Cohen A, Schwartz E
J Pediatr. 1978 Apr;92(4):659-62. doi: 10.1016/s0022-3476(78)80317-5.
Iron chelation with deferoxamine was studied in ten patients with sickle cell anemia who had received 2 to 37 liters of red blood cells. Urinary excretion of iron in response to 1.5 gm of deferoxamine administered intravenously ranged from 5.9 to 28.7 mg/24 hours and was closely related to the amount of iron acquired from transfusions. Administration of ascorbic acid did not improve deferoxamine-induced excretion of iron. Urinary excretion of iron in response to 0.75 gm of DFO intramuscularly was 4.7 to 6.9 mg/24 hours in three patients who had received 15 to 37 liters of red cells. The data indicate that measurement of DFO-induced excretion of iron is of value in detecting increased iron stores in children with sickle cell anemia who have received repeated transfusions and that chelation therapy will retard the accumulation of iron.
对10名镰状细胞贫血患者进行了去铁胺铁螯合治疗研究,这些患者已输注2至37升红细胞。静脉注射1.5克去铁胺后,尿铁排泄量为5.9至28.7毫克/24小时,且与输血获得的铁量密切相关。给予维生素C并不能改善去铁胺诱导的铁排泄。3名输注了15至37升红细胞的患者,肌肉注射0.75克去铁胺后的尿铁排泄量为4.7至6.9毫克/24小时。数据表明,检测去铁胺诱导的铁排泄量对检测接受反复输血的镰状细胞贫血儿童体内铁储存增加有价值,且螯合疗法将延缓铁的蓄积。