Literature DB >> 17970927

Quality of life related to oral versus subcutaneous iron chelation: a time trade-off study.

Richard H Osborne1, Richard De Abreu Lourenço, Andrew Dalton, Jennifer Houltram, David Dowton, Douglas Edgar Joshua, Robert Lindeman, Phoebe Joy Ho.   

Abstract

OBJECTIVE: To investigate the utility associated with subcutaneous infusion (deferoxamine) compared with once-daily oral administration (deferasirox) of iron chelation therapy.
METHODS: Interviews using the time trade-off technique were used to estimate preferences (utility) for health states by finding the point at which respondents were indifferent between a longer but lower quality of life (QoL) and a shorter time in full health. Participants (n = 110) were community-based, 51% women, median age 35 years, from four regions in Sydney, Australia. Respondents rated three health states involving equal outcomes for people with thalassemia but with different treatment modalities for iron chelation; an "anchor state" describing a patient receiving iron chelation without administration mode specified, anchor state plus iron chelation via subcutaneous infusion, and anchor state plus iron chelation through once-daily oral medication.
RESULTS: On an interval scale between 0 (death) and 1 (full health), median (interquartile range) utility of 0.80 (0.65-0.95) for the anchor state, 0.66 (0.45-0.87) for subcutaneous infusion, and 0.93 (0.80-0.97) for once-daily oral administration was obtained. The mean (median) difference of 0.23 (0.27) between the two treatments was statistically significant (Wilcoxon-signed rank test, P < 0.001). Subcutaneous infusion was associated with a mean (median) utility 0.13 (0.14) lower than the anchor state (P < 0.001), and once-daily oral treatment had a utility 0.10 (0.13) higher (P < 0.001).
CONCLUSION: Community respondents associate oral administration of an iron chelator such as deferasirox with enhanced QoL compared with subcutaneous treatment. Assuming equal safety and efficacy, QoL gains from once-daily oral treatment compared with subcutaneous infusion are significant.

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Year:  2007        PMID: 17970927     DOI: 10.1111/j.1524-4733.2007.00200.x

Source DB:  PubMed          Journal:  Value Health        ISSN: 1098-3015            Impact factor:   5.725


  24 in total

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Authors:  Victoria K Brennan; Simon Dixon
Journal:  Pharmacoeconomics       Date:  2013-08       Impact factor: 4.981

2.  Factors affecting health-related quality of life in Thai children with thalassemia.

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Review 3.  Valuing Meta-Health Effects for Use in Economic Evaluations to Inform Reimbursement Decisions: A Review of the Evidence.

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5.  Iron-chelating therapies in a transfusion-dependent thalassaemia population in Thailand: a cost-effectiveness study.

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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

7.  Allogeneic Hematopoietic Cell Transplantation for Children with Sickle Cell Disease Is Beneficial and Cost-Effective: A Single-Center Analysis.

Authors:  Staci D Arnold; Zhezhen Jin; Stephen Sands; Monica Bhatia; Andrew L Kung; Prakash Satwani
Journal:  Biol Blood Marrow Transplant       Date:  2015-01-20       Impact factor: 5.742

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

9.  A cost-utility and budget impact analysis of allogeneic hematopoietic stem cell transplantation for severe thalassemic patients in Thailand.

Authors:  Pattara Leelahavarong; Usa Chaikledkaew; Suradej Hongeng; Vijj Kasemsup; Yoel Lubell; Yot Teerawattananon
Journal:  BMC Health Serv Res       Date:  2010-07-16       Impact factor: 2.655

10.  Quality of life in patients with thalassemia major and intermedia in kerman-iran (I.R.).

Authors:  Hossein Safizadeh; Zahra Farahmandinia; Simin Soltani Nejad; Nasim Pourdamghan; Majid Araste
Journal:  Mediterr J Hematol Infect Dis       Date:  2012-10-03       Impact factor: 2.576

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