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#x203A; Attacks precipitated by fever can be epileptic or non-epileptic.
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› Children with febrile seizures (FSs) are not considered to have epilepsy since their seizure only occurs when the child is febrile (acute symptomatic seizure).
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› FSs do not constitute a homogeneous entity.
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› The cumulative incidence of FSs in most countries is 2–5%.
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› FSs usually occur between 6 months and 3 years. They peak at 18 months and it is rare for their onset to be after 6 years of age.
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› FSs are divided into simple and complex. The latter have focal features and/or are prolonged and/or are repeated in the same illness.
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› Viral illnesses, particularly human herpes virus 6, precipitate most FSs.
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› One third of children who have one FS will have at least one recurrence.
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› Recurrent FSs are more likely if the child was young at the time of the first seizure, the fever provoking the first seizure was relatively low, the child suffers from a lot of illness episodes and has a family history of FS.
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› The risk of epilepsy following FSs is 7% at 25 years.
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› Following one or more FS, risk factors for developing epilepsy are family history of epilepsy, neurodevelopmental problems and complex FS.
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› The risk that a child with a FS will have bacterial meningitis is 0-4%.
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› Routine brain imaging and EEG is not indicated following a FS.
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› Regular prophylactic medication to prevent recurrent FSs is not recommended but rectal diazepam or buccal midazolam may be useful to stop further prolonged FSs.
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(2009). Febrile Seizures. In: El-Radhi, A.S., Carroll, J., Klein, N. (eds) Clinical Manual of Fever in Children. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-540-78598-9_7
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