Desentrañando los misterios de la muerte súbita en epilepsia

dc.contributor.authorHampel, K.G.
dc.contributor.authorRocamora Zúñiga, Rodrigo Alberto
dc.contributor.authorQuesada, C.M.
dc.date.accessioned2018-07-05T07:22:57Z
dc.date.available2018-07-05T07:22:57Z
dc.date.issued2017
dc.description.abstractINTRODUCTION: Sudden unexpected death in epilepsy (SUDEP) is the most frequent cause of premature death in epileptic patients. Most SUDEP events occur at night and frequently go unnoticed; the exact pathophysiological mechanisms of this phenomenon therefore remain undetermined. Nevertheless, most cases of SUDEP are attributed to an infrequent yet extremely severe complication of epileptic seizures. DEVELOPMENT: We conducted a systematic literature search on PubMed. Our review article summarises scientific evidence on the classification, pathophysiological mechanisms, risk factors, biomarkers, and prevention of SUDEP. Likewise, we propose new lines of research and critically analyse findings that are relevant to clinical practice. CONCLUSIONS: Current knowledge suggests that SUDEP is a heterogeneous phenomenon caused by multiple factors. In most cases, however, SUDEP is thought to be due to postictal cardiorespiratory failure triggered by generalised tonic-clonic seizures and ultimately leading to cardiac arrest. The underlying pathophysiological mechanism involves multiple factors, ranging from genetic predisposition to environmental factors. Risk of SUDEP is higher in young adults with uncontrolled generalised tonic-clonic seizures. However, patients apparently at lower risk may also experience SUDEP. Current research focuses on identifying genetic and neuroimaging biomarkers that may help determine which patients are at high risk for SUDEP. Antiepileptic treatment is the only preventive measure proven effective to date. Night-time monitoring together with early resuscitation may reduce the risk of SUDEP.
dc.format.mimetypeapplication/pdf
dc.identifier.citationHampel KG, Rocamora Zuñiga R, Quesada CM. et al. Desentrañando los misterios de la muerte súbita en epilepsia. Neurologia. 2018 Oct;34(8):527-25. DOI: 10.1016/j.nrl.2017.02.004
dc.identifier.doihttp://dx.doi.org/10.1016/j.nrl.2017.02.004
dc.identifier.issn0213-4853
dc.identifier.urihttp://hdl.handle.net/10230/35034
dc.language.isospa
dc.publisherElsevierca
dc.relation.ispartofNeurologia. 2018 Oct;34(8):527-25
dc.rights0213-4853/© 2017 Sociedad Española de Neurología. Publicado por Elsevier España, S.L.U. Este es un artículo Open Access bajo la licencia CC BY-NC-ND (http://creativecommons.org/licenses/by-nc-nd/4.0/).
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subject.keywordCrisis epiléptica
dc.subject.keywordEpilepsia refractaria
dc.subject.keywordEpileptic seizure
dc.subject.keywordFactor de riesgo
dc.subject.keywordMortalidad
dc.subject.keywordMortality
dc.subject.keywordMuerte súbita en epilepsia
dc.subject.keywordRefractory epilepsy
dc.subject.keywordRisk factor
dc.subject.keywordSudden unexpected death in epilepsy
dc.subject.otherEpilèpsia -- Mort
dc.titleDesentrañando los misterios de la muerte súbita en epilepsiaca
dc.typeinfo:eu-repo/semantics/article
dc.type.versioninfo:eu-repo/semantics/acceptedVersion

Files

Original bundle

Now showing 1 - 1 of 1
Loading...
Thumbnail Image
Name:
hampel-neu-dese.pdf
Size:
771.01 KB
Format:
Adobe Portable Document Format

License

Rights