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Transition from oxcarbazepine to eslicarbazepine acetate: A single center study

OBJECTIVES: There is limited clinical evidence for comparison between oxcarbazepine (OXC) and eslicarbazepine acetate (ESL) in terms of tolerability, or how to execute the change from OXC to ESL. We report the process of transitioning patients with focal epilepsy from previous OXC treatment to ESL d...

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Autores principales: Mäkinen, Jussi, Rainesalo, Sirpa, Peltola, Jukka
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5346521/
https://www.ncbi.nlm.nih.gov/pubmed/28293474
http://dx.doi.org/10.1002/brb3.634
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author Mäkinen, Jussi
Rainesalo, Sirpa
Peltola, Jukka
author_facet Mäkinen, Jussi
Rainesalo, Sirpa
Peltola, Jukka
author_sort Mäkinen, Jussi
collection PubMed
description OBJECTIVES: There is limited clinical evidence for comparison between oxcarbazepine (OXC) and eslicarbazepine acetate (ESL) in terms of tolerability, or how to execute the change from OXC to ESL. We report the process of transitioning patients with focal epilepsy from previous OXC treatment to ESL due to tolerability problems. The rationale for change from OXC is reported, and the outcome with respective to this rationale is analyzed in terms of tolerability and efficacy. MATERIALS AND METHODS: The subjects were transitioned overnight from OXC to ESL in a hospital inpatient setting. An evaluation of the effects of the transition was made after 1 and 3 months. All adverse events (AEs) were recorded following the transition period. Subjects were classified by outcome in terms of AEs. RESULTS: Twenty‐three subjects were transitioned from OXC to ESL. Fifteen patients OXC‐related AEs reduced significantly after transition. Particularly, most of (93%) the AEs presented in the morning resolved after transition to ESL. No patient had an increase in seizure frequency following the transition. The incidence of ESL‐related AEs was 39% at 1 month and 13% at 3 month follow‐up; however, all patients continued ESL throughout the study period. CONCLUSIONS: This study demonstrates that patients suffering from OXC‐related AEs improve in terms of tolerability after a switch to ESL with maintaining seizure control. This improvement is more pronounced if the OXC‐related AEs are most evident following morning dosing of OXC. Transition can be safely executed in an outpatient setting.
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spelling pubmed-53465212017-03-14 Transition from oxcarbazepine to eslicarbazepine acetate: A single center study Mäkinen, Jussi Rainesalo, Sirpa Peltola, Jukka Brain Behav Original Research OBJECTIVES: There is limited clinical evidence for comparison between oxcarbazepine (OXC) and eslicarbazepine acetate (ESL) in terms of tolerability, or how to execute the change from OXC to ESL. We report the process of transitioning patients with focal epilepsy from previous OXC treatment to ESL due to tolerability problems. The rationale for change from OXC is reported, and the outcome with respective to this rationale is analyzed in terms of tolerability and efficacy. MATERIALS AND METHODS: The subjects were transitioned overnight from OXC to ESL in a hospital inpatient setting. An evaluation of the effects of the transition was made after 1 and 3 months. All adverse events (AEs) were recorded following the transition period. Subjects were classified by outcome in terms of AEs. RESULTS: Twenty‐three subjects were transitioned from OXC to ESL. Fifteen patients OXC‐related AEs reduced significantly after transition. Particularly, most of (93%) the AEs presented in the morning resolved after transition to ESL. No patient had an increase in seizure frequency following the transition. The incidence of ESL‐related AEs was 39% at 1 month and 13% at 3 month follow‐up; however, all patients continued ESL throughout the study period. CONCLUSIONS: This study demonstrates that patients suffering from OXC‐related AEs improve in terms of tolerability after a switch to ESL with maintaining seizure control. This improvement is more pronounced if the OXC‐related AEs are most evident following morning dosing of OXC. Transition can be safely executed in an outpatient setting. John Wiley and Sons Inc. 2017-01-27 /pmc/articles/PMC5346521/ /pubmed/28293474 http://dx.doi.org/10.1002/brb3.634 Text en © 2017 The Authors. Brain and Behavior published by Wiley Periodicals, Inc. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Mäkinen, Jussi
Rainesalo, Sirpa
Peltola, Jukka
Transition from oxcarbazepine to eslicarbazepine acetate: A single center study
title Transition from oxcarbazepine to eslicarbazepine acetate: A single center study
title_full Transition from oxcarbazepine to eslicarbazepine acetate: A single center study
title_fullStr Transition from oxcarbazepine to eslicarbazepine acetate: A single center study
title_full_unstemmed Transition from oxcarbazepine to eslicarbazepine acetate: A single center study
title_short Transition from oxcarbazepine to eslicarbazepine acetate: A single center study
title_sort transition from oxcarbazepine to eslicarbazepine acetate: a single center study
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5346521/
https://www.ncbi.nlm.nih.gov/pubmed/28293474
http://dx.doi.org/10.1002/brb3.634
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