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千足虫IRIS经导管二尖瓣环成形术的早期经验。

Early experience with Millipede IRIS transcatheter mitral annuloplasty.

作者信息

Rogers Jason H, Boyd Walter D, Smith Thomas W, Bolling Steven F

机构信息

Division of Cardiovascular Medicine, University of California, Davis Medical Center, Sacramento, CA, USA.

Division of Cardiothoracic Surgery, University of California, Davis Medical Center, Sacramento, CA, USA.

出版信息

Ann Cardiothorac Surg. 2018 Nov;7(6):780-786. doi: 10.21037/acs.2018.10.05.

Abstract

The IRIS mitral annuloplasty ring is a transcatheter, transfemoral and transseptal-delivered complete, semi-rigid annuloplasty ring. The IRIS system mimics surgical annuloplasty by reducing the mitral septal-lateral dimension and improving leaflet coaptation. We report the early experience with the IRIS system in seven patients. These patients had 3-4+ mitral regurgitation (MR) with annular dilation and were symptomatic NYHA II-IV with LV end systolic dimensions ≤65 mm. Patients were excluded for LVEF <20%, aortic valve disease, right-sided heart failure and PA systolic pressure >70 mmHg. Baseline and 30-day transthoracic echocardiography and CT imaging was performed. In phase 1, 4 patients had surgical IRIS mitral ring implantation. In phase 2, 3 patients had transfemoral, transseptal delivery of the IRIS mitral ring. There was no procedural death, or MI. The mitral SL diameter was reduced from 38.0±4.1 to 25.9±4.9 mm at 30 days (31.8% SL reduction, n=7). MR was reduced from baseline 3-4+ to 0-1+ in all patients at 30 days. There were improvements in NYHA class and there was a decrease in diastolic LV volumes from 182.4±54.3 to 115.3±98.8 mL at 30 days (36.8% reduction). Based on these initial positive findings, ongoing clinical trials are underway to further evaluate the safety and efficacy of the IRIS ring.

摘要

IRIS二尖瓣瓣环成形环是一种经导管、经股静脉和经房间隔输送的完整半刚性瓣环成形环。IRIS系统通过减小二尖瓣间隔-侧壁尺寸和改善瓣叶贴合来模拟外科瓣环成形术。我们报告了7例患者使用IRIS系统的早期经验。这些患者有3-4+级二尖瓣反流(MR)且瓣环扩张,纽约心脏协会(NYHA)心功能分级为II-IV级,左心室收缩末期内径≤65mm。左心室射血分数(LVEF)<20%、主动脉瓣疾病、右侧心力衰竭和肺动脉收缩压>70mmHg的患者被排除。进行了基线和30天的经胸超声心动图及CT成像检查。在第一阶段,4例患者接受了外科IRIS二尖瓣环植入术。在第二阶段,3例患者经股静脉、经房间隔植入了IRIS二尖瓣环。无手术死亡或心肌梗死发生。30天时二尖瓣间隔-侧壁直径从38.0±4.1mm减小至25.9±4.9mm(间隔-侧壁直径减小31.8%,n=7)。所有患者的MR在30天时从基线的3-4+级降至0-1+级。NYHA分级有所改善,30天时左心室舒张末期容积从182.4±54.3mL降至115.3±98.8mL(减少36.8%)。基于这些初步的阳性结果,正在进行临床试验以进一步评估IRIS环的安全性和有效性。

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