Ch 26 & 27 Seizures Flashcards
(55 cards)
How are seizures classified?
The ILAE 2017 operational classification of seizures is Focal, Generalised and Unknown. Focal seizures are divided into motor and non-motor and also into aware or impaired awareness. Generalised seizures are Motor or non-motor (absence). Unknown seizures are motor, non-motor or unclassified.
What are the different types of motor seizures?
Automatisms Atonic Tonic Clonic Myoclonic Epileptic spasms Hyperkinetic
What is the definition of a generalised seizure?
Bilateral hemispheric symmetrical and synchronous onset with loss of consciousness from the start (40% of all seizures)
What are clonic seizures?
Bilateral synchronous semirhythmic jerking with elbow flexion and knee extension
What are tonic seizures?
Sustained increase in tone. Characteristic cry or grunt.
What are absence seizures?
Impaired consciousness with no motor involvement and no post-ictal confusion. EEG shows 3 Hz spike and wave.
What are myoclonic seizures?
Shock-like body jerks with generalised EEG changes.
What are atonic seizures?
Sudden loss of tone that causes falls.
What are psychomotor seizures?
Alteration of awareness with automatisms and aura (usually epigastric rising sensation)
What is the characteristic feature of a seizure arising in the uncus?
Olfactory hallucinations - cacosmia = perception of a bad odour
What is the role of the hippocampus?
Spatial memory (dom), verbal memory (non-dom) and learning concepts
What are the common semiological features of a mesial temporal lobe seizure?
Behavioural arrest, staring, oral automatisms, posturing of the contralateral arm. Seizures last a few minutes and post-ictal confusion, amnesia and aphasia (if dominant side)
What are the characteristic EEG features in mesial temporal lobe epilepsy?
Rhythmic theta maximal in basal temporal electrodes
What is a wada test?
Intracarotid sodium amytal injection
What the features of juvenile myoclonic epilepsy?
Idiopathic generalised epilepsy syndrome characterised by myoclonic jerks after waking, generalised tonic-clonic seizures or absence. EEG shows polyspike discharges with the jerks. Strong family history. Responsive to valproate.
What is West syndrome?
Infantile spasms. Occurs in the first year of life with flexion and then extension of the trunk and limbs AKA salaam seizures. Seizures resolve by 5 years. Some may develop Lennox-Gastaut syndrome. HYPSARRHYTHMIA. Responds to ACTH or steroids.
What is HYPSARRHYTHMIA?
High amplitude spike and wave
What is Lennox-Gastaut syndrome?
Atonic seizures resulting in drop attacks
Medically refractory
Valproate reduces seizure frequency by 50%
Corpus callosotomy is treatment of choice
What factors lower seizure threshold?
Sleep deprivation
Hyperventilation
Photic stimulation
Infectins / Drugs / Metabolic disturbances
Trauma / Stroke
What is Todd’s paresis?
Post-ictal weakness due to involvement of the motor cortex in the functional deficit zone
What are the classes of antiepileptic medications?
Barbiturates - phenobarbital
Benzodiazepines - lorazepam / diazepam
GABA analogues - gabapentin
Voltage gated sodium channel blockage - phenytoin
Synaptic vesicle protein (SV2A) blockage - levetiracetam
Which antiepileptic drugs interfere with platelet function?
Valproate and Phenytoin
What is the drug of choice for GTCS?
Valproate
Phenytoin
What is the drug of choice for absence seizures?
Ethosuximide and valproate