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Published on: June 21, 2019
Epilepsy Due to Mild TBI in Children: An Experience at a Tertiary Referral Center
Jun T Park1,2,3, Sarah J DeLozier3, Harry T Chugani4
1Epilepsy Center, UH Rainbow Babies & Children's Hospital, Cleveland, OH 44106, USA.
Insights
Children with mild traumatic brain injury (TBI) are less likely to develop posttraumatic epilepsy (PTE) and often have normal head computed tomography (HCT) and electroencephalogram (EEG) results. This study highlights the distinct diagnostic profile of PTE in mild TBI cases.
Area of Science:
- Pediatric Neurology
- Neurotraumatology
- Epileptology
Background:
- Posttraumatic epilepsy (PTE) is a significant complication in children following traumatic brain injury (TBI), particularly severe TBI.
- Existing research predominantly focuses on severe TBI, leaving a gap in understanding PTE in mild TBI cases.
Purpose of the Study:
- To investigate the diagnostic utility of head computed tomography (HCT) and electroencephalogram (EEG) in children with mild TBI.
- To assess the risk of developing drug-resistant epilepsy in pediatric patients after mild TBI.
Main Methods:
- Retrospective analysis of 321 children with TBI over 10 years.
- Classification of TBI severity based on loss of consciousness/amnesia duration and imaging findings.
- Review of clinical variables including antiepileptic drug use, seizure control, and injury characteristics; EEG/video-EEG obtained at various time points.
Main Results:
- Eight children (17%) developed PTE after mild TBI, compared to 39 (83%) after severe TBI.
- Children with mild TBI were more likely to have normal EEGs (p=0.005) and HCT scans (p<0.0001) than those with severe TBI.
- No mild TBI patients with PTE had both abnormal EEG/HCT or were on more than one antiepileptic drug (p<0.005).
Conclusions:
- Children with epilepsy following mild TBI (LOC/amnesia < 30 min) typically present with normal HCT and EEG findings.
- These patients are less likely to require multiple antiepileptic drugs, suggesting a potentially different epilepsy profile.
- Further research is needed due to the small sample size and retrospective nature of this study on pediatric mild TBI-related epilepsy.
Rationale:
Posttraumatic epilepsy (PTE) is a common cause of morbidity in children after a traumatic brain injury (TBI), occurring in 10-20% of children following severe TBI. PTE is diagnosed after two or more unprovoked seizures occurring 1-week post TBI. More often, studies have focused on children with epilepsy due to severe TBI. We aim to understand the utility of head computed tomography (HCT), EEG, and the risk of developing drug-resistant epilepsy in children after mild TBI.
Method:
We retrospectively studied 321 children with TBI at a tertiary pediatric referral center during a 10-year period. Mild TBI was defined as loss of consciousness (LOC) or amnesia < 30 min, moderate TBI as LOC or amnesia between 30 min and 1 day, and severe TBI as LOC or amnesia > 1 day, subdural hemorrhage, or contusion. Multiple clinical variables were reviewed, including past and present antiepileptic drug(s), seizure control, and mode of injury. First and subsequent post-TBI EEGs/prolonged video-EEGs were obtained acutely, subacutely, and/or chronically (range, day 1-3 years, median 1 month). Descriptive analyses were conducted using medians and ranges for continuous data. Categorical data were reported using frequencies and percentages, while comparisons between groups were made using Fisher's exact test for small sample sizes.
Results:
Forty-seven children were diagnosed with posttraumatic epilepsy: eight children (17%) due to mild TBI, 39 children (83%) due to severe TBI. For the eight children with mild TBI whom all had an accidental trauma (non-inflicted), the median follow-up time was 25 months (range 1.5 months-84 months). The median age was 10 years (range 4-18 years), and the median age at the time of injury was seven years (range: 23 months-13 years). No relevant previous medical history was present for six patients (80%), and two patients' (20%) relevant previous medical histories were unknown. Seven patients (88%) had no history of seizures, and patient #6 (12%) had unknown seizure history. Six patients (75%) had normal routine EEG(s). Patient #6 (13%) had an abnormal VEEG 3 months after the initial normal routine EEG, while patient #1 (13%) had an initial prolonged EEG 8 months after TBI. Compared to the 39 patients with severe TBI, 31 (79%) of whom had abnormal EEGs (routine and/or prolonged with video), mild TBI patients were more likely to have normal EEGs, p = 0.005. Head CT scans were obtained acutely for seven patients (90%), all of which were normal. One patient only had brain magnetic resonance imaging (MRI) 8 months after the injury. Compared to the 39 patients with severe TBI, all of whom had abnormal HCTs, mild TBI patients were less likely to have abnormal HCTs, p < 0.0001. In patients with mild TBI, no patient had both abnormal EEG/VEEG and HCT, and no one was on more than one Antiepileptic drug (AED), p < 0.005. Six patients (75%) had MRIs, of which five (63%) were normal. Two patients (#1, 7) did not have MRIs, while one patient's (#4) MRI was unavailable. Five patients (63%) had a seizure <24 h post TBI, while the rest had seizures after the first week of injury.
Conclusion:
Children with epilepsy due to mild TBI, loss of consciousness, or amnesia < 30 min are more likely to have normal HCT and EEG and to be on 0-1 AED. Limitations of our study include the small sample size and retrospective design. The current findings add to the paucity of data in children who suffer from epilepsy due to mild TBI.
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