Erythropoietin in the treatment of anaemia of chronic renal failure

Erythropoietin in the treatment of anaemia of chronic renal failure

Human recombinant erythropoietin was administered subcutaneously to 26 chronic haemodialysis patients over a six month period, and the effect of erythropoiesis investigated. Initial therapy was 4000 units twice weekly with therapy titrated to individual response after 1 month. Mean EPO dosage was 150 ± 51 u/kg/week at the start of the study and 112 ± 50 u/kg/week at 6 months. The mean haemoglobin level rose from 6.7 ± 1.7 gr/dl at the start of treatment to 9.1 ± 1.9 gr/dl at 3 months (p<0.01) and 9.6 ± 1.9 gr/dl at 6 months. Simultaneously the mean haematocrit rose from 21 ± 4.8 to 28.3 ± 6.2 at 3 months (p<0.01) and 29.3 ± 4.6 at 6 months. Platelet count and white cell count were unaffected by therapy. Treatment failure occurred in 5 patients and seizures were seen in 4 patients. EPO therapy was not associated with increase in blood pressure.

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  • Fyhraqist F, Rosen lof K, Qronhagen R C, et al. Is renin substrate an erythropoietin precursor? nature 1984; 308:649-652.