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Beliefs about chelation among thalassemia patients

Authors :
Zahra Pakbaz
Janet L. Kwiatkowski
Nancy F. Olivieri
Rob Horne
Robert W. Grady
Lauren Mednick
Ellis J. Neufeld
Robert Yamashita
Alexis A. Thompson
Charles T. Quinn
Amy Sobota
Dru Haines
Felicia Trachtenberg
Source :
Health and Quality of Life Outcomes, Health and Quality of Life Outcomes, Vol 10, Iss 1, p 148 (2012)
Publication Year :
2012
Publisher :
BioMed Central, 2012.

Abstract

Background Understanding patients’ views about medication is crucial to maximize adherence. Thalassemia is a congenital blood disorder requiring chronic blood transfusions and daily iron chelation therapy. Methods The Beliefs in Medicine Questionnaire (BMQ) was used to assess beliefs in chelation in thalassemia patients from North America and London in the Thalassemia Longitudinal Cohort (TLC) of the Thalassemia Clinical Research Network (TCRN). Chelation adherence was based on patient report of doses administered out of those prescribed in the last four weeks. Results Of 371 patients (ages 5-58y, mean 24y), 93% were transfused and 92% receiving chelation (26% deferoxamine (DFO; a slow subcutaneous infusion via portable pump), 63% oral, 11% combination). Patients expressed high “necessity” for transfusion (96%), DFO chelation (92%) and oral chelation (89%), with lower “concern” about treatment (48%, 39%, 19% respectively). Concern about oral chelation was significantly lower than that of DFO (p Conclusions Despite their requirement for multimodal therapy, thalassemia patients have positive views about medicine, more so than in other disease populations. Patients may benefit from education about the tolerability of chelation and strategies to effectively cope with side effects, both of which might be beneficial in lowering body iron burden. Clinicaltrials.gov identifier NCT00661804

Details

Language :
English
ISSN :
14777525
Volume :
10
Database :
OpenAIRE
Journal :
Health and Quality of Life Outcomes
Accession number :
edsair.doi.dedup.....6b7f19627958d7dae4aa65e974ce6d37