Spinal cord stimulation delivers mild electrical impulses to the spinal cord that interrupt pain signals to the brain, replacing them with a tingling sensation.
These impulses are generated by a small device that is implanted under your skin. The stimulation to the spinal cord is delivered from the device through insulated wires called leads, which are placed adjacent to the spinal cord. Using a handheld device that works like a remote control, you can adjust the stimulator to specific areas and levels of pain, depending on your activities and how your pain changes during the day.
Spinal cord stimulation can be used to treat patients with severe, chronic pain due to a variety of conditions, including failed back surgery/arachnoiditis, neuropathic pain/neuropathy and complex regional pain syndrome/reflex sympathetic dystrophy.
Every patient experiences different pain relief from spinal cord stimulation, though most successful cases have a 50 to 70 percent decrease in pain. This may help you return to a more active lifestyle and reduce your use of pain medications.
There are two stages involved in the spinal cord stimulator procedure. The first is a trial stage, during which the leads are temporarily placed via needles to test the effectiveness of the device and whether you are comfortable with the tingling sensation it delivers. This is an outpatient procedure, and you will test the implant for approximately one week at home in your normal surroundings.
If you have a positive experience with the stimulator, we will perform a second procedure to permanently implant the device. This is a minor surgical procedure most often done as ambulatory surgery, although your doctor may decide to have you stay overnight in the hospital, depending on your individual circumstances.
To prepare for both procedures:
During the implantation of the trial device, you will receive a local anesthetic to numb the area and mild sedation to keep you relaxed. Insulated wires, called leads, are carefully placed through a needle into the epidural space, which is adjacent to the spine. The wires are then connected to a stimulator that remains outside your body for the duration of the trial. The leads are easily removed through the skin at the end of the trial with almost no discomfort.
If the device is successful at reducing your pain and you are comfortable with the tingling sensation it delivers, then you will have a permanent implantation procedure. This is very similar to the trial procedure. However, a small incision in the back is needed to allow the leads to be placed underneath the skin, and another small incision is needed for the stimulator to be implanted permanently under the skin, usually in the buttocks or abdominal area.
In most cases, the stimulator is barely visible underneath the skin. The stimulator usually has a rechargeable battery that lasts 5 to 10 years, depending on the model and how often it is used.
Serious side effects and complications are uncommon. The most common problem is pain for a few days at the site where the wires and stimulator were inserted. This is normal and your doctor can prescribe pain relief for a few days until the pain subsides. Other complications include infection, bleeding, nerve injury, spinal cord injury, dural puncture or tear, and migration or breakage of the wire.
Most people return to light levels of activity several days after the procedure. Lifting, bending and twisting should be limited for up to two months to allow the leads to heal in an appropriate position without moving.
Reviewed by health care specialists at UCSF Medical Center.
Pain Management Center
2255 Post St.
San Francisco, CA 94143-1654
Phone: (415) 885-PAIN (7246)
New Patients: (415) 885-3552
Current Patients: (415) 885-7533
Fax: (415) 885-3883