Department of Cardiovascular Sciences, University of Leicester, Leicester, England.
National Institute for Health Research Leicester Biomedical Research Centre, Glenfield Hospital, Leicester, England.
JAMA. 2022 May 17;327(19):1875-1887. doi: 10.1001/jama.2022.5776.
Transcatheter aortic valve implantation (TAVI) is a less invasive alternative to surgical aortic valve replacement and is the treatment of choice for patients at high operative risk. The role of TAVI in patients at lower risk is unclear.
To determine whether TAVI is noninferior to surgery in patients at moderately increased operative risk.
DESIGN, SETTING, AND PARTICIPANTS: In this randomized clinical trial conducted at 34 UK centers, 913 patients aged 70 years or older with severe, symptomatic aortic stenosis and moderately increased operative risk due to age or comorbidity were enrolled between April 2014 and April 2018 and followed up through April 2019.
TAVI using any valve with a CE mark (indicating conformity of the valve with all legal and safety requirements for sale throughout the European Economic Area) and any access route (n = 458) or surgical aortic valve replacement (surgery; n = 455).
The primary outcome was all-cause mortality at 1 year. The primary hypothesis was that TAVI was noninferior to surgery, with a noninferiority margin of 5% for the upper limit of the 1-sided 97.5% CI for the absolute between-group difference in mortality. There were 36 secondary outcomes (30 reported herein), including duration of hospital stay, major bleeding events, vascular complications, conduction disturbance requiring pacemaker implantation, and aortic regurgitation.
Among 913 patients randomized (median age, 81 years [IQR, 78 to 84 years]; 424 [46%] were female; median Society of Thoracic Surgeons mortality risk score, 2.6% [IQR, 2.0% to 3.4%]), 912 (99.9%) completed follow-up and were included in the noninferiority analysis. At 1 year, there were 21 deaths (4.6%) in the TAVI group and 30 deaths (6.6%) in the surgery group, with an adjusted absolute risk difference of -2.0% (1-sided 97.5% CI, -∞ to 1.2%; P < .001 for noninferiority). Of 30 prespecified secondary outcomes reported herein, 24 showed no significant difference at 1 year. TAVI was associated with significantly shorter postprocedural hospitalization (median of 3 days [IQR, 2 to 5 days] vs 8 days [IQR, 6 to 13 days] in the surgery group). At 1 year, there were significantly fewer major bleeding events after TAVI compared with surgery (7.2% vs 20.2%, respectively; adjusted hazard ratio [HR], 0.33 [95% CI, 0.24 to 0.45]) but significantly more vascular complications (10.3% vs 2.4%; adjusted HR, 4.42 [95% CI, 2.54 to 7.71]), conduction disturbances requiring pacemaker implantation (14.2% vs 7.3%; adjusted HR, 2.05 [95% CI, 1.43 to 2.94]), and mild (38.3% vs 11.7%) or moderate (2.3% vs 0.6%) aortic regurgitation (adjusted odds ratio for mild, moderate, or severe [no instance of severe reported] aortic regurgitation combined vs none, 4.89 [95% CI, 3.08 to 7.75]).
Among patients aged 70 years or older with severe, symptomatic aortic stenosis and moderately increased operative risk, TAVI was noninferior to surgery with respect to all-cause mortality at 1 year.
isrctn.com Identifier: ISRCTN57819173.
经导管主动脉瓣植入术(TAVI)是一种对主动脉瓣置换术具有侵入性较小的替代方法,是高手术风险患者的首选治疗方法。但 TAVI 在低风险患者中的作用尚不清楚。
确定 TAVI 对中度增加手术风险的患者是否不劣于手术。
设计、设置和参与者:在这项由 34 个英国中心进行的随机临床试验中,纳入了 913 名年龄在 70 岁或以上的严重、有症状的主动脉瓣狭窄患者,由于年龄或合并症而处于中度增加的手术风险,他们在 2014 年 4 月至 2018 年 4 月之间被招募并随访至 2019 年 4 月。
使用带有 CE 标志的任何瓣膜进行 TAVI(表示瓣膜符合整个欧洲经济区销售的所有法律和安全要求)和任何进入途径(n=458)或主动脉瓣置换手术(手术;n=455)。
主要结局是 1 年时的全因死亡率。主要假设是 TAVI 不劣于手术,死亡率绝对差值的单侧 97.5%CI 的上限为 5%,是组间差异的非劣效性边界。共有 36 个次要结局(本文报告了 30 个),包括住院时间、大出血事件、血管并发症、需要起搏器植入的传导障碍以及主动脉瓣反流。
在 913 名随机分组的患者中(中位年龄为 81 岁[IQR,78 至 84 岁];424[46%]为女性;中位胸外科医生死亡率风险评分,2.6%[IQR,2.0%至 3.4%]),912 名(99.9%)完成了随访并纳入了非劣效性分析。在 1 年时,TAVI 组有 21 例(4.6%)死亡,手术组有 30 例(6.6%)死亡,调整后的绝对风险差异为-2.0%(单侧 97.5%CI,-∞至 1.2%;P<0.001 用于非劣效性)。在本文报告的 30 个预先指定的次要结局中,有 24 个在 1 年时没有显著差异。TAVI 与术后住院时间明显缩短相关(中位数为 3 天[IQR,2 至 5 天],而手术组为 8 天[IQR,6 至 13 天])。在 1 年时,TAVI 组大出血事件的发生率明显低于手术组(分别为 7.2%和 20.2%;调整后的危险比[HR],0.33[95%CI,0.24 至 0.45]),但血管并发症明显更多(分别为 10.3%和 2.4%;调整后的 HR,4.42[95%CI,2.54 至 7.71]),需要起搏器植入的传导障碍(分别为 14.2%和 7.3%;调整后的 HR,2.05[95%CI,1.43 至 2.94]),以及轻度(38.3%)或中度(2.3%)主动脉瓣反流(轻度、中度或重度[无重度报告]主动脉瓣反流联合发生率的调整比值比,4.89[95%CI,3.08 至 7.75])。
在年龄为 70 岁或以上的严重、有症状的主动脉瓣狭窄且手术风险中度增加的患者中,TAVI 在 1 年时的全因死亡率方面不劣于手术。
isrctn.com 标识符:ISRCTN57819173。