Division of Cardiac Surgery, St Paul's Hospital, University of British Columbia, Vancouver, British Columbia, Canada.
J Thorac Cardiovasc Surg. 2010 May;139(5):1107-13, 1113.e1. doi: 10.1016/j.jtcvs.2009.10.056.
We performed the first human case of successful transapical transcatheter aortic valve implantation on a beating heart in October 2005, and therefore we have the longest follow-up on transapical aortic valve implantation in humans. We now report clinical and echocardiographic outcomes of transapical aortic valve implantation in 71 patients.
Between October 2005 and February 2009, 71 patients (44 female) underwent transcatheter transapical aortic valve implantation with either 23- or 26-mm Edwards Lifesciences transcatheter bioprostheses. All patients with symptomatic aortic stenosis were declined for conventional aortic valve replacement owing to unacceptable operative risks and were not candidates for transfemoral aortic valve implantation because of poor arterial access. Clinical and echocardiographic follow-ups were performed before discharge, at 1 and 6 months, and then yearly. The mean follow-up was 12.9 +/- 11.5 months with a total of 917.3 months of follow-up.
Mean age was 80.0 +/- 8.1 years and predicted operative mortality was 34.5% +/- 20.4% by logistic EuroSCORE and 12.1% +/- 7.7% by The Society of Thoracic Surgeons Risk Calculator. Valves were successfully implanted in all patients. Twelve patients died within 30 days (30-day mortality: 16.9% in all patients, 33% in the first 15 patients, and 12.5% in the remainder), and 10 patients died subsequently. Overall survival at 24 and 36 months was 66.3% +/- 6.4% and 58.0% +/- 9.5%, respectively. Among 59 patients who survived at least 30 days, 24- and 36-month survivals were 79.8% +/- 6.4% and 69.8% +/- 10.9%, respectively. Late valve-related complications were rare. New York Heart Association functional class improved significantly from preoperative 3.3 +/- 0.8 to 1.8 +/- 0.8 at 24 months. The aortic valve area and mean gradient remained stable at 24 months (1.6 +/- 0.3 cm(2) and 10.3 +/- 5.9 mm Hg, respectively).
Our outcome suggests that transapical transcatheter aortic valve implantation provides sustained clinical and hemodynamic benefits for up to 36 months in selected high-risk patients with symptomatic severe aortic stenosis.
我们于 2005 年 10 月首次成功地在跳动的心脏上进行了经心尖入路的经导管主动脉瓣植入术,因此我们拥有人类经心尖主动脉瓣植入术的最长随访记录。我们现在报告 71 例经心尖主动脉瓣植入术的临床和超声心动图结果。
2005 年 10 月至 2009 年 2 月期间,71 例患者(44 例为女性)接受了经导管经心尖主动脉瓣植入术,植入的瓣膜为爱德华生命科学公司的 23 或 26 毫米经导管生物瓣膜。所有有症状的主动脉瓣狭窄患者均因手术风险高而被拒绝进行传统的主动脉瓣置换术,且因动脉通路不佳而不适合经股动脉主动脉瓣植入术。在出院前、术后 1 个月和 6 个月以及之后每年进行临床和超声心动图随访。平均随访时间为 12.9±11.5 个月,总随访时间为 917.3 个月。
平均年龄为 80.0±8.1 岁,Logistic EuroSCORE 预测手术死亡率为 34.5%±20.4%,胸外科医生协会风险计算器预测手术死亡率为 12.1%±7.7%。所有患者均成功植入瓣膜。术后 30 天内有 12 例患者死亡(总死亡率为 16.9%,前 15 例患者死亡率为 33%,其余患者死亡率为 12.5%),随后又有 10 例患者死亡。总体 24 个月和 36 个月的生存率分别为 66.3%±6.4%和 58.0%±9.5%。在至少存活 30 天的 59 例患者中,24 个月和 36 个月的生存率分别为 79.8%±6.4%和 69.8%±10.9%。晚期瓣膜相关并发症罕见。纽约心脏协会功能分级从术前的 3.3±0.8 显著改善至术后 24 个月的 1.8±0.8。24 个月时主动脉瓣面积和平均梯度保持稳定(分别为 1.6±0.3cm2 和 10.3±5.9mmHg)。
我们的结果表明,在有症状的严重主动脉瓣狭窄高危患者中,经心尖入路的经导管主动脉瓣植入术可提供长达 36 个月的持续临床和血流动力学获益。