Hypersplenism is a very common complication in homozygous ,B thalassaemia. In regularly transfused patients it is suspected before the increased blood consumption and is sometimes associated with thrombocytopenia or leucopenia, or both. A high blood transfusion regimen usually delays this complication,' though it doesn't always suppress it. Splenectomy allows for the reduction of transfusional blood requirements thus reducing iron overload.2 However, this operation exposes patients, who are mainly under 5 years of age (but also older children and even adults), to the risk of overwhelming postsplenectomy infections.3 ' The severity of these infections has led to the search for alternative surgical techniques to replace total splenectomy so that blood requirements are reduced but the splenic contribution to the host defence against infections is preserved.We report our experience with 30 thalassaemic patients who underwent one of these alternative techniques, partial splenectomy.Patients and methods Thirty patients affected with homozygous ,B thalassaemia were included in the study; 24 had thalassaemia major and six thalassaemia intermedia. The diagnosis of thalassaemia major and intermedia was based on transfusion requirements.5 The patients' mean (SD) age was 7-9 (3 7) years (range 3-19 years) at the time of the partial splenectomy. Twenty five patients received a low transfusion regimen and five received a high transfusion regimen (table 1).In all patients about nine tenths of the total hypertrophied splenic mass was ablated at operation. The