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Does Ibuprofen increase neonatal hyperbilirubinemia?
Enrico Zecca1, Costantino Romagnoli, Maria Pia De Carolis
1Division of Neonatology, Department of Pediatrics, University Hospital A Gemelli, Catholic University of the Sacred Heart, Rome, Italy. enrizecca@rm.unicatt.it
Insights
Ibuprofen exposure in preterm infants was linked to higher bilirubin levels and increased need for phototherapy. This suggests a potential impact on infant jaundice management and treatment duration.
Area of Science:
- Neonatal Medicine
- Pharmacology
Background:
- Ibuprofen is used to prevent patent ductus arteriosus in preterm infants.
- Hyperbilirubinemia is a common concern in neonates.
Purpose of the Study:
- To investigate the association between ibuprofen exposure and hyperbilirubinemia in preterm infants.
Main Methods:
- Retrospective comparison of 418 infants receiving ibuprofen prophylaxis (2000-2007) versus 288 infants not exposed (1993-1999).
- Infants were all less than 30 weeks of gestation.
Main Results:
- The ibuprofen group showed significantly higher peak total serum bilirubin levels (9.0 vs 7.3 mg/dL).
- Increased need for and duration of phototherapy was observed in the ibuprofen group.
- No significant differences were found in gestational age, birth weight, G6PD deficiency, hypoalbuminemia, hemolytic isoimmunization, or exchange-transfusion rates.
Conclusions:
- Ibuprofen administration is associated with elevated peak total serum bilirubin levels in preterm infants.
- This can lead to more pronounced hyperbilirubinemia and necessitate longer phototherapy.
- Competition in the hepatic glucuronidation pathway is a potential mechanism.
Objective:
The aim of this study was to investigate whether ibuprofen exposure was associated with increased hyperbilirubinemia in preterm infants.
Methods:
Since 2000, ibuprofen has been administered to all infants at <30 weeks of gestation who are admitted to our unit, to prevent patent ductus arteriosus. We retrospectively compared data for 418 infants subjected to ibuprofen prophylaxis (2000-2007) and 288 infants not exposed to ibuprofen (1993-1999).
Results:
The ibuprofen group had a significantly higher peak total serum bilirubin level (9.0 +/- 2.5 mg/dL vs 7.3 +/- 3.3 mg/dL), more need for phototherapy (398 infants [95%] vs 254 infants [87.6%]), and a longer phototherapy duration (94.3 +/- 43.6 hours vs 87.2 +/- 38.6 hours). Groups did not differ with respect to gestational age, birth weight, gender ratio, glucose-6-phosphate dehydrogenase deficiency incidence, or hypoalbuminemia (<2.5 g/dL) incidence. Hemolytic isoimmunization was diagnosed with similar incidences (no-ibuprofen group: 7 of 288 infants; ibuprofen group: 8 of 418 infants). The rates of exchange-transfusion also were similar between the groups (no-ibuprofen group: 14 infants [4.8%]; ibuprofen group: 19 infants [4.5%]).
Conclusions:
Ibuprofen administration was associated with higher peak total serum bilirubin levels, and the more-pronounced hyperbilirubinemia led to longer phototherapy. The potential role of competition between ibuprofen and bilirubin in the hepatic glucuronidation pathway is discussed.
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