Why does MRI labelling matter?

Not all SCS devices offer the same MRI access.

Full-body MRI access is dependent on a number of variables. Inability to meet just one of these variables can restrict a patient’s access to this important scan.

In the end, certain SCS devices may not be as compatible as you think.
 

MRI labelling

The industry leader for MRI access

An independent study found that, after 5 years, 43% of MR conditional Abbott, Boston Scientific & Nevro patients may lose MR eligibility due to high electrode impedance.2

 

Risk of losing MRI eligibility at 5 years due to high electrode impedance

MRI labelling
MRI labelling

Listen to our expert panel

See the trailers below from our expert panel and log-in to our Medtronic Academy to watch the full webinar.

Dr. Peter Wright, PhD​

Clinical Scientist in MR and Non-ionising Imaging​
Director of HCST and Associate Director of Clinical Professions​
Healthcare Science and Technology, University Hospitals NHS Trust Plymouth, UK​

Dr. Cormac F. Mullins, MB, BCh, BAO, FCAI, FFPMCAI, MScHSM​

Pain Medicine and Anesthesiology Consultant​
Senior Clinical Lecturer​
South Infirmary Victoria University Hospital, Cork, Ireland​
Cork University Hospital, Cork, Ireland​
University College Cork, Ireland​

Dr. Peter Wright

Understanding the need for MRI in SCS patients​

Dr. Peter Wright

Discovering the fundamental difference between MR Conditionality and MRI Access​

Dr. Peter Wright

Understanding the differences in technology and the impact on the patient

Dr. Cormac Mullins

Explore the findings of "A retrospective review of elevated lead impedances in impedance-dependent magnetic resonance-conditional spinal cord stimulation devices"

Get in touch to talk about SCS MRI labelling

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References

1

Desai MJ, Hargens LM, Breitenfeldt MD, et al. The rate of magnetic resonance imaging in patients with spinal cord stimulation. Spine. 2015;40(9):E531-E537

2

Mullins CF, Harris S, Pang D. A retrospective review of elevated lead impedances in impedance-dependent magnetic resonance-conditional spinal cord stimulation devices. Pain Pract. 2023;00:1–8. https://doi.org/10.1111/papr.13301

Brief Statement:

This material should not be considered the exclusive source of information, it does not replace or supersede information contained in the device manual(s).  Please note that the intended use of a product may vary depending on geographical approvals.

See the device manual(s) for detailed information regarding the intended use, the implant procedure, indications, contraindications, warnings, precautions, and potential adverse events. For a MRI compatible device(s), consult the MRI information in the device manual(s) before performing a MRI.

If a device is eligible for eIFU usage, instructions for use can be found at Medtronic’s website manuals.medtronic.com. Manuals can be viewed using a current version of any major internet browser. For best results, use Adobe Acrobat® Reader with the browser.Medtronic products placed on European markets bear the CE mark and the UKCA mark (if applicable).

For any further information, contact your local Medtronic representative and/or consult Medtronic’s websites.