Seizures Flashcards
Atonic seizure
Generalized
Brief loss of muscle tome
May involve all musculature resulting in fall
May only involve nuchal musculature resulting in head drop
Use helmet
Overall generalized seizure characteristics
Entire brain
No aura-no warning
Postictal confusion-not absence or myoclonic
Bowel or bladder incontinence
Lateral tongue trauma
EEG-spike and slow wave discharges across all recording electrodes simultaneously
Absence seizure
Generalized seizure Pediatric epilepsy syndrome Resolves by adolescence Staring spell lasts 5-15 seconds Provoked by hyperventilation-diagnose No Postictal state EEG-Classic 3/second spike and slow wave discharges
Treatment: ethosuximide,valproic acid, lamotrigine
Myoclonic seizures
Generalized seizure
3 types: tonic clinic, myoclonic, staring spells
Adults:
Associated with anoxic injuries to brain
Treat with valproic acid, lamotrigine, levitiracetam, Topiramate
Overall Focal seizures characteristics
Partial seizure
Most commonly in medial temporal lobe
May have aura-smells, sights, voices
parietal= pain
occipital=unformed visual hallucinations: spots and zig zags
Temporal=formed visual hallucinations: actual objects
Frontal=motor activity, vocalizations, speech arrest
Simple
No alteration of consciousness
No postictal state
motor, sensory, autonomic, psychic (deja vu)
Complex Alteration in level of consciousness May have an aura Postictal confusion May have automatisms
EEG-spike and slow wave in focal area of recording electrodes
Treatment for all:
Carbamazepine, phenytoin, lamotrigine,
Add on: Topiramate, levitiracetam, gabapentin, pregabalin and zonisamide
Motor focal seizure
Tonic or clinic movements
Versive head or eye movements away from the side of the seizure
Autonomic focal seizure
Gustatory
Olfactory
Epigastric fullness
Nausea
Sensory focal seizures
Positive phenomena
Parathesias/dyathesias
Visual hallucinations
Psychic focal seizures
Déjà vu
Depersonalization
Febrile seizure
Associated with quickly acquiring high temp
Seen in children 6 months to 6 years old
Treatment: treat fever
Runs in families
Simple: no focal features to seizure
No increased risk of epilepsy
Complicated:
Focal features, increased risk of epilepsy
Status epilepticus
Recurrent or prolonged seizures; failure to return to baseline in between seizures
Causes: missed anticonvulsants-most common
Structural lesions-tumor, infection, stroke
Complications: hypertension, tachycardia, arrhythmias, lactic acidosis
Treatment: ABCs-metabolic issues 1st step: IV benzodiazepines-lorazepam 2nd step: IV anticonvulsant-phenytoin, Still seizing: phenoarbital still seizing: intubate and give anesthesia (midolzolam, propofol)
Juvenile Myoclonic Epilepsy
Juvenile myoclonic epilepsy-most common inherited seizure
JME-EEG generalized poly spike and slow wave discharges and photic sensitive
Lifetime duration
Otherwise healthy but present during adolescence with myoclonic seizure
Preservation of consciousnesss
Occur in first hour of waking and provoked by sleep deprivation
Treat with: valproic acid, lamatrigin, levetriacetam and topirimate
Epilepsy
Disorder of recurrent seizures
Give primidone
Tonic clonic
Alternating stiffening and movement
Tonic seizure
stiffening