Children with short bowel syndrome lack a functioning small intestine as the result of conditions including necrotizing enterocolitis (NEC), intestinal atresia, complicated gastroschisis, and volvulus. An insufficient length of small intestine can make it difficult or impossible for kids with short bowel syndrome to extract the nutrients they need to grow and thrive. For this reason, many children with the condition require parenteral nutrition through an intravenous (IV) line, enteral nutrition through a gastrostomy tube (G-tube), or both.
To lengthen the small intestine of children with short bowel syndrome, physicians at Boston Children's Hospital developed an operation called the serial transverse enteroplasty procedure (STEP). This procedure lengthens the small intestine to create more useable surface area and make a narrower space, which keeps food moving through your child's digestive tract at an appropriate pace to improve function.