Quantitative Aortography Analysis of JenaValve’s Trilogy Transcatheter Aortic Valve Implantation System in Patients With Aortic Regurgitation or Stenosis

IF 1.4 Q3 CARDIAC & CARDIOVASCULAR SYSTEMS Structural Heart Pub Date : 2024-09-01 DOI:10.1016/j.shj.2024.100346
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Abstract

Background

JenaValve’s Trilogy transcatheter heart valve (THV) (JenaValve Inc, Irvine, CA) is the only conformité européenne-marked THV system for the treatment of aortic regurgitation (AR) or aortic stenosis (AS). However, its efficacy has not been quantitatively investigated pre- and post-implantation using video-densitometric analysis.

Methods

Using the CAAS-A-Valve 2.1.2 software (Pie Medical Imaging, Maastricht, the Netherlands), an independent core lab retrospectively analyzed the aortograms of 88 consecutive patients (68 severe AR; 20 severe AS) receiving the JenaValve THV in three European centers. Video-densitometric AR was categorized by the regurgitant fraction (RF) as none/trace AR (RF ≤ 6%), mild (6% < RF ≤ 17%), and moderate/severe AR (RF > 17%).

Results

Pre- and post-THV aortograms were analyzable in 17 (22.4%) and 47 (54.0%) patients, respectively. The main reasons preventing analysis were the descending aorta overlap of the outflow tract (30%) and insufficient frame count (6%). The median RF pre- and post-THV implant was 31.0% (interquartile range 21.5-38.6%) and 5.0% (interquartile range 1.0-7.0%, p < 0.001), respectively. The post-THV incidence of none/trace AR was 72.3%, and of mild AR, 27.7%, with no cases of moderate/severe AR. Video-densitometry analysis of the 12 AR cases with paired pre- and post-THV showed a reduction in the RF of 21.8% ± 8.1%.

Conclusions

Quantitative aortography confirms the low rates of AR and the large reduction in RF following the implantation of Jenavalve’s Trilogy THV, irrespective of implant indication. However, these limited data need corroborating in prospective studies using standardized acquisition protocols.

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JenaValve的Trilogy经导管主动脉瓣植入系统对主动脉瓣反流或狭窄患者的定量主动脉造影分析
背景JenaValve公司的Trilogy经导管心脏瓣膜(THV)(JenaValve Inc, Irvine, CA)是唯一获得欧洲合格标志的THV系统,用于治疗主动脉瓣反流(AR)或主动脉瓣狭窄(AS)。方法利用 CAAS-A-Valve 2.1.2 软件(Pie Medical Imaging,荷兰马斯特里赫特),一个独立的核心实验室回顾性分析了在三个欧洲中心接受 JenaValve THV 治疗的 88 位连续患者(68 位重度 AR;20 位重度 AS)的主动脉造影。结果 THV前和THV后主动脉造影可分析的患者分别为17例(22.4%)和47例(54.0%)。无法分析的主要原因是降主动脉与流出道重叠(30%)和帧数不足(6%)。THV植入前后的射频中位数分别为31.0%(四分位距为21.5-38.6%)和5.0%(四分位距为1.0-7.0%,P< 0.001)。THV后无/微量AR发生率为72.3%,轻度AR发生率为27.7%,无中度/重度AR病例。结论定量主动脉造影证实,无论植入适应症如何,植入 Jenavalve Trilogy THV 后 AR 发生率低,RF 降低幅度大。然而,这些有限的数据还需要采用标准化采集方案的前瞻性研究加以证实。
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来源期刊
Structural Heart
Structural Heart Medicine-Cardiology and Cardiovascular Medicine
CiteScore
1.60
自引率
0.00%
发文量
81
期刊最新文献
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