Responsive Neurostimulation of Thalamic and Nonthalamic Targets in Pediatric and Young Adult Patients With Intractable Epilepsy
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Read the article on pubmed.ncbi.nlm.nih.gov ↗Article · Jun 2025 · 1 min read
In brief
In brief
This retrospective study evaluates responsive neurostimulation (RNS) outcomes in 24 pediatric and young adult patients with drug-resistant epilepsy unsuitable for resection. Both thalamic and nonthalamic lead placements achieved significant seizure reduction (74% overall), with comparable safety profiles across target locations.
Written by the GCMD Library team from the article.
Background And Objectives: Epilepsy is a significant cause of morbidity and has negative effects on cognitive and psychosocial development in pediatric and young adult patients. For pediatric patients who have epileptogenic foci that are poorly localized, deep, bilateral, or in eloquent regions and are not candidates for resection, responsive neurostimulation (RNS) may be an option. The study objective was to demonstrate safety and seizure outcomes from RNS in pediatric and young adults with intractable epilepsy with a specific focus on differences between thalamic and nonthalamic RNS lead implantation. Methods: The authors describe a single institution's experience with RNS in patients with drug-resistant epilepsy who were not candidates for seizure focus resection. An Institutional Review Board-approved retrospective review was conducted of all pediatric and young adult patients who underwent RNS implantation at Cincinnati Children's Hospital Medical Center between 2019 and 2023. Results: In total, 24 patients met the inclusion criteria for the study. Seven had thalamic targets whereas 17 had nonthalamic targets. The mean patient age at the time of surgery was 13.8 years (range 5-30), with a mean follow-up of 13 months. Thirteen patients (54%) had prior surgery for seizure control. The median global seizure percentage reduction was 68% in the nonthalamic group and 80% in the thalamic group, a nonsignificant difference, resulting in a reduction of 74% for all study patients
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