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DOI 10.1186/s13023-023-02796-1

Медицинская библиотека · Orphanet journal of rare diseases · 2023

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

СтатьяПоддержка исследования: вне правительства СШАConsensus StatementПеревод пока не подготовлен

Аннотация

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.

Для цитирования: 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.. Orphanet journal of rare diseases. 2023. DOI: 10.1186/s13023-023-02796-1.

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