Treatment-emergent adverse events and antiseizure medication actual drug load.
Adverse events
Antiepileptic drug
Antiseizure drug
Tolerability
Treatment discontinuation
Journal
Epilepsy & behavior : E&B
ISSN: 1525-5069
Titre abrégé: Epilepsy Behav
Pays: United States
ID NLM: 100892858
Informations de publication
Date de publication:
12 2022
12 2022
Historique:
received:
29
04
2022
revised:
05
10
2022
accepted:
27
10
2022
pubmed:
15
11
2022
medline:
30
11
2022
entrez:
14
11
2022
Statut:
ppublish
Résumé
The correlation between treatment-emergent adverse events (TEAE) and antiseizure medication (ASM) drug load is a controversial topic. Previous studies used daily defined dosage (DDD) to measure drug load. We aim to assess if ASM adjusted to body weight and plasma levels were associated with TEAE. We analyzed clinical visits of a trial on therapeutic drug monitoring in outpatients with epilepsy. TEAE, treatment, and its changes, as well as ASM plasma levels, were recorded at each visit. Each medication level was stratified according to its position in relation to its proposed reference range (below, in the lower half, upper half, or above). We analyzed 424 visits (151 participants). Treatment-emergent adverse events were reported in 84 (20%) visits. There was no significant difference when comparing visits with TEAE with those without TEAE in terms of ASM drug load (calculated with DDD), corrected for body weight, their changes since the last visit, as well as summed plasma levels compared to reference ranges. Actual drug load seems not to represent a major determinant of TEAE recorded during routine visits, even when accounting thoroughly for the patient's exposure to the treatment. The use of structured questionnaires and neuropsychometric tests may assess more accurately the potential consequences of drug loads.
Identifiants
pubmed: 36375306
pii: S1525-5050(22)00429-2
doi: 10.1016/j.yebeh.2022.108980
pii:
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
108980Informations de copyright
Copyright © 2022 The Author(s). Published by Elsevier Inc. All rights reserved.