Viganó S, Cattaneo M, Gervasoni W, Mannucci P M
Thromb Haemost. 1980 Oct 31;44(2):72-5.
Prothrombin complex concentrates (PCC) are known to carry a risk of thromboembolism. We have chosen to reassess the problem of detecting in vivo signs of activation of the clotting mechanism by assaying fibrinopeptide A (FpA) after PCC administration in hemophilic patients during bleeding episodes. FpA was significantly increased above baseline levels 15 to 60 min after the infusion of 19 doses of 5 different types of commercial PCC in 14 hemophilia B patients treated for bleeding episodes or dental extractions. A more marked increase followed 16 infusions of the activated PCC FEIBA and Auto IX in 4 hemophilia A patients with F. VIII inhibitors. There was no significant FpA change after F. VIII concentrates administered to a control group of 7 patients with hemophilia A. These findings suggest that circulation of thrombin occurs frequently after PCC administration, even though clinical manifestations of thromboembolism appear to be relatively rare.
凝血酶原复合物浓缩剂(PCC)已知存在血栓栓塞风险。我们选择在血友病患者出血发作期间给予PCC后,通过检测纤维蛋白肽A(FpA)来重新评估检测体内凝血机制激活迹象的问题。在14例因出血发作或拔牙接受治疗的B型血友病患者中,输注19剂5种不同类型的商用PCC后,FpA在输注后15至60分钟显著高于基线水平。在4例患有F. VIII抑制剂的A型血友病患者中,输注16剂活化的PCC FEIBA和Auto IX后,FpA升高更为明显。在7例A型血友病对照组患者给予F. VIII浓缩剂后,FpA无显著变化。这些发现表明,即使血栓栓塞的临床表现似乎相对罕见,但PCC给药后凝血酶循环仍频繁发生。