Duodenal atresia is a condition in which the first part of the small bowel (the
Causes, incidence, and risk factors
The cause of duodenal atresia is unknown, but it is thought to result from problems during an embryo’s development in which the duodenum does not normally change from a solid to a tube-like structure.
Duodenal atresia is seen in more than 1 in 10,000 live births. Approximately 20-30% of infants with duodenal atresia have Down syndrome. Duodenal atresia is often associated with other birth defects.
- Upper abdominal swelling may or may not be present
- Early vomiting of large amounts, which may be greenish (containing
- Continued vomiting even when infant has not been fed for several hours
- Absent urination after first few voidings
- Absent bowel movements after first few meconium stools
Signs and tests
A fetal ultrasound may show excessive amounts of
A tube is placed to decompress the stomach. Dehydration and electrolyte abnormalities are corrected by providing fluids through an intravenous tube. An evaluation for other congenital anomalies should be performed.
Surgery to correct the duodenal blockage is necessary, but is not an emergency. The surgical approach will depend on the nature of the abnormality. Associated problems (such as those related to Down syndrome) must be treated as appropriate.
Recovery from the duodenal atresia is expected after treatment. Untreated, the condition is deadly.
- Other birth defects
After surgery, there may be late complications such as:
Swelling of the first part of the small bowel (megaduodenum)
Problems with movement through the intestines
Calling your health care provider
Call your health care provider if your newborn is feeding poorly or not at all, vomiting (not simply spitting up), not urinating or stooling, or if the vomit is green.
There is no known prevention.