Alzemon: a prospective follow-up study of eslicarbazepine acetate monotherapy in patients with newly diagnosed epilepsy

Eslicarbazepine acetate is a novel sodium channel blocker for use in the treatment of focal onset seizures. Prospective studies on its effectiveness in monotherapy in patients with newly diagnosed partial epilepsy in routine clinical practice are scarce. To evaluate the effectiveness of eslicarbazep...

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Veröffentlicht in:Revista de neurologiá 2021-04, Vol.72 (8), p.263-268
Hauptverfasser: Hernández-Rubio, L, Asensio-Asensio, M, Tortosa-Conesa, D, Alfaro-Sáez, A, García-Escrivá, A, Díaz-Román, M, Montoya, J, Méndez-Miralles, M A, Bertol-Alegre, V, Castro-Vilanova, M D, Galiano, M L, Blanco-Cantó, M E, López-González, F
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container_issue 8
container_start_page 263
container_title Revista de neurologiá
container_volume 72
creator Hernández-Rubio, L
Asensio-Asensio, M
Tortosa-Conesa, D
Alfaro-Sáez, A
García-Escrivá, A
Díaz-Román, M
Montoya, J
Méndez-Miralles, M A
Bertol-Alegre, V
Castro-Vilanova, M D
Galiano, M L
Blanco-Cantó, M E
López-González, F
description Eslicarbazepine acetate is a novel sodium channel blocker for use in the treatment of focal onset seizures. Prospective studies on its effectiveness in monotherapy in patients with newly diagnosed partial epilepsy in routine clinical practice are scarce. To evaluate the effectiveness of eslicarbazepine as initial monotherapy in patients with newly diagnosed partial epilepsy in routine clinical practice. A prospective, multicentre, post-authorisation study. Patients with newly diagnosed partial epilepsy aged 18 years or older without previous treatment were included. The efficacy variables were: percentage of seizure-free patients, responders and reduction in monthly frequency of seizures. The safety variables analyse the 12-month retention rate and the occurrence of adverse effects. Fifty-three patients were included. The retention rate was 77.4%. At the end of the observation period, 83% of patients were seizure-free and 92.5% had reduced their baseline frequency by 50% or more. In addition, 68% of the patients reported some adverse effect and 7.5% of them dropped out of the study for this reason. The effectiveness analysis of the subgroup of patients aged 65 years or more showed no differences with respect to the overall population. Eslicarbazepine monotherapy in patients with newly diagnosed partial epilepsy, both in the general population and in the population over 65 years old, is effective and safe in routine clinical practice.
doi_str_mv 10.33588/rn.7208.2020593
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Prospective studies on its effectiveness in monotherapy in patients with newly diagnosed partial epilepsy in routine clinical practice are scarce. To evaluate the effectiveness of eslicarbazepine as initial monotherapy in patients with newly diagnosed partial epilepsy in routine clinical practice. A prospective, multicentre, post-authorisation study. Patients with newly diagnosed partial epilepsy aged 18 years or older without previous treatment were included. The efficacy variables were: percentage of seizure-free patients, responders and reduction in monthly frequency of seizures. The safety variables analyse the 12-month retention rate and the occurrence of adverse effects. Fifty-three patients were included. The retention rate was 77.4%. At the end of the observation period, 83% of patients were seizure-free and 92.5% had reduced their baseline frequency by 50% or more. 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source MEDLINE; EZB-FREE-00999 freely available EZB journals
subjects Adult
Aged
Anticonvulsants - therapeutic use
Dibenzazepines - therapeutic use
Epilepsy - drug therapy
Female
Follow-Up Studies
Humans
Male
Middle Aged
Prospective Studies
title Alzemon: a prospective follow-up study of eslicarbazepine acetate monotherapy in patients with newly diagnosed epilepsy
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