Management of the thalassemias
- PMID: 23732853
- PMCID: PMC3662352
- DOI: 10.1101/cshperspect.a011767
Management of the thalassemias
Abstract
During the last 30 years, in addition to the considerable progress made in control and prevention of thalassemias(3), there have also been major advances in their symptomatic management, at least in wealthier countries where appropriate facilities are available. Remarkable improvements in survival in the severe forms of thalassemia have followed the more judicious use of blood transfusion and, in particular, the ability to manage the iron accumulation resulting from transfusion with its severe and ultimately lethal effects on endocrine and cardiac function.
References
-
- Allen A, Fisher C, Premawardhena A, Peto T, Allen S, Arambepola M, Thayalsutha V, Olivieri N, Weatherall D 2010. Adaptation to anemia in hemoglobin E-ss thalassemia. Blood 116: 5368–5370 - PubMed
-
- Anderson LJ, Holden S, Davis B, Prescott E, Charrier CC, Bunce NH, Firmin DN, Wonke B, Porter J, Walker JM, et al. 2001. Cardiovascular T2-star (T2*) magnetic resonance for the early diagnosis of myocardial iron overload. Eur Heart J 22: 2171–2179 - PubMed
-
- Anderson LJ, Wonke B, Prescott E, Holden S, Walker JM, Pennell DJ 2002. Comparison of effects of oral deferiprone and subcutaneous desferrioxamine on myocardial iron concentrations and ventricular function in β-thalassaemia. Lancet 360: 516–520 - PubMed
-
- Anderson LJ, Westwood MA, Prescott E, Walker JM, Pennell DJ, Wonke B 2006. Development of thalassaemic iron overload cardiomyopathy despite low liver iron levels and meticulous compliance to desferrioxamine. Acta Haematol 115: 106–108 - PubMed
-
- Angelucci E, Brittenham GM, McLaren CE, Ripalti M, Baronciani D, Giardini C, Galimberti M, Polchi P, Lucarelli G 2000. Hepatic iron concentration and total body iron stores in thalassemia major. N Engl J Med 343: 327–331 - PubMed
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical