Anorectal malformations are birth defects in which the anus and rectum (the lower end of the digestive tract) did not develop properly. This can cause your child to have difficulty passing stool. The majority of babies with anorectal malformations will need to have surgery to correct the problem.
A PSARP is a type of pull-through procedure that is used to repair anorectal malformations in some children. This technique surgically creates the child’s anus within the sphincter muscle. Prior to surgery, if there is no opening for stool to come out, your child’s surgeon may use a type of X-ray called a colostogram to determine the severity and location of the malformation. The PSARP operation is usually done within the first year of your baby’s life.
Usually at birth, if needed, your child will already have undergone a colostomy procedure. In a colostomy, the large intestine is divided into two sections and the ends of intestine are brought through openings in the abdomen. The upper section allows stool to pass through the opening (called a stoma) and then into in a collection bag. The lower section allows mucus that is produced by the intestine to pass into a collection bag. By doing a colostomy, your baby’s digestion will not be impaired and they can grow before the time for the next operation.