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不适合行经导管二尖瓣置换术(TMVR)的患者的特征和结局:对未来器械创新的启示。

Characteristics and Outcomes of Patients Ineligible for Transcatheter Mitral Valve Replacement (TMVR): Implications for Future Device Innovation.

机构信息

Department of Cardiology, University Heart and Vascular Center Hamburg, Martinistrasse 52, 20246 Hamburg, Germany.

出版信息

J Invasive Cardiol. 2021 Apr;33(4):E294-E301. doi: 10.25270/jic/20.00407. Epub 2021 Feb 18.

Abstract

OBJECTIVES

Due to high rates of transcatheter mitral valve replacement (TMVR) screening failure, a substantial proportion of patients with severe mitral regurgitation (MR) remains on optimal medical treatment (OMT) only. Data on outcomes of these patients ineligible for mitral interventions are scarce. This study aimed to assess characteristics and outcomes of severe MR patients treated medically following TMVR screening failure.

METHODS

From 2016-2020, a total of 111 patients with severe MR underwent screening for TMVR. Screening failure occurred in 66 cases. Among these, 30 patients were treated with OMT only. Characteristics of these patients were analyzed, Kaplan-Meier estimates calculated, and univariate regression analysis performed. Median follow-up time was 2.26 years (95% confidence interval, 1.24-3.25).

RESULTS

Anatomical reasons for screening failure in the study cohort (n = 30) were left ventricular (LV) restraints, risk of LV outflow tract obstruction, mitral annulus calcification, and sizing issues. Median ejection fraction was 56.0% (interquartile range, 38.8%-60.0%). Concomitant tricuspid regurgitation and severe pulmonary hypertension were present in 36.7% and 46.2%, respectively. Intercommissural diameters ranged from 22.5-52.0 mm. Mortality was 23.6% after 6 months and 35.7% after 1 year. Factors associated with mortality were female sex, MR severity, ischemic MR, high N-terminal pro-brain natriuretic peptide levels, and small annulus diameters.

CONCLUSIONS

Despite growing experience with TMVR, the subset of MR patients anatomically eligible for TMVR is small and many patients are treated medically. Mortality in these patients remains high, underlining an unmet need for adequate therapeutic alternatives. TMVR devices adapting to broader annular size ranges with smaller ventricular profiles might fill this gap.

摘要

目的

由于经导管二尖瓣置换术(TMVR)筛选失败的比率较高,相当一部分严重二尖瓣反流(MR)患者仍仅接受最佳药物治疗(OMT)。关于这些不符合二尖瓣介入治疗标准的患者的结局数据较为匮乏。本研究旨在评估 TMVR 筛选失败后接受药物治疗的严重 MR 患者的特征和结局。

方法

2016 年至 2020 年,共有 111 例严重 MR 患者接受 TMVR 筛选。66 例筛选失败。其中,30 例患者仅接受 OMT 治疗。分析这些患者的特征,计算 Kaplan-Meier 估计值,并进行单因素回归分析。中位随访时间为 2.26 年(95%置信区间,1.24-3.25)。

结果

研究队列中(n=30)筛选失败的解剖学原因包括左心室(LV)限制、LV 流出道梗阻风险、二尖瓣环钙化和尺寸问题。中位射血分数为 56.0%(四分位间距,38.8%-60.0%)。同时存在三尖瓣反流和严重肺动脉高压的比例分别为 36.7%和 46.2%。房室环间直径范围为 22.5-52.0mm。6 个月后死亡率为 23.6%,1 年后死亡率为 35.7%。与死亡率相关的因素包括女性、MR 严重程度、缺血性 MR、高 N 末端脑利钠肽前体水平和小瓣环直径。

结论

尽管 TMVR 的经验不断增加,但解剖上适合 TMVR 的 MR 患者亚组很小,许多患者仍接受药物治疗。这些患者的死亡率仍然很高,突出表明需要有适当的治疗替代方案。具有更小心室轮廓、适应更广泛瓣环尺寸范围的 TMVR 装置可能会填补这一空白。

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