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Deep Brain Stimulation (DBS)

A Treatment For Drug-Resistant Epilepsy

  • Af-Soomaali PDF
  • Español PDF
  • Tiếng Việt PDF

What is DBS?

  • Deep Brain Stimulation (DBS) uses a small medical device that manages and treats seizures at their source. We implant the device in your child’s brain to reduce seizures and improve their quality of life.
  • DBS delivers controlled electrical stimulation directly to specific areas in your child’s brain. The device delivers stimulation to help control seizures.

Is DBS right for my child?

  • DBS is designed for patients whose seizures start on 1 side of the brain and then affect the entire brain (partial-onset seizures, with or without secondary generalization) and seizures that don’t respond to anti-seizure medicines.
  • We may recommend DBS in addition to seizure medicines (called adjunctive treatment).

What happens before surgery?

  • Your child’s provider will order a series of tests referred to as a Phase 1 evaluation. These tests are useful in learning about your child’s brain and seizures.
  • After Phase 1 testing is complete, your child’s provider will let you know if DBS is a good treatment option for your child.

How is this device implanted?

  • We implant the DBS device and wires in an operating room in a 2-step process. We will give your child medicine (anesthesia), so they are fully asleep during the surgery.
  • We place the DBS device under your child’s skin in the upper chest or abdomen. You cannot see the device after it is implanted.
  • The neurosurgeon then makes a small hole in your child’s skull. We place small electrodes through this hole into the target area in the brain. We pass a tiny wire under the neck skin and scalp, then connect the DBS device to the brain electrodes.

What happens after surgery?

Your child will stay in the hospital for up to 2 days and then return home.

Programming Phase:

  • A few weeks after surgery, a doctor who specializes in epilepsy (epileptologist) will turn the device on and adjust the stimulation settings. 
  • We program the device with a small computer tablet.
  • It will take several clinic visits to program the device settings and find the right setting for your child.
  • Your child’s provider will monitor how your child is doing very closely.

How do I use the patient programmer?

The patient programmer is a device like a smartphone. With help from your child’s provider, this programmer will allow you to:

  • Turn the device on and off 
  • Track seizures
  • Adjust stimulation at home
  • Check the device’s battery
  • Turn it off for MRIs (magnetic resonance imaging)

What are potential side effects?

Your child may:

  • Feel numb or tingling in their head
  • Feel dizzy
  • Have mood changes
  • Have trouble sleeping
  • Have memory problems
  • Have an increase in seizures

Are there safety issues?

This implanted device affects the ability to safely have an MRI. If your child needs an MRI, a provider needs to program the DBS device into a protective mode. Please call your child’s epilepsy provider before your child gets an MRI.

Where can I get more information?

You can read more:

  • Deep Brain Stimulation (DBS) – Epilepsy Foundation
    epilepsy.com/learn/treating-seizures-and-epilepsy/devices/deep-brainstimulation-dbs
  • DBS Therapy for Epilepsy - Medtronic
    medtronic.com/content/dam/medtroniccom/global/Patients/Documents/dbs-epilepsy-patient-brochure.pdf

To Learn More

  • Neurosciences Center
    206-987-2078
  • Ask your child’s healthcare provider
  • seattlechildrens.org/patient-education

Free Interpreter Services

  • In the hospital, ask your nurse.
  • From outside the hospital, call the toll-free Family Interpreting Line, 1-866-583-1527. Tell the interpreter the name or extension you need.
Seattle Children's Hospital

Seattle Children’s offers free interpreter services for patients, family members and legal representatives who are deaf or hard of hearing or speak a language other than English. Seattle Children’s will make this information available in alternate formats upon request. Call the Family Resource Center at 206-987-2201. This handout has been reviewed by clinical staff at Seattle Children’s. However, your needs are unique. Before you act or rely upon this information, please talk with your healthcare provider.

© 2026 Seattle Children’s, Seattle, Washington. All rights reserved.

07/01/2025
PE3703
Patient and Family Education | Neurosciences Center

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