Epilepsy with generalized tonic–clonic seizures alone: Electroclinical features and prognostic patterns.
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| Title: | Epilepsy with generalized tonic–clonic seizures alone: Electroclinical features and prognostic patterns. |
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| Authors: | Cerulli Irelli, Emanuele (AUTHOR), Gesche, Joanna (AUTHOR), Schlabitz, Sophie (AUTHOR), Fortunato, Francesco (AUTHOR), Catania, Cecilia (AUTHOR), Morano, Alessandra (AUTHOR), Labate, Angelo (AUTHOR), Vorderwülbecke, Bernd J. (AUTHOR), Gambardella, Antonio (AUTHOR), Baykan, Betül (AUTHOR), Holtkamp, Martin (AUTHOR), Di Bonaventura, Carlo (AUTHOR), Beier, Christoph P. (AUTHOR) |
| Source: | Epilepsia (Series 4). Jan2024, Vol. 65 Issue 1, p84-94. 11p. |
| Subjects: | Epilepsy, Seizures (Medicine), Termination of treatment, Patient experience, Prognosis, Patients' attitudes |
| Abstract: | Objective: Epilepsy with generalized tonic–clonic seizures alone (GTCA) is a common but poorly characterized idiopathic generalized epilepsy (IGE) syndrome. Hence, we investigated electroclinical features, seizure outcome, and antiseizure medication (ASM) withdrawal in a large cohort of GTCA patients. Methods: In this multicenter retrospective study, GTCA patients defined according to the diagnostic criteria of the International League Against Epilepsy (2022) were included. We investigated prognostic patterns, drug resistance at the last visit, and ASM withdrawal, along with their prognostic factors. Results: We included 247 patients with a median (interquartile range [IQR]) age at onset of 17 years (13–22) and a median follow‐up duration of 10 years (IQR = 5–20). Drug resistance at the last visit was observed in 40 (16.3%) patients, whereas the median latency to achieve 2‐year remission was 24 months (IQR = 24–46.5) with a median number of 1 (IQR = 1–2) ASM. During the long‐term follow‐up (i.e., 202 patients followed ≥5‐years after the first ASM trial), 69 (34.3%) patients displayed an early remission pattern and 36 (17.9%) patients displayed a late remission pattern, whereas 16 (8%) and 73 (36.3%) individuals had no‐remission and relapsing–remitting patterns, respectively. Catamenial seizures and morning predominance of generalized tonic–clonic seizures (GTCS) independently predicted drug resistance at the last visit according to multivariable logistic regression. Treatment withdrawal was attempted in 63 (25.5%) patients, with 59 (93.7%) of them having at least a 12‐month follow‐up after ASM discontinuation. At the last visit, 49 (83%) of those patients had experienced GTCS recurrence. A longer duration of seizure freedom was the only factor predicting a higher chance of successful ASM withdrawal according to multivariable Cox regression. Significance: GTCA could be considered a relatively easily manageable IGE syndrome, with a low rate of drug resistance and a high prevalence of early response to treatment. Nevertheless, a considerable proportion of patients experience relapsing patterns of seizure control, highlighting the need for appropriate counseling and lifestyle recommendations. [ABSTRACT FROM AUTHOR] |
| Copyright of Epilepsia (Series 4) is the property of Wiley-Blackwell and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.) | |
| Database: | Psychology and Behavioral Sciences Collection |
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| Header | DbId: pbh DbLabel: Psychology and Behavioral Sciences Collection An: 174782281 AccessLevel: 6 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Epilepsy with generalized tonic–clonic seizures alone: Electroclinical features and prognostic patterns. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AR" term="%22Cerulli Irelli%2C+Emanuele%22">Cerulli Irelli, Emanuele</searchLink> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Gesche%2C+Joanna%22">Gesche, Joanna</searchLink> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Schlabitz%2C+Sophie%22">Schlabitz, Sophie</searchLink> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Fortunato%2C+Francesco%22">Fortunato, Francesco</searchLink> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Catania%2C+Cecilia%22">Catania, Cecilia</searchLink> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Morano%2C+Alessandra%22">Morano, Alessandra</searchLink> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Labate%2C+Angelo%22">Labate, Angelo</searchLink> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Vorderwülbecke%2C+Bernd+J%2E%22">Vorderwülbecke, Bernd J.</searchLink> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Gambardella%2C+Antonio%22">Gambardella, Antonio</searchLink> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Baykan%2C+Betül%22">Baykan, Betül</searchLink> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Holtkamp%2C+Martin%22">Holtkamp, Martin</searchLink> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Di Bonaventura%2C+Carlo%22">Di Bonaventura, Carlo</searchLink> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Beier%2C+Christoph+P%2E%22">Beier, Christoph P.</searchLink> (AUTHOR) – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22Epilepsia+%28Series+4%29%22">Epilepsia (Series 4)</searchLink>. Jan2024, Vol. 65 Issue 1, p84-94. 11p. – Name: Subject Label: Subjects Group: Su Data: <searchLink fieldCode="DE" term="%22Epilepsy%22">Epilepsy</searchLink><br /><searchLink fieldCode="DE" term="%22Seizures+%28Medicine%29%22">Seizures (Medicine)</searchLink><br /><searchLink fieldCode="DE" term="%22Termination+of+treatment%22">Termination of treatment</searchLink><br /><searchLink fieldCode="DE" term="%22Patient+experience%22">Patient experience</searchLink><br /><searchLink fieldCode="DE" term="%22Prognosis%22">Prognosis</searchLink><br /><searchLink fieldCode="DE" term="%22Patients'+attitudes%22">Patients' attitudes</searchLink> – Name: Abstract Label: Abstract Group: Ab Data: Objective: Epilepsy with generalized tonic–clonic seizures alone (GTCA) is a common but poorly characterized idiopathic generalized epilepsy (IGE) syndrome. Hence, we investigated electroclinical features, seizure outcome, and antiseizure medication (ASM) withdrawal in a large cohort of GTCA patients. Methods: In this multicenter retrospective study, GTCA patients defined according to the diagnostic criteria of the International League Against Epilepsy (2022) were included. We investigated prognostic patterns, drug resistance at the last visit, and ASM withdrawal, along with their prognostic factors. Results: We included 247 patients with a median (interquartile range [IQR]) age at onset of 17 years (13–22) and a median follow‐up duration of 10 years (IQR = 5–20). Drug resistance at the last visit was observed in 40 (16.3%) patients, whereas the median latency to achieve 2‐year remission was 24 months (IQR = 24–46.5) with a median number of 1 (IQR = 1–2) ASM. During the long‐term follow‐up (i.e., 202 patients followed ≥5‐years after the first ASM trial), 69 (34.3%) patients displayed an early remission pattern and 36 (17.9%) patients displayed a late remission pattern, whereas 16 (8%) and 73 (36.3%) individuals had no‐remission and relapsing–remitting patterns, respectively. Catamenial seizures and morning predominance of generalized tonic–clonic seizures (GTCS) independently predicted drug resistance at the last visit according to multivariable logistic regression. Treatment withdrawal was attempted in 63 (25.5%) patients, with 59 (93.7%) of them having at least a 12‐month follow‐up after ASM discontinuation. At the last visit, 49 (83%) of those patients had experienced GTCS recurrence. A longer duration of seizure freedom was the only factor predicting a higher chance of successful ASM withdrawal according to multivariable Cox regression. Significance: GTCA could be considered a relatively easily manageable IGE syndrome, with a low rate of drug resistance and a high prevalence of early response to treatment. Nevertheless, a considerable proportion of patients experience relapsing patterns of seizure control, highlighting the need for appropriate counseling and lifestyle recommendations. [ABSTRACT FROM AUTHOR] – Name: AbstractSuppliedCopyright Label: Group: Ab Data: <i>Copyright of Epilepsia (Series 4) is the property of Wiley-Blackwell and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract.</i> (Copyright applies to all Abstracts.) |
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| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1111/epi.17809 Languages: – Code: eng Text: English PhysicalDescription: Pagination: PageCount: 11 StartPage: 84 Subjects: – SubjectFull: Epilepsy Type: general – SubjectFull: Seizures (Medicine) Type: general – SubjectFull: Termination of treatment Type: general – SubjectFull: Patient experience Type: general – SubjectFull: Prognosis Type: general – SubjectFull: Patients' attitudes Type: general Titles: – TitleFull: Epilepsy with generalized tonic–clonic seizures alone: Electroclinical features and prognostic patterns. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Cerulli Irelli, Emanuele – PersonEntity: Name: NameFull: Gesche, Joanna – PersonEntity: Name: NameFull: Schlabitz, Sophie – PersonEntity: Name: NameFull: Fortunato, Francesco – PersonEntity: Name: NameFull: Catania, Cecilia – PersonEntity: Name: NameFull: Morano, Alessandra – PersonEntity: Name: NameFull: Labate, Angelo – PersonEntity: Name: NameFull: Vorderwülbecke, Bernd J. – PersonEntity: Name: NameFull: Gambardella, Antonio – PersonEntity: Name: NameFull: Baykan, Betül – PersonEntity: Name: NameFull: Holtkamp, Martin – PersonEntity: Name: NameFull: Di Bonaventura, Carlo – PersonEntity: Name: NameFull: Beier, Christoph P. IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 01 Text: Jan2024 Type: published Y: 2024 Identifiers: – Type: issn-print Value: 00139580 Numbering: – Type: volume Value: 65 – Type: issue Value: 1 Titles: – TitleFull: Epilepsia (Series 4) Type: main |
| ResultId | 1 |