Department of Cardiology-Rhythmology, Marienhospital Siegen, Germany.
Department of Medicine-Cardiology, University Hospital Bonn, Venusberg-Campus 1, 53127, Bonn, Germany.
Clin Res Cardiol. 2024 Aug;113(8):1183-1199. doi: 10.1007/s00392-023-02319-9. Epub 2023 Nov 3.
Long-term oral anticoagulation (OAC) following successful catheter ablation of atrial fibrillation (AF) remains controversial. Prospective data are missing. The ODIn-AF study aimed to evaluate the effect of OAC on the incidence of silent cerebral embolic events and clinically relevant cardioembolic events in patients at intermediate to high risk for embolic events, free from AF after pulmonary vein isolation (PVI).
This prospective, randomized, multicenter, open-label, blinded endpoint interventional trial enrolled patients who were scheduled for PVI to treat paroxysmal or persistent AF. Six months after PVI, AF-free patients were randomized to receive either continued OAC with dabigatran or no OAC. The primary endpoint was the incidence of new silent micro- and macro-embolic lesions detected on brain MRI at 12 months of follow-up compared to baseline. Safety analysis included bleedings, clinically evident cardioembolic, and serious adverse events (SAE).
Between 2015 and 2021, 200 patients were randomized into 2 study arms (on OAC: n = 99, off OAC: n = 101). There was no significant difference in the occurrence of new cerebral microlesions between the on OAC and off OAC arm [2 (2%) versus 0 (0%); P = 0.1517] after 12 months. MRI showed no new macro-embolic lesion, no clinical apparent strokes were present in both groups. SAE were more frequent in the OAC arm [on OAC n = 34 (31.8%), off OAC n = 18 (19.4%); P = 0.0460]; bleedings did not differ.
Discontinuation of OAC after successful PVI was not found to be associated with an elevated risk of cerebral embolic events compared with continued OAC after a follow-up of 12 months.
成功进行导管消融心房颤动(AF)后,长期口服抗凝治疗(OAC)仍存在争议。目前缺乏前瞻性数据。ODIn-AF 研究旨在评估在无 AF 且已接受肺静脉隔离(PVI)的中高危栓塞事件患者中,OAC 是否会增加无症状性脑栓塞事件和临床相关心源性栓塞事件的发生率。
这项前瞻性、随机、多中心、开放标签、盲终点干预性试验纳入了计划接受 PVI 治疗阵发性或持续性 AF 的患者。PVI 后 6 个月,AF 无复发的患者被随机分配继续接受达比加群或不接受 OAC。主要终点是在 12 个月随访时与基线相比,脑 MRI 上检测到新的无症状性微栓子和大栓子病变的发生率。安全性分析包括出血、临床明显的心源性栓塞和严重不良事件(SAE)。
2015 年至 2021 年,200 例患者被随机分为 2 个研究组(OAC 组:n=99 例,无 OAC 组:n=101 例)。在 12 个月时,OAC 组和无 OAC 组新发生脑微梗死的发生率无显著差异[2(2%)对 0(0%);P=0.1517]。MRI 未显示新的大栓子病变,两组均未出现临床明显的中风。OAC 组 SAE 更为常见[OAC 组 n=34(31.8%),无 OAC 组 n=18(19.4%);P=0.0460];出血无差异。
与 12 个月时继续 OAC 相比,成功进行 PVI 后停用 OAC 并未发现与脑栓塞事件风险升高相关。