Understanding the treatment methods for pediatric biliary atresia, including surgical options and post-operative care.

The final symptoms of neonatal biliary atresia primarily include jaundice of the skin and eyes, along with darker urine and sometimes whitish stools. If the bile ducts are completely blocked due to congenital reasons leading to long-term bile duct obstruction, biliary cirrhosis may occur, causing liver function damage and leading to impaired absorption of fats and fat-soluble vitamins. If not treated promptly, most affected infants will die from liver failure within one year.

Learn about the treatment methods for pediatric biliary atresia, including surgical options and postoperative care tips.

The treatment options for congenital biliary atresia primarily include liver transplantation and the anastomosis of bile ducts and intestines.

Infant biliary atresia can lead to persistent jaundice, requiring timely surgery to reconstruct the bile duct drainage pathway

The reason children develop biliary atresia is due to the abnormal excretion of bilirubin into the intestines, leading to the accumulation of bilirubin in the body.

Causes, diagnosis, and treatment of neonatal biliary atresia

Discuss the prevalence and causes of biliary atresia in newborns, as well as the possible reasons for liver function abnormalities after surgery.

Treatment Options and Prognosis of Congenital Biliary Atresia

Congenital biliary atresia is one of the most important digestive surgical diseases in pediatric surgery and is also the most common indication for pediatric liver transplantation.