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Five-year Outcomes of the COMMENCE Trial Investigating Aortic Valve Replacement With RESILIA Tissue.
Bavaria, Joseph E; Griffith, Bartley; Heimansohn, David A; Rozanski, Jacek; Johnston, Douglas R; Bartus, Krzysztof; Girardi, Leonard N; Beaver, Thomas; Takayama, Hiroo; Mumtaz, Mubashir A; Rosengart, Todd K; Starnes, Vaughn; Timek, Tomasz A; Boateng, Percy; Ryan, William; Cornwell, Lorraine D; Blackstone, Eugene H; Borger, Michael A; Pibarot, Philippe; Thourani, Vinod H; Svensson, Lars G; Puskas, John D.
Afiliación
  • Bavaria JE; Department of Cardiovascular Surgery, Hospital of the University of Pennsylvania, Philadelphia, Pennsylvania. Electronic address: joseph.bavaria@pennmedicine.upenn.edu.
  • Griffith B; Department of Surgery, University of Maryland Medical Center, Baltimore, Maryland.
  • Heimansohn DA; Department of Cardiothoracic Surgery, St Vincent Heart Center, Indianapolis, Indiana.
  • Rozanski J; National Institute of Cardiology, Warsaw, Poland.
  • Johnston DR; Aortic Valve Center, Cleveland Clinic, Cleveland, Ohio.
  • Bartus K; Jagiellonian University, John Paul II Hospital, Krakow, Poland.
  • Girardi LN; Department of Cardiothoracic Surgery, Weill Cornell Medicine, New York, New York.
  • Beaver T; Department of Surgery, University of Florida, Gainesville, Florida.
  • Takayama H; Division of Cardiothoracic and Vascular Surgery, Department of Surgery, New York Presbyterian/Columbia University Medical Center, New York, New York.
  • Mumtaz MA; Department of Cardiovascular and Thoracic Surgery, UPMC Pinnacle, Harrisburg, Pennsylvania.
  • Rosengart TK; Michael E DeBakey Department of Surgery, Baylor College of Medicine, Houston, Texas.
  • Starnes V; Department of Surgery, University of Southern California, Los Angeles, California.
  • Timek TA; Division of Cardiothoracic Surgery, Spectrum Health Medical Group, Grand Rapids, Missouri.
  • Boateng P; Department of Cardiovascular Surgery, Mount Sinai Medical Center, New York, New York.
  • Ryan W; Department of Cardiovascular Surgery, Heart Hospital Baylor, Plano, Texas.
  • Cornwell LD; Department of Cardiovascular Surgery, Michael E DeBakey VA Medical Center, Houston, Texas.
  • Blackstone EH; Department of Thoracic and Cardiovascular Surgery, Cleveland Clinic, Cleveland, Ohio.
  • Borger MA; University Department of Cardiac Surgery, Heart Center Leipzig, Leipzig, Germany.
  • Pibarot P; Department of Cardiology, Québec Heart & Lung Institute, Laval University, Quebec, Quebec, Canada.
  • Thourani VH; Piedmont Heart Institute, Atlanta, Georgia.
  • Svensson LG; Department of Thoracic and Cardiovascular Surgery, Cleveland Clinic, Cleveland, Ohio.
  • Puskas JD; Department of Cardiovascular Surgery, Mount Sinai Saint Luke's, New York, New York.
Ann Thorac Surg ; 115(6): 1429-1436, 2023 06.
Article en En | MEDLINE | ID: mdl-35065065
BACKGROUND: The COMMENCE trial was conducted to evaluate the safety and effectiveness of aortic valve replacement using a bioprosthesis with novel RESILIA tissue (Edwards Lifesciences). RESILIA tissue is incorporated in the INSPIRIS RESILIA aortic valve (Edwards Lifesciences). METHODS: Patients underwent clinically indicated surgical aortic valve replacement with a bovine pericardial bioprosthesis (model 11000A; Edwards Lifesciences) in a prospective, multinational, multicenter (n = 27), US Food and Drug Administration Investigational Device Exemption trial. Events were adjudicated by an independent clinical events committee, and echocardiograms were analyzed by an independent core laboratory. Outcomes through an observational period of 5 years are reported. RESULTS: Between January 2013 and March 2016, 689 patients received the study valve. Mean patient age was 66.9 ± 11.6 years; Society of Thoracic Surgeons Predicted Risk of Mortality was 2.0% ± 1.8%; and 23.8%, 49.9%, and 24.4% of patients were New York Heart Association functional class I, II, and III at baseline, respectively. Through December 11, 2020 the follow-up duration was 4.3 ± 1.4 years, and the completeness of follow-up over the observational period was 95.5%. Early (<30 days) all-cause mortality was 1.2%, stroke 1.6%, and major paravalvular leak 0.1%. Five-year actuarial freedom from all-cause mortality, structural valve deterioration, and all-cause reintervention were 89.2%, 100%, and 98.7%, respectively. At 5 years the effective orifice area was 1.6 ± 0.5 cm2, mean gradient was 11.5 ± 6.0 mm Hg, 97.8% of patients were class I/II, and 97.8% and 96.3% of patients had none/trace paravalvular and transvalvular regurgitation, respectively. CONCLUSIONS: The safety and hemodynamic performance of this aortic bioprosthesis with RESILIA tissue through 5 years are encouraging, with clinically stable hemodynamics, minimal regurgitation, and no evidence of structural valve deterioration.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Estenosis de la Válvula Aórtica / Implantación de Prótesis de Válvulas Cardíacas Tipo de estudio: Clinical_trials / Prognostic_studies Límite: Aged / Animals / Humans / Middle aged Idioma: En Revista: Ann Thorac Surg Año: 2023 Tipo del documento: Article Pais de publicación: Países Bajos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Estenosis de la Válvula Aórtica / Implantación de Prótesis de Válvulas Cardíacas Tipo de estudio: Clinical_trials / Prognostic_studies Límite: Aged / Animals / Humans / Middle aged Idioma: En Revista: Ann Thorac Surg Año: 2023 Tipo del documento: Article Pais de publicación: Países Bajos