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Published on: October 16, 2015
Effect of ibuprofen on bilirubin-albumin binding affinity in premature infants
Sanjiv B Amin1, Nicholas Miravalle
1Division of Neonatology, Department of Pediatrics, University of Rochester Medical Center, Rochester, NY, USA. Sanjiv_Amin@urmc.rochester.edu
Insights
Ibuprofen did not significantly alter bilirubin-albumin binding or increase unbound bilirubin in premature infants with hyperbilirubinemia. This suggests ibuprofen is likely safe for this patient population regarding bilirubin displacement.
Area of Science:
- Neonatalogy
- Pharmacology
- Biochemistry
Background:
- Unconjugated hyperbilirubinemia is common in premature infants.
- Ibuprofen is used for patent ductus arteriosus in neonates.
- Concerns exist regarding ibuprofen's potential to displace bilirubin from albumin.
Purpose of the Study:
- To assess the impact of ibuprofen on bilirubin-albumin binding affinity.
- To determine if ibuprofen affects unbound bilirubin levels in premature infants.
Main Methods:
- Prospective study design with infants serving as their own controls.
- Inclusion of premature infants (<30 weeks gestational age) with unconjugated hyperbilirubinemia receiving ibuprofen.
- Measurement of total serum bilirubin and unbound bilirubin before and after ibuprofen initiation; calculation of bilirubin/albumin binding constant.
Main Results:
- Ten infants were studied.
- No significant changes in total serum bilirubin, unbound bilirubin, or bilirubin/albumin binding constant were observed after ibuprofen administration.
- The ratio of unbound bilirubin with and without ibuprofen (0.88) indicated no significant displacing effect.
Conclusions:
- Ibuprofen does not appear to displace bilirubin from albumin in stable premature infants with mild to moderate unconjugated hyperbilirubinemia.
- The findings suggest ibuprofen may be safely used in this population without increasing the risk of bilirubin-induced neurotoxicity due to displacement.
Aim:
To evaluate the effect of ibuprofen on bilirubin-albumin binding affinity and unbound bilirubin in premature infants.
Study Design:
A prospective study with subjects serving as their own controls was performed on <30 weeks' gestational age infants with unconjugated hyperbilirubinemia and who received ibuprofen for patent ductus arteriosus. Infants with congenital malformation, TORCH infections, and conjugated hyperbilirubinemia were excluded. Total serum bilirubin (TSB) and unbound bilirubin (modified peroxidase test) were measured prior to (baseline) and after (follow-up) initiation of ibuprofen. The bilirubin/albumin equilibrium association binding constant was calculated using albumin, TSB, and unbound bilirubin.
Results:
Ten infants were studied. The mean TSB between baseline (5.9±1.7 mg/dL) was higher than that at follow-up [4.9±1.7 mg/dL]. Mean unbound bilirubin at baseline (0.75±0.65 microg/dL) was similar to that at follow-up (0.63±0.46 microg/dL). No difference existed between mean baseline binding constant (49±50 L/micromol) and that at follow-up (44±36 L/micromol). The ratio of unbound bilirubin with and without ibuprofen, index of displacing effect, was 0.88 (95% CI 0.63-1.14).
Conclusions:
Ibuprofen may not be associated with bilirubin displacing effect in relatively stable premature infants with mild to moderate unconjugated hyperbilirubinemia.
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