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The era of comparable life expectancy between thalassaemia major and intermedia: Is it time to revisit the major‐intermedia dichotomy?

Summary In the last few decades, the life expectancy of regularly transfused β‐thalassaemia major (TM) patients has dramatically improved following the introduction of safe transfusion practices, iron chelation therapy, aggressive treatment of infections and improved management of cardiac complicati...

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Published in:British journal of haematology 2017-01, Vol.176 (1), p.124-130
Main Authors: Vitrano, Angela, Calvaruso, Giuseppina, Lai, Eliana, Colletta, Grazia, Quota, Alessandra, Gerardi, Calogera, Concetta Rigoli, Luciana, Pitrolo, Lorella, Cuccia, Liana, Gagliardotto, Francesco, Filosa, Aldo, Caruso, Vincenzo, Argento, Crocetta, Campisi, Saveria, Rizzo, Michele, Prossomariti, Luciano, Fidone, Carmelo, Fustaneo, Maria, Di Maggio, Rosario, Maggio, Aurelio
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Language:English
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Summary:Summary In the last few decades, the life expectancy of regularly transfused β‐thalassaemia major (TM) patients has dramatically improved following the introduction of safe transfusion practices, iron chelation therapy, aggressive treatment of infections and improved management of cardiac complications. How such changes, especially those attributed to the introduction of iron chelation therapy, improved the survival of TM patients to approach those with β‐thalassaemia intermedia (TI) remains unknown. Three hundred and seventy‐nine patients with TM (n = 284, dead 40) and TI (n = 95, dead 13) were followed retrospectively since birth until 30 June 2015 or death. Kaplan‐Meir curves showed statistically significant differences in TM and TI survival (P 
ISSN:0007-1048
1365-2141
DOI:10.1111/bjh.14381