Eisses Michael J, Velan Tomas, Aldea Gabriel S, Chandler Wayne L
Department of Anesthesiology, Children's Hospital and Regional Medical Center, University of Washington, Seattle, USA.
Thromb Res. 2006;117(6):689-703. doi: 10.1016/j.thromres.2005.05.028. Epub 2005 Jul 5.
We evaluated whether a modified protocol for cardiopulmonary bypass (CPB) could reduced the systemic hemostatic activation associated with this procedure.
The in vivo rates of thrombin, fibrin, plasmin and D-dimer generation were determined in each subject during CPB using measured levels of hemostatic factors combined with a computer model of the cardiovascular and hemostatic systems. A standard CPB group using uncoated circuits, standard heparin levels and direct shed blood reinfusion (n=9) was compared to a modified CPB group using heparin-coated circuits, shed blood collection, washing and reinfusion post-operatively, lower heparin levels and epsilon-amino-caproic acid (n=10).
Standard CPB increased average thrombin generation 9-fold, decreased fibrin generation 2-fold, increased plasmin generation 11-fold and increased fibrin degradation and D-dimer generation 19-fold. During CPB in the modified group thrombin generation was not increased beyond surgical levels, lower heparin concentrations allowed each thrombin to make more fibrin prior to inhibition, while fibrin degradation was suppressed by epsilon-amino-caproic acid. At baseline for every 100 fibrins formed only 1-2 were degraded to D-dimer. During standard CPB for every 100 fibrins generated on average 34 fibrins were degraded with some subjects showing a net fibrin loss. In contrast, in the modified CPB group for every 100 fibrins formed only 4 fibrins were degraded (p<0.0001 vs. standard group). Kinetic modeling of hemostasis in individual patients showed that a modified CPB protocol could reduce excessive thrombin generation during CPB and suppress fibrin degradation moving hemostatic regulation back towards normal.
我们评估了一种改良的体外循环(CPB)方案是否能够减少与该手术相关的全身止血激活。
在CPB期间,使用测量的止血因子水平结合心血管和止血系统的计算机模型,测定每个受试者体内凝血酶、纤维蛋白、纤溶酶和D-二聚体的生成速率。将使用未涂层回路、标准肝素水平和直接回输自体失血的标准CPB组(n = 9)与使用肝素涂层回路、术后收集、洗涤和回输自体失血、较低肝素水平和ε-氨基己酸的改良CPB组(n = 10)进行比较。
标准CPB使平均凝血酶生成增加9倍,纤维蛋白生成减少2倍,纤溶酶生成增加11倍,纤维蛋白降解和D-二聚体生成增加19倍。在改良组的CPB期间,凝血酶生成未超过手术水平,较低的肝素浓度使每个凝血酶在被抑制之前能够生成更多的纤维蛋白,而ε-氨基己酸抑制了纤维蛋白降解。在基线时,每形成100个纤维蛋白,只有1 - 2个降解为D-二聚体。在标准CPB期间,每生成100个纤维蛋白平均有34个被降解,一些受试者出现净纤维蛋白丢失。相比之下 在改良CPB组中,每形成100个纤维蛋白只有4个被降解(与标准组相比,p < 0.0001)。个体患者止血的动力学模型表明,改良的CPB方案可以减少CPB期间过度的凝血酶生成,并抑制纤维蛋白降解,使止血调节恢复正常。