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促红细胞生成素与铁

Erythropoietin and iron.

作者信息

Sunder-Plassmann G, Hörl W H

机构信息

Department of Medicine, University of Vienna, Austria.

出版信息

Clin Nephrol. 1997 Mar;47(3):141-57.

PMID:9105761
Abstract

Careful evaluation of iron status is of pivotal importance in end-stage renal disease patients before and during r-HuEPO therapy. Absolute (ferritin < 100 micrograms/l) and functional (ferritin normal or supranormal, transferrin saturation < 20%, hypochromic red blood cell [RBC] > 5%) iron deficiency are the main reasons for r-HuEPO hyporesponsiveness. Adequate iron supplementation allows significant reduction of r-HuEPO dosage and costs. Oral iron supplementation is recommended for predialysis and peritoneal dialysis patients with serum ferritin > 100 micrograms/l, whereas i.v. iron supplementation is the therapy of choice in hemodialysis patients. However, neutrophil impairment and other possible side-effects (e.g. cardiovascular complications, malignancy) as a result of i.v. iron therapy suggest that overtreatment with i.v. iron should be avoided.

摘要

在终末期肾病患者接受重组人促红细胞生成素(r-HuEPO)治疗之前及治疗期间,仔细评估铁状态至关重要。绝对铁缺乏(铁蛋白<100微克/升)和功能性铁缺乏(铁蛋白正常或高于正常,转铁蛋白饱和度<20%,低色素红细胞[RBC]>5%)是r-HuEPO反应低下的主要原因。充足的铁补充可显著降低r-HuEPO剂量和成本。对于血清铁蛋白>100微克/升的血液透析前和腹膜透析患者,建议口服铁补充剂,而静脉注射铁补充剂是血液透析患者的首选治疗方法。然而,静脉注射铁治疗导致的中性粒细胞损伤和其他可能的副作用(如心血管并发症、恶性肿瘤)表明,应避免静脉注射铁的过度治疗。

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