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Overnight switch from levetiracetam to brivaracetam. Safety and tolerability

Brivaracetam is a newer antiseizure medication than levetiracetam. It has a more selective action on the synaptic vesicle glycoprotein 2A binding site, and it seems to provide a more favorable neuropsychiatric profile. The aim of this study was to assess the safety and tolerability of an overnight s...

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Autores principales: Abraira, L., Salas-Puig, J., Quintana, M., Seijo-Raposo, I.M., Santamarina, E., Fonseca, E., Toledo, M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8640256/
https://www.ncbi.nlm.nih.gov/pubmed/34901817
http://dx.doi.org/10.1016/j.ebr.2021.100504
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author Abraira, L.
Salas-Puig, J.
Quintana, M.
Seijo-Raposo, I.M.
Santamarina, E.
Fonseca, E.
Toledo, M.
author_facet Abraira, L.
Salas-Puig, J.
Quintana, M.
Seijo-Raposo, I.M.
Santamarina, E.
Fonseca, E.
Toledo, M.
author_sort Abraira, L.
collection PubMed
description Brivaracetam is a newer antiseizure medication than levetiracetam. It has a more selective action on the synaptic vesicle glycoprotein 2A binding site, and it seems to provide a more favorable neuropsychiatric profile. The aim of this study was to assess the safety and tolerability of an overnight switch from levetiracetam to brivaracetam. This was a retrospective descriptive study including patients with epilepsy treated with levetiracetam, who switched due to inefficacy or previous adverse events (AEs). In total, forty-one patients were included (mean age 40.9 ± 17.8 years, women 48.8%). Focal epilepsy represented 75.6% (n = 31) of patients (structural cause [n = 25], unknown cause [n = 6]). Four patients had idiopathic generalized epilepsy, two had developmental and epileptic encephalopathy and four patients were unclassified. The reason to start brivaracetam was inefficacy in 53.7% (n = 22), AEs in 65.9% (25/27 neuropsychiatric) and both in 19.5% (n = 8). Brivaracetam-related AEs were reported in 24.4%. Neuropsychological AEs associated with the previous use of levetiracetam improved in 76% of patients. Treatment was discontinued in 19.5% patients. Patients’ reported seizure frequency improved, worsened and remained stable in 26.8%, 12.2%, and 61.0% of the cases, respectively. An overnight switching to brivaracetam is safe and well tolerated. This treatment can improve levetiracetam-related neuropsychiatric AEs.
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spelling pubmed-86402562021-12-09 Overnight switch from levetiracetam to brivaracetam. Safety and tolerability Abraira, L. Salas-Puig, J. Quintana, M. Seijo-Raposo, I.M. Santamarina, E. Fonseca, E. Toledo, M. Epilepsy Behav Rep Article Brivaracetam is a newer antiseizure medication than levetiracetam. It has a more selective action on the synaptic vesicle glycoprotein 2A binding site, and it seems to provide a more favorable neuropsychiatric profile. The aim of this study was to assess the safety and tolerability of an overnight switch from levetiracetam to brivaracetam. This was a retrospective descriptive study including patients with epilepsy treated with levetiracetam, who switched due to inefficacy or previous adverse events (AEs). In total, forty-one patients were included (mean age 40.9 ± 17.8 years, women 48.8%). Focal epilepsy represented 75.6% (n = 31) of patients (structural cause [n = 25], unknown cause [n = 6]). Four patients had idiopathic generalized epilepsy, two had developmental and epileptic encephalopathy and four patients were unclassified. The reason to start brivaracetam was inefficacy in 53.7% (n = 22), AEs in 65.9% (25/27 neuropsychiatric) and both in 19.5% (n = 8). Brivaracetam-related AEs were reported in 24.4%. Neuropsychological AEs associated with the previous use of levetiracetam improved in 76% of patients. Treatment was discontinued in 19.5% patients. Patients’ reported seizure frequency improved, worsened and remained stable in 26.8%, 12.2%, and 61.0% of the cases, respectively. An overnight switching to brivaracetam is safe and well tolerated. This treatment can improve levetiracetam-related neuropsychiatric AEs. Elsevier 2021-11-14 /pmc/articles/PMC8640256/ /pubmed/34901817 http://dx.doi.org/10.1016/j.ebr.2021.100504 Text en © 2021 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Abraira, L.
Salas-Puig, J.
Quintana, M.
Seijo-Raposo, I.M.
Santamarina, E.
Fonseca, E.
Toledo, M.
Overnight switch from levetiracetam to brivaracetam. Safety and tolerability
title Overnight switch from levetiracetam to brivaracetam. Safety and tolerability
title_full Overnight switch from levetiracetam to brivaracetam. Safety and tolerability
title_fullStr Overnight switch from levetiracetam to brivaracetam. Safety and tolerability
title_full_unstemmed Overnight switch from levetiracetam to brivaracetam. Safety and tolerability
title_short Overnight switch from levetiracetam to brivaracetam. Safety and tolerability
title_sort overnight switch from levetiracetam to brivaracetam. safety and tolerability
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8640256/
https://www.ncbi.nlm.nih.gov/pubmed/34901817
http://dx.doi.org/10.1016/j.ebr.2021.100504
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