Department of Cardiac Surgery and Cardiology, Quebec Heart and Lung Institute, Laval University, Canada (C.C., J.R.-C., E.D., D.D., R.D., J.-M.P., R.P., F.M., T.R.-G., D.K., S.M.).
Department of Cardiac Surgery and Cardiology, Hôpital Européen Georges Pompidou, Assistance Publique Hôpitaux de Paris, Université Paris Descartes, France (R.A.-A., D.B., C.S., J.-Y.P., A.L., N.K.).
Circ Cardiovasc Interv. 2018 Nov;11(11):e006388. doi: 10.1161/CIRCINTERVENTIONS.118.006388.
Background The optimal access for patients undergoing transcatheter aortic valve replacement (TAVR) who are not candidates for a transfemoral approach has not been elucidated. The purpose of this study was to compare the safety, feasibility, and early clinical outcomes of transcarotid TAVR compared with thoracic approaches. Methods and Results From a multicenter consecutive cohort of 329 alternative-access TAVR patients (2012-2017), we identified 101 patients who underwent transcarotid TAVR and 228 patients who underwent a transapical or transaortic TAVR. Preprocedural success and 30-day clinical outcomes were compared using multivariable propensity score analysis to account for between-group differences in baseline characteristics. All transcarotid cases were performed under general anesthesia, mainly using the left common carotid artery (97%). Propensity-matched groups had similar rates of 30-day all-cause mortality (2.1% versus 4.6%; P=0.37), stroke (2.1% versus 3.5%; P=0.67; transcarotid versus transapical/transaortic, respectively), new pacemaker implantation, and major vascular complications. Transcarotid TAVR was associated with significantly less new-onset atrial fibrillation (3.2% versus 19.0%; P=0.002), major or life-threatening bleeding (4.3% versus 19.9%; P=0.002), acute kidney injury (none versus 12.1%; P=0.002), and shorter median length of hospital stay (6 versus 8 days; P<0.001). Conclusions Transcarotid vascular access for TAVR is safe and feasible and is associated with encouraging short-term clinical outcomes. Our data suggest a clinical benefit of transcarotid TAVR with respect to atrial fibrillation, major bleeding, acute kidney injury, and length of stay compared with the more invasive transapical or transaortic strategies. Randomized studies are required to ascertain whether transcarotid TAVR yields equivalent results to other alternative vascular access routes.
对于不适合经股动脉入路的行经导管主动脉瓣置换术(TAVR)患者,最佳入路尚未阐明。本研究旨在比较经颈动脉 TAVR 与经胸入路的安全性、可行性和早期临床结果。
在一项多中心连续队列的 329 例经选择的 TAVR 患者(2012-2017 年)中,我们确定了 101 例行经颈动脉 TAVR 及 228 例行经心尖或经主动脉 TAVR 的患者。采用多变量倾向评分分析比较术前成功率和 30 天临床结果,以说明两组间基线特征的差异。所有经颈动脉病例均在全身麻醉下进行,主要使用左颈总动脉(97%)。倾向性匹配组的 30 天全因死亡率(2.1%对 4.6%;P=0.37)、卒中(2.1%对 3.5%;P=0.67;分别为经颈动脉与经心尖/经主动脉)、新植入起搏器和主要血管并发症发生率相似。经颈动脉 TAVR 与新发心房颤动(3.2%对 19.0%;P=0.002)、主要或危及生命的出血(4.3%对 19.9%;P=0.002)、急性肾损伤(无对 12.1%;P=0.002)和较短的中位住院时间(6 天对 8 天;P<0.001)显著相关。
经颈动脉 TAVR 血管入路安全可行,并与令人鼓舞的短期临床结果相关。与更具侵袭性的经心尖或经主动脉策略相比,我们的数据表明经颈动脉 TAVR 在心房颤动、大出血、急性肾损伤和住院时间方面具有临床获益。需要随机研究来确定经颈动脉 TAVR 是否与其他替代血管入路具有等效的结果。