North American Neuromodulation Society
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  • About
    • Leadership >
      • Call for Board Applications
    • Diversity, Equity, and Inclusion
    • International Neuromodulation Society
    • Institue of Neuromodulation >
      • ION Leadership
      • ION Projects
      • ION Publications
    • History >
      • Past Presidents
      • Past Award Recipients
    • Staff
  • Advocacy
    • News
    • Sign Up for Email
  • Annual Meeting
    • Registration
    • Hotel & Travel
    • For Exhibitors
    • For Faculty
    • Preliminary Program
    • CME and Accreditation
    • Receptions
    • Submit a Case: My Own Worst Complications >
      • For Attendings
      • For Fellows and Early Career Neuromodulators
    • Cadaver Lab >
      • Pain Cadaver Lab
      • Neurosurgery and Neurology Cadaver Lab
    • Abstracts
    • Apply for an Award or Grant
    • FAQ
  • Education & Events
    • Calendar of Events
    • Upcoming Webinars
    • Recorded Webinars
  • Membership
    • Member Login
    • Join
    • Benefits
    • Neuromodulation Journal
    • Get Involved >
      • Advanced Practice Providers
      • Diversity and Outreach Committee
      • Resident, Fellows, Students/Young Neuromodulators Committee
      • Women in Neuromodulation
    • Member Spotlight
    • Membership Assistance
  • For Patients
    • Deep Brain Stimulation
    • Drug Delivery
    • Neuroprosthetics
    • Peripheral Nerve Stimulation
    • Spinal Cord Stimulation

Implantation

Spinal Cord Stimulation
Non-Addictive Treatment
The Trial Period
Recovery
Following a successful trial, a specialist will insert the permanent device in an out-patient procedure (lasting 30-90 minutes), sometimes with sedation or general anesthesia. In a numbed area, the electrode lead is surgically implanted into the epidural space in the spine. Then, the generator or receiver is connected to the electrode lead and is surgically implanted nearby, usually in the upper buttock/back, upper chest wall, or abdominal wall area. During the procedure, the patient may be awakened for pain level feedback so that small adjustments can be made to ensure the stimulation is targeting the areas where pain is transmitted to provide optimal pain relief. Following the implantation, patients learn to use the handheld stimulator controller that turns the energy level up and down similar to a television remote controller to adjust the stimulation level.
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