Clinical Approach to the Hepatobiliary Patient: Chronic Liver Disease and Cirrhosis Flashcards

(44 cards)

1
Q

what is the time frame for chronic liver disease?

A

at least 6 months

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2
Q

What are 2 ways you can identify the presence or absence of fibrosis (cirrhosis) in chronic hepatitis?

A

serum fibrosure (lab) and/or ultrasound elastography (imaging)

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3
Q

Where is HBV endemic?

A

sub-saharan africa and southeast asia

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4
Q

What 3 things is HBV associated with?

A

glomerulonephritis, serum sickness, and polyarteritis nodosa

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5
Q

What are people with chronic HBV at substantial risk for?

A

cirrhosis (portal HTN) and hepatocellular carcinoma

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6
Q

How do you make the diagnosis of chronic HCV?

A

HCV Ab+ HCV RNA in serum

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7
Q

What is the most sensitive indicator of HCV infection?

A

HCV RNA

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8
Q

What indicates recovery from prior HCV infection?

A

anti-HCV in serum without HCV RNA in serum

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9
Q

What are 3 complications associated with chronic HCV?

A

cirrhosis, hepatocellular carcinoma, pathogenic factor in mixed cryoglobulinemia

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10
Q

What is the most common form of autoimmune hepatitis?

A

Type 1: classic: anti-smooth muscle and/or antinuclear antibodies (ANA)

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11
Q

what is the typical manifestation of classic autoimmune hepatitis?

A

female, 30-50 yo, healthy appearing young woman with stigmata of cirrhosis

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12
Q

What are the extrahepatic manifestations associated with autoimmune hepatitis?

A

rash, arthralgias, keratoconjunctivitis sicca, thyroiditis, hemolytic anemia, nephritis, ulcerative colitis

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13
Q

How do you make the diagnosis of autoimmune hepatitis?

A

look for serologic abnormalities: type I: SMA; type 2: anti-LKM antibody

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14
Q

How would you treat autoimmune hepatitis?

A

glucocorticoids, azathioprine, monitor liver function tests monthly, liver transplant may be required

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15
Q

How does alcoholic hepatitis present?

A

asymptomatic–> severe liver failure with jaundice, ascites, GI bleeding, and encephalopathy

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16
Q

what would a liver biopsy look like in a patient with alcohol-induced liver disease?

A

Mallory bodies (alcoholic hyaline)

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17
Q

how do you treat alcohol-induced liver disease with hypoglycemia?

A

abstinence from alcohol; daily multivitamin, thiamine, folic acid, zinc; you need to give thiamine first before glucose

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18
Q

what are 3 different scores used to assess prognosis of alcohol-induced liver disease?

A

A Maddrey’s discriminant function (DF); Glasgow alcoholic hepatitis score; a model for end-stage liver disease (MELD)

19
Q

what are the principal causes of NAFLD?

A

metabolic syndrome (obesity, DM, hypertriglyceridemia)

20
Q

What protects against NAFLD?

A

physical activity and coffee consumption

21
Q

What is the liver biopsy like in a patient with NAFLD?

A

it is indistinguishable from that of alcoholic hepatitis

22
Q

how does alpha-1 anti-trypsin deficiency present in young? in smokers?

A

pulmonary emphysema in lower lobes; pulmonary emphysema of upper lobes

23
Q

How do you diagnose alpha-1 anti-trypsin deficiency?

A

check alpha-1 antitrypsin phenotype; Pi gene on chromosome 14

24
Q

What is the classic tetrad associated with hemochromatosis?

A

cirrhosis with hepatomegaly, abnormal skin pigmentation, diabetes mellitus, cardiac dysfunction

25
Patients affected by hemochromatosis are at increased risk of infection with what?
yersinia enterocolitica, vibrio vulnificus, listeria monocytogenes, and siderophilic organisms
26
how do you treat hemochromatosis?
phlebotomy or the chelating agent deferoxamine
27
How do you make the diagnosis of wilson disease?
low serum ceruloplasmin
28
How do you treat wilson disease?
oral penicillamine or liver transplant
29
How does right heart failure affect the liver?
patients will have passive congestion of the liver (nutmeg liver)
30
What is ischemic hepatitis?
ischemic hepatopathy, hypoxic hepatitis, shock liver; when there is an acute fall in cardiac output due to acute MI, arrhythmia, or septic or hemorrhagic shock
31
What is the hallmark of ischemic hepatitis aka "shock liver"?
rapid and striking elevation of serum aminotransferase levels- often greater than 5000 units/L; early rapid rise in the serum lactate dehydrogenase (LDH) level
32
What is fibrosure and how does it work?
it is a noninvasive blood test of biochemical markers that provides fibrosis staging and necroinflammatory grading; low excludes advanced fibrosis; high predicts advanced fibrosis
33
How do you check/diagnose a spontaneous bacterial peritonitis in a patient with cirrhosis?
blood culture or paracentesis; check fluid for albumin, WBC with differential, culture and gram stain; if it is greater than 250 PMNs/mL think SBP
34
How do you determine the prognosis of cirrhosis?
you always calculate Child-turcotte-Pugh score and MELD/MELD-Na score
35
How do you screen for HCC?
alpha fetoprotein (AFP) and ultrasound every 6 months to screen for HCC
36
What is the most common cause of ascites?
portal hypertension (chronic liver disease)
37
How do you diagnose ascites?
abdominal ultrasound or abdominal paracentesis
38
What are the routine studies done on ascitic fluid?
1) cell count 2) albumin and total protein 3) culture and gram stain
39
What is primary spontaneous bacterial peritonitis?
it is most common among patients with cirrhosis; it is a hematogenous spread of organisms to ascitic fluid
40
how do you treat spontaneous bacterial peritonitis?
appropriate empirical antibiotic treatment: a third generation cephalosporin or piperacillin/tazobactam
41
What are the 4 risks of increased risk of bleeding from esophageal varices?
1) the size of the varices (larger than 5mm) 2) the presence at endoscopy of red wale markings 3) the severity of liver disease 4) active alcohol abuse
42
How do you prevent rebleeding of esophageal varices?
nonselective beta-adrenergic blockers (propranolol, nadolol)
43
How do you treat hepatic encephalopathy?
remove precipitants, correct electrolyte imbalances, lactulose
44
How do you diagnose HCC?
a patient with known liver disease develops an abnormality on ultrasound or rising alpha fetoprotein (AFP)