Heart and Vascular Institute, Cleveland Clinic Foundation, Cleveland, Ohio, USA.
Cardiovascular Institute, The Warren Alpert Medical School at Brown University, Providence, Rhode Island, USA.
J Am Coll Cardiol. 2021 Apr 13;77(14):1703-1713. doi: 10.1016/j.jacc.2021.02.032.
Patients with rheumatic aortic stenosis (AS) were excluded from transcatheter aortic valve replacement (TAVR) trials.
The authors sought to examine outcomes with TAVR versus surgical aortic valve replacement (SAVR) in patients with rheumatic AS, and versus TAVR in nonrheumatic AS.
The authors identified Medicare beneficiaries who underwent TAVR or SAVR from October 2015 to December 2017, and then identified patients with rheumatic AS using prior validated International Classification of Diseases, Version 10 codes. Overlap propensity score weighting analysis was used to adjust for measured confounders. The primary study outcome was all-cause mortality. Multiple secondary outcomes were also examined.
The final study cohort included 1,159 patients with rheumatic AS who underwent aortic valve replacement (SAVR, n = 554; TAVR, n = 605), and 88,554 patients with nonrheumatic AS who underwent TAVR. Patients in the SAVR group were younger and with lower prevalence of most comorbidities and frailty scores. After median follow-up of 19 months (interquartile range: 13 to 26 months), there was no difference in all-cause mortality with TAVR versus SAVR (11.2 vs. 7.0 per 100 person-year; adjusted hazard ratio: 1.53; 95% confidence interval: 0.84 to 2.79; p = 0.2). Compared with TAVR in nonrheumatic AS, TAVR for rheumatic AS was associated with similar mortality (15.2 vs. 17.7 deaths per 100 person-years (adjusted hazard ratio: 0.87; 95% confidence interval: 0.68 to 1.09; p = 0.2) after median follow-up of 17 months (interquartile range: 11 to 24 months). None of the rheumatic TAVR patients, <11 SAVR patients, and 242 nonrheumatic TAVR patients underwent repeat aortic valve replacement (124 redo-TAVR and 118 SAVR) at follow-up.
Compared with SAVR, TAVR could represent a viable and possibly durable option for patients with rheumatic AS.
患有风湿性主动脉瓣狭窄(AS)的患者被排除在经导管主动脉瓣置换术(TAVR)试验之外。
作者旨在研究 TAVR 与外科主动脉瓣置换术(SAVR)在风湿性 AS 患者中的疗效,并比较 TAVR 与非风湿性 AS 患者中的疗效。
作者从 2015 年 10 月至 2017 年 12 月期间确定了接受 TAVR 或 SAVR 的 Medicare 受益人的数据,并使用先前验证的国际疾病分类第 10 版(ICD-10)代码确定风湿性 AS 患者。采用重叠倾向评分加权分析来调整测量的混杂因素。主要研究结果是全因死亡率。还检查了多个次要结果。
最终的研究队列包括 1159 名接受主动脉瓣置换术(SAVR,n=554;TAVR,n=605)的风湿性 AS 患者,以及 88554 名接受 TAVR 的非风湿性 AS 患者。SAVR 组患者年龄较小,合并症和衰弱评分的发生率较低。中位随访 19 个月(四分位距:13 至 26 个月)后,TAVR 与 SAVR 的全因死亡率无差异(每 100 人年 11.2 与 7.0 例;校正后的危险比:1.53;95%置信区间:0.84 至 2.79;p=0.2)。与非风湿性 AS 患者的 TAVR 相比,风湿性 AS 患者的 TAVR 死亡率相似(每 100 人年 15.2 与 17.7 例(校正后的危险比:0.87;95%置信区间:0.68 至 1.09;p=0.2),中位随访 17 个月(四分位距:11 至 24 个月)。在随访期间,没有风湿性 TAVR 患者(<11 例 SAVR 患者)和 242 例非风湿性 TAVR 患者接受了再次主动脉瓣置换术(124 例再次 TAVR 和 118 例 SAVR)。
与 SAVR 相比,TAVR 可能是风湿性 AS 患者的一种可行且可能持久的选择。