Responsive Neurostimulation Therapy Outcomes in Two Small Bilateral Thalamic and Corticothalamic Subgroups of Patients with Drug-Resistant Epilepsy—A Single-Center Experience
Aug 2026· The Neuroscientist· Vol 7, pp. 92· 0 citations· 33 references
Medicine
TL;DR
Although bilateral thalamic targets were selected at the authors' center more often, both bilateral thalamic and corticothalamic RNS approaches provided seizure frequency reduction, and the majority of patients, including non-responders, reported seizure severity alleviation.
Abstract
Responsive neurostimulation (RNS) is a neuromodulation option for treatment of drug-resistant epilepsy (DRE). There is limited data reviewing bilateral thalamic and corticothalamic RNS therapy response. We performed a retrospective analysis of 21 patients undergoing RNS implantation with either bilateral thalamic (n = 17) or corticothalamic (n = 4) leads and ≥6 months of follow-up. Patients were classified as responders (≥50% seizure frequency reduction) vs. non-responders (<50% seizure frequency reduction). Among the bilateral thalamic cohort, 12/17 (70.6%) patients were responders, and 15/17 (88.2%) patients reported reduction in seizure severity. Pre-RNS seizure frequency was higher in bilateral thalamic nonresponders, although not found to be significant (median 13 vs. 30 seizures per month, p = 0.20). Among the corticothalamic cohort, 3/4 (75.0%) patients were responders, and all patients demonstrated improvement in seizure severity. These findings suggest that although bilateral thalamic targets were selected at our center more often, both bilateral thalamic and corticothalamic RNS approaches provided seizure frequency reduction. The majority of patients, including non-responders, reported seizure severity alleviation.
This study expands the limited literature on insular neuromodulation by demonstrating effectiveness of RNS and CSS, suggesting potential benefit from combined thalamocortical targeting, and defining parasagittal trajectories as a surgical approach for optimal lead proximity.
Raunak Singh, N. Gregg, K. Starnes et al.· Epilepsia· 0 citations
OBJECTIVE
Drug-resistant epilepsy (DRE) remains a significant clinical challenge, affecting approximately 30% of patients. Deep brain stimulation (DBS) of the centromedian thalamic nucleus (CM) has emerged as a viable therapy for generalized and multifocal seizures. Although high-frequency stimulation (HFS) is the clin...
Julia Vescovi Vieira, João Paulo Santiago Oliveira, R. Guimarães et al.· Epilepsia· 0 citations
Drug-resistant epilepsy affects approximately one-third of patients and is often not amenable to resective surgery due to the bilateral nature of the epileptogenic network, multifocality, or localization of the seizure onset zone within eloquent cortical areas. In such cases, neuromodulation techniques are preferable,...
D. Sevastyanov, A. Kholyavin· Vestnik nevrologii, psihiatr...· 0 citations
PURPOSE
Responsive neurostimulation (RNS) is an effective treatment for drug-resistant epilepsy, but optimal programming strategies remain undefined in pediatric populations. This study investigates the effect of programming parameter differences on time to > 50% seizure reduction. We aimed to determine the charge dens...
Taylor Walker, Paul S. Horn, A. Byars et al.· Epilepsy Research· 0 citations
OBJECTIVE
Deep brain stimulation (DBS) is an emerging treatment option for pediatric drug-resistant epilepsy (DRE), but evidence regarding its long-term efficacy and safety remains limited. We aimed to assess the long-term efficacy and safety of DBS in children with DRE at a minimum follow-up of 12 months.
METHODS
A...
Asmaa Mhanna, Michael A. Ciliberto, S. Ganganna et al.· Seizure· 0 citations
OBJECTIVE
Idiopathic generalized epilepsy (IGE) is a disorder of the cortico-subcortical networks. Continuous theta burst stimulation (cTBS) can target these networks to provide an innovative, noninvasive neuromodulation treatment. This study evaluated the safety and efficacy of multifocal cTBS in IGE.
METHODS
This s...
P. Leahu, A. Vataman, D. Ciolac et al.· Clinical Neurophysiology· 0 citations
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