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Child Health Guideline Identifier

Seizures - afebrile

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Principles and approach

  • Treat acute seizure (see Status epilepticus)
  • Is this a seizure? Take detailed history and exam to ascertain whether definitely or possibly a seizure. This includes:
    • Detailed history obtaining the sequence of events - including the presence or absence of focal features and the level of awareness throughout the seizure. Consider arrhythmic cause for generalized seizures especially occurring at night, or during or following exercise
    • Developmental history/assessment
    • Previous seizures? Including events that may not have been recognised as seizures (e.g. in sleep).
    • Family history of evidence of young sudden death, familial epilepsy or arrhythmic disorders.
    • Detailed physical examination, including BP, neurological, cardiac amd mental status examination
  • Order initial investigations based on presentation, and to rule out underlying or other conditions. Always consider blood glucose and calcium measurement, and ECG.  Consider toxicology/alcohol screen if ingestion possible.
  • Identify and manage any underlying or provoking condition that may have triggered seizure.
  • Neuro-imaging is not usually required acutely. Imaging should be considered for focal seizures, when new focal deficits are noted on examination, after a first status epilepticus, or if EEG suggests underlying structural pathology.
  • Consider diagnosis: e.g. epilepsy syndrome, non-syndrome epilepsy, febrile or other acute symptomatic seizure, or other condition mimicking seizure.
  • Use working diagnosis to guide further investigations, treatment, and timing of review.
  • Provide advice and prepared information for family and patient
  • Refer for follow up

Flowchart for first seizure

Flowchart

Follow up

OR

Admission criteria

  • Recurrent seizures in 24 hour period
  • Not recovering after a seizure
  • New onset focal deficit
  • Encephalopathic
  • Requiring further acute investigation/management
  • Family/social considerations

Recurrence risk

Epilepsy comprises a wide range of individual conditions.Risk of seizure recurrence after a first or subsequent afebrile seizure depends on the individual patient, the cause and type of their epilepsy.  Quoted risk rates vary between published studies with no single agreed rates.  Factors that can affect recurrence risk include:

  • Type of seizure (focal or generalized)
  • Underlying cause of the seizure (structural, genetic, etc)
  • Presence of other neurological abnormalities (developmental delay or abnormal examination)
  • Situation of the seizure (from sleep, due to photic stimulation, etc)
  • EEG findings (although EEG must be interpreted in light of other factors and clinical presentation) 

When discussing recurrence:

  • Defining the epilepsy type/syndrome gives the most useful guide to seizure recurrence, as well as prognosis, cognition, behaviour and motor outcome.  EEG and other investigations can assist with determining epilepsy type.
  • Seizures associated with underlying neurological or developmental abnormalities have a greater risk of recurrence.

The role of EEG following a first afebrile epileptic seizure is to help determine the seizure syndrome, hence why it should be requested once a paediatrician has determined that the seizure event is epileptic in nature.

Starting anticonvulsant medication

Regular anti-epileptic medication is not usually recommended after a first afebrile seizure. Whether to start medication, and the medication choice is determined by the seizure type or most likely seizure syndrome.  This is usually determined by the paediatrician providing ongoing management.

The New Zealand Epilepsy Guidelines gives recommendations for treatment based on epilepsy & seizure types.  Dosing advice and patient/carer information sheets are contained in the New Zealand Formulary for Children for the following medications. Adverse affects are also detailed in the NZ Formulary, however some specific issues are highlighted below.

  • Carbamazepine
    • Screen children of South East Asian origin for HLA-B*1502 haplotype via the Blood Bank prior to the initiation of carbamazepine - positive children should not receive carbamazepine (increased risk of Stevens Johnson Syndrome)
  • Sodium valproate
    • Teratogenetic risk - avoid if possible in young women of child-bearing potential.  Advise effective contraception if unavoidable.
  • Lamotrigine
  • Ethosuximide
  • Topirimate
  • Levetiracetam

Information for families

Family and patient information available from the New Zealand Child Neurology Network and Kidshealth includes:

Web information

Pamphlets

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Document Control

  • Date last published: 20 September 2018
  • Document type: Clinical Guideline
  • Services responsible: Paediatric Neurology, Children’s Emergency Department, General Paediatrics
  • Author(s): Greg Williams, Sarah Jamison, Suzanne Davis
  • Editor: Greg Williams
  • Review frequency: 2 years

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