Seizures and Epilepsy Flashcards
Paroxysmal, time-limited changes in motor activity and/or behavior that result from abnormal electrical activity in the brain
Transient occurrence of signs/symptoms resulting from ABNORMAL EXCESSIVE or SYNCHRONOUS neuronal activity in the brain
Seizures/convulsions
General term to include any one of the ff: epilepsy, febrile seizures secondary to metabolic, infectious or other etiologies
Seizure Disorder
Disorder of the brain characterized by an enduring PREDISPOSITION TO GENERATE SEIZURES and by the neurobiological, cognitive, psychological and social consequences of this condition
2 or more unprovoked seizures occurring in a time frame of >24 hrs
EPILEPSY
Disorder that manifests one or more specific seizure types and has a specific age of onset and prognosis
Epileptic syndrome
The primary determinant of the type of MEDICATIONS the patient is likely to respond to
Seizure type
Determines the TYPE OF PROGNOSIS one could expect
Epilepsy syndrome
ILAE 2017 Classification of Seizure Types
FOCAL (aware or impaired consciousness)
- Motor onset (automatisms, myoclonic etc)
- Non-motor onset (autonomic, emotional etc)
GENERALIZED
- Motor (tonic-clonic, tonic, clonic etc)
- Non-motor (absence)
UNKNOWN
- Motor
- Non-motor
- Unclassified
Partial seizure
Initial activation of a system of neurons LIMITED TO A PART OF ONE CEREBRAL HEMISPHERE
FOCAL SEIZURE
Focal seizure w/o impairment of consciousness
Focal seizure w/ impairment of consciousness (focal dyscognitive seizures)
Clinical and EEG changes indicate synchronous involvement of ALL OR BOTH HEMISPHERES
GENERALIZED SEIZURES
MC type of Benign Epilepsy Syndrome with Focal Seizures
- outgrown during adolescence
- focal seizure with buccal and throat tingling and tonic or clonic contractions of 1 side of the face, with drooling and inability to speak but with preserved consciousness and comprehension
Benign Epilepsy with Occipital Spikes
- Panayiotopoulos type
- Lennox-Gastaut type
TRIAD of West Syndrome
2-12 months (infancy stage)
Infantile epileptic spasms
Developmental regression
EEG - HYPSARRHYTHMIA
EEG in Benign Childhood Epilepsy with Centrotemporal Spike
broad based centrotemporal spikes
8 mo old boy
(+) truncal flexion (as if doing sit ups) multiple times throughout the day
lost of ability to sit w/o support which he was able to do a month ago
EEG - high voltage, slow, chaotic background w/ multifocal spike
West Syndrome
Later childhood (2-10 y/o)
complex partial seizure, visual auras, migraine headache
Lennox-Gastaut type
Triad of Lennox-Gastaut type
developmental delay
multiple seizure type
polyspike bursts in sleep and slow background in wakefulness
Early childhood
complex partial seizure with ictal vomiting
Panayiotopoulos type
AED for Focal seizures and Epilepsies
Oxcarbazepine
Carbamazepine