• J Cardiovasc Med (Hagerstown) · Oct 2015

    Assessing access to MRI of patients with magnetic resonance-conditional pacemaker and implantable cardioverter defibrillator systems: the Really ProMRI study design.

    • Giampiero Maglia, Antonio Curnis, Marco Brieda, Matteo Anaclerio, Vincenzo Caccavo, Paolo Bonfanti, Donato Melissano, Fabrizio Caravati, Lisa Giovene, Alessio Gargaro, and Really ProMRI Study Group.
    • aCardiology - Coronary Care Unit, Pugliese-Ciaccio Hospital, Catanzaro bElectrophysiology department, Spedali Civili, P.le Spedali Civili 1, Brescia cDepartment of Cardiology, S. Maria D.A. Hospital, Via Montereale 24, Pordenone dCardiology Department, A.O.U. Pol. Universitario di Bari, Piazza G. Cesare 11, eCardiology Department, Ente Ecclesiastico Miulli General Regional Hospital, SP 127 Acquaviva-Santeramo km 4, Acquaviva delle Fonti, Bari fDepartment of Cardiology II, Circolo e Fondazione Macchi Hospital, V.le Borri 57, Varese gCardiology Department, P.O. F. Ferrari, Via F. Ferrari, Casarano (Le) hDepartment of Cardiology I, Circolo e Fondazione Macchi Hospital, V.le Borri 57, Varese iClinical Office, Biotronik Italia S.p.a., V.le delle Industrie 11, Vimodrone (MI), Italy.
    • J Cardiovasc Med (Hagerstown). 2015 Oct 1; 16 (10): 715-20.

    BackgroundDespite the fact that magnetic resonance (MR)-conditional pacemaker and lead systems have been introduced more than 5 years ago, it is still not clear whether they have actually facilitated the access of pacemaker patients to this important diagnostic tool. Factors limiting MR scans in daily practice in patients with MR-conditional cardiac implantable electronic device (CIED) systems may be related to organizational, cultural and sometimes legal aspects. The Really ProMRI registry is an ongoing survey designed to assess the annual rate of MR examinations in patients with MR-conditional implants, with either pacemakers or implantable cardioverter defibrillators, and to detect the main factors limiting MRI.MethodsThe primary endpoint of the Really ProMRI registry is to assess the current access to MRI of patients with MR-conditional pacemaker or implantable cardioverter defibrillator systems during normal practice. Data in the literature reported a 17% annual incidence of medical conditions requiring MRI in CIED patients. The Really ProMRI registry has been designed to detect 4.5% absolute difference with an 80% statistical power, by recruiting 600 patients already implanted with MR-conditional CIED implant. Patients will be followed up for 1 year, during which they will be asked to refer any prescription, execution or denial of an MR examination by patient questionnaires and original source documents.ConclusionThe ongoing Really ProMRI registry will assess the actual rate of and factors limiting the access to MRI for patients with MR-conditional CIEDs.

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