The effects of recombinant human erythropoietin given immediately after delivery to women with anaemia

Curr Med Res Opin. 2003;19(4):346-9. doi: 10.1185/030079903125001802.

Abstract

Objective: Anaemia is a common problem during pregnancy and the puerperium. This study was designed to determine the efficacy and safety of giving recombinant human erythropoietin (EPO) to anaemic women during the puerperium.

Method: Thirty-seven women received a single dose of EPO (20 000 IU intravenously) immediately after delivery. A control population (n = 37) matched according to age and haemoglobin concentration was evaluated. All women received oral iron supplementation for 40 days after delivery. Haemoglobin concentrations were measured 4 and 40 days after delivery. Blood transfusions were given depending on clinical condition and haemoglobin level.

Results: Patients treated with EPO had a significantly higher mean haemoglobin concentration than control patients at days 4 and 40. No women in the EPO group required a transfusion, compared with six in the control group. No side-effects and fewer anaemia-related symptoms were observed during EPO treatment.

Conclusion: EPO given at delivery is effective in decreasing the need for blood transfusion and the incidence of problems associated with anaemia during the puerperium.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Anemia / blood
  • Anemia / prevention & control*
  • Delivery, Obstetric*
  • Erythropoietin / therapeutic use*
  • Female
  • Hemoglobins / analysis
  • Humans
  • Iron / therapeutic use
  • Postoperative Period
  • Postpartum Period
  • Pregnancy
  • Recombinant Proteins
  • Treatment Outcome

Substances

  • Hemoglobins
  • Recombinant Proteins
  • Erythropoietin
  • Iron