Cardiac pacemaker: in vitro assessment at 1.5 T
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Updated: Aug 13, 2026
Impact of Intracardiac Neurons on Cardiac Electrophysiology and Arrhythmogenesis in an Ex Vivo Langendorff System
Published on: May 22, 2018
Frank G Shellock1, David S Fieno, Louise J Thomson
1Department of Radiology, Keck School of Medicine, University of Southern California, Institute for Magnetic Resonance Safety, Education, and Research, Los Angeles, CA, USA. frank.shellock@gte.net
Background:
In vitro testing is used to determine safe parameters before performing magnetic resonance imaging (MRI) on a patient with an implant. Therefore, the objective of this study was to evaluate a cardiac pacemaker using a 1.5-T magnetic resonance (MR) system.
Methods:
A modern cardiac pacemaker (INSIGNIA I PLUS, Model 1298, and FINELINE II, Model 4471, pacing leads; Guidant Corporation, St Paul, MN) was evaluated for magnetic field interactions at 1.5 T. Magnetic resonance imaging-related heating was assessed using 3 different 1.5-T scanners operating at various levels of radio-frequency power and imaging conditions. Functional aspects of the pacemaker were evaluated immediately before and after MRI (9 different pulse sequences). Artifacts were also characterized.
Results:
Magnetic field interactions for the pacemaker were minor. Temperature changes measured in vitro were at levels that are not expected to pose a risk for specific MR conditions (< 4.0 degrees C). The function of the pacemaker was unaffected by MRI. Artifacts were minor for the leads and relatively large for the implantable pulse generator.
Conclusion:
The findings indicated that this pacemaker exhibited acceptable safety features relative to the use of a 1.5-T MR system. If induced currents do not occur for this device, it may be safe for a patient to undergo MRI by following specific conditions. The results are specific to the pacemaker tested, the MR systems, and conditions used in this evaluation.
