Transcarotid Transcatheter Aortic Valve Replacement Feasibility and Safety

被引:123
作者
Mylotte, Darren [1 ]
Sudre, Arnaud [2 ]
Teiger, Emmanuel [3 ]
Obadia, Jean Francois [4 ]
Lee, Marcus [1 ]
Spence, Mark [5 ]
Khamis, Hazem [6 ]
Al Nooryani, Arif [7 ]
Delhaye, Cedric [2 ]
Amr, Gilles [2 ]
Koussa, Mohamad [2 ]
Debry, Nicolas [2 ]
Piazza, Nicolo [8 ]
Modine, Thomas [2 ]
机构
[1] Univ Hosp Galway, Galway, Ireland
[2] CHRU Lille, Hop Cardiol, Dept Cardiol, F-59037 Lille, France
[3] Hop Henri Mondor, Paris, France
[4] Univ Lyon 1, Dept Cardiac Surg, Louis Pradel Cardiol Hosp, Hosp Civils Lyon, F-69365 Lyon, France
[5] Queens Univ Belfast, Royal Victoria Hosp, Belfast Trust, Belfast, Antrim, North Ireland
[6] October 6 Univ, Dept Cardiol, Cairo, Egypt
[7] Al Qassimi Hosp, Dept Cardiol, Dubai, U Arab Emirates
[8] McGill Univ, Ctr Hlth, Dept Intervent Cardiol, Montreal, PQ, Canada
关键词
aortic stenosis; carotid vascular access; transcatheter aortic valve replacement; CAROTID-ARTERY; IMPLANTATION; ACCESS; STENOSIS; EXPERIENCE; OUTCOMES; SURGERY; STROKE; RISK; FLOW;
D O I
10.1016/j.jcin.2015.11.045
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
OBJECTIVES The purpose of this study was to assess the feasibility and safety of transcarotid transcatheter aortic valve replacement (TAVR). BACKGROUND Many candidates for TAVR have challenging vascular anatomy that precludes transfemoral access. Transcarotid arterial access may be an option for such patients. METHODS 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. RESULTS 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%. CONCLUSIONS 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. (C) 2016 by the American College of Cardiology Foundation.
引用
收藏
页码:472 / 480
页数:9
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