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Biliary atresia



Digestive system
Digestive system
Bile produced in the liver
Bile produced in the liver


Biliary atresia

Treatment:

An operation called the Kasai procedure is done to connect the liver to the small intestine, bypassing the malformed ducts. It is most successful if performed before the baby is 10 - 12 weeks old. However, a liver transplant may still ultimately be required.


Expectations (prognosis):


Early surgical intervention will improve the survival of more than one-third of those affected by the condition. The long-term benefit of liver transplant is not yet known, but is expected to improve survival.


Complications:
  • Liver failure
  • Infection
  • Surgical complications
  • Failure of the Kasai procedure
  • Irreversible cirrhosis

Calling your health care provider:

Call your health care provider if your child appears jaundiced, or if other symptoms suggestive of this disorder develop.




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