Literature DB >> 18704280

Iron chelation therapy: clinical effectiveness, economic burden and quality of life in patients with iron overload.

Krista A Payne1, Diana Rofail, Jean-François Baladi, Muriel Viala, Linda Abetz, Marie-Pierre Desrosiers, Noreen Lordan, Khajak Ishak, Irina Proskorovsky.   

Abstract

INTRODUCTION: This study of UK patients examines clinical, health-related quality of life (HRQOL) and economic outcomes associated with iron chelation therapy (ICT). Desferrioxamine (DFO) (Desferal; Novartis, Switzerland) and Deferiprone (Ferriprox; Apotex, Canada) are ICTs used to treat iron overload. DFO requires 8-to 12-hour infusions a minimum of five times per week. Deferiprone is administered in an oral daily regimen. Although pharmacologically efficacious, clinical effectiveness of ICT within the real-world setting is yet to be fully elucidated.
METHODS: A naturalistic cohort study of 60 patients (beta-thalassaemia, n=40; sickle cell disease, n=14; myelodysplastic syndromes, n=6; 63% female) receiving ICT in four UK treatment centres was conducted. Serum ferritin level data were abstracted from medical charts. Compliance, HRQOL, satisfaction and resource utilisation data were collected from interviews. Maximum ICT costs were estimated using the resource utilisation data associated with DFO.
RESULTS: Mean serum ferritin levels, generally, remained elevated despite ICT. Compliance was suboptimal and HRQOL scores were lower than population norms. The total estimated mean weighted annual per-patient cost of DFO treatment was approximately pound19,000. DFO-related equipment, DFO drug, and home healthcare were estimated to account for 43%, 19% and 24% of costs, respectively. Other more minor components of total annual costs were for in-patient infusions, ICT home delivery services and monitoring costs.
CONCLUSION: Generally, patients are not achieving target serum ferritin thresholds despite chronic treatment for iron overload. ICT appears to negatively impact HRQOL; compliance with ICT is poor; and, in the case of DFO, treatment costs well exceed the cost of DFO alone. These results suggest that current ICT in the real-world setting is suboptimal with respect to various clinical, HRQOL and economic outcomes.

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Year:  2008        PMID: 18704280     DOI: 10.1007/s12325-008-0085-z

Source DB:  PubMed          Journal:  Adv Ther        ISSN: 0741-238X            Impact factor:   3.845


  27 in total

1.  Education and employment status of children and adults with thalassemia in North America.

Authors:  Zahra Pakbaz; Marsha Treadwell; Hae-Young Kim; Felicia Trachtenberg; Nagina Parmar; Janet L Kwiatkowski; Melody J Cunningham; Marie Martin; Nancy Sweeters; Ellis J Neufeld; Patricia J Giardina; Nancy Olivieri; Robert C Yamashita; Elliott Vichinsky
Journal:  Pediatr Blood Cancer       Date:  2010-10       Impact factor: 3.167

2.  Serum ferritin levels, socio-demographic factors and desferrioxamine therapy in multi-transfused thalassemia major patients at a government tertiary care hospital of Karachi, Pakistan.

Authors:  Haris Riaz; Talha Riaz; Muhammad Ubaid Khan; Sina Aziz; Faizan Ullah; Anis Rehman; Qandeel Zafar; Abdul Nafey Kazi
Journal:  BMC Res Notes       Date:  2011-08-11

3.  Relationship among chelator adherence, change in chelators, and quality of life in thalassemia.

Authors:  Felicia L Trachtenberg; Eric Gerstenberger; Yan Xu; Lauren Mednick; Amy Sobota; Hannah Ware; Alexis A Thompson; Ellis J Neufeld; Robert Yamashita
Journal:  Qual Life Res       Date:  2014-03-30       Impact factor: 4.147

Review 4.  Interventions for improving adherence to iron chelation therapy in people with sickle cell disease or thalassaemia.

Authors:  Patricia M Fortin; Karen V Madgwick; Marialena Trivella; Sally Hopewell; Carolyn Doree; Lise J Estcourt
Journal:  Cochrane Database Syst Rev       Date:  2016-09

5.  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

6.  Pain as an emergent issue in thalassemia.

Authors:  Felicia Trachtenberg; Dru Foote; Marie Martin; Susan Carson; Thomas Coates; Owen Beams; Olivia Vega; Manuela Merelles-Pulcini; Patricia J Giardina; Dorothy A Kleinert; Janet Kwiatkowski; Alexis A Thompson; Ellis J Neufeld; Leann Schilling; Vivek Thayalasuthan; Zahra Pakbaz; Robert Yamashita
Journal:  Am J Hematol       Date:  2010-05       Impact factor: 10.047

Review 7.  Pharmacoeconomic considerations in treating iron overload in patients with β-thalassaemia, sickle cell disease and myelodysplastic syndromes in the US: a literature review.

Authors:  Bin Zhang; Prina Z Donga; Mitra Corral; Medha Sasane; Jeffrey D Miller; Chris L Pashos
Journal:  Pharmacoeconomics       Date:  2011-06       Impact factor: 4.981

8.  Psychometric properties of the Specific Thalassemia Quality of Life Instrument for adults.

Authors:  Georgios N Lyrakos; Demetra Vini; Helen Aslani; Marouso Drosou-Servou
Journal:  Patient Prefer Adherence       Date:  2012-07-02       Impact factor: 2.711

Review 9.  Deferasirox: a review of its use for chronic iron overload in patients with non-transfusion-dependent thalassaemia.

Authors:  Matt Shirley; Greg L Plosker
Journal:  Drugs       Date:  2014-06       Impact factor: 9.546

10.  Adult sickle cell quality-of-life measurement information system (ASCQ-Me): conceptual model based on review of the literature and formative research.

Authors:  Marsha J Treadwell; Kathryn Hassell; Roger Levine; San Keller
Journal:  Clin J Pain       Date:  2014-10       Impact factor: 3.442

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