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Prospective US investigational device exemption trial of a sutureless aortic bioprosthesis: One-year outcomes.
Suri, Rakesh M; Javadikasgari, Hoda; Heimansohn, David A; Weissman, Neil J; Ailawadi, Gorav; Ad, Niv; Aldea, Gabriel S; Thourani, Vinod H; Szeto, Wilson Y; Michler, Robert E; Michelena, Hector I; Dabir, Reza; Fontana, Gregory P; Kessler, William F; Moront, Michael G; Brunsting, Louis A; Griffith, Bartley P; Montoya, Alvaro; Subramanian, Sreekumar; Mostovych, Mark A; Roselli, Eric E.
Afiliação
  • Suri RM; Department of Thoracic and Cardiovascular Surgery, Heart and Vascular Institute, Cleveland Clinic Abu Dhabi and Cleveland Clinic Foundation, Cleveland, Ohio. Electronic address: surir@ccf.org.
  • Javadikasgari H; Department of Thoracic and Cardiovascular Surgery, Heart and Vascular Institute, Cleveland Clinic Abu Dhabi and Cleveland Clinic Foundation, Cleveland, Ohio.
  • Heimansohn DA; Department of Cardiothoracic Surgery, St Vincent Heart Center of Indiana, Indianapolis, Ind.
  • Weissman NJ; Cardiovascular Core Laboratories, MedStar Health Research Institute, Washington, DC.
  • Ailawadi G; Section of Adult Cardiac Surgery, Advanced Cardiac Valve Center, University of Virginia, Charlottesville, Va.
  • Ad N; Cardiac Surgery, The Inova Heart and Vascular Institute, West Virginia University Medical Center, Morgantown, WVa.
  • Aldea GS; Division of Cardiothoracic Surgery, University of Washington Medical Center, Seattle, Wash.
  • Thourani VH; Cardiothoracic Surgery, Emory Midtown Hospital, Atlanta, Ga.
  • Szeto WY; Division of Cardiovascular Surgery, Department of Surgery, University of Pennsylvania Medical Center, Philadelphia, Pa.
  • Michler RE; Cardiothoracic Surgery and Surgery, Montefiore-Einstein Heart Center, New York, NY.
  • Michelena HI; Department of Cardiovascular Medicine, Mayo Clinic, Rochester, Minn.
  • Dabir R; Cardiovascular and Thoracic Surgery, Beaumont Hospital, Dearborn, Mich.
  • Fontana GP; Cardiothoracic Surgery, Cardiovascular Institute, Los Robles Hospital and Medical Center, Thousand Oaks CA Hospital Corporation of America, Nashville, Tenn.
  • Kessler WF; Cardiothoracic and Vascular Surgeons, Heart Hospital, Austin, Tex.
  • Moront MG; Cardiothoracic Surgery, The Toledo Hospital, Toledo, Ohio.
  • Brunsting LA; Heart and Lung Surgeons of East Alabama, East Alabama Medical Center (EAMC), Opelika, Ala.
  • Griffith BP; Division of Cardiac Surgery, University of Maryland, Baltimore, Md.
  • Montoya A; Cardiothoracic Surgery, Baptist Health, South Florida, Fla.
  • Subramanian S; Department of Cardiac Surgery, TriStar Centennial Medical Center, Nashville, Tenn.
  • Mostovych MA; Cardiac and Vascular Surgery, St Vincent's Medical Center, Jacksonville, Fla.
  • Roselli EE; Department of Thoracic and Cardiovascular Surgery, Heart and Vascular Institute, Cleveland Clinic Abu Dhabi and Cleveland Clinic Foundation, Cleveland, Ohio.
J Thorac Cardiovasc Surg ; 157(5): 1773-1782.e3, 2019 05.
Article em En | MEDLINE | ID: mdl-30553598
ABSTRACT

OBJECTIVES:

We performed a prospective, single-arm clinical trial approved under a Food and Drug Administration Investigational Device Exemption to assess safety and efficacy of Perceval, a sutureless bovine pericardial aortic valve representing the initial US experience.

METHODS:

From June 2013 to January 2015, 300 patients (mean age 76.7 ± 7.7 years, 54.3% men, 37.3% ≥80 years, median Society of Thoracic Surgeons Predicted Risk of Mortality 2.8%), underwent Perceval valve implantation at 18 centers across the United States. Twenty patients (6.7%) had a bicuspid aortic valve and 5 (1.7%) patients had previous aortic valve replacement. A minimally invasive approach was used in 80 (26.7%) and concomitant procedures were performed in 113 (37.8%) patients.

RESULTS:

Two hundred eighty-nine patients (96.3%) were successfully implanted. Operative mortality (≤30 days) was 1.3% (n = 4) (observed to expected ratio of 0.40). One-year results included all-cause mortality in 5.2% (n = 15), stroke in 1% (n = 3), and endocarditis in 1.7% (n = 5). New permanent periprocedural pacemaker rate was 10.7% (n = 30/281); 2.5% (n = 7/281) resulted from third-degree atrioventricular block. One-year valve-related reoperation was 2.1% (n = 6). At 1-year follow-up, 98% of patients were in New York Heart Association class I/II, left ventricular mass index decreased from 103.5 ± 30.1 g/m2 at discharge to 95.8 ± 27.1 g/m2 (P = .001), and 3 (1.3%) moderate paravalvular leaks were identified. Health-related quality of life score increased from 62.7 ± 21.8 before surgery to 85.5 ± 17.8 at 1 year (P < .001).

CONCLUSIONS:

These results confirm the safety and effectiveness of the Perceval sutureless aortic valve replacement in study patients with lower mortality than expected from a risk prediction model. Persistent hemodynamic benefit and improvement in quality of life at 1 year support the importance of this device in the management of aortic valve disease.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Valva Aórtica / Bioprótese / Próteses Valvulares Cardíacas / Implante de Prótese de Valva Cardíaca / Procedimentos Cirúrgicos sem Sutura / Doenças das Valvas Cardíacas Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Valva Aórtica / Bioprótese / Próteses Valvulares Cardíacas / Implante de Prótese de Valva Cardíaca / Procedimentos Cirúrgicos sem Sutura / Doenças das Valvas Cardíacas Idioma: En Ano de publicação: 2019 Tipo de documento: Article