The Superion™ Interspinous Spacer is indicated for those clients with impaired physical function who knowledge aid in flexion from symptoms of leg/buttock/groin pain, with or with no back pain, who have undergone not less than six months of non-operative treatment. The Superion Interspinous Spacer can be implanted at a few adjacent lumbar ranges in sufferers in whom treatment is indicated at no more than two ranges, from L1 to L5.
Warnings. Sufferers implanted with Boston Scientific Spinal Cord Stimulator Methods without having ImageReady™ MRI Technology should not be exposed to Magnetic Resonance Imaging (MRI). Publicity to MRI may well end in dislodgement in the stimulator or qualified prospects, heating of your stimulator, serious harm to the stimulator electronics and an unpleasant or jolting feeling. Being a Spinal Cord Stimulation affected person, you should not have diathermy as either a remedy for your clinical problem or as Component of a surgical procedure. Powerful electromagnetic fields, which include electricity turbines or theft detection techniques, can perhaps flip the stimulator off, or bring about awkward jolting stimulation. The system should not be charged even though sleeping. The Spinal Wire Stimulator procedure could interfere with the operation of implanted sensing stimulators including pacemakers or implanted cardiac defibrillators. Suggest your physician that there is a Spinal Twine Stimulator right before dealing with with other implantable system therapies so that professional medical selections can be produced and ideal safety measures taken.
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The Superion™ Interspinous Spacer is indicated for people clients with impaired physical perform who expertise relief in flexion from symptoms of leg/buttock/groin pain, with or without the need of back pain, who've gone through at the very least six months of non-operative treatment. The Superion Interspinous Spacer can be implanted at 1 or 2 adjacent lumbar ranges in people in whom remedy is indicated at not more than two levels, from L1 to L5.
Warnings. Patients implanted with Boston Scientific Spinal Twine Stimulator Devices without ImageReady™ MRI Technologies should not be exposed to Magnetic Resonance Imaging (MRI). Publicity to MRI may possibly end in dislodgement from the stimulator or sales opportunities, heating on the stimulator, significant damage to the stimulator electronics and an not comfortable or jolting sensation. As a Spinal Cord Stimulation affected individual, you should not have diathermy as both a remedy to get a healthcare ailment or as Section of a surgical course of action. Sturdy electromagnetic fields, including power generators or theft detection systems, can most likely switch the stimulator off, or lead to uncomfortable jolting stimulation. The process should find more not be billed although sleeping. The Spinal Twine Stimulator system might interfere with the Procedure of implanted sensing stimulators such as pacemakers or implanted cardiac defibrillators.
The Superion™ Interspinous Spacer is indicated for anyone people with impaired physical operate who working experience aid more info in flexion from symptoms of leg/buttock/groin pain, with or without the need of back pain, who may have been through at least 6 months of non-operative cure. The Superion Interspinous Spacer may very well be implanted at a couple of adjacent lumbar concentrations in individuals in whom treatment method is indicated at not more than two stages, from L1 to L5.
Warnings. For just a client that has a cardiac pacemaker, contact the pacemaker firm to determine whether or not the pacemaker needs for being transformed to fastened charge pacing during the radiofrequency method.
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Avoid arduous activity for six months after surgery, contact your physician if there is fluid leaking out of your incision, if you have pain, swelling or numbness with your legs or buttocks or for those who tumble. Make reference to the Guidelines for Use presented on For added Indications to be used, contraindications information and facts and possible adverse results, warnings, and precautions prior to utilizing this solution.
Warnings. For just a affected person using a cardiac pacemaker, contact the pacemaker corporation to ascertain whether or not click here to find out more the pacemaker needs for being converted to mounted level pacing during the radiofrequency process.
Keep away from arduous action for 6 months after surgery, contact your health practitioner if there is fluid leaking from a incision, When you have pain, check here swelling or numbness inside your legs or buttocks or in the event you fall. Make reference to the Directions to be used presented on for additional Indications to be used, contraindications data and prospective adverse consequences, warnings, and safeguards prior to applying this product or service.
Warnings. For the patient with a cardiac pacemaker, contact the pacemaker enterprise to find out whether the pacemaker needs to generally be converted to fixed amount pacing during the radiofrequency treatment.
Indications to be used: The Superion™ Oblique Decompression Program (IDS) is indicated to deal with skeletally experienced people struggling from pain, numbness, and/or cramping within the legs (neurogenic intermittent claudication) secondary into a prognosis of reasonable degenerative lumbar spinal stenosis, with or without the need of Quality one spondylolisthesis, having radiographic proof of thickened ligamentum flavum, narrowed lateral recess, and/or central canal or foraminal narrowing. The Superion™ Interspinous Spacer is indicated for the people patients with impaired physical function who knowledge reduction in flexion from symptoms of leg/buttock/groin pain, with or devoid of back pain, which have been through not less than six months of non-operative cure. The Superion Interspinous Spacer can be implanted at a couple of adjacent lumbar stages in sufferers in whom treatment method is best website indicated at no more than two levels, from L1 to L5. Contraindications, warnings, precautions, Negative effects.