Subcutaneous recombinant human erythropoietin in children with renal anemia on continuous ambulatory peritoneal dialysis

Acta Paediatr. 1993 Nov;82(11):959-62. doi: 10.1111/j.1651-2227.1993.tb12608.x.

Abstract

Subcutaneous recombinant human erythropoietin (rHuEpo) treatment of renal anemia was performed in four boys and eight girls on CAPD, aged 0.8-12.5 (mean 7.4) years. In contrast to previous studies, our therapeutic goal was not set with a hematocrit of 30% but with full correction of anemia. Following a maximum weekly rHuEpo dosage of median 120 (range 100-240) IU/kg body weight, hematocrit increased in 10 children from 24 (14-29)% within 12 (4-17) weeks to 40.1 (33.5-48.4)%. The weekly increase in hematocrit was 1.27 (0.5-3.1)%. The corrected reticulocyte count increased from 1.3 (0.7-1.8)% to 2.3 (1.4-3.9)% within 4 (2-6) weeks. Eight children fulfilled the protocol; six with an uncomplicated course were able to maintain a hematocrit of 37.1 (35.1-42.7)% with only one sc medication per week of approximately two-thirds of their highest weekly rHuEpo dosage. No serious adverse effect of rHuEpo therapy was observed.

MeSH terms

  • Anemia / blood
  • Anemia / drug therapy*
  • Anemia / etiology
  • Body Weight / drug effects
  • Child
  • Child, Preschool
  • Dose-Response Relationship, Drug
  • Erythropoietin / adverse effects
  • Erythropoietin / therapeutic use*
  • Female
  • Follow-Up Studies
  • Hematocrit
  • Humans
  • Infant
  • Injections, Subcutaneous
  • Kidney Failure, Chronic / blood
  • Kidney Failure, Chronic / complications*
  • Kidney Failure, Chronic / therapy
  • Male
  • Peritoneal Dialysis, Continuous Ambulatory*
  • Recombinant Proteins / adverse effects
  • Recombinant Proteins / therapeutic use
  • Reticulocyte Count / drug effects

Substances

  • Recombinant Proteins
  • Erythropoietin