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尼日利亚儿童镰状细胞贫血中的铁缺乏症

Iron deficiency in sickle cell anaemia in Nigerian children.

作者信息

Okeahialam T C, Obi G O

出版信息

Ann Trop Paediatr. 1982 Jun;2(2):89-92. doi: 10.1080/02724936.1982.11748234.

Abstract

The iron status in children with sickle cell anaemia has been studied in 45 patients. The mean haemoglobin level was 7.4 g/dl (s.d. 1.7) and the white cell count more than 11 X 10(9)/l in 35 (78%). Bone marrow examination showed depletion of iron stores of 21 (47%). The total iron binding capacity was elevated in most of the children and serum iron was below the normal mean level for age in 14 (31%) children. The possible causes of iron deficiency in some of these children include dietary deficiency, infections, malabsorption, blood loss through hookworm infestation and growth spurt. In the management of a child with sickle cell disease, iron administration is not recommended unless there is evidence of coexisting iron deficiency.

摘要

对45例镰状细胞贫血患儿的铁状态进行了研究。平均血红蛋白水平为7.4g/dl(标准差1.7),35例(78%)患儿白细胞计数超过11×10⁹/L。骨髓检查显示21例(47%)铁储备耗竭。大多数患儿总铁结合力升高,14例(31%)患儿血清铁低于年龄正常平均水平。这些患儿中部分缺铁的可能原因包括饮食缺乏、感染、吸收不良、钩虫感染导致的失血以及生长加速。在镰状细胞病患儿的管理中,除非有并存缺铁的证据,否则不建议给予铁剂。

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