Schipper Jan-Hendrik, Sommer Anne-Sophie, Nies Richard Julius, Metze Clemens, Meertens Max Maria, Wörmann Jonas, Dittrich Sebastian, van den Bruck Jan-Hendrik, Sultan Arian, Lüker Jakob, Steven Daniel, Hohmann Christopher, Pfister Roman, Baldus Stephan, Eitel Ingo, Frerker Christian, Schmidt Tobias
Faculty of Medicine and University Hospital Cologne, Clinic III for Internal Medicine University of Cologne Germany.
Heart Center, Department of Electrophysiology University Hospital Cologne Cologne Germany.
J Am Heart Assoc. 2025 Feb 4;14(3):e038834. doi: 10.1161/JAHA.124.038834. Epub 2025 Feb 3.
Mitral valve transcatheter edge-to-edge repair (M-TEER) has emerged as a viable therapy option in patients with severe mitral regurgitation and high surgical risk. Although atrial fibrillation is common among patients undergoing M-TEER, the optimal anticoagulatory treatment after the intervention is unknown.
A single-center retrospective observational analysis was conducted using data from the M-TEER registry at the University Hospital Cologne collected from 2019 untill 2021 including patients undergoing M-TEER between November 2012 and April 2019. Patients with atrial fibrillation receiving consistent anticoagulation following M-TEER were categorized into a direct oral anticoagulant or a vitamin K antagonist (VKA) group. The primary end point was a composite of ischemic cerebrovascular and bleeding events. Additionally, overall survival was assessed.
Among 613 patients undergoing M-TEER, 206 met the inclusion criteria, with 61 receiving direct oral anticoagulants and 145 receiving VKAs. After a median follow-up of 833 (interquartile range, 355-1271) days, the incidence of the composite primary end point did not differ between direct oral anticoagulant and VKA groups (hazard ratio [HR], 0.51 [95% CI, 0.23-1.12]; =0.07). Similarly, rates of ischemic cerebrovascular events and bleeding events were similar between groups. However, the overall mortality rate was higher in the VKA group (HR, 2.56 [95% CI, 1.54-4.26]; =0.002). In the multivariable analysis, oral anticoagulation with a VKA was an independent predictor for death (adjusted HR, 2.23 [95% CI, 1.08-5.06]; =0.03).
Our findings suggest that direct oral anticoagulants may offer comparable efficacy and safety to VKAs in preventing thromboembolic events following M-TEER in patients with atrial fibrillation. Further randomized trials are needed to confirm these results and establish optimal anticoagulation strategies in this patient population.
二尖瓣经导管缘对缘修复术(M-TEER)已成为严重二尖瓣反流且手术风险高的患者的一种可行治疗选择。尽管心房颤动在接受M-TEER的患者中很常见,但干预后的最佳抗凝治疗尚不清楚。
采用科隆大学医院M-TEER登记处2019年至2021年收集的数据进行单中心回顾性观察分析,包括2012年11月至2019年4月期间接受M-TEER的患者。M-TEER后接受持续抗凝治疗的心房颤动患者被分为直接口服抗凝剂组或维生素K拮抗剂(VKA)组。主要终点是缺血性脑血管事件和出血事件的复合终点。此外,评估总生存率。
在613例接受M-TEER的患者中,206例符合纳入标准,其中61例接受直接口服抗凝剂,145例接受VKA。中位随访833(四分位间距,355-1271)天后,直接口服抗凝剂组和VKA组的复合主要终点发生率无差异(风险比[HR],0.51[95%CI,0.23-1.12];P=0.07)。同样,两组间缺血性脑血管事件和出血事件的发生率相似。然而,VKA组的总死亡率更高(HR,2.56[95%CI,1.54-4.26];P=0.002)。在多变量分析中,使用VKA进行口服抗凝是死亡的独立预测因素(调整后HR,2.23[95%CI,1.08-5.06];P=0.03)。
我们的研究结果表明,在心房颤动患者M-TEER后预防血栓栓塞事件方面,直接口服抗凝剂可能与VKA具有相当的疗效和安全性。需要进一步的随机试验来证实这些结果,并确定该患者群体的最佳抗凝策略。