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Removal of cranial nerve (eg, vagus nerve) neurostimulator electrode array and pulse generator

CPT4 code

Name of the Procedure:

Removal of Cranial Nerve Neurostimulator Electrode Array and Pulse Generator (e.g., Vagus Nerve Stimulator Removal)

Summary

This procedure involves surgically removing a neurostimulator device, including the electrode array and pulse generator, from the cranial nerve, such as the vagus nerve. This device was originally implanted to manage conditions like epilepsy or depression but may need removal due to various reasons.

Purpose

The purpose of this procedure is to address issues related to the neurostimulator, such as malfunction, infection, or when the device is no longer needed by the patient. The goal is to safely extract the implanted components and resolve any complications or discomfort caused by the device.

Indications

  • Malfunction or failure of the neurostimulator device
  • Infection at the implantation site
  • Persistent pain or discomfort
  • Reduction or cessation of symptom control
  • Decision to discontinue neurostimulation therapy

Preparation

  • Patients may be required to fast for several hours before the procedure.
  • Medication adjustments, particularly if the patient is on blood thinners.
  • Pre-procedure diagnostic tests such as blood work, imaging scans, or evaluations to confirm the necessity for removal.

Procedure Description

  1. The patient is positioned and given appropriate anesthesia to ensure comfort and pain control.
  2. The surgeon makes an incision at the site of the implant, usually near the clavicle and neck where the electrode array is positioned.
  3. The electrode array and pulse generator are carefully extracted, taking care to avoid damage to the surrounding tissues and nerves.
  4. Incisions are closed with sutures or staples, and a sterile dressing is applied.

Duration

The procedure typically takes 1 to 2 hours, depending on the complexity of the removal.

Setting

The procedure is usually performed in a hospital operating room or an outpatient surgical center.

Personnel

  • Surgeon (usually a neurosurgeon or a specialized surgeon familiar with neurostimulator devices)
  • Anesthesiologist or nurse anesthetist
  • Surgical nurses and possibly a surgical technician

Risks and Complications

  • Infection
  • Bleeding
  • Nerve damage
  • Pain at the incision site
  • Adverse reactions to anesthesia
  • Incomplete removal of the device components

Benefits

  • Resolution of symptoms caused by the malfunctioning or problematic device
  • Reduced risk of infection or other complications associated with the implanted device
  • Improved comfort and quality of life for the patient

Recovery

  • Patients usually go home the same day or after an overnight observation.
  • Pain management typically involves over-the-counter pain relievers or prescribed medications.
  • Patients are advised to keep the surgical site clean and dry, follow specific care instructions, and attend follow-up appointments as directed.
  • Most patients can resume normal activities within a few weeks, with specific restrictions based on individual cases.

Alternatives

  • Reprogramming or adjusting the existing neurostimulator
  • Replacement of the pulse generator or electrode array instead of complete removal
  • Other medical treatments or therapies for the underlying condition (e.g., medication adjustments, alternative neuromodulation therapies)

Patient Experience

During the procedure, patients will be under anesthesia and should not feel any pain. Post-procedure, patients might experience mild to moderate pain at the surgical site, which can be managed with medications. Most patients report relief from the symptoms caused by the malfunctioning device within a short period, though some discomfort can be expected during the initial recovery phase.

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