2022
DOI: 10.1007/s11940-022-00727-2
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Predicting and Treating Post-traumatic Epilepsy

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Cited by 5 publications
(5 citation statements)
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“…A significant risk factor associated with epileptogenesis following ABI is the occurrence of acute symptomatic seizures (ASyS) (clinical or electrographic). [84][85][86] However, there are additional EEG features that can further stratify riskparticularly EAs, which have been associated with the development of epilepsy following any type of ABI. These patterns are thought to play a role in epileptogenesis by increasing metabolic demand of an area already at risk, leading to secondary brain injury, disruption of cortical connectivity, and hypersynchronization.…”
Section: Eeg As a Predictor Of Long-term Outcome And Recovery Of Cons...mentioning
confidence: 99%
“…A significant risk factor associated with epileptogenesis following ABI is the occurrence of acute symptomatic seizures (ASyS) (clinical or electrographic). [84][85][86] However, there are additional EEG features that can further stratify riskparticularly EAs, which have been associated with the development of epilepsy following any type of ABI. These patterns are thought to play a role in epileptogenesis by increasing metabolic demand of an area already at risk, leading to secondary brain injury, disruption of cortical connectivity, and hypersynchronization.…”
Section: Eeg As a Predictor Of Long-term Outcome And Recovery Of Cons...mentioning
confidence: 99%
“…If the therapy is ineffective or the patient does not tolerate it well, the doctor must employ an additional medication (monotherapy) or other drug combinations than those that have been previously utilized (add-on therapy). Innovative medicines provide a chance for a life devoid of epileptic seizures [ 91 , 95 ].…”
Section: Pharmacotherapymentioning
confidence: 99%
“…Retrospective case-controlled studies suggest some of these quantitative EEG features hold promise as predictive indicators for PTE [4][5][6][7] . However, these patients studies are face limitions such as poorly controlled environments, bias toward severe injury in participant selection, and insufficient consideration of patients' genetics, demographic information, comorbid conditions, or medication history 8 . Though animal models offer greater control over environmental variability, early animal studies of TBI commonly use rodent models with fixed genetic backgrounds, failing to capture the genetic diversity seen in humans 9,10 .…”
Section: Introductionmentioning
confidence: 99%