Quebec Heart and Lung Institute, Laval University, Quebec City, Quebec, Canada.
Centre Hospitalier Universitaire de Quebec, Quebec City, Quebec, Canada.
Am J Cardiol. 2019 May 1;123(9):1538-1545. doi: 10.1016/j.amjcard.2019.01.043. Epub 2019 Feb 8.
No data exist on the optimal duration of antithrombotic therapy (AT) following patent foramen ovale (PFO) closure. We sought to assess the safety of AT discontinuation following PFO closure in patients with a cryptogenic ischemic event. A total of 453 consecutive patients (mean age: 48 ± 13years, men: 51%) who underwent PFO closure due to a cryptogenic ischemic event were included. All patients were on AT following PFO closure (antiplatelet therapy: 92.7%, anticoagulation: 7.3%). Ischemic and bleeding events, and AT were assessed at a median follow-up of 8 (IQR: 4 to 11) years, and follow-up was complete in 96% of patients. Stroke and transient ischemic attack occurred in 4 (0.9%) and 12 (2.6%) patients, respectively, and 27 (6.0%) patients had bleeding events (major in 6 [1.3%] patients, including 4 episodes of intracranial hemorrhage). All major bleeding events occurred under aspirin therapy. A total of 82 patients (18%) stopped the AT at a median of 7 (IQR: 5 to 34) months post-PFO closure (due to a bleeding event or gastrointestinal symptoms: 13 patients, no specific reason: 69 patients), and none of them had any ischemic event after a median time of 7 (IQR 3 to 10) years without any AT. A propensity score matched analysis including 46 patients who discontinued the AT within 1-year post-PFO closure and 120 patients with an ongoing AT showed the lack of differences in ischemic events between groups (0 vs 0.2 stroke/transient ischemic attack per 100 patient-years in the no-AT and AT groups, respectively). In conclusion, in young patients who underwent PFO closure, bleeding events occurred in ∼6% of patients after a median follow-up of 8years. AT was discontinued in about one fifth of patients (most of them within the year following PFO closure), and this was not associated with any increase in ischemic events at long-term follow-up. These results suggest that, in patients without other co-morbidities increasing the risk of stroke, temporary AT following PFO closure may be a reasonable strategy.
目前尚无关于卵圆孔未闭(PFO)封堵术后抗栓治疗(AT)最佳持续时间的数据。我们旨在评估 PFO 封堵术后血栓栓塞事件患者停止 AT 的安全性。共纳入 453 例因隐源性缺血事件而接受 PFO 封堵术的连续患者(平均年龄:48 ± 13 岁,男性:51%)。所有患者在 PFO 封堵术后均接受 AT(抗血小板治疗:92.7%,抗凝治疗:7.3%)。在中位随访 8 年(IQR:4 至 11)时评估缺血和出血事件及 AT,96%的患者随访完整。4 例(0.9%)和 12 例(2.6%)患者分别发生卒中和短暂性脑缺血发作,27 例(6.0%)患者发生出血事件(6 例[1.3%]为大出血事件,包括 4 例颅内出血)。所有大出血事件均发生在阿司匹林治疗期间。共有 82 例(18%)患者在 PFO 封堵术后中位时间 7 个月(IQR:5 至 34)时停止 AT(因出血事件或胃肠道症状停药:13 例,无具体原因停药:69 例),且在中位时间 7 年后中位数时间 10 年无任何 AT 情况下,他们均未发生任何缺血事件。包括 46 例在 PFO 封堵后 1 年内停止 AT 和 120 例持续 AT 的患者在内的倾向评分匹配分析显示,两组间缺血事件无差异(无 AT 组和 AT 组的每 100 患者年分别为 0 例和 0.2 例卒中和短暂性脑缺血发作)。总之,在接受 PFO 封堵术的年轻患者中,中位随访 8 年后约有 6%的患者发生出血事件。约有五分之一的患者(其中大多数在 PFO 封堵后 1 年内)停止 AT,这与长期随访时缺血事件无增加无关。这些结果表明,在没有其他增加卒中风险的合并症的患者中,PFO 封堵术后的临时 AT 可能是一种合理的策略。