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First European consensus for diagnosis, management, and treatment of transthyretin familial amyloid polyneuropathy

机译:运甲状腺素蛋白家族性淀粉样蛋白多神经病的诊断,治疗和治疗的第一个欧洲共识

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摘要

Purpose of review Early and accurate diagnosis of transthyretin familial amyloid polyneuropathy (TTR-FAP) represents one of the major challenges faced by physicians when caring for patients with idiopathic progressive neuropathy. There is little consensus in diagnostic and management approaches across Europe. Recent findings The low prevalence of TTR-FAP across Europe and the high variation in both genotype and phenotypic expression of the disease means that recognizing symptoms can be difficult outside of a specialized diagnostic environment. The resulting delay in diagnosis and the possibility of misdiagnosis can misguide clinical decision-making and negatively impact subsequent treatment approaches and outcomes. Summary This review summarizes the findings from two meetings of the European Network for TTR-FAP (ATTReuNET). This is an emerging group comprising representatives from 10 European countries with expertise in the diagnosis and management of TTR-FAP, including nine National Reference Centres. The current review presents management strategies and a consensus on the gold standard for diagnosis of TTR-FAP as well as a structured approach to ongoing multidisciplinary care for the patient. Greater communication, not just between members of an individual patient's treatment team, but also between regional and national centres of expertise, is the key to the effective management of TTR-FAP.
机译:审查目的甲状腺素转运蛋白家族性淀粉样蛋白多神经病(TTR-FAP)的早期和准确诊断是医师在照顾特发性进行性神经病患者时面临的主要挑战之一。在欧洲,诊断和管理方法尚无共识。最近的发现TTR-FAP在欧洲的患病率较低,并且该疾病的基因型和表型表达差异很大,这意味着在专门的诊断环境之外很难识别症状。导致的诊断延迟和误诊的可能性可能会误导临床决策,并对后续治疗方法和结果产生负面影响。总结这篇综述总结了欧洲TTR-FAP网络(ATTReuNET)两次会议的调查结果。这个新兴小组由来自10个欧洲国家的代表组成,这些代表在TTR-FAP的诊断和管理方面具有专业知识,其中包括9个国家参考中心。本篇综述介绍了管理策略和关于诊断TTR-FAP的金标准的共识,以及针对患者进行持续多学科护理的结构化方法。 TTR-FAP有效管理的关键,不仅在单个患者治疗团队的成员之间,而且在区域和国家专业知识中心之间的更好的沟通。

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