Epilepsy Flashcards
Prevalence in children
4 in 1000
Defintion
chronic brain disorder characterized by recurrent (≥ 2), unprovoked seizures
A single seizure is not considered an epileptic seizure. Epilepsy is often idiopathic, but various brain disorders, such as malformations, strokes, and tumors, can cause symptomatic epilepsy.
Types of generalised seizures
absence (typical or atypical), myoclonic, clonic, tonic, tonic-clonic, and atonic (astatic) types
Types of partial seizures
Motor
Sensory
Autonomic
Psychiatric
What is a seizure
transient neurological dysfunction caused by excessive activity of cortical neurons,
resulting in paroxysmal alteration of behaviour and/or EEG changes
Describe an absent seizure
usually only seen in children, unresponsive for 5-10 s with arrest of activity, staring, blinking or eye-rolling, no post-ictal confusion; 3 Hz spike and slow wave
activity on EEG
Most common cause of late onset >50 yo seizures
dementia
Describe the presentations of simple->motor, sensory, psychiatric
simple (preserved LOC)
motor: postural, phonotory, forceful turning of eyes and/or head, focal muscle rigidity/jerking ± Jacksonian march (spreading to adjacent muscle groups)
sensory: unusual sensations affecting vision, hearing, smell, taste or touch
autonomic: epigastric discomfort, pallor, sweating, flushing, piloerection, pupillary dilatation
psychiatric: symptoms rarely occur without impairment of consciousness and are more
commonly complex partial
Presentation of complex seizures
complex (altered LOC)
patient may appear to be awake but with impairment of awareness
classic complex seizure is characterized by automatisms such as chewing, swallowing, lipsmacking,
scratching, fumbling, running, disrobing and other stereotypic movements
other forms: dysphasic, dysmnesic (déjà vu), cognitive (disorientation of time sense),
affective (fear, anger), illusions, structured hallucinations (music, scenes, taste, smells),
epigastric fullness
Compare motor activity in seizure vs pseudoseizure
Seizure:
Synchronous, stereotypic, automatisms, lateral
tongue biting, eyes rolled back
Pseudoseizure/conversion:
Opisthotonos, rigidity, forced eye closure, irregular extremity movements, shaking
head, pelvic thrust, crying, geotropic eye movements, tongue biting at the tip
Clinical features
Key diagnostic factors presence of risk factors (common) staring spells or inattention (common) tonic-clonic convulsions (common) brief, arrhythmic muscular jerking movements (common) unexplained falls (common) eyes rolling back in head (common) apnoea (common) intercurrent illness (common)
Other diagnostic factors incontinence (common) tongue biting (common) post-ictal phenomena (common) precipitated by fatigue or lack of sleep (common) precipitated by light or noise (common) developmental delay (common) neurocutaneous stigmata (uncommon)
Risk factors for generalised seizures
Strong genetic predisposition or FHx perinatal asphyxia metabolic/neurodegenerative disorders head trauma structural abnormalities of the CNS
Weak autistic spectrum disorder CNS infection neurocutaneous syndromes Hx of febrile seizures
How is diagnosis of epilepsy made
Clinical
Use of EEG has limited value is diagnostic process
Four key questions to ask with possible epilepsy
- Is the seizure epilepsy
- What type of seizure
- What type of epilepsy
- What is the cause of the epilepsy
Prognosis
Generally good
>70% will have resolution resolution when idiopathic