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可重定位自膨式经导管主动脉瓣置换术的临床结果:国际 FORWARD 研究。

Clinical Outcomes With a Repositionable Self-Expanding Transcatheter Aortic Valve Prosthesis: The International FORWARD Study.

机构信息

Department of Medicine, University of Bonn, Bonn, Germany.

Department of Cardiology, Erasmus Medical Centre Rotterdam, Rotterdam, the Netherlands.

出版信息

J Am Coll Cardiol. 2017 Aug 15;70(7):845-853. doi: 10.1016/j.jacc.2017.06.045.

Abstract

BACKGROUND

Clinical outcomes in large patient populations from real-world clinical practice with a next-generation self-expanding transcatheter aortic valve are lacking.

OBJECTIVES

This study sought to document the clinical and device performance outcomes of transcatheter aortic valve replacement (TAVR) with a next-generation, self-expanding transcatheter heart valve (THV) system in patients with severe symptomatic aortic stenosis (AS) in routine clinical practice.

METHODS

The FORWARD (CoreValve Evolut R FORWARD) study is a prospective, single-arm, multinational, multicenter, observational study. An independent clinical events committee adjudicated safety endpoints based on Valve Academic Research Consortium-2 definitions. An independent echocardiographic core laboratory evaluated all echocardiograms. From January 2016 to December 2016, TAVR with the next-generation self-expanding THV was attempted in 1,038 patients with symptomatic, severe AS at 53 centers on 4 continents.

RESULTS

Mean age was 81.8 ± 6.2 years, 64.9% were women, the mean Society of Thoracic Surgeons Predicted Risk of Mortality was 5.5 ± 4.5%, and 33.9% of patients were deemed frail. The repositioning feature of the THV was applied in 25.8% of patients. A single valve was implanted in the proper anatomic location in 98.9% of patients. The mean aortic valve gradient was 8.5 ± 5.6 mm Hg, and moderate or severe aortic regurgitation was 1.9% at discharge. All-cause mortality was 1.9%, and disabling stroke occurred in 1.8% at 30 days. The expected-to-observed early surgical mortality ratio was 0.35. A pacemaker was implanted in 17.5% of patients.

CONCLUSIONS

TAVR using the next-generation THV is clinically safe and effective for treating older patients with severe AS at increased operative risk. (CoreValve Evolut R FORWARD Study [FORWARD]; NCT02592369).

摘要

背景

缺乏在真实世界临床实践中使用下一代自膨式经导管主动脉瓣对大量患者的临床结局和器械性能进行评估的研究。

目的

本研究旨在评估在常规临床实践中,使用新一代自膨式经导管心脏瓣膜(THV)系统行经导管主动脉瓣置换术(TAVR)治疗有症状的严重主动脉瓣狭窄(AS)患者的临床结局和器械性能。

方法

前瞻性、单臂、多国、多中心、观察性的 FORWARD(CoreValve Evolut R FORWARD)研究。根据 Valve Academic Research Consortium-2 定义,独立临床事件委员会对安全性终点进行裁决。独立的超声心动图核心实验室对所有超声心动图进行评估。2016 年 1 月至 2016 年 12 月,在 4 大洲的 53 个中心对 1038 例有症状、严重 AS 的患者尝试进行了新一代自膨式 THV 的 TAVR。

结果

平均年龄为 81.8±6.2 岁,64.9%为女性,胸外科医师协会预测死亡率平均为 5.5±4.5%,33.9%的患者身体虚弱。THV 的重新定位功能在 25.8%的患者中应用。98.9%的患者的单个瓣膜均被正确植入到解剖位置。平均主动脉瓣跨瓣压差为 8.5±5.6mmHg,出院时中度或重度主动脉瓣反流发生率为 1.9%。全因死亡率为 1.9%,30 天内致残性卒中发生率为 1.8%。期望与观察到的早期手术死亡率比值为 0.35。17.5%的患者植入了起搏器。

结论

使用新一代 THV 的 TAVR 为治疗高手术风险的老年严重 AS 患者提供了一种安全有效的治疗方法。(CoreValve Evolut R FORWARD 研究[FORWARD];NCT02592369)。

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