Rocky Mountain Regional VA Medical Center, Aurora, CO (N.M.B.).
University of Colorado School of Medicine, Aurora (N.M.B., J.C.M.).
Circ Cardiovasc Interv. 2024 Sep;17(9):e013697. doi: 10.1161/CIRCINTERVENTIONS.123.013697. Epub 2024 Jun 5.
Cerebral embolic protection devices (EPDs) were developed to mitigate the risk of stroke during transcatheter aortic valve replacement (TAVR), but their benefit remains unproven. In the PROTECTED-TAVR trial (Stroke Protection With Sentinel During Transcatheter), EPD use did not reduce periprocedural stroke (primary study outcome) but led to a 62% reduction in the secondary end point of disabling stroke. Given these results, the impact of EPDs during TAVR remains unclear.
We used STS/ACC TVT registry data to examine the association between EPD use and a proxy for disabling stroke among transfemoral TAVR patients between January 2018 and June 2023. The primary outcome was in-hospital disabling stroke-defined as stroke associated with either in-hospital death or discharge to a nonhome location. We evaluated the association between EPD use and disabling stroke using instrumental variable analysis with a site-level preference for EPD use as the instrument-a quasi-experimental approach that can support causal inference. In addition, we performed a propensity score-based comparison using overlap weighting as a secondary analysis.
The study population consisted of 414 649 patients of whom 53 389 (12.9%) received an EPD. The unadjusted rate of in-hospital disabling stroke was 0.7% among the EPD group and 0.9% in the no-EPD group. EPD use was associated with a reduction in disabling stroke in both instrumental variable analysis (relative risk, 0.87 [95% CI, 0.73-1.00]) and propensity-weighted analysis (odds ratio, 0.79 [95% CI, 0.70-0.90]) but was not associated with a reduction in nondisabling stroke. In subgroup analyses, the benefit of EPD was greater among those with versus without prior stroke (<0.05 for both instrumental variable and propensity-weighted analyses).
In the largest study to date, among patients undergoing TAVR, EPD use was associated with a small, borderline significant reduction in stroke associated with death or discharge to a nonhome location (a proxy for disabling stroke) that is likely to be causal in nature. Taken together with previous mechanistic and clinical studies, these findings provide credible evidence that EPDs benefit patients undergoing TAVR.
脑栓子保护装置 (EPD) 的开发是为了降低经导管主动脉瓣置换术 (TAVR) 期间中风的风险,但它们的益处仍未得到证实。在 PROTECTED-TAVR 试验(经导管期间 Sentinel 用于中风保护)中,EPD 的使用并未降低围手术期中风(主要研究终点),但导致致残性中风的次要终点降低了 62%。鉴于这些结果,EPD 在 TAVR 中的作用仍不清楚。
我们使用 STS/ACC TVT 登记数据,检查 2018 年 1 月至 2023 年 6 月期间经股动脉 TAVR 患者中 EPD 使用与致残性中风替代指标之间的关联。主要结局是住院期间致残性中风——定义为与住院期间死亡或出院至非家庭地点相关的中风。我们使用基于仪器变量分析的方法评估 EPD 使用与致残性中风之间的关联,该方法使用 EPD 使用的站点级别偏好作为工具——一种支持因果推理的准实验方法。此外,我们使用重叠加权作为二次分析进行倾向评分匹配比较。
研究人群包括 414649 名患者,其中 53389 名(12.9%)接受了 EPD。EPD 组住院期间致残性中风的未调整发生率为 0.7%,无 EPD 组为 0.9%。在仪器变量分析(相对风险,0.87[95%CI,0.73-1.00])和倾向评分加权分析(优势比,0.79[95%CI,0.70-0.90])中,EPD 使用与降低致残性中风相关,但与降低非致残性中风无关。在亚组分析中,与无先前中风的患者相比,EPD 的益处更大(仪器变量和倾向评分加权分析均<0.05)。
在迄今为止最大的研究中,在接受 TAVR 的患者中,EPD 使用与与死亡或出院至非家庭地点相关的中风(致残性中风的替代指标)的小、边缘显著降低相关,这很可能具有因果关系。与之前的机制和临床研究相结合,这些发现提供了可信的证据,证明 EPD 使接受 TAVR 的患者受益。