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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.
Afiliación
  • Stepien KM; The Mark Holland Metabolic Unit, Salford Royal NHS Foundation Trust, Salford, UK. kstepien@doctors.org.uk.
  • Broomfield A; Willink Biochemical Genetics Unit, Manchester Centre for Genomic Medicine, St Mary's Hospital, Manchester University NHS Foundation Trust, Manchester, UK.
  • Cole D; Department of Medical Biochemistry and Immunology, University Hospital of Wales, Cardiff, Wales, UK.
  • Deegan PB; Lysosomal Disorders Unit, Addenbrooke's Hospital, Cambridge, UK.
  • Forshaw-Hulme S; The Mark Holland Metabolic Unit, Salford Royal NHS Foundation Trust, Salford, UK.
  • Hughes D; Lysosomal Storage Disorders Unit, Royal Free London NHS Foundation Trust, London, UK.
  • Jovanovic A; The Mark Holland Metabolic Unit, Salford Royal NHS Foundation Trust, Salford, UK.
  • Morris L; Lysosomal Disorders Unit, Addenbrooke's Hospital, Cambridge, UK.
  • Muir A; Belfast Heart Centre, Royal Victoria Hospital, Belfast, UK.
  • Ramaswami U; Lysosomal Storage Disorders Unit, Royal Free London NHS Foundation Trust, London, UK.
Orphanet J Rare Dis ; 18(1): 203, 2023 07 21.
Article en En | MEDLINE | ID: mdl-37480023
ABSTRACT

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.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Enfermedad de Fabry / Neuralgia Tipo de estudio: Diagnostic_studies / Etiology_studies / Guideline / Prognostic_studies / Qualitative_research Límite: Adult / Child / Female / Humans / Male País/Región como asunto: Europa Idioma: En Revista: Orphanet J Rare Dis Asunto de la revista: MEDICINA Año: 2023 Tipo del documento: Article País de afiliación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Enfermedad de Fabry / Neuralgia Tipo de estudio: Diagnostic_studies / Etiology_studies / Guideline / Prognostic_studies / Qualitative_research Límite: Adult / Child / Female / Humans / Male País/Región como asunto: Europa Idioma: En Revista: Orphanet J Rare Dis Asunto de la revista: MEDICINA Año: 2023 Tipo del documento: Article País de afiliación: Reino Unido