This resource outlines a standardized policy for safely performing MRI examinations in patients with legacy (non–MR conditional) or mixed cardiac implantable electronic device (CIED) systems. It defines patient eligibility criteria, device risk stratification, and MRI site requirements based on device characteristics and risk level. The policy includes a classification framework for legacy devices and describes multidisciplinary workflows involving radiology, electrophysiology, and cardiology to support safe MRI access.
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Publish Date or Last Revised
January 6, 2026
Resource Type
- Guidelines / Clinical Documents
Therapeutic Area
Device Management
Management
General / Comprehensive Management
Setting
Device Care, Inpatient, Outpatient
Quality Improvement Topic
Care Coordination, Implementation Science, Safety
Related Resources
Guidelines / Clinical Documents
+ 1 other(s)