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Indian Pediatr ; 1999 Jan; 36(1): 17-27
Article in English | IMSEAR | ID: sea-10758

ABSTRACT

OBJECTIVE: To evaluate safety and efficacy of recombinant human erythropoietin (r-HuEPO)in reducing the need for red cell transfusions in anemia of prematurity. METHODS: forty -two preterm infants (gestational age <32 weeks) were randomly assigned to a "treatment" group (r-HuEPO 400 units/kg every alternate day * 10 doses) or "no treatment" (control) group. All infants on enteral feeds received oral iron 3 mg/kg/day, graded up to 6 mg/kg/day. RESULTS: Higher reticulocyte counts in week 2 and 3 and higher hemoglobin levels in week 4 were noted after treatment with r-HuEPO. Despite stumulated erythropoiesis, the frequency of transfusions could not be reduced with r-HuEPO therapy.Overall, Phlebotomy losses, frequency and volume of redcell transfusions were significantly more in neonates with birthweight <1000 grams compared with those with birthweight >1000 grams (p<0.05). Associated side effects of r-HuEPO such as neutropenia,sepsis, hypertension or increased risk of late death did not occur. CONCLUSION:r-HuEPO therapy was safe without any side effects.Inability of r-HuEPO therapy to minimize red cell transfusions for anemia of prematurity may be explained by a relatively strict red-cell transfusion policy and the desired degree of treatment effect.


Subject(s)
Administration, Oral , Anemia/drug therapy , Birth Weight , Enteral Nutrition , Erythrocyte Count , Erythrocyte Transfusion , Erythropoiesis/drug effects , Erythropoietin/therapeutic use , Female , Follow-Up Studies , Hemoglobins/analysis , Humans , Hypertension/prevention & control , Infant, Newborn , Infant, Premature , Infant, Premature, Diseases/drug therapy , Infant, Very Low Birth Weight , Iron/administration & dosage , Male , Neutropenia/prevention & control , Phlebotomy/adverse effects , Reticulocytes/pathology , Safety , Sepsis/prevention & control , Survival Rate
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