Management of transfusion-dependent β-thalassemia (TDT): Expert insights and practical overview from the Middle East
- PMID: 37867006
- DOI: 10.1016/j.blre.2023.101138
Management of transfusion-dependent β-thalassemia (TDT): Expert insights and practical overview from the Middle East
Abstract
β-Thalassemia is one of the most common monogenetic diseases worldwide, with a particularly high prevalence in the Middle East region. As such, we have developed long-standing experience with disease management and devising solutions to address challenges attributed to resource limitations. The region has also participated in the majority of clinical trials and development programs of iron chelators and more novel ineffective erythropoiesis-targeted therapy. In this review, we provide a practical overview of management for patients with transfusion-dependent β-thalassemia, primarily driven by such experiences, with the aim of transferring knowledge to colleagues in other regions facing similar challenges.
Keywords: Complications; Management; Thalassemia; Transfusion; iron chelation.
Copyright © 2023 The Authors. Published by Elsevier Ltd.. All rights reserved.
Conflict of interest statement
Disclosures A.E-B. reports consultancy fees from Bristol Myers Squibb. H.D. reports consultancy fees from Bristol Myers Squibb, Novartis, and Chiesi; and research funding from Agios Pharmaceuticals. S.H. reports consultancy fees from Bristol Myers Squibb. S.A. reports consultancy fees from Bristol Myers Squibb and Novartis. A.A.T. reports consultancy fees from Bristol Myers Squibb. M.A.Y. reports consultancy fees from Bristol Myers Squibb. A.T.T. reports consultancy fees from Novartis, Celgene Corp (Bristol Myers Squibb), Agios Pharmaceuticals, Vifor Pharma, and Pharmacosmos; and research funding from Novartis, Celgene Corp (Bristol Myers Squibb), Agios Pharmaceuticals, Vifor Pharma, and Pharmacosmos.
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