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Updated: Jun 16, 2026

Tissue Engineering of the Intestine in a Murine Model
Published on: December 1, 2012
Medical management of pediatric intestinal failure
1University of Cincinnati College of Medicine, Nutrition and Intestinal Transplantation, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio 45229, USA. Samuel.kocoshis@cchmc.org
Insights
Outcomes for children with congenital enteropathies and short bowel syndrome have improved due to advances in understanding and treatment. New strategies, including nutritional support and therapies, enhance intestinal adaptation and reduce reliance on parenteral nutrition.
Area of Science:
- Pediatric Gastroenterology
- Intestinal Adaptation
- Congenital Enteropathies
Background:
- Significant improvements in outcomes for pediatric congenital enteropathies and short bowel syndrome over 20 years.
- Enhanced understanding of intractable diarrhea pathophysiology and genetic mutations.
- Advances in parenteral nutrition (TPN) and enteral alimentation strategies.
Purpose of the Study:
- To review advancements in managing congenital enteropathies and surgical short bowel syndrome.
- To highlight strategies promoting intestinal adaptation and independence from TPN.
- To discuss future therapeutic targets for improved outcomes.
Main Methods:
- Literature review of recent advancements in pediatric intestinal failure.
- Analysis of therapeutic strategies for congenital enteropathies and short bowel syndrome.
- Synthesis of current knowledge on intestinal adaptation mechanisms.
Main Results:
- Improved outcomes due to better understanding of disease mechanisms and targeted treatments.
- Enhanced nutritional support strategies (TPN and enteral) improve outcomes for short bowel syndrome.
- Ancillary therapies (acid suppression, antibiotics, prokinetics, fiber) accelerate adaptation.
Conclusions:
- Pediatric intestinal failure management has advanced significantly.
- Intestinal adaptation is key to improving outcomes and enabling emancipation from TPN.
- Future therapies including trophic hormones (EGF, GLP-2) hold promise for further improving outcomes.
Abstract:
The outcome for children with congenital enteropathies or massive surgical resections has improved significantly over the past two decades. Advances in understanding of the pathophysiology of intractable diarrhea and of the mutations causing many of the congenital enteropathies have enabled initiation of preventive measures for intractable diarrhea, and have enabled clinicians to provide focused treatment of immune-mediated congenital diarrheal illnesses. Children with surgical short bowel syndrome also face an improved outcome because of improvements in the composition of parenteral nutrition (TPN) and in enteral alimentation strategies. It is now recognized that, through adaptation, small intestinal surface area and absorptive function may improve over time to facilitate emancipation from parenteral nutrition. Beyond provision of enteral nutrition, ancillary therapies such as judicious use of acid suppression, antibiotics, prokinetic agents, and soluble fiber seem to accelerate the rate of adaptation in young children. In the future, trophic hormones such as epidermal growth factor (EGF) or glucagon-like peptide 2 (GLP-2) may become routine members of the therapeutic armamentarium for surgical short bowel syndrome, thus further improving outcomes.
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