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Abstract The aim of this study was to detect the prevalence of PHT and cardiac involvement among TI patients, its relationto various clinical and laboratory characteristics of those patients and the possible effects of different therapeutic strategies used in managementof TI patients on the development of PHT. This study was conducted in the Pediatric Hematology Clinic, New Children’s hospital, Cairo University. It included sixty patients with thalassemia intermedia (45 child and 15 adult). Allpatients were subjected to full history and through clinical examination with stress on: age at diagnosis, frequency of blood transfusion, splenectomy, cardiovascular symptoms and chelation therapy, the size of liver and spleen. Complete blood picture, differential leucocytic count, reticulocytic count, serum ferritin and lactate dehydrogenase (LDH), alanine transaminase (ALT), aspartate transaminase (AST) and serum bilirubin (total, direct), coagulation profile and Hb electrophoresis were done for all patients at the time of enrollement. Echocardiography examination was performed at Echocardiography Laboratory of Abu El-Reesh Hospital, Faculty of Medicine, Cairo University. Trans-thoracic two dimensional (2D) guided (M mode) and Doppler echocardiogram was performed for all patients. |