Interventional Structural and Congenital Heart Disease Programme, Invasive Cardiology Division of Cardiology, Ferrarotto Hospital, University of Catania, Catania, Italy.
Eur Heart J. 2012 Apr;33(8):969-76. doi: 10.1093/eurheartj/ehr491. Epub 2012 Jan 12.
The paucity of evidences about the long-term durability of currently available transcatheter prostheses is one of the main issues of transcatheter aortic valve implantation (TAVI). We sought to assess 3-year clinical and echocardiographic outcomes of patients undergoing TAVI with the third generation CoreValve prosthesis (Medtronic Incorporation, MN, USA).
From the Italian CoreValve registry, 181 who underwent TAVI from June 2007 to August 2008 and eligible for 3-year follow-up were analysed. All outcomes were defined according to the Valve Academic Research Consortium. All-cause mortality at 1, 2, and 3 years was 23.6, 30.3, and 34.8%, respectively. Cardiovascular death at 1, 2, and 3 years was 11.2, 12.1, and 13.5%, respectively. The actuarial survival free from a composite of death, major stroke, myocardial infarction, and life-threatening bleeding was 69.6% at 1 year, 63.5% at 2 years, and 59.7% at 3 years. Patients with renal insufficiency had a higher mortality at 3-year follow-up (49.0 vs. 29.2%, P = 0.007); moreover, patients experiencing post-procedural major or life-threatening bleeding had a higher rate of mortality already seen at 30 days (21.6 vs. 2.8%; P < 0.001) and this result was sustained at 3-year follow-up (62.2 vs. 27.7%; P < 0.001). Mean pressure gradients decreased from 52.2 ± 18.1 mmHg (pre-TAVI) to 10.3 ± 3.1 mmHg (1-year post-TAVI) (P < 0.001); aortic valve area increased from 0.6 ± 0.2 cm(2) (pre-TAVI) to 1.8 ± 0.4 cm(2) (1-year post-TAVI); these results remained stable over the 3 years of follow-up. Paravalvular leak was observed in the majority of patients. There were no cases of progression to moderate or severe regurgitation. No cases of structural valve deterioration were observed.
This multicentre study demonstrates that TAVI with the 18-Fr CoreValve ReValving System is associated with sustained clinical and functional cardiovascular benefits in high-risk patients with symptomatic aortic stenosis up to 3-year follow-up. Non-cardiac causes accounted for the majority of deaths at follow-up.
目前可用的经导管瓣膜假体的长期耐久性证据不足是经导管主动脉瓣置换术(TAVI)的主要问题之一。我们旨在评估第三代 CoreValve 假体(美敦力公司,明尼苏达州,美国)进行 TAVI 的患者 3 年的临床和超声心动图结果。
从 2007 年 6 月至 2008 年 8 月进行 TAVI 并符合 3 年随访条件的意大利 CoreValve 注册中,分析了 181 例患者。所有结果均根据瓣膜学术研究联盟定义。1、2 和 3 年的全因死亡率分别为 23.6%、30.3%和 34.8%。1、2 和 3 年的心血管死亡率分别为 11.2%、12.1%和 13.5%。1 年时无死亡、主要卒中、心肌梗死和危及生命的出血复合事件的 actuarial 生存率为 69.6%,2 年时为 63.5%,3 年时为 59.7%。肾功能不全患者在 3 年随访时死亡率更高(49.0%比 29.2%,P=0.007);此外,术后发生重大或危及生命的出血的患者在 30 天时死亡率更高(21.6%比 2.8%;P<0.001),这一结果在 3 年随访时仍持续存在(62.2%比 27.7%;P<0.001)。平均压力梯度从 52.2±18.1mmHg(TAVI 前)降至 10.3±3.1mmHg(TAVI 后 1 年)(P<0.001);主动脉瓣面积从 0.6±0.2cm²(TAVI 前)增加到 1.8±0.4cm²(TAVI 后 1 年);这些结果在 3 年的随访中保持稳定。大多数患者出现瓣周漏。无中度或重度反流进展的病例。未观察到结构性瓣膜恶化的病例。
这项多中心研究表明,在高危有症状的主动脉瓣狭窄患者中,使用 18Fr CoreValve ReValving 系统进行 TAVI 可带来持续的临床和功能心血管获益,可随访至 3 年。随访期间的大多数死亡是由非心脏原因引起的。