Ketamine in adult super-refractory status epilepticus: Efficacy analysis on a prospective registry.
Détails
Télécharger: 35274736_BIB_76BB5CCD9300.pdf (427.71 [Ko])
Etat: Public
Version: Final published version
Licence: CC BY-NC-ND 4.0
Etat: Public
Version: Final published version
Licence: CC BY-NC-ND 4.0
ID Serval
serval:BIB_76BB5CCD9300
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
Ketamine in adult super-refractory status epilepticus: Efficacy analysis on a prospective registry.
Périodique
Acta neurologica Scandinavica
ISSN
1600-0404 (Electronic)
ISSN-L
0001-6314
Statut éditorial
Publié
Date de publication
06/2022
Peer-reviewed
Oui
Volume
145
Numéro
6
Pages
737-742
Langue
anglais
Notes
Publication types: Journal Article
Publication Status: ppublish
Publication Status: ppublish
Résumé
Status epilepticus (SE) persisting despite two anti-seizures medications (ASM) and anesthetics is labeled super refractory (SRSE), correlating with important morbidity and mortality. Its treatment relies on expert opinions. Due to its pharmacological properties, ketamine (KET) has received increasing attention, but data are essentially retrospective.
To describe an unselected cohort of adults receiving KET for SRSE.
Analysis of a prospective registry of consecutive SE episodes, identifying SRSE patients receiving ketamine (KET). Comparison with recent adult series including more than 10 patients.
Eleven patients received KET after a median of 4 days (range: 2-20); median dose was 5 mg/kg/h (range: 2.5-15). KET provided permanent SE control in three (27%). Previous series, using KET administration delays and doses similar to our cohort, report KET efficacy in 28-96% of cases.
We found a lower SE control rate than existing literature, whose data are, however, often retrospective, potentially selecting patients with less severe SE forms or responding to KET. This might explain outcome differences, as KET administration modalities were comparable with our cohort. Since randomized controlled studies are lacking on this subject, the analysis of this prospective, unselected cohort, if confirmed, suggests a current overestimation of KET efficacy in SRSE.
To describe an unselected cohort of adults receiving KET for SRSE.
Analysis of a prospective registry of consecutive SE episodes, identifying SRSE patients receiving ketamine (KET). Comparison with recent adult series including more than 10 patients.
Eleven patients received KET after a median of 4 days (range: 2-20); median dose was 5 mg/kg/h (range: 2.5-15). KET provided permanent SE control in three (27%). Previous series, using KET administration delays and doses similar to our cohort, report KET efficacy in 28-96% of cases.
We found a lower SE control rate than existing literature, whose data are, however, often retrospective, potentially selecting patients with less severe SE forms or responding to KET. This might explain outcome differences, as KET administration modalities were comparable with our cohort. Since randomized controlled studies are lacking on this subject, the analysis of this prospective, unselected cohort, if confirmed, suggests a current overestimation of KET efficacy in SRSE.
Mots-clé
Adult, Anticonvulsants/therapeutic use, Cohort Studies, Humans, Ketamine/pharmacology, Ketamine/therapeutic use, Registries, Retrospective Studies, Status Epilepticus/drug therapy, coma, general anesthetic, ketamine, outcome, prognosis, refractory status epilepticus, therapeutic, treatment
Pubmed
Web of science
Open Access
Oui
Création de la notice
21/03/2022 8:50
Dernière modification de la notice
25/01/2024 7:38