All issues > Volume 57(9); 2014

Review Article

Published online: September 30, 2014

DOI: https://doi.org/10.3345/kjp.2014.57.9.384

Febrile seizures

Sajun Chung, MD

Department of Pediatrics, Kyung Hee University Medical Center, Kyung Hee University School of Medicine, Seoul, Korea.

Corresponding author: Sajun Chung, MD. Department of Pediatrics, Kyung Hee University Medical Center, Kyung Hee University School of Medicine, 23 Kyungheedae-ro, Dongdaemun-gu, Seoul 130-872, Korea. Tel: +82-2-958-8295, Fax: +82-2-958-8845, sajchung@khmc.or.kr

Received December 13, 2013       Accepted July 23, 2014

Copyright © 2014 by The Korean Pediatric Society

(open-access, http://creativecommons.org/licenses/by-nc/3.0/):

This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Febrile seizure (FS) is the most common seizure disorder of childhood, and occurs in an age-related manner. FS are classified into simple and complex. FS has a multifactorial inheritance, suggesting that both genetic and environmental factors are causative. Various animal models have elucidated the pathophysiological mechanisms of FS. Risk factors for a first FS are a family history of the disorder and a developmental delay. Risk factors for recurrent FS are a family history, age below 18 months at seizure onset, maximum temperature, and duration of fever. Risk factors for subsequent development of epilepsy are neurodevelopmental abnormality and complex FS. Clinicians evaluating children after a simple FS should concentrate on identifying the cause of the child's fever. Meningitis should be considered in the differential diagnosis for any febrile child. A simple FS does not usually require further evaluation such as ordering electroencephalography, neuroimaging, or other studies. Treatment is acute rescue therapy for prolonged FS. Antipyretics are not proven to reduce the recurrence risk for FS. Some evidence shows that both intermittent therapy with oral/rectal diazepam and continuous prophylaxis with oral phenobarbital or valproate are effective in reducing the risk of recurrence, but there is no evidence that these medications reduce the risk of subsequent epilepsy. Vaccine-induced FS is a rare event that does not lead to deleterious outcomes, but could affect patient and physician attitudes toward the safety of vaccination.

Key words: Febrile seizures, Classification, Child, Epilepsy

Introduction

Introduction

Febrile seizure (FS) is the most common type of childhood seizure disorder, which occurs in an age-specific manner, is associated with a fever of 38.0℃ or higher, and presents without evidence of any definite causative diseases, such as central nervous system (CNS) infection or metabolic abnormality1,²⁾. Most cases of FS are benign and self-limiting, and in general, treatment is not recommend³⁾. FS has been defined differently by the National Institutes of Health (NIH), the International League against Epilepsy (ILAE), and the American Academy of Pediatrics (AAP). The NIH (1980) defined FS as follows: an abnormal, sudden, excessive electrical discharge of neurons (gray matter) that propagates down the neuronal processes (white matter) to affect an end organ in a clinically measurable fashion, occurring in infancy or childhood, usually between 3 months and 5 years of age, associated with fever, but without evidence of intracranial infection or defined cause⁴⁾. The ILAE (1993) defined FS as a seizure occurring in childhood after age 1 month, associated with a febrile illness not caused by infection of the CNS, without previous neonatal seizures or a previous unprovoked seizure, and not meeting the criteria of other acute symptomatic seizures⁵⁾. Most recently, the AAP (2008) defined FS as a seizure occurring in febrile children between the ages of 6 and 60 months who do not have an intracranial infection, metabolic disturbance, or history of afebrile seizure¹⁾. FS is considered a "syndrome" because it fulfills several characteristics that are similar among affected children: (1) FS generally occurs within a restricted age range; (2) the majority of children with FS show normal neurological and structural development after the episode; and (3) FS is not associated with structural or developmental anomalies in the brain, although the existence of such pathology may enhance susceptibility to FS⁶⁾. Genetics, comorbidities (premature birth, fetal growth retardation), and environmental risk factors (exposure to nicotine in utero, or antihistamine use) may increase risk of FS in addition to the age factor7,⁸⁾.

Simple and complex FS-definition/terminology

Simple and complex FS-definition/terminology

Livingston et al.⁹⁾ first introduced the term "simple febrile convulsion" and "epileptic seizures precipitated by fever" to designate two groups on the basis of age of onset, seizure characteristics, electroencephalography (EEG) findings, frequency of seizures, and genetic factors. "Febrile seizures" can rationally be distinguished from "seizures with fever." The latter includes any convulsion in any child with a fever of any cause. Thus, children with seizures and fever, both with definite causes such as CNS infections or overt neurological disorders, have "seizures with fever" rather than "febrile seizures"¹⁰⁾.

Recently, clinicians have begun classifying FS as either simple or complex. Simple FS is defined as generalized, lasting less than 15 minutes, comprised of generalized tonic and clonic activity without a focal component, and without recurrence within 24 hours or within the same febrile illness¹⁾. Complex or complicated FS is defined as exhibiting one or more of the following features: (1) partial onset or focal features; (2) prolonged duration of more than 15 minutes; (3) recurrent febrile seizure within 24 hours of the first episode; and (4) association with postictal neurological abnormalities, as exemplified by Todd paresis10,¹¹⁾.

Incidence and prevalence

Incidence and prevalence

FSs occur in 2% to 5% of children 6 months to 5 years of age¹⁾. The peak incidence occurs at approximately 18 months of age and is low before 6 months or after 3 years of age²⁾. Generally, the incidence of FS decreases markedly after 4 years of age (and the condition rarely occurs in children older than 7 years of age2,¹²⁾. FS occurs more frequently in the Asian population, affecting 3.4%-9.3% of Japanese children²⁾ and 5%-10% of Indian children, but only 2%-5% of children in the United States (US) and Western Europe. The highest prevalence is 14% in Guam¹³⁾. Unfortunately, there is no epidemiological study in Korean children.

Males have consistently emerged as having a higher frequency of FS (male to female ratio, 1.1:1 to 2:1). However, some large studies have shown no significant gender difference¹⁴⁾.

There are two seasonal peaks in FS incidence: November-January, corresponding to the peak of viral upper respiratory infection, and June-August, when common viral gastrointestinal illnesses occur¹⁴⁾. Variation in prevalence is related to differences in case definitions, ascertainment methods, geography, and cultural factors¹⁵⁾.

In a study of children with a first FS, most seizures were simple, and at least one complex feature was noted in approximately 35% of cases, including features of focality (16.1%), multiple seizures (13.8%), prolonged duration (>15 minutes, 9.3%) and recurrent febrile seizure within 24 hours (16.2%); 6.5% showed two complex features, and 0.7% showed three complex features¹¹⁾. Febrile status epilepticus, that is, seizures that last more than 30 minutes, represents only 5% of FS¹⁶⁾, and represents about 25% of all episodes of childhood status epilepticus with more than two thirds of cases occurring at 2 years of age¹⁷⁾. Only 21% of children experience seizures either prior to or within 1 hour of the onset of fever; 57% have seizure after 1 to 24 hours of fever, and 22% experience febrile seizure more than 24 hours after the onset of fever18,¹⁹⁾.

FS is mostly generalized and convulsive in character, but approximately 5% of FS cases have nonconvulsive features presenting with unconsciousness, staring, eye deviation, atonia, or cyanosis²⁾.

Genetics

Genetics

These seizures have a familial tendency in some cases and are sporadic in others, suggesting that both genetic and environmental elements contribute to their generation²⁰⁾. The importance of genetic factors in FS has long been recognized. Population studies have demonstrated that FS occurs at a much higher-than-expected incidence in first- and second-degree relatives of children with FS²¹⁾. Family history also has a role in determining whether children have FS recurrences and subsequently develop afebrile seizures2,²¹⁾. Twenty-five to 40% of patients showed a positive family history for FS; the incidence of FS being 20.7% among siblings, 10.9% among parents, and 14.1% among first-degree relatives of probands²¹⁾. In a study done to compare these rates with those of control subjects, the incidence was 8.4% in siblings, 1.6% in parents, and 3.8% among first-degree relatives of the controls²¹⁾. Overall, there appears to be a multifactorial mode of inheritance for febrile convulsions, but there may be a subset of children with an autosomal-dominant mode of inheritance²²⁾.

Five areas of the genome have shown to be linked to FS in some way. Two of them, FEB1 and FEB2 , found on chromosomes 8 and 19p, are only involved in FS. Three others involve "generalized epilepsy with FS+" (GEFS+) syndrome21,²²⁾.

GEFS+ patients present with complex febrile seizures, which are often seen beyond 5 years of age, and develop afebrile seizures later in childhood²³⁾.

These children are reported to have a variety of mutations in the α-subunit of the sodium channel (SCN1A and B)22,²³⁾, and in the γ²-subunit of the γ-aminobutyric acid type A (GABAA) receptor (GABRG2)22,²⁴⁾.

Pathophysiology

Pathophysiology

Although the mechanism of FS remains unclear, animal models are informative²⁵⁾. First, elevated brain temperature alters many neuronal functions, including several temperature-sensitive ion channels²⁶⁾. This influences neuronal firing and increases the probability of generating massive neuronal activity, i.e., seizures. Also, an inflammatory process including secretion of cytokine in the periphery and in the brain is known to be a part of the mechanism²⁷⁾. Second, it was discovered that fever and hyperthermia share common mechanisms in provoking seizures: the fever-promoting pyrogen interleukin-1β contributes to fever generation and conversely, fever leads to the synthesis of this cytokine in the hippocampus28,²⁹⁾. In addition, interleukin-1β has been shown to increase neuronal excitability, acting via both glutamate and GABA³⁰⁾. In vivo, these actions of interleukin-1β enhance the actions of seizure-provoking agents³¹⁾. The importance of endogenous interleukin-1β in the occurrence of FS was supported by studies in mice that lacked the receptor for this cytokine³¹⁾. Fever of specific infectious etiologies, specifically human herpes virus 6 (HHV6), might influence the probability of generation of FS31,³²⁾. Third, hyperthermia-induced hyperventilation and alkalosis have been proposed as a pivotal element of FS generation in that alkalosis of the brain provokes neuronal excitability³³⁾ and contributes to seizure pathophysiology. However, human conditions associated with severe alkalosis, including prolonged crying and pyloric stenosis of infants, are not associated with the generation of seizures²⁵⁾.

Risk factors for recurrence and subsequent epilepsy

Risk factors for recurrence and subsequent epilepsy

1. Risk factors for first FS

1. Risk factors for first FS

Two studies have examined the risk factors associated with FS34,³⁵⁾. In one study, four factors were associated with an increased risk of FS: (1) a first- or second-degree relative with a history of FS; (2) a neonatal nursery stay of more than 30 days; (3) developmental delay; and (4) day-care attendance. Children with more than two risk factors have a chance of developing FS in approximately 28%³⁴⁾. In another multivariable analysis, significant independent risk factors were peak temperature and history of FS in a first- or higher-degree relative³⁵⁾. Gastroenteritis as the underlying illness appeared to have a significant inverse (i.e., protective) association with FS12,35,³⁶⁾.

2. Risk factors for recurrent FS

2. Risk factors for recurrent FS

Overall, approximately one-third of children with a first FS experience one or more recurrent FSs¹¹⁾ and 10% have three or more FSs18,19,37,38,39,40,⁴¹⁾.

The risk factors potentially associated with FS recurrence are summarized in Table 1. The most consistent risk factors reported are a family history of FS and onset of first FS at less than 18 months of age12,18,19,37,³⁸⁾. Two other definite risk factors for recurrence of FS are peak temperature and the duration of fever prior to seizure18,19,³⁸⁾. The higher the peak temperature, the lower the chance of recurrence; children with a peak temperature of 101℉ had a 42% recurrence risk at 1 year, compared with 29% for those with a peak temperature of 103℉, and only 12% for those with a peak temperature >105℉

The shorter the duration of recognized fever, the higher the chance of recurrence¹²⁾; the recurrence risk at 1 year was 46% in children who experienced FS within an hour of recognized onset of fever, compared to 25% in children with prior fever lasting 1 to 24 hours, and 15% in children with more than 24 hours of recognized fever prior to the FS¹²⁾. Children with multiple risk factors have the highest risk of recurrence¹⁸⁾. A child with two or more of the risk factors listed in Table 1 has a recurrence rate greater than 30% at 2 years; a child with three or more risk factors has a recurrence rate greater than 60%¹⁸⁾. In contrast, recurrence risk is less than 15% for a 2-year-old child with none of the risk factors mentioned in Table 112,¹⁸⁾. A recurrent FS is also more likely to be prolonged if the initial FS was prolonged11,⁴¹⁾. The existence of any relationship between a family history of unprovoked seizures or epilepsy and the overall risk of FS recurrence appears to be doubtful. Some studies report a modest increase in the risk of FS recurrence in children with a family history of unprovoked seizures, but a large study in Rochester, Minnesota, found no difference in recurrence risk between children with a family history of epilepsy (25%) and those with no such family history (23%)³⁷⁾. The presence of a neurodevelopmental abnormality in the child or a history of complex FS have not been shown to be significantly associated with an increased risk of subsequent FSs18,19,37,38,⁴¹⁾. Moreover, neither ethnicity nor sex associates with an increased risk of recurrent FSs¹²⁾.

3. Risk factors for subsequent epilepsy

3. Risk factors for subsequent epilepsy

The risk factors for developing subsequent epilepsy after FS are summarized in Table 2. Following a simple FS, the risk of developing epilepsy is no different from that in the general population16,⁴⁰⁾. Some studies on children with FS indicate that 2% to 10% of children who have FS will subsequently develop epilepsy. However, a family history of epilepsy and the occurrence of a complex FS were found to be associated with increased risk of subsequent epilepsy16,⁴⁰⁾. Repeated bouts of simple FS under the age of 12 months lead to a slight increase in epilepsy risk⁴²⁾. The occurrence of multiple FSs was also associated with a slight but statistically significant increase in the risk of subsequent epilepsy in two additional studies11,16,⁴³⁾. One study found that children with a FS that occurred within 1 hour of a recognized fever (i.e., at onset) had a higher risk for subsequent epilepsy than children with FS associated with longer duration of fever⁴⁰⁾. Two studies have found that prolonged FSs (i.e., febrile status epilepticus) were associated with an increased risk of subsequent epilepsy compared to a complex FS that was less prolonged16,⁴³⁾. The number of complex features in a FS may possibly affect the risk of recurrence. Although one study found that patients with two complex features (e.g., prolonged and focal) had an elevated risk of subsequent epilepsy, another study did not detect this association¹⁶⁾. A family history of FS, age at first FS, and the height of fever at first seizure are not associated with a differential risk of developing epilepsy16,40,⁴³⁾. The only common risk factor for both recurrent FSs and subsequent epilepsy was duration of fever prior to the FS16,18,¹⁹⁾. The types of subsequent epilepsy that develop are variable; however, the types of epilepsy that occur in children with prior FS are not significantly different from those that occur in children without such a history12,20,⁴³⁾. It is controversial whether FS is simply an age-specific marker of future seizure susceptibility or if it has a causal relationship with subsequent epilepsy¹²⁾. One study showed a 13% incidence of epilepsy caused by the presence of at least two of the following risk factors: (1) a family history of non-FSs; (2) abnormal neurologic or developmental status prior to FS; and (3) complex FS, such as a prolonged or focal seizure. Only 2 to 3% of children who have none or one of the above risk factors subsequently develop non-FSs⁴⁾.

Evaluation

Evaluation

Children should be promptly evaluated after an initial seizure. Most parents of patients with FS seek medical care within an hour of the seizure, but after resolution of the seizure and return of the patient to full alertness⁴⁴⁾.

The initial evaluation should focus on determining the source of the fever44,⁴⁵⁾. History taking should include documentation of any family history of FSs or epilepsy, status of immunizations, recent antibiotic use, duration of the seizure, any prolonged postictal phase, and any focal symptoms. On physical examination, attention should be given to the presence of meningeal signs and the child's level of consciousness³⁹⁾.

To begin, one must consider whether there is an infection of the CNS in the form of meningitis or encephalitis, particularly in younger infants in whom the signs can be more subtle. Therefore, the important issue for evaluation is whether a lumbar puncture is necessary to exclude meningitis. If meningitis is excluded, the next step is to consider what tests are needed to determine the cause of the febrile illness. Finally, consider whether there is a structural CNS abnormality that predisposed the child to having a seizure13,⁴⁶⁾.

1. Lumbar puncture

1. Lumbar puncture

Recommendations by the AAP (1966) for lumbar puncture (LP) in children with first simple FS were summarized as follows⁴⁷⁾: (1) In infants younger than 12 months, performance of an LP is strongly advised, because the clinical signs and symptoms associated with meningitis may be minimal or absent in this age group; (2) In a child between 12 and 18 months of age, an LP should be considered, because clinical signs and symptoms of meningitis may be subtle; (3) In a child older than 18 months, although an LP is not routinely warranted, it is recommended in the presence of meningeal signs and symptoms (i.e., neck stiffness and positive Kernig and Brudzinski signs); (4) In infants and children who have had FS and have received prior antibiotic treatment, clinicians should be aware that treatment might mask the signs and symptoms of meningitis. Therefore, an LP should be seriously considered. However, with the advent of Haemophilus influenzae type b (Hib) and Streptococcus pneumoniae conjugate vaccines in many countries, bacterial meningitis in children 6 months and older has become very rare42,48,49,50). In a retrospective review, children aged 6 to 18 months underwent an LP as part of the evaluation for a first simple FS⁴⁸⁾. Cerebrospinal fluid (CSF) pleocytosis was present in 10%, but no child had bacterial meningitis⁴⁸⁾. Another study assessed the rate of acute bacterial meningitis among 526 children aged 6 to 60 months, who presented with a first episode of complex FS. Only three of 14 children with CSF pleocytosis had acute bacterial meningitis (all S. pneumoniae), which would be a prevalence of 0.9%. Two of the three patients presented seizure prior to introduction of pneumococcal conjugated vaccine⁴⁹⁾. Investigators in India conducted a retrospective study of children aged 6 to 18 months admitted to a tertiary-care hospital for a first febrile seizure. The prevalence of meningitis in a first FS was 0.86%, compared with 4.8% in a complex FS⁴⁹⁾. Based on published evidence and consensus45,48,49,⁵⁰⁾, the recommendation for LP has recently changed to "strongly consider" in infants under 12 months.

The updated AAP guidelines for neurodiagnostic evaluation in children with simple FS are supported by evidence from some reviews⁴⁵⁾. Guidelines for LP in children with simple FS is summarized as follows: (1) LP should be performed in any child who presents with a seizure and fever and has meningeal signs and symptoms (e.g., neck stiffness, positive Kernig and Brudzinski signs), or in any child whose history or examination suggests the presence of meningitis or intracranial infection; (2) LP is an option in any infant between 6 and 12 months of age who presents with a seizure and fever when the child has not received scheduled immunization, if the child is considered deficient in Hib or S. pneumoniae immunizations or when immunization status cannot be determined because of an increased risk of bacterial meningitis; (3) LP is an option in a child who presents with a seizure and fever and was pretreated with antibiotics, because antibiotic treatment can mask the signs and symptoms of meningitis.

As a practical consequence, LP should not be performed routinely. As stated in the guidelines, current data no longer support routine LP in well-appearing, fully immunized children who present with a simple FS.

On the basis of published evidence48,49,50,⁵¹⁾, CSF is more likely to be abnormal in children initially seen with fevers and seizures who have had the following: (1) suspicious findings on physical and/or neurologic examinations, particularly meningeal signs; (2) complex FS; (3) previous physician visit within 48 hours before the seizure; (4) seizures on arrival to Emergency Departments; (5) prolonged postictal states; and (6) initial seizures after 3 years of age.

2. Electroencephalography

2. Electroencephalography

EEG is of limited value in the evaluation of children with FS12,⁴⁵⁾. EEG is more likely to be abnormal in older children with FS, children with a family history of FS, children with complex FS, or children with pre-existing neurodevelopmental abnormalities52,⁵³⁾. Although EEG abnormalities may be present in these children, their clinical significance is unclear.

There is no consistent evidence that routine EEG and/or abnormal EEGs after the first FS are predictive of either the risk of recurrence of FS or of the development of epilepsy⁴⁵⁾. Even studies that included children with complex FS and/or those with preexisting neurologic diseases (a group of children at higher risk of developing epilepsy) have failed to show EEG to be predictive of the development of epilepsy⁴⁷⁾. However, epileptiform discharges on the EEGs of patients with FS are important predictive risk factors for the development of epilepsy because the febrile illness lowers the seizure threshold, and patients with FS presenting with frontal paroxysmal EEG abnormalities may be at higher risk⁵⁴⁾.

Performing EEG within 24 hours of presentation can show generalized background slowing, which could make identifying possible epileptiform abnormalities difficult. Generalized slowing on EEG can be present up to 7 days after a child presents with febrile status epilepticus24,⁵⁵⁾. The reported incidence of EEG abnormalities in children with FS varies from 2% to 86%52,53,⁵⁴⁾. This wide range may be due to variable ages of the patients, variable criteria for selection of cases, differences in the definition of abnormalities, and variations in the time of EEG recording after seizures4,⁴⁵⁾. However, epileptic discharges do not correlate with recurrence and cannot predict the later development of epilepsy²⁾.

The AAP stated that EEG should not be a part of the routine evaluation in neurologically healthy children with a simple FS. However, this statement did not include patients with complex FS1,45,⁴⁷⁾.

3. Neuroimaging

3. Neuroimaging

Based on available evidence and consensus, the AAP recommended that neuroimaging not be included in the routine evaluation of a child with a first simple FS in both 1966 and 201145,⁴⁷⁾. There is no evidence to support the use of skull films in the evaluation of a child with a first FS⁴⁵⁾.

No data have been published that either support or negate the need for computed tomography (CT) or magnetic resonance imaging (MRI) in the evaluation of children with simple FS. However, some data show that CT scanning is associated with radiation exposure that may escalate future cancer risk. MRI is a burden because it requires sedation and is costly⁵⁶⁾. Neuroimaging has provided evidence that hippocampal injury (hippocampal edema and subsequent mesial temporal sclerosis) can occasionally occur during prolonged and focal FSs in infants who otherwise appear normal. However, it is not clear whether focality and long duration are independent factors⁵⁷⁾.

A pre-existing lesion can increase the propensity for further focally prolonged seizures and thus cause further hippocampal damage²⁴⁾. A recent study found MRI abnormalities in 14.8% of children with complex FS, while only 11.4% of 159 children with simple FS had imaging abnormalities; however, this was not statistically significant⁵⁸⁾. The most common abnormalities in MRI were subcortical focal hyperintensity, abnormal white matter signal, and focal cortical dysplasia.

As with EEG, neuroimaging may be considered in children with neurologic abnormalities on examination and in those with recurrent FS.

4. Other investigations

4. Other investigations

Based on available evidence and consensus, the AAP recommends that the following tests should not be performed routinely for the sole purpose of identifying the cause of a simple FS: measurement of serum electrolytes (calcium, phosphorus, or magnesium), blood glucose, or complete blood count. However, some children initially seen with FS are dehydrated and have low serum sodium concentration; therefore, they should be treated with overhydration with hypotonic fluid45,⁵⁹⁾. Complete blood counts may be useful in the evaluation of fever, particularly in young children, because the incidence of bacteremia in children younger than 2 years of age with or without FS is not different¹¹⁾. Therefore, laboratory testing in children with FS should be directed toward identifying the source of the fever rather than as a routine evaluation of the seizure itself. Causes of febrile illness in children with first FS, including the complex type, were the subject of two recent studies (one from a developed country and the other from a developing country) and are listed in Table 349,⁵⁰⁾. However, these studies did not consider the socioeconomic status, geographic differences, and immunization status of the population⁴⁶⁾. It can be seen that the majority of febrile illnesses are of undetermined etiology, a viral infection, or a bacterial respiratory tract infection. Occult bacteremia was a major reason for visits to the Emergency Department, but this has almost been eliminated by routine vaccination against S. pneumoniae and Hib in the US over the last two decades⁶⁰⁾. Moreover, even in an under immunized population, the likelihood of occult bacteremia is not higher in a child with a simple FS than in one with fever alone. Based on published evidence about the causes of fever in FS, it is evident that routine blood tests do not influence the management of the FS patient with no comorbidity⁴⁵⁾. There is also evidence that HHV 6 and 7 are one of the major causes of FS³²⁾.

In summary, most febrile illnesses in the FS-prone age group are of viral etiology, predominantly respiratory infections. Results of rapid viral diagnostic tests, notably those commonly available for HHV, respiratory syncytial virus and influenza, may aid in the management of a child during seasons when viruses are circulating in the population. However, there is no treatment for most viral infections⁴⁶⁾.

Treatments and prophylaxis

Treatments and prophylaxis

Parents may become extremely anxious when their child has FS, and concerned about the child's future because it can further interfere with the child's daily life¹⁵⁾. It is important that physicians play a vital role in reassuring families about the prognosis, including risks of seizure recurrence, neurologic morbidity, and mortality after FS, alleviate their anxiety, and let them return to normal life¹⁵⁾. Approaches to the treatment of FS are based on (1) the immediate treatment of prolonged or cluster seizures, (2) intermittent treatment at the time of illness, and (3) continuous anticonvulsant therapy for prophylaxis of FS12,²⁴⁾.

1. Immediate management

1. Immediate management

Treatment options for FS should include the use of a rescue seizure medication when the FS lasts longer than 5 minutes and when intravenous administration is not possible⁶¹⁾. Acute medications such as rectal diazepam (0.5 mg/kg) or buccal (0.4-0.5 mg/kg) or intranasal (0.2 mg/kg) midazolam administration are effective in stopping an ongoing seizure when intravenous access is not available, and can also be provided for home use in patients with initial prolonged febrile seizure and a high risk of recurrence62,⁶³⁾. Randomized, controlled trials have shown that midazolam has an efficacy superior to that of diazepam62,⁶³⁾. The choice of acute treatment depends on the formulations available in different countries⁴⁴⁾. In the acute setting, intravenous diazepam and lorazepam are the drugs of choice for aborting seizures or terminating continuous febrile or afebrile seizures¹⁰⁾. Diazepam is the fastest-acting benzodiazepine and rapidly crosses biological membranes, including the rectal mucosa and blood-brain barrier. A noteworthy disadvantage of diazepam is its short duration of action, the drug disappearing rapidly from the brain¹⁰⁾. Lorazepam has a more prolonged anticonvulsant action⁶⁴⁾. Lorazepam is widely used in many countries including Korea, probably because of the longer duration of action and fewer adverse effects, but its acute anticonvulsant action is less rapid than that of diazepam⁶⁵⁾. Intravenous lorazepam (Ativan) in a dose of 0.1 mg per kg is the treatment of choice for acute tonic-clonic pediatric seizures10,42,⁶⁴⁾.

2. Intermittent therapy at time of fever

2. Intermittent therapy at time of fever

By the evidence of many reported studies, intermittent use of antipyretics such as ibuprofen or acetaminophen at the onset of fever is not recommended for ongoing FS or for prevention of recurrent FSs⁴⁶⁾. However, antipyretics are usually administered for the purpose of making a child feel more comfortable. There are small relative risks of hepatotoxicity, metabolic acidosis, renal failure, or respiratory failure with acetaminophen; and coma with ibuprofen, when given in over-dose or with other risk factors present66,⁶⁷⁾. Diazepam, given orally or rectally at the onset of fever, has been demonstrated statistically to be effective in reducing the recurrence of simple and complex FS; however, the seizure could begin before the detection of fever, resulting in "failure" of the preemptive therapy68,69,⁷⁰⁾. Although intermittent use of oral diazepam at the onset of fever is effective at reducing recurrence of simple FS, the AAP does not recommend it because of potential adverse effects and because many cases of recurrent FS occur before the recognition of fever68,⁷⁰⁾. Intermittent, rather than regular, prophylaxis with phenobarbital or valproate at onset of fever is not proven effective in reducing the incidence of subsequent FS⁷¹⁾.

3. Continuous anticonvulsant therapy

3. Continuous anticonvulsant therapy

In most studies, phenobarbital and valproate have been proven effective in preventing recurrent FSs70,71,72,73,74,75,⁷⁶⁾. However, the NIH Consensus Statement concluded that febrile seizures are benign events and, in general, treatment is not recommended45,⁴⁷⁾. For children at higher risk for epilepsy (i.e., those with abnormal neurologic development, complex FS, or a family history of afebrile seizures), treatment with phenobarbital or valproic acid "might be considered." It also might be considered for children whose first FS occurred earlier than 12 months of age and who had multiple FSs³⁾. Controversy regarding the appropriate medical treatment of children with FS has been ongoing³⁾. According to a study comparing phenobarbital and a placebo group in children with FS, there is a significant benefit of phenobarbital; five percent of the treated children had a recurrence compared with 25% in the placebo group⁷²⁾. However, it must be given daily, and blood levels must be within the therapeutic range (serum concentration of 15 µg/mL or higher) for the effective use of this drug¹²⁾. Children receiving either intermittent or no phenobarbital showed no significant difference in recurrence; conversely, children receiving continuous phenobarbital on a daily basis showed a significant reduction in seizures. Therefore, if continuous phenobarbital shows no effect, it is likely to reflect noncompliance46,⁷¹⁾. In contrast to most studies, one study did not observe a significant advantage of phenobarbital even in children treated within the therapeutic range. Recurrence occurred in 19% of the control children, in 11% of those prescribed phenobarbital, and in 8% of those who completed treatment. Whether the inclusion of a larger number of subjects might have identified a significant benefit of phenobarbital is unclear⁷⁵⁾.

Daily treatment with valproic acid is effective in reducing the risk of recurrent FS. In randomized, controlled studies, only 4% of children taking valproic acid, as opposed to 35% of control subjects, had a subsequent FS. Therefore, valproic acid seems to be as effective in preventing recurrent simple FS as phenobarbital, and significantly more effective than placebo75,⁷⁶⁾. Several studies have compared valproic acid with phenobarbital in the prevention of recurrent FSs. In evaluation of three groups of children treated with phenobarbital, valproic acid, and no therapy⁷⁷⁾, valproic acid provided significantly better outcomes than the control group with no therapy. Of interest, significant differences were not identified in seizure prevention between those patients treated with phenobarbital and the control children⁷⁷⁾. However, a randomized study with children who had previous FS and were treated with valproic acid, phenobarbital, or placebo found a statistically significant difference among the three groups, with recurrence rates of 4%, 19%, and 35%, respectively. Therefore, significant differences were evident between the treatment groups (valproic acid versus phenobarbital) and between children treated with valproic acid and those treated with placebo72,⁷⁸⁾.

Carbamazepine and phenytoin are not effective in preventing recurrent FSs. Therefore, these medications should be avoided when considering treatment for simple or complex FS³⁾.

Although newer antiepileptic agents may prove to be safer and more effective in the treatment of recurrent or prolonged FSs, these medications have not yet been adequately studied in children with recurrent or complex FS²³⁾.

Levetiracetam can be an effective medication in preventing the recurrence of complex FS⁷⁹⁾.

A major disadvantage of continuous administration is the wide spectrum of adverse effects. Side effects and toxic reactions of phenobarbital are reported in up to 40% of infants or children receiving phenobarbital and are the cause of discontinuation of therapy in up to 25% of patients. Valproic acid causes few serious side effects or toxic reactions; however, gastrointestinal upset, toxic hepatitis, pancreatitis, and other side effects have been reported. Liver function should be monitored periodically in patients undergoing prolonged valproic acid therapy, particularly in infants 2 years and younger⁸⁰⁾. In another study, adverse effects were reported less often with valproate (24%) than with phenobarbital (61%), but the authors concluded that the risk-benefit ratio was insufficient to recommend either of these antiepileptic drugs for secondary prophylaxis⁸⁰⁾.

In summary, oral/intravenous diazepam and lorazepam are the drugs of choice for aborting a prolonged seizure in an acute setting. Although antipyretics may improve the children's comfort from fever, they should not be used to prevent FS prophylactically.

Although there is evidence that both continuous antiepileptic therapy with phenobarbital or valproic acid, and intermittent therapy with oral/rectal diazepam are effective in reducing the risk of recurrence, the AAP does not recommend that intermittent or continuous anticonvulsants be used to prevent recurrence of FS.

In situations in which parental anxiety associated with FS is severe, intermittent oral/rectal diazepam therapy at the onset of febrile illness to prevent recurrence may be advisable1,3,12,46,⁸⁰⁾.

Prognosis and outcome

Prognosis and outcome

Four potential adverse outcomes of FS that theoretically may be altered by an effective therapeutic agent are: (1) decline in IQ (intelligence quotient); (2) increased risk of epilepsy; (3) risk of recurrent FSs; and (4) death¹⁾. The first concern, a decline in IQ, low academic performance, neurocognitive inattention, or behavioral abnormalities, has not been shown to be a consequence of recurrent simple FSs⁸¹⁾. Children who experienced FS observed no significant difference in their learning compared with sibling controls. In a study of children with FSs compared with control children, no difference in learning was identified, except in those children who had neurologic abnormalities before their first seizure⁸¹⁾. The second concern, increased risk of epilepsy, is more complex. Children with simple FS have approximately the same risk (i.e., 1%) of developing epilepsy by the age of 7 as the general population³⁹⁾. However, children with a history of multiple simple FS, younger than 12 months at the time of their first FS, and a family history of epilepsy, are at higher risk, with generalized afebrile seizures developing by 25 years of age in 2.4%⁴³⁾. There currently is no evidence that simple FS causes structural damage to the brain¹⁾. The third concern, in contrast to the rare risk of developing epilepsy, is that children with simple FS have a high rate of recurrence. The risk varies with age. Children younger than 12 months at the time of their first simple FS have an approximately 50% probability of having recurrent FSs. Children older than 12 months at the time of their first event have an approximately 30% probability of a second FS¹⁸⁾. Finally, there is a theoretical risk of a child dying during a simple FS, but no case of this has yet been reported¹⁾.

Vaccination and FS

Vaccination and FS

Although vaccine-induced FS is a rare event that does not lead to deleterious outcomes, it could affect patient/parent and physician attitudes toward the safety of vaccination. Vaccine administration is the second most common medical event associated with FS82,⁸³⁾. Immunization has been associated with FS and an event occurring within 72 hours of immunization is commonly accepted as being associated with vaccine. Exceptions to this are the live attenuated vaccines for which events may be delayed until 7-14 days after vaccination⁸⁴⁾. Vaccines cause fever and may induce FS, but it is not clear whether a vaccine-induced fever is more epileptogenic than a fever due to other causes, such as a viral infection. Estimates of relative risk of seizure are dependent on vaccine type and components⁸⁴⁾. Seizure is more likely to occur after administration of certain vaccines, particularly live attenuated vaccines such as the measles, mumps, and rubella (MMR) vaccine, and toxin-containing or whole-cell preparations such as diphtheria-tetanus-acelluar pertussis (DTaP)85,86,⁸⁷⁾. Rates of all adverse events with acellular pertussis vaccines are estimated to be about one third of those of whole-cell preparations⁸⁸⁾.

As reported for simultaneous administration of influenza and pneumococcal vaccines, the associated risks could be increased when vaccines are administered in combination⁸³⁾. The recent multicomponent, recombinant meningococcal serogroup B (4CMenB) vaccine is an example. A recent study showed that increased reactogenicity is associated with this vaccine when it is administered concomitantly with routine vaccines (diphtheriatetanus-acellular pertussis, inactivated poliovirus, and hepatitis B plus Haemophilus influenzae type b [DTaP-IPV-HBV/Hib] and seven-valent pneumococcal vaccine [PCV7])⁸⁹⁾. Seventy-seven percent of infants had a fever of 38.5℃ or higher after 4CMenB injection, compared with only 45% after routine vaccinations alone and 47% with Neisseria meningitidis group C covaccination83,⁸⁹⁾. It needs to be kept in mind that children who experience FSs after immunization do not appear to be at higher risk for subsequent seizures or neurodevelopmental disability43,⁹⁰⁾. Although they are frequently reported, the adverse events following immunization such as FS are, nevertheless, rare events that may be attributable to DTaP and MMR vaccinations⁹⁰⁾. In comparison, measles disease itself results in 1 in 1000 infected children developing encephalitis, and 1 in 50 and 1 in 250 children with pertussis disease experience convulsions and encephalopathy, respectively⁸²⁾.

Therefore, despite the occurrence of this transient complication from fever after immunization, it needs to be emphasized that vaccination against measles and pertussis91,⁹²⁾, as well as invasive pneumococcus⁹³⁾ and Hib type b disease94,⁹⁵⁾, has significantly reduced not only the overall incidence of neurologic disorders associated with the diseases themselves, but also that of the associated serious and often permanent neurodevelopmental disabilities due to these diseases⁸¹⁾.

Administration of acetaminophen at the time of primary immunization with an inactivated-component vaccine (e.g., DTwP-polio) has been shown to significantly reduce or prevent the appearance of fever and has found wide acceptance96,⁹⁷⁾.

Ibuprofen and acetaminophen have been equally recommended for administration at the time of DTaP immunization, both prior to vaccination, and every 4 hours for 24 hours thereafter for children with a history of FS, to reduce the possibility of postvaccination fever⁸²⁾.

In summary²⁾: (1) None of the standard vaccinations is currently contraindicated for children with FS. All vaccinations of children with FS, and especially of children with a history of prolonged FS lasting >15 minutes, should be given individually under the supervision of the pediatrician or child neurologist who is responsible for providing information regarding the usefulness and potential side effects of any vaccination. (2) Children can be given a vaccination at least 2-3 months after the last episode of FS. This period may be shortened in light of the child's condition and the type of vaccine to be administered. (3) When a temperature of 37.5℃ or higher develops during the risk period for fever after vaccination, a suppository or oral diazepam can be administered prophylactically.

Guidelines for referral

Guidelines for referral

It is important to refer every child to a hospital after an episode at home, as there will be significant parental anxiety afterwards. A thorough and detailed history of the episode should be written down. Guidance for referral to a secondary or tertiary hospital is summarized in Table 413,¹⁷⁾.

Information for parents/guardians

Information for parents/guardians

To reduce anxiety and fear and to enable parents/guardians to cope with a child with FS, the following explanations must be given: (1) the natural history of FS, including incidence, age dependency, natural course, recurrence rate, incidence in siblings, difference between epilepsy and FS, the probability of onset of later epilepsy, and the prognosis for mental/behavioral development; (2) the possible measures to cope with fever and seizure episodes; and (3) a full explanation of the appropriate choice of antiepileptic drugs and potential side effects, and the need to avoid over-reliance on drug therapy2,44,⁹⁸⁾.

Acknowledgments

The author gratefully acknowledges data collection and language assistance rendered by Dr. Lee Eun Hye and medical student Lee You Jin.

Conflicts of interest

No potential conflict of interest relevant to this article was reported.

References

1. Steering Committee on Quality Improvement and Management. Subcommittee on Febrile Seizures American Academy of Pediatrics. Febrile seizures: clinical practice guideline for the long-term management of the child with simple febrile seizures. Pediatrics 2008;121:1281–1286.
[Article] [PubMed]

2. Sugai K. Current management of febrile seizures in Japan: an overview. Brain Dev 2010;32:64–70.
[Article] [PubMed]

3. Baumann RJ, Duffner PK. Treatment of children with simple febrile seizures: the AAP practice parameter. American Academy of Pediatrics. Pediatr Neurol 2000;23:11–17.
[Article] [PubMed]

4. National Institute of Health. Febrile seizures: long-term management of children with fever-associated seizures. Pediatrics 1980;66:1009–1012.
[Article]

5. Guidelines for epidemiologic studies on epilepsy. Commission on Epidemiology and Prognosis, International League Against Epilepsy. Epilepsia 1993;34:592–596.
[Article] [PubMed]

6. Germano IM, Zhang YF, Sperber EF, Moshe SL. Neuronal migration disorders increase susceptibility to hyperthermia-induced seizures in developing rats. Epilepsia 1996;37:902–910.
[Article] [PubMed]

7. Takano T, Sakaue Y, Sokoda T, Sawai C, Akabori S, Maruo Y, et al. Seizure susceptibility due to antihistamines in febrile seizures. Pediatr Neurol 2010;42:277–279.
[Article] [PubMed]

8. Vestergaard M, Christensen J. Register-based studies on febrile seizures in Denmark. Brain Dev 2009;31:372–377.
[Article] [PubMed]

9. Livingston S, Pauli LL, Pruce I, Kramer II. Febrile convulsions: diagnosis, treatment, and prognosis. Pediatr Ann 1979;8:133–153.
[PubMed]

10. Knudsen FU. Febrile seizures: treatment and outcome. Brain Dev 1996;18:438–449.
[Article] [PubMed]

11. Berg AT, Shinnar S. Complex febrile seizures. Epilepsia 1996;37:126–133.
[Article] [PubMed]

12. Shinnar S, Glauser TA. Febrile seizures. J Child Neurol 2002;17(Suppl 1): S44–S52.
[Article] [PubMed]

13. Paul SP, Blaikley S, Chinthapalli R. Clinical update: febrile convulsion in childhood. Community Pract 2012;85:36–38.

14. Stafstrom CE. The incidence and prevalence of febrile seizures. In: Baram TZ, Shinnar S, editors. Febrile seizures. San Diego: Academic Press, 2002:1–25.

15. Sadleir LG, Scheffer IE. Febrile seizures. BMJ 2007;334:307–311.
[Article] [PubMed] [PMC]

16. Berg AT, Shinnar S. Unprovoked seizures in children with febrile seizures: short-term outcome. Neurology 1996;47:562–568.
[Article] [PubMed]

17. Shinnar S, Pellock JM, Moshe SL, Maytal J, O'Dell C, Driscoll SM, et al. In whom does status epilepticus occur: age-related differences in children. Epilepsia 1997;38:907–914.
[Article] [PubMed]

18. Berg AT, Shinnar S, Darefsky AS, Holford TR, Shapiro ED, Salomon ME, et al. Predictors of recurrent febrile seizures. A prospective cohort study. Arch Pediatr Adolesc Med 1997;151:371–378.
[Article] [PubMed]

19. Berg AT, Shinnar S, Hauser WA, Alemany M, Shapiro ED, Salomon ME, et al. A prospective study of recurrent febrile seizures. N Engl J Med 1992;327:1122–1127.
[Article] [PubMed]

20. Berg AT, Shinnar S, Levy SR, Testa FM. Childhood-onset epilepsy with and without preceding febrile seizures. Neurology 1999;53:1742–1748.
[Article] [PubMed]

21. Greenberg DA, Holmes GL. The genetics of febrile seizures. In: Baram TZ, Shinnar S, editors. Febrile seizures. San Diego: Academic Press, 2002:249–261.

22. Wallace RH, Wang DW, Singh R, Scheffer IE, George AL Jr, Phillips HA, et al. Febrile seizures and generalized epilepsy associated with a mutation in the Na⁺-channel β1 subunit gene SCN1B. Nat Genet 1998;19:366–370.
[Article] [PubMed]

23. Herini ES, Gunadi , Harahap IS, Yusoff S, Morikawa S, Patria SY, et al. Generalized epilepsy with febrile seizures plus (GEFS+) spectrum: clinical manifestations and SCN1A mutations in Indonesian patients. Epilepsy Res 2010;90:132–139.
[Article] [PubMed]

24. Patel AD, Vidaurre J. Complex febrile seizures: a practical guide to evaluation and treatment. J Child Neurol 2013;28:762–767.
[Article] [PubMed]

25. Dube CM, Brewster AL, Baram TZ. Febrile seizures: mechanisms and relationship to epilepsy. Brain Dev 2009;31:366–371.
[Article] [PubMed] [PMC]

26. Shibasaki K, Suzuki M, Mizuno A, Tominaga M. Effects of body temperature on neural activity in the hippocampus: regulation of resting membrane potentials by transient receptor potential vanilloid 4. J Neurosci 2007;27:1566–1575.
[Article] [PubMed] [PMC]

27. Cartmell T, Luheshi GN, Rothwell NJ. Brain sites of action of endogenous interleukin-1 in the febrile response to localized inflammation in the rat. J Physiol 1999;518(Pt 2): 585–594.
[Article] [PubMed] [PMC]

28. Cartmell T, Southgate T, Rees GS, Castro MG, Lowenstein PR, Luheshi GN. Interleukin-1 mediates a rapid inflammatory response after injection of adenoviral vectors into the brain. J Neurosci 1999;19:1517–1523.
[Article] [PubMed] [PMC]

29. Ban E, Milon G, Prudhomme N, Fillion G, Haour F. Receptors for interleukin-1 (alpha and beta) in mouse brain: mapping and neuronal localization in hippocampus. Neuroscience 1991;43:21–30.
[Article] [PubMed]

30. Vezzani A, Granata T. Brain inflammation in epilepsy: experimental and clinical evidence. Epilepsia 2005;46:1724–1743.
[Article] [PubMed]

31. Dube C, Vezzani A, Behrens M, Bartfai T, Baram TZ. Interleukin-1 beta contributes to the generation of experimental febrile seizures. Ann Neurol 2005;57:152–155.
[Article] [PubMed] [PMC]

32. Barone SR, Kaplan MH, Krilov LR. Human herpesvirus-6 infection in children with first febrile seizures. J Pediatr 1995;127:95–97.
[Article] [PubMed]

33. Aram JA, Lodge D. Epileptiform activity induced by alkalosis in rat neocortical slices: block by antagonists of N-methyl-D-aspartate. Neurosci Lett 1987;83:345–350.
[Article] [PubMed]

34. Bethune P, Gordon K, Dooley J, Camfield C, Camfield P. Which child will have a febrile seizure. Am J Dis Child 1993;147:35–39.
[Article] [PubMed]

35. Berg AT, Shinnar S, Shapiro ED, Salomon ME, Crain EF, Hauser WA. Risk factors for a first febrile seizure: a matched case-control study. Epilepsia 1995;36:334–341.
[Article] [PubMed]

36. Lee EH, Chung S. A comparative study of febrile and afebrile seizures associated with mild gastroenteritis. Brain Dev 2013;35636–35640.

37. Annegers JF, Blakley SA, Hauser WA, Kurland LT. Recurrence of febrile convulsions in a population-based cohort. Epilepsy Res 1990;5:209–216.
[Article] [PubMed]

38. Berg AT, Shinnar S, Hauser WA, Leventhal JM. Predictors of recurrent febrile seizures: a metaanalytic review. J Pediatr 1990;116:329–337.
[Article] [PubMed]

39. Nelson KB, Ellenberg JH. Predictors of epilepsy in children who have experienced febrile seizures. N Engl J Med 1976;295:1029–1033.
[Article] [PubMed]

40. Verity CM, Golding J. Risk of epilepsy after febrile convulsions: a national cohort study. BMJ 1991;303:1373–1376.
[Article] [PubMed] [PMC]

41. Offringa M, Bossuyt PM, Lubsen J, Ellenberg JH, Nelson KB, Knudsen FU, et al. Risk factors for seizure recurrence in children with febrile seizures: a pooled analysis of individual patient data from five studies. J Pediatr 1994;124:574–584.
[Article] [PubMed]

42. French JA. Febrile seizures: possible outcomes. Neurology 2012;79:e80–e82.
[Article] [PubMed]

43. Annegers JF, Hauser WA, Shirts SB, Kurland LT. Factors prognostic of unprovoked seizures after febrile convulsions. N Engl J Med 1987;316:493–498.
[Article] [PubMed]

44. Graves RC, Oehler K, Tingle LE. Febrile seizures: risks, evaluation, and prognosis. Am Fam Physician 2012;85:149–153.
[PubMed]

45. Subcommittee on Febrile Seizures. American Academy of Pediatrics. Neurodiagnostic evaluation of the child with a simple febrile seizure. Pediatrics 2011;127:389–394.
[Article] [PubMed]

46. Oluwabusi T, Sood SK. Update on the management of simple febrile seizures: emphasis on minimal intervention. Curr Opin Pediatr 2012;24:259–265.
[Article] [PubMed]

47. Practice parameter: the neurodiagnostic evaluation of the child with a first simple febrile seizure. American Academy of Pediatrics. Provisional Committee on Quality Improvement, Subcommittee on Febrile Seizures. Pediatrics 1996;97:769–772.
[PubMed]

48. Kimia AA, Capraro AJ, Hummel D, Johnston P, Harper MB. Utility of lumbar puncture for first simple febrile seizure among children 6 to 18 months of age. Pediatrics 2009;123:6–12.
[Article] [PubMed]

49. Kimia A, Ben-Joseph EP, Rudloe T, Capraro A, Sarco D, Hummel D, et al. Yield of lumbar puncture among children who present with their first complex febrile seizure. Pediatrics 2010;126:62–69.
[Article] [PubMed]

50. Batra P, Gupta S, Gomber S, Saha A. Predictors of meningitis in children presenting with first febrile seizures. Pediatr Neurol 2011;44:35–39.
[Article] [PubMed]

51. Choi KC, Cho BS, Chung SJ, Choi YM, Ahn CI. Role of lumbar puncture in children with first febrile convulsion. J Korean Pediatr Soc 1984;27:718–724.

52. Kanemura H, Mizorogi S, Aoyagi K, Sugita K, Aihara M. EEG characteristics predict subsequent epilepsy in children with febrile seizure. Brain Dev 2012;34:302–307.
[Article] [PubMed]

53. Sofijanov N, Emoto S, Kuturec M, Dukovski M, Duma F, Ellenberg JH, et al. Febrile seizures: clinical characteristics and initial EEG. Epilepsia 1992;33:52–57.
[Article] [PubMed]

54. Wo SB, Lee JH, Lee YJ, Sung TJ, Lee KH, Kim SK. Risk for developing epilepsy and epileptiform discharges on EEG in patients with febrile seizures. Brain Dev 2013;35:307–311.
[Article] [PubMed]

55. Nordli DR, Moshe SL, Shinnar S. The role of EEG in febrile status epilepticus (FSE). Brain Dev 2010;32:37–41.
[Article] [PubMed]

56. Stein SC, Hurst RW, Sonnad SS. Meta-analysis of cranial CT scans in children: a mathematical model to predict radiation-induced tumors. Pediatr Neurosurg 2008;44:448–457.
[Article] [PubMed]

57. Janszky J, Schulz R, Ebner A. Clinical features and surgical outcome of medial temporal lobe epilepsy with a history of complex febrile convulsions. Epilepsy Res 2003;55:1–8.
[Article] [PubMed]

58. Hesdorffer DC, Chan S, Tian H, Allen Hauser W, Dayan P, Leary LD, et al. Are MRI-detected brain abnormalities associated with febrile seizure type? Epilepsia 2008;49:765–771.
[Article] [PubMed]

59. Thoman JE, Duffner PK, Shucard JL. Do serum sodium levels predict febrile seizure recurrence within 24 hours? Pediatr Neurol 2004;31:342–344.
[Article] [PubMed]

60. Stoll ML, Rubin LG. Incidence of occult bacteremia among highly febrile young children in the era of the pneumococcal conjugate vaccine: a study from a Children's Hospital Emergency Department and Urgent Care Center. Arch Pediatr Adolesc Med 2004;158:671–675.
[Article] [PubMed]

61. Hesdorffer DC, Shinnar S, Lewis DV, Moshe SL, Nordli DR Jr, Pellock JM, et al. Design and phenomenology of the FEBSTAT study. Epilepsia 2012;53:1471–1480.
[Article] [PubMed] [PMC]

62. McIntyre J, Robertson S, Norris E, Appleton R, Whitehouse WP, Phillips B, et al. Safety and efficacy of buccal midazolam versus rectal diazepam for emergency treatment of seizures in children: a randomised controlled trial. Lancet 2005;366:205–210.
[Article] [PubMed]

63. Bhattacharyya M, Kalra V, Gulati S. Intranasal midazolam vs rectal diazepam in acute childhood seizures. Pediatr Neurol 2006;34:355–359.
[Article] [PubMed]

64. Lacey DJ, Singer WD, Horwitz SJ, Gilmore H. Lorazepam therapy of status epilepticus in children and adolescents. J Pediatr 1986;108(5 Pt 1): 771–774.
[Article] [PubMed]

65. Giang DW, McBride MC. Lorazepam versus diazepam for the treatment of status epilepticus. Pediatr Neurol 1988;4:358–361.
[Article] [PubMed]

66. Easley RB, Altemeier WA 3rd. Central nervous system manifestations of an ibuprofen overdose reversed by naloxone. Pediatr Emerg Care 2000;16:39–41.
[Article] [PubMed]

67. American Academy of Pediatrics. Committee on Drugs. Acetaminophen toxicity in children. Pediatrics 2001;108:1020–1024.
[Article] [PubMed]

68. Verrotti A, Latini G, di Corcia G, Giannuzzi R, Salladini C, Trotta D, et al. Intermittent oral diazepam prophylaxis in febrile convulsions: its effectiveness for febrile seizure recurrence. Eur J Paediatr Neurol 2004;8:131–134.
[Article] [PubMed]

69. Autret E, Billard C, Bertrand P, Motte J, Pouplard F, Jonville AP. Double-blind, randomized trial of diazepam versus placebo for prevention of recurrence of febrile seizures. J Pediatr 1990;117:490–494.
[Article] [PubMed]

70. Knudsen FU, Vestermark S. Prophylactic diazepam or phenobarbitone in febrile convulsions: a prospective, controlled study. Arch Dis Child 1978;53:660–663.
[Article] [PubMed] [PMC]

71. Wolf SM, Carr A, Davis DC, Davidson S, Dale EP, Forsythe A, et al. The value of phenobarbital in the child who has had a single febrile seizure: a controlled prospective study. Pediatrics 1977;59:378–385.
[Article] [PubMed]

72. Camfield PR, Camfield CS, Shapiro SH, Cummings C. The first febrile seizure: antipyretic instruction plus either phenobarbital or placebo to prevent recurrence. J Pediatr 1980;97:16–21.
[Article] [PubMed]

73. Wallace SJ, Smith JA. Successful prophylaxis against febrile convulsions with valproic acid or phenobarbitone. Br Med J 1980;280:353–354.
[Article] [PubMed] [PMC]

74. Wolf SM. The effectiveness of phenobarbital in the prevention of recurrent febrile convulsions in children with and without a history of pre-, peri- and postnatal abnormalities. Acta Paediatr Scand 1977;66:585–587.
[Article] [PubMed]

75. Heckmatt JZ, Houston AB, Clow DJ, Strephenson JB, Dodd KL, Lealman GT, et al. Failure of phenobarbitone to prevent febrile convulsions. Br Med J 1976;1:559–561.
[Article] [PubMed] [PMC]

76. Bassan H, Barzilay M, Shinnar S, Shorer Z, Matoth I, Gross-Tsur V. Prolonged febrile seizures, clinical characteristics, and acute management. Epilepsia 2013;54:1092–1098.
[Article] [PubMed]

77. Lee K, Melchior JC. Sodium valproate versus phenobarbital in the prophylactic treatment of febrile convulsions in childhood. Eur J Pediatr 1981;137:151–153.
[Article] [PubMed]

78. Mamelle N, Mamelle JC, Plasse JC, Revol M, Gilly R. Prevention of recurrent febrile convulsions--a randomized therapeutic assay: sodium valproate, phenobarbital and placebo. Neuropediatrics 1984;15:37–42.
[Article]

79. Lynch BA, Lambeng N, Nocka K, Kensel-Hammes P, Bajjalieh SM, Matagne A, et al. The synaptic vesicle protein SV2A is the binding site for the antiepileptic drug levetiracetam. Proc Natl Acad Sci U S A 2004;101:9861–9866.
[Article] [PubMed] [PMC]

80. Herranz JL, Armijo JA, Arteaga R. Effectiveness and toxicity of phenobarbital, primidone, and sodium valproate in the prevention of febrile convulsions, controlled by plasma levels. Epilepsia 1984;25:89–95.
[Article] [PubMed]

81. Verity CM, Butler NR, Golding J. Febrile convulsions in a national cohort followed up from birth. II--Medical history and intellectual ability at 5 years of age. Br Med J (Clin Res Ed) 1985;290:1311–1315.
[Article] [PubMed] [PMC]

82. Kohl KS, Marcy SM, Blum M, Connell Jones M, Dagan R, Hansen J, et al. Fever after immunization: current concepts and improved future scientific understanding. Clin Infect Dis 2004;39:389–394.
[Article] [PubMed]

83. Principi N, Esposito S. Vaccines and febrile seizures. Expert Rev Vaccines 2013;12:885–892.
[Article] [PubMed]

84. Brown NJ, Berkovic SF, Scheffer IE. Vaccination, seizures and vaccine damage. Curr Opin Neurol 2007;20:181–187.
[Article] [PubMed]

85. Braun MM, Mootrey GT, Salive ME, Chen RT, Ellenberg SS. Infant immunization with acellular pertussis vaccines in the United States: assessment of the first two years' data from the Vaccine Adverse Event Reporting System (VAERS). Pediatrics 2000;106:E51
[Article] [PubMed]

86. Pollock TM, Miller E, Mortimer JY, Smith G. Symptoms after primary immunisation with DTP and with DT vaccine. Lancet 1984;2:146–149.
[PubMed]

87. Blumberg DA, Lewis K, Mink CM, Christenson PD, Chatfield P, Cherry JD. Severe reactions associated with diphtheria-tetanuspertussis vaccine: detailed study of children with seizures, hypotonic-hyporesponsive episodes, high fevers, and persistent crying. Pediatrics 1993;91:1158–1165.
[Article] [PubMed]

88. Rosenthal S, Chen R, Hadler S. The safety of acellular pertussis vaccine vs whole-cell pertussis vaccine: a postmarketing assessment. Arch Pediatr Adolesc Med 1996;150:457–460.
[Article] [PubMed]

89. Vesikari T, Esposito S, Prymula R, Ypma E, Kohl I, Toneatto D, et al. Immunogenicity and safety of an investigational multicomponent, recombinant, meningococcal serogroup B vaccine (4CMenB) administered concomitantly with routine infant and child vaccinations: results of two randomised trials. Lancet 2013;381:825–835.
[Article] [PubMed]

90. Barlow WE, Davis RL, Glasser JW, Rhodes PH, Thompson RS, Mullooly JP, et al. The risk of seizures after receipt of whole-cell pertussis or measles, mumps, and rubella vaccine. N Engl J Med 2001;345:656–661.
[Article] [PubMed]

91. Romanus V, Jonsell R, Bergquist SO. Pertussis in Sweden after the cessation of general immunization in 1979. Pediatr Infect Dis J 1987;6:364–371.
[Article] [PubMed]

92. Koskiniemi M, Korppi M, Mustonen K, Rantala H, Muttilainen M, Herrgard E, et al. Epidemiology of encephalitis in children: a prospective multicentre study. Eur J Pediatr 1997;156:541–545.
[Article] [PubMed]

93. Dagan R. Immunisation with a pneumococcal 7-valent conjugate vaccine. Int J Clin Pract 2002;56:287–291.
[Article] [PubMed]

94. Lee GM, Harper MB. Risk of bacteremia for febrile young children in the post-Haemophilus influenzae type b era. Arch Pediatr Adolesc Med 1998;152:624–628.
[PubMed]

95. Alpern ER, Alessandrini EA, Bell LM, Shaw KN, McGowan KL. Occult bacteremia from a pediatric emergency department: current prevalence, time to detection, and outcome. Pediatrics 2000;106:505–511.
[Article] [PubMed]

96. Lewis K, Cherry JD, Sachs MH, Woo DB, Hamilton RC, Tarle JM, et al. The effect of prophylactic acetaminophen administration on reactions to DTP vaccination. Am J Dis Child 1988;142:62–65.
[Article] [PubMed]

97. Ipp MM, Gold R, Greenberg S, Goldbach M, Kupfert BB, Lloyd DD, et al. Acetaminophen prophylaxis of adverse reactions following vaccination of infants with diphtheria-pertussis-tetanus toxoidspolio vaccine. Pediatr Infect Dis J 1987;6:721–725.
[Article] [PubMed]

98. Fukuyama Y, Seki T, Ohtsuka C, Miura H, Hara M. Practical guidelines for physicians in the management of febrile seizures. Brain Dev 1996;18:479–484.
[Article] [PubMed]

Table 1

Risk factors for recurrence of febrile seizure (FS)

Adapted from Shinnar S, et al. J Child Neurol 2002;17 Suppl 1:S44-52, with permission of SAGE Publication¹²⁾.

Table 2

Risk factors for subsequent epilepsy in children with febrile seizure (FS)

Adapted from Shinnar S, et al. J Child Neurol 2002;17 Suppl 1:S44-52, with permission of SAGE Publication¹²⁾.

Table 3

Causes of fever in children presenting with febrile seizure (FS)

Values are presented as number (% of total).

N/R, not recorded.

Table 4

Guidance for referral of children with febrile seizure (FS)13,¹⁷⁾