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Responsive Neurostimulation of the Anterior Thalamic Nuclei in Refractory Genetic Generalized Epilepsy: A Case Series

Genetic generalized epilepsies (GGEs) are thought to represent disorders of thalamocortical networks. There are currently no well-established non-pharmacologic treatment options for patients with drug-resistant GGE. NeuroPace’s Responsive Neurostimulation (RNS) System was approved by the United Stat...

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Autores principales: O’Donnell, Carly M., Swanson, Sara J., Carlson, Chad E., Raghavan, Manoj, Pahapill, Peter A., Anderson, Christopher Todd
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9954640/
https://www.ncbi.nlm.nih.gov/pubmed/36831867
http://dx.doi.org/10.3390/brainsci13020324
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author O’Donnell, Carly M.
Swanson, Sara J.
Carlson, Chad E.
Raghavan, Manoj
Pahapill, Peter A.
Anderson, Christopher Todd
author_facet O’Donnell, Carly M.
Swanson, Sara J.
Carlson, Chad E.
Raghavan, Manoj
Pahapill, Peter A.
Anderson, Christopher Todd
author_sort O’Donnell, Carly M.
collection PubMed
description Genetic generalized epilepsies (GGEs) are thought to represent disorders of thalamocortical networks. There are currently no well-established non-pharmacologic treatment options for patients with drug-resistant GGE. NeuroPace’s Responsive Neurostimulation (RNS) System was approved by the United States Food and Drug Administration to treat focal seizures with up to two ictal foci. We report on three adults with drug-resistant GGE who were treated with thalamic RNS. Given the severity of their epilepsies and the potential ictogenic role of the thalamus in the pathophysiology of GGE, the RNS System was palliatively implanted with leads in the bilateral anterior thalamic nuclei (ANT) of these patients. The ANT was selected because it was demonstrated to be a safe target. We retrospectively evaluated metrics including seizure frequency over 18–32 months. One patient required explantation due to infection. The other two patients were clinical responders. By the end of the observation period reported here, one patient was seizure-free for over 9 months. All three self-reported an improved quality of life. The clinical response observed in these patients provides ‘proof-of-principle’ that GGE may be treatable with responsive thalamic stimulation. Our results support proceeding to a larger study investigating the efficacy and safety of thalamic RNS in drug-resistant GGE.
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spelling pubmed-99546402023-02-25 Responsive Neurostimulation of the Anterior Thalamic Nuclei in Refractory Genetic Generalized Epilepsy: A Case Series O’Donnell, Carly M. Swanson, Sara J. Carlson, Chad E. Raghavan, Manoj Pahapill, Peter A. Anderson, Christopher Todd Brain Sci Case Report Genetic generalized epilepsies (GGEs) are thought to represent disorders of thalamocortical networks. There are currently no well-established non-pharmacologic treatment options for patients with drug-resistant GGE. NeuroPace’s Responsive Neurostimulation (RNS) System was approved by the United States Food and Drug Administration to treat focal seizures with up to two ictal foci. We report on three adults with drug-resistant GGE who were treated with thalamic RNS. Given the severity of their epilepsies and the potential ictogenic role of the thalamus in the pathophysiology of GGE, the RNS System was palliatively implanted with leads in the bilateral anterior thalamic nuclei (ANT) of these patients. The ANT was selected because it was demonstrated to be a safe target. We retrospectively evaluated metrics including seizure frequency over 18–32 months. One patient required explantation due to infection. The other two patients were clinical responders. By the end of the observation period reported here, one patient was seizure-free for over 9 months. All three self-reported an improved quality of life. The clinical response observed in these patients provides ‘proof-of-principle’ that GGE may be treatable with responsive thalamic stimulation. Our results support proceeding to a larger study investigating the efficacy and safety of thalamic RNS in drug-resistant GGE. MDPI 2023-02-14 /pmc/articles/PMC9954640/ /pubmed/36831867 http://dx.doi.org/10.3390/brainsci13020324 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Case Report
O’Donnell, Carly M.
Swanson, Sara J.
Carlson, Chad E.
Raghavan, Manoj
Pahapill, Peter A.
Anderson, Christopher Todd
Responsive Neurostimulation of the Anterior Thalamic Nuclei in Refractory Genetic Generalized Epilepsy: A Case Series
title Responsive Neurostimulation of the Anterior Thalamic Nuclei in Refractory Genetic Generalized Epilepsy: A Case Series
title_full Responsive Neurostimulation of the Anterior Thalamic Nuclei in Refractory Genetic Generalized Epilepsy: A Case Series
title_fullStr Responsive Neurostimulation of the Anterior Thalamic Nuclei in Refractory Genetic Generalized Epilepsy: A Case Series
title_full_unstemmed Responsive Neurostimulation of the Anterior Thalamic Nuclei in Refractory Genetic Generalized Epilepsy: A Case Series
title_short Responsive Neurostimulation of the Anterior Thalamic Nuclei in Refractory Genetic Generalized Epilepsy: A Case Series
title_sort responsive neurostimulation of the anterior thalamic nuclei in refractory genetic generalized epilepsy: a case series
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9954640/
https://www.ncbi.nlm.nih.gov/pubmed/36831867
http://dx.doi.org/10.3390/brainsci13020324
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