HartCentrum, Ziekenhuis Netwerk Antwerpen (ZNA) Middelheim, Antwerp, Belgium; Department of Experimental Medicine, University of Rome "Tor Vergata", Rome, Italy.
HartCentrum, Ziekenhuis Netwerk Antwerpen (ZNA) Middelheim, Antwerp, Belgium.
Am J Cardiol. 2024 Jun 15;221:102-109. doi: 10.1016/j.amjcard.2024.04.010. Epub 2024 Apr 17.
Transcatheter aortic valve implantation (TAVI) is an established treatment strategy in aortic valve disease. Infolding, as a nonuniform expansion of the prosthesis leading to introflection of part of the device circumference, is a complication specific to self-expandable prostheses. The aim of the study is to determine incidence, predictors, treatment strategy, and outcomes of infolding during Medtronic Evolut TAVI (Minneapolis, MN, US). Between January 2018 and March 2022, all patients treated with Evolut TAVI were included in a multicenter observational retrospective study. According to the occurrence of infolding, the enrolled cohort was divided into 2 groups; periprocedural characteristics and 30-day outcomes were compared. A total of 1,470 patients were included; 23 infolding cases (1.6%) were detected. Preprocedural imaging showed larger aortic anatomy and greater calcium burden in the infolding group. Infolding occurred mostly with Evolut Pro+ and size 34 mm and was diagnosed before full prosthesis release in 78.3%. The rate of moderate-to-severe paravalvular regurgitation was higher in the infolding group (21.7% vs 1.9%, p <0.001). Short-term follow-up showed greater all-cause and cardiovascular mortality (respectively, 4.3% vs 0.7% and 4.3% vs 0.6%, p <0.05) and higher rate of pacemaker implantation (33.3% vs 15.7%, p = 0.042) in case of infolding. High right cusp calcium score and resheathing maneuvers were independent predictors of infolding. In conclusion, prosthesis infolding is a TAVI complication burdened by worse cardiovascular outcomes. Prompt intraprocedural infolding diagnosis is pivotal, especially in case of great native valve calcium burden and resheathing maneuvers, to safely overcome this complication by prosthesis recapture or postdilation.
经导管主动脉瓣植入术(TAVI)是主动脉瓣疾病的一种既定治疗策略。折叠,作为一种导致部分器械周长内折的非均匀扩张,是自扩张假体特有的并发症。本研究旨在确定美敦力 Evolut TAVI(美国明尼苏达州明尼阿波利斯)期间折叠的发生率、预测因素、治疗策略和结果。在 2018 年 1 月至 2022 年 3 月期间,所有接受 Evolut TAVI 治疗的患者均被纳入一项多中心回顾性观察研究。根据折叠的发生情况,将纳入的队列分为 2 组;比较围手术期特征和 30 天结局。共纳入 1470 例患者;发现 23 例折叠病例(1.6%)。术前影像学显示折叠组的主动脉解剖结构较大,钙负荷较重。折叠主要发生在 Evolut Pro+和 34 毫米大小的情况下,在 78.3%的情况下在完全释放假体前诊断。折叠组的中度至重度瓣周反流发生率较高(21.7%比 1.9%,p <0.001)。短期随访显示,折叠组全因和心血管死亡率更高(分别为 4.3%比 0.7%和 4.3%比 0.6%,p <0.05),以及更高的起搏器植入率(33.3%比 15.7%,p = 0.042)。右冠瓣钙评分高和重新护套操作是折叠的独立预测因素。总之,假体折叠是 TAVI 并发症,心血管结局较差。在这种情况下,及时进行术中折叠诊断至关重要,特别是在存在大量原生瓣膜钙负荷和重新护套操作的情况下,通过假体捕获或后扩张安全克服这种并发症。