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经导管主动脉瓣植入术治疗重度主动脉瓣狭窄合并大瓣环患者,应用自膨式 31 毫米美敦力 CoreValve 瓣膜:初步临床经验。

Transcatheter aortic valve implantation in patients with severe aortic valve stenosis and large aortic annulus, using the self-expanding 31-mm Medtronic CoreValve prosthesis: first clinical experience.

机构信息

Department of Cardiology, University Medical Center Utrecht, Utrecht, The Netherlands.

Medisch Centrum Leeuwarden, Afdeling Hartcatheterisatie, Leeuwarden, The Netherlands.

出版信息

J Thorac Cardiovasc Surg. 2014 Aug;148(2):492-9.e1. doi: 10.1016/j.jtcvs.2013.09.059. Epub 2013 Nov 19.

Abstract

OBJECTIVES

With the introduction of the 31-mm Medtronic CoreValve prosthesis, patients with large aortic annulus have become eligible for transcatheter aortic valve implantation. The aim of this study was to evaluate the feasibility, efficacy, and safety of transcatheter aortic valve implantation using the 31-mm Medtronic CoreValve in patients with severe aortic valve stenosis and large aortic annulus.

METHODS

Five institutions in the Netherlands and Italy participated in a retrospective multicenter registry. Clinical, procedural, and imaging data of patients treated with the 31-mm Medtronic CoreValve were retrospectively collected in accordance with the Valve Academic Research Consortium-2 criteria.

RESULTS

Between August 2011 and November 2012, 47 patients (44 men, mean age 77.6 ± 8.9 years) received the 31-mm Medtronic CoreValve prosthesis for severe aortic stenosis. Device success (correct positioning of a single valve with intended performance and no all-cause 30-day mortality) was achieved in 31 patients (66.0%). Reasons for failing the device success criteria were significant prosthetic aortic regurgitation in 3 patients (6.4%), second valve implantation in 10 patients (21.2%) (8 cases of malpositioning with high-grade aortic regurgitation, 1 acute valve dislocation, and 1 delayed valve dislocation), 1 of whom died intrahospital, and in-hospital mortality in a further 3 patients (6.4%). Peak and mean transaortic gradients decreased significantly (P < .01). The rate of new pacemaker implantations was 41.7%.

CONCLUSIONS

In this retrospective multicenter registry, transcatheter treatment of severe aortic valve stenosis with the 31-mm Medtronic CoreValve seemed to be challenging, even in experienced hands. If the prosthesis is properly implanted, it offers adequate valve hemodynamics and proper functioning.

摘要

目的

随着 31 毫米美敦力 CoreValve 假体的引入,大主动脉瓣环的患者已符合经导管主动脉瓣植入术的条件。本研究旨在评估在大主动脉瓣环重度主动脉瓣狭窄患者中使用 31 毫米美敦力 CoreValve 进行经导管主动脉瓣植入术的可行性、疗效和安全性。

方法

荷兰和意大利的 5 家机构参与了一项回顾性多中心注册研究。根据 Valve Academic Research Consortium-2 标准,回顾性地收集了使用 31 毫米美敦力 CoreValve 治疗的患者的临床、手术和影像学数据。

结果

2011 年 8 月至 2012 年 11 月,47 名(44 名男性,平均年龄 77.6±8.9 岁)患者因严重主动脉瓣狭窄接受了 31 毫米美敦力 CoreValve 假体。31 名患者(66.0%)达到了器械成功(单一瓣膜正确定位,预期性能,无 30 天全因死亡率)。未能达到器械成功标准的原因包括 3 名患者(6.4%)出现显著的人工主动脉瓣反流,10 名患者(21.2%)需要植入第二枚瓣膜(8 例因主动脉瓣反流程度较高而定位不当,1 例急性瓣膜脱位,1 例延迟性瓣膜脱位),其中 1 例患者院内死亡,另有 3 例患者院内死亡(6.4%)。跨主动脉峰压和平均压明显降低(P<.01)。新植入起搏器的比例为 41.7%。

结论

在这项回顾性多中心注册研究中,即使在经验丰富的医生手中,使用 31 毫米美敦力 CoreValve 治疗严重主动脉瓣狭窄也具有挑战性。如果假体正确植入,它可以提供足够的瓣膜血流动力学和适当的功能。

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