Epilepsy Surgery

Surgery for epilepsy is advancing all the time, with new techniques, new equipment and an increasing number of surgeons interested in this area of epilepsy treatment. The result has been a steadily growing number of people undergoing this surgery and many of those people going on to enjoy a much better quality of life.

BrainThe success of modern surgery for epilepsy has caused a widespread interest in this type of treatment, with people seeing an operation as preferable to a lifetime on medication. However, only a small number of people with epilepsy are suitable for surgery and, even for those that are, there are no guarantees of success.

This page looks briefly at some aspects of surgery as a possible treatment for epilepsy.

Suitability

The first thing a doctor has to establish when considering surgery as an option is to establish the patients suitability. Will surgery be possible and, if so, will it be beneficial?

There are a number of different types of surgery for epilepsy but the most common is the removal of a small part of the brain which is the underlying cause of the epilepsy; the focus. During this type of surgery, the more tissue that is removed the higher the risk to the patient. Therefore, only those patients whose seizures consistently begin in one small area of the brain are suitable for surgery. Sadly, this means that for the many people with epilepsy whose condition cannot be traced to a specific area of damaged tissue, surgery is not currently an option.

Another consideration is the nature of the person’s epilepsy. Surgery is always a risk so the benefits have to be significant. For this reason, doctors tend to only recommend those patients whose epilepsy has a very negative impact on their lives. These tend to be people who still have regular seizures despite trying a variety of medication. The doctor will want to know that surgery will greatly improve seizure control.

It is the quality of a person’s life that will be a main factor in the decision. In some people, a relatively small number of seizures can have a dramatic impact on their lives while others can tolerate a much higher number of seizures without it significantly affecting their well being.

This decision is only the first step in what can be a long and frustrating journey.

Pre-surgery tests

Because the surgeon will be removing a part of the brain, it is vital that as much as possible is known about the patient’s brain and their epilepsy before surgery takes place. After many tests the patient needs to be aware that they could then be told that surgery is not possible - not an easy thing to accept after hoping for change.

While most people with epilepsy will have had a standard EEG test, they will be asked to go into hospital for a much more detailed version. The aim is to study the person having several seizures while the EEG is connected. This usually involves coming off medication and having the EEG continually recorded, sometimes for several days. In some instances, the surgeon may have to insert special electrodes onto the surface of the brain itself, although this is only done in a small number of cases. This involves using natural holes in the skull or having to create them. Throughout this type of test the patient receives a great deal of support and help from the hospital staff.

The surgeon will also want to have an up-to-date image of the patient’s brain and this means having an MRI scan (magnetic resonance imaging). This machine creates a picture of the brain which put together with the results from the EEG often enables the surgeon to pinpoint the exact part of the brain which is causing the epilepsy.

These tests will need to show that a single area of only one side of the brain is causing seizures. Some functions of the brain are shared by both sides of the brain, so removing one part on one side does not usually lead to a loss of that function. However, other functions are controlled only by one side of the brain, and the surgeon will need to be confident that these areas are not going to be damaged during any operation.

A new test, recenently developed is DTI (diffusion tensor imaging). This measures the actual movement of water in the brain, detecting areas where the flow of water is disrupted. DTI is in very early stages of development but offers an alternative investigatory method in cases where an MRI scan does not detect any abnormalities.

Other tests include PET (positron emission tomography) and SPET (single positron emission tomography), which involve injecting tiny traces of radio active substances into the body and watching which part of the brain they reach.

Other tests are undertaken, for example functions like memory are tested. This can involve the Wada Test or the Carotid Amytal Test and involves anaesthatising half of the brain and can be quite an ordeal for the patient.

All of these tests can be worrying or distressing for the patient, but the medical teams offer a great deal of help and support throughout.

After the tests the doctors will know whether an operation is the right way forward, offering the patient the best option for the future.

The assessment of any risks will be undertaken extremely carefully and will be discussed with the patient.

The operation

The type of surgery that a patient undergoes will depend greatly on what the surgeon hopes to achieve. The following is a list of some operations:

  • Selective amygdalo hippocampectomy - the removal of two structures in the temporal lobe which are commonly the site of seizure activity. Sometimes just the hippocampus part of the structure is removed.
  • Temporal lobectomy - a larger part of the temporal lobe is removed. This tends to be mainly the right side as the left side of the temporal lobe controls speech.
  • Sub-pial resection - fine cuts are made in the motor areas of the brain that do not affect the motor function but do prevent the spread of seizures.
  • Hemispherectomy - sometimes used to treat very severe epilepsy in children with damage to one whole side of the brain. The damaged side of the brain is removed.
  • Corpus callosotomy - again sometimes used to treat children with very severe epilepsy, this operation involves cutting the fibres that connect the two halves of the brain.
  • Removal of a lesion such as a tumour or a cyst.

 

After surgery

Despite the lengthy and very difficult nature of brain surgery, most patients make a rapid recovery and are usually up and about within a couple of days. Between eight and fifteen weeks later, most people are able to return to work. Some aspects, like waiting for the nerves that supply sensation to the skull, may take some time to recover.

The results

Some people may experience seizures just after the operation due to temporary swelling. This does not mean that the operation has failed.

Depending on the person’s own doctor, it may be some time before the patient can start reducing their medication. However, many patients notice a dramatic reduction in the number of seizures, many finding that their seizures appear to have stopped. They can then look at reducing or stopping their medication in consultation with their doctor.

One consequence of successful surgery that may surprise some people is the difficulty in coming to terms with life without seizures. Emotional reactions to this life change are common and can include quite severe temporary depression. Friends and family can also find it difficult to adjust to the person’s new found independence. This type of reaction will depend on how long the person has had epilepsy prior to having surgery.

As with most surgical techniques, there are no guarantees. Epilepsy surgery is no exception and a small number of people will find that surgery has not helped.

Further information on epilepsy surgery is available from Epilepsy Action by using the Email Helpline or if you live in the UK, by phoning the Freephone Helpline on 0808 800 5050.

 

Date last updated: 21 December 2007


We can provide references and information on the source material we use to write our epilepsy advice and information pages. Please contact our Epilepsy Helpline by email at helpline@epilepsy.org.uk.

Comments

I am 51 an I had a surgery to remove a cavernous hemangioma in the right temporal lobe of my brain which was causing epilepsy, two years and a half ago. I was having simple and complex partial seizures and occasionnaly absences.
Medication was not controlling my condition and my memory was getting poorer and poorer. I had to take a leave of absence from my work of Occupational therapist.

I had a MRI and WADA test before the surgery. Since that time I am seizure free. The neurologist reduced a lot my medication. And, what is wonderful, my memory got a lot better. I still have problem learning new things, but I remember what I did yesterday. And I can read a novel and remember what I read the day before, what I could not anymore before the surgery.
I am back to work. It is still hard, but I cope.

I had temprol lobe surgery nearly four years ago now due to my epilepsy and although my daytime siezures have improved 90% I now suffer from nocturnal siezures although they are only happening approx every 6 weeks or so.I am still on 1600mg daily of epi medication and also 1000mg of painkillers as I suffer from a constant headaches from the time I get up to the the time I go to bed.My GP has told me to face it, I will never work again which unfortunatly prompted me to have realy negative thoughts and I am now having to take antidepressants as well.My consultant says she intends to change my medication soon,to what I dont know?but unfortunatly I have started to rapidly loose weight recently so she wants my GP to carry out varios tests fo that before any decision is made.I am due yet another MRI scan in the next few weeks touch wood nothing shows out of order.

My son who is 15 has had surgery 2 weeks ago having found a lesion so far no fits was having 20 plus per day. Is now able to hold a conversation and follow what everyone is saying hopefully will go from strenth to strenth.

Had Right Temporal Lobectomy 7 years ago, had 1 seizure in post operation period before reducing medication and coming off it completely having had no seizures since.
you can read full story via www.justgiving.com/anthonywilliamsway and see for yourself how much it has improved my life.

I am so glad to read your story I have been looking for someone to talk to that has had the surgery I am looking at. I am 27 years old and I have a right temporal lobe hemangioma that causes complex partial seizures and in the past 3 years has caused a few GradMal seizures, the surgery frightens me and I am just scared of coming out of the surgery still having seizures or having memory loss or personality changes. Do you feel like you made the right decision having the surgery and would you have done it at my age if you were given the option?
Thanks for your time.

Hi I had my surgery just one and a half months before my 29th birthday and I've never looked back, also I know people as old as 40 when they had their surgery who have also never looked back so in my opinion your at the perfect age.
Right from the start of my 20s life as you've read about was a complete disaster, no employment, constant seizures, couldn't go out on my own etc, etc.
Now I have a good job, lots of friends, no seizures and even my own house which I've completely funded myself which at one time was something I never thought I'd ever have so yes a complete turnaround.
If there is anything I can do to help you please do stay in touch.
Anthony

My son, who is 15 now, has Sturge Weber Syndrome and at 2 and a half had a full right hemispherectomy due to the severe nature of his seizures. We have never looked back. Admittedly he has lost the use of his left arm (but great at putting on socks with one hand!) and his left side is a bit weaker, but he is doing really well. Due to his condition he does have learning difficulties, but is doing extremely well in his special school and having a go at 4 GCSEs. We never thought that would be the case as he could not talk until after the operation or walk. It has been a long journey, but he's learning to play the drums with one arm, has had two girlfriends already and wants to work with children! The operation for us, although risky, was the best for his future quality of life and if anyone reading this has a young child with Sturge Weber and their epilepsy is not under control, don't be afraid to find out all the options. For us, having the surgery as young as he did, meant he can't remember and has a great and happy quality of life.

I disagree with the part about post surgery depression due to their reasons...My post surgery was due to my inability to concentrate, my short term memory deficits, my inability to control my emotions, my inability to learn new things, etc. My IQ also was reduced 10 points. Until you have expierenced before and after...you couldn't imagine how those little things make such an enormous difference in day to day living. I will never alow my head to be worked on ever again, no matter what the problem....sad to say. -Mike