Durila Miroslav, Vajter Jaromir, Garaj Michal, Berousek Jan, Lischke Robert, Hlavacek Michal, Vymazal Tomas
Department of Anesthesiology and Intensive Care Medicine, Second Faculty of Medicine, Charles University and Motol University Hospital, Prague, Czech Republic.
Prague Lung Transplant Program, 3rd Department of Surgery, First Faculty of Medicine, Charles University and Motol University Hospital, Prague, Czech Republic.
Artif Organs. 2025 Mar;49(3):486-496. doi: 10.1111/aor.14879. Epub 2024 Oct 3.
Unfractionated heparin is used as the most common anticoagulation for venovenous extracorporeal membrane oxygenation (VV ECMO) patients. However, it is accompanied by frequent bleeding and thrombotic complications. The aim of the study was to demonstrate the feasibility of Enoxaparin anticoagulation for VV ECMO patients.
This study is a retrospective analysis of VV ECMO patients on continuous intravenous Enoxaparin anticoagulation. The primary outcome was the incidence of bleeding, thrombotic, and neurological complications during ECMO support. The secondary outcome was an analysis of secondary and primary hemostasis profiles.
Data from 38 patients were analyzed in this study. The incidence of bleeding complications was 5.3%, for thrombotic complications it was 2.6% and for neurological (bleeding/ischemic events) complications it was 10.5%. The targeted anti-Xa activity of 0.4-0.6 IU/mL was achieved and maintained during whole ECMO period in 28 patients (73.8%), not affecting the hemocoagulation profile represented by APTT-r 1.15 ± 0.2, TT 18.67 ± 3.35 s, PT/INR 1.21 ± 0.19, fibrinogen 5.39 ± 1.49 g/L, antithrombin, and platelet count. Primary hemostasis pathology was diagnosed in all patients by PFA 200 tests Col/EPI 279 ± 38 s and Col/ADP 249 ± 66 s. The running time of ECMO was 7.8 ± 3.4 days.
Enoxaparin anticoagulation appears to be feasible for VV ECMO patients without an increase in adverse events. Further larger-sampled and comparative studies are needed in the future to support our findings.
普通肝素是静脉-静脉体外膜肺氧合(VV ECMO)患者最常用的抗凝药物。然而,它常伴有出血和血栓形成并发症。本研究的目的是证明依诺肝素抗凝在VV ECMO患者中的可行性。
本研究是对接受持续静脉注射依诺肝素抗凝的VV ECMO患者的回顾性分析。主要结局是ECMO支持期间出血、血栓形成和神经并发症的发生率。次要结局是对 secondary 和 primary 止血指标的分析。
本研究分析了38例患者的数据。出血并发症的发生率为5.3%,血栓形成并发症的发生率为2.6%,神经(出血/缺血性事件)并发症的发生率为10.5%。28例患者(73.8%)在整个ECMO期间达到并维持了0.4 - 0.6 IU/mL的目标抗Xa活性,且未影响由活化部分凝血活酶时间比值(APTT-r)1.15 ± 0.2、凝血酶时间(TT)18.67 ± 3.35秒、凝血酶原时间/国际标准化比值(PT/INR)1.21 ± 0.19、纤维蛋白原5.39 ± 1.49 g/L、抗凝血酶和血小板计数所代表的血液凝固指标。通过血小板功能分析仪(PFA)200检测(胶原/肾上腺素279 ± 38秒和胶原/二磷酸腺苷249 ± 66秒)在所有患者中诊断出primary止血病理。ECMO的运行时间为7.8 ± 3.4天。
依诺肝素抗凝在VV ECMO患者中似乎是可行的,且不良事件未增加。未来需要进一步的大样本和对照研究来支持我们的发现。