last authored: April 2012, David LaPierre
last reviewed:
A seizure is a "sudden excessive discharge of gray matter", or a disturbance of electrical activity in the brain. Clinical features depend on where seizure begins and where the signals propogate to.
Epilepsy is a cluster of symptoms characterized by recurrent, spontaneous, unprovoked seizures. It affects 0.5-2% of the population. It tends to begin in children and adults, though 10-20% of cases begin after age 20. People can have a number of different seizures as a part of their epilepsy, though tend to have either partial or generalized. Epilepsy syndromes show the presence of some seizures, along with other findings, but do not meet the criteria for epilepsy.
Generalized seizures are much more likely to begin during childhood, with partial seizures affecting adults.
People have an 8% lifetime chance of seizure, most being provoked. Important causes include:
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It is important to rule out:
Benign Rolandic epilepsy
onset from ages 4-10
focal seizure, related to sleep
appears to be inherited in an AD fasion, with very incomplete penetrance
EEG has characteristic findings
always outgrown
Primary (generalized) seizures begin in the thalamus and spread across the brain, while secondary (partial) seizures begin in the cortex. Complex partials are the most common type of seizure.
Focal, partial, or secondary seizures, have a focal onset from a cortical problem. There are four main types, which can occur together or at different points of time. Depending on where the specific area of focus is, very discrete symptoms can occur.
Generalized seizures have global onset in both hemispheres. The mechanism likely depends on a diffusely hyperexcitable cortex and complex interactions between thalamus and cortex, possibly involving calcium channels. Generalized seizures are more likely to be genetics based.
Febrile seizures normally begin between 6 months-6 years, and are associated with a rapid rise in temperature. In order to make the diagnosis, it is important to determine:
Absence seizures can be distinguished from partial seizures based on age of onset (young), duration (brief), an often high frequency, lack of postictal phase, automatisms, and EEG findings.
Seizure >30 minutes, or no recovery post-ictally.
Overall recurrence is about 50% by 2 years.
Almost 20% of patients with 'first seizure' have experienced an unrecognized or incorrectly diagnosed tonic-clonic seizure (King et al, 1998). This is very very important, as having two seizures leads to much higher likelihood of a third seizure (80-90%).
Almost 30% had a prior non-convulsive seizure but not sought medical attention.
Seizure itself
Children
Evaluating possibility of past seizures:
Cardiac causes:
Precipitants include:
Prodromal symptoms can include:
Post-ictal symptoms can include:
Medications
neurologic history is very important from both patient and witness
ABC's ?Cushing's triad
Temperature
Neuro exam
Tongue: evidence of biting
Cardiovascular
Skin
For an acute, unexplained seizure, perform an immediate glucose check. Other bloodwork may include:
Ensure neurological exam is normal before performing lumbar puncture for meningitis.
In follow-up, serum dilantin levels should be measured, along with CBC.
For simple febrile seizures, no diagnostic studies are routinely indicated.
EEG can be used to localize seizure foci. Interictal (non-clinical) waves can sometimes be seen
Neuroimaging is helpful for determining aetiology. MRI is vastly superior than CT (King et al, 1998).
ECG to evaluate cardiac reasons.
Treatments are first to prevent injury and preserve life. They also have a substantial psychosocial role: people want to know their seizures are being managed.
Patients should not drive until they are seizure-free for one year.
Fatigue and stress can precriptate seizures; patients should be supported to live a life that is relaxing. A ketogenic diet may be helpful in reducing seizure likelihood, though being high fat, and low sugar, they are often poorly tolerated. Alcohol consumption can lower the seizure threshold and also decrease anticonvulsant blood levels.
Patients should be advised to speak with a physician about taking new medications.
Patients and their families should be advised as to proper seizure care.
Place NPA to open airway. Suction airway.
Place patient on 100% O2 with nonrebreather; reassess need for BMV.
Obtain vascular access, and provide IV dextrose.
Identify and treat the source of the fever. Antipyretics such as acetaminophen can help reduce fever.
Seizures do not damage the brain unless they are prolonged - over 30 minutes or so. As such, there is little need to urgently provide medications if an acute seizure begins while in a clinical setting.
As warranted, benzodiazepines such as diazepam or lorazepam can be used to end seizures.
For status epilepticus, lorazepam, midazolam, phenytoin, phenobarbitol, or valproate may be used.
In actively seizing children, investigate and treat underlying cause.
There are 12-15 anticonvulsant drugs. These should be attempted ONE drug at a time, with as low a dose at a time.
There are no drugs that prevent the development of seizure foci, ie following trauma.
Affirm the importance of compliance; many people struggle with the side effects.
cortical resection of focus, corpus callostomy (for atonic seizures), hemisperectomy (but only really for kids who have serious seizures
vagal nerve stimulation
Frontal and temporal lobes are very epileptogenic; parietal and occipital lobes are much more resistant. Possible mechanisms include excess 'excitation', diminished inhibition (ie GABA), hypersynchrony.
Any insult to cortex can cause seizures, and these can manifest years later.
Over 50% of cases have no known cause. However, the following are known precipitants:
Damage does not need to be dramatic; it is believed that disruption of only four neurons can start a seizure (ref).
Over 60% of patients will never have another seizure. Approximately 30% will have other febrile seizures, 3% will have seizures without fever, and 2% will develop epilepsy.
King MA et al. 1998. Lancet.
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