Revisiting ABO incompatibility as a risk factor for significant neonatal hyperbilirubinemia
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Updated: Jan 26, 2026

Assessment and Evaluation of the High Risk Neonate: The NICU Network Neurobehavioral Scale
Published on: August 25, 2014
Ritika Khurana1, Prerna Batra2, Mma Faridi3
11 Senior Resident, Department of Pediatrics, University College of Medical Sciences (University of Delhi) and Guru Tegh Bahadur Hospital, Delhi, India.
Insights
Newborns with ABO incompatibility do not require prolonged hospital stays. Bilirubin levels at 48 and 96 hours were similar in infants with and without ABO incompatibility, indicating no increased risk.
Area of Science:
- Neonatal Medicine
- Pediatrics
- Hematology
Background:
- ABO incompatibility is a common cause of neonatal jaundice.
- Current practices often involve frequent biochemical screening and extended hospital stays for affected infants.
Purpose of the Study:
- To compare serum bilirubin levels at 48 and 96 hours of age in neonates with and without ABO incompatibility.
- To evaluate the necessity of prolonged hospitalization for neonates with ABO incompatibility.
Main Methods:
- Prospective study of 184 neonates (≥34 weeks gestation), divided into groups with and without ABO incompatibility (92 each).
- Direct Coombs test performed on cord blood.
- Serum bilirubin, hematocrit, and reticulocyte counts were measured at 48 and 96 hours.
Main Results:
- Mean serum bilirubin and hematocrit levels were comparable between groups at 48 and 96 hours.
- Mean reticulocyte count was significantly higher in neonates with ABO incompatibility.
- No increased risk of significant hyperbilirubinemia observed in neonates with ABO incompatibility.
Conclusions:
- Late preterm and term neonates with and without ABO incompatibility exhibit similar bilirubin levels.
- Prolonged hospitalization for neonates with ABO incompatibility is likely unnecessary.
- Routine biochemical screening frequency may be re-evaluated for these infants.
Abstract:
Babies with ABO incompatibility are often advised frequent biochemical screening and prolonged hospital stay. Our primary objective of the study was to compare serum bilirubin levels at 48 h and 96 h of age in neonates with and without ABO incompatibility. Our prospective study included neonates with gestation ≥ 34 weeks, with or without ABO incompatibility (92 in each group). A direct Coombs test was performed on cord blood. The mean serum bilirubin and haematocrit levels in both groups at 48 h and 96 h were comparable. The mean reticulocyte count of babies with ABO incompatibility was, however, significantly higher. Late preterm and term neonates with and without ABO incompatibility have similar bilirubin levels and no increased risk of significant hyperbilirubinemia. Prolonged hospitalisation of these neonates appears to be unnecessary.
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