Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/31852
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dc.contributor.authorZographos, George A-
dc.contributor.authorRuss-Hall, Sophie J-
dc.contributor.authorScheffer, Ingrid E-
dc.date2022-
dc.date.accessioned2023-01-12T04:50:30Z-
dc.date.available2023-01-12T04:50:30Z-
dc.date.issued2022-12-
dc.identifier.citationAnnals of Clinical and t Translational Neurology 2022; 9(12)en_US
dc.identifier.issn2328-9503-
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/31852-
dc.description.abstractAnti-seizure medications that block sodium channels are generally considered contraindicated in Dravet syndrome. There is, however, considerable debate about the sodium-channel blocker phenytoin, which is often used for status epilepticus, a frequent feature of Dravet syndrome. We describe four patients with Dravet syndrome in whom long-term phenytoin therapy reduced seizure frequency and duration. In two patients, phenytoin produced prolonged periods without status epilepticus for the first time. Attempting to wean phenytoin in all patients after 1 to 20 years of use resulted in seizure exacerbation. Reintroducing phenytoin improved seizure control, suggesting phenytoin is beneficial in some patients with Dravet syndrome.en_US
dc.language.isoeng-
dc.titleDoes long-term phenytoin have a place in Dravet syndrome?en_US
dc.typeJournal Articleen_US
dc.identifier.journaltitleAnnals of Clinical and t Translational Neurologyen_US
dc.identifier.affiliationEpilepsy Research Centreen_US
dc.identifier.affiliationMedicine (University of Melbourne)en_US
dc.identifier.doi10.1002/acn3.51684en_US
dc.type.contentTexten_US
dc.identifier.orcid0000-0002-8768-9757en_US
dc.identifier.orcid0000-0002-4809-9340en_US
dc.identifier.orcid0000-0002-2311-2174en_US
dc.identifier.pubmedid36314457-
dc.description.volume9-
dc.description.issue12-
dc.description.startpage2036-
dc.description.endpage2040-
dc.subject.meshtermssecondaryPhenytoin/pharmacology-
dc.subject.meshtermssecondaryPhenytoin/therapeutic use-
dc.subject.meshtermssecondaryEpilepsies, Myoclonic/drug therapy-
dc.subject.meshtermssecondaryStatus Epilepticus/drug therapy-
local.name.researcherScheffer, Ingrid E
item.cerifentitytypePublications-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextNo Fulltext-
item.openairetypeJournal Article-
item.grantfulltextnone-
item.languageiso639-1en-
crisitem.author.deptEpilepsy Research Centre-
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