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DOI 10.3390/jcdd11100313

Медицинская библиотека · Journal of cardiovascular development and disease · 2024

Safety of Magnetic Resonance Imaging in Patients with Cardiac Implantable Electronic Devices.

Lanz Hugo, Strauß Katharina, Höpler Julia, Kraft Marie, Hoffmann Sabine, Binzenhöfer Leonhard, Gade Nils, Roden Daniel, Saleh Inas, Kääb Stefan, Lackermair Korbinian, Sadoni Sebastian, Hagl Christian, Massberg Steffen, Estner Heidi, Fichtner Stephanie, Lüsebrink Enzo

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Аннотация

BACKGROUND

MRI (magnetic resonance imaging) represents the diagnostic image modality of choice in several conditions. With an increasing number of patients requiring MRI for diagnostic purposes, the issue of safety in patients with cardiac implantable electronic devices (CIED) undergoing this imaging modality will play an ever more important role. The purpose of this study was to assess the safety and device function following MRI in an unrestricted real-world cohort of patients with a wide array of cardiac devices.

METHODS

We conducted a retrospective single-center study including 1010 MRI studies conducted in adult patients (≥18 years) with an implanted CIED treated in the University Hospital of Munich (LMU) between July 2012 and March 2024. Patients with non-MR conditionally labeled leads, abandoned or epicardial leads, as well as lead fragments, were included for analysis.

RESULTS

Across a total of 1010 MRIs (920 total MR-conditional device generators) performed in patients with an implanted CIED, there were no deaths, reports of discomfort, palpitations, heating, or ventricular arrythmias in the 24 h following MRI. Only 2/1010 MRIs were followed by a reported atrial arrhythmia within 24 h, both in patients with an MR-conditional pacemaker (PM) device without an abandoned lead. No significant changes in device function following MRI from baseline were observed across all included CIEDs. Lastly, no instances of severe malfunction, such as generator failure, loss of capture, electrical reset, or inappropriate inhibition of pacing, were found in post-MRI interrogation reports across all MRI studies.

CONCLUSIONS

Based on the analysis of 1010 MRIs undergone by patients with CIEDs, following standardized device interrogation, manufacturer-advised device programming, monitoring of vital function, and manufacturer-advised reprogramming, MRI can be performed safely and without adverse events or changes in device function.

Для цитирования: Lanz Hugo, Strauß Katharina, Höpler Julia, Kraft Marie, Hoffmann Sabine, Binzenhöfer Leonhard, Gade Nils, Roden Daniel, Saleh Inas, Kääb Stefan, Lackermair Korbinian, Sadoni Sebastian, Hagl Christian, Massberg Steffen, Estner Heidi, Fichtner Stephanie, Lüsebrink Enzo. Safety of Magnetic Resonance Imaging in Patients with Cardiac Implantable Electronic Devices.. Journal of cardiovascular development and disease. 2024. DOI: 10.3390/jcdd11100313.
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