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Dexmedetomidine depresses neuronal activity in the subthalamic nucleus during deep brain stimulation electrode implantation surgery

BACKGROUND: Micro-electrode recordings are often necessary during electrode implantation for deep brain stimulation of the subthalamic nucleus. Dexmedetomidine may be a useful sedative for these procedures, but there is limited information regarding its effect on neural activity in the subthalamic n...

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Autores principales: Amlong, Corey, Rusy, Deborah, Sanders, Robert D., Lake, Wendell, Raz, Aeyal
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10430856/
https://www.ncbi.nlm.nih.gov/pubmed/37588575
http://dx.doi.org/10.1016/j.bjao.2022.100088
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author Amlong, Corey
Rusy, Deborah
Sanders, Robert D.
Lake, Wendell
Raz, Aeyal
author_facet Amlong, Corey
Rusy, Deborah
Sanders, Robert D.
Lake, Wendell
Raz, Aeyal
author_sort Amlong, Corey
collection PubMed
description BACKGROUND: Micro-electrode recordings are often necessary during electrode implantation for deep brain stimulation of the subthalamic nucleus. Dexmedetomidine may be a useful sedative for these procedures, but there is limited information regarding its effect on neural activity in the subthalamic nucleus and on micro-electrode recording quality. METHODS: We recorded neural activity in five patients undergoing deep brain stimulation implantation to the subthalamic nucleus. Activity was recorded after subthalamic nucleus identification while patients received dexmedetomidine sedation (loading – 1 μg kg(−1) over 10–15 min, maintenance – 0.7 μg kg(−1) h(−1)). We compared the root-mean square (RMS) and beta band (13–30 Hz) oscillation power of multi-unit activity recorded by microelectrode before, during and after recovery from dexmedetomidine sedation. RMS was normalised to values recorded in the white matter. RESULTS: Multi-unit activity decreased during sedation in all five patients. Mean normalised RMS decreased from 2.8 (1.5) to 1.6 (1.1) during sedation (43% drop, p = 0.056). Beta band power dropped by 48.4%, but this was not significant (p = 0.15). Normalised RMS values failed to return to baseline levels during the time allocated for the study (30 min). CONCLUSIONS: In this small sample, we demonstrate that dexmedetomidine decreases neuronal firing in the subthalamic nucleus as expressed in the RMS of the multi-unit activity. As multi-unit activity is a factor in determining the subthalamic nucleus borders during micro-electrode recordings, dexmedetomidine should be used with caution for sedation during these procedures. CLINICAL TRIAL NUMBER: NCT01721460.
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spelling pubmed-104308562023-08-16 Dexmedetomidine depresses neuronal activity in the subthalamic nucleus during deep brain stimulation electrode implantation surgery Amlong, Corey Rusy, Deborah Sanders, Robert D. Lake, Wendell Raz, Aeyal BJA Open Original Research Article BACKGROUND: Micro-electrode recordings are often necessary during electrode implantation for deep brain stimulation of the subthalamic nucleus. Dexmedetomidine may be a useful sedative for these procedures, but there is limited information regarding its effect on neural activity in the subthalamic nucleus and on micro-electrode recording quality. METHODS: We recorded neural activity in five patients undergoing deep brain stimulation implantation to the subthalamic nucleus. Activity was recorded after subthalamic nucleus identification while patients received dexmedetomidine sedation (loading – 1 μg kg(−1) over 10–15 min, maintenance – 0.7 μg kg(−1) h(−1)). We compared the root-mean square (RMS) and beta band (13–30 Hz) oscillation power of multi-unit activity recorded by microelectrode before, during and after recovery from dexmedetomidine sedation. RMS was normalised to values recorded in the white matter. RESULTS: Multi-unit activity decreased during sedation in all five patients. Mean normalised RMS decreased from 2.8 (1.5) to 1.6 (1.1) during sedation (43% drop, p = 0.056). Beta band power dropped by 48.4%, but this was not significant (p = 0.15). Normalised RMS values failed to return to baseline levels during the time allocated for the study (30 min). CONCLUSIONS: In this small sample, we demonstrate that dexmedetomidine decreases neuronal firing in the subthalamic nucleus as expressed in the RMS of the multi-unit activity. As multi-unit activity is a factor in determining the subthalamic nucleus borders during micro-electrode recordings, dexmedetomidine should be used with caution for sedation during these procedures. CLINICAL TRIAL NUMBER: NCT01721460. Elsevier 2022-09-09 /pmc/articles/PMC10430856/ /pubmed/37588575 http://dx.doi.org/10.1016/j.bjao.2022.100088 Text en © 2022 The Author(s) https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Original Research Article
Amlong, Corey
Rusy, Deborah
Sanders, Robert D.
Lake, Wendell
Raz, Aeyal
Dexmedetomidine depresses neuronal activity in the subthalamic nucleus during deep brain stimulation electrode implantation surgery
title Dexmedetomidine depresses neuronal activity in the subthalamic nucleus during deep brain stimulation electrode implantation surgery
title_full Dexmedetomidine depresses neuronal activity in the subthalamic nucleus during deep brain stimulation electrode implantation surgery
title_fullStr Dexmedetomidine depresses neuronal activity in the subthalamic nucleus during deep brain stimulation electrode implantation surgery
title_full_unstemmed Dexmedetomidine depresses neuronal activity in the subthalamic nucleus during deep brain stimulation electrode implantation surgery
title_short Dexmedetomidine depresses neuronal activity in the subthalamic nucleus during deep brain stimulation electrode implantation surgery
title_sort dexmedetomidine depresses neuronal activity in the subthalamic nucleus during deep brain stimulation electrode implantation surgery
topic Original Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10430856/
https://www.ncbi.nlm.nih.gov/pubmed/37588575
http://dx.doi.org/10.1016/j.bjao.2022.100088
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