How Does Occipital Nerve Stimulation Work?

Occipital nerve stimulation relieves pain in the back of the head (occipital region) by producing a tingling sensation in the occipital area.

Occipital nerve stimulation relievespainin the back of the head (occipital region) by producing a tingling sensation in the occipital area. The electrical impulses from the pulse generator affect the occipital nerve’s function and block its transmission ofpainsignals to the brain.

Electrodes are placed into the tissues under the skin over the occipital nerve. The electrodes are connected with insulated leads to a battery-powered pulse generator that is implanted under the skin in the upper chest, abdomen or back. The non-rechargeable batteries last up to five years, and the rechargeable batteries last nearly 10 years.

The pulse generator is programmed by a clinical specialist and can be operated by the patient with a remote-control device. The device may be either programmed to provide continuous or intermittent stimulation. Based on individual needs, the patient can turn the device on or off, as well as adjust the stimulation parameters, such as voltage and frequency, for comfortable paresthesia.

Occipital nerve stimulation is performed in two stages, usually a week apart. In the first stage, the doctor places only the electrodes in thescalp, which are operated with an external battery. The patient uses the device for four to seven days, on a trial basis. If the patient experiences significant pain relief from the occipital nerve stimulation, implantation of the pulse generator follows.

A pain specialist or a neurosurgeon performs the procedure. The trial procedure is performed using local anesthesia and mild sedation, while the implantation of the pulse generator requires general anesthesia.

Stage I: Occipital nerve stimulation trial

Preparation

• Blood and imaging tests
• Historical data noted
  • Bleeding disorders
  • High blood pressure
  • Allergies
  • Any other health problems
  • Any regular medications taken
• Hair over electrode implantation site clipped

Procedure

The doctor

• Administers sedation and injects local anesthesia in the occipital area of the scalp.
• Makes a tiny incision in the scalp.
• Inserts the electrodes into the tissues under the skin using continuous X-ray (fluoroscopy) for guidance.
• Connects the leads to an external pulse generator.
• Tests the stimulator with response from the patient to ensure that the electrodes are placed optimally.
• Closes the incision withsutureswith the leads trailing out of the incision.

After the procedure

• 病人恢复roo的监控m for a few hours.
• The leads from the scalp are connected to the external pulse generator and settings are adjusted to suit the requirement of the patient.
• The patient uses the device for the next four to seven days as needed.
• The patient performs activities and eats food that usually triggermigrainesand maintains a pain diary, noting the stimulation effect.
• Implantation of the pulse generator is undertaken if the patient benefits from significant pain relief from occipital nerve stimulation.
• The trial stimulation may not prove useful with certain kinds ofheadaches, as the response to stimulation may take a few weeks or even months.

Stage II: Occipital nerve stimulator implantation

Preparation

• The patient must avoid eating and drinking for eight hours before the procedure.

Procedure

The doctor

• Attaches an IV line and administers general anesthesia.
• Opens the incision site in the scalp where the leads are implanted at the trial stage.
• Ensures the electrodes are firmly in place or adjusts the placement as necessary, with fluoroscopic guidance.
• Tunnels the leads subcutaneously to the pulse generator implant site.
• Creates a small pocket under the skin to implant the pulse generator.
• Connects the tunneled leads to the pulse generator.
• Tests the pulse generator to make sure it works properly.
• Places the pulse generator in the implant site and closes it with sutures.

After the procedure

• The patient is weaned off anesthesia and administered painkillers.
• 病人恢复roo的监控m for a few hours.

Recovery

• Most patients are discharged within a day or two.
• Complete recovery may take up to six weeks.
• Pain relief or reduction in pain intensity from the neurostimulation can occur variably in patients.
• Neurostimulation effects may take weeks or even months in some patients.

Implantation of occipital nerve stimulation devices is a relatively safe procedure with minimal complications. Studies show that most patients report significant reduction in the pain intensity, andheadachedays per month.

The complications include:

• Lead dislodgement or breakage
• Woundinfection
• Wound erosion (skin deterioration at the surgical site)
• Pain and numbness at the lead sites
• Hematoma
• Collection of fluid (seroma) in the incision sites
• Device malfunction
• Battery failure
• Lack of pain relief
• Insufficient stimulation coverage of pain area
• Need for revision surgery