Prospective Multicenter Evaluation of the Direct Flow Medical Transcatheter Aortic Valve System 12-Month Outcomes of the Evaluation of the Direct Flow Medical Percutaneous Aortic Valve 18F System for the Treatment of Patients With Severe Aortic Stenosis (DISCOVER) Study

被引:29
作者
Lefevre, Thierry [1 ,13 ]
Colombo, Antonio [2 ]
Tchetche, Didier [3 ]
Latib, Azeem [2 ]
Klugmann, Silvio [4 ]
Fajadet, Jean [3 ]
De Marco, Federico [4 ]
Maisano, Francesco [2 ]
Bruschi, Giuseppe [4 ]
Bijuklic, Klaudija [5 ]
Nava, Stefano [4 ]
Weissman, Neil [6 ]
Low, Reginald [7 ]
Thomas, Martyn [8 ]
Young, Christopher [8 ]
Redwood, Simon [8 ]
Mullen, Michael [9 ]
Yap, John [9 ]
Grube, Eberhard [10 ]
Nickenig, Georg [10 ]
Sinning, Jan-Malte [10 ]
Hauptmann, Karl Eugen [11 ]
Friedrich, Ivar [11 ]
Lauterbach, Michael [11 ]
Schmoeckel, Michael [12 ]
Davidson, Charles [13 ]
Schofer, Joachim [5 ]
机构
[1] Inst Cardiovasc Paris Sud, Hop Prive Jacques Cartier, F-91300 Massy, France
[2] Hosp San Raffaele, I-20132 Milan, Italy
[3] Clin Pasteur, Toulouse, France
[4] Azienda Osped Niguarda Ca Granda, Milan, Italy
[5] Univ Hamburg, Cardiovasc Ctr, Med Care Ctr, Hamburg, Germany
[6] Georgetown Univ, MedStar Hlth Res Inst, Washington, DC USA
[7] Univ Calif Davis, Davis, CA 95616 USA
[8] St Thomas Hosp, London, England
[9] Heart Hosp, London, England
[10] Univ Hosp Bonn, Bonn, Germany
[11] Krankenhaus Barmherzigen, Trier, Germany
[12] Asklepios Klin St Georg, Hamburg, Germany
[13] NW Mem Hosp, Chicago, IL 60611 USA
关键词
aortic stenosids; transcatheter aortic valve replacement; transfemoral transcatheter aortic valve replacement; HIGH-RISK PATIENTS; IMPLANTATION; REPLACEMENT; DEFINITIONS; PROSTHESIS; SURGERY;
D O I
10.1016/j.jcin.2015.09.027
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
OBJECTIVES The aim of this study was to assess the 1-year outcome after transcatheter aortic valve replacement (TAVR) of the Direct Flow Medical (DFM) valve in patients with severe symptomatic aortic stenosis who were contraindicated or high risk for surgery. BACKGROUND The DFM transcatheter heart valve is a new-generation, nonmetallic aortic valve with a pressurized support structure and conformable double-ring annular sealing delivered through an 18-F sheath. The device allows repositioning, retrieval, and assessment of valve performance before permanent implantation. METHODS A prospective multicenter European registry was set up to determine the safety and performance of the valve in 100 consecutive patients (10 centers). Echocardiographic and angiographic data were evaluated by an independent core laboratory, and adverse events were adjudicated by a clinical events committee using Valve Academic Research Consortium criteria. RESULTS Patients were 83.1 +/- 5.9 years of age and had a logistic EuroSCORE of 22.5 +/- 11.3% and a Society of Thoracic Surgeons score of 9.7 +/- 8.7%. Correct valve positioning was obtained in 99% of cases with a combined 30-day safety endpoint at 10%, including major stroke in 5.0%, major vascular complications in 2.0%, and death in 1%. At 12 months, 95% of patients were in New York Heart Association functional class I or II. Freedom from any death was 90%, and freedom from any death or major stroke was 85%. Echocardiography demonstrated none/trace to mild aortic regurgitation in 100% of patients and an unchanged mean aortic gradient of 12.2 +/- 6.6 mm Hg and effective orifice area of 1.6 +/- 0.4 cm(2). CONCLUSIONS At 1 year, the DFM transcatheter heart valve had durable hemodynamics. This study demonstrates that the low rate of early complications and the low risk of significant aortic regurgitation translated into m idterm clinical benefit. (J Am Coll Cardiol Intv 2016;9:68-75) (C) 2016 by the American College of Cardiology Foundation.
引用
收藏
页码:68 / 75
页数:8
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