Division of Cardiac Surgery, St. Paul's Hospital, University of British Columbia, Vancouver, British Columbia, Canada.
J Thorac Cardiovasc Surg. 2013 Jun;145(6):1554-62. doi: 10.1016/j.jtcvs.2012.05.016. Epub 2012 Jun 12.
The feasibility of transapical valve-in-valve aortic valve implantation into a failed aortic surgical bioprosthesis has been confirmed. The purpose of the present study was to investigate the clinical and hemodynamic outcomes more than 2 years after transapical valve-in-valve aortic valve implantation.
From April 2007 to May 2010, 8 consecutive patients underwent transapical valve-in-valve aortic valve implantation of either 23- or 26-mm Edwards-SAPIEN balloon-expandable bioprostheses into failed surgical tissue valves (21- to 25-mm valves). Clinical and echocardiographic follow-up was performed in all patients. The mean follow-up duration was 27.8 ± 15.7 months (range, 18-55 months).
Transapical valve-in-valve aortic valve implantation was successful in all patients (mean age, 84.1 ± 1.6 years). The predicted operative mortality was 42.1% ± 15.7% by logistic European System for Cardiac Operative Risk Evaluation and 14.4% ± 9.6% using the Society of Thoracic Surgeons risk calculator. The observed 30-day mortality was 12.5%. No strokes or valve embolization/migrations occurred. The mean hospital stay was 9.0 ± 9.1 days. The New York Heart Association class decreased from preoperative class III-IV to postoperative class I in 6 of 7 survivors. The 2-year survival was 87.5%. No late mortality occurred during the follow-up period. The echocardiographic results at 1 to 4 years of follow-up demonstrated stable valve position and function in all patients. The transaortic valve pressure gradients after valve-in-valve aortic valve implantation were greater than 20 mm Hg and less than 15 mm Hg in patients with 21- or 23-mm and 25-mm surgical valves, respectively.
Transapical valve-in-valve aortic valve implantation provides good clinical outcomes and stable valve function beyond 2 years of follow-up. The best hemodynamic and clinical outcomes can be achieved in the patients with a surgical valve size of 25 mm or greater. Valve-in-valve aortic valve implantation could become a viable approach for selected high-risk patients with failed surgical bioprostheses.
经心尖途径行主动脉瓣瓣中瓣植入术治疗主动脉瓣生物瓣衰败的可行性已得到证实。本研究旨在探讨经心尖途径行主动脉瓣瓣中瓣植入术 2 年以上的临床和血流动力学结果。
2007 年 4 月至 2010 年 5 月,连续 8 例患者在主动脉瓣生物瓣衰败后,行经心尖途径植入 23 或 26mm Edwards-SAPIEN 球扩式生物瓣,此前患者置换的主动脉瓣为 21-25mm 瓣膜(21-25mm 外科瓣)。所有患者均接受临床和超声心动图随访。平均随访时间为 27.8±15.7 个月(18-55 个月)。
所有患者(平均年龄 84.1±1.6 岁)均成功行经心尖途径行主动脉瓣瓣中瓣植入术。Logistic 欧洲心脏手术风险评估系统预测的手术死亡率为 42.1%±15.7%,胸外科医师协会风险计算系统预测的手术死亡率为 14.4%±9.6%。实际 30 天死亡率为 12.5%。无卒中或瓣环移位/脱出。平均住院时间为 9.0±9.1 天。7 例存活患者中,6 例术前纽约心脏协会心功能分级 III-IV 级,术后为 I 级。2 年生存率为 87.5%。随访期间无晚期死亡。术后 1-4 年的超声心动图结果显示,所有患者的瓣膜位置和功能均稳定。在外科瓣为 21-或 23-mm 及 25-mm 的患者中,主动脉瓣瓣中瓣植入术后跨瓣压差分别大于 20mmHg 且小于 15mmHg。
经心尖途径行主动脉瓣瓣中瓣植入术 2 年以上可获得良好的临床结果和稳定的瓣膜功能。外科瓣尺寸为 25mm 或更大的患者可获得最佳的血流动力学和临床结果。对于主动脉瓣生物瓣衰败的高危患者,瓣中瓣主动脉瓣植入术可能成为一种可行的方法。