A phase 1 open-label trial evaluating focused ultrasound unilateral anterior thalamotomy for focal onset epilepsy.
Autor: | Krishna V; Department of Neurosurgery, University of North Carolina, Chapel Hill, North Carolina, USA., Mindel J; Department of Neurology, Ohio State University, Columbus, Ohio, USA., Sammartino F; Department of Physical Medicine and Rehabilitation, Ohio State University, Columbus, Ohio, USA., Block C; Department of Neurology, Emory University, Atlanta, Georgia, USA., Dwivedi AK; Division of Biostatistics and Epidemiology, Texas Tech University Health Sciences Center, El Paso, Texas, USA., Van Gompel JJ; Department of Neurosurgery and Otorhinolaryngology, Mayo Clinic, Rochester, Minnesota, USA., Fountain N; Department of Neurology, University of Virginia, Charlottesville, Virginia, USA., Fisher R; Department of Neurology, Stanford University, Stanford, California, USA. |
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Jazyk: | angličtina |
Zdroj: | Epilepsia [Epilepsia] 2023 Apr; Vol. 64 (4), pp. 831-842. Date of Electronic Publication: 2023 Mar 01. |
DOI: | 10.1111/epi.17535 |
Abstrakt: | Objective: Focused ultrasound ablation (FUSA) is an emerging treatment for neurological and psychiatric diseases. We describe the initial experience from a pilot, open-label, single-center clinical trial of unilateral anterior nucleus of the thalamus (ANT) FUSA in patients with treatment-refractory epilepsy. Methods: Two adult subjects with treatment-refractory, focal onset epilepsy were recruited. The subjects received ANT FUSA using the Exablate Neuro (Insightec) system. We determined the safety and feasibility (primary outcomes), and changes in seizure frequency (secondary outcome) at 3, 6, and 12 months. Safety was assessed by the absence of side effects, that is, new onset neurological deficits or performance deterioration on neuropsychological testing. Feasibility was defined as the ability to create a lesion within the anterior nucleus. The monthly seizure frequency was compared between baseline and postthalamotomy. Results: The patients tolerated the procedure well, without neurological deficits or serious adverse events. One patient experienced a decline in verbal fluency, attention/working memory, and immediate verbal memory. Seizure frequency reduced significantly in both patients; one patient was seizure-free at 12 months, and in the second patient, the frequency reduced from 90-100 seizures per month to 3-6 seizures per month. Significance: This is the first known clinical trial to assess the safety, feasibility, and preliminary efficacy of ANT FUSA in adult patients with treatment-refractory focal onset epilepsy. (© 2023 International League Against Epilepsy.) |
Databáze: | MEDLINE |
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