Seek advice from the Instructions for Use offered with Boston Scientific generators, electrodes and cannulas for possible adverse outcomes, supplemental warnings and safeguards before utilizing these merchandise.

Avoid demanding exercise for six weeks after surgery, contact your medical doctor if there is fluid leaking from your incision, if you have pain, swelling or numbness in the legs or buttocks or in case you fall. Check with the Guidelines to be used supplied on For extra Indications for Use, contraindications details and possible adverse outcomes, warnings, and safeguards before working with this item.

Contraindications. The Spinal Cord Stimulator methods usually are not for sufferers who're not able to work the technique, have failed demo stimulation by failing to get powerful pain relief, are inadequate surgical risks, or are pregnant.

The Superion™ Interspinous Spacer is indicated for the people sufferers with impaired physical function who working experience relief in flexion from symptoms of leg/buttock/groin pain, with or without back pain, who've been through at the very least six months of non-operative therapy. The Superion Interspinous Spacer may very well be implanted at one or two adjacent lumbar degrees in sufferers in whom treatment is indicated at no more than two degrees, from L1 to L5.

Warnings. Clients implanted with Boston Scientific Spinal Twine Stimulator Techniques devoid of ImageReady™ MRI Technological know-how should not be exposed to Magnetic Resonance Imaging (MRI). Publicity to MRI may perhaps end in dislodgement with the stimulator or sales opportunities, heating on the stimulator, significant damage to the stimulator electronics and an uncomfortable or jolting feeling. For a Spinal Cord Stimulation patient, you should not have diathermy as possibly a remedy for any healthcare condition or as Element of a surgical technique. Robust electromagnetic fields, which include electric power generators or theft detection methods, can most likely change the stimulator off, or trigger uncomfortable jolting stimulation. The technique should not be billed whilst sleeping. The Spinal Cord Stimulator method may perhaps interfere Together with the Procedure of implanted sensing stimulators such as pacemakers or implanted cardiac defibrillators.

Contraindications. The Spinal Wire Stimulator programs will not be for sufferers who're not able to function the technique, have failed trial stimulation by failing to obtain successful pain relief, are weak surgical risks, or are pregnant.

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Contraindications. The Spinal Cord Stimulator systems usually are not for sufferers who're unable to operate the system, have unsuccessful trial stimulation by failing to receive successful pain relief, are bad surgical risks, or are Expecting.

Recommend your medical professional that you do have a Spinal Twine Stimulator just before experiencing with other implantable unit therapies so that health-related selections is often manufactured and acceptable safety steps taken. Sufferers making use of therapy that generates paresthesia should not operate motorized motor vehicles like automobiles or potentially risky machinery and machines Along with the stimulation on. Stimulation needs to be turned off to start with in these kinds of instances. For therapy that isn't going to produce paresthesia (i.e. subperception therapy) it is actually less likely that sudden stimulation changes causing distraction could happen when getting stimulation on when running moving cars, equipment, and gear. Your doctor may be able to give supplemental info on the Boston Scientific Spinal Wire Stimulator methods. For comprehensive indications for use, contraindications, warnings, safeguards, and Unwanted side effects, phone 866.360.4747 or stop by Pain.com.

Suggest your medical doctor that you have a Spinal Twine Stimulator just before dealing with with other implantable device therapies so that health care decisions can be designed and acceptable safety actions taken. People employing therapy that generates paresthesia should not work motorized autos resources such as automobiles or potentially risky equipment and tools with the stimulation on. Stimulation has to be turned off to start with in such situations. For therapy that would not produce paresthesia (i.e. subperception therapy) it can be less likely that sudden stimulation changes resulting in distraction could arise though having stimulation on official source when operating relocating autos, machinery, and products. Your health care provider may be able to offer extra information on the Boston Scientific Spinal Wire Stimulator systems. For go here complete indications to be used, contraindications, warnings, safeguards, and side effects, call 866.360.4747 or visit Pain.com.

Warnings. For the affected individual having a cardiac pacemaker, contact the pacemaker firm to find out if the pacemaker needs to generally be transformed to set fee pacing during the radiofrequency technique.

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Warnings. Individuals implanted with Boston Scientific Spinal Twine Stimulator Units with no ImageReady™ MRI Technologies should not be exposed to Magnetic Resonance Imaging (MRI). Exposure to MRI may well result in dislodgement in the stimulator or sales opportunities, heating of the stimulator, serious damage to the stimulator electronics and an unpleasant or jolting sensation. Being a Spinal Twine Stimulation individual, you should not have diathermy as both a cure for just a medical situation or as Portion of a surgical treatment. Solid electromagnetic fields, for instance How long will the results of spine surgery last? electric power turbines or theft detection programs, can perhaps switch the stimulator off, or trigger unpleasant jolting stimulation. The process should not be billed when sleeping. The Spinal Twine Stimulator process may possibly interfere Along with the operation of implanted sensing stimulators such as pacemakers or implanted cardiac defibrillators.

Indications to be used: The Superion™ Oblique Decompression Procedure (IDS) is indicated to treat skeletally experienced patients suffering from pain, numbness, and/or cramping within the legs (neurogenic intermittent claudication) secondary to a get more info diagnosis of moderate degenerative lumbar spinal stenosis, with or without having Grade 1 spondylolisthesis, having radiographic evidence of thickened ligamentum flavum, narrowed lateral recess, and/or central canal or foraminal narrowing. The Superion™ Interspinous Spacer is indicated for anyone sufferers with impaired physical operate who practical experience reduction in flexion from symptoms of leg/buttock/groin pain, with or with no back pain, who definitely have gone through at the least 6 months of non-operative treatment. The Superion Interspinous Spacer may be implanted at a few adjacent lumbar degrees in clients in whom treatment method is indicated at no more than two levels, from L1 to L5. Contraindications, warnings, safety measures, Uncomfortable side effects.