Epilepsy Flashcards
Seizure
sudden irregular discharge of electrical activity in the brain causing a physical manifestation such as sensory disturbance, unconsciousness or convulsions
Convulsion
uncontrolled shaking movements of the body due to rapid and repeated contraction and relaxation of muscles
Aura
perceptual disturbance experienced by some prior to a seizure, e.g. strange light, unpleasant smell, confusing thoughts
(not everyone w/ seizure gets Aura)
Epilepsy
neurological disorder marked by sudden recurrent episodes of sensory disturbance, LOC or convulsions, associated with abnormal electrical activity in the brain
What causes epilepsy? (4)
Increased excitatory activity
decreased inhibitory activity
Loss of homeostatic control
spread of neuronal activity
difference between primary and secondary causes of epilepsy
Primary: idiopathic
secondary: identifiable cause >> head trauma, hypoxia, tumor, stroke, infection, hypoglycemia, drugs
Status epilepticus
medical emergency.
It is defined as seizures lasting >5 mins or more than 3 seizures in one hour.
Management of status epileptics in the hospital:
Take an ABCDE approach:
- Secure the airway
- Give high-concentration oxygen
- Assess cardiac and respiratory function
- Check blood G levels
- IV access (insert a cannula)
- IV lorazepam 4mg, repeated after 10 minutes if the seizure continues
- If seizures persist: IV phenobarbital or phenytoin
- If no response (‘refractory status’) w/in 45 minutes from onset induction of GA
Medical options in the community:
- Buccal midazolam
- Rectal diazepam
CL ASSIFICATION OF SEIZURES
.generalized> “matat” il bint mn il seizure
PARTIAL VS GENERALISED
P
PARTIAL SEIZURES
how r their consciousness levels different?
.
most common partial seizure?
symptoms?
when does it commonly occur?
Temporal lobe epilepsy
– 1st/2nd decade in most people, following seizure with fever or an early injury to the brain
– auras –e.g. auditory hallucination, rush of memories
2nd common type of partial seizure
Frontol lope epilepsy
Abnormal movements when motor areas affected (contralateral side)
GENERALISED
.• Tonic-clonic: 2 parts - 1st tonic (muscles Tense), 2nd clonic (Convulsions)
• Absence: ‘daydreaming’
• Status epilepticus: medical emergency
• Myoclonic: brief shock-like muscle jerks
• Atonic: ‘without tone’ – drop attack
• Tonic: increased tone (stiff)
Having convo, them suddenly u stop…. and carry on then like nthn happened
tx?
Absence
1st line: sodium valproate or ethosuximide
Standing 3ady tsolfeen, faj2a ogaf wa i stretch my hands out, then contnue normal
Tonic
increase tone in hand
brief shock-like muscle jerks
Myoclonic Chna lama ag3D >> ba3dayn faj2a y7ooshny bard😂😂
1st line: sodium valproate
Other options: lamotrigine, levetiracetam or topiramate
typically happen in children as part of juvenile myoclonic epilepsy
Atonic Seizures
Mx
They may be indicative of Lennox-Gastaut syndrome.
Management is:
1st line: sodium valproate
Second line: lamotrigine
Infantile spasms
This is also known as West syndrome.
It is a rare (1 in 4000) disorder starting in infancy at around 6 months of age.
It is characterised by clusters of full body spasms.
poor prognosis: 1/3 die by age 25, however 1/3 are seizure free. It can be difficult to treat but
first line treatments are:
- Prednisolone
- Vigabatrin
INVESTIGATIONS (3)
• Clinical history
- EEG> can show typical patterns in different forms of epilepsy and support the diagnosis.
- MRI > used to diagnose structural problems that may be associated with seizures and other pathology such as tumours.
- ECG to exclude problems in the heart.
CLINICAL HISTORY
u wanna divide it into asking what happened (before, during ,after)