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Intestinal lengthening and growth hormone in extreme short bowel syndrome: a case report

B Velasco1, L Lassaletta, R Gracia

  • 1Departamento de Cirugía, Hospital Infantil Universitario La Paz, Madrid, Spain.

Insights

Recombinant growth hormone (GH) successfully treated an infant with extreme short bowel syndrome after intestinal lengthening. This treatment allowed complete weaning from parenteral nutrition, showing significant nutritional improvement.

Area of Science:

  • Pediatric Surgery
  • Gastroenterology
  • Endocrinology

Background:

  • Short bowel syndrome (SBS) is a malabsorptive condition often requiring long-term nutritional support.
  • Recombinant human growth hormone (rhGH) has shown efficacy in promoting intestinal adaptation in adults with SBS.
  • Extreme SBS in infants presents significant challenges for growth and nutritional management.

Observation:

  • A case report details an infant with intestinal atresia and only 14 cm of functional bowel.
  • Following a Bianchi procedure, the infant still required 50% of nutrition via parenteral route.
  • A short course of rhGH (0.5 U/kg for 4 weeks) was administered.

Findings:

  • The rhGH treatment led to dramatic nutritional improvement in the infant.
  • Total parenteral nutrition (TPN) was successfully discontinued 2 weeks post-treatment.
  • Stool frequency decreased from 7 to 2 daily, with no observed adverse effects.

Implications:

  • This case suggests rhGH may be a viable therapeutic option for infants with extreme SBS.
  • Further clinical trials are warranted to confirm the safety and efficacy of rhGH in this pediatric population.
  • rhGH could potentially improve outcomes and reduce the burden of TPN in infants with SBS.

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