Literature DB >> 17880620

Consequences and costs of noncompliance with iron chelation therapy in patients with transfusion-dependent thalassemia: a literature review.

Thomas E Delea1, John Edelsberg, Oleg Sofrygin, Simu K Thomas, Jean-Francois Baladi, Pradyumna D Phatak, Thomas D Coates.   

Abstract

BACKGROUND: Patients with thalassemia major require iron chelation therapy (ICT) to prevent complications from transfusional iron overload. Deferoxamine is effective, but requires administration as a slow continuous subcutaneous or intravenous infusion five to seven times per week. Deferiprone is a three-times-daily oral iron chelator, but has limited availability in the United States. Deferasirox is a once-daily oral iron chelator that was approved in the United States in 2005 for patients older than 2 years of age with transfusional iron overload. STUDY DESIGN AND METHODS: Published evidence on rates of compliance with ICT and the association between compliance, and the incidence and costs of complications of iron overload, in patients with thalassemia major was reviewed.
RESULTS: A total of 18 studies were identified reporting data on compliance with ICT, including 7 that examined deferoxamine only, 6 that examined deferiprone only, and 5 that compared deferoxamine and deferiprone; no studies reporting compliance with deferasirox were identified. In studies of deferoxamine only, estimated mean compliance ranged from 59 to 78 percent. Studies of deferiprone generally reported better compliance, ranging from 79 to 98 percent. Results of comparative studies of deferoxamine and deferiprone suggest that compliance may be better with oral therapy. Numerous studies demonstrate that that poor compliance with ICT results in increased risk of cardiac disease and endocrinopathies, as well as lower survival. Although data on the costs of noncompliance are limited, a recent model-based study estimated the lifetime costs of inadequate compliance with deferoxamine to be $33,142.
CONCLUSIONS: Inadequate compliance with ICT in thalassemia major is common and results in substantial morbidity and mortality, as well as increased costs.

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Year:  2007        PMID: 17880620     DOI: 10.1111/j.1537-2995.2007.01416.x

Source DB:  PubMed          Journal:  Transfusion        ISSN: 0041-1132            Impact factor:   3.157


  53 in total

Review 1.  Synthetic and natural iron chelators: therapeutic potential and clinical use.

Authors:  Heather C Hatcher; Ravi N Singh; Frank M Torti; Suzy V Torti
Journal:  Future Med Chem       Date:  2009-12       Impact factor: 3.808

2.  Cost-Utility Analysis of Three Iron Chelators Used in Monotherapy for the Treatment of Chronic Iron Overload in β-Thalassaemia Major Patients: An Italian Perspective.

Authors:  Alessia Pepe; Giuseppe Rossi; Anthony Bentley; Maria Caterina Putti; Ludovica Frizziero; Domenico Giuseppe D'Ascola; Liana Cuccia; Anna Spasiano; Aldo Filosa; Vincenzo Caruso; Aishah Hanif; Antonella Meloni
Journal:  Clin Drug Investig       Date:  2017-05       Impact factor: 2.859

Review 3.  An update on iron chelation therapy.

Authors:  Erika Poggiali; Elena Cassinerio; Laura Zanaboni; Maria Domenica Cappellini
Journal:  Blood Transfus       Date:  2012-06-27       Impact factor: 3.443

4.  Lifetime cost-utility analyses of deferasirox in beta-thalassaemia patients with chronic iron overload: a UK perspective.

Authors:  Jonathan Karnon; Keith Tolley; Joao Vieira; David Chandiwana
Journal:  Clin Drug Investig       Date:  2012-12       Impact factor: 2.859

Review 5.  Hydroxyurea for hemoglobin E/β-thalassemia: a systematic review and meta-analysis.

Authors:  Ali H Algiraigri; Aliya Kassam
Journal:  Int J Hematol       Date:  2017-08-07       Impact factor: 2.490

Review 6.  Iron overload in thalassemia: different organs at different rates.

Authors:  Ali T Taher; Antoine N Saliba
Journal:  Hematology Am Soc Hematol Educ Program       Date:  2017-12-08

Review 7.  Iron-chelating therapy for transfusional iron overload.

Authors:  Gary M Brittenham
Journal:  N Engl J Med       Date:  2011-01-13       Impact factor: 91.245

8.  Economic burden of beta-thalassemia/Hb E and beta-thalassemia major in Thai children.

Authors:  Arthorn Riewpaiboon; Issarang Nuchprayoon; Kitti Torcharus; Kaemthong Indaratna; Montarat Thavorncharoensap; Bang-On Ubol
Journal:  BMC Res Notes       Date:  2010-01-30

9.  d-Propranolol protects against oxidative stress and progressive cardiac dysfunction in iron overloaded rats.

Authors:  Jay H Kramer; Christopher F Spurney; Micaela Iantorno; Constantine Tziros; Joanna J Chmielinska; I Tong Mak; William B Weglicki
Journal:  Can J Physiol Pharmacol       Date:  2012-08-22       Impact factor: 2.273

10.  Update on the use of deferasirox in the management of iron overload.

Authors:  Ali Taher; Maria Domenica Cappellini
Journal:  Ther Clin Risk Manag       Date:  2009-11-02       Impact factor: 2.423

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