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经导管主动脉瓣置换术中带瓣支架置入治疗与不带瓣支架置入治疗合并生物瓣破裂的结果。

Outcomes of valve-in-valve transcatheter aortic valve implantation with and without bioprosthetic valve fracture.

机构信息

MVZ Department Structural Heart Disease, Asklepios St. Georg, Hamburg, Germany.

出版信息

EuroIntervention. 2021 Nov 19;17(10):848-855. doi: 10.4244/EIJ-D-21-00254.

Abstract

BACKGROUND

Bioprosthetic valve fracture (BVF) is a technique to reduce gradients in valve-in-valve transcatheter aortic valve implantation (VIV-TAVI) procedures. The outcome of VIV-TAVI with BVF has not been compared with VIV-TAVI without BVF.

AIMS

The aim of this study was to evaluate the outcome of VIV-TAVI with BVF compared to VIV-TAVI without BVF.

METHODS

In total, 81 cases of BVF VIV-TAVI (BVF group) from 14 centres were compared to 79 cases of VIV-TAVI without BVF (control group).

RESULTS

VARC-2-defined device success was 93% in the BVF group and 68.4% in the control group (p<0.001). The mean transvalvular gradient decreased from 37±13 mmHg to 10.8±5.9 mmHg (p<0.001) in the BVF group and from 35±16 mmHg to 15.8±6.8 mmHg (p<0.001) in the control group with a significantly higher final gradient in the control group (p<0.001). The transvalvular gradients did not change significantly over time. In-hospital major adverse events occurred in 3.7% in the BVF group and 7.6% in the control group (p=0.325). A linear mixed model identified BVF, self-expanding transcatheter heart valves (THVs) and other surgical aortic valve (SAV) types other than Mitroflow as predictors of lower transvalvular gradients.

CONCLUSIONS

Compared to VIV-TAVI alone, VIV-TAVI with BVF resulted in a significantly lower transvalvular gradient acutely and at follow-up. Independent predictors of lower gradients were the use of self-expanding THVs and the treatment of SAVs other than Mitroflow, irrespective of BVF performance. BVF significantly reduced the gradient independently from transcatheter or surgical valve type.

摘要

背景

生物瓣假体破裂(BVF)是一种用于降低经导管主动脉瓣植入术中经瓣中瓣(VIV-TAVI)技术梯度的方法。使用 BVF 的 VIV-TAVI 的结果尚未与未使用 BVF 的 VIV-TAVI 进行比较。

目的

本研究旨在评估 VIV-TAVI 中使用 BVF 与不使用 BVF 的结果。

方法

共比较了 14 个中心的 81 例 BVF VIV-TAVI(BVF 组)与 79 例未使用 BVF 的 VIV-TAVI(对照组)。

结果

BVF 组 VARC-2 定义的器械成功率为 93%,对照组为 68.4%(p<0.001)。在 BVF 组,跨瓣梯度从 37±13mmHg 降低至 10.8±5.9mmHg(p<0.001),在对照组从 35±16mmHg 降低至 15.8±6.8mmHg(p<0.001),对照组的最终梯度明显更高(p<0.001)。跨瓣梯度在随访期间没有明显变化。在 BVF 组中,住院期间发生主要不良事件的比例为 3.7%,在对照组中为 7.6%(p=0.325)。线性混合模型确定 BVF、自膨式经导管心脏瓣膜(THV)和 Mitroflow 以外的其他外科主动脉瓣(SAV)类型是降低跨瓣梯度的预测因素。

结论

与单独 VIV-TAVI 相比,VIV-TAVI 中使用 BVF 可显著降低急性和随访时的跨瓣梯度。较低梯度的独立预测因素是使用自膨式 THV 和治疗除 Mitroflow 以外的 SAV,而与 BVF 性能无关。BVF 可独立于经导管或外科瓣膜类型显著降低梯度。

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