Pabinger-Fasching Ingrid
Haematology and Haemostaseology Division, Department of Internal Medicine I, Medical University of Vienna, Vienna, Austria.
Thromb Res. 2008;122 Suppl 2:S19-22. doi: 10.1016/S0049-3848(08)70005-7.
Bleeding can be a major problem in patients on oral anticoagulation therapy. Beriplex P/N is a prothrombin complex concentrate (PCC) that has been developed for the rapid reversal of anticoagulation in patients requiring immediate haemostatic control. Beriplex P/N contains high concentrations of the coagulation factors II, VII, IX and X, together with the inhibitors protein C and protein S, and it can be rapidly prepared and administered at an infusion rate of up to 8.0 mL/min. The efficacy of Beriplex P/N in patients requiring emergency reversal of oral anticoagulation has been demonstrated in a prospective, open-label, uncontrolled study involving 43 patients; 17 with acute bleeding and 26 requiring emergency surgery. Beriplex P/N was administered at a dose of 25-50 IU/kg, according to baseline international normalised ratio (INR) in conjunction with vitamin K. Mean INR 30 minutes post-infusion was 1.18, and 93% of patients achieved an INR of <or=1.3. Clinical efficacy was rated as satisfactory or very good in 98% of patients. Therapy was found to be well tolerated. There were no adverse events related to the rapid rate of infusion and, of the 8 serious adverse events reported; only 1 was regarded as being possibly related to treatment. No virus transmission was observed and changes in thrombogenicity markers were found to be transient and did not correspond to any clinically observed thromboembolic events. In conclusion, Beriplex P/N is an effective and well-tolerated therapy for rapid, complete and predictable reversal of anticoagulation in patients with acute bleeding or requiring emergency surgery.
出血可能是接受口服抗凝治疗患者的一个主要问题。倍利凝血因子复合物(Beriplex P/N)是一种凝血酶原复合物浓缩剂(PCC),已被开发用于在需要立即止血控制的患者中快速逆转抗凝作用。倍利凝血因子复合物(Beriplex P/N)含有高浓度的凝血因子II、VII、IX和X,以及抑制剂蛋白C和蛋白S,并且可以快速配制并以高达8.0 mL/分钟的输注速率给药。一项涉及43例患者的前瞻性、开放标签、非对照研究证明了倍利凝血因子复合物(Beriplex P/N)在需要紧急逆转口服抗凝作用患者中的疗效;其中17例有急性出血,26例需要急诊手术。根据基线国际标准化比值(INR)并联合维生素K,以25 - 50 IU/kg的剂量给予倍利凝血因子复合物(Beriplex P/N)。输注后30分钟的平均INR为1.18,93%的患者INR≤1.3。98%的患者临床疗效被评为满意或非常好。发现该治疗耐受性良好。未观察到与快速输注速率相关的不良事件,在报告的8例严重不良事件中,只有1例被认为可能与治疗有关。未观察到病毒传播,并且发现血栓形成标志物的变化是短暂的,与任何临床观察到的血栓栓塞事件均不相符。总之,倍利凝血因子复合物(Beriplex P/N)是一种有效且耐受性良好的治疗方法,可在急性出血或需要急诊手术的患者中快速、完全且可预测地逆转抗凝作用。