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Combined chelation therapy with deferoxamine and deferiprone in β-thalassemia major: compliance and opinions of young thalassemic patients.

TitleCombined chelation therapy with deferoxamine and deferiprone in β-thalassemia major: compliance and opinions of young thalassemic patients.
Publication TypeJournal Article
Year of Publication2014
AuthorsHatzipantelis, E. S., Karasmanis K., Perifanis V., Vlachaki E., Tziomalos K., & Economou M.
JournalHemoglobin
Volume38
Issue2
Pagination111-4
Date Published2014
ISSN1532-432X
KeywordsAdolescent, Adult, beta-Thalassemia, Chelation Therapy, Chi-Square Distribution, Child, Deferoxamine, Drug Therapy, Combination, Health Knowledge, Attitudes, Practice, Humans, Iron Chelating Agents, Patient Compliance, Public Opinion, Pyridones, Surveys and Questionnaires, Young Adult
Abstract

Treatment of β-thalassemia major (β-TM) includes regular blood transfusions and iron chelation with subcutaneous injection of deferoxamine (DFO). During the last decade, a new chelation agent, deferiprone (L1), was introduced. The purpose of our study was to determine the level of awareness/education regarding chelation therapy, the degree of compliance to this therapy and their views of L1 in patients with β-TM. A relevant questionnaire was administered to 36 patients (12-26 years old) who were on combination chelation therapy with both DFO and L1. The majority of patients was well aware/educated about chelation therapy (76.6%), was compliant with this therapy (74.4%) and had a positive view towards oral chelation (86.0%). In conclusion, most patients with β-TM who were on combination chelation therapy with DFO and L1 were satisfied with this treatment and this results in high compliance rates.

DOI10.3109/03630269.2013.867407
Alternate JournalHemoglobin
PubMed ID24351163

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