Interventional Cardiology, Cardiologicum Hamburg, Schloßgarten 3-7, 22401 Hamburg, Germany.
J Invasive Cardiol. 2022 May;34(5):E348-E355. doi: 10.25270/jic/21.00240.
Left atrial appendage occlusion (LAAO) is recommended for patients with atrial fibrillation at increased stroke risk, where effective long-term oral anticoagulation (OAC) is not feasible. In order to assess long-term safety of LAAO with aspirin monotherapy or no therapy, we aimed to report on patients with the Watchman LAAO device (Boston Scientific) once postimplantation intensified antiplatelet or anticoagulation therapy is discontinued.
A total of 1025 patients scheduled for elective LAAO therapy prospectively consented for participation in the EWOLUTION registry; 1005 patients received a successful implant and were followed for 2 years. We identified 766 patients in EWOLUTION on single-antiplatelet therapy (SAPT; n = 639) or no therapy (n = 127) for ≥1 year following LAAO.
Three to 6 months after LAAO, 766 patients were switched to SAPT or no therapy and were followed for at least 1 year until the study's conclusion or with events while on SAPT/ no therapy; mean time on SAPT/no therapy was 536.56 ± 177.59 days. Patients experienced 1.4 ischemic strokes per 100 patient years (PY) despite a CHA2DS2-VASC score of 4.3 ± 1.6. Major nonprocedural bleeding rates were low, with 1.3 major bleeds per 100 PY with a mean HAS-BLED score of 2.2 ± 1.2. Furthermore, the ischemic stroke rate in the SAPT/no-therapy subgroup was similar to the whole EWOLUTION collective and high-risk subgroups; the bleeding rate was even lower. When analyzed separately, strokes (2.1/100 PY) and bleedings (1.4/100 PY) of the no-therapy subgroup were similar to patients on SAPT (strokes 0.7/100 PY [P=.70]; bleedings 1.4/100 PY [P=.90]).
Outcome data of patients on SAPT/no therapy for ≥1 year following Watchman implantation in the EWOLUTION registry suggest the efficacy and safety of LAAO.
左心耳封堵术(LAAO)适用于存在卒中风险且无法长期有效口服抗凝治疗(OAC)的房颤患者。为了评估 LAAO 术后应用阿司匹林单药或无抗栓治疗的长期安全性,我们旨在报告 Watchman LAAO 装置(波士顿科学公司)植入后一旦停止强化抗血小板或抗凝治疗的患者情况。
共有 1025 例拟行择期 LAAO 治疗的患者前瞻性同意参与 EWOLUTION 注册研究;1005 例患者成功植入并随访 2 年。我们在 EWOLUTION 中识别出 766 例 LAAO 术后接受至少 1 年单抗血小板治疗(SAPT;n = 639)或无治疗(n = 127)的患者。
LAAO 术后 3-6 个月,766 例患者转换为 SAPT 或无治疗,并至少随访 1 年直至研究结束或 SAPT/无治疗期间出现事件;SAPT/无治疗的中位时间为 536.56±177.59 天。尽管 CHA2DS2-VASC 评分为 4.3±1.6,但患者仍发生 1.4 例/100 患者年的缺血性卒中。主要非手术出血发生率较低,每 100 患者年发生 1.3 例大出血,平均 HAS-BLED 评分为 2.2±1.2。此外,SAPT/无治疗亚组的缺血性卒中发生率与 EWOLUTION 全体和高危亚组相似;出血率甚至更低。单独分析时,无治疗亚组的卒中(2.1/100 患者年)和出血(1.4/100 患者年)与 SAPT 组相似(卒中 0.7/100 患者年[P=.70];出血 1.4/100 患者年[P=.90])。
EWOLUTION 注册研究中 Watchman 植入后接受 SAPT/无治疗至少 1 年的患者数据表明 LAAO 的疗效和安全性。