Why the study?
Increasing demand for MRI in CEID carriers and persistent risks despite MR-conditional technology necessitate standardized institutional workflows, monitoring, and device programming.
This joint position paper provides standardized recommendations for the safe performance of MRI in patients with cardiac electronic implantable devices, emphasizing specific programming and monitoring protocols.
Magnetic resonance imaging (MRI) has become the reference imaging for the management of a large number of diseases. The number of MR examinations increases every year, simultaneously with the number of patients receiving a cardiac electronic implantable device (CEID). A CEID was considered an absolute contraindication for MRI for years. The progressive replacement of conventional pacemakers and defibrillators by MR-conditional CEIDs and recent data on the safety of MRI in patients with "MR-nonconditional" CEIDs have progressively increased the demand for MRI in patients with a CEID. However, some risks are associated with MRI in CEID carriers, even with "MR-conditional" devices because these devices are not "MR-safe". A specific programing of the device in "MR-mode" and monitoring patients during MRI remain mandatory for all patients with a CEID. A standardized patient workflow based on an institutional protocol should be established in each institution performing such examinations. This joint position paper of the Working Group of Pacing and Electrophysiology of the French Society of Cardiology and the Société française d'imagerie cardiaque et vasculaire diagnostique et interventionnelle (SFICV) describes the effect and risks associated with MRI in CEID carriers. We propose recommendations for patient workflow and monitoring and CEID programming in MR-conditional, "MR-conditional nonguaranteed" and MR-nonconditional devices.
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Dacher et al. (2020) conducted a review in Patients with cardiac electronic implantable devices (CEID) requiring MRI. Magnetic resonance imaging (MRI) and CEID programming was evaluated. This joint position paper provides recommendations for patient workflow, monitoring, and device programming to safely perform MRI in patients with cardiac electronic implantable devices.
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