Cardiovascular Division, University of Pennsylvania, Philadelphia.
Department of Medicine, Laval University, Quebec City, Quebec, Canada.
JAMA Cardiol. 2016 Aug 1;1(5):584-92. doi: 10.1001/jamacardio.2016.0759.
Low-flow (LF) severe aortic stenosis (AS) is an independent predictor of mortality in patients undergoing aortic valve replacement (AVR). Little is known about improvement in flow after AVR and its effects on survival.
To determine whether higher flow (left-ventricular stroke volume index [LVSVI]) after transcatheter AVR (TAVR) would indicate better clinical outcomes in this at-risk population.
DESIGN, SETTING, AND PARTICIPANTS: A substudy analysis of data from the Placement of Aortic Transcatheter Valves (PARTNER) randomized clinical trial and continued-access registry was conducted. A total of 984 participants with evaluable echocardiograms and baseline LF AS (LVSVI ≤35 mL/m2) were included. The trial was conducted at 26 sites in the United States and Canada. Patients were stratified after TAVR into tertiles by discharge LVSVI status (severe low flow [SLF], moderate low flow [MLF], and normal flow [(NF]). The present study was conducted from May 11, 2007, to January 9, 2012, with data analysis performed from April 25, 2014, to January 21, 2016.
The primary end point was all-cause mortality at 1 year.
Baseline characteristics of 984 patients with LF AS included mean (SD) age, 84 (7) years; 582 (59.1%) men; mean Society of Thoracic Surgeons (STS) score, 11.4% (4.0%); and mean LVSVI, 27.6 (5.0) mL/m2. The discharge LVSVI values by group were SLF, 23.1 (3.5) mL/m2; MLF, 31.7 (2.2) mL/m2; and NF, 43.1 (7.0). All-cause mortality at 1 year was SLF, 26.5%; MLF, 20.1%; and NF, 19.6% (P = .045). Mean LVSVI normalized by 6 months in the MLF (35.9 [9.3] mL/m2) and NF (38.8 [11.1] mL/m2) groups, but remained low in the SLF group at 6 months and 1 year (31.4 [8.4] and 33.0 [8.3] mL/m2], respectively) (P < .001 for all groups). Reported as multivariate hazard ratio, mortality at 1 year was higher in the SLF group compared with the other groups (1.61; 95% CI, 1.17-2.23; P = .004). In addition to SLF, sex (1.59; 95% CI, 1.18-2.13; P = .002), presence of atrial fibrillation (1.41; 95% CI, 1.06-1.87; P = .02), STS score (1.03; 95% CI, 1.01-1.06; P = .02), presence of moderate or severe mitral regurgitation at discharge (1.65; 95% CI, 1.21-2.26; P = .001), pre-TAVR mean transvalvular gradient (0.98; 95% CI, 0.97-0.99; P = .004), and effective orifice area index (1.87; 95% CI, 1.09-3.19; P = .02) were independent predictors of 1-year mortality.
Severe LF at discharge is associated with an increased risk of mortality following TAVR in patients with severe AS and preexisting LF. The identification of remedial causes of persistent LF after TAVR may represent an opportunity to improve the outcome of these patients.
clinicaltrials.gov Identifier: NCT00530894.
在接受主动脉瓣置换术 (AVR) 的患者中,低流量 (LF) 严重主动脉瓣狭窄 (AS) 是死亡率的独立预测因素。关于 AVR 后流量的改善及其对生存的影响知之甚少。
确定经导管主动脉瓣置换术 (TAVR) 后较高的流量 (左心室每搏量指数 [LVSVI]) 是否会在这一高危人群中预示更好的临床结局。
设计、地点和参与者:对来自 Placement of Aortic Transcatheter Valves (PARTNER) 随机临床试验和持续准入注册的研究数据进行了子研究分析。共纳入了 984 名可评估超声心动图和基线 LF AS(LVSVI≤35 mL/m2)的患者。该试验在美国和加拿大的 26 个地点进行。根据出院时 LVSVI 状态,患者在 TAVR 后分层为 3 个三分位数(严重低流量 [SLF]、中度低流量 [MLF] 和正常流量 [NF])。本研究于 2007 年 5 月 11 日至 2012 年 1 月 9 日进行,数据分析于 2014 年 4 月 25 日至 2016 年 1 月 21 日进行。
主要终点为 1 年时的全因死亡率。
984 例 LF AS 患者的基线特征包括平均(标准差)年龄为 84(7)岁;582 名(59.1%)男性;平均胸外科医生协会(STS)评分 11.4%(4.0%);平均 LVSVI 为 27.6(5.0)mL/m2。各组出院时的 LVSVI 值分别为 SLF:23.1(3.5)mL/m2;MLF:31.7(2.2)mL/m2;NF:43.1(7.0)mL/m2。1 年时的全因死亡率分别为 SLF:26.5%;MLF:20.1%;NF:19.6%(P=0.045)。MLF(35.9[9.3]mL/m2)和 NF(38.8[11.1]mL/m2)组的 LVSVI 在 6 个月时得到正常化,但 SLF 组在 6 个月和 1 年时仍较低,分别为 31.4(8.4)和 33.0(8.3)mL/m2(P<0.001 所有组)。作为多变量危险比,与其他组相比,SLF 组 1 年时的死亡率更高(1.61;95%CI,1.17-2.23;P=0.004)。除了 SLF,性别(1.59;95%CI,1.18-2.13;P=0.002)、房颤(1.41;95%CI,1.06-1.87;P=0.02)、STS 评分(1.03;95%CI,1.01-1.06;P=0.02)、出院时存在中度或重度二尖瓣反流(1.65;95%CI,1.21-2.26;P=0.001)、术前跨瓣梯度(0.98;95%CI,0.97-0.99;P=0.004)和有效瓣口面积指数(1.87;95%CI,1.09-3.19;P=0.02)是 1 年死亡率的独立预测因素。
严重 AS 合并 LF 的患者在接受 TAVR 后出现严重 LF 与死亡率增加相关。确定 TAVR 后持续存在 LF 的补救原因可能代表改善这些患者结局的机会。
clinicaltrials.gov 标识符:NCT00530894。