Five-Year Clinical and Echocardiographic Outcomes from the NOTION Randomized Clinical Trial in Patients at Lower Surgical Risk

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

  • Hans Gustav Hørsted Thyregod
  • Nikolaj Ihlemann
  • Troels Højsgaard Jørgensen
  • Henrik Nissen
  • Bo Juel Kjeldsen
  • Petur Petursson
  • Yanping Chang
  • Olaf Walter Franzen
  • Engstrøm, Thomas
  • Peter Clemmensen
  • Peter Bo Hansen
  • Lars Willy Andersen
  • Daniel Andreas Steinbruüchel
  • Peter Skov Olsen
  • Søndergaard, Lars

Background: The NOTION trial (Nordic Aortic Valve Intervention) was designed to compare transcatheter aortic valve replacement (TAVR) with surgical aortic valve replacement (SAVR) in patients ≥70 years old with isolated severe aortic valve stenosis. Clinical and echocardiographic outcomes are presented after 5 years. Methods: Patients were enrolled at 3 Nordic centers and randomized 1:1 to TAVR using the self-expanding CoreValve prosthesis (n=145) or SAVR using any stented bioprostheses (n=135). The primary composite outcome was the rate of all-cause mortality, stroke, or myocardial infarction at 1 year defined according to Valve Academic Research Consortium-2 criteria. Results: Baseline characteristics were similar. The mean age was 79.1±4.8 years and mean Society of Thoracic Surgeons Predicted Risk of Mortality score was 3.0%±1.7%. After 5 years, there were no differences between TAVR and SAVR in the composite outcome (Kaplan-Meier estimates 38.0% versus 36.3%, log-rank test P=0.86) or any of its components. TAVR patients had larger prosthetic valve area (1.7 cm2 versus 1.2 cm2, P<0.001) with a lower mean transprosthetic gradient (8.2 mm Hg versus 13.7 mm Hg, P<0.001), both unchanged over time. More TAVR patients had moderate/severe total aortic regurgitation (8.2% versus 0.0%, P<0.001) and a new pacemaker (43.7% versus 8.7%, P<0.001). Four patients had prosthetic reintervention and no difference was found for functional outcomes. Conclusions: These are currently the longest follow-up data comparing TAVR and SAVR in lower risk patients, demonstrating no statistical difference for major clinical outcomes 5 years after TAVR with a self-expanding prosthesis compared to SAVR. Higher rates of prosthetic regurgitation and pacemaker implantation were seen after TAVR. Clinical Trial Registration: URL: Https://clinicaltrials.gov. Unique identifier: NCT01057173.

OriginalsprogEngelsk
TidsskriftCirculation
Vol/bind139
Udgave nummer24
Sider (fra-til)2714-2723
Antal sider10
ISSN0009-7322
DOI
StatusUdgivet - 2019

ID: 236662523