Polyclinic of Bari-Hospital, Department of Cardiology, Bari, Italy.
Vivantes Klinikum im Friedrichshain, Department of Anaesthesia & Intensive Care Medicine, Emergency Medicine, and Pain Therapy, Berlin, Germany.
Clin Cardiol. 2020 Jul;43(7):769-780. doi: 10.1002/clc.23379. Epub 2020 May 14.
Guidance for periprocedural anticoagulant management is mainly based on limited data from Phase III or observational studies and expert opinion.
EMIT-AF/VTE was designed to document the risks of bleeding and thromboembolic events in more than 1000 patients on edoxaban undergoing diagnostic and therapeutic procedures in clinical practice.
Routine care in a multinational multicenter, prospective observational study. Participants were adult patients with atrial fibrillation and/or venous thromboembolism treated with edoxaban for stroke prevention or for secondary prevention in venous thromboembolic disease, undergoing a wide range of diagnostic and therapeutic procedures. Edoxaban therapy was interrupted periprocedurally at the treating physician's discretion. Patients were evaluated from 5 days pre- until 30 days postprocedure. Primary outcome was the incidence of International Society on Thrombosis and Haemostasis defined major bleeding; secondary outcomes included incidence of clinically relevant non-major bleeding, acute coronary syndrome, and acute thromboembolic events.
Outcomes and management are reported for the first procedures in 1155 unselected patients. Five cases of major bleeding (0.4%) and eight of clinically relevant non-major bleeding (0.7%) were documented, five (38%) of which occurred outside the period of likely edoxaban effect (last edoxaban dose ≥3 days prior to bleeding). Five (0.4%) deaths from any cause, seven acute thromboembolic events (0.6%) including two cardiac deaths (0.2%) in six patients, and one acute coronary event (0.1%) occurred.
The periprocedural bleeding and acute thromboembolic event risks for patients treated with edoxaban were low. This can help inform both clinical routine and guidelines for the periprocedural management of edoxaban.
围手术期抗凝管理指南主要基于 III 期研究或观察性研究以及专家意见的有限数据。
EMIT-AF/VTE 旨在记录 1000 多名接受依度沙班治疗的患者在接受诊断和治疗程序时发生出血和血栓栓塞事件的风险,这些患者的房颤和/或静脉血栓栓塞症在临床实践中接受依度沙班治疗。
这是一项多中心、前瞻性观察性研究。参与者为接受依度沙班治疗的房颤和/或静脉血栓栓塞症患者,用于预防卒中和静脉血栓栓塞性疾病的二级预防,接受广泛的诊断和治疗程序。依度沙班治疗在治疗医生的决定下在围手术期中断。患者从术前 5 天到术后 30 天进行评估。主要结局是国际血栓与止血学会定义的大出血发生率;次要结局包括临床相关非大出血、急性冠状动脉综合征和急性血栓栓塞事件的发生率。
报告了 1155 例未选择患者的首次手术的结果和管理。记录了 5 例大出血(0.4%)和 8 例临床相关非大出血(0.7%),其中 5 例(38%)发生在可能的依度沙班作用时间之外(最后一次依度沙班剂量在出血前≥3 天)。5 例(0.4%)任何原因导致的死亡,7 例急性血栓栓塞事件(0.6%),包括 6 例中的 2 例心脏死亡(0.2%)和 1 例急性冠状动脉事件(0.1%)。
接受依度沙班治疗的患者围手术期出血和急性血栓栓塞事件风险较低。这有助于为依度沙班的围手术期管理提供临床常规和指南信息。