“…Although case reports have published instances of bizarre CRMD behavior in the setting of intraoperative EMI, [9][10][11][12] prior reports suggest that most instances of intraoperative EMI occur when electrocautery is used in close proximity to the device. 6,9,13,14 In addition, several small crosssectional studies have not shown any evidence of device malfunction other than minor changes in sensing or threshold measurements. 6,7,15,16 After appropriate precautions were taken (magnet use and reprogramming certain CRMDs to a safety mode), the patients in either cohort of our study had similar outcomes to the ones in these previous reports (i.e., an absence of inappropriate device function).…”