Key result
Magnetic resonance imaging was safely performed without adverse events or changes in device parameters in a patient with an MRI-compatible temporary external pacemaker and active fixation lead.
Why the study?
Patients with temporary external pacemakers may be denied MRI due to limited data regarding device safety profiles.
Does a 1.5 T brain MRI cause adverse events or device malfunction in a patient with a temporary externalized MRI-compatible pacemaker?
Case Report (n=1)
No
Does a 1.5 T brain MRI cause adverse events or device malfunction in a patient with a temporary externalized MRI-compatible pacemaker?
Brain MRI can be safely performed in selected patients with MRI-compatible temporary external pacemakers using appropriate multidisciplinary precautions and device programming.
Supports MRI feasibility with select temporary external pacemakers; leaves open need for prospective safety data before routine use.
Temporary external pacemakers are frequently used in critically ill patients who are not candidates for a permanent device.1,2 While patients with cardiac implantable electronic devices (CIEDs) meeting specific criteria have been approved by the Food and Drug Administration to undergo magnetic resonance imaging (MRI) studies, patients with temporary external devices may be denied the opportunity for MRI given the limited data regarding the safety profile of these devices.3–5
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Kovach et al. (2020) conducted a case report in Prosthetic valve endocarditis with complete heart block (n=1). Magnetic resonance imaging (MRI) was evaluated on Safety and feasibility of MRI. Magnetic resonance imaging was safely performed without adverse events or changes in device parameters in a patient with an MRI-compatible temporary external pacemaker and active fixation lead.
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