Grubitzsch Herko, Zobel Sebastian, Christ Torsten, Holinski Sebastian, Stangl Karl, Treskatsch Sascha, Falk Volkmar, Laule Michael
Department of Cardiovascular Surgery, Campus Charité Mitte, Charité - Universitätsmedizin Berlin, Berlin, Germany.
Department of Cardiology, Campus Charité Mitte, Charité - Universitätsmedizin Berlin, Berlin, Germany.
Eur J Cardiothorac Surg. 2017 Apr 1;51(4):653-659. doi: 10.1093/ejcts/ezw397.
This study evaluates reinterventions for degenerated stentless aortic xenografts.
Between 2010 and 2015, 52 consecutive patients (age 72.3 ± 9.7 years, EuroSCORE II 11.1 ± 8.9%) underwent reintervention for failed stentless aortic valves (60% porcine, 40% pericardial, 87% sub-coronary, 81% isolated/combined regurgitation).
Based on age, EuroSCORE II, the presence of pulmonary hypertension, renal failure, a patent internal mammary artery graft and required concomitant procedures, the heart team assigned 25 patients to reoperation and 27 to valve-in-valve transcatheter aortic valve implantation (ViV-TAVI). Valve implantation was successful in all surgical (24% root replacement) and in 24 transcatheter cases (93% trans-femoral, 56% balloon-expandable). Procedural complications were aortic dissection ( n = 1) during reoperation and coronary obstruction ( n = 4), device malpositioning ( n = 3), deployment of >1 valve ( n = 2) and vascular access site complications ( n = 2) during ViV-TAVI. Thirty-day mortality (10%, three ViV-TAVI patients, two surgical patients, P = 1.0) was associated with preoperative renal failure, >1 concomitant procedure, life-threatening bleeding, coronary obstruction and necessity for prolonged circulatory support. ViV-TAVI was beneficial regarding ventilation time, transfusion requirements and the incidence of sepsis. Overall, functional (94% New York Heart Association Class I/II) and echocardiographic results (indexed effective orifice area 0.95 ± 0.27 cm 2 /m 2 , mean transvalvular gradient 14 ± 6.8 mmHg) were favourable. After ViV-TAVI, aortic regurgitation was mild and moderate in two and three patients. One-year survival was 82.3 ± 5.4% and similar after surgery (83.1 ± 7.7%) and ViV-TAVI (81.5 ± 7.5%, P = 0.76).
Reinterventions for degenerated stentless aortic valves are challenging. Although ViV-TAVI is appropriate in high-risk patients, limitations and potential complications must be considered. Redo surgery has its place in low-risk patients and if concomitant procedures are required.
本研究评估对退化的无支架主动脉异种移植物的再次干预措施。
在2010年至2015年期间,52例连续患者(年龄72.3±9.7岁,欧洲心脏手术风险评估系统II 11.1±8.9%)因无支架主动脉瓣功能衰竭接受了再次干预(60%为猪主动脉瓣,40%为心包主动脉瓣,87%为冠状动脉下型,81%为单纯/合并反流)。
根据年龄、欧洲心脏手术风险评估系统II、是否存在肺动脉高压、肾衰竭、胸廓内动脉桥血管通畅情况以及所需的同期手术,心脏团队将25例患者分配至再次手术组,27例患者分配至经导管主动脉瓣置入术(ViV-TAVI)组。瓣膜置入在所有手术病例(24%为根部置换)和24例经导管病例中均成功(93%经股动脉入路,56%为球囊扩张型)。手术并发症包括再次手术期间发生的主动脉夹层(n = 1)以及ViV-TAVI期间发生的冠状动脉阻塞(n = 4)、装置位置不当(n = 3)、置入>1个瓣膜(n = 2)和血管入路部位并发症(n = 2)。30天死亡率(10%,3例ViV-TAVI患者,2例手术患者,P = 1.0)与术前肾衰竭、>1项同期手术、危及生命的出血、冠状动脉阻塞以及需要延长循环支持有关。ViV-TAVI在通气时间、输血需求和脓毒症发生率方面具有优势。总体而言,功能(94%为纽约心脏协会I/II级)和超声心动图结果(指数化有效瓣口面积0.95±0.27cm²/m²,平均跨瓣压差14±6.8mmHg)良好。ViV-TAVI后,2例患者存在轻度主动脉反流,3例患者存在中度主动脉反流。1年生存率为82.3±5.4%,手术组(83.1±7.7%)和ViV-TAVI组(81.5±7.5%)相似(P = 0.76)。
对退化的无支架主动脉瓣进行再次干预具有挑战性。尽管ViV-TAVI适用于高危患者,但必须考虑其局限性和潜在并发症。再次手术在低危患者以及需要同期手术时仍有其应用价值。