Transcatheter Valve-in-Valve Replacement With Balloon- Versus Self-Expanding Valves in Patients With Degenerated Stentless Aortic Bioprosthesis

IF 2.3 3区 医学 Q2 CARDIAC & CARDIOVASCULAR SYSTEMS American Journal of Cardiology Pub Date : 2024-08-06 DOI:10.1016/j.amjcard.2024.08.001
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Abstract

Valve-in-valve (ViV) transcatheter aortic valve replacement (TAVR) has been associated with favorable outcomes in patients with degenerated stentless bioprosthesis. However, whether the outcomes after ViV TAVR for failed stentless bioprosthesis differ between balloon-expandable valves (BEVs) and self-expanding valves (SEVs) remains unknown. Therefore, we retrospectively analyzed 59 consecutive patients who underwent ViV TAVR for failed stentless bioprsothesis with BEVs (n = 42) versus SEVs (n = 17) in a single–health care system between 2013 and 2022. Overall, the mean age was 70.8 years and 74.6% were men. The mean transcatheter valve size was 26.3 ± 2.2 mm for BEVs and 26.4 ± 4 mm for SEVs (p = 0.93). The mean Society of Thoracic Surgeons score was 6.0 ± 3.6 for BEVs and 7.5 ± 5.5 for SEVs (p = 0.22). Compared with patients who received BEVs, those who received SEVs had higher rates of device malposition (2.4% vs 23.5%, p <0.01), postdeployment balloon dilation (11.9% vs 35.5%, p = 0.04) and need for a second transcatheter device (2.4% vs 35.5%, p <0.01). However, both groups showed similar improvement in aortic valve function at 30-day and 1-year follow-up (incidence of 1-year severe patient-prosthesis mismatch in BEVs: 17.6% vs 14.3% in SEVs, p = 0.78). The 1- and 3-year mortality did not differ between BEVs and SEVs (11.9% vs 11.8% and 25% vs 30%, respectively, Log rank p = 0.9). In conclusion, performing ViV TAVR for failed stentless bioprsothesis is technically challenging, especially when using SEVs; however, satisfactory positioning is possible in most cases, with excellent hemodynamic and clinical outcomes with BEVs and SEVs.

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在无支架主动脉生物假体退化患者中使用球囊瓣膜与自扩张瓣膜进行经导管瓣中瓣膜置换术
瓣中瓣(ViV)经导管主动脉瓣置换术(TAVR)与无支架生物前列腺瓣膜退化患者的良好预后有关。然而,无支架生物瓣膜置换术(TAVR)失败后,球囊扩张瓣膜(BEV)和自扩张瓣膜(SEV)的疗效是否存在差异仍是未知数。因此,我们回顾性分析了 2013 年至 2022 年间在单一医疗保健系统中因无支架生物假体失败而接受 ViV TAVR 的 59 例连续患者,他们分别接受了 BEV(42 例)和 SEV(17 例)治疗。总体而言,平均年龄为 70.8 岁,74.6% 为男性。BEV和SEV的平均经导管瓣膜尺寸分别为26.3 ±2.2 mm和26.4 ±4 mm(P= 0.93)。BEV和SEV的平均STS评分分别为(6.0 ± 3.6)和(7.5 ± 5.5)(P= 0.22)。与接受 BEV 的患者相比,接受 SEV 的患者发生装置错位(2.4% vs. 23.5%;p< 0.01)、部署后球囊扩张(11.9% vs. 35.5%;p= 0.04)和需要第二个经导管装置(2.4% vs. 35.5%;p< 0.01)的比例更高。不过,两组患者在 30 天和 1 年随访中的主动脉瓣功能改善情况相似(BEV 患者 1 年严重患者-假体不匹配发生率:17.6% 对 SEV:14.3%;P= 0.78)。BEV 和 SEV 的 1 年和 3 年死亡率没有差异(分别为 11.9% 对 11.8% 和 25% 对 30%;对数秩 p=0.9)。总之,为无支架生物假说失败的患者实施 ViV TAVR 在技术上具有挑战性,尤其是在使用 SEV 时,但在大多数情况下都能获得满意的定位,BEV 和 SEV 均能获得极佳的血流动力学和临床效果。
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来源期刊
American Journal of Cardiology
American Journal of Cardiology 医学-心血管系统
CiteScore
4.00
自引率
3.60%
发文量
698
审稿时长
33 days
期刊介绍: Published 24 times a year, The American Journal of Cardiology® is an independent journal designed for cardiovascular disease specialists and internists with a subspecialty in cardiology throughout the world. AJC is an independent, scientific, peer-reviewed journal of original articles that focus on the practical, clinical approach to the diagnosis and treatment of cardiovascular disease. AJC has one of the fastest acceptance to publication times in Cardiology. Features report on systemic hypertension, methodology, drugs, pacing, arrhythmia, preventive cardiology, congestive heart failure, valvular heart disease, congenital heart disease, and cardiomyopathy. Also included are editorials, readers'' comments, and symposia.
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