Publication:
The efficacy and adverse effects of topiramate in Add on therapy in children with intractable epilepsy

dc.contributor.authorÖzdemir, Özlem
dc.contributor.authorOkan, Mehmet
dc.contributor.authorBeyazıt, Aysun N.
dc.contributor.buuauthorÖzdemir, Özlem
dc.contributor.buuauthorOKAN, MEHMET SAİT
dc.contributor.buuauthorBeyazıt, Aysun N.
dc.contributor.departmentUludağ Üniversitesi/Tıp Fakültesi/Çocuk Sağlığı Hastalıkları Anabilim Dalı/Çocuk Noroloji Bilim Dalı.
dc.contributor.departmentUludağ Üniversitesi/Tıp Fakültesi/Çocuk Sağlığı Hastalıkları Anabilim Dalı.
dc.contributor.researcheridFPY-3754-2022
dc.contributor.researcheridIMZ-1723-2023
dc.contributor.researcheridEOB-0702-2022
dc.date.accessioned2024-10-24T11:11:32Z
dc.date.available2024-10-24T11:11:32Z
dc.date.issued2009-12-01
dc.description.abstractIntroduction: The aim of this study was to evaluate the efficacy and adverse effects of topiramate add on therapy in children with intractable epilepsy.Materials and Method: The efficacy and adverse events of topiramate were evaluated in 166 children (67 girls, 99 boys). The classification of the epilepsies were as follows: partial 82 (49.4%), generalized 8 (4.8%), secondarily generalized 6 (3.8%), myoclonic 24 (14.5%) and epileptic syndromes 34 (27.7%). Topiramate was initiated at a daily dose of 0.5-1 mg/kg, up to an approximate daily dose of 9 mg/kg. The patients were assessed for the seizure frequency, duration and adverse events during the follow-up. Response to treatment was classified as good (complete, > 75%), moderately (25-75%) and poor (0-25%).Results: Response to treatment among 166 patients were as follows: 85 (51.2%) good, 39 (23.5%) moderately and 42 (25.3%) poor. The efficacy rates according to the seizure types were 45 (54.9%) good, 22 (26.8%) moderately, 15 (18.3%) poor for partial seizures; 8 (100%) good for generalized whereas 10 (41.7%) good, 4 (16.7%) moderately and 10 (41.7%) poor for myoclonic seizures. Generally topiramate appeared to be more effective in partial epilepsy than generalized and myoclonic epilepsy (p=0.008 and p=0.024). Adverse events were present in 33 patients (19.9%), mostly as somnolence (n=9, 5.4%). Topiramate was discontinued because of poor response in 33 patients (19.9%), severe adverse events in 4 (2.4%), increase in the frequency of seizures in 3 (1.8%) and long term seizure free follow-up in 2 (1.2%).Conclusion: Topiramate seems to be highly effective and safe in intractable epileptic patients. However, the drug specific adverse events should always be kept in mind during the follow-up.
dc.identifier.endpage129
dc.identifier.issn1304-9054
dc.identifier.issue3
dc.identifier.startpage125
dc.identifier.urihttps://hdl.handle.net/11452/47014
dc.identifier.volume7
dc.identifier.wos000422255500004
dc.indexed.wosWOS.ESCI
dc.language.isoen
dc.publisherGalenos Yayıncılık
dc.relation.journalGüncel Pediatri-Journal of Current Pediatrics
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectTopiramate
dc.subjectChildhood
dc.subjectIntractable epilepsy
dc.subjectAdverse event
dc.subjectPediatrics
dc.titleThe efficacy and adverse effects of topiramate in Add on therapy in children with intractable epilepsy
dc.typeArticle
dspace.entity.typePublication
relation.isAuthorOfPublicationafcf2981-c150-42de-b600-f72b3ff95317
relation.isAuthorOfPublication.latestForDiscoveryafcf2981-c150-42de-b600-f72b3ff95317

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