Kasai Procedure: Pre-Op & Post-Op Care
A coordinated approach with timely diagnosis, careful preparation, precise surgery, and close post-operative monitoring helps improve bile flow, support liver function, and enhance recovery outcomes.
Pre-operative Care
Before performing the Kasai procedure, a thorough evaluation is essential to confirm biliary atresia and assess the infant’s overall health. This includes blood tests (liver function tests, coagulation profile), imaging studies such as ultrasound or hepatobiliary scans, and sometimes a liver biopsy. Nutritional status is carefully optimized, as many infants may have poor weight gain. Vitamin supplementation (especially fat-soluble vitamins A, D, E, and K) is often started. Parents are counseled about the procedure, expected outcomes, and the possibility of future liver transplantation if needed.
Intra-operative Care
During the surgery, the infant is placed under general anesthesia with continuous monitoring of vital parameters. The surgeon removes the damaged bile ducts and exposes the porta hepatis, where microscopic bile channels may still be present. A segment of the small intestine is then fashioned into a Roux-en-Y loop and connected directly to the liver to allow bile drainage. Strict sterile techniques are followed to reduce infection risk, and meticulous surgical precision is required to preserve liver tissue and ensure proper bile flow. The procedure typically takes several hours and is performed by experienced pediatric surgeons.
Post-operative Care
After surgery, the infant is closely monitored in a pediatric intensive care or recovery unit. Pain management, fluid balance, and nutritional support are carefully maintained. Antibiotics may be given to prevent infections such as cholangitis, and medications like ursodeoxycholic acid may be prescribed to improve bile flow. Feeding is gradually reintroduced, often with specialized high-calorie formulas. Regular follow-up is essential to monitor liver function, growth, and signs of complications. Parents are educated to watch for symptoms like fever, pale stools, or jaundice. Long-term care is crucial, as some children may still require liver transplantation later in life.