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右旋糖酐铁治疗血液透析患者缺铁的疗效。

The efficacy of iron dextran for the treatment of iron deficiency in hemodialysis patients.

作者信息

Fishbane S, Lynn R I

机构信息

Division of Nephrology, Winthrop-University Hospital, Mineola, New York, USA.

出版信息

Clin Nephrol. 1995 Oct;44(4):238-40.

PMID:8575123
Abstract

We prospectively evaluated the efficacy of intravenous iron dextran for the replacement of iron stores in iron deficient hemodialysis patients. Twenty-eight patients with serum ferritin < 100 ng/ml were treated with 100 mg intravenous iron dextran for ten consecutive hemodialysis treatments. Therapy was considered successful if the serum ferritin remained > 100 ng/ml for 4 months after treatment. Mean hematocrit increased from 29.1 +/- 0.9% at baseline to 33.6 +/- 1.8% at ten weeks (p < 0.05). The mean erythropoietin dose decreased from 94.1 +/- 5.3 U/kg body weight per treatment at baseline to 82.6 +/- 4.4 U/kg body weight per treatment at 10 weeks (p < 0.05). The mean serum ferritin at baseline was 38.3 +/- 5.5 ng/ml, at 2 weeks 135.9 +/- 19.7 ng/ml, at 6 weeks 114.1 +/- 22.4 ng/ml, and 86.6 +/- 17.7 ng/ml at 10 weeks. The number of patients at the therapeutic target (serum ferritin > 100 ng/ml) was 13 of 28 at 2 weeks after therapy, 9 of 28 at 6 weeks, and 8 of 28 at 10 weeks. The initial serum ferritin was the variable most predictive of successful therapy. None of 15 patients with baseline serum ferritin less than 28 ng/ml had a serum ferritin > 100 ng/ml at 4 months, compared with 8 of 13 (61%) with initial ferritins > or = 28 ng/ml. Baseline hematocrit and transferrin saturation were not predictive of therapeutic success. In summary, this regimen for administration of intravenous iron dextran resulted in improved erythropoiesis, however, at study completion iron stores remained inadequate in the majority of patients. Baseline serum ferritin < 28 ng/ml was highly predictive of patients who failed to reach the therapeutic target.

摘要

我们前瞻性评估了静脉注射右旋糖酐铁用于补充缺铁血液透析患者铁储备的疗效。28例血清铁蛋白<100 ng/ml的患者连续10次血液透析治疗中接受100 mg静脉注射右旋糖酐铁治疗。若治疗后4个月血清铁蛋白仍>100 ng/ml,则认为治疗成功。平均血细胞比容从基线时的29.1±0.9%升至10周时的33.6±1.8%(p<0.05)。平均促红细胞生成素剂量从基线时每次治疗94.1±5.3 U/kg体重降至10周时的82.6±4.4 U/kg体重(p<0.05)。基线时平均血清铁蛋白为38.3±5.5 ng/ml,2周时为135.9±19.7 ng/ml,6周时为114.1±22.4 ng/ml,10周时为86.6±17.7 ng/ml。治疗后2周达到治疗目标(血清铁蛋白>100 ng/ml)的患者有13/28,6周时为9/28,10周时为8/28。初始血清铁蛋白是最能预测治疗成功的变量。15例基线血清铁蛋白低于28 ng/ml的患者在4个月时血清铁蛋白均未>100 ng/ml,相比之下,初始铁蛋白>或=28 ng/ml的13例患者中有8例(61%)达到此水平。基线血细胞比容和转铁蛋白饱和度不能预测治疗成功。总之,这种静脉注射右旋糖酐铁的给药方案改善了红细胞生成,然而,在研究结束时,大多数患者的铁储备仍然不足。基线血清铁蛋白<28 ng/ml高度预测患者无法达到治疗目标。

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