Treatments

Diagnosing epilepsy and treating seizures successfully requires a team effort between you, your family and your health care team. It is important to consult with a Neurologist if you have epilepsy or seizures because a Neurologist is trained to care for people with neurological disorders.

For some people it may be easy to diagnose and control seizures and epilepsy. For others diagnosing and treating epilepsy may be difficult. When seizures and epilepsy are difficult to diagnose or when the person is not responding to standard therapy (medication), it is recommended to consult with a neurologist who specializes in epilepsy who is called an Epileptologist.

The following treatments are the most studied and commonly used in western medicine. There are many alternative treatments that may be of benefit to individuals living with epilepsy but the options listed below are the most researched, common types of seizure control.

 

To find a Neurologist or Epileptologist near you in Northern California please visit our ‘Resources’ tab.

 

Managing your Epilepsy:
Participating in your treatment and being an advocate for yourself can impact your results. We encourage you to do a few simple things to effectively participate and advocate for yourself.

  • Take your medicine on time, every day, exactly as prescribed by your doctor.
  • See a specialist if your seizures are not controlled.
  • Keep a health diary of seizures, test results, medications, and questions for your doctor.
  • Track your seizures.
  • Know your seizure triggers – For many people, sleep deprivation or stress can trigger seizure activity.
  • Create and share your own seizure action plan – Get your doctor’s input and share this with your employer, school, family and friends.


Specialized Treatment

You should ask for a referral to an epilepsy center if one of these statements is TRUE:

Statement

  1. Continue to have seizures despite treatment with two different seizure medications
  2. Take multiple seizure medications daily and have unacceptable side effects
  3. Need advanced testing to confirm the diagnosis of epilepsy or find another cause for symptoms
  4. Need a team approach to epilepsy and other medical conditions such as depression, learning disabilities, anxiety, or problems with memory or thinking
  5. Want to learn about non-medication treatments for seizures – the ketogenic diet, responsive neurostimulation, vagus nerve stimulator, epilepsy surgery, and other new therapies
  6. Have seizures secondary to genetic disorders or other rare diseases
  7. Are pregnant or want to learn more about effects of epilepsy and seizure medications on pregnancy and the developing baby
  8. Are interested in participating in clinical trials of new experimental medical or device treatments for seizures

Adopted from Guidelines for epilepsy care designation level: http://www.naec-epilepsy.org/documents/NAECBrochureinPDF.pdf.


Specific Medications

Most epilepsy medicines are taken by mouth. The doctor’s choice of which drug to prescribe depends on what kind of seizure a person is having. People react to medicines in different ways. Some experience side effects while others may not. Some people’s seizures will respond well to a particular drug, while someone else will have seizures that continue. It may take some time to find exactly the right dose of the right drug for each person with epilepsy.

Whenever possible, doctors try to prevent seizures with a single medication. This is called monotherapy. However, some people may require polytherapy, the use of more than one medication to achieve seizure control.When selecting a drug, your doctor will consider the type of seizures you have. Not all medications work for all types of seizures.

Like all drugs, epilepsy medicines have side effects. Some are dose-related, and become more likely as the dose increases. For a comprehensive list of anti-epileptic drugs please click here.

 

Surgery

When antiepileptic drugs fail to control or substantially reduce seizures, surgery on the brain may be considered. Although some of the techniques are recent, surgical removal of seizure-producing areas of the brain has been an accepted form of treatment for more than 50 years. Most surgical patients are adults who have fought long and unsuccessful battles for seizure control. However, children with severe seizures are also being treated with surgery.
Brain surgery can be a successful way of treating epilepsy. Surgery is most likely to be considered when someone with epilepsy:

  • Has documented epileptic seizures and not pseudoseizures.
  • Has already tried the standard medicines without success (or has bad reactions to them).
  • Has seizures that always start in just one part of the brain.
  • Has seizures in a part of the brain that can be removed without damaging important things like speech, memory or eyesight.

People who are going to have epilepsy surgery may have several tests first. In some cases, electrodes have to be implanted in a separate operation to locate seizure sites deep in the brain. Sometimes these tests take days or even weeks to complete.

 

Types of surgeries:

  • Craniotomy
  • Laser Ablation
  • Gamma knife

Afterwards some seizure medications may have to be continued usually for a year or two. Then if no further seizures occur the medicine may be slowly withdrawn. At this point, chances of living free of seizures and free of medication are good. However, many people will have to continue with medication and some do not benefit from surgery.

 

Vagal Nerve Stimulator  (Download Brochure)

Vagal nerve stimulation therapy is another form of treatment that may be tried when medications fail to stop seizures. It is currently approved for use in adults and children over the age of 12 who have partial seizures that resist control by other methods. The therapy is designed to prevent seizures, by sending regular small pulses of electrical energy to the brain via the vagal nerve, a large nerve in the neck.

The energy is delivered by a flat round battery about the size of a silver dollar, which is surgically implanted in the chest wall. Thin wires (electrodes) are threaded under the skin and wound around the vagal nerve in the neck. The battery is programmed by your health team to send a few seconds of electrical energy to the vagal nerve every few minutes. If the person with the system feels a seizure coming on, he or she can activate the discharge by passing a small magnet over the battery. In some people this has the effect of stopping the seizure. It is also possible to turn the device off by holding the magnet over it.

 

Responsive Neurostimulation (More Info)
Responsive neurostimulation is a new approach to treating medically uncontrolled partial onset seizures. The RNS® System is the first device to provide responsive neurostimulation, automatically monitoring brain signals and providing stimulation to abnormal electrical brain events just when it is needed. The system is approved by FDA as an adjunctive treatment for adults with medically refractory partial seizures that come from one or two seizure targets identified by your doctor. The RNS Neurostimulator is placed under the scalp and within the skull by a surgeon. One or two leads are then placed at the seizure target and connected to the neurostimulator. After the scalp heals, the neurostimulator should not be noticeable to others. The neurostimulator continuously monitors the brain’s activity and is programmed by the epilepsy doctor to detect and record specific patterns that could lead to a seizure. When these patterns are detected, the neurostimulator responds with brief pulses of stimulation intended to disrupt the abnormal brain activity before a seizure occurs. Detection and stimulation settings are individualized for each patient’s patterns and so that stimulation is not felt. In addition, each patient gets a take- home monitor so that brain activity data can be sent to the epilepsy doctor between office visits.

The RNS System is manufactured by NeuroPace, Inc.

 

Ketogenic Diet (Download Brochure)
Normally our bodies run on energy from glucose which we get from food. We can’t store large amounts of glucose because we only have about a 24-hour supply. When a child has no food for 24 hours — which is the way the diet begins usually in a hospital — he or she uses up all the stored glucose. With no more glucose to provide energy, the child’s body begins to burn stored fat.

The ketogenic diet keeps this process going. It forces the child’s body to burn fat round the clock by keeping calories low and making fat products the primary food that the child is getting. In fact, the diet gets most (80 percent) of its calories from fat. The rest comes from carbohydrates and protein. Each meal has about four times as much fat as protein or carbohydrates. The amount of food and liquid at each meal have to be carefully worked out and weighed for each person.

Doctors don’t know precisely why a diet that mimics starvation by burning fat for energy should prevent seizures, although this is being studied. Nor do they know why the same diet works for some children and not for others.

Trying to put a child on the diet without medical guidance puts a child at risk of serious consequences. Every step of the ketogenic diet process must be managed by an experienced treatment team usually based at a specialized medical center.

 

Making the Decision

Most experts say the diet is worth trying, when two or more medications have failed to control seizures, or when medications cause side effects that are having a harmful effect on a child’s life. It also helps to have a child who is willing to try foods that he might otherwise not be enthusiastic about, and is tolerant and not fussy about eating.

The diet seems to work for more than one kind of seizure, and for children who have a lot of seizures or a few seizures. But most doctors say it shouldn’t be used instead of medications, if the drugs are working and the child is not having bad side effects. Parents generally decide to try the diet because they hope it will give their child a better chance for a normal life.

However, the diet can be a barrier to some normal life experiences for children, especially those that revolve around food and holidays. And, like other treatments for epilepsy, it also can have side effects that affect some children more than others. So, as with any kind of treatment, there’s a lot to think about before deciding to try the diet.

Going over all the possibilities with your doctor is the best way to make the decision. It may also be helpful to talk with other parents whose children have been on the diet.