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在英国临床环境下管理法布雷病的疼痛:来自专家 Delphi 小组的共识结果。

Management of pain in Fabry disease in the UK clinical setting: consensus findings from an expert Delphi panel.

机构信息

The Mark Holland Metabolic Unit, Salford Royal NHS Foundation Trust, Salford, UK.

Willink Biochemical Genetics Unit, Manchester Centre for Genomic Medicine, St Mary's Hospital, Manchester University NHS Foundation Trust, Manchester, UK.

出版信息

Orphanet J Rare Dis. 2023 Jul 21;18(1):203. doi: 10.1186/s13023-023-02796-1.

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.

摘要

背景

法布瑞病是一种罕见的 X 连锁遗传性溶酶体贮积病,表现为一种具有肾、心和神经系统受累的异质性疾病。法布瑞病患者最常见的疼痛是神经痛,高达 80%的经典半合子男性患者和高达 65%的杂合子女性患者都会出现这种疼痛。由于缺乏基于临床实践和临床经验的共识,英国临床实践中法布瑞病疼痛的评估和管理尚无明确共识。在这里,我们描述了一项改良 Delphi 倡议,以建立英国临床环境中法布瑞病疼痛管理的专家共识。

方法

德尔菲小组的成员是根据他们在英国管理成年或儿科法布瑞病患者的专业知识确定的,并由独立的第三方管理员招募。10 名专家小组成员同意参加两轮调查,在此期间,他们彼此保持匿名。调查问卷的循环以及小组回复的收集和处理是在 2021 年 9 月至 2021 年 12 月之间进行的。所有问题都需要回答。

结果

德尔菲小组就法布瑞病疼痛评估和管理的 41 个方面中的 21 个方面达成了共识。这些方面涵盖了从治疗目标到整体支持的护理路径中的各个步骤,包括加巴喷丁和卡马西平作为治疗法布瑞病神经痛的一线镇痛药物的使用,以及对与法布瑞疼痛相关的焦虑和/或抑郁症状的积极管理。

结论

这里报告的共识小组结果强调了英国当前临床实践中的优势,以及进一步研究和达成共识的未满足需求。这项共识旨在推动制定临床指南的下一步工作。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/99b4/10362568/6682e41e125c/13023_2023_2796_Fig1_HTML.jpg

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