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Dr Mergan Naidoo
Seizures
A seizure is a change in movement, attention or level of awareness that is sustained or repetitive and occurs as a result of abnormal neuronal discharges within the brain. When seizures are recurrent or typical of a specific syndrome, then the term epilepsy is used and specific management applies.
Epidemiology
Incidence of epilepsy: 30 50 /100 000 Prevalence of epilepsy: 0.5 0.8 % partial epilepsy 60% generalized epilepsy 25% absence epilepsy10%
Poisoning
accidental ingestion of medicines medicine withdrawal in infancy environmental toxins
Infections
meningitis encephalitis brain abscess febrile convulsion (Commonest cause)
Metabolic conditions
hypoglycaemia hypocalcaemia hypomagnesaemia hyponatraemia hypernatraemia inborn errors of metabolism
Systemic disorders
vasculitis Hypertensive encephalopathy uraemia (renal failure) Hyperammonaemia (liver failure)
Generalised seizures:
The epileptic focus arises centrally and spreads to the rest of the brain
Generalised seizures may be: tonic-clonic (grand-mal convulsion) absence clonic tonic myoclonic Generalised Tonic Clonic Seizures (GTCS) that continue for more than 30 minutes are called Convulsive Status Epilepticus
Partial seizures:
The epileptic activity arises from a particular focus within the brain.
Simple partial seizure: a focal seizure with retained consciousness. Complex partial seizure: a focal seizure with spread of the seizure to involve the whole cerebral cortex, resulting in an altered level of consciousness
DIAGNOSTIC CRITERIA
Clinical
History: Eye witness account, aura Perinatal history, developmental history, school record and family history Environment Examine to exclude obvious aetiology, but in particular look for occult causes: General: skin abnormalities, e.g. Sturge Weber and tuberous sclerosis CNS examination for loss of consciousness, localising signs, head growth, Developmental milestones and fundi CVS examination: blood pressure
Investigations
Always consider hypoglycaemia as a primary or aggravating cause of any seizure
Blood glucose thick/thin film electrolytes serology culture metabolic screen FBC toxicology urinalysis: blood and protein in renal hypertension, MCS for UTI Lumbar puncture: if meningitis is suspected and for first febrile generalised tonic clonic seizures in children < 2 years old Note: Lumbar puncture is contra indicated in the presence of the following: Increased intracranial pressure GCS < 12/15 (paediatric coma scale reduced by 3 points or more) Focal neurological signs/seizures. If the seizure has progressed to status
Other Investigations
CT/MRI scan: if persistently reduced coma score (GCS < 12/15) without known cause, raised intracranial pressure or focal intracranial pathology is suspected EEG: is only indicated for recurrent or syndromic seizures where diagnosis cannot be made on clinical grounds alone. The EEG is to be delayed for at least one week after the convulsive episode.
NON-DRUG TREATMENT
Ensure an open airway and administer oxygen, if available Position to prevent aspiration of vomitus, i.e. head up position Check glucose during the seizure and blood pressure after the seizure Obtain intravenous access if seizure duration > 5 minutes Keep child nil per os and intravenous fluid volumes at maintenance rates Control fever with tepid sponging Aetiology will determine further management
EPILEPSY
A condition characterised by recurrent seizures associated with abnormal paroxysmal neuronal discharges
Seizures are managed according to type (i.e. generalised or partial) and also according to specific syndromes.
Epileptic syndromes:
Infantile spasms (Wests Syndrome)
An infantile onset encephalopathy with epileptic spasms associated with hypsarrhythmia on the EEG and developmental regression It is a neurological emergency diagnosis, treatment and referral must not be delayed. Early intervention reduces the subsequent neurodisability. Clinically, the child appears to stare, give a sudden flexion of the trunk and head, with the limbs either flung in or out but held in this tonic spasm for a few seconds Events occur in runs and are most common when the infant is going to sleep or rousing The episodes are distressing to the infant and he will often appear red in the face and may cry out Events are often confused with colic
Primary generalised absence seizure of childhood (petit mal) Short spells of motor arrest of maximum 15 seconds duration with little or no associated movements, no post-ictal effect Onset 46 years Generalised epilepsy with febrile seizures plus (GEFS+) Children with febrile convulsions which persist beyond 6 years Occasionally associated with afebrile convulsions These children have epilepsy triggered by fever and may warrant anticonvulsant intervention Often family history of febrile convulsions
DIAGNOSTIC CRITERIA
A child may be diagnosed: With a specific anatomical or systemic cause for the seizure type As having an epileptic syndrome, i.e. a specific seizure type associated with a characteristic EEG, natural history, response to therapy and prognosis With idiopathic epilepsy
LONG TERM
Minimise the impact of the epilepsy by obtaining complete seizure control to maximising childs full potential Educate the patient and caregiver about epilepsy and associated complications, i.e. learning difficulties and ADHD
DRUG TREATMENT
TREAT MENT
Generalised Tonic and/ or clonic Partial
SEIZURE TYPE
Infantile Spasms Absence Myoclonic
1st line
Refer
sodium valproate
refer
Sodium valproate, oral, 2040 mg/kg/24 hours in 23 divided doses The slow release formulation enable school going children to take medication in a manner such that is does not sedate them with peaks and troughs and can be taken twice a day i.e. not at school. Monitor for hepatotoxicity in children under two years of age. Carbamazepine, oral, 1520 mg/kg/24 hours in 23 divided doses Initiate slowly over a period of 23 weeks. Exacerbates myoclonic seizures and absence seizures.
Lamotrigine, oral, 0.2 mg/kg/day Use as a third line agent, specialist initiated. Increase dose incrementing to 5 mg/kg/day slowly in conjunction with valproate. Lamotrigine is given as add-on therapy for many seizure types drug-resistant paediatric epileptic syndromes, such as LennoxGastaut syndrome. Phenobarbital, oral, 35 mg/kg/24 hours as single dose at night May be used in children under six months of age. Is not recommended as maintenance therapy for children older than 2 years due to undesirable side effects such as sedation, behaviour disturbances, hyperkinesia and dependence, except in situations where there is poor adherence to other drugs. Exacerbates absence seizures
Generalised seizures
absence myoclonus tonic/atonic primary T/C
Partial seizures
simple partial complex partial 2dry T-C
ethosuximide
Carbamazepine life = 12 20 hrs Phenytoin life = 20 30 hrs Phenobarbitone life = 100 hrs Valproate life = 10 20 hrs
Drug level
Time
adverse effects and cost 2) Choose a low starting dose and titrate slowly 3) Increase the dose until seizures controlled or side effects occur 4) If seizures not controlled, start another appropriate AED 5) Most drug interactions are based on induction of P450 system 6) Drug levels are for compliance and toxicity
Dosage
REFERRAL
Suspected secondary cause Partial seizures for neuroimaging if facilities or expertise not available Generalised seizures other than typical febrile convulsions in children < 2 years Seizures that are not controlled within 2 months on one agent with minimal side effects Neuroregression Mixed seizure types within one patient. All myoclonic seizures and infantile spasms at presentation
FEBRILE SEIZURES
DESCRIPTION Seizures occurring in children between the ages of 3 months and 5 years associated with a rapid rise in temperature at the beginning of an extracranial illness. Febrile seizures can be simple or complex febrile seizures.
DIAGNOSTIC CRITERIA
Clinical Exclude intracranial, extracranial and biochemical causes Signs of meningism are unreliable in children under 2 years If raised intracranial pressure or meningitis cannot be excluded then the diagnosis of febrile seizures cannot be made. Treat children empirically for meningitis.
Investigations A lumbar puncture is indicated in: Children under 2 years for exclusion of intracranial infection even when signs of meningism are absent All children who have no focus of infection, particularly those who have received antibiotics prior to the event In children older than 2 years, where a focus of extracranial infection is present and intra-cranial infection has been excluded clinically, no further investigation is required. All children with complex seizures and persistent lethargy should have a ct scan and then a lumbar puncture if raised intracranial pressure can be reliably excluded An EEG is of no value in simple febrile seizures
Non-drug treatment Control fever with tepid sponging Reassure parents and caregivers Educate parents and caregivers regarding the management of future episodes of fever Drug treatment For fever: administered by parents Paracetamol, oral, 1015 mg/kg/dose 46 hourly until fever subsides
Status Epilepticus
Diazepam 0.5mg/kg rectally
Still convulsing after 10 minutes
Lorazepam 0.1mg/kg IVI Still convulsing after 10 minutes Phenytoin 18mg/kg over 30 min in N/S Cardiac Monitoring Still convulsing at the end of phenytoin infusion Refer for ICU admission. Intubation with thiopental Sodium. Start infusion of midalolam 0.5-5ug/kg/min
References
Hospital Level Paediatrics STGs and EDL 2006 DOH Professor P.A. Bill Lecture notes EMU UKZN 2007 APLS