[重组红细胞生成素在血液透析肾功能不全终末期继发性贫血中的应用]。

Acta medica Iugoslavica Pub Date : 1990-01-01
V Gasparović, Z Puretić, B Vrhovac, M Gjurasin, D Puljević
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引用次数: 0

摘要

本组6例终末期肾功能不全患者接受血液透析治疗,给予50 IU/kg体重的促红细胞生成素(EPO)静脉滴注,每周定期随访血象,每月进行其他实验室评价。研究开始时,红细胞数量为2.2 +/- 0.3 × 10(12)/l。4周后为2.3 +/- 0.4 (p = 0.001), 8周后为2.8 +/- 0.4 (p = 0.007), 12周后为3.2 +/- 0.3。开始时血红蛋白为70 +/- 8 g/l, 4周后为76.3 +/- 13.7 (NS), 8周后为95.7 +/- 14.3 (p = 0.008), 12周后为102.2 +/- 12 (p = 0.001)。12周后,红细胞压积值从研究开始时的21.4 +/- 3.4上升到32.1 +/- 3.6 (p = 0.001)。试验显示EPO对血清钾无显著影响,试验开始时为5.3 +/- 0.4 mmol/l, 12周后为5.6 +/- 0.8 mmol/l;血小板从132.8 +/- 2.4 × 10(9)/l上升到155.2 +/- 42.2的速率也不显著。结果表明,在肾功能不全终末期接受促红细胞生成素治疗的患者红细胞有明显改善,并对其一般状况有影响。一名女性患者因严重的骨痛被排除在研究参与之外。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Use of recombinant erythropoietin on secondary anemia in patients in the terminal phase of renal insufficiency on hemodialysis].

A group of 6 patients with a history of end-stage renal insufficiency on hemodialysis was receiving erythropoietin (EPO) in a dosage of 50 IU/kg body weight i. v. The hemogram values were followed regularly every week and the patients underwent other laboratory evaluations every month. At the beginning of the study, the number of erythrocytes amounted to 2.2 +/- 0.3 x 10(12)/l. After 4 weeks it was 2.3 +/- 0.4 (NS) (p = 0.001), after 8 weeks 2.8 +/- 0.4 (p = 0.007), and after 12 weeks 3.2 +/- 0.3. At the beginning, hemoglobin was 70 +/- 8 g/l, after 4 weeks 76.3 +/- 13.7 (NS), after 8 weeks 95.7 +/- 14.3 (p = 0.008), and after 12 weeks 102.2 +/- 12 (p = 0.001). The hematocrit value rose from 21.4 +/- 3.4 at the beginning of the study to 32.1 +/- 3.6 (p = 0.001) after 12 weeks. The trial showed no significant effect of EPO on serum potassium which amounted to 5.3 +/- 0.4 mmol/l at the beginning of the trial and 5.6 +/- 0.8 (NS) after 12 weeks; the rate of the rise of platelets from 132.8 +/- 2.4 x 10(9)/l to 155.2 +/- 42.2 was not significant either. The results demonstrate a marked improvement in the red blood cells of patients receiving EPO in the end-stage of renal insufficiency and its influence on their general condition. One female patient was excluded from the study participation because of a severe bone pain.

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