Has Baystate Hospital in Springfield, MA, ever performed MRI scans on patients with non-compliant pacemaker (artificial cardiac pacing device) leads?

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Last updated: July 11, 2025View editorial policy

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MRI Safety for Patients with Non-Compliant Pacemaker Leads at Baystate Hospital

Based on the available evidence, there is no specific information indicating whether Baystate Hospital in Springfield, MA has ever performed MRI scans on patients with non-compliant pacemaker leads. However, I can provide guidance on the safety and protocols for performing MRI in patients with non-compliant cardiac devices according to current guidelines.

Safety of MRI in Patients with Non-Compliant Pacemaker Leads

The 2013 European Society of Cardiology (ESC) guidelines state that MRI at 1.5 Tesla can be performed with a low risk of complications in patients with conventional (non-MRI-conditional) cardiac devices if appropriate precautions are taken 1. This represents a Class IIb recommendation with Level B evidence.

Key Safety Considerations:

  • Patient Selection:

    • Exclude patients with leads implanted less than 6 weeks before the scan
    • Exclude patients with abandoned or epicardial leads (prone to heating)
    • Assess pacemaker dependency status
  • Device Programming Protocol:

    • For pacemaker-dependent patients: Program to asynchronous mode (VOO/DOO)
    • For non-dependent patients: Program to inhibited mode (VVI/DDI)
    • Deactivate other pacing functions (magnet, rate, noise, PVC response)
    • Deactivate tachyarrhythmia monitoring and therapies in ICDs
  • Monitoring Requirements:

    • Qualified personnel must monitor the patient during MRI
    • Record device parameters before and after MRI (lead impedance, thresholds, sensing amplitude, battery voltage)
    • Continuous ECG monitoring during the procedure
    • Restore original programming immediately after MRI

Evidence Supporting MRI Safety in Non-Compliant Devices

A 2020 systematic review and meta-analysis of 35 cohort studies including 5,625 patients with non-conditional cardiac devices who underwent 7,196 MRI scans (0.5-3T) found 2:

  • No deaths or ICD shocks occurred
  • Extremely low incidence of lead or device-related complications
  • Lead failure, electrical reset, arrhythmia, and inappropriate pacing occurred in only 0-1.43% of cases
  • Increase in pacing threshold >0.5V occurred in only 1.1% of cases

Similarly, a 2017 study of 1,500 patients (1,000 with pacemakers, 500 with ICDs) undergoing non-thoracic MRI found no deaths, lead failures, loss of capture, or ventricular arrhythmias when following a standardized protocol 3.

Special Considerations

  1. Battery Status: Caution is advised for devices with nearly depleted batteries. A 2017 study showed that while ICDs with nearly depleted batteries had no issues during MRI, older pacemakers (pre-2005) experienced power-on-reset events 4.

  2. Pacemaker Dependency: Higher risk but can be managed. A 2005 study of 10 pacemaker-dependent patients who underwent 11 MRI scans of the head and neck showed no adverse events when using appropriate reprogramming (VOO/DOO), monitoring, and modified MRI pulse sequences 5.

  3. Benefit vs. Risk: The 2010 safety guidance in anesthesia notes that approximately 50-75% of patients with implanted cardiac devices will need an MRI scan during the lifetime of their device 1. When MRI is necessary for clinical management of serious diseases, the benefit might outweigh the risk.

Practical Approach

If a patient with a non-compliant pacemaker lead requires an MRI at Baystate Hospital:

  1. Consult with an electrophysiology specialist
  2. Assess if alternative imaging techniques could provide the needed information
  3. If MRI is deemed necessary, follow the comprehensive safety protocol outlined in the ESC guidelines
  4. Consider limiting the scan to 1.5T field strength (no data exists for >1.5T even for MRI-compatible devices)
  5. Ensure continuous monitoring and have resuscitation equipment readily available

While the evidence suggests MRI can be performed with acceptable risk in patients with non-compliant devices when following strict protocols, the decision should be based on a careful assessment of clinical necessity and available expertise.

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Research

Magnetic resonance imaging in non-conditional pacemakers and implantable cardioverter-defibrillators: a systematic review and meta-analysis.

Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology, 2020

Research

Strategies for the safe magnetic resonance imaging of pacemaker-dependent patients.

Pacing and clinical electrophysiology : PACE, 2005

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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