Recombinant erythropoietin in the prevention of late anaemia in intrauterine transfused neonates with Rh-haemolytic disease

Fetal Diagn Ther. 1999 Sep-Oct;14(5):270-4. doi: 10.1159/000020937.

Abstract

Objective: To evaluate the efficacy of recombinant human erythropoietin (rHuEPO) in prevention of late anaemia due to Rh-haemolytic disease in neonates subjected to one or more intrauterine transfusions (IUTs).

Study design: Six neonates (GA 28-38 weeks, BW 980-3,360 g), subjected to one or more IUTs for Rh-haemolytic disease, were treated for 3 weeks with rHuEPO (200 U/kg/day, s.c.) after the second week of life to prevent late anaemia and consequently reduce the need for blood transfusions. All treated neonates were supplemented weekly with iron, vitamin E and folinic acid, intramuscularly.

Results: Of the 6 patients studied, 4 preterm neonates, after commencement of rHuEPO treatment, showed a decrease in Hct values with persistent reticulocytopenia, and consequent need for one or more transfusions with packed and filtered red cells (PFRC). These 4 neonates had received a greater blood volume with IUTs than the 2 other term neonates, who, after starting rHuEPO treatment, showed an increase in Hct values and in reticulocyte count, with no transfusion requirements after birth (247 +/- 47 vs. 84 +/- 76 ml).

Conclusions: Our results seem to correlate the efficacy of erythropoietin treatment in prevention of late anaemia resulting from Rh-haemolytic disease to the severity of intrauterine anaemia and to gestational age. Erythropoietin, in fact, was less effective in cases of severe intrauterine anaemia requiring a high volume of PFRC; it was also less effective in the preterm babies, because of the simultaneous presence of anaemia of prematurity and other major diseases.

MeSH terms

  • Anemia / prevention & control*
  • Blood Transfusion, Intrauterine*
  • Erythroblastosis, Fetal / therapy*
  • Erythrocyte Transfusion
  • Erythropoietin / therapeutic use*
  • Hematocrit
  • Humans
  • Infant, Newborn
  • Infant, Premature / blood
  • Recombinant Proteins / therapeutic use
  • Reticulocyte Count / drug effects
  • Retreatment
  • Rh Isoimmunization / therapy*

Substances

  • Recombinant Proteins
  • Erythropoietin