Effectiveness and safety of early add-on therapy with brivaracetam in patients with poorly controlled focal seizures in routine clinical practice: BRIV-add study

Other authors

Institut Català de la Salut

[Serrano-Castro PJ] Instituto de Investigación Biomédica de Málaga (IBIMA-Plataforma Bionand), Málaga, Spain. Málaga Regional University Hospital, Málaga, Spain. Departamento de Medicina y Dermatología, Universidad de Málaga, Málaga, Spain. [Caballero-Martínez F] Faculty of Medicine, Universidad Francisco de Vitoria, Madrid, Spain. [Campos-Lucas FJ] Health Research, Universidad Francisco de Vitoria, Madrid, Spain. [Campos-Fernández D, Gifreu A, Toledo-Argany M] Vall d’Hebron Hospital Universitari, Barcelona, Spain. [de Aguilar-Amat MJ] La Paz University Hospital, Madrid, Spain. [García A] Central University Hospital of Asturias, Oviedo, Asturias, Spain

Vall d'Hebron Barcelona Hospital Campus

Publication date

2025-11-06T12:10:52Z

2025-11-06T12:10:52Z

2025-10



Abstract

Antiseizure medication; Brivaracetam; Drug therapy


Medicació anticonvulsiva; Brivaracetam; Teràpia farmacològica


Medicación anticonvulsiva; Brivaracetam; Terapia farmacológica


Objective: To evaluate the effectiveness and safety of brivaracetam (BRV) as an add-on therapy in patients with focal onset seizures who did not achieve seizure freedom with antiseizure medication (ASM) monotherapy in routine clinical practice. Methods: This was a retrospective, observational, multicenter study conducted across 17 neurology centers in Spain. We evaluated adult patients with focal onset epilepsy who had inadequate seizure control after at least 3 months of ASM monotherapy and were treated with dual therapy, combining BRV with their previous ASM, with the intention of maintaining this treatment for at least 6 months. Data were collected from medical records on seizure frequency, ASM doses, and adverse events (AEs), taking into account the end of this 6-month period of dual therapy. The primary efficacy outcomes were the proportion of patients achieving ≥50% reduction in seizure frequency and those achieving seizure freedom. Safety outcomes included the incidence of treatment-related AEs. Results: A total of 195 patients (mean age: 43.2 years; 52.3% male; mean disease duration: 11.5 years) were included in the study. The main location of epilepsy was identified (53.8%) as the frontal lobe (27.7%). The mean number of seizures during the last 3 months of ASM monotherapy was 12.1 (SD 39.5), which decreased to 6.4 (SD 21.2) after 6 months of BRV add-on therapy. A ≥ 50% reduction in seizure frequency was achieved by 90.8% of patients, while 49.7% reached seizure freedom. The most common AEs were related to the central nervous system, reported by 22.1% of patients, with a treatment discontinuation rate due to AEs of 12.8%. Significance: BRV as an add-on therapy is effective in reducing seizure frequency and is well-tolerated in patients with focal onset seizures. This study supports the use of BRV as an add-on option in patients who do not achieve adequate seizure control with ASM monotherapy. Plain language summary: This study evaluated how effective and safe brivaracetam (BRV) is when added to another medication for patients with focal onset seizures. The results showed that adding BRV helped many patients reduce the number of seizures, and some patients stopped having seizures completely. Side effects were generally mild.


This study has been funded by the Universidad Francisco de Vitoria-UCB Chair in Epilepsy and Movement Disorders.

Document Type

Article


Published version

Language

English

Subjects and keywords

Avaluació de resultats (Assistència sanitària); Epilèpsia - Tractament; Convulsions - Tractament; Anticonvulsius - Ús terapèutic; ANALYTICAL, DIAGNOSTIC AND THERAPEUTIC TECHNIQUES, AND EQUIPMENT::Diagnosis::Prognosis::Treatment Outcome; DISEASES::Nervous System Diseases::Neurologic Manifestations::Seizures; Other subheadings::Other subheadings::Other subheadings::/drug therapy; CHEMICALS AND DRUGS::Chemical Actions and Uses::Pharmacologic Actions::Therapeutic Uses::Central Nervous System Agents::Anticonvulsants; Other subheadings::Other subheadings::/therapeutic use; ANALYTICAL, DIAGNOSTIC AND THERAPEUTIC TECHNIQUES, AND EQUIPMENT::Therapeutics::Drug Therapy::Drug Therapy, Combination; DISEASES::Nervous System Diseases::Central Nervous System Diseases::Brain Diseases::Epilepsy; TÉCNICAS Y EQUIPOS ANALÍTICOS, DIAGNÓSTICOS Y TERAPÉUTICOS::diagnóstico::pronóstico::resultado del tratamiento; ENFERMEDADES::enfermedades del sistema nervioso::manifestaciones neurológicas::convulsiones; Otros calificadores::Otros calificadores::Otros calificadores::/farmacoterapia; COMPUESTOS QUÍMICOS Y DROGAS::acciones y usos químicos::acciones farmacológicas::usos terapéuticos::fármacos del sistema nervioso central::anticonvulsivantes; Otros calificadores::Otros calificadores::/uso terapéutico; TÉCNICAS Y EQUIPOS ANALÍTICOS, DIAGNÓSTICOS Y TERAPÉUTICOS::terapéutica::farmacoterapia::farmacoterapia combinada; ENFERMEDADES::enfermedades del sistema nervioso::enfermedades del sistema nervioso central::enfermedades cerebrales::epilepsia

Publisher

Wiley

Related items

Epilepsia Open;10(5)

https://doi.org/10.1002/epi4.70073

Recommended citation

This citation was generated automatically.

Rights

Attribution-NonCommercial-NoDerivatives 4.0 International

http://creativecommons.org/licenses/by-nc-nd/4.0/

This item appears in the following Collection(s)