Febrile seizure
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| Febrile seizure Classification and external resources | |
| ICD-10 | R56.0 |
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| ICD-9 | 780.3 |
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Overview
A febrile seizure, also known as a fever fit or febrile convulsion is a generalized convulsion caused by elevated body temperature. They most commonly occur in children below the age of three and should not be diagnosed in children under the age of 6 months or over the age of 6 years. In many cases, the first sign of fever is the onset of the seizure. It has been theorized that the seizure is triggered by the rapidity of the rise in temperature, rather than the actual temperature reached.
Classification
Simple
- Seizure less than 15 minutes
- Generalized
- Does not reoccur in same febrile illness
Complex
- Focal features
- Prolonged past 15 minutes
- Reoccurs with 24 hours
Febrile seizures represent the meeting point between a low seizure threshold (genetically and age determined) - some children have a greater tendency to have a seizure under certain circumstances - and a trigger: fever. The genetic causes of febrile seizures are still being researched. Some mutations that cause a neuronal hyperexcitability and could be responsible for febrile seizures have already been discovered.
Diagnosis
The diagnosis is one that must be arrived at by eliminating more serious causes of seizure: in particular, meningitis and encephalitis must be ruled out. Therefore a doctor's opinion should be sought and in many cases the child would be admitted to hospital overnight for observation and/or tests. As a general rule, if the child returns to a normal state of health soon after the seizure, a nervous system infection is unlikely. Even in cases where the diagnosis is febrile seizure, doctors will try to identify and treat the source of fever. In particular, it is useful to distinguish the event as a simple febrile seizure - in which the seizure lasts less than 15 minutes, does not recur in the next 24 hours, and involves the entire body (classically a generalized tonic-clonic seizure). The complex febrile seizure is characterized by long duration, recurrence, or focus on only part of the body. The simple seizure represents the majority of cases and is considered to be less of a cause for concern than the complex. It is reassuring if the cause of seizure can indeed be determined to have been fever, as simple febrile seizures generally do not cause permanent brain injury; do not tend to recur frequently, as children tend to 'out-grow' them; and do not make the development of adult epilepsy significantly more likely (less than 3-5% which is similar to that of the general public).
Children with febrile convulsions who are destined to suffer from afebrile epileptic attacks in the future will usually exhibit the following:
- A family history of afebrile convulsions in first degree relatives (a parent or sibling)
- A pre-convulsion history of abnormal neurological signs or developmental delay
- A febrile convulsion lasting longer than 15 minutes
- A febrile convulsion with strong indications of focal features before, during or afterward
Management
Early use of antipyretics for fever seems useful and effective. Applying cold (tepid sponging) is no longer recommended, as it does not appear to offer any advantage over antipyretic medications. The commonly given advice to give anti-pyretic drugs to reduce fever in the hope of reducing the risk of febrile convulsion following childhood immunization lacks good evidence of effectiveness.[1]
For children who present with a prolonged seizure, rectal diazepam may be used at home in the event of another prolonged (e.g. more than 5 minutes) seizure is an option. Some children have frequent episodes, and although it is tempting to prescribe anti-epileptic medication to prevent stress and inconvenience, it is hard to justify the risk:benefit ratio.
Prognosis
Following a first febrile convulsion, 2-4% of children will have an unprovoked (i.e. afebrile) seizure - this is 4 x the risk in general population). Most of these children will subsequently develop epilepsy. Other risk factors for developing epilepsy:
- Family history of epilepsy
- Complex features
- Presence of early onset neuro-developmental abnormalities
Genetic basis but multiple chromosomes, so complex and not strictly autosomal dominant. Current opinion supports an association between prolonged febrile convulsion and lesions in the temporal lobe (especially hippocampal sclerosis; in the past it was thought febrile convulsions might predispose to temporal lobe epilepsy, but the brain lesions probably pre-exists and increases the likelihood of febrile convulsion.
Prognosis is generally good. One third of children presenting with a febrile convulsion will have another one (recurrence); age would appear to be the single, strongest, and most consistent risk factor: the younger you are when you have your first, the more likely you are to have another before you grow out of it! Most recurrences will occur during the first year after the initial episode and over 90% recur within two years. Other risks - family history of febrile seizures (but not epilepsy) in a first degree relative, children whose initial seizure occurred with a relatively low fever, multiple initial seizures occurring during the same febrile episode. Surprisingly, status epilepticus in an otherwise normal child does not appear to significantly increase the risk for further febrile seizures or the development of epilepsy.
See also
References
Additional Resource
- Wilkinson, I.M.S. Neurology. Blackwell Science. ISBN 0-86542-854-9
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Acknowledgement and Attribution Regarding Sources of Content
Some of the initial content on this page may be incorporated in part from copyleft sources in the public domain including wikis such as Wikipedia and AskDrWiki. Drug information for patients came from the The National Library of Medicine. Infectious disease information may have come from the Centers for Disease Control (CDC). Differential Diagnoses are drawn from clinicians as well as an amalgamation of 3 sources: 1.The Disease Database; 2. Kahan, Scott, Smith, Ellen G. In A Page: Signs and Symptoms. Malden, Massachusetts: Blackwell Publishing, 2004:3; 3. Sailer, Christian, Wasner, Susanne. Differential Diagnosis Pocket. Hermosa Beach, CA: Borm Bruckmeir Publishing LLC, 2002:7 .
