Heart Rhythm Center, Okayama Heart Clinic, 54-1, Takeda, Naka Ward, Okayama, 703-8251, Okayama, Japan.
Department of Medical Technology, Okayama University Graduate School of Health Sciences, 2-5-1, Shikata-cho, Kita-ku, Okayama, 700-8558, Okayma, Japan.
J Cardiovasc Electrophysiol. 2018 Jun;29(6):835-843. doi: 10.1111/jce.13483. Epub 2018 Mar 30.
Different target activated clotting times (ACTs) during atrial fibrillation (AF) ablation have been proposed. Moreover, relationships between initial bolus dose of heparin at the start of AF ablation in patients receiving edoxaban anticoagulation therapy and ACT are unclear.
Patients who received anticoagulation with uninterrupted warfarin (control; n = 120) or interrupted edoxaban (n = 120) on the morning of day of ablation were studied. An initial dose of 100 U/kg heparin was administered as a reliable control for warfarin. Initial heparin doses of 120, 130, 140, or 150 U/kg were randomly administered to the edoxaban group.
Edoxaban group showed shorter baseline ACT before the procedure (130 ± 16 seconds) than the warfarin group (152 ± 26 seconds, P < 0.0001). In the warfarin group, 100 U/kg heparin showed 361 ± 48 seconds 15-minute ACT. In the edoxaban group, an increase in initial dose induced prolongation of 15-minute ACT (i.e., 15-minute ACTs of 293 ± 56, 306 ± 39, 311 ± 45, and 319 ± 45 seconds for 120, 130, 140, and 150 U/kg initial doses, respectively). The total heparin required during the procedure was higher in the edoxaban group than in the warfarin group (109 ± 37 vs. 77 ± 21 U/kg/h, P < 0.0001). The 120-150 U/kg dose of heparin in edoxaban group did not cause thromboembolic or major bleeding complications.
Edoxaban interrupted on the day of ablation showed a shorter baseline ACT than uninterrupted warfarin. Edoxaban required a higher initial heparin dose to achieve a similar 15-minute ACT to warfarin. These results are useful for determining the initial heparin dose required to achieve variable target ACTs.
在心房颤动(AF)消融期间,已经提出了不同的目标激活凝血时间(ACT)。此外,在接受依度沙班抗凝治疗的患者中,AF 消融开始时肝素初始推注剂量与 ACT 之间的关系尚不清楚。
研究了在消融日上午接受不间断华法林(对照组;n=120)或间断依度沙班(n=120)抗凝治疗的患者。作为华法林的可靠对照,给予 100 U/kg 肝素初始剂量。依度沙班组随机给予 120、130、140 或 150 U/kg 的初始肝素剂量。
依度沙班组的基线 ACT 术前更短(130±16 秒),而华法林组为 152±26 秒(P<0.0001)。华法林组 100 U/kg 肝素可使 15 分钟 ACT 达到 361±48 秒。依度沙班组中,初始剂量的增加可延长 15 分钟 ACT(即初始剂量为 120、130、140 和 150 U/kg 时,15 分钟 ACT 分别为 293±56、306±39、311±45 和 319±45 秒)。与华法林组相比,依度沙班组术中所需肝素总量更高(109±37 比 77±21 U/kg/h,P<0.0001)。依度沙班组中 120-150 U/kg 的肝素剂量未引起血栓栓塞或大出血并发症。
AF 消融日中断的依度沙班的基线 ACT 短于不间断的华法林。依度沙班需要更高的初始肝素剂量才能达到与华法林相似的 15 分钟 ACT。这些结果对于确定达到不同目标 ACT 所需的初始肝素剂量很有用。