Arrhythmia Section, Cardiovascular Clinic Institute, Hospital Clínic, University of Barcelona, Barcelona, Catalonia, Spain; Centro de Investigación Biomédica en Red Enfermedades Cardiovasculares (CIBERCV), Madrid, Spain.
Arrhythmia Section, Cardiovascular Clinic Institute, Hospital Clínic, University of Barcelona, Barcelona, Catalonia, Spain.
Heart Rhythm. 2019 Dec;16(12):1849-1854. doi: 10.1016/j.hrthm.2019.05.016. Epub 2019 May 22.
The Micra transcatheter pacing system (Micra TPS) is often implanted in patients with atrial fibrillation and thus with increased thromboembolic risk. It is unknown whether the use of anticoagulants, associated with the use of a large venous introducer, implies an increased risk of bleeding in this group of patients.
The purpose of this study was to assess the incidence of bleeding and thromboembolic complications after Micra TPS implantation with and without therapeutic anticoagulation.
This single-center observational study included 107 consecutive patients receiving the Micra TPS from 2014 to 2018. At procedure completion, a figure-of-eight suture was placed at the femoral puncture site after sheath withdrawal and was maintained for 24 hours. In patients receiving enoxaparin or new oral anticoagulants, treatment was discontinued 12 or 24 hours before the procedure, respectively, and was reinitiated 4-6 hours postprocedure. In those receiving vitamin K antagonists (VKAs), dosing was not discontinued and the procedure was performed if the international normalized ratio was less than 3.
Sixty-four patients (60%) did not receive anticoagulants. Of the 43 (40%) who did, 29 (67%) received VKAs, 8 (19%) received new oral anticoagulants, and 6 (14%) received enoxaparin. Two patients presented hemorrhagic or thromboembolic complications during short-term follow-up: 1 woman receiving VKAs presented hemorrhagic pericardial effusion without tamponade and 1 woman not receiving anticoagulants presented thrombosis of the ipsilateral saphenous vein.
Bleeding and thromboembolic complications after receiving Micra TPSs are infrequent. The use of anticoagulant therapy, regardless of the type, does not increase the complications associated with the procedure.
Micra 经导管起搏系统(Micra TPS)通常植入有房性颤动且血栓栓塞风险增加的患者体内。目前尚不清楚在这群患者中,使用抗凝药物联合大静脉导入器是否会增加出血风险。
本研究旨在评估 Micra TPS 植入术有无抗凝治疗情况下的出血和血栓栓塞并发症发生率。
本单中心观察性研究纳入了 2014 年至 2018 年间接受 Micra TPS 治疗的 107 例连续患者。在手术完成时,在鞘管退出后在股动脉穿刺部位放置 8 字形缝线,并维持 24 小时。在接受依诺肝素或新型口服抗凝剂的患者中,分别在术前 12 或 24 小时停止治疗,并在术后 4-6 小时重新开始治疗。在接受维生素 K 拮抗剂(VKA)治疗的患者中,不停止剂量,INR < 3 时进行手术。
64 例(60%)患者未接受抗凝治疗。在接受抗凝治疗的 43 例(40%)患者中,29 例(67%)接受 VKA,8 例(19%)接受新型口服抗凝剂,6 例(14%)接受依诺肝素。在短期随访期间,有 2 例患者出现出血或血栓栓塞并发症:1 例接受 VKA 的女性出现无填塞的心包积血,1 例未接受抗凝治疗的女性出现同侧隐静脉血栓形成。
接受 Micra TPS 后出血和血栓栓塞并发症较为少见。使用抗凝治疗(无论类型如何)并不会增加与手术相关的并发症。