Paeds: Epilepsy georgie Flashcards
AED for partial seizures
• Carbamezapine (first libe treatment) • Sodium valporate • Lamotrigine • Topiramate Levetiracetam
AEDs for Generalized
• Sodium valporate (first line teatment)
• Lamotrigine
• Topiramate
Levetiracetam
Complex partial
Prevalence
60%
Prevalence Secondary generalized tonic-clonic
60%
Prevalence Primary generalized tonic-clonic
30%
Prevalence Generalized absence
5%
Prevalence Generalized myoclonus
5%
Simple partial Prevalence
rare
West syndrome
age and comments
4-6 months
• Violent flexor spasms of the head, trunk and limbs followed by extension of the arms (so-called ‘salaam spasms’). Flexor spasms last 1–2 s, often multiple bursts of 20–30 spasms, often on waking, but may occur many times a day.
• Many causes; two-thirds have underlying neurological cause.
Most will subsequently lose skills and develop learning disability or epilepsy
Management of west syndorme
• Treatment is with vigabatrin or corticosteroids good response in 30-40%
•
Childhood absence syndrome
4-12 Years
• It is associated with brief interruptions of 3-5s in awareness, with minimal or no motor manifestation
• Accounts for 2% of epilepsy
• Prognosis is good, with 95% remission in adolescence; 5–10% may develop tonic-clonic seizures in adult life
•
childhood absence syndrome management
It responds to sodium valporate or ethosuximide
Juvenile myoclonic epilepsy age and presentation
- Associated with early morning myoclonic jerks
- Generalized tonic-clonic seizures occur in most
- Childhood absence seizures in 30%
- Precipitants: sleep deprivation, alcohol
Juvenile myoclonic epilepsy management
Best response to sodium valproate
Tonic-clonic generalised seizures first-line Rx
Valproate, carbamazepine