Armbruster Heather L, Lindsley John P, Moranville Michael P, Habibi Mohammadali, Khurram Irfan M, Spragg David D, Berger Ronald D, Calkins Hugh, Marine Joseph E
The Johns Hopkins Hospital, Baltimore, MD, USA
The Johns Hopkins Hospital, Baltimore, MD, USA.
Ann Pharmacother. 2015 Mar;49(3):278-84. doi: 10.1177/1060028014563950. Epub 2014 Dec 16.
The novel oral anticoagulants (NOACs) are used for stroke prevention in atrial fibrillation (AF), but their safety and efficacy in the periablation period are not well established. Additionally, no standard procedure for managing periprocedural and intraprocedural anticoagulation has been established.
To evaluate the frequency of hemorrhagic and thrombotic events as well as periprocedural management strategies of NOACs compared with warfarin as anticoagulation therapy for AF ablation.
This was a retrospective cohort study from a prospective AF ablation registry maintained at a large, academic medical center.
A total of 374 cases (173 warfarin, 123 dabigatran, 61 rivaroxaban, and 17 apixaban) were included in the analysis. The overall hemorrhagic/thrombotic event rate was 14.2 % (major hemorrhage 2.7%, minor hemorrhage 11.2%, thrombotic stroke 0.5%). The frequency of minor hemorrhage was significantly higher with warfarin compared with dabigatran (15% vs 5.7%, P = 0.012). The average heparin dose required to reach the goal activated clotting time (ACT) was 5600 units for warfarin, 12 900 units for dabigatran (P < 0.001), 15 100 units for rivaroxaban (P < 0.001), and 14 700 units for apixaban (P < 0.001). The average time in minutes to reach the goal ACT was significantly longer, compared with warfarin, for dabigatran (57 vs 28, P < 0.001), rivaroxaban (63 vs 28, P < 0.001), and apixaban (72 vs 28, P < 0.001).
Compared with warfarin, periprocedural anticoagulation with dabigatran resulted in fewer minor hemorrhages and total adverse events after AF ablation. Patients anticoagulated with NOACs required larger doses of heparin and took longer to reach the goal ACT compared with patients anticoagulated with warfarin.
新型口服抗凝药(NOACs)用于心房颤动(AF)的卒中预防,但其在消融围手术期的安全性和有效性尚未明确。此外,尚未建立围手术期和手术过程中抗凝管理的标准程序。
评估与华法林相比,NOACs作为AF消融抗凝治疗时出血和血栓形成事件的发生率以及围手术期管理策略。
这是一项回顾性队列研究,数据来自于一家大型学术医疗中心前瞻性维护的AF消融登记系统。
分析共纳入374例患者(173例使用华法林,123例使用达比加群,61例使用利伐沙班,17例使用阿哌沙班)。总体出血/血栓形成事件发生率为14.2%(大出血2.7%,小出血11.2%,血栓性卒中0.5%)。与达比加群相比,华法林导致的小出血发生率显著更高(15%对5.7%,P = 0.012)。达到目标活化凝血时间(ACT)所需的平均肝素剂量,华法林为5600单位,达比加群为12900单位(P < 0.001),利伐沙班为15100单位(P < 0.001),阿哌沙班为14700单位(P < 0.001)。与华法林相比,达比加群(57分钟对28分钟,P < 0.001)、利伐沙班(63分钟对28分钟,P < 0.001)和阿哌沙班(72分钟对28分钟,P < 0.001)达到目标ACT的平均时间显著更长。
与华法林相比,AF消融术后使用达比加群进行围手术期抗凝导致的小出血和总不良事件更少。与使用华法林抗凝的患者相比,使用NOACs抗凝的患者需要更大剂量的肝素,且达到目标ACT的时间更长。