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[重组人促红细胞生成素治疗慢性肾功能不全血液透析患者贫血:12个月经验]

[Treatment of anemia in patients with chronic renal insufficiency undergoing hemodialysis with recombinant human erythropoietin: 12 months' experience].

作者信息

de Sousa F T, Prata M M, Barbas J V, dos Santos J P

机构信息

Departamento de Nefrologia, Hospital de Santa Maria, Lisboa.

出版信息

Acta Med Port. 1990 Nov-Dec;3(6):347-52.

PMID:2089856
Abstract

In this study we analyse the effects of the administration of recombinant human erythropoietin (rHuEpo) during 12 months to correct the anaemia in a group of 17 patients (9 men and 8 women; mean age 52.7 +/- 13.7; range 23 to 68 years) with end-stage renal disease (ESRD) on chronic haemodialysis (HD) for a range of 14 to 126 months (mean 43.1 +/- 29.6). In the correction period the rHuEpo was started at 50 U/Kg i.v. 3 times a week, immediately after each HD. This dose was maintained during 4 weeks and then increased in 25 U/Kg steps until haemoglobin (Hb) levels of 12 g/dl or a maximum dose of 100 U/Kg were reached. During the long-term maintenance period the individual rHuEpo dose was adjusted to keep the Hb constant at the target level of 10-12 g/dl. Baseline blood tests were done before the beginning of the treatment and every months afterwards. The levels of Hb increased significantly in week 4 and at the end of the first 3 month only 4 patients had no answer to rHuEpo. These patients had baseline serum ferritin levels below 100 ng/ml and responded well when this defficiency was corrected with oral iron. When levels of 30-35 vol% haematocrit (Hct) were reached the dose of rHuEpo could be reduced (150 to 200 U/Kg/week). The serum ferritin levels decreased 51% from a mean baseline level of 247.8 +/- 196 to 121.1 +/- 154.9 ng/ml with the onset of the maintenance phase (p less than 0.05).

摘要

在本研究中,我们分析了对一组17例(9例男性和8例女性;平均年龄52.7±13.7岁;范围23至68岁)接受慢性血液透析(HD)14至126个月(平均43.1±29.6个月)的终末期肾病(ESRD)患者,给予重组人促红细胞生成素(rHuEpo)治疗12个月以纠正贫血的效果。在纠正期,rHuEpo以50 U/Kg静脉注射,每周3次,每次HD后立即给药。该剂量维持4周,然后以25 U/Kg的幅度增加,直至血红蛋白(Hb)水平达到12 g/dl或最大剂量100 U/Kg。在长期维持期,调整个体rHuEpo剂量以将Hb维持在10 - 12 g/dl的目标水平。在治疗开始前及之后每月进行基线血液检查。Hb水平在第4周显著升高,在最初3个月末只有4例患者对rHuEpo无反应。这些患者的基线血清铁蛋白水平低于100 ng/ml,当用口服铁纠正这种缺乏时反应良好。当血细胞比容(Hct)达到30 - 35 vol%时,rHuEpo剂量可减少(150至200 U/Kg/周)。随着维持期开始,血清铁蛋白水平从平均基线水平247.8±196降至121.1±154.9 ng/ml,下降了51%(p<0.05)。

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