在接受经导管主动脉瓣置换术的 0 型双尖瓣主动脉瓣狭窄患者中,比较缩小尺寸策略(HANGZHOU Solution)和标准瓣环尺寸策略:随机临床试验的原理与设计。

IF 3.7 2区 医学 Q1 CARDIAC & CARDIOVASCULAR SYSTEMS American heart journal Pub Date : 2024-05-01 DOI:10.1016/j.ahj.2024.04.011
Yuchao Guo MD , Xianbao Liu MD , Ranxi Li BM , Stella Ng BM , Qiong Liu PhD , Lihan Wang MMed , Po Hu MMed , Kaida Ren MD , Jubo Jiang MMed , Jiaqi Fan MD , Yuxin He MD , Qifeng Zhu MD , Xinping Lin MMed , Huajun Li MMed , Jian'an Wang MD
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引用次数: 0

摘要

背景:对于接受经导管主动脉瓣置换术(TAVR)的0型双尖瓣主动脉瓣狭窄(AS)患者的人工瓣膜尺寸策略尚未达成共识。由于其独特的解剖学特征,可能需要对标准瓣环尺寸策略进行修改。我们专门为 0 型双尖瓣 AS 患者设计了一种使用自扩张瓣膜进行 TAVR 的向下尺寸调整策略。本研究的主要目的是比较 "缩小瓣膜尺寸策略 "与 "标准瓣环尺寸策略 "在 0 型双尖瓣强直性脊柱炎患者 TAVR 中的安全性和有效性:这是一项前瞻性、多中心、优越性、单盲、随机对照试验,在接受经导管主动脉瓣置换术的 0 型双尖瓣主动脉瓣狭窄患者中比较 Down Sizing 策略和 Standard Annulus Sizing 策略。符合条件的参与者将包括重度 0 型双尖瓣 AS 患者,其标准包括主动脉瓣平均梯度≥40 mmHg、主动脉喷射速度峰值≥4.0 m/s、主动脉瓣面积 (AVA) ≤1.0 cm²,或 AVA 指数≤0.6 cm2/m²。这些患者将按 1:1 的比例随机分配到 "缩小尺寸策略 "组或 "标准尺寸策略 "组。在缩小尺寸策略组中,如果在球囊预扩张过程中出现 "腰围征 "并伴有轻度以下反流,则植入小一号的瓣膜。研究的主要终点是 VARC-3 定义的设备成功率、没有因高度房室传导阻滞和新发完全左束支传导阻滞而植入永久起搏器:这项研究将比较 "向下尺寸选择策略 "与 "标准瓣环尺寸选择策略 "的安全性和有效性,并为 0 型双尖瓣 AS TAVR 患者的最佳尺寸选择方法提供有价值的见解。我们假设,与标准瓣环大小策略相比,向下大小策略将显示出优越性。(双尖瓣主动脉瓣狭窄(0 型)TAVR 的向下尺寸策略(杭州方案)与标准尺寸策略(TAILOR-TAVR),NCT05511792)。
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Comparison of downsizing strategy (HANGZHOU Solution) and standard annulus sizing strategy in type 0 bicuspid aortic stenosis patients undergoing transcatheter aortic valve replacement: Rationale and design of a randomized clinical trial

Background

There has not been a consensus on the prothesis sizing strategy in type 0 bicuspid aortic stenosis (AS) patients undergoing transcatheter aortic valve replacement (TAVR). Modifications to standard annular sizing strategies might be required due to the distinct anatomical characteristics. We have devised a downsizing strategy for TAVR using a self-expanding valve specifically for patients with type 0 bicuspid AS. The primary aim of this study is to compare the safety and efficacy of downsizing strategy with the Standard Annulus Sizing Strategy in TAVR for patients with type 0 bicuspid AS.

Trial design

It is a prospective, multi-center, superiority, single-blinded, randomized controlled trial comparing the Down Sizing and Standard Annulus Sizing Strategy in patients with type 0 bicuspid aortic stenosis undergoing transcatheter aortic valve replacement. Eligible participants will include patients with severe type 0 bicuspid AS, as defined by criteria such as mean gradient across aortic valve ≥40 mmHg, peak aortic jet velocity ≥4.0 m/s, aortic valve area (AVA) ≤1.0 cm², or AVA index ≤0.6 cm2/m2. These patients will be randomly assigned, in a 1:1 ratio, to either the Down Sizing Strategy group or the Standard Sizing Strategy group. In the Down Sizing Strategy group, a valve one size smaller will be implanted if the “waist sign” manifests along with less than mild regurgitation during balloon pre-dilatation. The primary end point of the study is a composite of VARC-3 defined device success, absence of both permanent pacemaker implantation due to high-degree atrioventricular block and new-onset complete left bundle branch block.

Conclusion

This study will compare the safety and efficacy of Down Sizing Strategy with the Standard Annulus Sizing Strategy and provide valuable insights into the optimal approach for sizing in TAVR patients with type 0 bicuspid AS. We hypothesize that the Down Sizing Strategy will demonstrate superiority when compared to the Standard Annulus Sizing Strategy. (Down Sizing Strategy (HANGZHOU Solution) vs Standard Sizing Strategy TAVR in Bicuspid Aortic Stenosis (Type 0) (TAILOR-TAVR), NCT05511792).

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来源期刊
American heart journal
American heart journal 医学-心血管系统
CiteScore
8.20
自引率
2.10%
发文量
214
审稿时长
38 days
期刊介绍: The American Heart Journal will consider for publication suitable articles on topics pertaining to the broad discipline of cardiovascular disease. Our goal is to provide the reader primary investigation, scholarly review, and opinion concerning the practice of cardiovascular medicine. We especially encourage submission of 3 types of reports that are not frequently seen in cardiovascular journals: negative clinical studies, reports on study designs, and studies involving the organization of medical care. The Journal does not accept individual case reports or original articles involving bench laboratory or animal research.
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