2003
DOI: 10.1053/apmr.2003.50022
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Analyzing risk factors for late posttraumatic seizures: A prospective, multicenter investigation

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Cited by 325 publications
(311 citation statements)
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“…9,17,[20][21][22] Despite a decreasing risk of developing seizures and epilepsy over time, the risk persists for up to 10 years, which could be one explanation for the negative influence on long-term functional outcome. 4 Predictors of seizures in elderly patients were a low GCS score 24 hours after operation and a left-sided hematoma, similar to the previously published results by Rabinstein et al 21 Since elderly patients with comorbidities have clinical fluctuation more often than younger patients, the diagnosis of seizure may …”
Section: Discussionsupporting
confidence: 83%
“…9,17,[20][21][22] Despite a decreasing risk of developing seizures and epilepsy over time, the risk persists for up to 10 years, which could be one explanation for the negative influence on long-term functional outcome. 4 Predictors of seizures in elderly patients were a low GCS score 24 hours after operation and a left-sided hematoma, similar to the previously published results by Rabinstein et al 21 Since elderly patients with comorbidities have clinical fluctuation more often than younger patients, the diagnosis of seizure may …”
Section: Discussionsupporting
confidence: 83%
“…The onset of seizures after TBI has been categorized into immediate (<24 hours after TBI), early (within a week after TBI), and late (>1 week after TBI) onset 5. Focal brain lesions in the frontal, temporal and parietal lobes, bilateral contusions, depressed fractures, midline shift >5 mm, subdural hematomas, decreased brain volume, intraparenchymal hemorrhage, and occurrence of seizures within the first week after TBI are important risk factors for PTE in humans 5, 6, 7, 8. Traumatic brain injury in dogs recently has been associated with significant risk of developing PTE with an incidence up to 6.8% 9, 10.…”
mentioning
confidence: 99%
“…Human studies have revealed that TBI is a major risk factor in the development of temporal lobe epilepsy (Englander et al, 2003). Hippocampal mossy fibers are composed of excitatory axons derived from DG granule cells, projecting to the CA3 region and forming part of the trisynaptic hippocampal circuit.…”
mentioning
confidence: 99%