Moerer Onnen, Huber-Petersen Jan Felix, Schaeper Joern, Binder Claudia, Wand Saskia
Department of Anesthesiology, University Medical Center Goettingen, 37075 Goettingen, Germany.
Department of Hematology and Oncology, University Medical Center Goettingen, Robert-Koch-Str. 40, 37075 Goettingen, Germany.
J Clin Med. 2021 Mar 14;10(6):1203. doi: 10.3390/jcm10061203.
Direct complications in patients receiving extracorporeal (veno-venous) membrane oxygenation (vvECMO) are mainly either due to bleeding or thromboembolism. We aimed to evaluate the course of routine coagulation parameters and the activity of different coagulation factors-with special focus on factor XIII (F XIII)-before, during and after vvECMO in acute respiratory distress syndrome (ARDS) patients. The activity of coagulation factors and rotational thrombelastometry were analyzed in 20 ECMO patients before (T-1) and 6 h (T0), one (T1), three (T3) and seven days (T7) after the implantation, as well as one and three days after the termination of ECMO. F XIII activity was already severely decreased to 37% (30/49) before ECMO. F XIII activity was the only coagulation factor continuously declining during vvECMO, being significantly decreased at T3 (31% (26/45) vs. 24% (18/42), = 0.0079) and T7 (31% (26/45) vs. 23% (17/37), = 0.0037) compared to T0. Three days after termination of vvECMO, platelet count and fibrinogen nearly doubled and factors II, V, XI and XIII showed spontaneous significant increases. Severe ARDS patients showed a considerably diminished factor XIII activity before vvECMO initiation and its activity continuously declined later on. Thus, incorporation of F XIII monitoring into the regular hemostaseologic routine during vvECMO therapy seems advisable. Due to the potential development of a hypercoagulatory state after the termination of vvECMO, tight hemostasiologic monitoring should persist in the initial phase after ECMO termination.
接受体外(静脉 - 静脉)膜肺氧合(vvECMO)治疗的患者直接并发症主要是出血或血栓栓塞。我们旨在评估急性呼吸窘迫综合征(ARDS)患者在vvECMO治疗前、治疗期间及治疗后常规凝血参数的变化过程以及不同凝血因子的活性,特别关注因子XIII(F XIII)。对20例接受ECMO治疗的患者在植入前(T - 1)、植入后6小时(T0)、1天(T1)、3天(T3)和7天(T7)以及ECMO终止后1天和3天分析凝血因子活性和旋转血栓弹力图。在ECMO治疗前,F XIII活性已严重下降至37%(30/49)。F XIII活性是vvECMO治疗期间唯一持续下降的凝血因子,与T0相比,在T3时显著降低(31%(26/45)对24%(18/42),P = 0.0079),在T7时也显著降低(31%(26/45)对23%(17/37),P = 0.0037)。vvECMO终止三天后,血小板计数和纤维蛋白原几乎翻倍,因子II、V、XI和XIII显示出自发性显著增加。严重ARDS患者在vvECMO开始前F XIII活性明显降低,且随后其活性持续下降。因此,在vvECMO治疗期间将F XIII监测纳入常规止血学检查似乎是可取的。由于vvECMO终止后可能出现高凝状态,在ECMO终止后的初始阶段应持续进行严格的止血学监测。