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Prospective US investigational device exemption trial of a sutureless aortic bioprosthesis: One-year outcomes

  • Rakesh M. Suri
  • , Hoda Javadikasgari
  • , David A. Heimansohn
  • , Neil J. Weissman
  • , Gorav Ailawadi
  • , Niv Ad
  • , Gabriel S. Aldea
  • , Vinod H. Thourani
  • , Wilson Y. Szeto
  • , Robert E. Michler
  • , Hector I. Michelena
  • , Reza Dabir
  • , Gregory P. Fontana
  • , William F. Kessler
  • , Michael G. Moront
  • , Louis A. Brunsting
  • , Bartley P. Griffith
  • , Alvaro Montoya
  • , Sreekumar Subramanian
  • , Mark A. Mostovych
  • Eric E. Roselli

Research output: Contribution to journalArticlepeer-review

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.

Original languageEnglish (US)
Pages (from-to)1773-1782.e3
JournalJournal of Thoracic and Cardiovascular Surgery
Volume157
Issue number5
DOIs
StatePublished - May 2019

Keywords

  • aortic stenosis
  • aortic valve replacement
  • concomitant procedures
  • hemodynamics
  • minimally invasive surgery
  • quality of life
  • sutureless valve

ASJC Scopus subject areas

  • Surgery
  • Pulmonary and Respiratory Medicine
  • Cardiology and Cardiovascular Medicine

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