Intravenous Corticosteroids as an Adjunctive Treatment for Refractory and Super-Refractory Status Epilepticus: An Observational Cohort Study.

Détails

ID Serval
serval:BIB_D5B26CBEC812
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
Intravenous Corticosteroids as an Adjunctive Treatment for Refractory and Super-Refractory Status Epilepticus: An Observational Cohort Study.
Périodique
CNS drugs
Auteur⸱e⸱s
Pantazou V., Novy J., Rossetti A.O.
ISSN
1179-1934 (Electronic)
ISSN-L
1172-7047
Statut éditorial
Publié
Date de publication
02/2019
Peer-reviewed
Oui
Volume
33
Numéro
2
Pages
187-192
Langue
anglais
Notes
Publication types: Journal Article ; Observational Study
Publication Status: ppublish
Résumé
Status epilepticus (SE) represents a neurological emergency that leads to considerable morbidity and mortality. Following failure of first-line therapy, usually with benzodiazepines, there is no clear evidence to guide treatment of refractory SE, although a wide variety of approaches has been described anecdotally.
The aim of this study was to assess the clinical response to corticosteroids in adults with refractory and super-refractory SE, describing, to the best of our knowledge, the first adult SE cohort treated with corticosteroids.
We retrospectively analysed our adult SE registry (2006-2017), identifying 15 out of 987 episodes (1.5%) in which corticosteroids were prescribed de novo as adjuvant therapy to a variety of antiepileptic drug regimens. We analysed incident episodes and defined clinical response as SE ceasing within 1 week of administration, without any other medical intervention.
Out of 987 SE episodes, 15 (1.5%) were treated with de novo corticosteroids, corresponding to 12 patients, with increasing prevalence as the SE became refractory (10/411; 2.4% of episodes) and super-refractory (5/108; 4.6% of episodes). One patient (a woman with Rasmussen encephalitis) presented with four SE episodes over a period of 3 years, so only her index SE episode was included in subsequent analyses. The episodes treated were predominantly of inflammatory origin (6/12), such as autoimmune or Rasmussen encephalitis. In five out of 12 (42%) of the considered incident episodes, SE resolved following corticosteroids (all within 3 days). The outcome was better in this responders group (for 2/5 episodes, patients did not have a new handicap at discharge, versus 0/7 in non-responders). In patients with inflammatory and acute symptomatic causes, global prognosis was better than in those with progressive or neurodegenerative aetiologies (6/8 vs. 4/4 had a new handicap at discharge or died).
Our observations seem to support the use of corticosteroids, especially for acute SE of putative inflammatory origin; these compounds, however, were prescribed infrequently.
Mots-clé
Adrenal Cortex Hormones/administration & dosage, Adrenal Cortex Hormones/therapeutic use, Anticonvulsants/administration & dosage, Anticonvulsants/therapeutic use, Chemotherapy, Adjuvant, Cohort Studies, Drug Therapy, Combination, Female, Humans, Injections, Intravenous, Male, Middle Aged, Retrospective Studies, Status Epilepticus/drug therapy, Status Epilepticus/immunology, Treatment Outcome
Pubmed
Web of science
Création de la notice
10/02/2019 16:35
Dernière modification de la notice
26/06/2020 6:21
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