Olusan Adeogo Akinwale, Rajendra Raj, Roberts Elved, Kovac Jan
Department of Cardiology, Glenfield Hospital, Leicester, UK.
University of Leicester, Leicester, UK.
Catheter Cardiovasc Interv. 2025 Aug;106(2):992-1001. doi: 10.1002/ccd.31625. Epub 2025 Jun 2.
Valve-in-valve (ViV) Transcatheter aortic valve replacement (TAVR) has emerged as a valid treatment option in symptomatic patients with failed aortic bioprosthetic valves, most especially in those with intermediate, high or prohibitive risk of surgery. Due to the unique design of stentless bioprosthetic valves with absence of visible posts and stent frame, they present with challenges during ViV TAVR procedure. Our case series assessed the safety, feasibility, and early outcomes of ViV TAVR in patients with failed bioprosthetic aortic valve replacement (AVR) using self-expanding valve platform (Acurate Neo 2/AN2 valve) between March and September 2024 with minimalist approach. Procedural success, complications and early outcomes (mortality and functional status) were evaluated. A total number of three patients, mean age 75 ± 7 years, 67% female were included in the case series with high Society of Thoracic Surgeons (STS) and European System of Cardiac Operative Risk Evaluation II (EuroSCORE II) score. The mean time from initial surgery to ViV procedure was 18 ± 1 years. ViV procedure was successfully completed in all patients with no major complication, and no more than trivial trans/paravalvular regurgitation on discharge. There was no requirement for permanent pacemaker implantation, no stroke or mortality at 30-day and there was significant improvement in functional class alongside symptomatic improvement. We report our experience in ViV TAVR using AN2 valve in Shelhigh supra stentless aortic bioprosthesis and that this procedure despite anatomical and procedural challenges is feasible and safe.
瓣中瓣(ViV)经导管主动脉瓣置换术(TAVR)已成为有症状的主动脉生物瓣功能衰竭患者的一种有效治疗选择,尤其是那些手术风险为中度、高度或禁忌的患者。由于无支架生物瓣的独特设计,没有可见的支柱和支架框架,它们在ViV TAVR手术过程中带来了挑战。我们的病例系列评估了2024年3月至9月期间使用自膨胀瓣膜平台(Acurate Neo 2/AN2瓣膜)对生物瓣主动脉瓣置换术(AVR)失败患者进行ViV TAVR的安全性、可行性和早期结果,采用了极简主义方法。评估了手术成功率、并发症和早期结果(死亡率和功能状态)。该病例系列共纳入3例患者,平均年龄75±7岁,67%为女性,胸外科医师协会(STS)和欧洲心脏手术风险评估系统II(EuroSCORE II)评分较高。从初次手术到ViV手术的平均时间为18±1年。所有患者均成功完成ViV手术,无重大并发症,出院时经瓣/瓣周反流不超过轻度。无需植入永久性起搏器,30天内无中风或死亡,功能分级有显著改善,症状也有所改善。我们报告了我们在使用AN2瓣膜对Shelhigh supra无支架主动脉生物瓣进行ViV TAVR方面的经验,并且尽管存在解剖和手术挑战,但该手术是可行且安全的。