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Transapical Mitral Valve Replacement: 1-Year Results of the Real-World Tendyne European Experience Registry.经导管二尖瓣置换术: Tendyne 欧洲真实世界经验注册研究的 1 年结果。
JACC Cardiovasc Interv. 2024 Mar 11;17(5):648-661. doi: 10.1016/j.jcin.2023.12.027. Epub 2024 Feb 21.
2
Clinical outcomes of transcatheter mitral valve replacement: two-year results of the CHOICE-MI Registry.经导管二尖瓣置换术的临床结局:CHOICE-MI 注册研究的两年结果。
EuroIntervention. 2023 Aug 21;19(6):512-525. doi: 10.4244/EIJ-D-22-01037.
3
Transcatheter Mitral Valve Replacement Versus Medical Therapy for Secondary Mitral Regurgitation: A Propensity Score-Matched Comparison.经导管二尖瓣置换术与药物治疗继发性二尖瓣反流:倾向评分匹配比较。
Circ Cardiovasc Interv. 2023 Jun;16(6):e013045. doi: 10.1161/CIRCINTERVENTIONS.123.013045. Epub 2023 May 16.
4
Transcatheter mitral valve replacement or repair for secondary mitral regurgitation: a propensity score-matched analysis.经导管二尖瓣置换或修复治疗继发性二尖瓣反流:一项倾向评分匹配分析。
Eur J Heart Fail. 2023 Mar;25(3):399-410. doi: 10.1002/ejhf.2797. Epub 2023 Mar 8.
5
Characteristics and outcomes of patients screened for transcatheter mitral valve implantation: 1-year results from the CHOICE-MI registry.经筛选接受经导管二尖瓣植入术患者的特征和结局:CHOICE-MI 注册研究的 1 年结果。
Eur J Heart Fail. 2022 May;24(5):887-898. doi: 10.1002/ejhf.2492. Epub 2022 Apr 17.
6
Management of patients with mitral regurgitation ineligible for standard therapy undergoing TMVI screening.对不符合标准治疗条件且正在接受经导管二尖瓣植入术(TMVI)筛查的二尖瓣反流患者的管理。
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2021 ESC/EACTS Guidelines for the management of valvular heart disease.2021年欧洲心脏病学会/欧洲心胸外科学会心脏瓣膜病管理指南。
EuroIntervention. 2022 Feb 4;17(14):e1126-e1196. doi: 10.4244/EIJ-E-21-00009.
8
30-Day Outcomes Following Transfemoral Transseptal Transcatheter Mitral Valve Replacement: Intrepid TMVR Early Feasibility Study Results.经股静脉经房间隔经导管二尖瓣置换术后 30 天的结果:IntrepidTMVR 早期可行性研究结果。
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Transcatheter Mitral Valve Therapy in the United States: A Report From the STS-ACC TVT Registry.经导管二尖瓣治疗在美国:来自 STS-ACC TVT 注册中心的报告。
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经心尖经导管二尖瓣置换术的临床结果和预测因素: Tendyne 扩展临床研究。

Clinical outcomes and predictors of transapical transcatheter mitral valve replacement: the Tendyne Expanded Clinical Study.

机构信息

Department of Cardiovascular Surgery, University Heart & Vascular Center Hamburg, Hamburg, Germany.

German Center for Cardiovascular Research (DZHK), partner site Hamburg/Kiel/Lübeck, Hamburg, Germany.

出版信息

EuroIntervention. 2024 Jul 15;20(14):e887-e897. doi: 10.4244/EIJ-D-23-00904.

DOI:10.4244/EIJ-D-23-00904
PMID:39007829
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11228541/
Abstract

BACKGROUND

Transcatheter mitral valve replacement (TMVR) is a therapeutic option for patients with severe mitral regurgitation (MR) who are ineligible for conventional surgery. There are limited data on the outcomes of large patient cohorts treated with TMVR.

AIMS

This study aimed to investigate the outcomes and predictors of mortality for patients treated with transapical TMVR.

METHODS

This analysis represents the clinical experience of all patients enrolled in the Tendyne Expanded Clinical Study. Patients with symptomatic MR underwent transapical TMVR with the Tendyne system between November 2014 and June 2020. Outcomes and adverse events up to 2 years, as well as predictors of short-term mortality, were assessed.

RESULTS

A total of 191 patients were treated (74.1±8.0 years, 62.8% male, Society of Thoracic Surgeons Predicted Risk of Mortality 7.7±6.6%). Technical success was achieved in 96.9% (185/191), and there were no intraprocedural deaths. At 30-day, 1- and 2-year follow-up, the rates of all-cause mortality were 7.9%, 30.8% and 40.5%, respectively. Complete MR elimination (MR <1+) was observed in 99.3%, 99.1% and 96.3% of patients, respectively. TMVR treatment resulted in consistent improvement of New York Heart Association Functional Class and quality of life up to 2 years (both p<0.001). Independent predictors of early mortality were age (odds ratio [OR] 1.11; p=0.003), pulmonary hypertension (OR 3.83; p=0.007), and institutional experience (OR 0.40; p=0.047).

CONCLUSIONS

This study investigated clinical outcomes in the full cohort of patients included in the Tendyne Expanded Clinical Study. The Tendyne TMVR system successfully eliminated MR with no intraprocedural deaths, resulting in an improvement in symptoms and quality of life. Continued refinement of clinical and echocardiographic risks will be important to optimise longitudinal outcomes.

摘要

背景

经导管二尖瓣置换术(TMVR)是一种治疗严重二尖瓣反流(MR)患者的方法,这些患者不适合接受传统手术。目前关于接受 TMVR 治疗的大量患者队列的结果数据有限。

目的

本研究旨在探讨经心尖 TMVR 治疗患者的结局和死亡率预测因素。

方法

本分析代表了 2014 年 11 月至 2020 年 6 月期间接受 Tendyne 系统经心尖 TMVR 治疗的所有入组患者的临床经验。有症状的 MR 患者接受经心尖 TMVR 治疗,Tendyne 系统治疗。评估了 2 年内的结局和不良事件,以及短期死亡率的预测因素。

结果

共治疗了 191 例患者(74.1±8.0 岁,62.8%为男性,胸外科医师协会预测死亡率为 7.7±6.6%)。技术成功率达到 96.9%(185/191),术中无死亡。30 天、1 年和 2 年随访时,全因死亡率分别为 7.9%、30.8%和 40.5%。分别有 99.3%、99.1%和 96.3%的患者完全消除了二尖瓣反流(MR <1+)。TMVR 治疗可持续改善纽约心脏协会功能分级和生活质量,直至 2 年(均 p<0.001)。早期死亡率的独立预测因素是年龄(优势比[OR] 1.11;p=0.003)、肺动脉高压(OR 3.83;p=0.007)和机构经验(OR 0.40;p=0.047)。

结论

本研究调查了 Tendyne 扩大临床试验中所有入组患者的临床结局。Tendyne TMVR 系统成功消除了二尖瓣反流,且无术中死亡,从而改善了症状和生活质量。进一步完善临床和超声心动图风险将对优化长期结局至关重要。