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经导管瓣中瓣植入术与外科再次行主动脉根部置换术治疗退行性 Freestyle 生物瓣的比较。

Transcatheter valve-in-valve implantation versus surgical redo aortic root replacement in patients with degenerated freestyle aortic bioprosthesis.

机构信息

Klinik für Kardiologie, Herz- und Gefäßzentrum Bad Bevensen, Bad Bevensen, Germany.

Klinik für Herz-Thorax-Chirurgie, Herz- und Gefäßzentrum Bad Bevensen, Bad Bevensen, Germany.

出版信息

Catheter Cardiovasc Interv. 2021 Jun 1;97(7):1472-1478. doi: 10.1002/ccd.29507. Epub 2021 Feb 1.

Abstract

BACKGROUND

Transcatheter aortic valve-in-valve implantation (ViV TAVI) represents a new treatment option for patients with degenerated aortic bioprosthesis. Comparative data to redo surgical aortic valve replacement (redo SAVR) are limited.

OBJECTIVE

We investigated feasibility and outcome of ViV TAVI versus redo SAVR in patients with symptomatic degenerated Medtronic Freestyle aortic bioprosthesis (FSB).

METHODS

Between January 2002 and February 2020, 25 patients with failed FSB underwent ViV TAVI and 10 patients with failed FSB underwent redo SAVR. Endpoints were defined according to the Valve Academic Research Consortium-2 (VARC-2) criteria.

RESULTS

Age and logistic EuroSCORE II were higher in patients with ViV TAVI (75.4 ± 1.7 vs. 62.9 ± 5.1 years, p = .019; 11.5 ± 1.6 vs. 5.6 ± 5.6%, p = .007). Valve implantation was successful in all cases. Mean transvalvular pressure gradients were significantly lower in patients with redo SAVR than ViV TAVI (7.6 ± 1.0 vs. 10.3 ± 0.8 mmHg, p = .037). Aortic valve regurgitation was absent in 91% and 100% of patients with ViV TAVI and redo SAVR, respectively. Thirty-day mortality rates were 12% in the ViV TAVI cohort versus 0% in the redo SAVR cohort (p = .542). Within the first year after hospital discharge, one patient after ViV TAVI had redo surgical intervention.

CONCLUSIONS

ViV TAVI and redo SAVR lead to excellent functional results in patients with degenerated FSB. Post-procedural early complications must be considered particularly in patients with ViV TAVI because of higher clinical risk profiles.

摘要

背景

经导管主动脉瓣瓣中瓣植入术(ViV TAVI)为退行性生物瓣主动脉瓣患者提供了一种新的治疗选择。与再次开胸主动脉瓣置换术(redo SAVR)相比,相关比较数据有限。

目的

我们研究了 ViV TAVI 与 redo SAVR 在退行性美敦力弗雷斯特瓣膜(FSB)患者中的可行性和结局。

方法

2002 年 1 月至 2020 年 2 月,25 例 FSB 失败的患者接受了 ViV TAVI,10 例 FSB 失败的患者接受了 redo SAVR。终点根据 Valve Academic Research Consortium-2(VARC-2)标准定义。

结果

ViV TAVI 组患者年龄和逻辑 EuroSCORE II 更高(75.4 ± 1.7 岁 vs. 62.9 ± 5.1 岁,p = 0.019;11.5 ± 1.6% vs. 5.6 ± 5.6%,p = 0.007)。所有病例的瓣膜植入均成功。 redo SAVR 组患者的跨瓣压差明显低于 ViV TAVI 组(7.6 ± 1.0 毫米汞柱 vs. 10.3 ± 0.8 毫米汞柱,p = 0.037)。ViV TAVI 和 redo SAVR 组患者的主动脉瓣反流均为 0%(91%和 100%)。ViV TAVI 组 30 天死亡率为 12%,redo SAVR 组为 0%(p = 0.542)。出院后 1 年内,ViV TAVI 组有 1 例患者再次行手术干预。

结论

ViV TAVI 和 redo SAVR 可使退行性 FSB 患者获得极佳的功能结果。由于临床风险较高,尤其应考虑 ViV TAVI 患者术后早期并发症。

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