Exam 2 CM3 Biliary dz Flashcards

1
Q

What is bile, it’s composition/function

A

500 mL secreted daily by liver, concentrated in GB
Composition: water, electrolytes, bile salts, phospholipids, bilirubin & cholesterol
Function: digestion and absorption of fats (bile salts); vehicle for excretion of bilirubin, excess chol and metab by products

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2
Q

Cholelithiasis

A

Stones in gallbladder

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3
Q

Cholecystitis

A

Inflammation of the GB

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4
Q

Choledocholithiasis

A

Stones in CBD

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5
Q

Cholangitis

A

Inflammation of the bile ducts

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6
Q

Cholestasis

A

Disruption of bile flow, regardless of cause

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7
Q

Risk factors for Cholelithiasis

A
Four F’s (female, fluffy/obese, Forty, Fertile/Estrogen)
Female
>40
Pregnancy (hormones change bile consistency)
Obesity
Rapid weight loss (bile not being used)
Estrogen (birth control)
Ethnicity (Native Americans)
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8
Q

What are the different types of gallbladder stones (Cholelithiasis)

A
  1. Cholesterol (most common) >80%

2. Pigment – bilirubin, calcium, proteins Black or Brown

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9
Q

What are the various outcomes/prognoses for Cholelithiasis

A
Asymptomatic (most)
Symptomatic
Biliary colic
Complications
Acute Cholecystitis (inflam of GB)
Acute Choledocholithiasis (Stones in CBD)
Ascending Cholangitis (inflam of bile duct)
Acute Pancreatitis
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10
Q

How do you diagnose Cholelithiasis (initial study then others)

A

Initial study = UTZ
*UTZ is initial TOC in eval of biliary dz; inexpensive/noninvasive
*May show gallstones, wall thickening, pericholecystic fluid (fluid surrounding gallbladder)
Abdominal Plain film
Only + in ~10% pt’s with gallstones
CT abdomen
Will show majority of gallstones (50-80%) but higher cost, radiation exposure and less sensitive than UTZ

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11
Q

How do you treat Cholelithiasis

A

Asymptomatic Cholelithiasis incidental finding w/ no sx then Cholecystectomy (CCY) is NOT RECOMMENDED
Symptomatic Cholelithiasis sx biliary disease (biliary colic, cholecystitis, choledocholithiasis, ascending cholangitis) CCY recommended

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12
Q

What is Biliary Colic? Sx? Triggers?

A

Biliary Colic = TEMPORARY obstruction of cystic duct
Usually caused by gallstone (cholelithiasis); pressure rises in gallbladder causing pain
Colicky, dull constant RUQ pain, possibly radiating to R shoulder blade; assoc N/V, diaphoresis
As gallbladder relaxes, obstruction is relieved; no associated inflammation (thus NO FEVER, NO LEUKOCYTOSIS)
Triggers: fatty meal
Sx temporary, do not last more than 4-6 hr

Often initial presentation of sx gallbladder dz

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13
Q

In a pt with Biliary Colic, what PE findings would be present?

A

Gen: do not appear acutely ill
Skin: NO EVIDENCE of JAUNDICE (bc stone in cystic duct, NOT bile duct)
Eyes: anicteric (bc no jaundice)
Vitals: normal (no fever/tachy)
Abd exam: Fairly benign with possible RUQ tenderness, no evidence of peritonitis (rebound pain) and negative Murphy’s sign

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14
Q

What studies/results help dx BILIARY COLIC?

A

Lab: CBC, LFT, Amylase, Lipase ALL WNL!
UTZ: preferred initial test in eval of suspected biliary dz
Gallstones and/or sludge (bc temporary cystic duct obstruction)

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15
Q

How do you treat/manage BILIARY COLIC?

A

Considered sx biliary dz Prophylactic CCY (cholecystectomy) IS RECOMMENDED to prevent recurrent sx and complications
Be sure to r/o alternative dx

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16
Q

What is Biliary Dyskinesia and who should be considered for this dx?

A

Biliary dyskinesisa = functional gallbladder disorder, likely a motility disorder of gallbladder
Consider in pt presenting with typical biliary colic (dull constant RUQ pain that may radiate to R shoulder blade) who:
Has no evidence of Gallstones or sludge on UTZ
No CBC, LFT, amylase or lipase abnormalities
Other causes of sx r/o
Consider performing HIDA w CCK

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17
Q

What is a HIDA scan with CCK and what is it used to evaluate?

A

HIDA: inject 99 technetium labeled derivative or hepatic iminodiacetic acid (HIDA) dye which is excreted in bile and taken up by gallbladder if cystic duct is patent. Normal gallbladder fills in 30 min, radioactivity measured in gallbladder. CCK given to stim contraction, EF calculated to see how well gallbladder is functioning. Want at least 35-40% ejection fraction upon stimulation or CCK, less than 35-45% EF may indicate Biliary Dyskinesia)
Used to eval BILIARY DYSKINESIA
*NOTE: do NOT given CCK if pt has gallstones (contractions stimulate attack)

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18
Q

How should you manage/treat biliary dyskinesia

A

CCY if…
Typical biliary sx (RUQ pain, may radiate to R shoulder)
HIDA w/ CCK <35-40%
R/o other dx (PUD, gastritis, GERD, cardiac ischemia etc) need good H&P

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19
Q

What is ACUTE CHOLECYSTITIS and what is the cause? Sx?

A

Etiology: acute inflammation of the gall bladder secondary to sustained obstruction of the cystic duct
Most commonly caused by cholesterol stones (Overall mortality: 3%)
Often prior hx of biliary colic
Sx: Steady severe RUQ pain +/- radiation to R shoulder/flank;
Assoc N,V, diaphoresis, FEVER!!
Sx are PERSISTENT, often longer than 4-6 hr (unlike Biliary colic with sx <4-6hr)
Trigger: fatty meal

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20
Q

PE findings associated with Acute Cholecystitis

A

Gen: ILL appearance
Vitals: FEVER, tachy (biliary colic, no fever or tachy)
Eyes: Anicteric (in cystic duct)
Skin: No jaundice (in cystic duct)
Abd exam: RUQ tender, Palpable tender gall bladder in 30-40%, possible guarding and rebound, +MURPHYS (unlike biliary colic)

21
Q

What complications are associated with acute cholecystitis?

A

Gangrene (up to 20%): often in elderly, immunosuppressed, people who get delayed tx
Look for signs of sepsis
Perforation
Generalized Peritonitis
Cholcystoenteric fistula (bw small bowel and gallbladder)
Gallstone ileus

22
Q

What lab/imaging studies are helpful to dx acute cholecystitis?

A

CBC (elevated WBC with LEFT shift)
LFT: usually normal
Possible mild increase in AST/ALT, alk phos, bilirubin
If significant elevations in alk phosbilirubin, r/o CHOLANGITIS (CBD obstruction)
UA: elevated uroblinogen
Pancreatic Enzymes
Possible mild elevation of amylase

UTZ (preferred) gallstones, wall thickening (>4-5mm), Pericholescystic fluid, + sonographic Murphys
HIDA: used to confirm dx if in question
Failure to fill gallbladder in setting of cystic duct obstruction

23
Q

How do you manage/tx acute cholecystitis?

A

Admit All
Analgesia (Ketorolac, morphine, meperidine or NSAID)
NPO (don’t want to stim gallbladder)
IV fluids w/ electrolyte
IV ABX (similar as diverticulitis)
Monotx: Zosyn, Unasyn, Timentin IV or Combo (Rocephin & Flagyl or Cipro & Flagyl)
Early CCY (most laparoscopic)
Recommended during initial hospitalization in healthy low risk ASA I or II pt
Emergent CCY if severe complication (gangrene, perf, peritonitis etc) or clinical deterioration despite supportive tx
IF HIGH RISK (ASA III-V) continue supportive tx, weight risk vs. benefit via specialist
if med tx fails then possible percutaneous CCY tube for decompression

24
Q

What is chroniccholecystitis and how is it dx?

A

Chronic inflammation of the gallbladder
Associated with mechanical irritation from gallstones or repeated episodes of acute cholecystistis
Typically dx made upon review of histology ie post CCY

25
Q

What is Acalculous Cholecystitis, who gets it and how it it dx/tx?

A

Common in critically ill pt (most are hospitalized), associated with stasis and ischemia
Presents similar to acute Cholecystitis except no gallstones; may have jaundice (if inflammation is sign enough to extend into cystic and into common bile duct)
Dx: UTZ, LFT, CBC
Prompt tx is imperative
CCY vs. cholecystostomy
Secondary infection of gallbladder is common: monitor blood, start broad spectrum abx, risk of gallbladder gangrene
Worse prognosis

26
Q

What is choldedocholithiasis? How do patients present?

A

Stone in common bile duct (CBD); Will black bile flow and cause jaundice
Most present with biliary type pain RUQ or epigastric pain, N/V
Some are asymptomatic
Some have jaundice: pruritis, tea colored urine, light colored stool

27
Q

PE findings in a patient with choledocholithiasis

A

UNCOMPLICATED (no cholangitis present)
May be in some discomfort
Vitals: NO FEVER OR TACHY, NO hypoTN
Skin: Jaundic
Eyes Sclearl Icterus
Abd: +/- RUQ tenderness, no peritoneal signs (neg Murphy)
If fever, jaundice, leukocytosis and more prominent abdominal tenderness present, think cholangitis

28
Q

Lab findings in pt with Choledocholethiasis (uncomplicated) would show? How do you confirm dx of Choledocholethiasis?

A

CBC: no leukocytosis
Pancreatic enzymes: normal amylase and lipase
LFT (cholestasis): conjugated bilirubin, alk phos

Confirm Dx with imaging:
RUQ UTZ = initial test of choice
UTZ will should CBD stone, Dilated CBD (>6mm), gallstones in gallbladder
If dx is uncertain, consider MRCP
Shows biliary and pancreatic duct (dye contrast), to confirm dx of CBD stone will show massive dilation

29
Q

How do you manage/tx a patient with Choledocholethiasis (stone in CBD)

A

Need to remove stone to prevent cholangitis or pancreatitis
Consider prophylactic ABX (same coverage as cholecystisis
Cipro/flagyl or Rocephin/flagyl or unasyn/zosyn/timentin
ERCP is the preferred therapeutic test remove stones, insert stents, perform sphincterotomy
Then CCY to follow

30
Q

What is ascending cholangitis and what is it associated with?

A

Ascending Cholangitis = infection of the biliary tract, most commonly the CBD
Associated with biliary obstruction (CBD stone)
Bacteria infects bile (ascending infection from duodenum)
Pus under pressure!! = SURGICAL emergency, early intervention is imperative!!!!

31
Q

What are sx, PE findings in a pt with ascending cholangitis

A

Sx: RUQ/epigastric abdominal pain, jaundice, fever, hx of biliary colic or disease
Charcot’s triad!: Fever/chills, RUQ pain, Jaundice
Charcot’s triad + hypoTN and mental status changes = Reynolds Pentad (50% mortality rate)
Look for signs of peritonitis and sepsis
PE:
Gen: acutely ill appearing, diaphoretic
Vitals: Fever, tachy, hypoTN
Skin: Jaundice
Eyes: Icterus
Abd: RUQ/epigastric tenderness, guarding
Neuro: mental status changes

32
Q

What is Charcot’s triad

A

Acute presentation of ascending cholangitis fever, pain, jaundice
Fever/chills
RUQ pain
Jaundice

33
Q

What is Reynolds Pentad?

A
  1. Charcot’s triad (Fever/chills, RUQ pain, Jaundice)
  2. HypoTN
  3. Mental status changes
    Suggest ascending cholangitis
34
Q

What lab studies suggest ascending cholangitis

A

CBC: Marked leukocytosis (typically >20,000)
LFTs: cholestasis: conjugated bili, alk phos
Pancreatic enzymes: normal/mild elev
UA: urobilinogen
Blood cultures

35
Q

In pt with dx of ascending cholangitis in question, what studies should be pursued? How do you manage a pt with ascending cholangitis?

A

UTZ
MRCP (CBD dilation, CBD stone)

Mgmt
Admit to hospital
Consult GI (emergent)
NPO/IV fluids
Broad spectrum abx to cover G+ and G- bacteria (Rocephin/Flagyl; Cipro/Flagyl**, Piperacillin/Tazobactam)
Relief of biliary obstruction imperative ERCP w/ sphincterotomy and stone extraction, +/- stent (gush of pus into duodenum
Follow with CCY

36
Q

Summary of Biliary colic vs Acute Cholecystitis and Choledocholithiasis vs Ascending Cholangitis summary

A

Biliary colic: temporary RUQ pain, No fever, No leukocytosis, No jaundice
Acute Cholecystitis: Persistent RUQ pain, Fever, Leukocytosis, No jaundice
Choledocholithiasis: RUQ pain, NO fever/leukocytosis, Jaundice
Ascending Cholangitis: RUQ pain, Fever, Leukocytosis, Jaundice

37
Q

Dx approach: how to approach Biliary disease?

A

Get CBC with differential r/o infection (cholangitis, acute Cholecystitis)
Get Amylase and lipase r/o pancreatitis (may be mild elevation in acute biliary disease)
LFTs: Alk phos/conjugated bilirubin = Cholestasis
Biliary obstruction (choledocholithiasis)
AST/ALT may have transient elevations
UTZ: initial TOC in eval of biliary dz; may show gallstones, wall thickening, pericholecystic fluid, ductal dilation, CBD stones
MRCP: helpful for dx stones/obstruction in CBD when UTZ is non dx
Additional studies:
HIDA scan: to confirm cystic duct obstruction in Cholecystitis
Can use CCK to measure EF for biliary dyskinesia
ERCP: used to relieve CBD obstruction (choledocholithiasis, cholangitis)

38
Q

What is Primary Biliary Cirrhosis (PBC), who does it affect, and what are the sx?

A

Autoimmune destruction of small intrahepatic bile ducts which causes cholestasis (progress to cirrhosis and failure)
Primarily females 35-60 yo
Presentation
Fatigue, pruritis, arthritis,
RUQ pain, CREST sx (Calcinosis, Raynauds phenomenon, Esophageal dysmotility, sclerodactyly, telangiectasia)
Skin hyperpigmentation, xanthomas, hepatomegaly

39
Q

What lab findings are indicative of PBC

A
LFTs (cholestatis pattern): Alk Phos ( conjugated bilirubin later in disease) and  GGT, 5-NT
AMA (95%)***
ANA (70%)
IgM
Hyperlipidemia (50%)
40
Q

How do you dx PBC? Tx?

A
LIVER BIOPSY (dx and stage)
Will show florid bile duct lesion

Mgmt: Urso (detox bile) and monitor bone density (DEXA) bc increased risk of OP

41
Q

What is Primary Sclerosing Cholangitis (PSC), what can it progress to and who does it affect?

A

PSC = Inflammation/fibrosis of medium and larger intra/extra hepatic ducts
Progresses to CIRRHOSIS (median survival 10-12 yr following dx)
Mostly MEN, >75% have IBD mostly ulcerative colitis
Sx: asymp, fatigue, pruritis, jaundice, steatorrhea, OP

42
Q

What are potential complications of PSC (Primary Sclerosing Cholangitis)

A
Biliary stricture
Cholangitis
Cholangiocarcinoma (cancer of CBD)
Gallbladder CA
Colon CA
THINK CANCERS AND STRICTURE
BGCCC are PSC complications (biliary stricture, gallbladder cancer, cholangitis, CBD/Colon CA)
43
Q

How do you dx PSC

A

Abnormal LFTs (Cholestatic pattern: Alk phos and CB)
P-ANCA, ASMA, ANA, IgM
Imaging
ERCP: dx and therapeutic
MRCP: dx multifocal structuring with intrahepatic/extrahepatic ductal dilation
Liver Bx: usually non dx

44
Q

How do you manage/tx PSC?

A

Monitor bone density DEXA
Manage biliary strictures with ERCP (Biliary ductal dilation or stenting)
Monitor for complications (cholangiocarcinoma, cholangitis etc)
Liver transplant with advanced dz

45
Q

What is Gilbert’s Syndrome? Who should we suspect for having it?

A

Deficiency in enzyme for Glucuronidation of bilirubin in liver (conjugation)
9% of population is homozygous for Gilbert’s
Suspect in pt with unconjugated hyperbilirubinemia in absence of hemolysis
Normal CBC, blood smear, Reticulocyte count
Remainder of LFTs normal

46
Q

What risk factors are there for Gallbladder CA, and what presenting sx are associated?

A

> 50% of biliary tract CA’s
Risks: Cholelithiasis, Gallbladder polyps >1cm, Salmonella
Presentation:
Can be indistinguishable from Cholelithiasis
May be asymptomatic
May have sx suggestive of malignancy (anorexia, wt. loss)

47
Q

What is Cholangiocarcinoma, what is it associated with, and how does it present?

A

Adenocarcinoma of bile ducts (intra/extra hepatic)
- Assoc with PSC and choledochal cysts
Presentation
Jaundice, vague upper abd pain, anorexia, weight loss, pruritis
Labs: cholestasis (obstructive pattern) elevated CB and Alk PHos (remember, Gilberts is UCB)
CA 19-9 (know that this tumor marker is assoc with Cholangiocarcinoma)

48
Q

What is Ampullary Cancer

A

Rare
Associated with Familial Adenomatous Polyposis (FAP) and Hereditary Non-polyposis colon cancer (HNPCC)
Presentation: OBSTRUCTIVE JAUNDICE (most common), occult GIB with microcytic anemia, abdominal pain