Gastroschisis

This code represents a congenital malformation characterized by a defect in the abdominal wall, typically to the right of the umbilical cord, through which the intestines and sometimes other abdominal organs protrude. The herniated organs are not covered by a peritoneal sac or skin.

Assign this code for neonates diagnosed with an omphalocele where the abdominal contents are freely exposed. Documentation should clearly indicate the absence of a covering sac over the eviscerated organs. This code is typically used in the perinatal period and for subsequent care related to the condition.

• Differentiate carefully from omphalocele, where the herniated organs are covered by a sac.
• Ensure documentation specifies the location and nature of the abdominal wall defect.
• Consider additional codes for any associated congenital anomalies or complications, such as intestinal atresia or infection.