The Kasai procedure is a surgical treatment for infants with biliary atresia. Your baby’s surgeon removes blocked ducts in your baby’s liver, using a portion of their small intestine to create a new path for bile to drain properly. By improving bile flow, the Kasai procedure may help prevent liver failure and a liver transplant.
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The Kasai procedure is a surgical treatment for biliary atresia. During the Kasai procedure, your baby’s provider will remove the blocked bile ducts outside their liver. They’ll use a portion of your baby’s small intestine to create a new pathway for bile to drain out of their liver. Other names for the Kasai Procedure are hepatoportoenterostomy, biliary atresia surgery and biliary atresia operation.
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Kasai surgery can slow — and sometimes stop — the progression of biliary atresia. Healthcare providers usually diagnose babies with biliary atresia within the first two months of life. If your baby has the condition, a blockage in their bile ducts stops bile from flowing into their bowel. The blocked bile damages and scars their liver cells (cirrhosis).
If untreated, biliary atresia usually leads to liver failure. But in some cases, the Kasai procedure can slow or prevent it.
Your baby’s provider will prepare them for surgery by giving your baby intravenous (IV) fluids to keep them hydrated, maintain their sugar levels and provide nutrients. They’ll also give your baby antibiotics intravenously to reduce the risk of infection. During surgery, your baby might also need blood products, like red blood cells or platelets.
Before starting the Kasai procedure, your baby’s surgeon needs to make sure they have biliary atresia. To do that, they perform a cholangiogram, a procedure that allows the surgeon to inspect your baby’s bile ducts.
To start the cholangiogram, the surgeon makes an incision below your baby’s ribs on the right side of their belly. Or, using laparoscopic surgery, they place a small tube into your baby’s gallbladder. Then, the surgeon injects medication that helps find the bile ducts using an X-ray machine. If your baby has a blocked gallbladder and bile ducts that prevent bile from draining from their liver, your baby has biliary atresia.
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During the Kasai procedure, the surgeon removes your baby’s gallbladder and abnormal bile ducts, where they connect with the liver. They then use a piece of your baby’s small intestine — called the jejunum — to replace the damaged bile ducts, making a connection between their liver and their intestine.
If successful, this connection allows bile to drain into your baby’s intestine, stopping the effects of biliary atresia.
The surgery may take several hours.
Following the Kasai procedure, your baby will spend five to 10 days in intensive care to recover. They won’t eat for the first few days after the procedure, giving their internal wounds a better chance to heal. Your baby’s providers will deliver nutrients intravenously these first days. After, they’ll feed through a nasogastric tube (a feeding tube inserted through their nose). Gradually, your baby will begin to take food through their mouth. Their surgeon will also put surgical drains around your baby’s incision to help remove fluids from the wound and promote healing. They’ll take the drains out before your baby leaves the hospital.
While in the hospital, providers watch your baby closely for signs of bleeding, bile leakage, gas and pooping. These indicate that bile is draining correctly from their liver into their intestines. Your baby may need some medications to help improve the drainage. Once your baby’s intestine starts functioning again, they can start feeding. The surgeon will let your baby go home once their incision begins to heal, their liver functions improve, and they can tolerate formula or breastfeeding (chestfeeding).
The benefits of the Kasai procedure include:
The success rate of the Kasai procedure is highest when your baby is between 6 weeks and 2 months old, has minimal liver damage and has a skilled and experienced surgeon. Under these conditions, the Kasai procedure can reduce biliary atresia symptoms — especially jaundice — in more than 60% of infants.
Signs of a successful surgery include the return of normal color to your baby’s poop and improved liver functioning test results. Your baby’s healthcare team considers the Kasai procedure a success if your baby doesn’t have jaundice for six months after surgery.
A common complication after the Kasai procedure is a liver infection called cholangitis. Your baby’s provider may prescribe antibiotics after surgery to help prevent this. If an infection occurs, your baby’s doctor will treat it with intravenous antibiotics.
If the Kasai procedure doesn’t work and your baby’s bile ducts are still blocked, they’ll likely need a liver transplant. It’s not uncommon. In fact, about half of babies who have the surgery will need a liver transplant by age 2.
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It will take about three to four months for your baby to recover from the Kasai procedure. Here are some steps you can take to speed up their recovery and avoid problems once they get home:
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Contact your provider immediately if you notice any signs of infection or liver disease in the days and weeks following the Kasai procedure, including:
If you recently found out your baby has biliary atresia and needs the Kasai procedure, you’re probably still in shock. With everything moving so fast, you’re going to need support. Allow your family, friends and loved ones to help you. Look for and join support groups of parents who have babies with liver conditions. You’re not alone in this.
Remember to be kind to yourself in this journey. Stay hopeful, stay informed, and lean on the community around you, both near and far.
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Last reviewed on 10/16/2024.
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