Smidt Heart Institute, Cedars-Sinai Medical Center, Los Angeles, California.
Columbia University Medical Center, New York, New York.
JAMA. 2019 Jun 11;321(22):2193-2202. doi: 10.1001/jama.2019.7108.
Transcatheter aortic valve replacement (TAVR) indications are expanding, leading to an increasing number of patients with bicuspid aortic stenosis undergoing TAVR. Pivotal randomized trials conducted to obtain US Food and Drug Administration approval excluded bicuspid anatomy.
To compare the outcomes of TAVR with a balloon-expandable valve for bicuspid vs tricuspid aortic stenosis.
DESIGN, SETTING, AND PARTICIPANTS: Registry-based prospective cohort study of patients undergoing TAVR at 552 US centers. Participants were enrolled in the Society of Thoracic Surgeons (STS)/American College of Cardiology (ACC) Transcatheter Valve Therapies Registry from June 2015 to November 2018.
TAVR for bicuspid vs tricuspid aortic stenosis.
Primary outcomes were 30-day and 1-year mortality and stroke. Secondary outcomes included procedural complications, valve hemodynamics, and quality of life assessment.
Of 81 822 consecutive patients with aortic stenosis (2726 bicuspid; 79 096 tricuspid), 2691 propensity-score matched pairs of bicuspid and tricuspid aortic stenosis were analyzed (median age, 74 years [interquartile range {IQR}, 66-81 years]; 39.1%, women; mean [SD] STS-predicted risk of mortality, 4.9% [4.0%] and 5.1% [4.2%], respectively). All-cause mortality was not significantly different between patients with bicuspid and tricuspid aortic stenosis at 30 days (2.6% vs 2.5%; hazard ratio [HR], 1.04, [95% CI, 0.74-1.47]) and 1 year (10.5% vs 12.0%; HR, 0.90 [95% CI, 0.73-1.10]). The 30-day stroke rate was significantly higher for bicuspid vs tricuspid aortic stenosis (2.5% vs 1.6%; HR, 1.57 [95% CI, 1.06-2.33]). The risk of procedural complications requiring open heart surgery was significantly higher in the bicuspid vs tricuspid cohort (0.9% vs 0.4%, respectively; absolute risk difference [RD], 0.5% [95% CI, 0%-0.9%]). There were no significant differences in valve hemodynamics. There were no significant differences in moderate or severe paravalvular leak at 30 days (2.0% vs 2.4%; absolute RD, 0.3% [95% CI, -1.3% to 0.7%]) and 1 year (3.2% vs 2.5%; absolute RD, 0.7% [95% CI, -1.3% to 2.7%]). At 1 year there was no significant difference in improvement in quality of life between the groups (difference in improvement in the Kansas City Cardiomyopathy Questionnaire overall summary score, -2.4 [95% CI, -5.1 to 0.3]; P = .08).
In this preliminary, registry-based study of propensity-matched patients who had undergone transcatheter aortic valve replacement for aortic stenosis, patients with bicuspid vs tricuspid aortic stenosis had no significant difference in 30-day or 1-year mortality but had increased 30-day risk for stroke. Because of the potential for selection bias and the absence of a control group treated surgically for bicuspid stenosis, randomized trials are needed to adequately assess the efficacy and safety of transcatheter aortic valve replacement for bicuspid aortic stenosis.
重要性:经导管主动脉瓣置换术(TAVR)的适应证不断扩大,导致越来越多的二叶式主动脉瓣狭窄患者接受 TAVR。为获得美国食品和药物管理局的批准而进行的关键随机试验排除了二叶式解剖结构。
目的:比较 TAVR 治疗二叶式与三叶式主动脉瓣狭窄的结果。
设计、地点和参与者:这是一项基于注册的前瞻性队列研究,在 552 个美国中心进行 TAVR。参与者于 2015 年 6 月至 2018 年 11 月期间被纳入胸外科医师学会(STS)/美国心脏病学会(ACC)经导管瓣膜治疗登记处。
暴露情况:二叶式 vs 三叶式主动脉瓣狭窄的 TAVR。
主要结果和措施:主要结局为 30 天和 1 年死亡率和卒中。次要结局包括手术并发症、瓣膜血流动力学和生活质量评估。
结果:在连续 81822 例主动脉瓣狭窄患者中(2726 例二叶式;79096 例三叶式),分析了 2691 对倾向性评分匹配的二叶式和三叶式主动脉瓣狭窄患者(中位年龄 74 岁[四分位距 {IQR} ,66-81 岁];39.1%为女性;平均 [标准差] STS 预测死亡率分别为 4.9%[4.0%]和 5.1%[4.2%])。二叶式和三叶式主动脉瓣狭窄患者的全因死亡率在 30 天(2.6%比 2.5%;危险比[HR],1.04[95%置信区间 {CI} ,0.74-1.47])和 1 年(10.5%比 12.0%;HR,0.90[95%CI,0.73-1.10])时无显著差异。二叶式主动脉瓣狭窄患者的 30 天卒中发生率显著高于三叶式主动脉瓣狭窄患者(2.5%比 1.6%;HR,1.57[95%CI,1.06-2.33])。二叶式主动脉瓣狭窄患者需要开胸手术的手术并发症风险显著高于三叶式主动脉瓣狭窄患者(0.9%比 0.4%;绝对风险差异 [RD],0.5%[95%CI,0%-0.9%])。瓣膜血流动力学无显著差异。30 天中度或重度瓣周漏的发生率无显著差异(2.0%比 2.4%;绝对 RD,0.3%[95%CI,-1.3%至 0.7%])和 1 年(3.2%比 2.5%;绝对 RD,0.7%[95%CI,-1.3%至 2.7%])。1 年时,两组之间的生活质量改善程度没有显著差异(堪萨斯城心肌病问卷整体综合评分的改善差异,-2.4[95%CI,-5.1 至 0.3];P=0.08)。
结论和相关性:在这项初步的、基于注册的研究中,对接受主动脉瓣狭窄 TAVR 的二叶式和三叶式患者进行倾向性匹配,二叶式主动脉瓣狭窄患者与三叶式主动脉瓣狭窄患者在 30 天或 1 年死亡率方面无显著差异,但 30 天卒中风险增加。由于存在选择偏倚的潜在风险和缺乏二叶式狭窄的外科治疗对照组,需要进行随机试验来充分评估 TAVR 治疗二叶式主动脉瓣狭窄的疗效和安全性。