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Cognitive and behavioural development in children presenting with complex febrile seizures: at onset and school age
Emilie Sheppard1, Eve Lalancette1, Fanny Thébault-Dagher1
1Department of Psychology, University of Montreal, Marie Victorin Building, 90 Vincent-D'Indy Avenue, Montreal, Quebec, H2V 2S9, Canada, CHU Sainte-Justine, 3175 Côte Ste-Catherine, Montreal, Qc., H3T 1C5, Canada.
Insights
Children with complex febrile seizures (FS) show normal early development, but may face executive functioning and memory challenges later. Long-term follow-up is crucial for understanding outcomes after febrile seizures.
Area of Science:
- Pediatric Neurology
- Developmental Neuroscience
Background:
- Febrile seizures (FS) are common in childhood.
- Complex FS carry potential risks for neurodevelopment.
- Early assessment is key to identifying developmental trajectories.
Purpose of the Study:
- To assess neurodevelopment, cognition, and behavior after initial complex FS.
- To compare outcomes at infancy and school age.
- To investigate the impact of risk factors on cognitive development.
Main Methods:
- Two cohorts: infants and school-age children with complex FS and controls.
- Infants assessed for cognitive, motor, language, and emotional development.
- School-age children assessed for intelligence, executive function, learning, memory, and behavior.
Main Results:
- Infants with complex FS showed normal development within the first year.
- School-age children with complex FS had lower executive functioning and memory.
- Complex FS correlated with attentional problems, anxiety, and hyperactivity.
Conclusions:
- Early development in complex FS infants appears normal.
- Cognitive challenges, particularly in executive function and memory, emerge by school age.
- Long-term follow-up is essential to understand the full impact of complex FS.
Objective:
Our goal was to assess development, cognition and behaviour following an initial complex febrile seizure (FS), at onset and school age, in the context of known risk factors for cognitive development.
Methods:
Two cohorts were recruited. Thirty-five infants with an initial complex FS were assessed within the first year post-seizure and compared to 30 controls (simple FS) based on measures of cognitive, motor and language development, behaviour and emotions. Additionally, 19 school-age children with previous complex FS (11 multiple, eight prolonged) were assessed and compared to 19 controls (simple FS) based on measures of intelligence, learning/memory, executive functioning, behaviour and emotions.
Results:
Within the first year post-onset, infants with complex FS did not significantly differ from controls based on developmental measures. Seizure duration and age at seizure onset did not impact developmental outcome. School-age children with complex FS showed unaltered global intelligence, but lower executive functioning, compared to controls. Children with prolonged FS also showed evidence of a lower level of learning and memory abilities. Neuropsychological scores correlated with seizure duration. Children with complex FS showed more attentional problems and anxious/depressed symptomatology at onset and school age, and more hyperactivity at school age.
Significance:
Infants with complex FS seemed to show normal development within the first year post-seizure onset. However, challenges in executive functioning, learning and memory at school age were found in children with a history of FS. Hence, at school age, cognitive challenges cannot be excluded based on undifferentiated early cognitive development, and may occur even in the absence of the most severe form of FS (i.e., FSE). Beyond the limits of this study (i.e., small sample size, use of parental questionnaires for emotional/behavioural outcome, absence of focal cases in the school-age cohort), our results suggest that a follow-up is necessary beyond the early preschool years in order to understand the long-term outcome.
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