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Vagus nerve stimulation for refractory epilepsy: experience from Saudi Arabia

BACKGROUND: Vagus nerve stimulation (VNS) has been approved for the treatment of refractory partial epilepsy in adults and children over 12 years of age. Later on, its application expanded to include younger children and other types of epilepsy. We report our experience with this treatment modality...

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Autores principales: Al-Said, Youssef, Baeesa, Saleh, Khalid, Muhammad, Abdeen, Mohamed, Kayyali, Husam R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: King Faisal Specialist Hospital and Research Centre 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6152542/
https://www.ncbi.nlm.nih.gov/pubmed/26142937
http://dx.doi.org/10.5144/0256-4947.2015.41
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author Al-Said, Youssef
Baeesa, Saleh
Khalid, Muhammad
Abdeen, Mohamed
Kayyali, Husam R.
author_facet Al-Said, Youssef
Baeesa, Saleh
Khalid, Muhammad
Abdeen, Mohamed
Kayyali, Husam R.
author_sort Al-Said, Youssef
collection PubMed
description BACKGROUND: Vagus nerve stimulation (VNS) has been approved for the treatment of refractory partial epilepsy in adults and children over 12 years of age. Later on, its application expanded to include younger children and other types of epilepsy. We report our experience with this treatment modality for refractory epilepsy in Saudi Arabia. DESIGN AND SETTINGS: Open-label, uncontrolled, retrospective study of patients with refractory epilepsy, who were treated with VNS in a tertiary care hospital from January 2010 to June 2013. PATIENTS AND METHODS: Collected data included 26 patients’ demographics, epilepsy characteristics, seizure frequency, and treatment history. Patients with a follow-up duration of minimum 12 months were included in the analysis. The examined outcome measures were seizure reduction rates, antiepileptic drugs (AEDs) burden, and impact on patients’ quality of life (QOL). RESULTS: Onset of seizures was from birth to 30 years. Patients’ ages at VNS implantation ranged from 4 to 38 years (18.9 [8.7] years). Epilepsy was classified as focal in 8 patients (30%), multifocal in 9 patients (35%), and generalized in 9 patients (35%). The average number of AEDs failed before VNS was 4.2 (1.4). Greater than 50% seizure reduction was achieved in 50% of patients at 3 months, 67% at 6 months, 73% at 12 months, and 78% at 24 months. There was no significant reduction in AEDs burden during the same period. Subjective QOL improvement was reported by 72% of patients at 3 months, 83% at 6 months, 78% at 12 months, and 73% at 24 months after VNS. Minor adverse effects were reported in 27% of patients. One patient had the device replaced due to malfunction. CONCLUSION: The experience with VNS in a single center in Saudi Arabia confirms that it is a safe and effective adjunctive therapy for refractory epilepsy in adult and pediatric patients.
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spelling pubmed-61525422018-09-25 Vagus nerve stimulation for refractory epilepsy: experience from Saudi Arabia Al-Said, Youssef Baeesa, Saleh Khalid, Muhammad Abdeen, Mohamed Kayyali, Husam R. Ann Saudi Med Original Article BACKGROUND: Vagus nerve stimulation (VNS) has been approved for the treatment of refractory partial epilepsy in adults and children over 12 years of age. Later on, its application expanded to include younger children and other types of epilepsy. We report our experience with this treatment modality for refractory epilepsy in Saudi Arabia. DESIGN AND SETTINGS: Open-label, uncontrolled, retrospective study of patients with refractory epilepsy, who were treated with VNS in a tertiary care hospital from January 2010 to June 2013. PATIENTS AND METHODS: Collected data included 26 patients’ demographics, epilepsy characteristics, seizure frequency, and treatment history. Patients with a follow-up duration of minimum 12 months were included in the analysis. The examined outcome measures were seizure reduction rates, antiepileptic drugs (AEDs) burden, and impact on patients’ quality of life (QOL). RESULTS: Onset of seizures was from birth to 30 years. Patients’ ages at VNS implantation ranged from 4 to 38 years (18.9 [8.7] years). Epilepsy was classified as focal in 8 patients (30%), multifocal in 9 patients (35%), and generalized in 9 patients (35%). The average number of AEDs failed before VNS was 4.2 (1.4). Greater than 50% seizure reduction was achieved in 50% of patients at 3 months, 67% at 6 months, 73% at 12 months, and 78% at 24 months. There was no significant reduction in AEDs burden during the same period. Subjective QOL improvement was reported by 72% of patients at 3 months, 83% at 6 months, 78% at 12 months, and 73% at 24 months after VNS. Minor adverse effects were reported in 27% of patients. One patient had the device replaced due to malfunction. CONCLUSION: The experience with VNS in a single center in Saudi Arabia confirms that it is a safe and effective adjunctive therapy for refractory epilepsy in adult and pediatric patients. King Faisal Specialist Hospital and Research Centre 2015 /pmc/articles/PMC6152542/ /pubmed/26142937 http://dx.doi.org/10.5144/0256-4947.2015.41 Text en Copyright © 2015, Annals of Saudi Medicine This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Original Article
Al-Said, Youssef
Baeesa, Saleh
Khalid, Muhammad
Abdeen, Mohamed
Kayyali, Husam R.
Vagus nerve stimulation for refractory epilepsy: experience from Saudi Arabia
title Vagus nerve stimulation for refractory epilepsy: experience from Saudi Arabia
title_full Vagus nerve stimulation for refractory epilepsy: experience from Saudi Arabia
title_fullStr Vagus nerve stimulation for refractory epilepsy: experience from Saudi Arabia
title_full_unstemmed Vagus nerve stimulation for refractory epilepsy: experience from Saudi Arabia
title_short Vagus nerve stimulation for refractory epilepsy: experience from Saudi Arabia
title_sort vagus nerve stimulation for refractory epilepsy: experience from saudi arabia
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6152542/
https://www.ncbi.nlm.nih.gov/pubmed/26142937
http://dx.doi.org/10.5144/0256-4947.2015.41
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