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Dibenzazepine Agents in Epilepsy: How Does Eslicarbazepine Acetate Differ?

Carbamazepine (CBZ), oxcarbazepine (OXC), and eslicarbazepine acetate (ESL) belong to the dibenzazepine family of antiepileptic drugs and are all thought to primarily act as sodium channel blockers (SCBs). However, ESL is structurally distinct from CBZ and OXC, resulting in differences in metabolism...

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Autores principales: Lawthom, Charlotte, Peltola, Jukka, McMurray, Rob, Dodd, Emma, Villanueva, Vicente
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Healthcare 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6283801/
https://www.ncbi.nlm.nih.gov/pubmed/30251237
http://dx.doi.org/10.1007/s40120-018-0111-2
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author Lawthom, Charlotte
Peltola, Jukka
McMurray, Rob
Dodd, Emma
Villanueva, Vicente
author_facet Lawthom, Charlotte
Peltola, Jukka
McMurray, Rob
Dodd, Emma
Villanueva, Vicente
author_sort Lawthom, Charlotte
collection PubMed
description Carbamazepine (CBZ), oxcarbazepine (OXC), and eslicarbazepine acetate (ESL) belong to the dibenzazepine family of antiepileptic drugs and are all thought to primarily act as sodium channel blockers (SCBs). However, ESL is structurally distinct from CBZ and OXC, resulting in differences in metabolism, pharmacokinetics, and pharmacodynamics. Despite a lack of direct comparative data, evidence for potential differences in effectiveness and tolerability within the dibenzazepine family has emerged from studies in which patients being treated with one dibenzazepine agent have received adjunctive treatment with another (having achieved insufficient seizure control with the first) or have transitioned from one dibenzazepine agent to another because of lack of effectiveness or poor tolerability. Most of these studies have been conducted in the real-world clinical practice setting. ESL has been shown to be effective as adjunctive therapy in patients who have previously achieved inadequate seizure control with CBZ, indicating that the use of different dibenzazepine agents in combination can provide additive effectiveness benefits, which may reflect underlying differences in their mechanisms of action. Similarly, ESL monotherapy can be effective in patients who have switched from another dibenzazepine, such as CBZ or OXC, because of inadequate efficacy. There is also considerable evidence to demonstrate that patients transitioning from OXC or CBZ to ESL as a result of adverse events experience improvements in tolerability, which may also be associated with improvements in quality of life, alertness, and/or lipid profiles. Current evidence therefore demonstrates that ESL differs from other dibenzazepine agents in terms of effectiveness and tolerability. Funding: Eisai Ltd.
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spelling pubmed-62838012018-12-26 Dibenzazepine Agents in Epilepsy: How Does Eslicarbazepine Acetate Differ? Lawthom, Charlotte Peltola, Jukka McMurray, Rob Dodd, Emma Villanueva, Vicente Neurol Ther Commentary Carbamazepine (CBZ), oxcarbazepine (OXC), and eslicarbazepine acetate (ESL) belong to the dibenzazepine family of antiepileptic drugs and are all thought to primarily act as sodium channel blockers (SCBs). However, ESL is structurally distinct from CBZ and OXC, resulting in differences in metabolism, pharmacokinetics, and pharmacodynamics. Despite a lack of direct comparative data, evidence for potential differences in effectiveness and tolerability within the dibenzazepine family has emerged from studies in which patients being treated with one dibenzazepine agent have received adjunctive treatment with another (having achieved insufficient seizure control with the first) or have transitioned from one dibenzazepine agent to another because of lack of effectiveness or poor tolerability. Most of these studies have been conducted in the real-world clinical practice setting. ESL has been shown to be effective as adjunctive therapy in patients who have previously achieved inadequate seizure control with CBZ, indicating that the use of different dibenzazepine agents in combination can provide additive effectiveness benefits, which may reflect underlying differences in their mechanisms of action. Similarly, ESL monotherapy can be effective in patients who have switched from another dibenzazepine, such as CBZ or OXC, because of inadequate efficacy. There is also considerable evidence to demonstrate that patients transitioning from OXC or CBZ to ESL as a result of adverse events experience improvements in tolerability, which may also be associated with improvements in quality of life, alertness, and/or lipid profiles. Current evidence therefore demonstrates that ESL differs from other dibenzazepine agents in terms of effectiveness and tolerability. Funding: Eisai Ltd. Springer Healthcare 2018-09-24 /pmc/articles/PMC6283801/ /pubmed/30251237 http://dx.doi.org/10.1007/s40120-018-0111-2 Text en © The Author(s) 2018 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits any noncommercial use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Commentary
Lawthom, Charlotte
Peltola, Jukka
McMurray, Rob
Dodd, Emma
Villanueva, Vicente
Dibenzazepine Agents in Epilepsy: How Does Eslicarbazepine Acetate Differ?
title Dibenzazepine Agents in Epilepsy: How Does Eslicarbazepine Acetate Differ?
title_full Dibenzazepine Agents in Epilepsy: How Does Eslicarbazepine Acetate Differ?
title_fullStr Dibenzazepine Agents in Epilepsy: How Does Eslicarbazepine Acetate Differ?
title_full_unstemmed Dibenzazepine Agents in Epilepsy: How Does Eslicarbazepine Acetate Differ?
title_short Dibenzazepine Agents in Epilepsy: How Does Eslicarbazepine Acetate Differ?
title_sort dibenzazepine agents in epilepsy: how does eslicarbazepine acetate differ?
topic Commentary
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6283801/
https://www.ncbi.nlm.nih.gov/pubmed/30251237
http://dx.doi.org/10.1007/s40120-018-0111-2
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