Beth Israel Deaconess Medical Center, Boston, Massachusetts.
Mount Sinai Medical Center, New York, New York.
J Am Coll Cardiol. 2014 May 20;63(19):1972-81. doi: 10.1016/j.jacc.2014.02.556. Epub 2014 Mar 19.
This study sought to evaluate the safety and efficacy of the CoreValve transcatheter heart valve (THV) for the treatment of severe aortic stenosis in patients at extreme risk for surgery.
Untreated severe aortic stenosis is a progressive disease with a poor prognosis. Transcatheter aortic valve replacement (TAVR) with a self-expanding bioprosthesis is a potentially effective therapy.
We performed a prospective, multicenter, nonrandomized investigation evaluating the safety and efficacy of self-expanding TAVR in patients with symptomatic severe aortic stenosis with prohibitive risks for surgery. The primary endpoint was a composite of all-cause mortality or major stroke at 12 months, which was compared with a pre-specified objective performance goal (OPG).
A total of 41 sites in the United States recruited 506 patients, of whom 489 underwent attempted treatment with the CoreValve THV. The rate of all-cause mortality or major stroke at 12 months was 26.0% (upper 2-sided 95% confidence bound: 29.9%) versus 43.0% with the OPG (p < 0.0001). Individual 30-day and 12-month events included all-cause mortality (8.4% and 24.3%, respectively) and major stroke (2.3% and 4.3%, respectively). Procedural events at 30 days included life-threatening/disabling bleeding (12.7%), major vascular complications (8.2%), and need for permanent pacemaker placement (21.6%). The frequency of moderate or severe paravalvular aortic regurgitation was lower 12 months after self-expanding TAVR (4.2%) than at discharge (10.7%; p = 0.004 for paired analysis).
TAVR with a self-expanding bioprosthesis was safe and effective in patients with symptomatic severe aortic stenosis at prohibitive risk for surgical valve replacement. (Safety and Efficacy Study of the Medtronic CoreValve System in the Treatment of Symptomatic Severe Aortic Stenosis in High Risk and Very High Risk Subjects Who Need Aortic Valve Replacement; NCT01240902).
本研究旨在评估 CoreValve 经导管心脏瓣膜(THV)治疗手术高危极高危重度主动脉瓣狭窄患者的安全性和疗效。
未经治疗的重度主动脉瓣狭窄是一种进行性疾病,预后不良。经导管主动脉瓣置换术(TAVR)联合自膨式生物瓣是一种潜在有效的治疗方法。
我们进行了一项前瞻性、多中心、非随机研究,评估自膨式 TAVR 治疗有手术禁忌极高危症状性重度主动脉瓣狭窄患者的安全性和疗效。主要终点是 12 个月时全因死亡率或主要卒中的复合终点,与预先设定的客观绩效目标(OPG)进行比较。
美国 41 个中心共招募了 506 名患者,其中 489 名患者接受了 CoreValve THV 的尝试性治疗。12 个月时全因死亡率或主要卒中的发生率为 26.0%(双侧 95%置信区间上限:29.9%),而 OPG 为 43.0%(p<0.0001)。30 天和 12 个月的单个事件包括全因死亡率(分别为 8.4%和 24.3%)和主要卒中(分别为 2.3%和 4.3%)。30 天的手术相关事件包括危及生命/致残性出血(12.7%)、大血管并发症(8.2%)和需要永久性起搏器植入(21.6%)。自膨式 TAVR 后 12 个月时中度或重度瓣周主动脉反流的发生率低于出院时(分别为 4.2%和 10.7%;配对分析 p=0.004)。
在手术瓣膜置换高危极高危的有症状重度主动脉瓣狭窄患者中,自膨式生物瓣的 TAVR 是安全有效的。(经导管心脏瓣膜治疗高危极高危症状性重度主动脉瓣狭窄患者的安全性和疗效研究;NCT01240902)