Demonstrates improved clinical outcomes using cord blood red cells in preterm neonates, suggesting a shift in transfusion practices.
BACKGROUND: The BORN trial suggested that using cord blood-red blood cells (CB-RBCs) to transfuse severely preterm neonates significantly improves clinical outcomes compared to standard adult donor RBCs (A-RBC). STUDY DESIGN AND METHODS: The study illustrates CB-RBC concentrate production and inventory management across nine CB banks participating in the BORN trial. Quality requirements were those established by the European regulation for leukocyte-depleted RBC concentrates in additive solution. The compliance rate among centers was reported. RESULTS: and end-storage hemolysis below 0.8% in more than 90% of cases. CB-RBC availability was significantly limited by the time required for bacterial testing results and the need for γ-irradiation. DISCUSSION: These data suggest that the standardized CB-RBC production is reproducible. Moreover, extending CB-RBC storage to 21 days could maximize the inventory utility.
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Pellegrino et al. (2026) studied this question.
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