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Ketamine as an adjuvant in sympathetic blocks for management of central sensitization following peripheral nerve injury
Proliferation of NMDA receptors and role of glutamate in producing central sensitization and 'wind up' phenomena in CRPS [complex regional pain syndrome] forms a strong basis for the use of Ketamine to block the cellular mechanisms that initiate and maintain these changes. In this case ser...
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2008
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2584055/ https://www.ncbi.nlm.nih.gov/pubmed/18950516 http://dx.doi.org/10.1186/1749-7221-3-22 |
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author | Sunder, Rani A Toshniwal, Gokul Dureja, GP |
author_facet | Sunder, Rani A Toshniwal, Gokul Dureja, GP |
author_sort | Sunder, Rani A |
collection | PubMed |
description | Proliferation of NMDA receptors and role of glutamate in producing central sensitization and 'wind up' phenomena in CRPS [complex regional pain syndrome] forms a strong basis for the use of Ketamine to block the cellular mechanisms that initiate and maintain these changes. In this case series, we describe 3 patients of CRPS Type II with debilitating central sensitization, heat/mechano allodynia and cognitive symptoms that we termed 'vicarious pain'. Each of these patients had dramatic relief with addition of Ketamine as an adjuvant to the sympathetic blocks after conventional therapy failed. CASE REPORTS: All 3 patients suffered gunshot wounds and developed characteristic features of CRPS Type II. Within 2–3 weeks they developed extraterritorial symptoms typical of central sensitization. The generalized mechanical allodynia and debilitating heat allodynia described to be rare in human subjects had life altering affect on their daily life. Case 2 and 3 also described an unusual cognitive phenomenon i.e. visual stimuli of friction would evoke severe pain in the affected limb that we have termed as 'vicarious pain'. They responded positively to sympathetic blocks but the sympatholysis did not bring relief to the heat and mechanical allodynia. Addition of Ketamine 0.5 mg/kg to the sympathetic blocks elicited resulted in marked relief in the allodynia. CONCLUSION: Ketamine has a special role in patients with debilitating heat allodynia and positive cognitive symptoms via its action on central pain pathway. As an adjuvant in sympatholytic blocks it has a targeted action without significant neuropsychiatric side effects. |
format | Text |
id | pubmed-2584055 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-25840552008-11-18 Ketamine as an adjuvant in sympathetic blocks for management of central sensitization following peripheral nerve injury Sunder, Rani A Toshniwal, Gokul Dureja, GP J Brachial Plex Peripher Nerve Inj Case Study Proliferation of NMDA receptors and role of glutamate in producing central sensitization and 'wind up' phenomena in CRPS [complex regional pain syndrome] forms a strong basis for the use of Ketamine to block the cellular mechanisms that initiate and maintain these changes. In this case series, we describe 3 patients of CRPS Type II with debilitating central sensitization, heat/mechano allodynia and cognitive symptoms that we termed 'vicarious pain'. Each of these patients had dramatic relief with addition of Ketamine as an adjuvant to the sympathetic blocks after conventional therapy failed. CASE REPORTS: All 3 patients suffered gunshot wounds and developed characteristic features of CRPS Type II. Within 2–3 weeks they developed extraterritorial symptoms typical of central sensitization. The generalized mechanical allodynia and debilitating heat allodynia described to be rare in human subjects had life altering affect on their daily life. Case 2 and 3 also described an unusual cognitive phenomenon i.e. visual stimuli of friction would evoke severe pain in the affected limb that we have termed as 'vicarious pain'. They responded positively to sympathetic blocks but the sympatholysis did not bring relief to the heat and mechanical allodynia. Addition of Ketamine 0.5 mg/kg to the sympathetic blocks elicited resulted in marked relief in the allodynia. CONCLUSION: Ketamine has a special role in patients with debilitating heat allodynia and positive cognitive symptoms via its action on central pain pathway. As an adjuvant in sympatholytic blocks it has a targeted action without significant neuropsychiatric side effects. BioMed Central 2008-10-25 /pmc/articles/PMC2584055/ /pubmed/18950516 http://dx.doi.org/10.1186/1749-7221-3-22 Text en Copyright © 2008 Sunder et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Study Sunder, Rani A Toshniwal, Gokul Dureja, GP Ketamine as an adjuvant in sympathetic blocks for management of central sensitization following peripheral nerve injury |
title | Ketamine as an adjuvant in sympathetic blocks for management of central sensitization following peripheral nerve injury |
title_full | Ketamine as an adjuvant in sympathetic blocks for management of central sensitization following peripheral nerve injury |
title_fullStr | Ketamine as an adjuvant in sympathetic blocks for management of central sensitization following peripheral nerve injury |
title_full_unstemmed | Ketamine as an adjuvant in sympathetic blocks for management of central sensitization following peripheral nerve injury |
title_short | Ketamine as an adjuvant in sympathetic blocks for management of central sensitization following peripheral nerve injury |
title_sort | ketamine as an adjuvant in sympathetic blocks for management of central sensitization following peripheral nerve injury |
topic | Case Study |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2584055/ https://www.ncbi.nlm.nih.gov/pubmed/18950516 http://dx.doi.org/10.1186/1749-7221-3-22 |
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