Magnetic Resonance Perfusion or Fractional Flow Reserve in Coronary Disease

Eike Nagel1, John P Greenwood1, Gerry P McCann1

  • 1From the Institute for Experimental and Translational Cardiovascular Imaging, DZHK (German Center for Cardiovascular Research) Center for Cardiovascular Imaging, Goethe University, and the Department of Cardiology, University Hospital Frankfurt, Frankfurt am Main (E.N., V.O.P.), Pharmtrace (W.-S.R.), Schwenke Consulting (C.S.), and Charité-Universitätsmedizin Berlin, Freie Universität Berlin, Humboldt Universität zu Berlin, Berlin Institute of Health, DZHK, and Helios Kliniken Berlin-Buch (J.S.-M.), Berlin, and the Clinic for Cardiology, Angiology, and Pulmonology, University Hospital Heidelberg, Heidelberg (H.S.) - all in Germany; the Division of Biomedical Engineering and Imaging Sciences (E.N., S.T.H., S.P., M.P.) and British Heart Foundation Centre (A.M.S., D.P., M.M.), King's College London, Barts Heart Centre, St. Bartholomew's Hospital (M.A.W.), the Hatter Cardiovascular Institute, Institute of Cardiovascular Science, University College London (D.J.H.), and the National Institute for Health Research (NIHR) University College London Hospitals Biomedical Research Centre (D.J.H.), London, Leeds Institute of Cardiovascular and Metabolic Medicine, University of Leeds, Leeds (J.P.G., S.P.), the Department of Cardiovascular Sciences, University of Leicester and the NIHR Leicester Biomedical Research Centre, Glenfield Hospital (G.P.M.), and the Department of Cardiology, Glenfield Hospital (S.T.H.), Leicester, Bristol Heart Institute, University of Bristol and Bristol NIHR Biomedical Research Centre, Bristol (C.B.-D.), the Faculty of Health and Life Sciences, Northumbria University, and Freeman Hospital, Newcastle-upon-Tyne (R.D.), the Department of Cardiology, Royal Brompton and Harefield NHS Foundation Trust, Harefield Hospital, Uxbridge (J.W.), and the British Heart Foundation Glasgow Cardiovascular Research Centre, University of Glasgow, Glasgow (C.B.) - all in the United Kingdom; Cardiovascular Research and Development Unit, Faculty of Medicine, University of Porto, Porto, Portugal (N.B.); Kardiologie, Herzzentrum Luzern, Luzerner Kantonsspital, Lucerne, Switzerland (M.P.); and the Cardiovascular and Metabolic Disorders Program, Duke-National University of Singapore Medical School, and the National Heart Research Institute Singapore, National Heart Center, Yong Loo Lin School of Medicine, National University of Singapore, Singapore (D.J.H.).

Insights

Myocardial-perfusion cardiovascular MRI is a noninferior strategy to fractional flow reserve (FFR) for managing stable angina. This approach reduces revascularization rates without increasing major adverse cardiac events, offering a valuable alternative for patient care.

Area of Science:

  • Cardiology
  • Medical Imaging
  • Interventional Cardiology

Background:

  • Stable angina management often involves guiding revascularization using either myocardial-perfusion cardiovascular magnetic resonance imaging (MRI) or invasive angiography with fractional flow reserve (FFR) measurement.
  • The noninferiority of a cardiovascular MRI-based strategy compared to an FFR-based strategy concerning major adverse cardiac events has not been previously established.

Purpose of the Study:

  • To determine if a cardiovascular MRI-based strategy is noninferior to an FFR-based strategy in patients with stable angina.
  • To compare the rates of major adverse cardiac events between the two strategies.

Main Methods:

  • An unblinded, multicenter clinical-effectiveness trial randomly assigned 918 patients with typical angina and risk factors to either a cardiovascular MRI-based or an FFR-based strategy.
  • Revascularization was recommended based on specific criteria for ischemia (cardiovascular MRI) or FFR values (≤0.8).
  • The primary outcome was a composite of death, nonfatal myocardial infarction, or target-vessel revascularization within 1 year, with a noninferiority margin of 6 percentage points.

Main Results:

  • Fewer patients in the cardiovascular MRI group (35.7%) underwent revascularization compared to the FFR group (45.0%) (P=0.005).
  • The primary outcome occurred in 3.6% of the cardiovascular MRI group and 3.7% of the FFR group, meeting the noninferiority threshold (risk difference, -0.2 percentage points).
  • No significant difference was observed in the percentage of patients free from angina at 12 months between the groups (49.2% vs. 43.8%).

Conclusions:

  • In patients with stable angina, myocardial-perfusion cardiovascular MRI is associated with a lower incidence of coronary revascularization compared to FFR.
  • The cardiovascular MRI strategy was found to be noninferior to the FFR strategy regarding major adverse cardiac events.
  • This study suggests that cardiovascular MRI is a viable alternative strategy for guiding revascularization in stable angina patients.
Abstract

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