Transthyretin amyloidosis: Testing strategies and model for center of excellence support.

Centre of excellence Rare disease Testing strategies Transthyretin amyloidosis

Journal

Clinica chimica acta; international journal of clinical chemistry
ISSN: 1873-3492
Titre abrégé: Clin Chim Acta
Pays: Netherlands
ID NLM: 1302422

Informations de publication

Date de publication:
Oct 2020
Historique:
received: 16 04 2020
revised: 14 06 2020
accepted: 16 06 2020
pubmed: 23 6 2020
medline: 22 6 2021
entrez: 23 6 2020
Statut: ppublish

Résumé

Appropriate testing strategies and strict model for Center Of Excellence (CoE) support are essential for the correct diagnosis, follow-up strategy and treatment plan for transthyretin (ATTR) amyloidosis. CoE is defined as a programme within a healthcare institution established to provide an exceptionally high concentration of expertise and related resources centred on a particular area of medicine, delivering associated care in a comprehensive, interdisciplinary fashion to afford the best patient outcome. Ideally, CoEs provide regular education and training for healthcare professionals and share knowledge and learning with other CoEs and specialists to ensure the highest standards of care. CoEs and testing strategies are of significant value to those with rare diseases and their families, as there is naturally low awareness among healthcare professionals, a phenomenon that potentially delays diagnosis and treatment. In this review, we focus on the importance of performing the most appropriate testing strategies for ATTR amyloidosis and establishing a CoE for this rare disease. We highlight our experience in establishing a CoE in Sofia, Bulgaria and define the fundamental steps needed to successfully launch a programme.

Identifiants

pubmed: 32564944
pii: S0009-8981(20)30293-X
doi: 10.1016/j.cca.2020.06.029
pii:
doi:

Substances chimiques

Prealbumin 0

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

228-234

Informations de copyright

Copyright © 2020 Elsevier B.V. All rights reserved.

Auteurs

Radislav Nakov (R)

Clinic of Gastroenterology, Tsaritsa Joanna University Hospital, Medical University - Sofia, Bulgaria. Electronic address: radislav.nakov@gmail.com.

Stayko Sarafov (S)

Clinic of Nervous Diseases, Alexandrovska University Hospital, Medical University - Sofia, Bulgaria.

Mariana Gospodinova (M)

Clinic of Cardiology, Medical Institute of Ministry of Interior, Sofia, Bulgaria.

Andrey Kirov (A)

Genetic and Medico-diagnostic Laboratory "Genica", Sofia, Bulgaria; Department of Medical Chemistry and Biochemistry, Medical University - Sofia, Bulgaria.

Teodora Chamova (T)

Clinic of Gastroenterology, Tsaritsa Joanna University Hospital, Medical University - Sofia, Bulgaria.

Tihomir Todorov (T)

Genetic and Medico-diagnostic Laboratory "Genica", Sofia, Bulgaria.

Albena Todorova (A)

Genetic and Medico-diagnostic Laboratory "Genica", Sofia, Bulgaria; Department of Medical Chemistry and Biochemistry, Medical University - Sofia, Bulgaria.

Ivailo Tournev (I)

Clinic of Nervous Diseases, Alexandrovska University Hospital, Medical University - Sofia, Bulgaria; Department of Cognitive Science and Psychology, New Bulgarian University, Sofia, Bulgaria.

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Classifications MeSH