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This information is designed to provide you with helpful educational information but is for information purposes only, is not medical advice, and should not be used as an alternative to speaking with your doctor. No representation is made that the information provided is current, complete, or accurate. Medtronic does not assume any responsibility for persons relying on the information provided. Be sure to discuss questions specific to your health and treatments with a healthcare professional. For more information please speak to your healthcare professional.
This information is designed to provide you with helpful educational information but is for information purposes only, is not medical advice, and should not be used as an alternative to speaking with your doctor. No representation is made that the information provided is current, complete, or accurate. Medtronic does not assume any responsibility for persons relying on the information provided. Be sure to discuss questions specific to your health and treatments with a healthcare professional. For more information please speak to your healthcare professional.
Refer to technical manual and Instruction for Use (IFU) for complete list of indications, contraindications, warnings and precautions.
The Physician will require approval from the insurer before a trial and implant of the neurostimulator. Workers Compensation my also be approved and will need approval prior to treatment.
The spinal cord stimulator trial is designed to mimic what the experience with the implanted device. The Medtronic SCS may be adjusted.
Many people experience significant pain reduction in regions such as their extremities, leg, and/or back with spinal cord stimulation.1 However, the therapy doesn’t treat the source of pain, so the degree of pain reduction will vary from person to person. Medtronic SCS is recommended as an aid in the management of chronic, intractable pain of the trunk and/or limbs.
A doctor will program the settings based on the needs and preferences, but adjustment can occur at many time with the hand held patient controller.
Treatment-related information is stored on the device, so the patient can be treated at any clinic that uses the Medtronic neurostimulators.
Approximately 82% of patients implanted with a spinal cord stimulator will need an MRI within five years to diagnose an unrelated condition. Medtronic SureScan™ MRI Technology allows access to MRI scans anywhere on the body.†
Depending on the neurostimulator it may need to be replaced in the future due to malfunction or depletion. The device with Medtronic Overdrive™ battery technology maintains nearly full capacity (less than 5% fade) at 9 years, at which point replacement is recommended. At this point, the SCS device should be replaced.
Published studies have shown that when used by patients with chronic intractable pain, spinal cord stimulation may offer the following benefits:
Approximately 82% of patients implanted with a spinal cord stimulator will need an MRI within five years to diagnose an unrelated condition. Medtronic SureScan™ MRI Technology allows the access to MRI scans anywhere on the body.
Under specific conditions. Talk to your doctor and refer to product labeling for full list of conditions.
Kumar K, Taylor RS, Jacques L, et al. The effects of spinal cord stimulation in neuropathic pain are sustained: a 24-month follow-up of the prospective randomized controlled multicenter trial of the effectiveness of spinal cord stimulation. Neurosurgery. 2008;63(4):762-770; discussion 770.
Harke H, Gretenkort P, Ladleif HU, Rahman S. Spinal cord stimulation in sympathetically maintained complex regional pain syndrome type I with severe disability. A prospective clinical study. Eur J Pain. 2005:9(4);363-373.
North RB, Kidd DH, Farrokhi F, Piantadosi SA. Spinal cord stimulation versus repeated lumbosacral spine surgery for chronic pain: a randomized, controlled trial. Neurosurgery. 2005;56(1):98-107.
North RB, Kidd D, Shipley J, Taylor RS. Spinal cord stimulation versus reoperation for failed back surgery syndrome: a cost effectiveness and cost utility analysis based on a randomized, controlled trial. Neurosurgery. 2007;61(2):361-369.