Abstract
Patients with pacemakers or internal cardioverter-defibrillators (ICDs) are at risk for device malfunction on exposure to electromagnetic interference (EMI) from monopolar cautery, magnetic resonance imaging (MRI), or radiofrequency ablation and therapeutic radiation. The most common and potentially life-threatening adverse effects of EMI are inhibition of cardiac pacing (leading to bradycardia or asystole) and inadvertent shocks if ICD interprets the EMI as a heart rate higher than the therapy trigger rate. Most experts recommend that a plan for device management for surgery be made by a qualified individual with the recommendation based on knowledge of the proposed surgery and the information gleaned from a recent interrogation of the device.
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Rooke, G.A. (2015). Implantable Cardiac Electronic Devices. In: Jackson, M.B., Mookherjee, S., Hamlin, N.P. (eds) The Perioperative Medicine Consult Handbook. Springer, Cham. https://doi.org/10.1007/978-3-319-09366-6_12
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DOI: https://doi.org/10.1007/978-3-319-09366-6_12
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