Safinamide in Clinical Practice: A Spanish Multicenter Cohort Study

Background: Safinamide is an approved drug for the treatment of motor fluctuations of Parkinson's Disease (PD) patients with a potential benefit on non-motor symptoms (NMS). Methods: A retrospective multicenter cohort study was conducted, in which the clinical effect of safinamide on both motor...

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Detalhes bibliográficos
Autores: Martí-Andrés, G. (Gloria)|||/items/3d001d3e-a3cc-4105-a1c4-198602fb28b4, Jiménez-Bolaños, R. (Rayco)|||/items/e03cbed9-2f08-4429-88a8-a361be5eb2ee, Arbelo-González, J.M. (José Matías)|||/items/21116843-e426-4991-9ec1-b4161240ed13, Pagonabarraga, J. (Javier)|||/items/11fa7b60-f13e-4cc2-bb32-eb486349545d, Durán-Herrera, C. (Carmen)|||/items/9c13f10d-25a5-44bc-bb99-48c8b92f106c, Valentí-Azcarate, R. (Rafael)|||/items/1bc97f69-206c-4e9b-84ff-3f55fd6ead95, Luquin-Piudo, M.R. (María Rosario)|||/items/6449c359-8b33-4ca4-9ff1-ca1505be7ed3
Formato: artículo
Fecha de publicación:2019
País:España
Recursos:Universidad de Navarra
Repositorio:Dadun. Depósito Académico Digital de la Universidad de Navarra
Idioma:inglés
OAI Identifier:oai:dadun.unav.edu:10171/62132
Acesso em linha:https://hdl.handle.net/10171/62132
Access Level:acceso abierto
Palavra-chave:Materias Investigacion::Ciencias de la Salud::Neurología
Adverse drug event
Drug-Induced
Dyskinesia
Motor complications
Parkinson-™s Disease
Safinamide
Neurología
Descrição
Resumo:Background: Safinamide is an approved drug for the treatment of motor fluctuations of Parkinson's Disease (PD) patients with a potential benefit on non-motor symptoms (NMS). Methods: A retrospective multicenter cohort study was conducted, in which the clinical effect of safinamide on both motor and NMS was assessed by the Clinical Global Impression of Change scale. Furthermore, we assessed the appearance of adverse events (AEs) and its effect on dyskinesia, that were also recorded in non-fluctuating PD patients and in those previously treated with rasagiline. Results: We included 213 PD patients who received safinamide in addition to their regular levodopa therapy. Thirty-five withdrew prematurely from safinamide, mainly because of AEs. Out of 178, clinical improvement on motor and NMS was found in 76.4% and 26.2%, respectively. A total of 44 reported AEs of mild intensity. We did not find a difference concerning the clinical benefit or AEs when comparing either patients who had or had not been taking Monoamine Oxidase B Inhibitor (MAOB-I) previously or between patients with and without motor complications. Conclusions: Safinamide is an effective and safe add-on to levodopa drug for PD patients. Moreover, safinamide could elicit an additional clinical improvement in PD patients previously treated with other MAOB-I and in non- fluctuating patients with suboptimal motor control.