Epilepsy and Other Causes of Seizure

last authored: April 2012, David LaPierre
last reviewed:

 

 

Introduction

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.

 

 

 

The Case of...

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Differential Diagnosis

People have an 8% lifetime chance of seizure, most being provoked. Important causes include:

  • epilepsy
  • brain tumours
  • intracranial hemorrhage
  • hippocampal sclerosis
  • cavernous angiomas and other vascular malformations
  • disorders of cortical development
  • evidence of remote trauma
  • eclampsia
  • inborn errors of metabolism

 

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

 

 

 

Types of Seizure

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.

  • Partial
  • Generalized

Focal/Partial Seizures

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.

 

simple partial motor seizure

  • no loss of consciousness
  • focal clonic jerks that can spread (Jacksonian march)
  • focal tonic (ie head turing, eye deviation)

 

simple partial sensory seizure

  • numbness or tingling (somatic cortex)
  • visual elementary shapes, colours (occipital)
  • auditory: elementary sounds (superior temporal lobe)
    • usually very stereotyped; more complex hallucinations suggests psychosis
  • olfactory, gustatory (medial temporal lobe)
  • multimodal experiential or 'psychic' (temporal lobe)

 

complex partial

  • usually affects temporal or frontal lobe
  • one of the most common
  • onset at any age
  • huge range of clinical expression
  • stop and stare: impaired awareness
  • memory loss
  • automatisms (lip smacking, chewing, verbal, complicated gestures
  • subcortical functions (walking, driving!) can continue during this loss of consciousness
  • typically last 1-2 minutes, but can last hours
  • often weird sensation beginning above epigastrium and traveling behind sternum

 

secondary generalized tonic-clonic

  • spead from localized area through limbic system to rest of cortex
  • often begins with "cry"
  • may have cyanosis
  • may or may not have aura
  • loss of consciousness
  • tonic - rigid; clonic - shaking
  • bilateral motor involvement with consciousness cannot be seizure, as if both hemispheres are seizing, LOC will occur
  • urinary incontience, tongue biting

Generalized

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 seizure

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:

  • no neurological abnormalities before or after (suggesting CNS infection)
  • no history of non-febrile seizures
  • typical: generalized tonic-clonic, less than 15 minutes duration, no recurrence in 24 hours
  • atypical: focal origin, more than 15 minutes duration, more than one in 24 hours

 

 

Absence

  • relatively unusual
  • childhood onset
  • brief periods (10-15s) with no warning
  • arrest of behaviour; simple automatisms (blinking) sometimes
  • no postictal phase
  • may have dozens per day
  • EEG shows characteristic "3 per second spike and wave"
  • can use calcium channel active anticonvulsants

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.

 

 

Generalized tonic-clonic

  • full-body flexion-contraction
  • onset in childhood or adolescence
  • interictal EEG can show generalized spike waves
  • can occur on its own or with other general seizure types

 

 

Myoclonic Seizures

  • brief lightening-like jerks
  • isolated or repetitive showers
  • can have "epileptic" and "nonepileptic" myoclonus; can occur with diverse clinical conditions
  • very complicated physiology
  • juvenile myoclonic seizures respond extremely well to valproic acid

 

 

Atonic Seizures

  • also called drop seizures, result from brief loss of muscle tone
  • short lasting - less than 15 seconds - with full recovery
  • begin in childhood and may persist

 

Status Epilepticus

Seizure >30 minutes, or no recovery post-ictally.

 

 

 

Evaluating First seizures

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.

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History and Physical Exam

  • history
  • physical exam

History

Seizure itself

  • duration
  • body parts affected, in which order
  • premonitory signs
  • neurological symptoms

Children

 

Evaluating possibility of past seizures:

  • ever chewed your tongue severely at night?
  • ever lost control of your bladder or bowels?
  • every woken up with a dislocated shoulder or compression fracture?

 

Cardiac causes:

  • family history
  • developmental delay in children

 

Precipitants include:

  • sleep deprivation
  • alcohol
  • drugs
  • TV screen
  • strobe light
  • emotional upset
  • head trauma
  • toxic exposure

Prodromal symptoms can include:

  • aura
  • smells

Post-ictal symptoms can include:

  • decreased level of consciousness
  • headache
  • sensory abnormalities
  • tongue pain
  • limb pain
  • Todd's paresis: if during the postictal phase they can't speak, it suggests the language centre is the area of focus

Medications

  • what medications are being used?
  • duration
  • compliance

 

neurologic history is very important from both patient and witness

 

Physical Exam

ABC's ?Cushing's triad

Temperature

 

Neuro exam

  • MMSE
  • cranial nerves
  • bulk, tone, strength
  • sensation
  • reflexes
  • cerebellar

Tongue: evidence of biting

Cardiovascular

  • carotid and cranial bruits

Skin

  • neurocutaneous syndromes: tuberous sclerosis, NF1

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Investigations

  • lab investigations
  • diagnostic imaging

Lab Investigations

For an acute, unexplained seizure, perform an immediate glucose check. Other bloodwork may include:

  • CBC (especially in pediatrics: hemolytic uremic syndrome)
  • electrolytes

Ensure neurological exam is normal before performing lumbar puncture for meningitis.

 

In follow-up, serum dilantin levels should be measured, along with CBC.

Diagnostic Imaging

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.

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Management

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.

 

 

First Aid for a Seizure

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.

 

 

Febrile seizures

Identify and treat the source of the fever. Antipyretics such as acetaminophen can help reduce fever.

 

Stopping a Seizure

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.

 

 

Prophylactic Medications

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.

 

Surgery

cortical resection of focus, corpus callostomy (for atonic seizures), hemisperectomy (but only really for kids who have serious seizures

 

vagal nerve stimulation

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Pathophysiology

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).

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Consequences and Course

Febrile seizure

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.

 

 

 

Resources and References

King MA et al. 1998. Lancet.

 

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Topic Development

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