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Pain management strategies for neuropathic pain in Fabry disease - a systematic review

BACKGROUND: Neuropathic pain is one of the key features of (classical) Fabry disease (FD). No randomized clinical trials comparing effectiveness of different pain management strategies have been performed. This review aims to give an overview of existing pain management strategies. METHODS: PubMed a...

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Autores principales: Schuller, Y., Linthorst, G. E., Hollak, C. E. M., Van Schaik, I. N., Biegstraaten, M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4766720/
https://www.ncbi.nlm.nih.gov/pubmed/26911544
http://dx.doi.org/10.1186/s12883-016-0549-8
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author Schuller, Y.
Linthorst, G. E.
Hollak, C. E. M.
Van Schaik, I. N.
Biegstraaten, M.
author_facet Schuller, Y.
Linthorst, G. E.
Hollak, C. E. M.
Van Schaik, I. N.
Biegstraaten, M.
author_sort Schuller, Y.
collection PubMed
description BACKGROUND: Neuropathic pain is one of the key features of (classical) Fabry disease (FD). No randomized clinical trials comparing effectiveness of different pain management strategies have been performed. This review aims to give an overview of existing pain management strategies. METHODS: PubMed and Embase were searched up to September 2014 for relevant articles on treatment of neuropathic pain in FD. RESULTS: Seven-hundred-thirty-one articles were identified of which 26 were included in the analysis. Studies reported on 55 individuals in total, with group-sizes ranging from 1 to 8. Carbamazepine appeared most beneficial: complete pain relief in 5/25, partial relief in 17/25, and no benefit in 3/25 patients. Phenytoin resulted in complete relief in 1/27, partial relief in 12/27 and no benefit in 6/27 patients. In 8 patients a significant reduction in the frequency of pain attacks was described. Gabapentin caused partial relief in 6/7 and no relief in 1/7 patients. Little evidence was reported for SSNRI’s or treatment combinations. Adverse-effects were reported in all treatment strategies. CONCLUSIONS: Only for carbamazepine, phenytoin and gabapentin there is evidence of effectiveness in neuropathic pain due to FD, but comparison of effectiveness between these drugs is lacking. In routine clinical practice adverse-effects may discourage use of carbamazepine and phenytoin in favor of second-generation antiepileptic drugs, but this is currently not supported by clinical evidence. This review suffers greatly from incomplete outcome reports and a predominance of case reports, which emphasizes the need for robust clinical trials and observational cohort studies.
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spelling pubmed-47667202016-02-26 Pain management strategies for neuropathic pain in Fabry disease - a systematic review Schuller, Y. Linthorst, G. E. Hollak, C. E. M. Van Schaik, I. N. Biegstraaten, M. BMC Neurol Research Article BACKGROUND: Neuropathic pain is one of the key features of (classical) Fabry disease (FD). No randomized clinical trials comparing effectiveness of different pain management strategies have been performed. This review aims to give an overview of existing pain management strategies. METHODS: PubMed and Embase were searched up to September 2014 for relevant articles on treatment of neuropathic pain in FD. RESULTS: Seven-hundred-thirty-one articles were identified of which 26 were included in the analysis. Studies reported on 55 individuals in total, with group-sizes ranging from 1 to 8. Carbamazepine appeared most beneficial: complete pain relief in 5/25, partial relief in 17/25, and no benefit in 3/25 patients. Phenytoin resulted in complete relief in 1/27, partial relief in 12/27 and no benefit in 6/27 patients. In 8 patients a significant reduction in the frequency of pain attacks was described. Gabapentin caused partial relief in 6/7 and no relief in 1/7 patients. Little evidence was reported for SSNRI’s or treatment combinations. Adverse-effects were reported in all treatment strategies. CONCLUSIONS: Only for carbamazepine, phenytoin and gabapentin there is evidence of effectiveness in neuropathic pain due to FD, but comparison of effectiveness between these drugs is lacking. In routine clinical practice adverse-effects may discourage use of carbamazepine and phenytoin in favor of second-generation antiepileptic drugs, but this is currently not supported by clinical evidence. This review suffers greatly from incomplete outcome reports and a predominance of case reports, which emphasizes the need for robust clinical trials and observational cohort studies. BioMed Central 2016-02-24 /pmc/articles/PMC4766720/ /pubmed/26911544 http://dx.doi.org/10.1186/s12883-016-0549-8 Text en © Schuller et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Schuller, Y.
Linthorst, G. E.
Hollak, C. E. M.
Van Schaik, I. N.
Biegstraaten, M.
Pain management strategies for neuropathic pain in Fabry disease - a systematic review
title Pain management strategies for neuropathic pain in Fabry disease - a systematic review
title_full Pain management strategies for neuropathic pain in Fabry disease - a systematic review
title_fullStr Pain management strategies for neuropathic pain in Fabry disease - a systematic review
title_full_unstemmed Pain management strategies for neuropathic pain in Fabry disease - a systematic review
title_short Pain management strategies for neuropathic pain in Fabry disease - a systematic review
title_sort pain management strategies for neuropathic pain in fabry disease - a systematic review
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4766720/
https://www.ncbi.nlm.nih.gov/pubmed/26911544
http://dx.doi.org/10.1186/s12883-016-0549-8
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