MétaCan
← all works

<scp>ILAE</scp> classification of the epilepsies: Position paper of the <scp>ILAE</scp> Commission for Classification and Terminology

2017· article· en· 4,881 citations· W2592509339 on OpenAlex· 10.1111/epi.13709

Why is this work in the frame?

A frame that forgets how it found something cannot be audited. These are the routes that admitted this work.

Canadian affiliationAn author listed a Canadian institution. This is the only route the usual frame has.
Canadian funderA Canadian agency funded it. The work may carry no Canadian affiliation at all.

Abstract

The 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.

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

The record

Venue
Epilepsia
Topic
Epilepsy research and treatment
Field
Medicine
Canadian institutions
University of CalgaryBC Children's HospitalUniversity of British Columbia
Funders
CilagUCB PharmaNational Health and Medical Research CouncilMedical Research CouncilCanadian Institutes of Health ResearchUniversity of California, Los AngelesSun PharmaUniversidade Católica de BrasíliaFundação BialEisaiEpilepsy Research UKNeuroPaceNational Institutes of HealthMylanSupernus PharmaceuticalsZynerba PharmaceuticalsUpsher-SmithDivision of Arctic SciencesSage TherapeuticsEpilepsiatutkimussäätiöDravet Syndrome UKZogenixAlva FoundationLundbeckfondenU.S. Department of DefenseYorkhill Children’s CharityGW PharmaceuticalsSanofiCitizens United for Research in EpilepsyNovartisAcorda TherapeuticsStockholms Läns LandstingTakeda Pharmaceuticals U.S.A.PfizerHumanities Research Center, Rice UniversityUltragenyx PharmaceuticalGlaxoSmithKlineVertex PharmaceuticalsMarch of Dimes FoundationNational Institute of Neurological Disorders and StrokeCURE Childhood CancerH. Lundbeck A/SSunovion
Keywords
EpilepsyTerminologyEtiologyMedicineEpilepsy syndromesGeneralized epilepsyPediatricsIntensive care medicinePsychiatry
Has abstract in OpenAlex
yes