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Seizures Mark Wahba August 7, 2003

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Seizures. Mark Wahba August 7, 2003. Statistics. 10% of population will have 1 seizure in their lifetime 6% of population will have at least 1 afebrile seizure in their lifetime Incidence of epilepsy in the population is

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Page 1: Seizures

Seizures

Mark WahbaAugust 7, 2003

Page 2: Seizures

Statistics• 10% of population will have 1 seizure in

their lifetime• 6% of population will have at least 1

afebrile seizure in their lifetime• Incidence of epilepsy in the population

is <1%• 1% of ED visits is for seizures

Page 3: Seizures

Sub-presentations

• Status epilepticus• Febrile Seizures• Medical

management acute and chronic

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Outline• Definitions• Classification of seizures• Pathophysiology• Clinical Features• Postictal state• Emergency Department Management• Summary

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Definitions

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Seizure• “clinical manifestation of excessive,

abnormal cortical neuron activity” Rosen’s p.1445

• Not a diagnosis but a series of signs and symptoms

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Epilepsy• “recurring seizures without consistent

provocation” Rosen’s p1445

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Ictal• “pertaining to, marked by, or due to a

stroke or an acute epileptic seizure” Dorland’s Pocket Medical Dictionary 25th Ed. 1995 W.B. Saunders Company

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Classification of Seizures

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Primary and Secondary• Primary seizure• Idiopathic/Genetic• Epilepsy

• Secondary seizure• aka reactive seizure• Response to certain

toxic, pathophysiologic, or environmental stress

• Not epilepsy

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Generalized and Partial• Generalized• Electrical activity

simultaneously involves both cerebral hemispheres

• Loss of consciousness

• Partial (Focal )• Electrical activity

limited to part of one cerebral hemisphere

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Partial Seizure

• Partial with secondary Generalization• Starts partial then becomes generalized

• Complex Partial• Consciousness is

impaired

• Simple Partial• Consciousness is

maintained

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Cryptogenic Seizure• Thought to be secondary but identifiable

cause found

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Febrile Seizure• Most common pediatric seizure• 2-5% of children between 6mo -5years• 20-30% have at least 1 recurrence• Impt. to differentiate febrile seizure from

seizure with fever

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Pathophysiology

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Page 17: Seizures

Pathophysiology• Not completely

understood• Knowledge is from

animal studies• Electrical or

pharmacologic stimulation applied to the brain cortex

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Recruitment• Generalized:• “when the initiating neurons’ abnormal,

increased electrical activity activates adjacent neurons and propagates until the thalamus and other subcortical structures are recruited” Rosen’s p.1446

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Recruitment• Partial:• Less recruitment and ictal activity does not

cross the midline

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Why?• Unclear• Disruption of normal structure:

congenital, maturational, acquired• Disruption of local metabolic or

biochemical function

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Neurotransmitters• acetylcholine-excitatory to cortical

neurons• gamma-aminobutyric acid (GABA)-

inhibitory to cortical neurons• changes in concentration of these NTs

may produce membrane depolarization, then hyperpolarization, then recruitment

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Why is consciousness altered?• Ictal discharge reaches below the

cortex• Enters brainstem and effects the

reticular activating system

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Why does the seizure stop?• hyperpolarization subsides• electrical discharges terminate• “Due to reflex inhibition, loss of

synchrony, neuronal exhaustion, alteration of the local balance of ACH and GABA in favor of inhibition” Rosen’s p. 1446

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How are seizures confirmed?• Electroencephalography (EEG)

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Clinical Features

Primary Seizures

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Simple Partial• Specific function of initiating neurons

determines the clinical manifestation of the ictal event

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Features• motor

• somato-sensory• special sensory

• autonomic• psychic

• focal clonic movements

• paresthesias• visual, auditory,

olfactory, gustatory• sweating, flushing• sense of déjà vu,

fear

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Complex Partial• Impairment but not loss of

consciousness• Amnesia, but may be responsive during

seizure• Automatisms: lip smacking, swallowing• Aura: taste, smell, visual • Maintain high cortical functioning

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Generalized Seizures• Loss of consciousness• No aura• May have a vague prodrome or

dysphoric state prior• Convulsive or Non-Convulsive

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Convulsive Generalized Seizures• ‘Grand-Mal’• generalized hypertonus• “rhythmic, violent contractions of

multiple, bilateral, symmetric muscle groups”

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• posterior shoulder dislocation, # thoracic spine vertebral bodies

• transient apnea• incontinence: urinary > fecal• followed by postictal state, headache,

drowsiness that may last for hours

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Nonconvulsive Generalized Seizures• Absence or ‘Petit mal’• Myoclonic• Tonic• Atonic

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Absence Seizures• Begin in childhood• Sudden cessation of normal, conscious

activity• dissociative state lasting secs to min• sudden termination of such state• No postictal state

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Myoclonic and Tonic Seizures• Sudden, brief muscle group

contractions• If entire body involved: ‘drop attack’• No postictal state

Page 36: Seizures

Atonic Seizure• Loss of muscle tone• May cause ‘drop attack’

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Clinical Features

Secondary seizures

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Caused by Metabolic Derangements

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Hypoglycemia• Most common metabolic cause of

seizure activity• Plasma glucose level <45mg/dL or

2.5mmol/L• Extremes of age particularly susceptible

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Ketotic Hypoglycemia• Most common cause of childhood

hypoglycemia• Small for age kids• “Episodes of symptomatic hypoglycemia

during periods of caloric deprivation or under provocation by a ketogenic diet” Rosen’s p.1448

• Hypoglycemia and ketonuria• Dietary management

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Osmolar Disorders• Hyponatremia Na<120mmol/l• Rate of decline is factor• Treat slowly: increase Na by 0.5mmol/h• Treat with 3% NaCl only if seizing

Page 42: Seizures

Osmolar Disorders• Hypernatremia Na>160mmol/l• Usually due to dehydrating illness• Correct slowly

Page 43: Seizures

others• Hypocalcemia, Hypoparathyroidism• Hypomagnesemia• Nonketotic Hyperosmolar Hyperglycemia• Uremic Encephalopathy in renal failure• Hypothyroidism• Thyrotoxicosis• High anion gap acidosis• Hypertensive Encephalopathy• Acute Intermittent Porphyria

Page 44: Seizures

Infectious Causes

Page 45: Seizures

Infectious Causes• Independent of febrile mechanism• Usually CNS infections

Page 46: Seizures

Meningitis• 15-40% of pts will seize• More common at extremes of age• Partial seizures > general

Page 47: Seizures

Meningoencephalitides• Usually partial motor• Postictal paralysis common esp. with

herpetic infections• Presenting sign in 1/3 of cerebral

abscesses

Page 48: Seizures

Other• Neurocysticercosis: parasite in

immigrants from Latin America• Latent syphilis• Primary HIV disease and its infections

Page 49: Seizures

Drugs and Toxins

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Drugs and Toxins• Antimicrobials• Neuroleptics• Sympathomimetics• Anticholinergics:

tricyclics, antihistamines

• cocaine• amphetamines• PCP

• Withdrawal:alcohol, BZD

• Overdose: ASA,theophylline, INH, Li, phenytoin

• Insecticides• Rodenticides• hydrocarbons

Page 51: Seizures

Cocaine induced Seizures• Fever• Rhabdomyolysis• Arrhythmias• Rx: BZD

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EtOH Associated seizures• Overdose• Withdrawal• Must r/o other causes• Rx: BZD• “substitute for the GABA enhancing

effect of ethanol in the CNS” Rosen’s p.1449

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Trauma Associated Seizures

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Early• <1 week post injury• Epi + Sub dural hematomas• Intracerebral Hemorrhage• SAH

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Late• >1week post injury• 1 year after significant head trauma,

incidence of seizures is increased 12 x• Severity of head injury is directly

proportional to likelihood of seizures• 10-15% will develop post traumatic

epilepsy

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Malignancy Associated Seizures

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Malignancy Associated Seizures• Primary tumors or metastases• Usually partial with secondary

generalization

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Vasculitic Associated Seizures

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Vasculitic Associated Seizures• Systemic Lupus Erythematosus• Polyarteritis Nodosa• Complex partial

Page 60: Seizures

Other Neurologic Causes

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• Stroke: incidence of seizures 4-15%• Incidence of epilepsy post stroke is 4-

9%• Aneurysm and AVM• Migrainous activation of an epileptic

focus• MS - 5% of patients

Page 62: Seizures

• Neurofibromatosis: café au lait, axillary freckling

• Tuberous Sclerosis: ash leaf spots, adenoma sebaceum

• Sturge-Weber syndrome: facial port wine nevus

• Alzheimer’s Dementia

Page 63: Seizures

Gestational Seizures

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Gestational Seizures• Gestational epilepsy• Hormonal and metabolic changes

unmask underlying epilepsy• Eclampsia• Seizures, hypertension, proteinuria,

edema, coma

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Pseudoseizures

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Pseudoseizures• Functional• Not the result of abnormal CNS

electrical activity• “lower intelligence and have an

underlying anxiety or hysterical personality disorder” Rosen’s P.1450

• ED evaluation is difficult• Can co-exist with seizures

Page 67: Seizures

Post ictal state

Page 68: Seizures

Postictal State• Decreased level of arousal and

consciousness• Amnesia• Headache• Minutes to hours

Page 69: Seizures

• Must monitor and investigate altered mental status after a seizure

• Airway, pulse oximetry, blood glucose, cardiac monitoring

• Monitor until recovery

Page 70: Seizures

Postictal Paralysis• “Todd’s Paralysis”• May follow generalized or complex

partial• Focal motor deficit • Lasts up to 24h• High likelihood of an underlying

structural cause

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Neurogenic Pulmonary Edema• Common, but often subclinical feature of any

CNS insult• “centrally mediated sympathetic discharge

and generalized vasoconstriction, coupled with increased pulmonary capillary membrane permeability” Rosen’s p.1451

• May appear like aspiration pneumonia• Ventilatory support if necessary

Page 72: Seizures

Emergency Department Management

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http://www.seizurerobots.com/

Page 74: Seizures

Diagnosis• Hx of ictal event, known or potential

precipitants and exposures and PMHx• Thorough Physical Examination

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History taking• 1. Hx of seizures?• 2. If no, was the event witnessed?

Page 76: Seizures

Differential Diagnosis• Syncope• Hyperventilation• Breath holding• Toxic state: DTs• Metabolic state:

hypoglycemia

• TIA• Narcolepsy• Movement disorders• Psychogenic illness

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COLD• Character-type of seizure• Onset-when, what was pt doing• Location-where• Duration-how long

Page 78: Seizures

seizure• Abrupt onset-no aura• Brief duration-usually <120s• Altered mental status• Purposeless activity• Unprovoked• Postictal state

Page 79: Seizures

Previous Seizures• Focus on:• Anticonvusant level, med

noncompliance, med change• Drugs, etoh• Drug-drug interactions• Change in ictal pattern• Cause for lowered seizure threshold

Page 80: Seizures

Physical Examination• Medic alert• Hypertension,

tachycardia, tachypnea• Tongue biting• Shoulder dislocation• Back pain• Urinary or fecal

incontinence• Neurocutaneous signs

Page 81: Seizures

Lab• Stat glucose is vital• in neurologically N, healthy pt: little

value• Medically ill: labs• Anticonvulsant levels• Tox screen if suspicion of abuse• BHCG if eclampsia suspected• Meningitis or SAH: LP if no inc. ICP

Page 82: Seizures

Lab abnormalities• Hypoglycemia- cause/effect?• Lactic Acidosis• Rhabdomyolysis

Page 83: Seizures

First time seizure• Never assume it is idiopathic• 46% will need admission• Focus on medical, toxicologic,

neurologic cause

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First time seizure:CT scan in the department?

• if you suspect a ‘serious structural lesion’

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Suspect a ‘serious structural lesion’?• New focal deficit• Persistent altered

metal status• Fever• Trauma• Persistent headache

• History of cancer• Anticoagulant use• Suspicion or known

AIDS• Age > 40• Partial onset seizure• Increased ICP

Page 86: Seizures

First time Seizure• Scan as an outpatient if:• Complete recovery and no apparent

cause of seizure found• If follow up questionable: scan in ED

Page 87: Seizures

Recurrent Seizures• Initial stabilization same• Most common cause is med noncompliance• Must measure anticonvulsant levels• Supratherapeutic levels of phenytoin and

carbamazepine may cause seizures• Be careful about giving loading dose before

checking a serum level• Hx and PE

Page 88: Seizures

Known or Recurrent Epilepsy:CT scan in dept?• Same considerations as with first time

seizure• Also: • Change in seizure pattern• Prolonged post-ictal state

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Management

Page 90: Seizures
Page 91: Seizures

Stabilization• Monitored bed• Oxygen• Pulse oximetry• Heart rate monitor, BP cuff• IV access

Page 92: Seizures

Airway• Anticipatory• Gag reflex suppressed• +/- vomiting• Left lateral decubitus• ?Bite block to prevent tongue biting and

to allow suctioning• +/- nasopharyngeal airway

Page 93: Seizures

Apneic or airway threat• If O2 sat<90% or inability to protect

airway• Endotracheally intubate• BZD for induction• If trismus, may need neuromuscular

blockade

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Think:• If seizure lasts longer than 5 minutes it

is unlikely to stop• should start thinking about status

epilepticus• Treat ASAP

Page 95: Seizures

stolen from Dr. S. Bernbaum

Drug Rx of SE

• Starting Rx ASAP has been correlated with a better response rate to drug Rx, and lower morbidity– Lowenstein DH, Alldredge BK

Neurology 1993 (43): 483-8• < 30 min - 80% stopped• > 120 min - < 40% stopped

but - retrospective review; • ? groups comparable

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Reversible causes• Hypoglycemia• Isoniazid• Eclampsia

• Dextrose• Pyridoxine• Magnesium

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Medications• First Line: Benzodiazepines IV• Directly enhance GABA-mediated neuronal

inhibition• affect both clinical and electrical

manifestations of seizures • Terminate seizure activity in 75-90% of pts• May cause hypotension and respiratory

depression

Page 98: Seizures

Lorazepam (Ativan)• 0.1mg/kg/IV• 1-2mg/min• Up to 10mg• Peds: 0.05mg to 0.1mg/kg IV• Longer duration of seizure suppression

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Diazepam (Valium)• 0.2mg/kg IV• at 2mg/min• up to 20mg• Peds: 0.2-0.5mg/kg IV/IO/ET or 0.5-

1.0mg PR• Works well rectally, endotracheally,

interosseously

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Midazolam (Versed)• 2.5-5.0mg IV• 0.2mg/kg IM• Peds: 0.15mg/kg IV then 2-10ug/kg/min• Works well IM

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Second line• anticonvulsants

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Phenytoin (Dilantin)• suppresses neuronal recruitment • does not suppress electrical activity at

the ictogenic focus• No sedation or resp depression• May cause hypotension if given rapid IV• Takes 30min to infuse

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Phenytoin• 20mg/kg IV at <50mg/min• Peds: 20mg/kg IV at 1mg/kg/min

• If pt subtherapeutic:• May give loading dose IV or PO to

boost serum levels

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Fosphenytoin• Phenytoin prodrug• Water soluble• May be administered quickly• Better tolerated, more safe, more stable

than phenytoin• More difficult to monitor, delayed

hypotension

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Fosphenytoin• 15-20 PE/kg at 100-150mg PE/min• PE: phenytoin sodium equivalent• Peds: not established

Page 106: Seizures

Phenobarbital• third-line• in pediatrics is second-line therapy• CNS depressant decreases both ictal

and physiologic cortical electrical activity

• anticipate: sedation and depression of respiratory drive and BP

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Phenobarbital• 20mg/kg IV at 60-100mg/min• Ped: same• May give as IM loading dose

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Eclampsia• Magnesium is not an anticonvulsant• 4-6g IV followed by 1-2g/h infusion with

hydralazine• Unexplained efficacy• BZD effective short term• Phenytoin may be efficacious-teratogenic• Should consult Obs/Gyn or have established

protocol

Page 109: Seizures

stolen from Dr. S. Bernbuam

Status Epilepticus• continuous or rapidly repeating seizures• no consensus on exact definition - “abn prolonged”

– “no recovery between attacks”– “20-30 min” --> injury to CNS neurons– more practical definition: since isolated tonic -

clonic seizures rarely last > few minutes ... consider Status if sz > 5 min or 2 discrete sz with no regaining of consciousness between

• vs. serial sz - close together - regained consciousness in between

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stolen from Dr. S. Bernbaum

CNS damage can occur• uncontrolled neuronal firing• excess glutamate (exitatory NT)• this sustained high influx of calcium ions

into neurons leads to cell death (“excitotoxicity”)

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Management of ‘Status’• Valproate: PR, increases GABA conc.• Valproate IV 25mg/kg in future• Barbiturate Coma

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Barbiturate coma• works well but suppresses all brainstem function• Neuro, ICU consults recommended: resp arrest,

myocardial depression, hypotension, dec ICP, dec cerebral perfusion

• phenobarbital 20mg/kg IV at 60mg/min• pentobarbital 10-15mg/kg IV load then 0.5-

1.0mg/kg/hr infusion• Need intubation and ventilatory support, cardiac

monitoring, invasive hemodynamic monitoring, +/- pressors = ICU

Page 113: Seizures

Midazolam and Propofol• midazolam 0.2mg/kg bolus then

0.045mg/kg/h infusion• propofol 1mg/kg bolus then 2mg/kg/h

infusion• Hypotension• Intubation and ICU

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Isoflurane Anaesthesia• Final alternative in refractory status• Anaesthesia involved• BZD induction agent + lidocaine

pretreatment• ICU

Page 115: Seizures

Not moving = Not seizing?• NO• Visual manifestations of convulsive

ictus are extinguished by neuromuscular blockade.

• Need electroencephalographic monitoring arranged

Page 116: Seizures

Disposition• Individualized for pt.• Home, home with GP follow, neuro

consult in ED, neuro follow up• Shouldn’t drive for 6 months• Law varies from province to province

Page 117: Seizures

Summary• Several types of and many causes for

seizures• History is important• First seizure likely needs imaging• Treat immediately• If seizure lasts >5min think status

epilepticus• “Sub” areas to consider: febrile seizures,

status epilepticus

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References• Dorland’s Pocket Medical Dictionary 25th Ed. 1995 W.B.

Saunders Company• Neuroimaging in the emergency department patient presenting

with seizures, Neurology 47:26, 1996.• Rosen’s Emergency Medicine 5th edition, Marx et al. Mosby,

Toronto, 2002• Emergency Medicine Secrets 3rd Ed. Markovchick et al. Hanley

& Belfus, Philadelphia 2003• Seizures in the Emergency Department, Nicholl J.S. et al

http://www.emedicine.com/neuro/topic694.htm• Status Epilepticus, Stan Bernbaum MD CCFP-EM, May 31,

2001, http://www.calgaryhealthregion.ca/em/