MVZ Department Structural Heart Disease, Asklepios St. Georg, Hamburg, Germany.
EuroIntervention. 2021 Nov 19;17(10):848-855. doi: 10.4244/EIJ-D-21-00254.
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.
The aim of this study was to evaluate the outcome of VIV-TAVI with BVF compared to VIV-TAVI without BVF.
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).
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.
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.
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。
本研究旨在评估 VIV-TAVI 中使用 BVF 与不使用 BVF 的结果。
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)。
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。
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。