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Kasai Procedure
Surgery in Hyderabad

Get Comprehensive Kasai Procedure Care at Yashoda Hospitals with Advanced Pediatric Surgical Expertise

  • Expert Pediatric Surgeons & Liver Specialists
  • Early Intervention for Better Outcomes
  • Safe & Precision-Driven Surgical Care
  • Personalized Treatment & Nutritional Support
  • Advanced Pediatric & Surgical Infrastructure
  • Comprehensive Pre- & Post-Operative Care

The Kasai procedure, also known as hepatoportoenterostomy, is a specialized surgery performed in infants with biliary atresia, a condition where the bile ducts are absent or blocked, preventing bile from flowing from the liver to the intestine. During the procedure, the surgeon removes the damaged bile ducts and connects a loop of the small intestine directly to the liver at the porta hepatis, allowing bile to drain into the intestine. It is typically performed under general anesthesia and is most effective when done early in life (ideally before 2–3 months of age). The surgery usually takes about 3 to 4 hours. After the procedure, infants may require medications, nutritional support, and close monitoring for complications such as infection or cholangitis. While the Kasai procedure can restore bile flow and delay liver damage, some children may still eventually require a liver transplant later in life.

What is a Kasai Procedure (Hepatoportoenterostomy)?

The Kasai procedure, also known as hepatoportoenterostomy, is a surgical treatment performed in infants with biliary atresia, a condition in which the bile ducts are blocked or absent, preventing bile from flowing from the liver to the intestine. In this procedure, the damaged bile ducts are removed, and a loop of the small intestine is directly connected to the liver at the porta hepatis to allow bile drainage into the intestine. It is performed under general anesthesia and is most effective when done early in life, ideally within the first 2 to 3 months, as it helps improve bile flow, supports digestion, and delays liver damage, although some children may still require a liver transplant later in life.

Types of Kasai Procedure (Hepatoportoenterostomy):

The Kasai Procedure (Hepatoportoenterostomy) is not a single uniform technique but can be performed in different ways depending on the child’s condition, the stage of biliary atresia, and the surgeon’s approach. Each type is designed to improve bile drainage from the liver and delay liver damage, though the method and extent of surgery may vary.

  • Standard (Classic) Kasai Procedure: This is the most widely used approach. In this method, the surgeon removes the blocked or damaged bile ducts outside the liver and carefully exposes the area called the porta hepatis, where tiny bile channels may still be present. A segment of the small intestine (usually arranged as a Roux-en-Y loop) is then connected directly to this area, creating a new pathway for bile to flow from the liver into the intestine. This technique is considered the foundation of treatment and offers the best outcomes when performed early.
  • Extended Kasai Procedure: The extended version involves a more detailed and wider dissection at the porta hepatis. The surgeon removes additional fibrous tissue to uncover as many microscopic bile ductules as possible, which may improve bile drainage in some infants. This approach is often considered when the disease is more advanced, and maximizing bile flow is critical. However, it may also carry a slightly higher risk of bleeding or complications due to the deeper dissection.
  • Laparoscopic Kasai Procedure: This is a minimally invasive variation where the surgery is performed using small incisions, a camera, and specialized instruments. The same principle of connecting the intestine to the liver is followed, but with less tissue disruption. Potential benefits include smaller scars, reduced pain, and faster recovery. However, it is technically demanding and may not be suitable for all cases, especially in very small infants or advanced disease stages.
  • Revision (Redo) Kasai Procedure: In some cases, the initial Kasai procedure may not provide adequate bile drainage, or its effectiveness may decrease over time. A revision or redo of the Kasai may be attempted to restore bile flow by revising the previous connection or removing additional scar tissue. This is typically considered selectively, as outcomes can vary, and many children may ultimately require liver transplantation.

Overall, the choice of technique depends on early diagnosis, surgical expertise, and the individual child’s liver condition, with the primary goal being to establish effective bile drainage and preserve liver function for as long as possible.

 

Procedure Name Kasai Procedure
Type of Surgery Major pediatric abdominal surgery
Anesthesia General Anesthesia
Duration 3–4 hours
Recovery 2–4 weeks (with ongoing follow-up care)

Specialist Doctors

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.

Benefits of Kasai Procedure at Yashoda Hospitals

The Kasai Procedure (Hepatoportoenterostomy) offers several important benefits for infants diagnosed with biliary atresia, especially when performed early:

  • Restores Bile Flow: Creates a new pathway for bile to drain from the liver into the intestine, improving digestion.
  • Reduces Jaundice: Helps decrease yellowing of the skin and eyes by improving bile excretion.
  • Prevents or Delays Liver Damage: Slows the progression of liver scarring (cirrhosis).
  • Improves Growth and Nutrition: Better bile flow aids the absorption of fats and essential vitamins.
  • Enhances Quality of Life: Allows many infants to grow and develop more normally.
  • Delays Need for Liver Transplant: In many cases, it postpones or reduces the immediate need for transplantation.

Testimonials

Discover what patients have to say about their experience with Coronary Angiography at Yashoda Hospitals.

 

Pallavi Jha

“I underwent Coronary Angiography at Yashoda Hospitals, and I couldn't be happier with the care I received. The medical team was highly skilled and made me feel comfortable throughout the procedure.”

 

Pallavi Jha 2

“I underwent Coronary Angiography at Yashoda Hospitals, and I couldn't be happier with the care I received. The medical team was highly skilled and made me feel comfortable throughout the procedure.”

 

Pallavi Jha 3

“I underwent Coronary Angiography at Yashoda Hospitals, and I couldn't be happier with the care I received. The medical team was highly skilled and made me feel comfortable throughout the procedure.”

 

Insurance Assistance for Kasai Procedure

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Free Second Opinion for Kasai Procedure

Getting a free second opinion for the Kasai Procedure (Hepatoportoenterostomy) can help parents make well-informed decisions when their child is diagnosed with Biliary Atresia. It allows confirmation of the diagnosis, assessment of the urgency of surgery, and a clearer understanding of the most suitable treatment approach based on the child’s condition.
Consulting experienced pediatric liver specialists also provides insights into surgical outcomes, potential risks, and long-term care, including the possibility of future liver transplantation. A second opinion offers reassurance, clarity, and confidence in choosing the best course of treatment for the child’s health.

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Why Choose Yashoda Hospitals for Kasai Procedure?

Expertise in Pediatric Surgery & Hepatology:

Yashoda Hospitals has highly experienced pediatric surgeons and liver specialists skilled in performing the Kasai procedure with precision, ensuring effective management of biliary atresia while prioritizing the safety and well-being of infants.

Comprehensive Evaluation & Diagnosis:

Infants undergo thorough clinical assessment along with advanced diagnostic tests such as liver function tests, ultrasound, and hepatobiliary imaging to accurately confirm the condition and plan timely surgical intervention.

Advanced Surgical Infrastructure:

The hospital is equipped with modern operation theatres, specialized pediatric anesthesia support, and advanced surgical techniques that enable precise and safe hepatoportoenterostomy with optimal outcomes.

Integrated Post-operative Care:

Yashoda Hospitals provides complete post-surgical care, including NICU support, nutritional management, infection prevention, regular follow-ups, and long-term monitoring to ensure better recovery and improved liver function.

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Our Locations

  • Malakpet Location

    Malakpet

  • Somajiguda Location

    Somajiguda

  • Secunderabad Location

    Secunderabad

  • Hitec City Location

    Hitec City

FAQ's

The Kasai procedure (hepatoportoenterostomy) is a surgery used to treat Biliary Atresia in infants. It creates a new pathway for bile to flow from the liver into the intestine, helping improve liver function.

The best time to perform the Kasai procedure is before 2 to 3 months of age. Early surgery increases the chances of successful bile drainage and better outcomes.

After the procedure, the baby is closely monitored and given medications along with nutritional support. Regular follow-ups are needed, and some children may still require a liver transplant later in life.

The Kasai procedure is not a complete cure but helps restore bile flow and improve liver function. It can delay disease progression and reduce the need for early liver transplantation.

The surgery typically takes about 3 to 4 hours to complete. The duration may vary depending on the infant’s condition and surgical complexity.

Possible risks include infection, bleeding, and a condition called cholangitis (bile duct infection). Long-term risks may include progressive liver damage despite surgery.

Most infants stay in the hospital for about 1 to 2 weeks after the procedure. The duration depends on recovery, feeding tolerance, and absence of complications.

Yes, babies often require high-calorie feeds and vitamin supplements to support growth. Special formulas and fat-soluble vitamins may be recommended.

Success rates vary, but many infants achieve improved bile flow if the surgery is done early. However, some children may still need a liver transplant later in life.

Parents should monitor for fever, worsening jaundice, pale stools, or poor feeding. These signs may indicate complications and require immediate medical attention.
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