Jaundice Flashcards

1
Q

Jaundice associated with RUQ pain & fever with a history of travel & food is most probably due to?

A

Hepatitis

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2
Q

What will be found in lab investigations of hepatitis patient presenting with jaundice?

A
  • increase WBC -> lymphocytes
  • AST in 1000s
  • increase in total & direct bilirubin
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3
Q

What are the prehepatic causes of jaundice?

A
  • HEMOLYSIS
  • increased bilirubin production -> massive blood transfusions
  • side effect of medication -> impaired hepatic uptake of bilirubin
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4
Q

What are the different etiologies of hemolysis leading to jaundice?

A
  • G6PD deficiency
  • structural defects: sickle cell anemia, hereditary spherocytosis
  • autoimmune hemolytic anemia
  • hemolytic transfusion reaction
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5
Q

How is autoimmune & non-autoimmune hemolysis differentiated?

A

COOMBS TEST

  • if positive -> autoimmune
  • if negative -> non-autoimmune
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6
Q

What findings will be seen in jaundice due to hemolysis?

A
  • increased INDIRECT bilirubin
  • reticulocytes > 45
  • increase LDH
  • decreased hepatoglobin
  • anemia
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7
Q

What are the intrahepatic causes of jaundice?

A
  • Gilbert syndrome -> impaired bilirubin conjugation (INDIRECT BILIRUBIN HIGH)
  • hepatocellular injury -> MIXED indirect & direct bilirubin
    (viral hepatitis, alcoholic hepatitis, NASH, cirrhosis, drug toxicity)
  • impaired hepatic excretion & intrahepatic cholestasis -> DIRECT BILIRUBIN
    (intrahepatic biliary tract disorders -> primary biliary cholangitis & primary sclerosing cholangitis)
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8
Q

What are the post hepatic causes of jaundice?

A
  • malignancy -> pancreatic head cancer, cholangiocarcinoma
  • gallbladder & gallstone disease
  • inflammation -> primary sclerosing cholangitis
  • infection
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9
Q

How is Gilbert syndrome identified?

A
  • fluctuating levels of bilirubin triggered by stress, strain, dehydration
  • history of flu
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10
Q

What level does bilirubin have to reach so jaundice becomes apparent?

A
  • serum bilirubin > 2 - 3 mg/dL -> scleral icterus

- serum bilirubin > 4 - 5 mg/dL -> skin discoloration

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11
Q

What clinical features are associated with cholestasis or post-hepatic?

A
  • pale, clay colored stool
  • dark urine
  • pruritis
  • fat malabsorption (steatorrhea)
  • RUQ abdominal pain
  • chronic biliary obstruction -> backflow of bile -> inflammation & hepatomegaly
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12
Q

What features are seen with jaundice due to hemolysis?

A
  • pallor
  • fatigue
  • exertional dyspnea
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13
Q

What features are seen with jaundice due to liver failure?

A
  • anorexia
  • fatigue
  • nausea
  • abdominal pain
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14
Q

What is seen on labs of prehepatic jaundice?

A
  • indirect bilirubin -> increased
  • direct bilirubin, AST & ALT, ALP & GGT, & urinary bilirubin -> normal
  • urinary urobilinogen -> increased
  • stool color -> dark
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15
Q

What is seen on labs of intrahepatic jaundice?

A
  • indirect bilirubin -> increased
  • direct bilirubin -> increased
  • AST & ALT -> increased
  • ALP & GGT -> increased
  • urine -> dark, increased bilirubin, normal or increased urobilinogen
  • stool -> dark or pale
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16
Q

What is seen on labs of extrahepatic jaundice?

A
  • indirect bilirubin -> normal
  • direct bilirubin -> increased
  • AST & ALT -> normal
  • ALP & GGT -> increased
  • urine -> very dark, increased bilirubin, decreased urobilinogen
  • stool -> pale, clay-colored
17
Q

What is the first line radiological investigation that should be done in all patients with jaundice?

A

1- abdominal ultrasound
2- MRCP
3- ERCP

18
Q

What are the findings of abdominal ultrasound in extrahepatic jaundice?

A
  • dilated CBD
  • double-duct sign
  • visualization of cause of obstruction
19
Q

What are the diagnostic findings of autoimmune hemolytic anemia?

A
  • decreased Hb, Hct, & RBC count
  • decreased heptoglobin
  • increased LDH
  • positive Coombs test

TREAT WITH STEROIDS

20
Q

Which causes of jaundice require NO TREATMENT?

A
  • Gilbert syndrome

- Hepatitis A

21
Q

How should alcoholic hepatitis be treated?

A

stop alcohol

22
Q

How is acetominophen toxicity be treated?

A

N-acetylcysteine

23
Q

How is Wilson’s disease detected & treated?

A
  • decreased serum ceruloplasmin
  • increased urine copper excretion (24 hrs)

use copper chelating agents