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Deep brain stimulation may be a viable option for resistant to treatment aggression in children with intellectual disability

INTRODUCTION: Deep brain stimulation (DBS) is a surgical technique used to manage aggression in patients who do not improve despite the use of appropriate drug treatment. OBJECTIVE: The objective of this study is to assess the impact of DBS on aggressive behavior refractory to the pharmacological an...

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Autores principales: Benedetti‐Isaac, Juan Carlos, Camargo, Loida, Torres Zambrano, Martin, Perea‐Castro, Esther, Castillo‐Tamara, Edgard, Caldichoury, Nicole, Herrera‐Pino, Jorge, Flórez, Yuliana, Porto, María, López, Norman
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10324351/
https://www.ncbi.nlm.nih.gov/pubmed/36890650
http://dx.doi.org/10.1111/cns.14156
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author Benedetti‐Isaac, Juan Carlos
Camargo, Loida
Torres Zambrano, Martin
Perea‐Castro, Esther
Castillo‐Tamara, Edgard
Caldichoury, Nicole
Herrera‐Pino, Jorge
Flórez, Yuliana
Porto, María
López, Norman
author_facet Benedetti‐Isaac, Juan Carlos
Camargo, Loida
Torres Zambrano, Martin
Perea‐Castro, Esther
Castillo‐Tamara, Edgard
Caldichoury, Nicole
Herrera‐Pino, Jorge
Flórez, Yuliana
Porto, María
López, Norman
author_sort Benedetti‐Isaac, Juan Carlos
collection PubMed
description INTRODUCTION: Deep brain stimulation (DBS) is a surgical technique used to manage aggression in patients who do not improve despite the use of appropriate drug treatment. OBJECTIVE: The objective of this study is to assess the impact of DBS on aggressive behavior refractory to the pharmacological and behavioral treatment of patients with Intellectual Disabilities (ID). METHODS: A follow‐up was conducted on a cohort of 12 patients with severe ID, undergoing DBS in posteromedial hypothalamic nuclei; evaluated with the Overt Aggression Scale (OAS), before the intervention, at 6, 12, and 18 months of medical follow‐up. RESULTS: After the surgical procedure, there was a significant reduction in the aggressiveness of patients in the follow‐up medical evaluation at 6 months (t = 10.14; p < 0.01), 12 months (t = 14.06; p < 0.01), and 18 months (t = 15.34; p < 0.01), respect to the initial measurement; with a very large effect size (6 months: d = 2.71; 12 months: d = 3.75; 18 months: d = 4.10). From 12 months onward, emotional control stabilized and is sustained at 18 months (t = 1.24; p > 0.05). CONCLUSION: DBS in posteromedial hypothalamic nuclei may be an effective treatment for the management of aggression in patients with ID refractory to pharmacological treatment.
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spelling pubmed-103243512023-07-07 Deep brain stimulation may be a viable option for resistant to treatment aggression in children with intellectual disability Benedetti‐Isaac, Juan Carlos Camargo, Loida Torres Zambrano, Martin Perea‐Castro, Esther Castillo‐Tamara, Edgard Caldichoury, Nicole Herrera‐Pino, Jorge Flórez, Yuliana Porto, María López, Norman CNS Neurosci Ther Original Articles INTRODUCTION: Deep brain stimulation (DBS) is a surgical technique used to manage aggression in patients who do not improve despite the use of appropriate drug treatment. OBJECTIVE: The objective of this study is to assess the impact of DBS on aggressive behavior refractory to the pharmacological and behavioral treatment of patients with Intellectual Disabilities (ID). METHODS: A follow‐up was conducted on a cohort of 12 patients with severe ID, undergoing DBS in posteromedial hypothalamic nuclei; evaluated with the Overt Aggression Scale (OAS), before the intervention, at 6, 12, and 18 months of medical follow‐up. RESULTS: After the surgical procedure, there was a significant reduction in the aggressiveness of patients in the follow‐up medical evaluation at 6 months (t = 10.14; p < 0.01), 12 months (t = 14.06; p < 0.01), and 18 months (t = 15.34; p < 0.01), respect to the initial measurement; with a very large effect size (6 months: d = 2.71; 12 months: d = 3.75; 18 months: d = 4.10). From 12 months onward, emotional control stabilized and is sustained at 18 months (t = 1.24; p > 0.05). CONCLUSION: DBS in posteromedial hypothalamic nuclei may be an effective treatment for the management of aggression in patients with ID refractory to pharmacological treatment. John Wiley and Sons Inc. 2023-03-08 /pmc/articles/PMC10324351/ /pubmed/36890650 http://dx.doi.org/10.1111/cns.14156 Text en © 2023 The Authors. CNS Neuroscience & Therapeutics published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Benedetti‐Isaac, Juan Carlos
Camargo, Loida
Torres Zambrano, Martin
Perea‐Castro, Esther
Castillo‐Tamara, Edgard
Caldichoury, Nicole
Herrera‐Pino, Jorge
Flórez, Yuliana
Porto, María
López, Norman
Deep brain stimulation may be a viable option for resistant to treatment aggression in children with intellectual disability
title Deep brain stimulation may be a viable option for resistant to treatment aggression in children with intellectual disability
title_full Deep brain stimulation may be a viable option for resistant to treatment aggression in children with intellectual disability
title_fullStr Deep brain stimulation may be a viable option for resistant to treatment aggression in children with intellectual disability
title_full_unstemmed Deep brain stimulation may be a viable option for resistant to treatment aggression in children with intellectual disability
title_short Deep brain stimulation may be a viable option for resistant to treatment aggression in children with intellectual disability
title_sort deep brain stimulation may be a viable option for resistant to treatment aggression in children with intellectual disability
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10324351/
https://www.ncbi.nlm.nih.gov/pubmed/36890650
http://dx.doi.org/10.1111/cns.14156
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