Hirschsprung's Disease - Topic Overview
How is it treated?
Children with Hirschsprung's
disease need surgery to remove the diseased part of the large intestine.
Surgery is often done within the first days or month of life, soon after the
disease is found. Treatment may involve one or two
- The first surgery removes the damaged part of the intestine and may create a colostomy or ileostomy so that the intestine can heal. (With an ostomy, stool leaves the body through an opening in the belly and collects in a bag.)
- If your baby gets an ostomy during the first surgery (not all babies do), a second surgery will be done to close the ostomy. This will allow stool to pass through the body normally again.
Most babies are in the hospital from a couple of days up to 1 week. Being involved in your baby's care while he or she is in the hospital may help you feel more comfortable when you take your baby home. Talk with the doctor about how to feed and care for your baby at home, and make sure you know what problems to watch for. It's normal to feel nervous, but don't be afraid to hold and handle your baby.
Some children have long-term (chronic) problems with stomachaches and
bowel problems after surgery. But most of the time, these problems
aren't severe. Depending on the problem, there are a number of treatment
options. These include medicine,
cognitive-behavioral therapy, and more surgery.
In a few cases, emergency surgery may be needed if a dangerous problem
such as serious swelling of the small and large intestines (enterocolitis)