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Published on: November 8, 2018
Therapeutic indicators of acute encephalopathy in patients with complex febrile seizures
Hiroaki Nagase1, Taku Nakagawa, Kazunori Aoki
1Department of Neurology, Hyogo Prefectural Kobe Children's Hospital, Kobe, Japan. nagasehiroaki@msn.com
Insights
Predicting neurologic damage in children with febrile seizures is possible within 6 hours using identified risk factors. Early identification of severe febrile seizures (SFS) aids in managing potential acute encephalopathy.
Area of Science:
- Pediatric Neurology
- Neuroscience
- Clinical Medicine
Background:
- Febrile seizures are common in children, but predictors of neurologic damage require identification.
- Altered consciousness within 6 hours of seizure onset is a critical period for assessment.
Purpose of the Study:
- To identify early predictors of neurologic damage in children experiencing febrile seizures or altered consciousness.
- To establish criteria for identifying children at high risk for poor neurologic outcomes.
Main Methods:
- A cohort of 86 children (4-159 months) with complex febrile seizures were analyzed.
- Children were classified into good (PCPC=1) and poor (PCPC=2-6) outcome groups.
- Clinical and laboratory data were compared between outcome groups.
Main Results:
- Three key predictors of poor neurologic outcome were identified within 6 hours: consciousness disturbance/hemiplegia, refractory status epilepticus, and elevated aspartate aminotransferase (>90 IU/L).
- These factors achieved 94% sensitivity and 67% specificity for identifying poor outcomes (OR=36.6).
- Children meeting these criteria and diagnosed with acute encephalopathy had poor outcomes.
Conclusions:
- Neurologic damage in complex febrile seizures can be predicted early using identified risk factors.
- The study proposes the concept of severe febrile seizures (SFS) for children meeting these risk factors.
- SFS criteria can facilitate the design of interventional studies for acute encephalopathy.
Background:
The aim of this study was to identify predictors of neurologic damage in children with febrile seizures or altered consciousness within 6 h of seizure onset.
Methods:
The present study included 86 children (age range, 4-159 months old), who fulfilled the diagnostic criteria for complex febrile seizures on admission between October 2002 and November 2008. Using the Pediatric Cerebral Performance Category Scale (PCPC), the children were classified into two groups: poor outcome (PCPC = 2-6) and good outcome (PCPC = 1). Clinical profiles and laboratory findings were compared between the groups.
Results:
Of the 86 children, 17 fell into the poor outcome and 69 into the good outcome group. Using univariate analysis, three early risk factors for poor outcome were identified: (i) consciousness disturbance or hemiplegia at 6 h from onset; (ii) refractory status epilepticus; and (iii) elevation of aspartate aminotransferase to >90 IU/L within 6 h of onset. Using these criteria, children in the poor outcome group were identified with a 94% sensitivity and 67% specificity rate (odds ratio, 36.6; 95% confidence interval: 4.87-1560). During the study period, the inpatients who met the criteria for acute encephalopathy also fell into the poor outcome group.
Conclusions:
The development of neurologic damage in children with complex febrile seizures can be predicted within 6 h of onset, using the identified risk factors. The authors propose an assumption of severe febrile seizures (SFS) in children who fulfill these risk factors. Using SFS as an inclusion criterion, an interventional study for acute encephalopathy can be designed.
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