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Like any chronic pain treatment, there are both appreciable advantages and risks/disadvantages involved with spinal cord stimulation. In general, the biggest risk of this treatment is that it does not work for everyone—most studies show that about 50-60% of patients who try neurostimulation find meaningful pain relief (e.g. reduction of pain of at least 50%).
A trial can test patient response before the patient commits to a permanent implant.
It has few side effects and is easily reversible; if it doesn’t work or is no longer needed it can be removed.
Implantation of the system is minimally invasive, requiring a relatively minor surgical procedure on an outpatient basis.
Leads are inserted just under the skin, and patients can travel anywhere, and participate in any recreational activities, including swimming.
Achieving pain relief with spinal cord stimulation or peripheral nerve field stimulation can allow patients to reduce or eliminate their use of narcotic drugs.
Ongoing advances in neurostimulator technology give patients more control to adjust the stimulation if their pain changes in location or severity.
Continual improvements in the design of electrodes and longer lasting, rechargeable batteries mean that implantable systems can be placed in locations to give optimal and more efficient pain control than other modalities.
Spinal cord stimulation does not work for everyone. Most studies show that 50% to 60% of people find meaningful pain relief with spinal cord stimulation.
It does not eliminate the pain. A successful outcome of spinal cord stimulation is considered to be pain relief of 50% or more.
Spinal cord stimulation does not address the source of the pain. The system is designed to interrupt pain signals being sent to the brain, but it does not correct any underlying anatomical problem. For many people with chronic pain, this is the right approach to treatment. However, for those with a correctable anatomic lesion, treatments to address the source of the pain should be tried first.
The treatment involves an implant and surgery. As with any surgical procedure and implant, there are certain risks and potential complications associated with spinal cord stimulation and peripheral nerve field stimulation, discussed below.
Allergic reaction to the implanted materials
Bleeding
Infection
Pain at the incision site (usually resolves in a few weeks)
Weakness, numbness, clumsiness, paralysis
Battery failure and/or battery leakage requiring a surgical incision to remove and replace the battery
Fluid leak from the spinal cord, causing headache
Undesirable changes in stimulation may occur over time due to scar tissue forming around the leads, or movement of the lead position
Undesirable or unpleasant stimulation of the chest or rib area as a result of nerve root involvement
Migration of the electrode may occur, resulting in a loss or change of stimulation
Skin breakdown over the generator or electrode site
Stimulation may work for a period of time and then lose effectiveness after 1-2 years
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