Department of Anaesthesiology and Intensive Care, Skåne University Hospital and Lund University , Lund , Sweden.
Scand J Clin Lab Invest. 2013 Oct;73(7):553-62. doi: 10.3109/00365513.2013.821710. Epub 2013 Sep 5.
Natural colloid albumin induces a lesser degree of dilutional coagulopathy than synthetic colloids. Fibrinogen concentrate has emerged as a promising strategy to treat coagulopathy, and factor XIII (FXIII) works synergistically with fibrinogen to correct coagulopathy following haemodilution with crystalloids. Our objectives were to examine the ability of fibrinogen and FXIII concentrates to reverse albumin-induced dilutional coagulopathy.
High and low concentrations of both fibrinogen and FXIII were used to reverse coagulopathy induced by 1:1 dilution in vitro with 5% albumin of blood samples from healthy volunteers, monitored by rotational thromboelastometry (ROTEM).
Haemodilution with albumin significantly attenuated EXTEM maximum clot firmness (MCF), alpha angle (AA), clotting time (CT) and clot formation time (CFT), and FIBTEM MCF (p < 0.001). Following haemodilution, both doses of fibrinogen significantly corrected all ROTEM parameters (p ≤ 0.02), except the lower dose did not correct AA. Compared to the lower dose, the higher dose of fibrinogen significantly improved FIBTEM MCF and EXTEM MCF, AA and CFT (p < 0.001). The lower dose of FXIII did not significantly correct any of the ROTEM parameters, and the high dose only improved EXTEM CT (p = 0.004). All combinations of high/low concentrations of fibrinogen/FXIII significantly improved all ROTEM parameters examined (p ≤ 0.001). Fibrinogen concentration generally had a greater effect on each parameter than did FXIII concentration; the best correction of ROTEM parameters was achieved with high-dose fibrinogen concentrate and either low- or high-dose FXIII.
Fibrinogen concentrate successfully corrected initiation, propagation and clot firmness deficits induced by haemodilution with albumin, and FXIII synergistically improved fibrin-based clot strength.
天然胶体白蛋白引起的稀释性凝血功能障碍程度低于合成胶体。纤维蛋白原浓缩物已成为治疗凝血功能障碍的一种有前途的策略,而因子 XIII (FXIII) 与纤维蛋白原协同作用,可纠正晶体稀释后引起的凝血功能障碍。我们的目的是研究纤维蛋白原和 FXIII 浓缩物逆转白蛋白诱导的稀释性凝血功能障碍的能力。
使用高浓度和低浓度的纤维蛋白原和 FXIII 来逆转健康志愿者血液样本在体外与 5%白蛋白以 1:1 稀释时引起的凝血功能障碍,通过旋转血栓弹性测定法(ROTEM)进行监测。
白蛋白稀释显著减弱 EXTEM 最大凝块硬度(MCF)、α角(AA)、凝血时间(CT)和凝块形成时间(CFT)以及 FIBTEM MCF(p < 0.001)。稀释后,两种剂量的纤维蛋白原均显著纠正了所有 ROTEM 参数(p ≤ 0.02),除了低剂量未能纠正 AA。与低剂量相比,高剂量的纤维蛋白原显著改善了 FIBTEM MCF 和 EXTEM MCF、AA 和 CFT(p < 0.001)。低剂量的 FXIII 并未显著纠正任何 ROTEM 参数,而高剂量仅改善 EXTEM CT(p = 0.004)。高/低浓度的纤维蛋白原/FXIII 的所有组合均显著改善了所检查的所有 ROTEM 参数(p ≤ 0.001)。纤维蛋白原浓度对每个参数的影响通常大于 FXIII 浓度;高剂量纤维蛋白原浓缩物与低或高剂量 FXIII 联合使用可实现对 ROTEM 参数的最佳纠正。
纤维蛋白原浓缩物成功纠正了白蛋白稀释引起的起始、扩展和凝块硬度缺陷,而 FXIII 则协同增强了纤维蛋白基凝块的强度。