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Persistent abnormal liver fibrosis after weaning off parenteral nutrition in pediatric intestinal failure
Annika Mutanen1, Jouko Lohi, Päivi Heikkilä
1Section of Pediatric Surgery, Children's Hospital, Helsinki University Central Hospital, University of Helsinki, Helsinki, Finland. annika.mutanen@helsinki.fi
Insights
Pediatric intestinal failure (IF) can cause long-term liver damage, including fibrosis and steatosis, even after parenteral nutrition (PN) cessation. Extensive small bowel resection is a key predictor of liver fibrosis in these patients.
Area of Science:
- Hepatology
- Pediatric Gastroenterology
- Intestinal Failure Management
Background:
- Pediatric intestinal failure (IF) poses significant long-term health challenges.
- Liver disease is a known complication of IF, particularly in patients requiring parenteral nutrition (PN).
- Understanding the persistent effects of IF on liver histology is crucial for patient management.
Purpose of the Study:
- To evaluate the long-term impact of pediatric intestinal failure (IF) on liver histology.
- To assess the persistence of liver abnormalities after weaning from parenteral nutrition (PN).
- To identify predictors of liver fibrosis in patients with IF.
Main Methods:
- Liver biopsy, gastroscopy, abdominal ultrasound, and laboratory tests were performed on 38 IF patients.
- Patients were categorized into those currently on PN and those weaned off PN.
- A control group of 15 transplant donor livers was included for comparison.
Main Results:
- Abnormal liver histology was prevalent in 94% of patients on PN and 77% of those weaned off PN.
- Cholestasis and portal inflammation were significantly more common in patients on PN.
- Liver fibrosis and steatosis were common in both groups, with fibrosis stage associated with small bowel length and septic episodes.
Conclusions:
- Significant liver fibrosis and steatosis persist long-term after weaning from PN in pediatric IF patients.
- While cholestasis and portal inflammation may resolve, fibrosis remains a concern.
- Extensive small intestinal resection emerged as the primary predictor for liver fibrosis stage.
Unlabelled:
The aim of this study was to evaluate the long-term effects of pediatric intestinal failure (IF) on liver histology. Altogether, 38 IF patients (median age: 7.2 years; range, 0.2-27) underwent liver biopsy, gastroscopy, abdominal ultrasound, and laboratory tests. Sixteen patients were on parenteral nutrition (PN) after 74 PN months (range, 2.5-204). Twenty-two had weaned off PN 8.8 years (range, 0.3-27) earlier, after 35 PN months (range, 0.7-250). Fifteen transplant donor livers served as controls. Abnormal liver histology was found in 94% of patients on PN and 77% of patients weaned off PN (P = 0.370). During PN, liver histology weighted with cholestasis (38% of patients on PN versus 0% of patients weaned off PN; P = 0.003) and portal inflammation (38% versus 9%; P = 0.050) were found. Fibrosis (88% versus 64%; P = 0.143; Metavir stage: 1.6 [range, 0-4] versus 1.1 [range, 0-2]; P = 0.089) and steatosis (50% versus 45%; P = 1.000) were equally common during and after weaning off PN. Plasma alanine aminotransferase (78 U/L [range, 19-204] versus 34 [range, 9-129]; P = 0.009) and conjugated bilirubin (43 μmol/L [range, 1-215] versus 4 [range, 1-23]; P = 0.037) were significantly higher during than after weaning off PN. Esophageal varices were encountered in 1 patient after weaning off PN. Metavir stage was associated with small bowel length (r = -0.486; P = 0.002) and number of septic episodes (r = 0.480; P = 0.002). In a multivariate analysis, age-adjusted small bowel length (ß = -0.533; P = 0.001), portal inflammation (ß = 0.291; P = 0.030), and absence of an ileocecal valve (ß = 0.267; P = 0.048) were predictive for fibrosis stage.
Conclusion:
Despite resolution of cholestasis and portal inflammation, significant liver fibrosis and steatosis persist after weaning off PN. Extensive small intestinal resection was the major predictor for liver fibrosis stage.
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