经心尖经导管二尖瓣置换术治疗二尖瓣疾病:伊比利亚的经验。

IF 7.2 2区 医学 Q1 CARDIAC & CARDIOVASCULAR SYSTEMS Revista española de cardiología (English ed.) Pub Date : 2025-03-01 DOI:10.1016/j.rec.2024.07.004
Eva Gutiérrez-Ortiz , Javier Cobiella , Christian Muñoz-Guijosa , Rui C. Teles , Rodrigo Estévez-Loureiro , Vanessa Moñivas , Ander Regueiro , Sara Blasco-Turrión , Patricia Mahía , Danela Figuereo Beltre , Pedro Freitas , Miguel Piñón , Ignacio J Amat-Santos , Ignasi Julià Amill , Tiago Nolasco , Daniel Pereda , Carlos Martín López , Luis Nombela-Franco
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引用次数: 0

摘要

导言和目标:经导管二尖瓣置换术(TMVR)是一种新兴的二尖瓣疾病替代治疗方法,适用于不符合手术干预或边缘对边缘修复条件的患者。本研究旨在评估该手术的短期和中期疗效:我们进行了一项前瞻性登记,纳入了伊比利亚半岛 7 个中心使用经心尖 Tendyne 系统接受 TMVR 的连续无症状患者的初步经验。收集了基线临床和成像数据、围手术期信息以及 1 个月和 1 年的随访评估:共有 40 名患者(平均年龄 78.5 岁 [76-82],47.5% 为男性)接受了 TMVR。大多数患者有重大手术风险、合并症和功能分级较高。所有患者均有明显的二尖瓣反流(MR),只有两名患者有严重狭窄。曾接受过中风介入治疗和标示外手术指征的患者分别为 4 人(10.0%)和 8 人(20.0%)。30天内,技术成功率为100%,设备成功率为95.0%,手术成功率为85.0%。随访1个月和1年时的全因死亡率分别为2.5%和17.5%。1年后,分别有93.9%和87.9%的幸存者观察到MR降低(≤1)和功能分级改善(NYHA I-II):结论:TMVR治疗可持久缓解中风疾病,随访1年后功能明显改善。该手术的早期安全性令人满意,但在这一高风险人群中,1年死亡率仍然相对较高。
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Transapical transcatheter mitral valve replacement for mitral valve disease: an Iberian experience

Introduction and objectives

Transcatheter mitral valve replacement (TMVR) is an emerging treatment alternative for mitral valve (MV) disease in patients who were ineligible for surgical intervention or edge-to-edge repair. This study aimed to assess the short- and mid-term outcomes of this procedure.

Methods

We conducted a prospective registry to include the initial experience with symptomatic, consecutive patients who underwent TMVR using the transapical Tendyne system at 7 centers in the Iberian Peninsula. Baseline clinical and imaging data, periprocedural information, and follow-up assessments were collected at 1 month and 1 year.

Results

A total of 40 patients (mean age 78.5 years [76-82], 47,5% males) underwent TMVR. The majority had significant surgical risk, comorbidities, and advanced functional class. All patients had significant mitral regurgitation (MR), except for 2 with severe stenosis. Previous MV intervention and off-label indication for the procedure were present in 4 (10.0%) and 8 (20.0%) patients, respectively. Technical success was recorded in 100%, device success in 95.0%, and procedural success in 85.0% at 30-day. All-cause mortality was 2.5% and 17.5% at the 1-month and 1-year follow-up, respectively. MR reduction (≤ 1) and functional class improvement (NYHA I-II) were observed at 1 year in 93.9% and 87.9% of survivors, respectively.

Conclusions

Treatment with TMVR produced enduring resolution of MV disease and notable functional enhancement at 1 year of follow-up. The procedure demonstrated a satisfactory early safety profile, although 1-year mortality remained relatively high in this high-risk population.
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