Management and outcomes among older adults with generalized epilepsy in routine clinical practice

Abstract Generalized epilepsy is classically thought of as a disease of the young and adolescent, with rarely reported cases among older adults. We aimed to analyze management and outcomes in a population sparsely described in the literature through a retrospective single‐center cohort design. After...

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Main Authors: MarieElena Byrnes, Majed Alzahrany, Vineet Punia
Format: Article
Language:English
Published: Wiley 2025-02-01
Series:Epilepsia Open
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Online Access:https://doi.org/10.1002/epi4.13123
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author MarieElena Byrnes
Majed Alzahrany
Vineet Punia
author_facet MarieElena Byrnes
Majed Alzahrany
Vineet Punia
author_sort MarieElena Byrnes
collection DOAJ
description Abstract Generalized epilepsy is classically thought of as a disease of the young and adolescent, with rarely reported cases among older adults. We aimed to analyze management and outcomes in a population sparsely described in the literature through a retrospective single‐center cohort design. After excluding individuals without follow‐up, we identified 151 people ≥50 years at the time of electrographically confirmed generalized epilepsy. Just over a quarter were late‐onset (≥26 years), and 77% were diagnosed with genetic generalized epilepsy (GGE). Active seizures (in the last year of follow‐up) were present in 57% of individuals, despite most of them having experienced prolonged seizure remission periods (median 7 years) in the past. Only five people were off antiseizure medication (ASM) at their last appointment, with most on an average of 2 ASMs. The odds of active epilepsy at the last follow‐up were significantly higher among those with polyspikes (odds ratio [OR] = 2.42; 95% confidence interval [CI] = 1.01–6.01), myoclonic seizure history (OR = 2.88, 1.23–6.96), and developmental delay (OR = 4.75, 1.45–19.3). The odds were 60% lower in older adults with family history (OR = 0.4, 0.17–5.68). Our findings suggest that most older adults with generalized epilepsy achieve years of seizure remission, but the likelihood of epilepsy resolution is low. Plain Language Summary Generalized epilepsy is seldom seen in older adults. We looked at 151 patients diagnosed with generalized epilepsy over the age of 50 to see how they are managed and what influences their outcomes. We found that although these patients can control their seizures with medication, the chance that their epilepsy resolves is low. Patients with certain characteristics classically seen in an epilepsy called “Juvenile Myoclonic Epilepsy” (JME) may have a more intractable course.
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spelling doaj-art-e58d5afdd4f34ae0af0c13b996f7d1d12025-02-07T09:12:45ZengWileyEpilepsia Open2470-92392025-02-0110135536010.1002/epi4.13123Management and outcomes among older adults with generalized epilepsy in routine clinical practiceMarieElena Byrnes0Majed Alzahrany1Vineet Punia2Epilepsy Center, Neurological Institute Cleveland Clinic Cleveland Ohio USADepartment of Neurology King Abdulaziz University Jeddah Saudi ArabiaEpilepsy Center, Neurological Institute Cleveland Clinic Cleveland Ohio USAAbstract Generalized epilepsy is classically thought of as a disease of the young and adolescent, with rarely reported cases among older adults. We aimed to analyze management and outcomes in a population sparsely described in the literature through a retrospective single‐center cohort design. After excluding individuals without follow‐up, we identified 151 people ≥50 years at the time of electrographically confirmed generalized epilepsy. Just over a quarter were late‐onset (≥26 years), and 77% were diagnosed with genetic generalized epilepsy (GGE). Active seizures (in the last year of follow‐up) were present in 57% of individuals, despite most of them having experienced prolonged seizure remission periods (median 7 years) in the past. Only five people were off antiseizure medication (ASM) at their last appointment, with most on an average of 2 ASMs. The odds of active epilepsy at the last follow‐up were significantly higher among those with polyspikes (odds ratio [OR] = 2.42; 95% confidence interval [CI] = 1.01–6.01), myoclonic seizure history (OR = 2.88, 1.23–6.96), and developmental delay (OR = 4.75, 1.45–19.3). The odds were 60% lower in older adults with family history (OR = 0.4, 0.17–5.68). Our findings suggest that most older adults with generalized epilepsy achieve years of seizure remission, but the likelihood of epilepsy resolution is low. Plain Language Summary Generalized epilepsy is seldom seen in older adults. We looked at 151 patients diagnosed with generalized epilepsy over the age of 50 to see how they are managed and what influences their outcomes. We found that although these patients can control their seizures with medication, the chance that their epilepsy resolves is low. Patients with certain characteristics classically seen in an epilepsy called “Juvenile Myoclonic Epilepsy” (JME) may have a more intractable course.https://doi.org/10.1002/epi4.13123active epilepsyelderlygenetic epilepsyidiopathic epilepsyseizure remission
spellingShingle MarieElena Byrnes
Majed Alzahrany
Vineet Punia
Management and outcomes among older adults with generalized epilepsy in routine clinical practice
Epilepsia Open
active epilepsy
elderly
genetic epilepsy
idiopathic epilepsy
seizure remission
title Management and outcomes among older adults with generalized epilepsy in routine clinical practice
title_full Management and outcomes among older adults with generalized epilepsy in routine clinical practice
title_fullStr Management and outcomes among older adults with generalized epilepsy in routine clinical practice
title_full_unstemmed Management and outcomes among older adults with generalized epilepsy in routine clinical practice
title_short Management and outcomes among older adults with generalized epilepsy in routine clinical practice
title_sort management and outcomes among older adults with generalized epilepsy in routine clinical practice
topic active epilepsy
elderly
genetic epilepsy
idiopathic epilepsy
seizure remission
url https://doi.org/10.1002/epi4.13123
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