Mylotte Darren, Sudre Arnaud, Teiger Emmanuel, Obadia Jean François, Lee Marcus, Spence Mark, Khamis Hazem, Al Nooryani Arif, Delhaye Cedric, Amr Gilles, Koussa Mohamad, Debry Nicolas, Piazza Nicolo, Modine Thomas
University Hospital Galway, Galway, Ireland.
Department of Cardiology, Hôpital Cardiologique, CHRU de Lille, Lille, France.
JACC Cardiovasc Interv. 2016 Mar 14;9(5):472-80. doi: 10.1016/j.jcin.2015.11.045.
The purpose of this study was to assess the feasibility and safety of transcarotid transcatheter aortic valve replacement (TAVR).
Many candidates for TAVR have challenging vascular anatomy that precludes transfemoral access. Transcarotid arterial access may be an option for such patients.
The French Transcarotid TAVR Registry is a voluntary database that prospectively collected patient demographics, procedural characteristics, and clinical outcomes among patients undergoing transcarotid TAVR. Outcomes are reported according to the updated Valve Academic Research Consortium criteria.
Among 96 patients undergoing transcarotid TAVR at 3 French sites (2009 to 2013), the mean age and Society of Thoracic Surgeons predicted risk of mortality were 79.4 ± 9.2 years and 7.1 ± 4.1%, respectively. Successful carotid artery access was achieved in all patients. The Medtronic CoreValve (Medtronic, Inc., Minneapolis, Minnesota) (n = 89; 92.7%) and Edwards SAPIEN valves (Edwards Lifesciences, Irvine, California) (n = 7; 7.3%) were used. Procedural complications included: valve embolization (3.1%), requirement for a second valve (3.1%), and tamponade (4.2%). There were no major bleeds or major vascular complications related to the access site. There were 3 (3.1%) procedural deaths and 6 (6.3%) deaths at 30 days. The 1-year mortality rate was 16.7%. There were 3 (3.1%) cases of Valve Academic Research Consortium-defined in-hospital stroke (n = 0) or transient ischemic attack (TIA) (n = 3). None of these patients achieved the criteria for stroke and none manifested new ischemic lesions on cerebral computed tomography or magnetic resonance imaging. At 30 days, a further 3 TIAs were observed, giving an overall stroke/TIA rate of 6.3%.
Transcarotid vascular access for TAVR is feasible and is associated with encouraging short- and medium-term clinical outcomes. Prospective studies are required to ascertain if transcarotid TAVR yields equivalent results to other nonfemoral vascular access routes.
本研究旨在评估经颈动脉经导管主动脉瓣置换术(TAVR)的可行性和安全性。
许多TAVR候选患者的血管解剖结构复杂,无法进行经股动脉入路。经颈动脉入路可能是这类患者的一种选择。
法国经颈动脉TAVR注册研究是一个自愿性数据库,前瞻性收集了接受经颈动脉TAVR患者的人口统计学资料、手术特征和临床结局。结局根据更新后的瓣膜学术研究联盟标准进行报告。
在法国3个中心(2009年至2013年)接受经颈动脉TAVR的96例患者中,平均年龄和胸外科医师协会预测的死亡风险分别为79.4±9.2岁和7.1±4.1%。所有患者均成功实现颈动脉入路。使用了美敦力CoreValve瓣膜(美敦力公司,明尼阿波利斯,明尼苏达州)(n = 89;92.7%)和爱德华SAPIEN瓣膜(爱德华生命科学公司,尔湾,加利福尼亚州)(n = 7;7.3%)。手术并发症包括:瓣膜栓塞(3.1%)、需要植入第二个瓣膜(3.1%)和心包填塞(4.2%)。未发生与入路部位相关的严重出血或严重血管并发症。有3例(3.1%)手术死亡,30天时有6例(6.3%)死亡。1年死亡率为16.7%。有3例(3.1%)符合瓣膜学术研究联盟定义的院内卒中(n = 0)或短暂性脑缺血发作(TIA)(n = 3)。这些患者均未达到卒中标准,且在脑部计算机断层扫描或磁共振成像上均未显示新的缺血性病变。在30天时,又观察到3例TIA,使总体卒中/TIA发生率为6.3%。
经颈动脉血管入路进行TAVR是可行的,且与令人鼓舞的短期和中期临床结局相关。需要进行前瞻性研究以确定经颈动脉TAVR是否能产生与其他非股动脉血管入路相同的结果。