Short bowel syndrome occurs after extensive loss of small bowel leading to a status of intestinal failure characterized by significant problems in digesting and absorbing enteral nutrition. A very complex adaptation process of the intestine allows that 90% of the patients can be weaned after a long-term period from parenteral nutrition. A small number of patients will finally need surgical interventions either to reduce a very fast passage time or to lengthen the dilated intestinal remnants. Some patients will need intestinal or combined intestinal/ liver transplantation either after nearly total loss of small bowel or after severe complication such as intestinal failure-associated liver insufficiency. The therapeutic decisions have to be tailored to each individual patient depending which parts of the intestine are lost or which dysfunctions of the intestinal remnants need a special treatment. Survival rates reach today nearly 90% including some children with long-term home parenteral support, additionally to the enteral nutrition.
CITATION STYLE
Höllwarth, M. E. (2020). Short Bowel Syndrome. In Pediatric Surgery: General Principles and Newborn Surgery: Volume 1 (Vol. 1, pp. 1107–1124). Springer Berlin Heidelberg. https://doi.org/10.1007/978-3-662-43588-5_80
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