Long term outcomes of no gut syndrome in children - A multicentre study

Elena Cernat1, Susan Hill2, Rachel Wood3

  • 1Paediatric Gastroenterology Department, Leeds Teaching Hospitals NHS Trust, Leeds, UK.

PubMed

Insights

Children with No Gut Syndrome (NGS) are surviving thanks to parenteral nutrition advancements. Most attend school, demonstrating positive long-term outcomes and improved quality of life for these young patients.

Area of Science:

  • Pediatric Gastroenterology
  • Intestinal Failure Management
  • Parenteral Nutrition

Background:

  • Extreme short bowel syndrome, termed No Gut Syndrome (NGS), presents significant challenges for pediatric patients.
  • Advancements in parenteral nutrition (PN) and medical care have led to increased survival rates in children with NGS.

Purpose of the Study:

  • To describe the population characteristics of children diagnosed with NGS.
  • To evaluate the long-term outcomes for pediatric patients with NGS.

Main Methods:

  • A questionnaire was distributed to UK pediatric intestinal failure (IF) centers to identify patients with NGS on PN.
  • Inclusion criteria included infants and children under 18 with minimal remaining small bowel (duodenum plus up to 5 cm jejunum) and colon.
  • Follow-up data was collected two years post-recruitment.

Main Results:

  • Out of 379 home parenteral nutrition (HPN) patients across 19 centers, 14 (4%) were identified with NGS.
  • The primary etiologies for NGS were midgut volvulus (64%), bowel ischemia (22%), necrotizing enterocolitis (7%), and jejuno-ileal atresia (7%).
  • Most patients (93%) remained stable on PN, with one weaned after a small bowel transplant; 61% tolerated some enteral nutrition, and 79% were attending school.

Conclusions:

  • Improved PN and healthcare have enhanced long-term survival for children with NGS.
  • Pediatric NGS patients demonstrate positive long-term outcomes, including school attendance and participation in daily activities.
Abstract

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