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Preventive effect of ursodeoxycholic acid on parenteral nutrition-associated liver disease in infants
Insights
Ursodeoxycholic acid (UDCA) treatment delayed the onset of parenteral nutrition-associated cholestasis in newborns. UDCA also reduced cholestasis symptoms and duration in infants receiving long-term parenteral nutrition (PN).
Area of Science:
- Neonatology
- Pediatric Gastroenterology
- Hepatology
Background:
- Parenteral nutrition-associated cholestasis is a recognized complication in infants requiring long-term nutritional support.
- Infants receiving prolonged parenteral nutrition (PN) are at risk for developing cholestasis.
Purpose of the Study:
- To evaluate the efficacy of ursodeoxycholic acid (UDCA) in preventing and treating cholestasis in newborns on extended PN.
- To assess the impact of UDCA on the timing and severity of cholestasis in infants.
Main Methods:
- Retrospective study of 56 infants receiving prolonged PN.
- Comparison between a control group (lower birth weight infants) and groups treated with UDCA (pediatric and surgical patients).
- Monitoring of blood chemistries, including bilirubin, AST, ALT, and alkaline phosphatase.
Main Results:
- Cholestasis onset was significantly delayed in UDCA-treated infants compared to controls (39 and 34 days vs. 25 days).
- Peak levels of conjugated bilirubin, AST, ALT, and alkaline phosphatase were significantly lower in UDCA-treated groups.
- Duration of cholestasis was significantly reduced in all UDCA-treated infants.
Conclusions:
- Ursodeoxycholic acid (UDCA) is effective in delaying the onset and reducing the severity of parenteral nutrition-associated cholestasis in newborns.
- UDCA treatment significantly shortens the duration of cholestasis in infants on prolonged PN.
- The study did not find a difference in UDCA efficacy between lower and higher birth weight infants.
Introduction:
Parenteral nutrition-associated cholestasis is well recognized phenomenon in the term and preterm infant receiving long-term parenteral nutrition.
Objectives:
The aim of this study was to evaluate the effect of ursodeoxycholic acid (UDCA) use on cholestasis in newborns on prolonged TPN.
Methods:
A total of 56 infants were enrolled in this retrospective study: control group consisted of lower (1500 g) birth weight infants (n = 30), as well as the group of pediatric (n = 11) and surgical patients (n = 15) treated with UDCA. Blood chemistries were obtained two times weekly.
Results:
All of 56 newborns developed cholestasis but duration of parenteral nutrition (PN) before onset of cholestasis was significantly longer in UDCA treated patients. Average duration of PN before the onset of cholestasis in control group of patients was 25 days in distinction from treated pediatric and surgical patients (39 and 34 days, respectively).The peak serum conjugated bilirubin (CB), AST, ALT and alkaline phosphatase (AP) levels were significantly lower in the treated groups.There was no significant difference among treated pediatric and surgical patients and between lower and higher birth weight infants considering the CB, ALT, AST and AP peak. Duration of cholestasis was significantly decreased in all treated groups.There was a significant difference in time needed to achieve complete enteral intake between pediatric and surgical patient group.
Conclusion:
Cholestasis developed significantly later in treated groups than in the controls. UDCA appears to be very successful in reducing the symptoms of cholestasis. The difference in efficacy of UDCA treatment between lower and higher birth weight infants could not be proven.
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