Recombinant human erythropoietin in preterm infants: evaluation of one year of experience

Citation
As. Trentesaux et al., Recombinant human erythropoietin in preterm infants: evaluation of one year of experience, ARCH PED, 6(9), 1999, pp. 944-951
Citations number
28
Categorie Soggetti
Pediatrics
Journal title
ARCHIVES DE PEDIATRIE
ISSN journal
0929693X → ACNP
Volume
6
Issue
9
Year of publication
1999
Pages
944 - 951
Database
ISI
SICI code
0929-693X(199909)6:9<944:RHEIPI>2.0.ZU;2-U
Abstract
Recently, recombinant human erythropoietin (rhEPO) has been claimed to dimi nish red Blood cell transfusions in premature infants. After a year of expe rience, we investigated whether early rhEPO treatment would reduce the need for transfusion. Patients and methods. - Fifty premature infants of gestational age less tha n or equal to 32 weeks admitted to our NICU in 1997, received rhEPO 750 UI/ kg/week from day 3 to 5 for six weeks. They were compared with 50 untreated controls admitted in 1996. Results. - The treatment and control groups did not differ for gestational age, weight at birth, CRIB score, and blood losses. We were not able to det ect any difference in the number of transfused infants, and in the number o f transfusions per infant until discharge. However, treated infants receive d significantly fewer transfusions per infant between day 16 and day 45 (0. 42 +/- 0.67 vs. 0.8 +/- 0.99). Infants with a birth weight between 1,000-1, 250 g received fewer transfusions in the EPO group. Conclusion. - rhEPO treatment can be useful. but in association with other procedures: conservative transfusion criteria, ;minimization of phlebotomy losses and early iron supplementation. (C) 1999 Elsevier, Paris.