Redo surgical aortic valve replacement versus valve-in-valve transcatheter aortic valve replacement with balloon valve fracture: Short-term clinical outcomes.

JTCVS structural and endovascular Pub Date : 2026-05-03 eCollection Date: 2026-06-01 DOI:10.1016/j.xjse.2026.100127
Rahul Kanade, Marco Tagliafierro, Isao Anzai, Fady Soliman, William M Mitchell, Darina Kirilina, Paul Kurlansky, Rebecca T Hahn, Susheel Kodali, Tamim M Nazif, Torsten P Vahl, Arnar Geirsson, Michael Argenziano, Isaac George, Luigi Pirelli
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Abstract

Objective: To evaluate short-term outcomes of redo surgical aortic valve replacement (SAVR) versus valve-in-valve transcatheter aortic valve replacement (ViV-TAVR) with bioprosthetic valve fracture (ViVBVF) in patients with bioprosthetic structural valve deterioration undergoing reintervention.

Methods: This retrospective single-center study was conducted between 2015 and 2025. Data were obtained from institutional registries. A total of 128 consecutive patients met the inclusion criteria (75 with redo-SAVR and 53 with ViVBVF). Patients requiring concomitant cardiac procedures, mechanical valves, or unsuitable anatomy for ViV were excluded. The primary endpoints were 30-day mortality, stroke, and readmission; secondary endpoints included echocardiographic changes and postoperative complications. Overlap propensity score weighting to adjust baseline differences was performed.

Results: Compared to the redo-SAVR patients, the ViVBVF patients were older and had a higher predicted risk of mortality. The rates of 30-day mortality, stroke, and readmission were similar in the 2 groups. ViVBVF achieved significantly greater reductions in mean gradient (-26.0 mm Hg vs -17.4 mm Hg; P =.003), peak gradient (-39.2 mm Hg vs -23.3 mm Hg; P =.004), and peak velocity. After matching, 30-day mortality was higher after redo-SAVR (8.9% vs 0%; P < .001). The ViVBVF group showed a greater reduction in peak velocity but more frequent pacemaker implantation.

Conclusions: In patients with bioprosthetic valves requiring reintervention, ViVBVF offers greater gradient reduction, with a perioperative safety advantage suggested in the adjusted analysis.

重做手术主动脉瓣置换术与经导管主动脉瓣置换术并发球囊瓣膜骨折:短期临床结果
目的:评价再介入治疗生物假体结构瓣膜恶化患者的重做手术主动脉瓣置换术(SAVR)与经导管瓣中瓣主动脉瓣置换术(ViV-TAVR)合并生物假体瓣膜骨折(ViVBVF)的短期疗效。方法:2015 - 2025年进行回顾性单中心研究。数据来自机构登记处。共有128例连续患者符合纳入标准(75例为redo-SAVR, 53例为ViVBVF)。需要合并心脏手术、机械瓣膜或不适合ViV解剖的患者被排除在外。主要终点为30天死亡率、卒中和再入院;次要终点包括超声心动图变化和术后并发症。重叠倾向评分加权来调整基线差异。结果:与redo-SAVR患者相比,ViVBVF患者年龄更大,预测死亡风险更高。两组患者的30天死亡率、卒中和再入院率相似。ViVBVF显著降低了平均梯度(-26.0 mm Hg vs -17.4 mm Hg, P = 0.003)、峰梯度(-39.2 mm Hg vs -23.3 mm Hg, P = 0.004)和峰流速。匹配后,重做savr后30天死亡率更高(8.9% vs 0%; P < 0.001)。ViVBVF组心率峰值下降幅度更大,但起搏器植入频率更高。结论:在需要再干预的生物瓣膜患者中,ViVBVF提供了更大的梯度降低,在调整分析中表明具有围手术期安全优势。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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