Seizure Disorders Flashcards
Seizure Types
Not all seizures = epilepsy
Symptomatic Seizure
Cryptogenic Seizure
Acute vs Remote
Prevalence of Seizures
1 in 10 adults will have had a seizure
Seizure where cause is identified
Symptomatic Seizure
No cause of seizure is identified
Cryptogenic Seizure
Pathophysiology of Seizure
Basis for neuronal excitation is the action potential
Seizure results from increased frequency burst of action potentials- spikes
Glutamate- excitatory neurotransmitter- allows Ca++ influx which keeps Na+ voltage gated channels open (perpetuates depolarization)
Depolarization activates NMDA channels open which allows further Ca++ influx
GABA- inhibitory neurotransmitter
Old theory: loss of inhibitory neurons (GABA)
New theories:
- loss of excitatory neurons (that stimulate the inhibitory neurons)
- Injury leads to axonal “sprouting” to other excitatory neurons
Causes of Non-epileptic Seizure
> 70-80% Idiopathic
Neurogenic: Brain tumor, CVA, trauma
Electrolyte/Metabolic imbalances
Hypoglycemia, hyponatremia, hypocalcemia
Hyperthyroidism
Acute renal or hepatic failure
Medication overdoses
Antidepressants, antipsychotics, cyclosporine, interferon, INH, Lithium, Demerol, tramadol (Ultram), quinolone atbs
Drug withdrawal
Drugs: Cocain, m-amphetamine, nitrous oxide, IV contrast dye, lead or mercury poisoning, acetylcholinesterase inhibitors
Infection and/or fever
Common seizure causes <10 yo
Idiopathic
congenital
birth injury
metabolic disorders
Common seizure causes 10-40 yo
Idiopathic, congenital, birth injury, metabolic disorders
Common seizure causes 40-60 yo
Brain Tumor
Head Trauma
Common seizure causes >60 yo
CVA brain tumor subdural hematoma CNS infection Alzheimers metabolic disturbance
Age of Febrile Seizure Occurance
6 mo - 5 yo
Peak age 2 yo
Prevalence of Febrile Seizures
66% male
3-5% children <5
First Febrile Seizure Risk Factors
Fever >38 (100.4)
Day care attendance
Developmental delay
Neonatal nursery >30 days
FH (sibling- 10% risk)
Viral infections (HHV6, influenza, others)
Vaccinations (influenza, DTP, MMR (fever))
Common Viral pathogen for Febrile Seizures
HH6
Influenza
Recurrent Febrile Seizure Risk Factors
30-50% will experience subsequent szs
Age <104F)
First degree relative with febrile
Simple Febrile Seizure
last less than 15 min; no underlying neuro problems, ie. Cerebral palsy
Evaluation of Febrile Seizure
History & Physical: FH PMH HPI Recent vaccines Meningeal irritation - If yes, LP
Imaging?
Most do not require. MRI preferred (due to less radiation)
Management of Febrile Seizures
Antipyretics Tylenol/ibuprofen -For comfort -Do NOT prevent seizure Recurrence likely No increased morbidity/mortality No behavioral/developmental disorders No prophylaxis required- adverse effects, lack of efficacy
Febrile Seizure Prognosis
By age 5 - 98% seizure free
Risk of developing later seizures after febrile seizure:
Underlying neuro disease (cerebral palsy)
FH epilepsy
Complex seizures
Types of Seizures
Partial
Generalized
Partial Seizures
Simple
Complex
Generalized Seizures
Absence (“Petit Mal”)
Generalized tonic-clonic (“Grand Mal”)
Myoclonic
Atonic
Causes of Absence Seizures
Inherited idiopathic disorder
Secondary disorder: AVM, neoplasm, ID
Absence seizures vs Partial-complex seizures
AGE is critical.
In adult, with similar symptoms, think partial-complex seizures.
Tx different!
Age of onset of Absence Seizures
age 5-18
Rare under age 2 or beyond adolescense
Signs and Symptoms of Absence Seizures
NO AURA!!!
Vacant, dazed expression
Staring
Pallor
Timing: 10 seconds max
Multiple times throughout day (50-100x)
Other: eye blinking, head movements, autonomic movements (incontinent stool or urine)
Post-ictal: brief recovery, picking clothes, pursing lips
EEG: diffuse 3Hz spike pattern (see later)
What are absence seizures mistaken for?
Often escape detection.
Mistaken for ADHD, daydreaming.
Treatment of Absence Seizures
Usually cease by age 20
Progress (if untreated) to generalized tonic-clonic seizures in 33%
Treatment:
Ethosuximide (Zarontin)
Valproic acid (Depakote)
+/- clonazepam (historically)
Pharmacologic Treatment of Absence Seizures
Ethosuximide (Zarontin)
Valproic acid (Depakote)
+/- clonazepam (historically)
Tonic Clonic Seizures AKA
Grand Mal
What often proceeds Tonic Clonic seizures?
Aura
Aura symptoms
Irritability Apathy HA Scintillating scotoma nausea choking sensation paresthesias
Signs of Tonic Clonic seizures
Aura (often precedes Sudden LOC Tonic- muscular rigidity (adduction and flexion of arms; extension of legs) Clonic- jerking Incontinence Tongue biting
Treatment of Tonic Clonic Seizures
Valproic acid (Depakote) (first line)
Phenytoin (Dilantin)
Carbamazepine (Tegretol)
+/- phenobarbital
Others: Primidone (Mysoline) Lamotrigine (Lamictal) Topiramate (Topamax) Zonsisamide (Zonegran) Levetiracetam (Keppra)
Myoclonic Seizures feel like
Sudden, single or multiple jerks
Myoclonic seizures and chidren manfest as
“Infantile spasms”
S/S Atonic Seizures
LOC
Head drops, loss of posture
“drop attack”
Falls cause Injury
Treatment for Atonic Seizures
Resistant to drug therapy