flashcards_biliary_atresia

1
Q

When is surgical intervention recommended for biliary atresia?

A

Surgical intervention is recommended immediately, ideally within the first 60 days of life.

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2
Q

What is the Kasai hepatoportoenterostomy?

A

Kasai hepatoportoenterostomy involves ligating the fibrous ducts above the join with the duodenum, dissecting proximally to the porta hepatis, and joining a loop of jejunum directly to the porta hepatis of the liver to facilitate bile duct drainage.

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3
Q

What is required during the first year of life after a Kasai procedure?

A

Antibiotic cover for the first year of life.

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4
Q

When is liver transplantation considered for biliary atresia?

A

If the Kasai procedure is unsuccessful or infants present with end-stage liver disease.

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5
Q

What are the complications of biliary atresia?

A

Complications include growth failure, portal hypertension, cholangitis, and ascites.

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6
Q

How is bile flow promoted in biliary atresia management?

A

Ursodeoxycholic acid promotes bile flow.

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7
Q

What nutritional supplementation is recommended during the first year of life for biliary atresia?

A

Either breast milk or medium-chain triglyceride-enriched formula with monthly monitoring and nutritional status.

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8
Q

What type of vitamins are given to all children with biliary atresia?

A

Fat-soluble vitamins, with levels monitored and doses adjusted accordingly.

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9
Q

How is cholangitis prevented during the first year of life in biliary atresia patients?

A

Prophylactic antibiotics (usually co-trimoxazole).

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