N. Mohamed et N. Jackson, SEVERE THALASSEMIA-INTERMEDIA - CLINICAL PROBLEMS IN THE ABSENCE OF HYPERTRANSFUSION, Blood reviews, 12(3), 1998, pp. 163-170
In many of the parts of the world where thalassaemia is common, the bl
ood supply is inadequate or unsafe, and desferrioxamine is too expensi
ve for routine use. We classify some patients as having 'severe thalas
saemia intermedia', i.e, those with moderately severe thalassaemia who
can survive without regular transfusions, but who are at risk of many
complications which are reviewed here. These include bone deformity a
nd fractures, extramedullary haemopoietic tumours, leg ulcers, autoimm
une haemolysis and, especially after splenectomy, thromboembolism and
infection. An increase in the quality and safety of the blood supply,
and a cheaper and/or oral iron chelator, would enable more of these pa
tients to be treated as thalassaemia major and have improved survival
and quality of life.