Posterior Sagittal Anorectoplasty (PSARP)

Our experienced pediatric surgeons are skilled in posterior sagittal anorectoplasty (PSARP), surgery to correct structural problems in a child’s anal opening. At the Colorectal and Pelvic Center at Children's Health℠, our multidisciplinary team specializes in caring for children with complex conditions of the intestines, urinary tract and reproductive organs. We provide expert, compassionate care to support your child’s health, well-being and quality of life.

What is PSARP surgery?

A PSARP is a surgical procedure to repair several types of anorectal malformations (ARMs). An ARM is a congenital (present at birth) condition that occurs when a baby’s rectum and anus (lower end of the large intestine) don’t develop properly before birth.

In a PSARP, our surgeons perform reconstructive surgery through an approach from the bottom to create an opening through which a child can pass stool (poop). The procedure involves moving the rectum into the correct position and creating an anus within the child’s sphincter muscles. Children usually have PSARP surgery within the first few months of life.

What are the benefits of PSARP?

The goal of PSARP surgery is to reposition the rectum into an ideal position with a normal anal opening while avoiding damage to nearby tissues, nerves, urinary tract and reproductive organs. This procedure will allow your child to pass stool naturally through an anus. Our pediatric colorectal surgeons are experienced in this procedure, which gives babies the best chance for good bowel control later in life.

What questions should I ask my provider about PSARP?

  • Are there other treatment options for the type of ARM my child has?
  • What medications should my child stop taking before PSARP?
  • How soon will I be able to see my child after PSARP?
  • How long will my child need to stay in the hospital after PSARP?
  • Will my child go home with any special equipment after PSARP?

Posterior Sagittal Anorectoplasty (PSARP) Doctors and Providers

Our team brings experts together from multiple medical specialties to treat children with even the most complex ARMs. These conditions can require years of treatment and follow-up care, and we’ll stay by your side and deliver the care your child needs, every step of the way.

Frequently Asked Questions

  • Why might a child need PSARP surgery?

    PSARP surgery can benefit children who have an ARM, including:

  • What is the outlook for my child after PSARP to repair an anorectal malformation?

    Most children heal well from surgery and have no complications. For toilet training your child, you can start at the usual age, when they are age 2 to 3. Children with more complex conditions are more likely to have difficulty with urinary (pee) and bowel (poop) function later in life.

    A child who has had an ARM may need to use a catheter to help with urinary continence (bladder control). Some children may be slower than others to control bowel movements, and most will experience long-term constipation.

    At our Pediatric Colorectal and Pelvic Center, we offer a comprehensive bowel management program to help your child achieve bowel control and avoid future accidents. We work closely with you and your child to customize a program specifically for their unique needs.

  • Will my child need lifelong care after PSARP for an anorectal malformation?

    Children born with an ARM have a higher risk of certain urological and colorectal conditions, so they need ongoing follow-up care. Some children may experience constipation, urinary tract infections (UTI), and bowel and urinary incontinence, which can lead to more serious conditions if left untreated.

    Your child may need additional surgeries later in life to treat these conditions. It’s important to continue to bring them to the Colorectal and Pelvic Center for follow-up care, where we adjust their care plan as needed.

    Some children may develop issues with body self-image and may benefit from psychological support. Our center offers access to pediatric psychologists, Child Life specialists and social workers for therapy and other services. With a proactive approach, young adults can feel empowered to take a larger role in managing their condition, offering lifelong health benefits.

    Your child’s health needs will change over time as they become an adult. We can help your child transition to an adult care provider with experience treating people who have had ARMs. Some adults who received care for an ARM as children may develop bowel and kidney issues, so it’s critical that they receive ongoing care throughout their lives.

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