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Evidence based guidelines for complex regional pain syndrome type 1
BACKGROUND: Treatment of complex regional pain syndrome type I (CRPS-I) is subject to discussion. The purpose of this study was to develop multidisciplinary guidelines for treatment of CRPS-I. METHOD: A multidisciplinary task force graded literature evaluating treatment effects for CRPS-I according...
Autores principales: | , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2861029/ https://www.ncbi.nlm.nih.gov/pubmed/20356382 http://dx.doi.org/10.1186/1471-2377-10-20 |
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author | Perez, Roberto S Zollinger, Paul E Dijkstra, Pieter U Thomassen-Hilgersom, Ilona L Zuurmond, Wouter W Rosenbrand, Kitty CJ Geertzen, Jan H |
author_facet | Perez, Roberto S Zollinger, Paul E Dijkstra, Pieter U Thomassen-Hilgersom, Ilona L Zuurmond, Wouter W Rosenbrand, Kitty CJ Geertzen, Jan H |
author_sort | Perez, Roberto S |
collection | PubMed |
description | BACKGROUND: Treatment of complex regional pain syndrome type I (CRPS-I) is subject to discussion. The purpose of this study was to develop multidisciplinary guidelines for treatment of CRPS-I. METHOD: A multidisciplinary task force graded literature evaluating treatment effects for CRPS-I according to their strength of evidence, published between 1980 to June 2005. Treatment recommendations based on the literature findings were formulated and formally approved by all Dutch professional associations involved in CRPS-I treatment. RESULTS: For pain treatment, the WHO analgesic ladder is advised with the exception of strong opioids. For neuropathic pain, anticonvulsants and tricyclic antidepressants may be considered. For inflammatory symptoms, free-radical scavengers (dimethylsulphoxide or acetylcysteine) are advised. To promote peripheral blood flow, vasodilatory medication may be considered. Percutaneous sympathetic blockades may be used to increase blood flow in case vasodilatory medication has insufficient effect. To decrease functional limitations, standardised physiotherapy and occupational therapy are advised. To prevent the occurrence of CRPS-I after wrist fractures, vitamin C is recommended. Adequate perioperative analgesia, limitation of operating time, limited use of tourniquet, and use of regional anaesthetic techniques are recommended for secondary prevention of CRPS-I. CONCLUSIONS: Based on the literature identified and the extent of evidence found for therapeutic interventions for CRPS-I, we conclude that further research is needed into each of the therapeutic modalities discussed in the guidelines. |
format | Text |
id | pubmed-2861029 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-28610292010-04-29 Evidence based guidelines for complex regional pain syndrome type 1 Perez, Roberto S Zollinger, Paul E Dijkstra, Pieter U Thomassen-Hilgersom, Ilona L Zuurmond, Wouter W Rosenbrand, Kitty CJ Geertzen, Jan H BMC Neurol Research article BACKGROUND: Treatment of complex regional pain syndrome type I (CRPS-I) is subject to discussion. The purpose of this study was to develop multidisciplinary guidelines for treatment of CRPS-I. METHOD: A multidisciplinary task force graded literature evaluating treatment effects for CRPS-I according to their strength of evidence, published between 1980 to June 2005. Treatment recommendations based on the literature findings were formulated and formally approved by all Dutch professional associations involved in CRPS-I treatment. RESULTS: For pain treatment, the WHO analgesic ladder is advised with the exception of strong opioids. For neuropathic pain, anticonvulsants and tricyclic antidepressants may be considered. For inflammatory symptoms, free-radical scavengers (dimethylsulphoxide or acetylcysteine) are advised. To promote peripheral blood flow, vasodilatory medication may be considered. Percutaneous sympathetic blockades may be used to increase blood flow in case vasodilatory medication has insufficient effect. To decrease functional limitations, standardised physiotherapy and occupational therapy are advised. To prevent the occurrence of CRPS-I after wrist fractures, vitamin C is recommended. Adequate perioperative analgesia, limitation of operating time, limited use of tourniquet, and use of regional anaesthetic techniques are recommended for secondary prevention of CRPS-I. CONCLUSIONS: Based on the literature identified and the extent of evidence found for therapeutic interventions for CRPS-I, we conclude that further research is needed into each of the therapeutic modalities discussed in the guidelines. BioMed Central 2010-03-31 /pmc/articles/PMC2861029/ /pubmed/20356382 http://dx.doi.org/10.1186/1471-2377-10-20 Text en Copyright ©2010 Perez 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 | Research article Perez, Roberto S Zollinger, Paul E Dijkstra, Pieter U Thomassen-Hilgersom, Ilona L Zuurmond, Wouter W Rosenbrand, Kitty CJ Geertzen, Jan H Evidence based guidelines for complex regional pain syndrome type 1 |
title | Evidence based guidelines for complex regional pain syndrome type 1 |
title_full | Evidence based guidelines for complex regional pain syndrome type 1 |
title_fullStr | Evidence based guidelines for complex regional pain syndrome type 1 |
title_full_unstemmed | Evidence based guidelines for complex regional pain syndrome type 1 |
title_short | Evidence based guidelines for complex regional pain syndrome type 1 |
title_sort | evidence based guidelines for complex regional pain syndrome type 1 |
topic | Research article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2861029/ https://www.ncbi.nlm.nih.gov/pubmed/20356382 http://dx.doi.org/10.1186/1471-2377-10-20 |
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