An approach to using recombinant erythropoietin for neuroprotection in very preterm infants

Pediatrics. 2008 Aug;122(2):375-82. doi: 10.1542/peds.2007-2591.

Abstract

Objective: Erythropoietin has been shown to be protective against hypoxic-ischemic and inflammatory injuries in cell culture, animal models of brain injury, and clinical trials of adult humans. The rationale for our study was that early administration of high-dose recombinant human erythropoietin may reduce perinatal brain injury (intraventricular hemorrhage and periventricular leukomalacia) in very preterm infants and improve neurodevelopmental outcome. We investigated whether administration of high-dose recombinant human erythropoietin to very preterm infants shortly after birth and subsequently during the first 2 days is safe in terms of short-term outcome.

Methods: This was a randomized, double-masked, single-center trial with a 2:1 allocation in favor of recombinant human erythropoietin. Preterm infants (gestational age: 24 to 31 weeks) were given recombinant human erythropoietin or NaCl 0.9% intravenously 3, 12 to 18, and 36 to 42 hours after birth.

Results: The percentage of infants who survived without brain injury or retinopathy was 53% in the recombinant human erythropoietin group and 60% in the placebo group. There were no relevant differences regarding short-term outcomes such as intraventricular hemorrhage, retinopathy, sepsis, necrotizing enterocolitis, and bronchopulmonary dysplasia. For 5 infants who were in the recombinant human erythropoietin group and had a gestational age of <26 weeks, withdrawal of intensive care was decided (3 of 5 with severe bilateral intraventricular hemorrhage, 2 of 5 with pulmonary insufficiency); no infant of the control group died. Recombinant human erythropoietin treatment did not result in significant differences in blood pressure, cerebral oxygenation, hemoglobin, leukocyte, and platelet count.

Conclusions: No significant adverse effects of early high-dose recombinant human erythropoietin treatment in very preterm infants were identified. These results enable us to embark on a large multicenter trial with the aim of determining whether early high-dose administration of recombinant human erythropoietin to very preterm infants improves neurodevelopmental outcome at 24 months' and 5 years' corrected age.

Publication types

  • Clinical Trial, Phase II
  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Apgar Score
  • Brain Diseases / drug therapy
  • Brain Diseases / mortality
  • Brain Diseases / prevention & control*
  • Cerebral Hemorrhage / drug therapy
  • Cerebral Hemorrhage / mortality
  • Cerebral Hemorrhage / prevention & control
  • Developmental Disabilities / drug therapy
  • Developmental Disabilities / mortality
  • Developmental Disabilities / prevention & control*
  • Dose-Response Relationship, Drug
  • Double-Blind Method
  • Drug Administration Schedule
  • Erythropoietin / administration & dosage*
  • Female
  • Follow-Up Studies
  • Gestational Age
  • Humans
  • Infant, Newborn
  • Infant, Premature, Diseases / diagnosis
  • Infant, Premature, Diseases / drug therapy*
  • Infant, Premature, Diseases / mortality
  • Infant, Very Low Birth Weight*
  • Intensive Care Units, Neonatal
  • Male
  • Maximum Tolerated Dose
  • Probability
  • Recombinant Proteins
  • Reference Values
  • Retinopathy of Prematurity / drug therapy
  • Retinopathy of Prematurity / prevention & control
  • Risk Assessment
  • Survival Analysis
  • Treatment Outcome

Substances

  • Recombinant Proteins
  • Erythropoietin