Cedars-Sinai Medical Center, Heart Institute, Los Angeles, California, USA.
Heart Institute, Cedars Sinai Medical Center, Los Angeles, California, US.
Heart. 2019 Nov;105(21):1622-1628. doi: 10.1136/heartjnl-2017-312605. Epub 2018 Aug 4.
This study evaluates the 5-year clinical outcomes of transcatheter mitral valve (MV) repair with the MitraClip device in patients at high risk for MV surgery treated in the Endovascular Valve Edge-to-Edge Repair (EVEREST) II High Risk Study (HRS).
Patients with mitral regurgitation (MR) 3+ or 4+ and predicted surgical mortality risk ≥12% or surgeon assessment based on prespecified high-risk factors were enrolled. Patients prospectively consented to 5 years of follow-up.
At 5 years, clinical follow-up was achieved in 90% of 78 enrolled patients. The rate of postprocedural adverse events declined from 30 days to 1 year follow-up and was stable thereafter through 5 years. Two patients (2.6%) developed mitral stenosis (MS). Two patients underwent MV surgery, including one due to MS. A total of 42 deaths were reported through 5 years. Effectiveness measures at 5 years showed reductions in MR severity to ≤2+ in 75% of patients (p=0.0107), left ventricular (LV) end-diastolic volume (-38.2 mL; 95% CI -55.0 to -21.4; p<0.0001) and LV end-systolic volume (-14.6 mL; 95% CI -27.7 to -1.5; p=0.0303) compared with baseline. The New York Heart Association (NYHA) functional class improved from baseline to 5 years (p<0.005), and septal-lateral annular dimensions remained stable with no indication of mitral annular dilation through 5 years.
The EVEREST II HRS demonstrated long-term safety and efficacy of MitraClip in high-surgical-risk patients through 5 years. The observed mortality was most likely a consequence of the advanced age and comorbidity profile of the enrolled patients, while improvements in NYHA class in surviving patients were durable through long-term follow-up.
NCT01940120.
本研究评估了在血管内瓣缘对缘修复(EVEREST)Ⅱ高风险研究(HRS)中接受治疗的高危二尖瓣(MV)手术患者中,使用 MitraClip 装置进行经导管 MV 修复的 5 年临床结果。
纳入 MR 3+或 4+且预测手术死亡率风险≥12%或基于预定高危因素的外科医生评估的 MV 反流患者。患者前瞻性同意进行 5 年随访。
78 名入组患者中,90%的患者获得了 5 年临床随访。术后不良事件发生率从 30 天下降至 1 年随访,此后至 5 年保持稳定。2 例(2.6%)发生二尖瓣狭窄(MS)。2 例患者接受了 MV 手术,其中 1 例因 MS 而行手术。通过 5 年共报告了 42 例死亡。5 年时的有效性测量结果显示,75%的患者 MR 严重程度降低至≤2+(p=0.0107),左心室(LV)舒张末期容积(-38.2ml;95%置信区间-55.0 至-21.4;p<0.0001)和 LV 收缩末期容积(-14.6ml;95%置信区间-27.7 至-1.5;p=0.0303)与基线相比均减少。与基线相比,纽约心脏协会(NYHA)功能分级从基线改善至 5 年(p<0.005),并且通过 5 年的随访,室间隔-侧壁环形尺寸保持稳定,没有二尖瓣环扩张的迹象。
EVEREST Ⅱ HRS 表明,在高危患者中,MitraClip 在 5 年内具有长期的安全性和有效性。观察到的死亡率很可能是由于入组患者的高龄和合并症情况所致,而存活患者的 NYHA 分级改善在长期随访中是持久的。
NCT01940120。