Apixaban or Warfarin in Patients with an On-X Mechanical Aortic Valve.

Richard C Becker, John H Alexander, Hector I Michelena, Ashraf A Sabe, Ibrahim Sultan, Allen Graeve, J Alan Wolfe, Alberto Pochettino, John A Elefteriades, David G Cable, Hussein R Al-Khalidi, John Puskas, Vinod Thourani, Tracy Y Wang, Eugene H Blackstone, Marc Ruel, Alma Chavez, Renato D Lopes, Doug Johnston, Michael Moront, Vijay U Rao, Marc Gerdisch, Andrew Vekstein, Jun Wen, Lars G Svensson

Journal: NEJM evidence 2024;2(7):EVIDoa2300067

PMID: 38320162

Abstract

BACKGROUND: Vitamin K antagonists are the only oral anticoagulants approved to prevent valve thrombosis and valve-related thromboembolism in patients with mechanical heart valves. Whether patients with an On-X mechanical aortic valve can be safely anticoagulated with apixaban is unknown. METHODS: Patients with an On-X aortic valve implanted at least 3 months before enrollment were randomly assigned to receive apixaban 5 mg twice daily or warfarin (target international normalized ratio 2.0 to 3.0). The primary efficacy end point was the composite of valve thrombosis or valve-related thromboembolism with coprimary analyses comparing apixaban with warfarin for noninferiority and comparing the apixaban event rate with an objective performance criterion (OPC). RESULTS: The trial was stopped after 863 participants were enrolled owing to an excess of thromboembolic events in the apixaban group. Most (94%) participants took aspirin. A total of 26 primary end-point events occurred, 20 (in 16 participants) in the apixaban group (4.2%/patient-year; 95% confidence interval [CI], 2.3 to 6.0) and 6 (in 6 participants) in the warfarin group (1.3%/patient-year; 95% CI, 0.3 to 2.3). The difference in primary end-point rates between the apixaban and warfarin groups was 2.9 (95% CI, 0.8 to 5.0); noninferiority and OPC success criteria were not met. Major bleeding rates were 3.6%/patient-year with apixaban and 4.5%/patient-year with warfarin. CONCLUSIONS: Apixaban did not demonstrate noninferiority to warfarin and is less effective than warfarin for the prevention of valve thrombosis or thromboembolism in patients with an On-X mechanical aortic valve. (Funded by Artivion; ClinicalTrials.gov number, NCT04142658.)

Address: Duke Clinical Research Institute, Duke University School of Medicine, Durham, NC.; Cleveland Clinic, Cleveland.; Franciscian Health, Indianapolis.; ProMedica Toledo Hospital, Toledo, OH.; University of Ottawa Heart Institute, Ottawa, ON.; University of Cincinnati College of Medicine, Cincinnati.; Piedmont Heart Institute, Atlanta.; Mount Sinai Morningside Hospital, New York.; OSF HealthCare Cardiovascular Institute, Rockford, IL.; Yale University School of Medicine, New Haven, CT.; Mayo Clinic, Rochester, MN.; Northeast Georgia Medical Center, Gainesville, GA.; MultiCare Institute for Research and Innovation, Tacoma, WA.; University of Pittsburgh Medical Center, Pittsburgh.; Brigham and Women's Hospital, Harvard Medical School, Boston.
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