The Superion™ Interspinous Spacer is indicated for those individuals with impaired physical purpose who working experience aid in flexion from symptoms of leg/buttock/groin pain, with or without back pain, who've gone through no less than 6 months of non-operative procedure. The Superion Interspinous Spacer could be implanted at a couple of adjacent lumbar levels in sufferers in whom remedy is indicated at not more than two levels, from L1 to L5.
Contraindications. The Spinal Cord Stimulator methods usually are not for individuals who will be unable to function the method, have unsuccessful demo stimulation by failing to obtain effective pain reduction, are inadequate surgical risks, or are Expecting.
Prevent strenuous exercise for six weeks after surgery, contact your medical doctor if there is fluid leaking out of your incision, Should you have pain, swelling or numbness with your legs or buttocks or for those who fall. Consult with the Guidance to be used presented on For extra Indications for Use, contraindications information and facts and opportunity adverse results, warnings, and precautions prior to working with this solution.
Warnings. Clients implanted with Boston Scientific Spinal Cord Stimulator Units devoid of ImageReady™ MRI Engineering should not be subjected to Magnetic Resonance Imaging (MRI). Exposure to MRI may perhaps cause dislodgement on the stimulator or sales opportunities, heating with the stimulator, serious harm to the stimulator electronics and an not comfortable or jolting sensation. Being a Spinal Twine Stimulation affected person, you should not have diathermy as both a treatment for the medical issue or as Element of a surgical procedure. Robust electromagnetic fields, for instance power generators or theft detection units, can probably convert the stimulator off, or induce uncomfortable jolting stimulation. The method should not be charged while sleeping. The Spinal Wire Stimulator system may interfere Using the operation of implanted sensing stimulators for instance pacemakers or implanted cardiac defibrillators.
Contraindications. The Spinal Wire Stimulator techniques are usually not for individuals that are not able to work the technique, have unsuccessful demo stimulation by failing to acquire powerful pain aid, are inadequate surgical risks, or are pregnant.
Warnings. To get a client having a cardiac pacemaker, contact the pacemaker organization to find out whether or not the pacemaker needs for being converted to mounted amount pacing during the radiofrequency procedure.
Refer to the Instructions to be used supplied with Boston Scientific generators, electrodes and cannulas for opportunity adverse effects, extra warnings and safety measures ahead of read here using these products.
Refer to the Directions for Use presented with Boston Scientific turbines, electrodes and cannulas for potential adverse effects, further warnings and safety article measures prior to making use of these solutions.
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Consult with the Guidelines for Use supplied with Boston Scientific turbines, electrodes and cannulas for opportunity adverse outcomes, added warnings and safeguards before employing these products and solutions.
Warnings. For any affected individual by using a cardiac pacemaker, contact the article pacemaker enterprise to determine whether the pacemaker needs to get transformed to fastened rate pacing during the radiofrequency course of action.
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Pain management professionals are Physicians who focus on all kinds of pain. They obtain decades of Innovative training in pain management and center on managing patients with extreme pain.
Indications for Use: The Superion™ Indirect Decompression Procedure (IDS) is indicated to treat useful content skeletally mature sufferers suffering from pain, numbness, and/or cramping during the legs (neurogenic intermittent claudication) secondary to a diagnosis of moderate degenerative lumbar spinal stenosis, with or devoid of Quality one spondylolisthesis, getting radiographic evidence of thickened ligamentum flavum, narrowed lateral recess, and/or central canal or foraminal narrowing. The Superion™ Interspinous Spacer is indicated for anyone clients with impaired physical functionality who encounter relief in flexion from symptoms of leg/buttock/groin pain, with or with no back pain, who definitely have been through at least six months of non-operative procedure. The Superion Interspinous Spacer may very well be implanted at a few go here adjacent lumbar concentrations in people in whom treatment is indicated at not more than two concentrations, from L1 to L5. Contraindications, warnings, safety measures, Unintended effects.