Pre exchange Albumin Administration in Neonates with Hyperbilirubinemia: A Randomized Controlled Trial

Indian Pediatr. 2015 Sep;52(9):763-7. doi: 10.1007/s13312-015-0713-z.

Abstract

Objective: To evaluate the efficacy of pre-exchange transfusion albumin priming in neonates with non-hemolytic hyperbilirubinemia.

Design: Single center, randomized controlled trial.

Setting: Level III Neonatal unit.

Participants: Fifty healthy term and late preterm neonates with non-hemolytic hyperbilirubinemia requiring exchange transfusion.

Interventions: 5 mL/kg of either 20% human albumin (n=23) or 0.9% saline (n=27) infusion one hour prior to exchange transfusion.

Main outcome measure: Post-exchange transfusion phototherapy duration.

Results: The post-exchange transfusion phototherapy duration was not different between albumin and saline groups [Median (IQR): 29 (24-48) h vs. 33 (24-43) h; P=0.76]. The total amount of bilirubin removed during exchange transfusion was also similar [Median (IQR): 34 (28-46) mg vs. 33 (27-38) mg; P=0.46]. Serial changes in total serum bilirubin following exchange transfusion and need for repeat exchange transfusion were comparable between the groups.

Conclusions: In healthy late preterm and term neonates with non-hemolytic hyperbilirubinemia, priming with 1 g/kg of 20% albumin prior to exchange transfusion is not superior to equi-volume 0.9% saline in reducing post- exchange transfusion phototherapy duration or amount of bilirubin mass removed.

Publication types

  • Randomized Controlled Trial

MeSH terms

  • Albumins / administration & dosage*
  • Albumins / therapeutic use
  • Exchange Transfusion, Whole Blood / methods*
  • Humans
  • Hyperbilirubinemia, Neonatal / therapy*
  • Infant, Newborn
  • Phytotherapy

Substances

  • Albumins