<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-04-13T01:12:06Z</responseDate><request verb="GetRecord" identifier="oai:www.recercat.cat:11351/7571" metadataPrefix="oai_dc">https://recercat.cat/oai/request</request><GetRecord><record><header><identifier>oai:recercat.cat:11351/7571</identifier><datestamp>2025-10-24T10:31:49Z</datestamp><setSpec>com_2072_378070</setSpec><setSpec>com_2072_378040</setSpec><setSpec>col_2072_378092</setSpec></header><metadata><oai_dc:dc xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:doc="http://www.lyncode.com/xoai" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
   <dc:title>Overnight switch from levetiracetam to brivaracetam: safety and tolerability</dc:title>
   <dc:creator>Salas Puig, Xavier</dc:creator>
   <dc:creator>Quintana Luque, Manuel</dc:creator>
   <dc:creator>Seijo Raposo, Ivan Manuel</dc:creator>
   <dc:creator>Santamarina Pérez, Estevo</dc:creator>
   <dc:creator>Fonseca Hernandez, Elena</dc:creator>
   <dc:creator>Toledo Argany, Manuel</dc:creator>
   <dc:creator>Abraira del Fresno, Laura</dc:creator>
   <dc:contributor>Institut Català de la Salut</dc:contributor>
   <dc:contributor>Unitat d’Epilèpsia, Servei de Neurologia, Vall d’Hebron Hospital Universitari, Barcelona, Spain</dc:contributor>
   <dc:contributor>Vall d'Hebron Barcelona Hospital Campus</dc:contributor>
   <dc:subject>Anticonvulsius - Ús terapèutic</dc:subject>
   <dc:subject>Epilèpsia - Tractament</dc:subject>
   <dc:subject>Avaluació de resultats (Assistència sanitària)</dc:subject>
   <dc:subject>CHEMICALS AND DRUGS::Chemical Actions and Uses::Pharmacologic Actions::Therapeutic Uses::Central Nervous System Agents::Anticonvulsants</dc:subject>
   <dc:subject>Other subheadings::Other subheadings::Other subheadings::/administration &amp; dosage</dc:subject>
   <dc:subject>ANALYTICAL, DIAGNOSTIC AND THERAPEUTIC TECHNIQUES, AND EQUIPMENT::Diagnosis::Prognosis::Treatment Outcome</dc:subject>
   <dc:subject>DISEASES::Nervous System Diseases::Central Nervous System Diseases::Brain Diseases::Epilepsy</dc:subject>
   <dc:subject>COMPUESTOS QUÍMICOS Y DROGAS::acciones y usos químicos::acciones farmacológicas::usos terapéuticos::fármacos del sistema nervioso central::anticonvulsivantes</dc:subject>
   <dc:subject>Otros calificadores::Otros calificadores::Otros calificadores::/administración &amp; dosificación</dc:subject>
   <dc:subject>TÉCNICAS Y EQUIPOS ANALÍTICOS, DIAGNÓSTICOS Y TERAPÉUTICOS::diagnóstico::pronóstico::resultado del tratamiento</dc:subject>
   <dc:subject>ENFERMEDADES::enfermedades del sistema nervioso::enfermedades del sistema nervioso central::enfermedades cerebrales::epilepsia</dc:subject>
   <dc:description>Brivaracetam; Epilepsy; Tolerability</dc:description>
   <dc:description>Brivaracetam; Epilepsia; Tolerabilidad</dc:description>
   <dc:description>Brivaracetam; Epilèpsia; Tolerabilitat</dc:description>
   <dc: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.&#xd;
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.&#xd;
An overnight switching to brivaracetam is safe and well tolerated. This treatment can improve levetiracetam-related neuropsychiatric AEs.</dc:description>
   <dc:date>2022-05-24T06:57:29Z</dc:date>
   <dc:date>2022-05-24T06:57:29Z</dc:date>
   <dc:date>2021</dc:date>
   <dc:type>info:eu-repo/semantics/article</dc:type>
   <dc:type>info:eu-repo/semantics/publishedVersion</dc:type>
   <dc:identifier>Abraira L, Salas-Puig J, Quintana M, Seijo-Raposo IM, Santamarina E, Fonseca E, et al. Overnight switch from levetiracetam to brivaracetam: safety and tolerability. Epilepsy Behav Reports. 2021;16:100504.</dc:identifier>
   <dc:identifier>2589-9864</dc:identifier>
   <dc:identifier>https://hdl.handle.net/11351/7571</dc:identifier>
   <dc:identifier>10.1016/j.ebr.2021.100504</dc:identifier>
   <dc:identifier>34901817</dc:identifier>
   <dc:identifier>000730415800003</dc:identifier>
   <dc:identifier>http://hdl.handle.net/11351/7571</dc:identifier>
   <dc:language>eng</dc:language>
   <dc:relation>Epilepsy &amp; Behavior Reports;16</dc:relation>
   <dc:relation>https://doi.org/10.1016/j.ebr.2021.100504</dc:relation>
   <dc:rights>Attribution-NonCommercial-NoDerivatives 4.0 International</dc:rights>
   <dc:rights>http://creativecommons.org/licenses/by-nc-nd/4.0/</dc:rights>
   <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
   <dc:format>application/pdf</dc:format>
   <dc:publisher>Elsevier</dc:publisher>
   <dc:source>Scientia</dc:source>
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