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Clofibrate for unconjugated hyperbilirubinemia in neonates: a systematic review
Tao Xiong1, Dapeng Chen, Zhoujin Duan
1Department of Pediatrics, West China Second University Hospital, Sichuan University, Chengdu, China.
Insights
Clofibrate may reduce the need for and duration of phototherapy in newborns with unconjugated hyperbilirubinemia. Further research is needed to confirm its long-term safety and efficacy.
Area of Science:
- Neonatal Medicine
- Pharmacology
- Evidence-Based Medicine
Background:
- Unconjugated hyperbilirubinemia is a common condition in newborns.
- Phototherapy is a standard treatment, but may have limitations.
- Alternative or adjunctive treatments are being explored.
Purpose of the Study:
- To systematically review and meta-analyze the efficacy of clofibrate for treating unconjugated hyperbilirubinemia in neonates.
- To assess the impact of clofibrate on phototherapy requirements and bilirubin levels.
Main Methods:
- Systematic review and meta-analysis of randomized controlled trials (RCTs) and quasi-RCTs.
- Adherence to Cochrane review group guidelines and PRISMA statement.
- Inclusion of 13 studies involving 867 infants.
Main Results:
- Clofibrate administration decreased the need for phototherapy (RR: 0.38) and shortened its duration.
- Reduced peak total serum bilirubin levels were observed with clofibrate treatment.
- Benefits were more pronounced in term infants and those without hemolytic diseases.
Conclusions:
- Clofibrate shows potential short-term benefits for neonatal hyperbilirubinemia, particularly in specific infant populations.
- Further large-scale RCTs with long-term follow-up are necessary to establish safety and long-term effects.
- The study did not provide data on mortality or kernicterus.
Objective:
To evaluate the effect of clofibrate for unconjugated hyperbilirubinemia in neonates.
Methods:
A systematic review with meta-analysis of randomized controlled trials or quasi-randomized controlled trials was conducted to evaluate the clofibrate treatment in neonates with unconjugated hyperbilirubinemia. We followed the guidelines from the Cochrane review group and the PRISMA statement.
Results:
Of 148 studies identified, a total of 13 studies on 867 infants were included. A single oral administration of clofibrate was associated with decreased need of phototherapy (RR:.38, 95% CI: 0.21 to 0.68), shortened duration of phototherapy (mean duration: 23.88 h, 95% CI: 33.03 to -14.72 h) and reduced peak total serum bilirubin (mean duration: -1.62 mg/dL, 95% CI: 2.13 to -1.11 mg/dL). These effects were especially obvious in term infants and infants without hemolytic diseases. Data regarding mortality or kernicterus were not available from included studies.
Conclusions:
Clofibrate may have short-term benefits for the infants with hyperbilirubinaemia, especially for population of term infants and infants without hemolytic diseases. Large RCTs with long-term followup are required to verify the safety of clofibrate and assess its long-term effects.
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