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首页> 外文期刊>Clinical nephrology >Targeting higher ferritin concentrations with intravenous iron dextran lowers erythropoietin requirement in hemodialysis patients.
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Targeting higher ferritin concentrations with intravenous iron dextran lowers erythropoietin requirement in hemodialysis patients.

机译:通过静脉内右旋糖酐铁靶向更高的铁蛋白浓度可降低血液透析患者的促红细胞生成素需求。

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INTRODUCTION: Although clinical use of recombinant human erythropoietin (rHuEPO) since 1989 has improved anemia in most end-stage renal disease patients, there are still many hemodialysis patients unable to maintain an adequate hematocrit (HCT) without large doses of rHuEPO. This suggests that anemia is not solely a consequence of rHuEPO deficiency, but may be due to other factors including functional iron deficiency. Since the optimal prescription for iron replacement is not yet known, we evaluated the effect of intravenous iron dextran (IVFe) infusion on serum ferritin (SFer) concentration and rHuEPO dose. Our objective was to raise and maintain serum ferritin concentrations to 2 different levels above the National Kidney Foundation Dialysis Outcome Quality Initiative standard of 100 ng/ml to determine whether, and by what degree rHuEPO dose could be lowered. METHODS: HD patients on i.v. rHuEPO with a SFer concentration > or = 70 ng/ml and an HCT of < or = 33% were enrolled. Subjects were divided as follows: Group 1: target SFer of 200 ng/ml, Group 2: target SFer of 400 ng/ml. Each subject below the target level received IVFe in up to 10 divided doses during consecutive dialysis sessions as needed to reach the target. HCT was maintained between 32.5% and 36% by adjusting rHuEPO dosage. RESULTS: Mean SFer concentration at the study conclusion in Group 1: 261 ng/ml; Group 2: 387 ng/ml. The mean decrease in rHuEPO dose for Group 1 was 31 U/kg body weight/week (250 - 219 U/kg bw/wk) while in Group 2 it was 154 U/kg body weight/week (312 - 158 U/kg bw/wk) (p < 0.001). There was no difference in HCT between groups. Our results suggest that higher target serum ferritin concentrations can be well tolerated and lower rHuEPO requirements.
机译:简介:尽管从1989年开始临床使用重组人促红细胞生成素(rHuEPO)可以改善大多数终末期肾病患者的贫血,但是仍有许多血液透析患者在不使用大剂量rHuEPO的情况下无法维持足够的血细胞比容(HCT)。这表明贫血不仅是rHuEPO缺乏的结果,还可能是由于其他因素包括功能性铁缺乏引起的。由于尚不清楚铁替代的最佳处方,我们评估了静脉内右旋糖酐铁(IVFe)输注对血清铁蛋白(SFer)浓度和rHuEPO剂量的影响。我们的目标是将血清铁蛋白浓度提高并维持在高于国家肾脏基金会透析结果质量倡议100 ng / ml的标准的2个不同水平,以确定是否可以降低rHuEPO剂量以及在何种程度上可以降低rHuEPO剂量。方法:高清患者通过静脉入选SFer浓度≥70 ng / ml且HCT≤33%的rHuEPO。按照以下方式对受试者进行划分:第1组:目标SFer为200 ng / ml,第2组:目标SFer为400 ng / ml。低于目标水平的每个受试者在连续透析期间,均需要达到目标达到10次分剂量的IVFe。通过调整rHuEPO剂量,HCT维持在32.5%至36%之间。结果:第1组研究结论的平均SFer浓度为261 ng / ml;第2组:387 ng / ml。第1组的rHuEPO剂量平均减少量为31 U / kg体重/周(250-219 U / kg bw / wk),而第2组则为154 U / kg体重/周(312-158 U / kg bw / wk)(p <0.001)。两组之间的HCT没有差异。我们的结果表明,较高的目标血清铁蛋白浓度可以被很好地耐受,而较低的rHuEPO要求。

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