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Updated: Feb 14, 2026

Ex Vivo Hepatic Perfusion Through the Portal Vein in Mouse
Published on: March 9, 2022
Metabolic profile of children with extrahepatic portal vein obstruction undergoing meso-Rex bypass
Timothy B Lautz1, Simon Eaton2, Lisa Keys1
1Department of Surgery, Ann & Robert H Lurie Children's Hospital of Chicago, Feinberg School of Medicine of Northwestern University, Chicago, Illinois.
Insights
Extrahepatic portal vein obstruction (EHPVO) in children causes malnutrition and growth hormone resistance, leading to growth restriction. A meso-Rex bypass improves nutritional markers like prealbumin and insulin-like growth factor 1 (IGF-1), aiding growth recovery.
Area of Science:
- Pediatric surgery
- Gastroenterology
- Endocrinology
Background:
- Extrahepatic portal vein obstruction (EHPVO) is linked to growth restriction in children.
- The underlying physiological mechanism for this growth delay remains unclear.
Purpose of the Study:
- To investigate the mechanism of growth delay in children with EHPVO.
- To detail the metabolic and nutritional profiles before and after meso-Rex bypass surgery.
Main Methods:
- Prospective study of 20 children with EHPVO before and 1 year after meso-Rex bypass.
- Assessment of caloric balance (intake, expenditure, stool loss) and laboratory markers of nutrition and growth hormone resistance.
Main Results:
- Successful bypass in 15 children improved low prealbumin levels (P=0.026).
- Insulin-like growth factor 1 (IGF-1) levels, initially low, increased significantly post-surgery (P=0.047).
- Caloric intake, energy expenditure, and stool losses were within normal ranges.
Conclusions:
- Children with EHPVO exhibit malnutrition and growth hormone resistance contributing to growth restriction.
- Meso-Rex bypass positively impacts prealbumin and IGF-1 levels, suggesting a mechanism for improved growth.
Background:
Extrahepatic portal vein obstruction (EHPVO) in children is often associated with growth restriction, which improves after the restoration of portal venous flow with a meso-Rex bypass, but the physiologic mechanism is unknown. The purpose of this study was to investigate the mechanism of growth delay in children with EHPVO by detailing the metabolic and nutritional profile before and after meso-Rex bypass.
Methods:
Twenty consecutive children with EHPVO were prospectively studied before and 1 year after meso-Rex bypass. Caloric balance was determined by investigating caloric intake via a calorie count, total energy expenditure via a doubly labeled water isotope assay and stool caloric loss by bomb calorimetry. Laboratory markers of nutrition and growth hormone resistance were tested.
Results:
Fifteen of the 20 children underwent successful meso-Rex bypass at a median age of 4.3 years. Prealbumin level was abnormally low (14.6 ± 3.0 mg/dL) at surgery but improved (17.0 ± 4.3 mg/dL) 1 year later (P = 0.026). Mean insulin-like growth factor 1 (IGF-1) level at baseline was 1.57 standard deviations below normal. IGF-1 levels increased from 88.3 ± 38.9 to 117.3 ± 54.5 ng/mL in the year after surgery (P = 0.047). Caloric intake divided by basal metabolic rate (1.90 ± 0.61), total energy expenditure (97.2 ± 15.0% of expected), and stool caloric losses (3.7 ± 1.8% of caloric intake) were all normal at baseline.
Conclusions:
Children with EHPVO suffer from malnutrition and growth hormone resistance, which may explain their well-established finding of growth restriction. Prealbumin and IGF-1 levels improve after a successful meso-Rex bypass.
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