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Three-year outcomes after transcatheter or surgical aortic valve replacement in low-risk patients with aortic stenosis

  • John K Forrest
  • , G Michael Deeb
  • , Steven J Yakubov
  • , Hemal Gada
  • , Mubashir A Mumtaz
  • , Basel Ramlawi
  • , Tanvir Bajwa
  • , Paul S Teirstein
  • , Michael DeFrain
  • , Murali Muppala
  • , Bruce J Rutkin
  • , Atul Chawla
  • , Bart Jenson
  • , Stanley J Chetcuti
  • , Robert C Stoler
  • , Marie-France Poulin
  • , Kamal Khabbaz
  • , Melissa Levack
  • , Kashish Goel
  • , Didier Tchétché
  • Ka Yan Lam, Pim A Tonino, Saki Ito, Jae K Oh, Jian Huang, Jeffrey J Popma, Neal Kleiman, Michael J Reardon
  • Yale University School of Medicine, New Haven, CT. Electronic address: [email protected].
  • University of Michigan Health Systems Ok - University Hospital, Ann Arbor, MI.
  • OhioHealth Riverside Methodist Hospital, Columbus, OH.
  • University of Pittsburgh Medical Center, Harrisburg, PA.
  • Lankenau Heart Institute, Philadelphia, PA.
  • Scripps Clinic, La Jolla, CA.
  • HealthPark Medical Center, Fort Myers, FL.
  • North Shore University Hospital, Manhasset, NY.
  • Mercy Medical Center, Iowa Heart, Des Moines, IA.
  • Baylor Heart and Vascular Hospital, Dallas, TX.
  • Beth Israel Deaconess Medical Center, Boston, MA.
  • Vanderbilt University Medical Center, Nashville, TN.
  • Clinique Pasteur, Toulouse, France.
  • Catharina Ziekenhuis, Eindhoven, Netherlands.
  • Echocardiography Core Laboratory, Mayo Clinic, Rochester, MN.
  • Medtronic, Mounds View, MN.
  • Methodist DeBakey Heart and Vascular Center, Houston, TX.

Research output: Contribution to journalArticlepeer-review

Abstract

Background: Randomized data comparing outcomes of transcatheter aortic valve replacement (TAVR) with surgery in low–surgical risk patients at time points beyond 2 years is limited. This presents an unknown for physicians striving to educate patients as part of a shared decision-making process. Objectives: The authors evaluated 3-year clinical and echocardiographic outcomes from the Evolut Low Risk trial. Methods: Low-risk patients were randomized to TAVR with a self-expanding, supra-annular valve or surgery. The primary endpoint of all-cause mortality or disabling stroke and several secondary endpoints were assessed at 3 years. Results: There were 1,414 attempted implantations (730 TAVR; 684 surgery). Patients had a mean age of 74 years and 35% were women. At 3 years, the primary endpoint occurred in 7.4% of TAVR patients and 10.4% of surgery patients (HR: 0.70; 95% CI: 0.49-1.00; P = 0.051). The difference between treatment arms for all-cause mortality or disabling stroke remained broadly consistent over time: −1.8% at year 1; −2.0% at year 2; and −2.9% at year 3. The incidence of mild paravalvular regurgitation (20.3% TAVR vs 2.5% surgery) and pacemaker placement (23.2% TAVR vs 9.1% surgery; P < 0.001) were lower in the surgery group. Rates of moderate or greater paravalvular regurgitation for both groups were <1% and not significantly different. Patients who underwent TAVR had significantly improved valve hemodynamics (mean gradient 9.1 mm Hg TAVR vs 12.1 mm Hg surgery; P < 0.001) at 3 years. Conclusions: Within the Evolut Low Risk study, TAVR at 3 years showed durable benefits compared with surgery with respect to all-cause mortality or disabling stroke.

Original languageAmerican English
JournalJournal of the American College of Cardiology
DOIs
StatusPublished - Mar 5 2023

Keywords

  • SAVR
  • TAVR
  • aortic stenosis
  • aortic valve replacement

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