Please use this identifier to cite or link to this item: https://dora.health.qld.gov.au/qldresearchjspui/handle/1/4226
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dc.contributor.authorAnink, J.en
dc.contributor.authorKotulska, K.en
dc.contributor.authorKwiatkowski, D. J.en
dc.contributor.authorCuratolo, P.en
dc.contributor.authorWeschke, B.en
dc.contributor.authorRiney, K.en
dc.contributor.authorJansen, F.en
dc.contributor.authorFeucht, M.en
dc.contributor.authorKrsek, P.en
dc.contributor.authorNabbout, R.en
dc.contributor.authorJansen, A. C.en
dc.contributor.authorWojdan, K.en
dc.contributor.authorSijko, K.en
dc.contributor.authorGłowacka-Walas, J.en
dc.contributor.authorBorkowska, J.en
dc.contributor.authorSadowski, K.en
dc.contributor.authorDomańska-Pakieła, D.en
dc.contributor.authorMoavero, R.en
dc.contributor.authorHertzberg, C.en
dc.contributor.authorHulshof, H.en
dc.contributor.authorScholl, T.en
dc.contributor.authorBenova, B.en
dc.contributor.authorAronica, E.en
dc.contributor.authorde Ridder, J.en
dc.contributor.authorLagae, L.en
dc.contributor.authorJóźwiak, S.en
dc.contributor.authorBenvenuto, A.en
dc.contributor.authorBlazejczyk, M.en
dc.contributor.authorBongaerts, A.en
dc.contributor.authorBreuillard, D.en
dc.contributor.authorChmielewski, D.en
dc.contributor.authorDabrowska, M.en
dc.contributor.authorGiannikou, K.en
dc.contributor.authorHamieh, L.en
dc.contributor.authorHarȩza, A.en
dc.contributor.authorHuschner, F.en
dc.contributor.authorIyer, A.en
dc.contributor.authorJansen, A.en
dc.contributor.authorJanssen, B.en
dc.contributor.authorJaworski, J.en
dc.contributor.authorJùźwiak, S.en
dc.contributor.authorKaczorowska-Frontczak, M.en
dc.contributor.authorKwiatkowski, D.en
dc.contributor.authorLehmann, K.en
dc.contributor.authorLeusman, A.en
dc.contributor.authorMaćkowiak, N.en
dc.contributor.authorMills, J.en
dc.contributor.authorMuelebner, A.en
dc.contributor.authorSamueli, S.en
dc.contributor.authorScheldeman, C.en
dc.contributor.authorSciuto, A.en
dc.contributor.authorSłowińska, M.en
dc.contributor.authorTempes, A.en
dc.contributor.authorvan Scheppingen, J.en
dc.contributor.authorVerhelle, B.en
dc.contributor.authorVervisch, J.en
dc.contributor.authorUrbańska, M.en
dc.date.accessioned2022-11-07T23:50:38Z-
dc.date.available2022-11-07T23:50:38Z-
dc.date.issued2021en
dc.identifier.citation89, (2), 2021, p. 304-314en
dc.identifier.otherRISen
dc.identifier.urihttp://dora.health.qld.gov.au/qldresearchjspui/handle/1/4226-
dc.description.abstractObjective: Epilepsy develops in 70 to 90% of children with tuberous sclerosis complex (TSC) and is often resistant to medication. Recently, the concept of preventive antiepileptic treatment to modify the natural history of epilepsy has been proposed. EPISTOP was a clinical trial designed to compare preventive versus conventional antiepileptic treatment in TSC infants. Methods: In this multicenter study, 94 infants with TSC without seizure history were followed with monthly video electroencephalography (EEG), and received vigabatrin either as conventional antiepileptic treatment, started after the first electrographic or clinical seizure, or preventively when epileptiform EEG activity before seizures was detected. At 6 sites, subjects were randomly allocated to treatment in a 1:1 ratio in a randomized controlled trial (RCT). At 4 sites, treatment allocation was fixed; this was denoted an open-label trial (OLT). Subjects were followed until 2 years of age. The primary endpoint was the time to first clinical seizure. Results: In 54 subjects, epileptiform EEG abnormalities were identified before seizures. Twenty-seven were included in the RCT and 27 in the OLT. The time to the first clinical seizure was significantly longer with preventive than conventional treatment [RCT: 364 days (95% confidence interval [CI] = 223–535) vs 124 days (95% CI = 33–149); OLT: 426 days (95% CI = 258–628) vs 106 days (95% CI = 11–149)]. At 24 months, our pooled analysis showed preventive treatment reduced the risk of clinical seizures (odds ratio [OR] = 0.21, p = 0.032), drug-resistant epilepsy (OR = 0.23, p = 0.022), and infantile spasms (OR = 0, p < 0.001). No adverse events related to preventive treatment were noted. Interpretation: Preventive treatment with vigabatrin was safe and modified the natural history of seizures in TSC, reducing the risk and severity of epilepsy. ANN NEUROL 2021;89:304–314.L20073971332020-12-01 <br />2021-03-09 <br />en
dc.language.isoenen
dc.relation.ispartofAnnals of Neurologyen
dc.titlePrevention of Epilepsy in Infants with Tuberous Sclerosis Complex in the EPISTOP Trialen
dc.typeArticleen
dc.identifier.doi10.1002/ana.25956en
dc.subject.keywordsEEG abnormalityen
dc.subject.keywordselectroencephalogramen
dc.subject.keywordselectroencephalographyen
dc.subject.keywordsepilepsyen
dc.subject.keywordsepileptic stateen
dc.subject.keywordsfebrile convulsionen
dc.subject.keywordsfeeding difficultyen
dc.subject.keywordsfemaleen
dc.subject.keywordsfollow upen
dc.subject.keywordsheart arresten
dc.subject.keywordsheart arrhythmiaen
dc.subject.keywordsheart tumoren
dc.subject.keywordshumanen
dc.subject.keywordshyperkeratosisen
dc.subject.keywordshypsarrhythmiaen
dc.subject.keywordsinfanten
dc.subject.keywordsinfant mortalityen
dc.subject.keywordsinfantile spasmen
dc.subject.keywordsinfluenzaen
dc.subject.keywordsintellectual impairmenten
dc.subject.keywordsintermethod comparisonen
dc.subject.keywordskidney tumoren
dc.subject.keywordsmajor clinical studyen
dc.subject.keywordsmaleen
dc.subject.keywordsnewbornen
dc.subject.keywordsopen studyen
dc.subject.keywordsparallel designen
dc.subject.keywordspneumoniaen
dc.subject.keywordspriority journalen
dc.subject.keywordsprophylaxisen
dc.subject.keywordsrandomized controlled trialen
dc.subject.keywordsseizureen
dc.subject.keywordssubependymal giant cell astrocytomaen
dc.subject.keywordstreatment durationen
dc.subject.keywordstuberous sclerosisen
dc.subject.keywordsupper respiratory tract infectionen
dc.subject.keywordsvideorecordingen
dc.subject.keywordsside effecten
dc.subject.keywordsNCT02098759vigabatrinen
dc.subject.keywordsanticonvulsant therapyen
dc.subject.keywordsarticleen
dc.subject.keywordsBayley Scales of Infant Developmenten
dc.subject.keywordscancer surgeryen
dc.subject.keywordsclinical outcomeen
dc.subject.keywordscontrolled studyen
dc.subject.keywordsdevelopmental delayen
dc.subject.keywordsdrug dose reductionen
dc.subject.keywordsdrug efficacyen
dc.subject.keywordsdrug resistant epilepsyen
dc.subject.keywordsdrug safetyen
dc.relation.urlhttps://www.embase.com/search/results?subaction=viewrecord&id=L2007397133&from=exporthttp://dx.doi.org/10.1002/ana.25956 |en
dc.identifier.risid2844en
dc.description.pages304-314en
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextNo Fulltext-
item.languageiso639-1en-
item.grantfulltextnone-
item.cerifentitytypePublications-
item.openairetypeArticle-
Appears in Sites:Children's Health Queensland Publications
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