About This Document
This manual provides critical information regarding Magnetic Resonance Imaging (MRI) examinations for patients who have implanted Medtronic Deep Brain Stimulation (DBS) systems. It is essential for healthcare professionals to thoroughly review these guidelines before conducting any MRI procedure on such patients. For inquiries, Medtronic representatives are available for assistance.
Key Information for MRI Procedures
The document outlines the conditions under which Medtronic DBS systems are considered 'MR Conditional', detailing specific requirements for both full-body and head-only MRI scans. It covers essential aspects such as:
- MRI scan eligibility criteria for various Medtronic DBS system components.
- Precautions and contraindications to ensure patient safety during MRI.
- Explanation of symbols used on product labeling related to MRI compatibility.
- Information on potential interactions between MRI environments and implanted DBS devices.
- Guidance for clinicians, radiologists, and MRI technologists on patient preparation and scan execution.
Always ensure you are using the most current MRI guidelines, available at www.medtronic.com/mri.
Medtronic DBS System Components
Medtronic DBS systems typically include a lead, an extension, and a neurostimulator. Some systems may also include a pocket adaptor. These guidelines apply to both implanted neurostimulation systems and lead-only systems.
Safety and Compliance
Adherence to these guidelines is paramount to prevent serious injury, including tissue damage, unintended stimulation, or device malfunction. Medtronic DBS systems are designed with specific MRI compatibility in mind, but proper protocol must always be followed.
