klöcking H P, Klessen C, Jablonowski C, Meerbach W, Dornheim G
Folia Haematol Int Mag Klin Morphol Blutforsch. 1984;111(5):645-61.
A prothrombin complex concentrate produced according to a new procedure was tested for potential thrombogenicity in vitro and in vivo. The results obtained by in vitro methods (NAPTT, TGt50, determination of the hydrolytic index) were not in the critical range of thrombogenicity. An effective dose of 175 U/kg for thrombus formation assessed in the stasis model of Wessler suggested comparatively low thrombogenicity. In the non stasis model no changes in the haemostaseological variables indicative of consumption reaction were observed after infusion of 125 U/kg for 30 min in rabbits. In the organs investigated (heart, liver, kidneys, adrenals) no thrombin were detected morphologically.
按照一种新方法生产的凝血酶原复合物浓缩物在体外和体内进行了潜在致血栓形成性测试。通过体外方法(活化部分凝血活酶时间、血栓形成时间50、水解指数测定)获得的结果不在致血栓形成性的临界范围内。在韦氏勒停滞模型中评估的血栓形成有效剂量为175 U/kg,表明致血栓形成性相对较低。在非停滞模型中,给兔子输注125 U/kg 30分钟后,未观察到表明消耗反应的血液学变量有变化。在所研究的器官(心脏、肝脏、肾脏、肾上腺)中,未在形态学上检测到凝血酶。