Professional Documents
Culture Documents
Objectives
Review the clinical presentation and
differential diagnosis
Discuss pathophysiologic implications on
clinical presentation
Review etiology
Apply this information to evaluation and
treatment
Discuss prognosis
Clinical Classification
Focal/Multifocal Clonic
Not generalized
Migratory
Not necessarily focal etiology
Focal Tonic
Not usually generalized
Generalized Myoclonic
Clinical Classification
Subtle (Hypomotor)
Motor activity arrest
Apnea
Eye deviation
Autonomic changes
Motor automatisms
Oral-buccal-lingual movements
Swimming
Bicycling
Causes.
24-72 hours
Meningitis/sepsis
In premature infants: IVH
In full-term infants: infarction, venous
thrombosis
Cerebral dysgenesis
Causes.
72 hours to 1 week
Above causes
Inborn errors of metabolism
Hypocalcemia
Familial neonatal seizures
1 week to 4 weeks
Above causes
HSV
Other Syndromes
Benign idiopathic neonatal convulsions
(BINC or Fifth-day fits)
Benign familial neonatal convulsions
(BFNC)
Early myoclonic encephalopathy (EME)
Early infantile epileptic encephalopathy
(EIEE)
Glucose transporter type I
Tox screen
CT or MRI of brain
?metabolic w/u, congenital infection w/u
Phenytoin 20 mg/kg
Lorazepam 0.1 mg/kg
Pyridoxine 50-100 mg IV with EEG
Outcome
45 % controlled after either phenobarb or
phosphenytoin
60 % controlled with both
30% of survivors develop epilepsy
WORSE: HIE, meningitis, dysplasia
WORSE: electrographic seizures
BETTER: hypoCa, BINC, BIFC, stroke