Learn about how the body may not get enough nutrients when the small intestine is short because of surgery or a condition present at birth.
Update Date: 25.07.2026
Short bowel syndrome is a condition in which the small intestine cannot take in enough nutrients from foods because it's shorter than a typical small intestine or because its ability to absorb nutrients is decreased.
One role of the small intestine, also called the small bowel, is to absorb nutrients and fluids from food. The nutrients then circulate through the bloodstream. A short bowel may not be able to absorb enough nutrients for the body's needs.
Short bowel syndrome can happen when:
Treatment of short bowel syndrome usually involves getting nutrition through a tube placed in a vein or through a feeding tube to the stomach. The condition also may be managed with a special diet and nutritional supplements. In some cases, surgery is needed.
Short bowel syndrome also is called short gut syndrome.
Common signs and symptoms of short bowel syndrome may include:
Short bowel syndrome also may cause low fluid levels, called dehydration. Symptoms of dehydration include:
Several conditions of the small intestine are treated by surgery to remove damaged or diseased tissues. These conditions include:
A shortened small intestine after surgery may not be able to absorb enough nutrients and fluids. The type and amount of nutrition loss depend on how much of the small intestine was removed and what section was removed.
Risk factors for short bowel syndrome include the following:
A lack of essential vitamins and minerals can cause many complications:
Long-term complications can include:
Your healthcare professional will do a physical exam and ask questions about symptoms, diet and medical history. This includes a history of any surgery to remove part of the small intestine.
Several tests can help diagnose short bowel syndrome or rule out other causes of symptoms. These include:
Treatment options vary depending on what section of the small intestine was removed or is not functioning well. In general, the treatment goals are to make sure you receive the nutrition your body needs and to manage complications.
The hope is for the small intestine to adapt as much as possible and absorb the nutrition you need.
For adults, it takes about two years for the small intestine to adapt. In children, it takes longer.
How far someone progresses with treatment varies. Some people may need a feeding tube for all or some of their nutritional needs. Some people will be able to eat a carefully planned diet to make sure they get enough vitamins, minerals and fluids.
Medicines to treat short bowel syndrome include the following:
Surgery may be necessary for people who depend on getting nutrition through an IV line. Procedures include:
If you or your child has had surgery to remove part of the small intestine, an ongoing part of care is watching for complications, including short bowel syndrome. Your healthcare team will likely include a specialist in digestive diseases, called a gastroenterologist; a surgical team; and a nutrition specialist.
For children who have symptoms of short bowel syndrome but have not had surgery, an appointment will likely start with your pediatrician or family healthcare professional.
The following tips can help you make the best use of the time with your healthcare team.
Before any appointment with your team, make a list of:
If possible, bring a friend or family member who can take notes during appointments. If you get a diagnosis of short bowel syndrome, ask if there are any brochures or websites that provide useful information.
Questions from your healthcare professional may include:
Questions about your child may include:
© 2026 Mayo Foundation for Medical Education and Research. All rights reserved. Terms of Use