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经导管植入 MONARC 冠状窦装置治疗二尖瓣反流:EVOLUTION 阶段 I 研究的 1 年结果(经皮爱德华兹生命科学二尖瓣环成形术系统治疗二尖瓣反流的临床评估)。

Transcatheter implantation of the MONARC coronary sinus device for mitral regurgitation: 1-year results from the EVOLUTION phase I study (Clinical Evaluation of the Edwards Lifesciences Percutaneous Mitral Annuloplasty System for the Treatment of Mitral Regurgitation).

机构信息

Department of Coronary Heart Disease, Skane University Hospital, Lund, Sweden.

出版信息

JACC Cardiovasc Interv. 2011 Jan;4(1):115-22. doi: 10.1016/j.jcin.2010.08.027.

Abstract

OBJECTIVES

This study sought to assess the safety and efficacy of transcatheter valve annuloplasty in patients with mitral regurgitation (MR).

BACKGROUND

Mitral regurgitation is associated with a worsened prognosis in patients with dilated cardiomyopathy. Surgical mitral annuloplasty reduces the septal-lateral dimension of the mitral annulus resulting in improved leaflet coaptation with a reduction in regurgitation. Percutaneous annuloplasty with the MONARC device (Edwards Lifesciences, Irvine, California) implanted within the coronary sinus is designed to reduce mitral regurgitation through a similar mechanism.

METHODS

A total of 72 patients with MR grade ≥ 2 were enrolled at 8 participating centers in 4 countries. Clinical evaluation and transthoracic echocardiography were performed at baseline and at 3, 6, and 12 months. Multislice cardiac computed tomography and coronary angiography were performed at baseline and 3 months.

RESULTS

The MONARC device was implanted in 59 of 72 patients (82%). The primary safety end point (freedom from death, tamponade, or myocardial infarction at 30 days) was met in 91% of patients at 30 days and in 82% at 1 year. Computed tomography imaging documented passage of the great cardiac vein over an obtuse marginal artery in 55% of patients and was associated with angiographic coronary artery compression in 15 patients and myocardial infarction in 2 patients (3.4%). At 12 months, a reduction in MR by ≥ 1 grade was observed in 50.0% of 22 implanted patients with matched echocardiograms and in 85.7% of 7 patients with baseline MR grade ≥ 3.

CONCLUSIONS

Implantation of the MONARC device in the coronary sinus is feasible and may reduce MR. However, coronary artery compression may occur in patients in whom the great cardiac vein passes over a coronary artery, necessitating strategies in future studies to avoid this occurrence.

摘要

目的

本研究旨在评估经导管瓣环成形术治疗二尖瓣反流(MR)患者的安全性和疗效。

背景

MR 与扩张型心肌病患者的预后恶化相关。二尖瓣环成形术通过缩小二尖瓣环的间隔-侧壁尺寸,改善瓣叶对合,减少反流,从而降低二尖瓣反流。MONARC 装置(爱德华兹生命科学公司,加利福尼亚州欧文)通过经冠状窦植入,通过类似的机制降低二尖瓣反流。

方法

共有 72 名 MR 分级≥2 级的患者在 4 个国家的 8 个参与中心入组。在基线、3、6 和 12 个月时进行临床评估和经胸超声心动图检查。在基线和 3 个月时进行多层心脏 CT 和冠状动脉造影。

结果

72 例患者中有 59 例(82%)植入了 MONARC 装置。30 天时主要安全性终点(30 天内无死亡、心脏压塞或心肌梗死)在 91%的患者中得到满足,1 年后在 82%的患者中得到满足。心脏 CT 成像显示 55%的患者大心静脉穿过钝角缘动脉,15 例患者存在血管造影冠状动脉受压,2 例患者(3.4%)发生心肌梗死。在 12 个月时,22 例有匹配超声心动图的植入患者中有 50.0%的患者 MR 分级至少降低 1 级,7 例基线 MR 分级≥3 级的患者中有 85.7%的患者 MR 分级降低。

结论

经冠状窦植入 MONARC 装置是可行的,可能会降低 MR。然而,大心静脉穿过冠状动脉的患者可能会发生冠状动脉受压,未来的研究中需要制定策略来避免这种情况的发生。

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