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经导管将主动脉瓣假体植入退化的二尖瓣生物假体和失效的瓣环成形环:根据入路和二尖瓣学术研究联盟(MVARC)标准的结果

Transcatheter implantation of aortic valve prostheses into degenerated mitral valve bioprostheses and failed annuloplasty rings: outcomes according to access route and Mitral Valve Academic Research Consortium (MVARC) criteria.

作者信息

Frerker Christian, Schmidt Tobias, Schlüter Michael, Bader Ralf, Schewel Jury, Schewel Dimitry, Thielsen Thomas, Kreidel Felix, Alessandrini Hannes, Schlingloff Friederike, Schäfer Ulrich, Kuck Karl-Heinz

机构信息

Department of Cardiology, Asklepios Klinik St. Georg, Hamburg, Germany.

出版信息

EuroIntervention. 2016 Dec 20;12(12):1520-1526. doi: 10.4244/EIJ-D-16-00209.

Abstract

AIMS

The study sought to assess outcomes of transcatheter mitral valve-in-valve implantation (TMVIV) for degenerated bioprostheses and transcatheter mitral valve-in-ring implantation (TMVIR) for failed annuloplasty rings according to access route and the Mitral Valve Academic Research Consortium (MVARC) criteria.

METHODS AND RESULTS

Twenty-four patients (72±13 years; eight men [33%]) underwent TMVIV (n=14) or TMVIR (n=10) for mitral regurgitation (MR; n=17) or stenosis (n=7) using balloon-expandable bioprostheses. Transapical (TA) access was chosen in 13, and transseptal (TS) access in 11 patients. MVARC technical success, device success and procedural success were 95.8%, 41.7% and 33.3%, respectively, with no differences between access routes. Cardiac output (CO) increased significantly by 1.1±0.8 l/min in TS patients, but not in TA patients (ΔCO=0.0±0.5 l/min; p=0.0051). Overall three-year survival was estimated at 57.6% (95% confidence interval: 33.9-81.3; TA 35.5% [5.2-65.9]; TS 90.9% [73.9-100]). Survival up to four years according to vascular access showed a clear benefit in patients treated transseptally (p=0.045).

CONCLUSIONS

Regardless of the access route, TMVIV/TMVIR was associated with high technical success yet impaired device success. In the long term, TA access had a significant adverse impact on survival.

摘要

目的

本研究旨在根据入路途径和二尖瓣学术研究联盟(MVARC)标准,评估经导管二尖瓣瓣中瓣植入术(TMVIV)治疗退化生物瓣膜以及经导管二尖瓣瓣环内植入术(TMVIR)治疗失败瓣环成形环的疗效。

方法与结果

24例患者(72±13岁;8例男性[33%])因二尖瓣反流(MR;n = 17)或狭窄(n = 7)接受了TMVIV(n = 14)或TMVIR(n = 10)治疗,使用球囊扩张生物瓣膜。13例患者选择经心尖(TA)入路,11例患者选择经房间隔(TS)入路。MVARC技术成功率、器械成功率和手术成功率分别为95.8%、41.7%和33.3%,入路途径之间无差异。TS入路患者的心输出量(CO)显著增加1.1±0.8 l/min,而TA入路患者未增加(ΔCO = 0.0±0.5 l/min;p = 0.0051)。总体三年生存率估计为57.6%(95%置信区间:33.9 - 81.3;TA 35.5% [5.2 - 65.9];TS 90.9% [73.9 - 100])。根据血管入路的四年生存率显示,经房间隔治疗的患者有明显益处(p = 0.045)。

结论

无论入路途径如何,TMVIV/TMVIR技术成功率高,但器械成功率受损。从长期来看,TA入路对生存率有显著不利影响。

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