Place Your Advertisement Here
 
UPDATED: Thu, 11/08/2007 - 12:12am

  • Epilepsy First Aid
  • Seizure Medication
  • Animation of a Seizure
  • Seizure Diary
  • Find a Doctor
  • Epilepsy Centers
  • Clinical Trials
  • Event Calendar

Place Your Advertisement Here

Vagus Nerve Stimulation

Vagus nerve stimulation (VNS) is designed to prevent seizures by sending regular, mild pulses of electrical energy to the brain via the vagus nerve. These pulses are supplied by a device something like a pacemaker.

The VNS device is sometimes referred to as a "pacemaker for the brain." It is placed under the skin on the chest wall and a wire runs from it to the vagus nerve in the neck.

The vagus nerve is part of the autonomic nervous system, which controls functions of the body that are not under voluntary control, such as the heart rate. The vagus nerve passes through the neck as it travels between the chest and abdomen and the lower part of the brain.

What is the surgery like?

The surgeon first makes an incision along the outer side of the chest on the left side, and the device is implanted under the skin. Then a second incision is made horizontally in the lower neck, along a crease of skin, and the wire from the stimulator is wound around the vagus nerve in the left side of the neck. The brain itself is not involved in the surgery.

The device (also called an implant) is a flat, round battery, about the size of a silver dollar—that is, about an inch and a half (4 cm) across—and 10 to 13 millimeters thick, depending on the model used. Newer models may be somewhat smaller.

The procedure usually lasts about 50 to 90 minutes with the patient under general anesthesia. Sometimes a hospital stay of one night is required. Some surgeons have performed the procedure with local anesthesia and the patient has been discharged the same day.

How is VNS used?

The neurologist programs the strength and timing of the impulses according to each patient's individual needs. The settings can be programmed and changed without entering the body, just by using a programming wand connected to a laptop computer.

For all patients, the device is programmed to go on for a certain period (for example, 7 seconds or 30 seconds) and then to go off for another period (for example, 14 seconds or 5 minutes). The device runs continuously, usually with 30 seconds of stimulation alternating with 5 minutes of no stimulation. The patient is usually not aware that it's operating.

Holding a special magnet near the implanted device causes the device to become active outside of the programmed interval. For people with warnings (auras) before their seizures, activating the stimulator with the magnet when the warning occurs may help to stop the seizure. Many patients without auras also experience improved seizure control, however.

Settings (also called stimulation parameters) set by the neurologist typically include a stimulation amplitude of 1.0 to 3.0 mA (milliamperes), a stimulation frequency of 30 Hz (hertz), and a pulse width of 500 microseconds. By adjusting these settings, the doctor not only may be able to control more of the patient's seizures, but often can also relieve side effects. One study, for instance, found that changing the pulse width eliminated pain that some patients were experiencing.

The battery for the stimulator lasts approximately 5-10 years.

Resources

The VNS implant devices are built by Cyberonics, Inc. Additional information for patients and physicians is available at their website (www.cyberonics.com).

Topic Editor: Steven C. Schachter, M.D.
Last Reviewed:12/15/06


This content is user-generated. Content is not monitored nor consistently reviewed by the epilepsy.com Editorial Board. Epilepsy.com therefore cannot guarantee the accuracy of any content edited with the Wiki sections. While epilepsy.com, the Epilepsy Therapy Project, and its partners encourage visitor interaction and publishing within these sections, users should use caution when exploring content, especially as it pertains to health concerns. No content on epilepsy.com is intended to replace the care of a doctor. We encourage you to contact your own health care provider for individual medical advice. We cannot provide second opinions or make specific recommendations regarding therapy, nor does this Wiki content constitute a recommendation for any diagnosis or treatment options.




Title Posted
??  
debys
CDKL5 disorders  
cdkl5mum
newly diagnosed 9 month old  
widdletigger
Does this sound like seizure?? Delays??  
kaitlynsmom
Wondering about Kappra  
nanny53
sex drive  
rosegirl
So Overwhelming...  
SaBrinah_D
If I could change 1 thing on epilepsy.com it would be . . .  
kdredske
EPI_HELP (patty) is now calling all teeni-boppers and teenagers to get together.  
sophia_hill
Metformin and Epilepsy  
pan06
View all Forums

Title Page Views
my.epilepsy.com Updates  
epi_help
topamax and weight loss  
alexia mom
kepra  
brian mattingly
Possible cure for absence seizures  
pdl1
Epilepsy and marijuana  
cjad234
Sexual Side Effects  
George R
How exactly do aura's feel  
WendyBendy
MEDICAL ALERT I.D.'s  
picnupthepcs
Over 40 Different Types Of Seizures - Revised  
spiz
electrical shock in head?  
Maggie
View all Forums

Title Posted
AND OUR GUEST ARTIST TONIGHT IS . . .  
Adz
I just wanted to say . . .  
Adz
aggravation  
scratch
comp  
scratch
NOTHING MORE TO SAY?  
ROCKNROLL
Epilepsy takes everything away...  
thumper29
Transitions  
davita
Epilepsy and Bipolar Disorder  
thepenfairy
mothers  
davita
Input is welcome/More photos's (tables)  
woodland
View all Blogs

Title Page Views
Inspirational Quote - My Own Personal Inner Thoughts  
Butterflygrl
my partial complex seizures  
Zanna1211
Topomax... The Dreaded.........  
Dr Jason
Brain Zaps, tics & twitches  
JudiS
side effects of phenobarb.  
pksmom
Feeling Sick  
JBJ1984
Tegretol XR and ANXIETY meds  
Butterflygrl
How can you tell if a sleep seizure happens?  
epl_controller
Nonepileptic "Events" vs. "Seizures"  
teft
TYLENOL, AEDs & SEIZURES  
cmscribbles
View all Blogs

Title Posted
Along came a hurdle  
june03
My Epilepsy and effects on my life.  
Lovebuggs
My name is Dyanna & this is my story with Epilepsy  
dyanna
Emily's epilepsy story  
Lemondrop
SILENT BUT DEADLY...  
deonycewlk
Diagnosed of epilepsy,but reports seem normal.  
nitya
newly diagnosed  
AuntAnna
living with epilepsy..  
nareema
Mr  
elijahmuchiri
sEE52  
skohtz
View all Stories

Place Your Advertisement Here

What should the Epilepsy Therapy Project focus on as most important?

Helping scientists to develop new treatments for epilepsy.
51% (40 votes)
Providing information about the newest medications to doctors.
4% (3 votes)
Providing information about all treatments to patients and families.
32% (25 votes)
Adding more discussions and groups to the MyEpilepsy community
1% (1 vote)
Adding more videos to www.epilepsy.com
1% (1 vote)
Expanding the seizure and medication diary
4% (3 votes)
Adding more discussions to the MyEpilepsy community
8% (6 votes)
Total votes: 79

View results
View past poll results