首页> 外文期刊>The American heart journal >Treatment of functional mitral valve regurgitation with the permanent percutaneous transvenous mitral annuloplasty system: Results of the multicenter international Percutaneous Transvenous Mitral Annuloplasty System to Reduce Mitral Valve Regurgitation in Patients with Heart Failure trial
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Treatment of functional mitral valve regurgitation with the permanent percutaneous transvenous mitral annuloplasty system: Results of the multicenter international Percutaneous Transvenous Mitral Annuloplasty System to Reduce Mitral Valve Regurgitation in Patients with Heart Failure trial

机译:用永久性经皮吞咽二尖瓣瓣膜成形术治疗功能二尖瓣反渗透系统:多中心国际经皮吞咽二尖瓣瓣膜成形术的结果,减少心力衰竭患者二尖瓣反流

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摘要

Objectives PTOLEMY-2 was a prospective multicenter phase I single-arm feasibility trial to evaluate the second-generation permanent percutaneous transvenous mitral annuloplasty (PTMA) device in reducing functional mitral regurgitation (MR). Background Percutaneous MR reduction has been performed through a direct method of clipping and securing the mitral leaflets together or an indirect approach of reducing mitral annular dimension via the coronary sinus. The PTMA device is the only coronary sinus mitral repair device without a static fixation element. Methods Patients with at least moderate functional MR, New York Heart Association functional class II to IV, and left ventricular ejection fraction of 20% to 50% were enrolled at 14 centers in 5 countries. Device effects on patients were assessed by serial echocardiography, quality of life (QOL), and exercise capacity metrics. Results A total of 43 patients were recruited, and 30 patients (70%) were implanted with a permanent PTMA device with a mean follow-up of 5.8 ± 3.8 months. The primary safety end point (freedom from death, myocardial infarction, stroke, or emergency surgery) at 30 days was met in 28 patients, whereas 2 patients died of device-related complications. The primary efficacy end point (MR reduction of at least 1.0 grade or reduction of regurgitant orifice area by 0.1 cm2 or regurgitant volume by 15 mL or regurgitant fraction by 10% compared with baseline) was obtained in 13 patients. No significant changes were noted in MR parameters, ventricular volumes, or QOL. Distance walked on 6 minutes testing at 6-month follow-up increased from 331 ± 167 m to 417 ± 132 m (P =.65). Compared with nonresponders, responders had a higher baseline regurgitant orifice area 0.2 cm2 (P =.001) and less prior history of myocardial infarction (P =.02), coronary artery bypass surgery (P =.03), and ischemic MR (P =.04). Conclusions Overall, PTMA had mild impact on MR reduction, left ventricular remodeling, QOL, and exercise capacity. During follow-up, the risk/benefit ratio remained suboptimal.
机译:目标Ptolemy-2是一种前瞻性多中心阶段I单臂可行性试验,以评估减少功能二尖瓣流动(MR)的第二代永久经皮吞咽二尖瓣瓣膜成形术(PTMA)装置。背景技术经皮MR通过直接夹持和固定二尖瓣尖端的直接方法或通过冠状动脉窦减少二尖瓣尺寸的间接方法进行。 PTMA器件是唯一没有静态固定元件的冠状窦二尖瓣修复装置。方法患有至少适度的功能性Mr,纽约心脏关联功能II级至IV的患者,左心室喷射分数为20%至50%,在5个国家的14个中心注册。通过连续超声心动图,寿命质量(QOL)和运动能力指标评估患者的设备效果。结果共募集了43名患者,植入了30名患者(70%),用永久性PTMA装置植入,平均随访5.8±3.8个月。在28名患者中满足了30天的主要安全终点(死亡,心肌梗死,中风或急诊手术),而2名患者死于与器件相关的并发症。在13例患者中获得了13例初级疗效终点(将至少1.0级或再凝血孔面积的至少1.0℃或再凝固孔口,或再刺激体积减少15ml或再刺激物体积,或再刺激物体积与基线相比的级别为10%)。 MR参数,心室卷或QOL中没有明显改变。距离在6分钟的测试中散步6个月的随访时间从331±167米增加到417±132 m(p = .65)。与非反应者相比,响应者具有较高的基线反弧孔口区域& 0.2cm 2(p = .001)和较少的心肌梗死历史(p = .02),冠状动脉旁路手术(p = .03)和缺血先生(p = .04)。结论总体而言,PTMA对MR减少,左心室重塑,QOL和运动能力有轻微的影响。在随访期间,风险/效益比仍然是次优。

著录项

  • 来源
    《The American heart journal》 |2013年第5期|共9页
  • 作者单位

    Institut Universitaire de Cardiologie et de Pneumologie de Québec Quebec City QC Canada;

    Royal Victoria Hospital Montreal QC Canada;

    Rheinisch-Westfalische Technische Hochschule Universit?tsklinikum Aachen Aachen Germany;

    Klinikum Schwabing St?dtisches Klinikum München GmbH Munich Germany;

    CardioVascular Center Frankfurt Sankt Katharinen Frankfurt Germany;

    Institut Klinicke A Experimentalni Mediciny Prague Czech Republic;

    Albert-Ludwigs-Universit?t Freiburg Medizinische Universit?tsklinik Freiburg Germany;

    Thoraxcentrum Erasmus Medisch Centrum Rotterdam Netherlands;

    Institut Universitaire de Cardiologie et de Pneumologie de Québec Quebec City QC Canada;

    Duke University Medical Center Durham NC United States;

    Institut Universitaire de Cardiologie et de Pneumologie de Québec Quebec City QC Canada;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 心脏、血管(循环系)疾病;
  • 关键词

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