Nascimento José Carlos Rodrigues, Freitas Luiz Henrique, Pinto Daniel Vieira, Souza Antônia Lima, Aquino Cristhyane Costa, Santos Denise Teixeira, Nunes Rogean Rodrigues
Universidade da Integração Internacional da Lusofonia Afro-Brasileira, Institute of Health Sciences - Redenção (CE), Brazil.
Hospital Geral de Fortaleza, Department of Anesthesia and Liver Transplantation - Fortaleza (CE), Brazil.
Arq Bras Cir Dig. 2025 Aug 18;38:e1891. doi: 10.1590/0102-67202025000022e1891. eCollection 2025.
Orthotopic liver transplantation (OLT) is a highly complex procedure.
OLT can be difficult to control intraoperative bleeding in patients with coagulopathies.
OLT may result in a high need for transfusion of blood products.
Epsilon aminocaproic acid (EACA) can reduce the need for transfusion of Hood products.
EACA can be safe with regard to complications such as thrombosis.
A total of 105 patients were assessed for eligibility, and 55 were excluded. The remaining 50 patients were randomized, of which 24 patients were allocated to the intervention group and the other 26 to the saline placebo group. In the analysis of the fibrinolytic and hemostatic coagulation profile by rotational thromboelastometry, fibrinolysis was significantly less frequent in patients treated with epsilon aminocaproic acid (p<0.001) compared to those in the placebo group during the anhepatic phase. In the other analyses using thromboelastometry assays such as extrinsic pathway thromboelastometry (EXTEM) (clotting time [CT], clot formation time, alpha angle, amplitude of clot firmness 10 min after CT [A10], and maximum clot firmness [MCF]) and fibrinogen-specific thromboelastometry (FIBTEM) (A10 and MCF), there was no significant difference nor postoperative complications in both groups.
Some studies have shown that epsilon aminocaproic acid (EACA) inhibits the binding of plasminogen to lysine residues on the surface of fibrin and prevents conversion of plasminogen to plasmin and the degradation of glycoprotein Ib receptors, thus preserving platelet function. Although EACA did not reduce blood product transfusion, the drug effectively treated all cases and was not associated with any complications of increased risk of hepatic artery and vein thrombosis or mortality within 3 months after orthotopic liver transplantation (OLT). These results support the safety of EACA as the antifibrinolytic drug of choice in OLT. However, future studies involving larger randomized clinical trials and higher doses are needed to further investigate the results.
Orthotopic liver transplantation (OLT) is a highly complex procedure, which can be difficult to control intraoperatively in patients with coagulopathies.
The aim of this study was to evaluate the prophylactic administration of epsilon aminocaproic acid (EACA) to reduce the need for transfusion of blood products and its relevance for thrombosis.
Patients were randomized into two groups: one group received EACA (20 mg/kg/h) before surgical incision until the end of OLT and a control group received a similar volume of 0.9% saline solution. Blood was collected to analyze fibrinolysis and coagulation disorders using rotational thromboelastometry (ROTEM®).
A total of 24 patients received EACA and 26 patients received saline solution. In the analysis of the fibrinolytic and hemostatic coagulation profile by ROTEM®, fibrinolysis was significantly less frequent in the group of patients treated with EACA (p<0.001) in the anhepatic phase. There were no significant differences in the other extrinsic pathway thromboelastometry and fibrinogen-specific thromboelastometry analyses. In addition, there were no significant differences between both groups regarding the average and percentage transfusion of blood products, postoperative complications, patients who were discharged from the hospital, and those who died within 3 months after liver transplantation.
Although the administration of EACA did not reduce the transfusion of blood products, this drug effectively treated fibrinolysis and was not associated with any complications with increased risk of vein and hepatic artery thrombosis or mortality within 3 months after liver transplantation.
原位肝移植(OLT)是一项高度复杂的手术。
OLT术中可能难以控制凝血功能障碍患者的出血。
OLT可能导致对血液制品的大量需求。
ε-氨基己酸(EACA)可减少血液制品的输注需求。
EACA在血栓形成等并发症方面是安全的。
共有105例患者接受资格评估,55例被排除。其余50例患者被随机分组,其中24例患者被分配到干预组,另外26例被分配到生理盐水安慰剂组。在通过旋转血栓弹力图分析纤维蛋白溶解和止血凝血情况时,与安慰剂组相比,在无肝期接受ε-氨基己酸治疗的患者纤维蛋白溶解明显较少(p<0.001)。在使用血栓弹力图分析方法如外源性途径血栓弹力图(EXTEM)(凝血时间[CT]、凝血形成时间、α角、CT后10分钟时的血凝块硬度振幅[A10]和最大血凝块硬度[MCF])和纤维蛋白原特异性血栓弹力图(FIBTEM)(A10和MCF)的其他分析中,两组之间无显著差异,术后并发症也无差异。
一些研究表明,ε-氨基己酸(EACA)可抑制纤溶酶原与纤维蛋白表面赖氨酸残基的结合,防止纤溶酶原转化为纤溶酶以及糖蛋白Ib受体的降解,从而保留血小板功能。尽管EACA并未减少血液制品的输注,但该药物有效治疗了所有病例,且与原位肝移植(OLT)后3个月内肝动脉和静脉血栓形成风险增加或死亡率的任何并发症均无关。这些结果支持EACA作为OLT中抗纤维蛋白溶解药物选择的安全性。然而,需要未来涉及更大规模随机临床试验和更高剂量的研究来进一步探究结果。
原位肝移植(OLT)是一项高度复杂的手术,对于凝血功能障碍患者,术中可能难以控制出血。
本研究的目的是评估预防性给予ε-氨基己酸(EACA)以减少血液制品的输注需求及其与血栓形成的相关性。
患者被随机分为两组:一组在手术切口前至OLT结束时接受EACA(20mg/kg/h),对照组接受相同体积的0.9%盐水溶液。采集血液,使用旋转血栓弹力图(ROTEM®)分析纤维蛋白溶解和凝血障碍。
共有24例患者接受EACA治疗,26例患者接受盐水溶液治疗。在通过ROTEM®分析纤维蛋白溶解和止血凝血情况时,在无肝期接受EACA治疗的患者组中纤维蛋白溶解明显较少(p<0.001)。在其他外源性途径血栓弹力图和纤维蛋白原特异性血栓弹力图分析中无显著差异。此外,两组在血液制品的平均输注量和输注百分比、术后并发症、出院患者以及肝移植后3个月内死亡患者方面均无显著差异。
尽管给予EACA并未减少血液制品的输注,但该药物有效治疗了纤维蛋白溶解,且与肝移植后3个月内静脉和肝动脉血栓形成风险增加或死亡率的任何并发症均无关。