Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/19075
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dc.contributor.authorScheffer, Ingrid E-
dc.contributor.authorBerkovic, Samuel F-
dc.contributor.authorCapovilla, Giuseppe-
dc.contributor.authorConnolly, Mary B-
dc.contributor.authorFrench, Jacqueline-
dc.contributor.authorGuilhoto, Laura-
dc.contributor.authorHirsch, Edouard-
dc.contributor.authorJain, Satish-
dc.contributor.authorMathern, Gary W-
dc.contributor.authorMoshé, Solomon L-
dc.contributor.authorNordli, Douglas R-
dc.contributor.authorPerucca, Emilio-
dc.contributor.authorTomson, Torbjörn-
dc.contributor.authorWiebe, Samuel-
dc.contributor.authorZhang, Yue-Hua-
dc.contributor.authorZuberi, Sameer M-
dc.date2017-03-08-
dc.date.accessioned2018-09-13T00:14:47Z-
dc.date.available2018-09-13T00:14:47Z-
dc.date.issued2017-04-
dc.identifier.citationEpilepsia 2017; 58(4): 512-521-
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/19075-
dc.description.abstractThe International League Against Epilepsy (ILAE) Classification of the Epilepsies has been updated to reflect our gain in understanding of the epilepsies and their underlying mechanisms following the major scientific advances that have taken place since the last ratified classification in 1989. As a critical tool for the practicing clinician, epilepsy classification must be relevant and dynamic to changes in thinking, yet robust and translatable to all areas of the globe. Its primary purpose is for diagnosis of patients, but it is also critical for epilepsy research, development of antiepileptic therapies, and communication around the world. The new classification originates from a draft document submitted for public comments in 2013, which was revised to incorporate extensive feedback from the international epilepsy community over several rounds of consultation. It presents three levels, starting with seizure type, where it assumes that the patient is having epileptic seizures as defined by the new 2017 ILAE Seizure Classification. After diagnosis of the seizure type, the next step is diagnosis of epilepsy type, including focal epilepsy, generalized epilepsy, combined generalized, and focal epilepsy, and also an unknown epilepsy group. The third level is that of epilepsy syndrome, where a specific syndromic diagnosis can be made. The new classification incorporates etiology along each stage, emphasizing the need to consider etiology at each step of diagnosis, as it often carries significant treatment implications. Etiology is broken into six subgroups, selected because of their potential therapeutic consequences. New terminology is introduced such as developmental and epileptic encephalopathy. The term benign is replaced by the terms self-limited and pharmacoresponsive, to be used where appropriate. It is hoped that this new framework will assist in improving epilepsy care and research in the 21st century.-
dc.language.isoeng-
dc.subjectClassification-
dc.subjectEpilepsy syndromes-
dc.subjectEtiology-
dc.subjectTerminology-
dc.titleILAE classification of the epilepsies: Position paper of the ILAE Commission for Classification and Terminology.-
dc.typeJournal Article-
dc.identifier.journaltitleEpilepsia-
dc.identifier.affiliationSchool of Medicine, University of Glasgow, Glasgow, United Kingdomen
dc.identifier.affiliationDepartment of Pediatrics, Peking University First Hospital, Beijing, Chinaen
dc.identifier.affiliationPaediatric Neurosciences Research Group, Fraser of Allander Neurosciences Unit, Royal Hospital for Children, Glasgow, United Kingdomen
dc.identifier.affiliationDepartment of Medicine, Austin Health, The University of Melbourne, Heidelberg, Victoria, Australiaen
dc.identifier.affiliationDepartment of Paediatrics, Royal Children's Hospital, The University of Melbourne, Melbourne, Victoria, Australiaen
dc.identifier.affiliationFlorey Institute, Melbourne, Victoria, Australiaen
dc.identifier.affiliationChild Neuropsychiatry Department, Epilepsy Center, C. Poma Hospital, Mantova, Italyen
dc.identifier.affiliationDepartment of Pediatrics, British Columbia's Children's Hospital, University of British Columbia, Vancouver, British Columbia, Canadaen
dc.identifier.affiliationDepartment of Neurology, NYU School of Medicine, New York, New York, U.S.Aen
dc.identifier.affiliationDepartment of Neurology, Federal University of São Paulo; University Hospital, University of São Paulo, São Paulo, Brazilen
dc.identifier.affiliationUniversity Hospital INSERM U 964, Strasbourg, Franceen
dc.identifier.affiliationIDÉE, Lyon, Franceen
dc.identifier.affiliationIndian Epilepsy Centre, New Delhi, Indiaen
dc.identifier.affiliationDepartments of Neurosurgery, Psychiatry and Biobehavioral Medicine, David Geffen School of Medicine, UCLA, Los Angeles, California, U.S.Aen
dc.identifier.affiliationSaul R. Korey Department of Neurology, Dominick P. Purpura Department of Neuroscience and Department of Pediatrics, Albert Einstein College of Medicine and Montefiore Medical Center, Bronx, New York, U.S.Aen
dc.identifier.affiliationDivision of Neurology, Children's Hospital Los Angeles, Los Angeles, California, U.S.Aen
dc.identifier.affiliationC. Mondino National Neurological Institute and Clinical Pharmacology Unit, University of Pavia, Pavia, Italyen
dc.identifier.affiliationDepartment of Clinical Neuroscience, Karolinska Institute, Stockholm, Swedenen
dc.identifier.affiliationDepartments of Clinical Neurosciences and Community Health Sciences, University of Calgary, Calgary, Alberta, Canadaen
dc.identifier.doi10.1111/epi.13709-
dc.identifier.orcid0000-0002-2311-2174en
dc.identifier.orcid0000-0003-4580-841Xen
dc.identifier.pubmedid28276062-
dc.type.austinJournal Article-
local.name.researcherBerkovic, Samuel F
item.openairetypeJournal Article-
item.cerifentitytypePublications-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextNo Fulltext-
item.grantfulltextnone-
item.languageiso639-1en-
crisitem.author.deptEpilepsy Research Centre-
crisitem.author.deptEpilepsy Research Centre-
crisitem.author.deptNeurology-
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