Patients who have not responded to other treatments for chronic pain can undergo minimally invasive dorsal root ganglion stimulation (DRG). An electrical impulse is delivered to the dorsal root ganglion, a cluster of nerve cells that transmit pain signals to the brain, by implanting a small device near the spinal cord. Various types of chronic pain, including complex regional pain syndrome (CRPS), neuropathic pain, and post-surgical pain, can be relieved through DRG stimulation.
Before undergoing DRG stimulation:
Patients undergo a thorough medical evaluation, including physical examinations and imaging studies, to determine the cause and severity of their chronic pain.
Patient consultation with a pain management specialist: Patients discuss their treatment options with a pain management specialist, including the benefits and risks of DRG stimulation, and determine if the procedure is right for them.
Some patients may undergo a psychological assessment to determine their expectations, coping mechanisms, and psychological readiness for surgery.
During DRG stimulation:
In order to ensure comfort during the procedure, the patient is placed under local anesthesia, conscious sedation, or general anesthesia.
Using fluoroscopy (real-time X-ray imaging), thin wire leads are guided to the targeted dorsal root ganglion through a small incision near the spine.
Occasionally, patients may undergo a temporary stimulation trial before permanent implantation to assess the effectiveness of DRG stimulation.
A small pulse generator device is implanted under the skin, typically in the lower back or buttock area, and delivers electrical impulses to the dorsal root ganglion.
After implantation, the device is programmed by a pain management specialist to deliver electrical stimulation at the appropriate settings.
After DRG stimulation:
Patient Monitoring: Following the procedure, patients are monitored for a short period to ensure stability and assess pain relief.
To allow the incision site to heal, patients may be advised to avoid strenuous activities and heavy lifting for a brief period after the procedure.
A pain management specialist will schedule regular follow-up appointments to monitor pain relief, adjust stimulation settings if necessary, and address any concerns.
DRG stimulation carries certain risks and potential complications, including:
An infection may occur at the site of the incision or around the implanted device, which may require antibiotic treatment or removal of the device.
Migration of leads may result in reduced stimulation effectiveness or discomfort over time.
The implanted pulse generator or leads may malfunction or require replacement due to technical issues or battery drain.
After DRG stimulation, patients are advised to:
Adhere to postoperative instructions provided by the pain management specialist, including medication management, activity restrictions, and wound care.
Maintain Follow-Up Appointments: Attend all scheduled follow-up appointments to monitor pain relief, evaluate device function, and adjust stimulation settings if necessary.
If the implantation site experiences worsening pain, discomfort, or signs of infection, notify the healthcare provider immediately.
For those suffering from chronic pain who have not responded to other treatments, DRG stimulation can be an effective treatment option. Following DRG stimulation, patients can experience significant relief and improve their quality of life with proper preparation, diligent postoperative care, and ongoing management by a pain management specialist.
