Intravenous lacosamide in status epilepticus: Correlation between loading dose, serum levels, and clinical response.
Détails
Etat: Public
Version: de l'auteur⸱e
Licence: Non spécifiée
ID Serval
serval:BIB_4B7DEF70D1C9
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
Intravenous lacosamide in status epilepticus: Correlation between loading dose, serum levels, and clinical response.
Périodique
Epilepsy Research
ISSN
1872-6844 (Electronic)
ISSN-L
0920-1211
Statut éditorial
Publié
Date de publication
2017
Peer-reviewed
Oui
Volume
135
Pages
38-42
Langue
anglais
Résumé
Intravenous lacosamide (LCM) is increasingly used in the treatment of status epilepticus (SE), but optimal loading dose and target serum levels are unclear. We analysed the correlation between LCM serum levels after intravenous loading dose and clinical response.
Retrospective study in two centres from December 2014 to May 2016 including consecutive SE patients treated with LCM, in which trough serum levels after intravenous loading dose were available. Trough levels were correlated with the loading dose and the clinical response, defined as LCM introduction terminating SE without the need of further treatment. Correlations were adjusted for other SE characteristics.
Among 40 patients, 16 (40%) responded to LCM. LCM serum concentrations within the reference interval (10-20mg/l) were associated with loading doses of >9mg/kg (p=0.003; χ2). However, we observed no difference between LCM serum levels in responders (median 10.4mg/l) versus non-responders (median 9.5mg/l; p=0.36; U test), even after adjusting for other predictors of clinical outcome (SE severity, aetiology, and number of previous treatment).
High intravenous LCM loading doses (>9mg/kg) were associated with serum levels within the reference interval, there was however no correlation with the clinical response. Prospective studies are needed to evaluate the benefit of increasing the LCM loading dose in SE.
Retrospective study in two centres from December 2014 to May 2016 including consecutive SE patients treated with LCM, in which trough serum levels after intravenous loading dose were available. Trough levels were correlated with the loading dose and the clinical response, defined as LCM introduction terminating SE without the need of further treatment. Correlations were adjusted for other SE characteristics.
Among 40 patients, 16 (40%) responded to LCM. LCM serum concentrations within the reference interval (10-20mg/l) were associated with loading doses of >9mg/kg (p=0.003; χ2). However, we observed no difference between LCM serum levels in responders (median 10.4mg/l) versus non-responders (median 9.5mg/l; p=0.36; U test), even after adjusting for other predictors of clinical outcome (SE severity, aetiology, and number of previous treatment).
High intravenous LCM loading doses (>9mg/kg) were associated with serum levels within the reference interval, there was however no correlation with the clinical response. Prospective studies are needed to evaluate the benefit of increasing the LCM loading dose in SE.
Mots-clé
Acetamides/administration & dosage, Acetamides/blood, Administration, Intravenous, Adult, Aged, Aged, 80 and over, Anticonvulsants/administration & dosage, Anticonvulsants/blood, Dose-Response Relationship, Drug, Female, Humans, Male, Middle Aged, Retrospective Studies, Status Epilepticus/blood, Status Epilepticus/drug therapy, Status Epilepticus/mortality, Treatment Outcome, Critical care, Outcome, Retrospective, Therapeutic drug monitoring
Pubmed
Web of science
Création de la notice
27/06/2017 17:25
Dernière modification de la notice
21/11/2022 9:22