Schaefer R M, Kürner B, Zech M, Krahn R, Heidland A
Abteilung Nephrologie, Medizinische Universitätsklinik Würzburg.
Dtsch Med Wochenschr. 1988 Jan 29;113(4):125-9. doi: 10.1055/s-2008-1067605.
The effectiveness of recombinant human erythropoietin (r-HEPO) was tested in 15 haemodialysis patients. The dosage was started at 24 IU/kg three times weekly, as an intravenous bolus at the end of the dialysis session, and then doubled every two weeks as long as the rise in haemoglobin was less than 2 g/dl. During treatment the reticulocyte count rose from 31 +/- 5 x 10(3)/microliters to 152 +/- 11 x 10(3)/microliters after 16 weeks. The haematocrit rose from 0.24 +/- 0.01 to 0.36 +/- 0.002. At the beginning of treatment the haemoglobin level was 7.3 +/- 0.3 g/dl and rose during treatment to 11.3 +/- 0.2 g/dl. Three patients developed hypertension and in two their Cimino shunt closed. but there were no toxic side effects, organ damage, allergic reactions or antibodies against the hormone. The results show that the anaemia of patients on chronic dialysis can be treated effectively and without serious side effects with r-HEPO.
在15名血液透析患者中测试了重组人促红细胞生成素(r-HEPO)的有效性。剂量从每周三次、每次24国际单位/千克开始,在透析 session结束时静脉推注,然后每两周加倍,只要血红蛋白升高小于2克/分升。治疗期间,网织红细胞计数在16周后从31±5×10³/微升升至152±11×10³/微升。血细胞比容从0.24±0.01升至0.36±0.002。治疗开始时血红蛋白水平为7.3±0.3克/分升,治疗期间升至11.3±0.2克/分升。三名患者出现高血压,两名患者的Cimino分流关闭。但未出现毒性副作用、器官损伤、过敏反应或针对该激素的抗体。结果表明,慢性透析患者的贫血可用r-HEPO有效治疗且无严重副作用。