INSERM UMRS 765, Paris, France.
Br J Anaesth. 2012 Apr;108(4):586-93. doi: 10.1093/bja/aer450. Epub 2012 Jan 18.
Recombinant activated factor VII (rFVIIa) is indicated in bleeding patients when a life-threatening haemorrhage occurs. Prothrombin complex concentrates (PCCs) are also used for this indication in several countries, without any evidence-based rationale. Our objective was to compare the efficacy and safety of PCC and rFVIIa in a model of bleeding and thrombosis in haemodiluted rabbits.
Forty-eight rabbits were randomly allocated into four groups: a control group and three treatment groups, in which animals were haemodiluted with hydroxyethyl starch 130/0.4 then administered either placebo, 160 µg kg(-1) rFVIIa, or 25 IU FIX kg(-1) PCC. The primary endpoint was hepatosplenic (HS) blood loss. Secondary endpoints were: (i) ear immersion bleeding time (IBT); (ii) thrombosis risk assessed by cyclic flow reductions (CFRs) of the carotid artery; and (iii) activated partial thromboplastin time (aPTT), and progress of thrombin activity.
Haemodilution increased HS blood loss by 80% from 8 g (5-16) (control group) to 14 g (8-45) (placebo group) (P<0.01). HS blood loss was not different in animals receiving either rFVIIa [10 g (7-22)] or PCC [15 g (4-33)] (P<0.05) compared with the placebo group. Ear IBT was reduced with both rFVIIa and PCC. CFRs disappeared after haemodilution and were not restored with any treatment. Although PCC nearly doubled the total amount of thrombin generated, no significant change in the total amount of thrombin was seen in animals treated with rFVIIa.
Neither rVIIa nor PCC reduced HS blood loss, whereas they both controlled the bleeding time, without increasing the thrombosis risk.
在发生危及生命的大出血时,重组活化因子 VII(rFVIIa)被用于出血患者。在一些国家,凝血酶原复合物浓缩物(PCC)也被用于该适应证,但没有任何基于证据的理由。我们的目的是在兔血液稀释模型中比较 PCC 和 rFVIIa 在出血和血栓形成方面的疗效和安全性。
48 只兔子随机分为 4 组:对照组和 3 个治疗组,其中动物用羟乙基淀粉 130/0.4 血液稀释,然后分别给予安慰剂、160µg/kg rFVIIa 或 25IU FIX/kg PCC。主要终点是肝脾(HS)失血。次要终点为:(i)耳部浸浴出血时间(IBT);(ii)颈动脉循环血流减少(CFRs)评估的血栓形成风险;(iii)活化部分凝血活酶时间(aPTT)和凝血酶活性进展。
血液稀释使 HS 失血增加 80%,从 8g(5-16)(对照组)增加到 14g(8-45)(安慰剂组)(P<0.01)。与安慰剂组相比,接受 rFVIIa [10g(7-22)]或 PCC [15g(4-33)]的动物 HS 失血无差异(P<0.05)。rFVIIa 和 PCC 均缩短了耳部 IBT。血液稀释后 CFRs 消失,任何治疗均未恢复。尽管 PCC 使生成的总凝血酶量增加近一倍,但 rFVIIa 治疗的动物总凝血酶量没有明显变化。
rVIIa 和 PCC 均不能减少 HS 失血,虽然它们都控制了出血时间,但没有增加血栓形成风险。