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Updated: Aug 25, 2026

Intravenous Injections in Neonatal Mice
Published on: November 11, 2014
[Erythropoietin administration to preterm infants: comparison between subcutaneous and intravenous route]
V Rigourd1, F Kieffer, M A Dommergues
1Service de réanimation néonatale, institut de puériculture et de périnatalogie, 26, boulevard Brune, 75014 Paris, France. ipp.rigourd@free.fr
Insights
Subcutaneous recombinant human erythropoietin (rHuEpo) significantly reduces transfusions in preterm infants compared to intravenous routes. This finding supports subcutaneous administration for treating anemia of prematurity.
Area of Science:
- Neonatal Medicine
- Hematology
- Pharmacology
Background:
- Anemia of prematurity is a common complication in preterm infants.
- Recombinant human erythropoietin (rHuEpo) is used to stimulate red blood cell production.
- The optimal administration route for rHuEpo in preterm infants remains debated.
Purpose of the Study:
- To compare the effectiveness of one-month rHuEpo treatment based on administration route.
- To evaluate the impact of subcutaneous, continuous infusion, and direct intravenous rHuEpo on hematological parameters and transfusion needs.
Main Methods:
- Retrospective study of 64 preterm infants.
- Three groups received weekly rHuEpo: subcutaneous injections (750 IU/kg), continuous infusion in TPN (1050 IU/kg), or direct intravenous injections (750 IU/kg).
- Effectiveness assessed by reticulocyte count, hemoglobin levels, and blood transfusion incidence.
Main Results:
- Subcutaneous rHuEpo resulted in significantly higher hemoglobin levels (10.3 g/dl) and reticulocyte counts (216,000/mm3) compared to continuous infusion (8.8 g/dl, 123,000/mm3) and intravenous routes (9.6 g/dl, 190,000/mm3).
- The incidence of blood transfusions was significantly lower with subcutaneous administration (21.2%) versus continuous infusion (40%) and intravenous routes (75%).
- Ferritin levels and phlebotomy losses did not differ significantly between groups.
Conclusions:
- Subcutaneous administration of rHuEpo is more effective in reducing transfusion requirements in preterm infants compared to intravenous routes.
- The study recommends subcutaneous rHuEpo (250 IU/kg three times weekly) for treating anemia of prematurity pending further research.
- Further studies and new molecules are needed to optimize anemia treatment in preterm infants.
Objective:
Our aim was to compare the effectiveness of a one-month treatment with recombinant human erythropoietine (rHuEpo) according to the administration route.
Methods:
Retrospective study based on the data collection from medical files of 64 preterm infant hospitalized in the "institut de puériculture et de périnatalogie" (Paris) between January 13th, 2002 and April 13th, 2002. The first group (N =33) was treated by subcutaneous rHuEpo 750 IU/kg per week, in three injections by week, for one month. The second group (N =15) was treated by continuous infusion of rHuEpo in total parenteral nutrition 1050 IU/kg per week (30% augmentation to compensate the amount absorbed by the filter). The third group (N =16) received 750 IU/kg per week of rHuEpo in three direct intravenous injections. The effectiveness of rHuEpo was evaluated by the absolute reticulocyte count, the level of hemoglobin and the incidence of blood transfusion (multiple logistic analysis of variant and regression).
Results:
The absolute reticulocyte count and hemoglobin level were significantly reduced after one month of treatment by continuous infusion of rHuEpo in total parenteral nutrition and direct intravenous injections compared with a one-month treatment by subcutaneous rHuEpo. Hemoglobine level were at 8.8 and 9.6 g/dl vs 10.3 g/dl (P =0.02) and absolute reticulocyte count at 123,000/mm3 and 190,000/mm3 vs 216,000/mm3 (p =0.001). The number of transfused infants was significantly increased with utilization of continuous (40%) and direct intravenous (75%) compared with those treated by subcutaneous route (21.2%) while the ferritin level and phlebotomy losses were not significantly different in the three groups. The number of blood transfusion was significantly linked to phlebotomy losses and administration route of rHuEpo.
Conclusion:
Our study tends to demonstrate that rHuEpo administered subcutaneously reduces significantly the number of transfusion in contrary to intravenous routes. Waiting for pilot study and new molecules, we recommend subcutaneous administration of rHuEpo to preterm infants 250 IU/kg three times weekly in the treatment of anemia of prematurity.
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