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Eur J Heart Fail ; 9(3): 320-2, 2007 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-17029959

RESUMO

Despite usual iron chelating therapy based on desferrioxamine, patients affected by beta-thalassemia major (beta-TM) often develop progressive heart failure caused by myocardial iron overload, which is the leading cause of mortality within the third decade of life. Heart transplantation is a limited therapeutic option, as very often these patients have multi-organ iron deposits and infective complications (particularly hepatitis C), secondary to frequent blood transfusions. We report the case of a 26-year-old male affected by beta-TM with end-stage heart failure, who showed a dramatic improvement in symptoms and myocardial function when a new oral iron chelating agent, deferiprone, was added to standard therapy with desferrioxamine.


Assuntos
Cardiomiopatia Dilatada/tratamento farmacológico , Desferroxamina/uso terapêutico , Quelantes de Ferro/uso terapêutico , Piridonas/uso terapêutico , Talassemia beta/tratamento farmacológico , Adulto , Cardiomiopatia Dilatada/etiologia , Deferiprona , Quimioterapia Combinada , Ferritinas/sangue , Humanos , Masculino , Recuperação de Função Fisiológica , Talassemia beta/complicações
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