Introduction
Epilepsy is a neurological disorder that targets 1 in 100 people in North America. Epilepsy is one of very few diseases without a definite cure. In fact scientists to this day cannot figure out what triggers these seizures. This is quite amazing considering the modern technologies medicine uses today. Throughout my paper I will explain what epilepsy is and what happens during an epileptic seizure, I will cover the different categories of seizures, how doctors diagnose epilepsy, and different types of treatment to help the patients with epilepsy.
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What is epilepsy?
Epilepsy is a neurological disorder that attacks the nervous system. Another term for epilepsy is “seizure disorder” (www.epilepsy.com). To this day the exact factor that triggers an epileptic seizure is unknown. In other words epileptic seizures are idiopathic (Ogden, 2005). Seizures occur when too many brain cells get excited at the same time. A seizure is like an electrical storm in your brain. During this electrical storm your brain cannot perform its usual tasks, causing sudden changes in behaviour, sensations, movement, and awareness (www.epilepsysociety.org.uk). A typical seizure usually last between a few seconds, to a few minutes. Once the seizure is finished the victim enters a “post-ictal period. (The greek word “post” meaning “after”, and the Greek work “ictal” meaning “seizure” [http://www.behindthename.com]). During this post-ictal period, which can last from seconds to hours, the brain begins recovering, and the victim’s awareness will gradually increase. It is common to experience confusion and drowsiness during this phase.
Diagnosis
Epilepsy is the conditions of having spontaneous seizures. This means having one seizure is not enough to be diagnosed with epilepsy, there must be two or more. To be considered an epileptic seizure the seizure must occur spontaneously, without a direct factor (www.epilepsy.com). Doctors use three main ways to diagnose epilepsy.
Neurological History – Doctors must be given specific description of previous seizures in the past. Such as; how long they lasted, what were you doing when the seizure occurred, what was your body’s behaviour/feeling before the seizure took place, and your body’s behaviour after the seizure ended (www.modernmedicine.com) People who suffer from having seizures do not remember what happens while a seizure takes place. That being said a description from a witness to your seizures could be very beneficial (www.epilepsyfoundation.org).
Electroencephalograph – An electroencephalograph or an EEG is the most common tool used to diagnose epilepsy. An EEG measures the electrical signals passed from one neuron to another within the brain (www.epilepsyfoundation.org) ( see image 1).
To measure these electrical signals doctors attach wires, known as electrodes, on the patients scalp (www.chp.edu). During an EEG no electricity is taken from the patient’s brain, and no electricity is injected into the patients brain. The EEG simply measures the electrical current travelling through the patient’s brain.
Magnetic Resonance Imaging – a magnetic resonance imaging or MRI is a procedure used to create detailed images of the damaged area of your body. When diagnosing epilepsy an MRI can show damaged regions of your frontal lobe. (see figure 2) Wu XingXiaovi WangFangfang Xie Weihua, L. (2013) An MRI is done by using a large field of radio waves. An MRI is much more effective than an EEG, the neuron images created from an MRI shows exactly where the damaged area of the brain is (Robert F. LaPrade) From there procedures can made to repair or remove the damaged section of the frontal lobe that is causing epileptic seizures.
Types of Epileptic Seizures
Epileptic seizures are a very broad term. When diagnosing the type of epileptic seizures doctors categorize in two main categories; partial seizures, and primary generalized seizures. Within these two main categories there are more specific types of seizures (Stephen C. Schachter).
The first category is “primary generalized seizures”. When a primary generalized seizure takes place both sides of the brain are affected at once, with a large amount of electrical discharge at the same time. The body is then accompanied by sudden movements, loss of awareness, or loss of consciousness. There are three types of primary generalized seizures:
Clonic seizure (Grand Mal) – This type of seizure that most people visualize when they hear the word “seizure”. When a clonic seizure takes place the victim will stiffen and lose consciousness. – This is the “tonic phase”. The tonic phase usually lasts from thirty seconds, to a couple minutes (www.hopkinsmedicine.org). Next the body’s muscles then start to contract and back will begin to arch, and elbows and legs will start the flex. The last phase of the clonic seizure is jerking. The victim will lose all control of their body and will begin to jerk uncontrollably, this phase usually lasts around two or three minutes (www.nlm.nih.gov).
Absence seizures (Petit Mal) – Absence seizures disconnect the victim from the world for a matter of a few seconds. This type of seizure is triggered from abnormal activity in the brain. Absence seizures occur mostly in children (www.epilepsy.com). There are two types of absence; Simple absence seizures, and Complex absence seizures.
Simple Absence seizure – Usually last ten seconds or less. During these ten seconds the person “zones out” or stares off into the distance. This type of seizure is very difficult to diagnose (www.mayoclinic.org).
Complex absence seizures – Usually lasts twenty seconds or less. During this time period then victim will “zone out” but will also be doing some sort of movement, such as; chewing, blinking, hand motions, or rubbing their fingers. (www.epilepsy.com).
Myoclonic seizures – A myoclonic seizure is very brief, only lasting a matter of seconds. During this few seconds both sides of your body has sudden jerks at exactly the same time. During a myoclonic seizure the patient does not lose consciousness and does not have any memory loss (Orrin Devinsky, 7/2013). A myoclonic seizure can be compared to being in contact with a single jolt of electricity, sudden hiccups, or the jolt of waking up from sleep state very quickly (www.hopkinsmedicine.org) (Orrin Devinsky, 7/2013). Like absence seizures, myoclonic seizures are hard to diagnose and usually over looked because the seizures are so brief.
The second category is “partial seizures”. When partial seizure takes place there is a large amount of electrical discharge in a certain area of the brain (Mary Ellen Ellis, July 25, 2012). Since only a specific location of the brain is effected, only a specific location of the body will be effected, depending on the location of the seizure in the brain. There are two types of partial seizures; Complex partial seizures, and simple partial seizures.
Simple partial seizures: A typical simple partial seizure usually last between 30 seconds to two minutes (emedicine.medscape.com). When a patient has a simple partial seizure they are fully awake, alert, and able to interact with peers around them. The patient might lose one of their senses temporarily, be unable to move one of their fingers, or even stiffen one of their body parts (www.epilepsy.com). For the seizure to be considered a “simple partial seizure” memory, awareness, and consciousness must be preserved.
Complex partial seizure – Similar to simple partial seizures, a complex partial seizure typically last between 30 seconds and two minutes (emedicine.medscape.com). During a complex partial seizure there are symptoms known as automatisms. Automatisms consist of lip-smacking, chewing, walking or pacing back and forth, swallowing, patting or fumbling (emedicine.medscape.com). A main difference between the two types of partial seizures is; consciousness, awareness, or memory is impaired.
Unlike primary generalized seizures, partial seizures usually have a warning sign to inform the patient a seizure is near. This warning sign is called an “aura” (Columbia University, P. (2013)). An aura usually takes place a few seconds, or a few minutes before the seizure occurs. Aura’s can come in many different ways, such as; numbness, headaches, being light-headed, upset stomach, dizziness, the sensation of fear, forced thinking, abnormal sensations, or unusual tingle in a certain area of your body. When an epileptic patient senses one or more of these symptoms there is high probability a partial seizure will be soon to follow (William H. Blahd, Jr, August 25, 2011).
Types of Epileptic Treatment
The most common type of epileptic treatment is anti-epileptic drugs or AEG’s. With over twenty different choices seventy percent of epileptic patients choose anti-epileptic drugs. Although these medications to not cure epilepsy, it only suppresses the seizures (see figure #3, located on the top of the next page) (www.webmd.com). The way this medication works is by lowering the amount of electricity each neuron passes in the brain. This type of treatment is very useful in cases of generalized seizures. The only down fall from using anti-epileptic drugs is the side effects and because the medication acts on the brain and the body there is numerous side effects. The main four side effects are headaches, balancing troubles, more difficult to focus your eyes, and trouble thinking properly. This medication is not guaranteed to work; in some cases patients experience both seizures and side effects. When this occurs a new treatment is needed. This can be a switch to a different anti-epileptic drug or a non-medicated treatment (Juan G Ochoa, Selim R Benbadis). If a patient does not have a seizure for two years and shows no sign of epilepsy on an EEG the doctor will slowly begin to ease off the medication. (FAULKNER M. A. (2014))
The other option of treatment for patients with epilepsy is the non-pharmaceutical route. Although anti-epileptic drugs have the highest success rate, non-medicated treatment has substantial research to support it (www.epilepsyontario.org). Brain surgery is the most common non-medicated treatment; the only issue with brain surgery is that it only works for partial seizures. The reason why is only works on partial seizures is because doctors can locate the specific area of the brain and remove sections of it. On grand mal seizures both hemispheres are triggered at the same time, in order to fix the epileptic problems doctors would have to remove too much of the brain, the patient would not live (www.epilepsyontario.org). New research always shows diet can be very beneficial; his is called the ketogenic diet. Its takes a lot of commitments considering no sweets or treats are allowed and 80 percent of the diet must be fatty foods, but low in carbohydrates. The ketogenic diet has success rates from 30 percent up to 50 percent (www.epilepsyontario.com).
Further research
Epilepsy has become more and more common in the past 20 years. Now that it has become more common scientists all over the world are beginning to test for a cure, weather that is a new class of medicine, gene therapy, or a non-medicated cure. The newest research for curing epilepsy is gene therapy. In 2009 scientist were able to figure out that the gene for epilepsy is located on chromosome 15 also known as “15q13.3”. (www.sciencedaily.com). With this knowledge and the proper technologies scientists can inject a virus containing the normal gene into chromosome where the epileptic mutation is. From there the normal gene will splice into the DNA strand, fixing the abnormal gene. In result epilepsy will be cured from the patient, and when they reproduce they can pass on a normal gene to their children. With this being said we can potentially remove epilepsy from our society. So far scientists have been able to cure rats with epilepsy using gene therapy, and now they have also been successful in Border Collie dogs. (Keijiro MizukamiAkira Yabukihye-Sook ChangUddin, M.) Another example of further research is new drug classes for epilepsy that are advancing each year. A good example of this is: September 2013 a new epileptic drug called Perampanel was released in United States. This new drug showed up to 35 percent more responsive outcomes than any other drug on the market. (www.ncbi.nlm.nih.gov). The only factor that is holding science back from curing epilepsy is funding. There is not enough funding going into epilepsy research. With the proper amount of Government funding or public donations epilepsy would be cured within the matter of five years from now.
Physiological Issues with Epileptic patients
Epilepsy does not affect the patient only physically, but also mentally and emotionally. Patients who suffer from epilepsy also have to deal with low self-esteem. Low self-esteem and epilepsy go hand and hand because patients with epilepsy are afraid of going out in public, or even doing the normal day to day things because the thought of having a seizure in public. (Ogden, 2005) It is extremely embarrassing for a patient suffering from epilepsy to have a seizure in front of their friends, family, or even strangers. Another emotional barrier that is part of suffering from epilepsy is the thought of never getting a driver’s license. Not getting a driver’s license makes everything in a normal adult life difficult. From getting to work, or getting groceries, or any sort of transportation. In some cases epilepsy makes the patient one hundred percent dependent on other people.
Conclusion
Life with epilepsy makes any day to day task more difficult. Epilepsy has impacted millions of people in a negative manner but further research is getting close to a cure, by using gene therapy research, and finding new classes of medicine. With the proper funding from the government epileptic medicine will continue to grow and be redefined. The research going into epilepsy is constantly growing, at this rate epilepsy will have a definite cure within the next decade, and using gene therapy epilepsy will also be removed from our society all together, allowing everyone to live epileptic free.
Resources
http://www.behindthename.com/names/usage/greek-mythology
http://epilepsy.com/learn/epilepsy-101/what-epilepsy
Ogden, 2005
http://www.epilepsysociety.org.uk/what-epilepsy#.UzXDJPnIZ5V
http://www.professinals.epilepsy.com/page/after_ab_pos
http://www.epilepsyfoundation.org/aboutepilepsy
http://cedars-sinai.edu/Patients/Programs-and-Services/Epilepsy-Program/Diagnosing-Epilepsy/
http://www.modernmedicine.com/modern-medicine/news/neurological-assessment-refresher
http://web.a.ebscohost.com/ehost/detail?vid=11&sid=467a451f-9d21-4962-a627-675ecbe6d893%40sessionmgr4004&hid=4204&bdata=JnNpdGU9ZWhvc3QtbGl2ZQ%3d%3d#db=aqh&AN=94116054
http://web.a.ebscohost.com/ehost/detail?vid=3&sid=867d5b74-4a00-46de-86e1-686c17975c83%40sessionmgr4003&hid=4112&bdata=JnNpdGU9ZWhvc3QtbGl2ZQ%3d%3d#db=aqh&AN=85968889
Figure 2 – http://www.webmd.com/epilepsy/seizure-mri
http://www.epilepsy.com/learn/types-seizures http://www.hopkinsmedicine.org
http://nlm.nih.gov/medlineplus/ency/article/000695
http://epilepsy.com/learn/types-seizures/absense-seizures
http://mayoclinic.org/diseases-conditions/petit-mal-seizure/basics/definition/con-20021252
http://www.epilepsy.com/learn/types-seizures/myoclonic-seizures http://www.hopkinsmedicine.org/neurology_neurosurgery/specialty_areas/epilepsy/seizures/types/myoclinc-seizures.html
http://emedicine.medscape.com/article/1183962-overview
http://emedicine.medscape.com/article/1183853-overview
http://web.b.ebscohost.com/ehost/detail?vid=4&sid=e018e8f4-ed9b-4c77-929f-f00e8685f286%40sessionmgr115&hid=103&bdata=JnNpdGU9ZWhvc3QtbGl2ZQ%3d%3d#db=khh&AN=39005165 (EBSCO #3)
http://www.webmd.com/epilepsy/aura-and-seizures
http://www.webmd.com/epilepsy/aura-and-seizures  William H. Blahd, Jr
http://web.a.ebscohost.com/ehost/imageQuickView?sid=b73438ba-bb51-48e9-9b98-e729f8f2a7e9@sessionmgr4005&vid=5&ui=16088672&id=59600950&parentui=59600950&tag=AN&db=aqh  Image #3
http://www.emedicine.medscape.com/article/1187334-overview  Juan G Ochoa, Selim R Benbadis
http://epilepsyontario.org/non-pharmaceutical-treatments/
http://web.b.ebscohost.com/ehost/detail?vid=4&sid=b0940d9f-1c3e-465e-af24-23be73f63bc7%40sessionmgr110&hid=122&bdata=JnNpdGU9ZWhvc3QtbGl2ZQ%3d%3d#db=aqh&AN=15877590 http://www.sciencedaily.com/releases/2009/01/090114075919.htm
http://web.a.ebscohost.com/ehost/detail?vid=3&sid=d6e55ff9-b6e5-4a6d-ab81-7e59cc92f267%40sessionmgr4001&hid=4209&bdata=JnNpdGU9ZWhvc3QtbGl2ZQ%3d%3d#db=aqh&AN=95333447
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