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Management of pain in Fabry disease in the UK clinical setting: consensus findings from an expert Delphi panel
BACKGROUND: Fabry disease is a rare, X-linked inherited lysosomal storage disorder, that manifests as a heterogeneous disease with renal, cardiac and nervous system involvement. The most common pain experienced by people with Fabry disease are episodes of neuropathic pain reported in up to 80% of cl...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10362568/ https://www.ncbi.nlm.nih.gov/pubmed/37480023 http://dx.doi.org/10.1186/s13023-023-02796-1 |
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author | Stepien, Karolina M. Broomfield, Alexander Cole, Duncan Deegan, Patrick B. Forshaw-Hulme, Stuart Hughes, Derralynn Jovanovic, Ana Morris, Liz Muir, Alison Ramaswami, Uma |
author_facet | Stepien, Karolina M. Broomfield, Alexander Cole, Duncan Deegan, Patrick B. Forshaw-Hulme, Stuart Hughes, Derralynn Jovanovic, Ana Morris, Liz Muir, Alison Ramaswami, Uma |
author_sort | Stepien, Karolina M. |
collection | PubMed |
description | BACKGROUND: Fabry disease is a rare, X-linked inherited lysosomal storage disorder, that manifests as a heterogeneous disease with renal, cardiac and nervous system involvement. The most common pain experienced by people with Fabry disease are episodes of neuropathic pain reported in up to 80% of classical hemizygous male patients and up to 65% of heterozygous female patients. No clear consensus exists within UK clinical practice for the assessment and management of pain in Fabry disease based on agreed clinical practice and clinical experience. Here we describe a modified Delphi initiative to establish expert consensus on management of pain in Fabry disease in the UK clinical setting. METHODS: Delphi panel members were identified based on their demonstrated expertise in managing adult or paediatric patients with Fabry disease in the UK and recruited by an independent third-party administrator. Ten expert panellists agreed to participate in two survey rounds, during which they remained anonymous to each other. Circulation of the questionnaires, and collection and processing of the panel’s responses were conducted between September 2021 and December 2021. All questions required an answer. RESULTS: The Delphi panel reached a consensus on 21 out of 41 aspects of pain assessment and management of pain in Fabry disease. These encompassed steps in the care pathway from the goals of therapy through to holistic support, including the use of gabapentin and carbamazepine as first-line analgesic medications for the treatment of neuropathic pain in Fabry disease, as well as the proactive management of symptoms of anxiety and/or depression associated with Fabry pain. CONCLUSIONS: The consensus panel outcomes reported here have highlighted strengths in current UK clinical practice, along with unmet needs for further research and agreement. This consensus is intended to prompt the next steps towards developing clinical guidelines. |
format | Online Article Text |
id | pubmed-10362568 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-103625682023-07-23 Management of pain in Fabry disease in the UK clinical setting: consensus findings from an expert Delphi panel Stepien, Karolina M. Broomfield, Alexander Cole, Duncan Deegan, Patrick B. Forshaw-Hulme, Stuart Hughes, Derralynn Jovanovic, Ana Morris, Liz Muir, Alison Ramaswami, Uma Orphanet J Rare Dis Research BACKGROUND: Fabry disease is a rare, X-linked inherited lysosomal storage disorder, that manifests as a heterogeneous disease with renal, cardiac and nervous system involvement. The most common pain experienced by people with Fabry disease are episodes of neuropathic pain reported in up to 80% of classical hemizygous male patients and up to 65% of heterozygous female patients. No clear consensus exists within UK clinical practice for the assessment and management of pain in Fabry disease based on agreed clinical practice and clinical experience. Here we describe a modified Delphi initiative to establish expert consensus on management of pain in Fabry disease in the UK clinical setting. METHODS: Delphi panel members were identified based on their demonstrated expertise in managing adult or paediatric patients with Fabry disease in the UK and recruited by an independent third-party administrator. Ten expert panellists agreed to participate in two survey rounds, during which they remained anonymous to each other. Circulation of the questionnaires, and collection and processing of the panel’s responses were conducted between September 2021 and December 2021. All questions required an answer. RESULTS: The Delphi panel reached a consensus on 21 out of 41 aspects of pain assessment and management of pain in Fabry disease. These encompassed steps in the care pathway from the goals of therapy through to holistic support, including the use of gabapentin and carbamazepine as first-line analgesic medications for the treatment of neuropathic pain in Fabry disease, as well as the proactive management of symptoms of anxiety and/or depression associated with Fabry pain. CONCLUSIONS: The consensus panel outcomes reported here have highlighted strengths in current UK clinical practice, along with unmet needs for further research and agreement. This consensus is intended to prompt the next steps towards developing clinical guidelines. BioMed Central 2023-07-21 /pmc/articles/PMC10362568/ /pubmed/37480023 http://dx.doi.org/10.1186/s13023-023-02796-1 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Stepien, Karolina M. Broomfield, Alexander Cole, Duncan Deegan, Patrick B. Forshaw-Hulme, Stuart Hughes, Derralynn Jovanovic, Ana Morris, Liz Muir, Alison Ramaswami, Uma Management of pain in Fabry disease in the UK clinical setting: consensus findings from an expert Delphi panel |
title | Management of pain in Fabry disease in the UK clinical setting: consensus findings from an expert Delphi panel |
title_full | Management of pain in Fabry disease in the UK clinical setting: consensus findings from an expert Delphi panel |
title_fullStr | Management of pain in Fabry disease in the UK clinical setting: consensus findings from an expert Delphi panel |
title_full_unstemmed | Management of pain in Fabry disease in the UK clinical setting: consensus findings from an expert Delphi panel |
title_short | Management of pain in Fabry disease in the UK clinical setting: consensus findings from an expert Delphi panel |
title_sort | management of pain in fabry disease in the uk clinical setting: consensus findings from an expert delphi panel |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10362568/ https://www.ncbi.nlm.nih.gov/pubmed/37480023 http://dx.doi.org/10.1186/s13023-023-02796-1 |
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