Efficacy and safety of the long-term Vagus Nerve Stimulation: Preliminary report in adult patients with drug-resistant focal epilepsy

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Objective: To report the efficacy and long-term safety of the Vagus Nerve Stimulation (VNS), in a series of adult patients with drug-resistant focal epilepsy, treated in a hospital of Peru’s Social Security System. Methods: Data of the Adult Epilepsy Unit at Edgardo Reba...

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Autores: Barreto-Acevedo, Elliot, Barreto-Barra, Leila, Villafuerte-Espinoza, Mirla, Díaz-Vásquez, Alberto, Becerra-Zegarra, Alicia, Hernández-Vizarreta, José, Llaja-Rojas, Victoria
Formato: artículo
Fecha de Publicación:2019
Institución:Universidad Peruana Cayetano Heredia
Repositorio:Revistas - Universidad Peruana Cayetano Heredia
Lenguaje:español
OAI Identifier:oai:revistas.upch.edu.pe:article/3571
Enlace del recurso:https://revistas.upch.edu.pe/index.php/RNP/article/view/3571
Nivel de acceso:acceso abierto
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network_name_str Revistas - Universidad Peruana Cayetano Heredia
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dc.title.none.fl_str_mv Efficacy and safety of the long-term Vagus Nerve Stimulation: Preliminary report in adult patients with drug-resistant focal epilepsy
Eficacia y seguridad a largo plazo de la estimulación del nervio vago: Reporte preliminar en pacientes adultos con epilepsia focal fármacorresistente.
title Efficacy and safety of the long-term Vagus Nerve Stimulation: Preliminary report in adult patients with drug-resistant focal epilepsy
spellingShingle Efficacy and safety of the long-term Vagus Nerve Stimulation: Preliminary report in adult patients with drug-resistant focal epilepsy
Barreto-Acevedo, Elliot
title_short Efficacy and safety of the long-term Vagus Nerve Stimulation: Preliminary report in adult patients with drug-resistant focal epilepsy
title_full Efficacy and safety of the long-term Vagus Nerve Stimulation: Preliminary report in adult patients with drug-resistant focal epilepsy
title_fullStr Efficacy and safety of the long-term Vagus Nerve Stimulation: Preliminary report in adult patients with drug-resistant focal epilepsy
title_full_unstemmed Efficacy and safety of the long-term Vagus Nerve Stimulation: Preliminary report in adult patients with drug-resistant focal epilepsy
title_sort Efficacy and safety of the long-term Vagus Nerve Stimulation: Preliminary report in adult patients with drug-resistant focal epilepsy
dc.creator.none.fl_str_mv Barreto-Acevedo, Elliot
Barreto-Barra, Leila
Villafuerte-Espinoza, Mirla
Díaz-Vásquez, Alberto
Becerra-Zegarra, Alicia
Hernández-Vizarreta, José
Llaja-Rojas, Victoria
author Barreto-Acevedo, Elliot
author_facet Barreto-Acevedo, Elliot
Barreto-Barra, Leila
Villafuerte-Espinoza, Mirla
Díaz-Vásquez, Alberto
Becerra-Zegarra, Alicia
Hernández-Vizarreta, José
Llaja-Rojas, Victoria
author_role author
author2 Barreto-Barra, Leila
Villafuerte-Espinoza, Mirla
Díaz-Vásquez, Alberto
Becerra-Zegarra, Alicia
Hernández-Vizarreta, José
Llaja-Rojas, Victoria
author2_role author
author
author
author
author
author
description Objective: To report the efficacy and long-term safety of the Vagus Nerve Stimulation (VNS), in a series of adult patients with drug-resistant focal epilepsy, treated in a hospital of Peru’s Social Security System. Methods: Data of the Adult Epilepsy Unit at Edgardo Rebagliati National Hospital, from June 2016 to June 2019, were reviewed in order to identify patients who had been implanted with VNS. Frequency of seizures and antiepileptic drugs (AED), prior to implantation with VNS, at 3 and 6 months, and at the end of the follow-up period were recorded, as were the average percentage change in the frequency of seizures, response rates of ≥ 50%, ≥75%, and changes in AED and adverse effects. Results: Five patients with drug-resistant multifocal epilepsy who were implanted with VNS for not being candidates to resective epilepsy surgery were identified. The average age was 20.6 years old. The average duration of follow-up from the implant was 21 months and the average percentage in the reduction of the seizure frequency at 3, and 6 months, and at the end of the follow-up period (21 months), was 24%, 45% and 69%, respectively. The response rates of ≥ 50% and ≥ 75% were 80% and 40%. There was a partial reduction of AED in only 1 patient. The main adverse effect was hoarseness. Conclusions: The experience with VNS, reported for the first time in Peru, demonstrates its efficacy as palliative therapy, and good safety profile in adults with drug-resistant multifocal epilepsy. The effectiveness is significantly higher with sustained long-term stimulation.
publishDate 2019
dc.date.none.fl_str_mv 2019-10-01
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.none.fl_str_mv https://revistas.upch.edu.pe/index.php/RNP/article/view/3571
10.20453/rnp.v82i3.3571
url https://revistas.upch.edu.pe/index.php/RNP/article/view/3571
identifier_str_mv 10.20453/rnp.v82i3.3571
dc.language.none.fl_str_mv spa
language spa
dc.relation.none.fl_str_mv https://revistas.upch.edu.pe/index.php/RNP/article/view/3571/3956
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Universidad Peruana Cayetano Heredia
publisher.none.fl_str_mv Universidad Peruana Cayetano Heredia
dc.source.none.fl_str_mv Revista de Neuro-Psiquiatria; Vol. 82 No. 3 (2019): July - September; 183-191
Revista de Neuro-Psiquiatría; Vol. 82 Núm. 3 (2019): Julio - Setiembre; 183-191
Revista de Neuro-Psiquiatria; v. 82 n. 3 (2019): Julio - Setiembre; 183-191
1609-7394
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spelling Efficacy and safety of the long-term Vagus Nerve Stimulation: Preliminary report in adult patients with drug-resistant focal epilepsyEficacia y seguridad a largo plazo de la estimulación del nervio vago: Reporte preliminar en pacientes adultos con epilepsia focal fármacorresistente.Barreto-Acevedo, ElliotBarreto-Barra, LeilaVillafuerte-Espinoza, MirlaDíaz-Vásquez, AlbertoBecerra-Zegarra, AliciaHernández-Vizarreta, JoséLlaja-Rojas, VictoriaObjective: To report the efficacy and long-term safety of the Vagus Nerve Stimulation (VNS), in a series of adult patients with drug-resistant focal epilepsy, treated in a hospital of Peru’s Social Security System. Methods: Data of the Adult Epilepsy Unit at Edgardo Rebagliati National Hospital, from June 2016 to June 2019, were reviewed in order to identify patients who had been implanted with VNS. Frequency of seizures and antiepileptic drugs (AED), prior to implantation with VNS, at 3 and 6 months, and at the end of the follow-up period were recorded, as were the average percentage change in the frequency of seizures, response rates of ≥ 50%, ≥75%, and changes in AED and adverse effects. Results: Five patients with drug-resistant multifocal epilepsy who were implanted with VNS for not being candidates to resective epilepsy surgery were identified. The average age was 20.6 years old. The average duration of follow-up from the implant was 21 months and the average percentage in the reduction of the seizure frequency at 3, and 6 months, and at the end of the follow-up period (21 months), was 24%, 45% and 69%, respectively. The response rates of ≥ 50% and ≥ 75% were 80% and 40%. There was a partial reduction of AED in only 1 patient. The main adverse effect was hoarseness. Conclusions: The experience with VNS, reported for the first time in Peru, demonstrates its efficacy as palliative therapy, and good safety profile in adults with drug-resistant multifocal epilepsy. The effectiveness is significantly higher with sustained long-term stimulation.Objetivo: Reportar la experiencia en eficacia y seguridad a largo plazo de la estimulación del nervio vago (ENV), en una serie de pacientes adultos con epilepsia focal fármacorresistente, tratados en un hospital del Seguro Social del Perú. Material y Métodos: Se revisó la base de datos de la Unidad de Epilepsia de Adultos del Hospital Nacional Edgardo Rebagliati, de junio 2016 a junio 2019, a efecto de identificar pacientes a quienes se había implantados el estimulador. Se registraron las características clínicas y de manejo de la epilepsia (i.e., frecuencia de las crisis y regímenes de antiepilépticos (DAE), previas al implante, a los 3 y 6 meses del mismo y al final del periodo de seguimiento. Igualmente, el cambio porcentual promedio en la frecuencia de crisis en cada periodo, analizándose las tasas de respuesta ≥ 50%, ≥75% y los cambios en DAE, así como los efectos adversos al final del periodo de seguimiento. Resultados: Cinco pacientes con epilepsia multifocal fármacorresistente recibieron implante de ENV por no ser candidatos a cirugía resectiva de epilepsia. La edad promedio fue de 20,6 años, el promedio de duración del seguimiento fue de 21 meses y el promedio porcentual en la reducción de frecuencia de las crisis a los 3 meses, 6 meses y al final del seguimiento (21 meses) fue de 24%, 45% y 69%, respectivamente. Las tasa de respuesta ≥ 50% y ≥ 75%, fueron 80% y 40%. Se evidenció una reducción parcial de DAE en solo 1 paciente. El principal efecto adverso fue la ronquera. Conclusiones: La experiencia con ENV, reportada por primera vez en el Perú, demuestra su eficacia como terapia paliativa y un buen perfil de seguridad en adultos con epilepsia multifocal fármacorresistente. La eficacia es significativamente mayor con la estimulación sostenida a largo plazo.Universidad Peruana Cayetano Heredia2019-10-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://revistas.upch.edu.pe/index.php/RNP/article/view/357110.20453/rnp.v82i3.3571Revista de Neuro-Psiquiatria; Vol. 82 No. 3 (2019): July - September; 183-191Revista de Neuro-Psiquiatría; Vol. 82 Núm. 3 (2019): Julio - Setiembre; 183-191Revista de Neuro-Psiquiatria; v. 82 n. 3 (2019): Julio - Setiembre; 183-1911609-73940034-8597reponame:Revistas - Universidad Peruana Cayetano Herediainstname:Universidad Peruana Cayetano Herediainstacron:UPCHspahttps://revistas.upch.edu.pe/index.php/RNP/article/view/3571/3956info:eu-repo/semantics/openAccessoai:revistas.upch.edu.pe:article/35712020-06-09T20:45:29Z
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