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

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 acr...

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Autores principales: Adams, David, Suhr, Ole B., Hund, Ernst, Obici, Laura, Tournev, Ivailo, Campistol, Josep M., Slama, Michel S., Hazenberg, Bouke P., Coelho, Teresa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4739312/
https://www.ncbi.nlm.nih.gov/pubmed/26734952
http://dx.doi.org/10.1097/WCO.0000000000000289
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author Adams, David
Suhr, Ole B.
Hund, Ernst
Obici, Laura
Tournev, Ivailo
Campistol, Josep M.
Slama, Michel S.
Hazenberg, Bouke P.
Coelho, Teresa
author_facet Adams, David
Suhr, Ole B.
Hund, Ernst
Obici, Laura
Tournev, Ivailo
Campistol, Josep M.
Slama, Michel S.
Hazenberg, Bouke P.
Coelho, Teresa
author_sort Adams, David
collection PubMed
description 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.
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spelling pubmed-47393122016-02-17 First European consensus for diagnosis, management, and treatment of transthyretin familial amyloid polyneuropathy Adams, David Suhr, Ole B. Hund, Ernst Obici, Laura Tournev, Ivailo Campistol, Josep M. Slama, Michel S. Hazenberg, Bouke P. Coelho, Teresa Curr Opin Neurol Supplement Article 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. Lippincott Williams & Wilkins 2016-02 2016-02-01 /pmc/articles/PMC4739312/ /pubmed/26734952 http://dx.doi.org/10.1097/WCO.0000000000000289 Text en Copyright © 2016 Wolters Kluwer Health, Inc. All rights reserved. http://creativecommons.org/licenses/by-nc-nd/4.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 License, where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially. http://creativecommons.org/licenses/by-nc-nd/4.0
spellingShingle Supplement Article
Adams, David
Suhr, Ole B.
Hund, Ernst
Obici, Laura
Tournev, Ivailo
Campistol, Josep M.
Slama, Michel S.
Hazenberg, Bouke P.
Coelho, Teresa
First European consensus for diagnosis, management, and treatment of transthyretin familial amyloid polyneuropathy
title First European consensus for diagnosis, management, and treatment of transthyretin familial amyloid polyneuropathy
title_full First European consensus for diagnosis, management, and treatment of transthyretin familial amyloid polyneuropathy
title_fullStr First European consensus for diagnosis, management, and treatment of transthyretin familial amyloid polyneuropathy
title_full_unstemmed First European consensus for diagnosis, management, and treatment of transthyretin familial amyloid polyneuropathy
title_short First European consensus for diagnosis, management, and treatment of transthyretin familial amyloid polyneuropathy
title_sort first european consensus for diagnosis, management, and treatment of transthyretin familial amyloid polyneuropathy
topic Supplement Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4739312/
https://www.ncbi.nlm.nih.gov/pubmed/26734952
http://dx.doi.org/10.1097/WCO.0000000000000289
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