Bile Secretion and Gall Stone Disease Flashcards

1
Q

What kinds of bile flow are there?

A

bile acid dependent or bile acid independent.
dependent: hepatocytes secrete bile into ducts and water follows the osmotic gradient.
Independent: ducts secrete bicarb and mucin fluid into the ducts in a secretin/CCK-mediated pathway

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2
Q

Roles of the gallbladder

A
  1. store bile when the body is fasting
  2. release bile in response to fat consumption
  3. concentrate stored bile
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3
Q

Main types of gallstones

A

cholesterol stones (enveloped shaped) and bilirubin stones

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4
Q

Bilirubin metab

A

Heme from RBCs and muscles converted to biliverdin, CO, and Fe3+ by heme oxygenase. biliverdin is converted to bilirubin and is transported in the serum associated with albumin (unconjugated bilirubin)
Liver takes up bilirubin and binds it to Y protein.
Bilrubin + Y protein go to the endoplasmic reticulum.
UGT1A1 addes side chains to bilirubin –> water soluble and ready for excretion.
Conjugated bilirubin is excreted in the bile. Bacteria in the bowel convert conjugated bilirubin to stercobilinogen/urobilinogen. Some excteted in the urine. Stercobilinogen is oxidized to stercobilin

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5
Q

Gilbert’s syndrome

A

UGT1A1 doesn’t work- unconjugated bilirubinemia. dangerous in neonates. can’t give these pts ironitecan

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6
Q

What are bile acids

A

made by hepatocytes from cholesterol and then conjugated with amino acids. amphipathic detergents. important for helping fat digestion via emulsification and incr. surface area; incr. absorption of fat soluble vitamins; decr. bacterial overgrowth in the small intestine

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7
Q

types of bile acids

A

cholic and chenodeoxycholic acid. bacteria convert bile acids to secondary (bad) bile acids deoxycholic and ithocholic acids– toxic and lithogenic.

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8
Q

what is the enterohepatic ciculation of bile acids

A

bile acids made by liver, stored in gall bladder, released in gut, reabsorbed and returned to liver via protal vein.

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9
Q

risks and types of gallstones disease

A

risks: female, overweight, pregnant, OCPs, Native American, sudden weight loss, hemolytic anemias
types: yellow cholesterol stones with Ca.
black calcium bilirubinate from chronic hemolysis
brown stones from bacterail action on bile

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10
Q

when do cholesterol stones occur in the gallbladder?

A
  1. Oversaturation with cholesterol or not enough bile acids: obesity, high fat diet, acute weight loss, liver disease
  2. Seeding of a stone (cholesterol monohydrate crystal nucleation)- from bacterial or mucin seed
  3. gallbladder stasis: fasting, TPN
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11
Q

Clinical presentation of gallstones

A

usually asymptomatic- no tx needed

others: RUQ epigastric pain post-prandially, often associated with nausea and vomiting. lasts 1-6 hrs.

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12
Q

Complications of gallstones

A

acute cholecystitis, bile duct obstruction and jaundice, infection, gallstone pancreatitis

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13
Q

Dx and Tx of gallstone disease

A

Dx: ultrasound
Tx: none if asymptomatic. If symptomatic, do elective cholecystectomy. Or, give URSODIOL if pt not gandidate for surgery. works better with less calcium, small stones, if gallbladder fills and empties well.

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14
Q

What is acute cholecystitis?

A

acute infection/inflammation of the gallbladder, usually due to blockage of the cystic duct by a gallstone. If bacteria grow, you may see abscesses, fever, chills, peritonitis.
This is a surgical emergency and requires immediate cholecystectomy

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15
Q

Dx of acute cholecystitis

A

biliary cholic and RUQ pain
exam: RUQ pain, rebound tenderness.
U/S shows gallstones and sludge, thickened distended bladder.
may do a TC99 taged HIDA with nonvisualization of gallbladder with contrast going from liver into the bowel.
Tx: cholecystectomy. give abx, IV fluids, pain meds

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16
Q

What is choledocholithiasis

A

Stones in the bile duct. may be asymptomatic, or pts may present with serous complications like pancreatitis or cholangitis

17
Q

Clinical signs of choledocholithiasis

A

Pain. Charcot’s triad: pain, fever, jaundice is suggestive of ascending cholangitis

18
Q

Dx of choledocholithiasis

A

labs and imaging w/ U/S, CT, MRCP. ERCP is more invasive, but if you make the diagnosis, you can also treat

19
Q

Tx of choledocolithiasis

A

URGENT
IV fluids, abx, biliary decompression/drainage.
ERCP (best) or percutaneous transhepatic cholangiography

20
Q

What is primary sclerosing cholangitis

A

chronic inflammatory disease that affects the large and medium sized bile ducts. may lead to fibrosis, cirrhosis and liver failure

21
Q

Epi of primary sclerosing cholangitis

A

more in men than women

associated with IBD, esp. ulcerative colitis. one dx may precede the other.

22
Q

Pathogenesis and markers for primary sclerosing cholangitis

A

auto-immune with pANCA and ANA.

poor progonsis: 10-12 yrs w/o transplant

23
Q

Presentation of primary sclerosing cholangiits

A

usually in pts aged 20-40
jaundice, pruritis, fatigue and/or mixed cholestatic hepatic enzyme elevation. may presents with ascending cholangitis or sepsis. occasionally presents with cholangiocarcinoma.

24
Q

Dx of primary sclerosing cholangitis

A

imaging of the bile ducts via MRCP or ERCP.
Beading, dilation, and strictures of the main bile duct or branches
may need liver biopsy
classically, see periductal onion skinning.

25
Q

Management of primary sclerosing cholangiitis

A

nothing, really. treat complications. look for IBD. manage cirrhosis. Maybe liver transplant, though disease frequently recurs.
many develop cholangiocarcinoma
do colonoscopy to look for asymptomatic IBD; if present, do additional screening for colon CA