Long term outcomes of intestinal rehabilitation in children with neonatal very short bowel syndrome: Parenteral nutrition or intestinal transplantation

Summary Background & aims Intestinal rehabilitation is the preferred treatment for children with short bowel syndrome (SBS) whatever the residual bowel length, and depends on the accurate management of long-term parenteral nutrition (PN). If nutritional failure develops, intestinal transplantation (ITx) should be discussed and may be life-saving. This study aimed to evaluate survival, PN dependency and nutritional status in children with neonatal very SBS on PN or after ITx, in order to define indications and timing of both treatments. Patients and methods This retrospective cross-sectional study enrolled 36 children with very SBS ( Results All the children on long-term PN ( n  = 16) survived with a follow-up of 17 years (9–20). Six of them were eventually weaned off PN. Twenty children underwent ITx: eight children died (40%) 29 months (0–127) after Tx. The others 12 patients were weaned off PN 73 days (13–330) after Tx. Follow-up after transplantation was 14 years (6–28). Seven out of 8 (88%) patients with a history of gastroschisis required ITx. Patients who required ITx had longer stoma duration. Conclusion Survival rate of children with very short bowel was excellent if no life-threatening complications requiring transplantation developed. Gastroschisis and delayed ostomy closure are confirmed as risk factor for nutritional failure. Intestinal rehabilitation may allow a total weaning of PN before adulthood. A follow-up by a multidisciplinary team is necessary to avoid PN complications in order to minimize indications for ITx.