61885 Insertion or replacement of cranial neurostimulator pulse generator or receiver, direct or inductive coupling; with connection to a single electrode array

Name of the Procedure:

Insertion or Replacement of Cranial Neurostimulator Pulse Generator or Receiver, Direct or Inductive Coupling; with Connection to a Single Electrode Array

Summary

This procedure involves placing or replacing a device known as a cranial neurostimulator, which is used to send electrical impulses to the brain. The device connects to an array of electrodes that stimulates specific areas of the brain to help manage certain neurological conditions.

Purpose

This procedure is typically performed to manage chronic pain, movement disorders, or other neurological conditions that have not responded well to conventional treatments. The goal is to improve symptoms and enhance the patient’s quality of life by modulating brain activity.

Indications

• Chronic pain conditions (such as severe neuropathic pain)
• Movement disorders (such as Parkinson’s disease)
• Epilepsy
• Essential tremor
• Other neurological disorders that are unresponsive to medication

Preparation

• Fasting for 8 hours before the procedure may be required.
• Adjustments to current medications as guided by the healthcare provider.
• Pre-procedure tests such as MRI or CT scans to map brain areas.
• Blood tests may be needed to ensure there are no contraindications.

Procedure Description

1. The patient is given anesthesia or sedation.
2. An incision is made in the scalp.
3. A small hole is drilled into the skull to access the brain.
4. The electrode array is carefully placed in the targeted brain area.
5. The pulse generator or receiver is implanted, usually under the skin near the clavicle.
6. The device is connected to the electrode array via extensions.
7. The incision site is closed and dressed.

Tools used may include imaging devices like MRI or CT for guidance, surgical drills, and neurostimulators.

Duration

The procedure typically takes 2-5 hours depending on complexity.

Setting

This procedure is usually performed in a hospital operating room or specialized surgical center.

Personnel

• Neurosurgeon
• Surgical nurses
• Anesthesiologist
• Neurophysiologist (in some cases)

Risks and Complications

• Infection at the incision site
• Bleeding or hemorrhage in the brain
• Device malfunction or migration
• Allergic reaction to materials in the neurostimulator
• Temporary or permanent neurological deficits
• Seizures

Benefits

• Reduction or elimination of chronic pain or tremors
• Improved quality of life and functional outcomes
• Better management of symptoms in conditions like Parkinson’s disease or epilepsy

Recovery

• Hospital stay for 1-2 days post-procedure.
• Instructions on wound care and activity restrictions.
• Follow-up appointments to check the device settings and adjust them if needed.
• Full recovery typically takes several weeks, during which activity should be limited to avoid dislodging the device.

Alternatives

• Medication management (although this might have been insufficient)
• Physical therapy and rehabilitation
• Less invasive nerve stimulation techniques
• Surgical options such as ablative procedures

Each alternative has its own benefits and downsides and may not be as effective as a neurostimulator for certain conditions.

Patient Experience

During the procedure, the patient will be under anesthesia and should not feel pain. Post-procedure, the patient may experience some discomfort at the incision sites, managed with pain medications. Swelling and bruising are common initially. The patient should avoid strenuous activities for a few weeks to ensure proper healing and device stability.