Magnetic resonance in patients with cardiovascular devices. SEC-GT CRMTC/SEC-Heart Rhythm Association/SERAM/SEICAT consensus document
M. Barreiro-Pérez a, B. Cabeza b c, D. Calvo d e, J.L. Reyes-Juárez f, T. Datino g h i, E. Vañó Galván c, A.M. Maceira González j k, C. Delgado Sánchez-Gracián l, S. Prat-González m, R.J. Perea n, G. Bastarrika o, M. Sánchez n, L.J. Jiménez-Borreguero p, C. Fernández-Golfín Lobán q r, J.F. Rodríguez Palomares r s, J.M. Tolosana r s, J.A. Hidalgo Pérez t, E. Pérez-David r u, V. Bertomeu-González r v, H. Cuéllar f
Magnetic resonance has become a first-line imaging modality in various clinical scenarios. The number of patients with different cardiovascular devices, including cardiac implantable electronic devices, has increased exponentially.
Although there have been reports of risks associated with exposure to magnetic resonance in these patients, the clinical evidence now supports the safety of performing these studies under specific conditions and following recommendations to minimize possible risks.
This document was written by the Working Group on Cardiac Magnetic Resonance Imaging and Cardiac Computed Tomography of the Spanish Society of Cardiology (SEC-GT CRMTC), the Heart Rhythm Association of the Spanish Society of Cardiology (SEC-Heart Rhythm Association), the Spanish Society of Medical Radiology (SERAM), and the Spanish Society of Cardiothoracic Imaging (SEICAT).
The document reviews the clinical evidence available in this field and establishes a series of recommendations so that patients with cardiovascular devices can safely access this diagnostic tool.
CITATION Radiologia (Engl Ed). 2023 May-Jun;65(3):269-284. doi: 10.1016/j.rxeng.2022.09.014