Testa Luca, Giannini Cristina, Costa Giulia, Fiorina Claudia, Adamo Marianna, Massussi Mauro, Bruschi Giuseppe, Merlanti Bruno, Montorfano Matteo, Bellini Barbara, Poli Arnaldo, Ferrara Erica, Sisinni Antonio, Squillace Mattia, De Felice Francesco, Musto Carmine, Mazzapicchi Alessandro, Brambilla Nedy, Palmerini Tullio, De Carlo Marco, Bedogni Francesco
Cardiology Department, IRCCS Policlinico S. Donato, S. Donato Milanese, Italy.
Cardiothoracic and Vascular Department, University of Pisa, Pisa, Italy.
Cardiovasc Revasc Med. 2025 Apr;73:23-30. doi: 10.1016/j.carrev.2024.07.013. Epub 2024 Jul 27.
Transcatheter aortic valve replacement (TAVR) determined a paradigm shift in the treatment of patients with severe symptomatic aortic stenosis but data on very long-term durability are lacking. We sought to evaluate the clinical and hemodynamic outcomes of the CoreValve porcine pericardial self-expanding bioprosthesis at 12-year follow-up.
882 inoperable or high-risk patients were treated with the CoreValve bioprosthesis in 8 Italian high-volume centers between 2007 and 2011. The endpoints were 12-year all-cause and cardiovascular mortality, and Cumulative Incidence Functions (CIFs) for severe Structural Valve Deterioration (SVD), Bioprosthetic Valve Dysfunction (BVD), Bioprosthetic Valve Failure (BVF), and severe Hemodynamic Valve Deterioration (HVD). VARC-3 definitions were applied.
Baseline characteristics included a mean age of 83 ± 6 years, and NYHA class III or IV in 76.3 % of patients. The actuarial risk of death at 12 years after TAVR was 95.5 % (CI 93.5 %- 97.1 %). The actual risk of cardiovascular death, weighted against the risk of non-cardiac death at 12 years was 23.9 % (21.0 %-26.8 %). The 12-year actual risk of BVD was 7.0 % (5.3 %-8.9 %), of SVD was 3.6 % (2.5 %-5.2 %), of BVF was 3.12 % (2.02 %-4.57 %), and of severe HVD was 1.7 % (0.9 %-2.9 %). Mean transaortic gradient significantly decreased after the procedure (52 ± 15 mmHg vs 9 ± 5 mmHg, p < 0.001), and remained stable up to 12 years (12 ± 4 mmHg, P = 0.08 vs. discharge).
The first-generation CoreValve bioprosthesis showed reassuring clinical and hemodynamic performance at 12-year follow-up.
经导管主动脉瓣置换术(TAVR)使严重症状性主动脉瓣狭窄患者的治疗发生了范式转变,但缺乏关于其长期耐久性的数据。我们试图评估CoreValve猪心包自膨胀生物假体在12年随访时的临床和血流动力学结果。
2007年至2011年期间,882例无法手术或高危患者在意大利8个大容量中心接受了CoreValve生物假体治疗。终点指标为12年全因死亡率和心血管死亡率,以及严重结构性瓣膜退变(SVD)、生物假体瓣膜功能障碍(BVD)、生物假体瓣膜衰竭(BVF)和严重血流动力学瓣膜退变(HVD)的累积发生率函数(CIFs)。采用VARC-3定义。
基线特征包括平均年龄83±6岁,76.3%的患者为纽约心脏协会(NYHA)III或IV级。TAVR术后12年的精算死亡风险为95.5%(93.5%-97.1%置信区间)。12年时心血管死亡的实际风险,加权非心血管死亡风险后为23.9%(21.0%-26.8%)。12年时BVD的实际风险为7.0%(5.3%-8.9%),SVD为3.6%(2.5%-5.2%),BVF为3.12%(2.02%-4.57%),严重HVD为1.7%(0.9%-2.9%)。术后平均跨主动脉压差显著降低(52±15mmHg对9±5mmHg,p<0.001),并在12年内保持稳定(12±4mmHg,与出院时相比P=0.08)。
第一代CoreValve生物假体在12年随访时显示出令人放心的临床和血流动力学性能。