25: Chronic Liver Dz And Cirrhosis Flashcards

1
Q

Major complication associated with Hep B vs Hep C

A

Hep B: polyarteritis nodosa

Hep C: mixed cryoglobulinemia

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2
Q

Major lab + imaging to ID fibrosis due to cirrhosis

A
  1. Serum fibrosure lab

2. US elastography

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3
Q

Risk of an HBV positive mother transmitting to infant at time of delivery

A

90%

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4
Q

Leukopenia in alcoholics

A

Occasionally seen but resolves after cessation of drinking

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5
Q

CBC issues possibly seen in alcoholics

A
  1. high or low WBCs
  2. Anemia
  3. Folic acid deficiency
  4. Thrombocytopenia
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6
Q

Mallory (Mallory-Denk) bodies

A

Alcoholic hyaline seen on liver biopsy in alcoholic liver disease

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7
Q

What happens if you administer glucose without thiamine in alcohol-induced liver disease

A

Can precipitate Wernicke Korsakoff

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8
Q

Three major treatments for severe alcoholic hepatitis

A
  1. Steroids
  2. Pentoxifylline
  3. Liver transplant
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9
Q

Requirement for liver transplant for alcohol-induced liver disease

A

Must abstain from alcohol for 6mo to be considered

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10
Q

Three scores for severity of alcohol-induced liver disease + the score that indicates a poor prognosis

A
  1. Maddrey’s discrimination function (DF): 32
  2. Glasgow Alcoholic hepatitis score: 9
  3. MELD: model for end-stage liver disease: 21
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11
Q

Wernicke Korsakoff sx

A

AMS, ataxia, involuntary eye movements (nystagmus)

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12
Q

Korsakoff sx

A

Severe memory issues, confabulation

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13
Q

Treatment for Wernicke encephalopathy

A

Thiamine

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14
Q

Two things that protect against NAFLD

A
  1. physical activity

2. Coffee consumption

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15
Q

What is seen on liver biopsy in NAFLD

A

Macrovesicular steatosis +/- inflammation and fibrosis, PMN infiltrate, Mallory hyaline - indistinguishable from alcoholic steatohepatitis

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16
Q

Lung disease seen in a1 antitrypsin deficiency

A

Pan-acinar emphysema in lower lobes (smokers get emphysema in upper lobes)

17
Q

Most commonly diagnosed inherited hepatic disorder in infants/children

A

A1 antitrypsin deficiency

18
Q

PiM, PIS, PiZ and PiZZ phenotypes in a1AT deficiency

A
  1. PiM: normal, most common
  2. PIS: mildly reduced levels
  3. PiZ: severe reduction
  4. PiZZ: most severe reduction
19
Q

What is iron stored as + where is it stored in hemochromatosis

A

Hemosiderin -> liver, panc, heart, adrenals, testes, pituitary, kidneys

20
Q

Neurological manifestations in Wilson disease

A

Parkinson’s, tremor, ataxia, dysarthria, dysphagia, spasticity, migraines, insomnia, seizure

21
Q

How to check for SBP?

A

Paracentesis

22
Q

Two major scores to calculate for cirrhosis

A
  1. Child-Turcotte Pugh

2. MELD

23
Q

What to order for MELD vs Child-Turcotte-Pugh

A

MELD: bili, creat, Na, INR
CTP: bili, INR, albumin, assess for encephalopathy and ascites

24
Q

What two things should be monitored every 6 months in cirrhosis to monitor for HCC?

A

Alpha fetoprotein, US

25
Q

Three treatments for NAFLD

A
  1. Weight reduction
  2. Exercise
  3. Control metabolic syndrome
26
Q

Three pt populations that need paracentesis for ascites

A
  1. New onset ascites
  2. Pts admitted to hospital with ascites
  3. Known ascites deterioration
27
Q

What level of PMN suggests SBP in ascites?

A

250 mcL

28
Q

What does SAAG stand for?

A

Serum albumin- ascites gradient

29
Q

Four things that increase severity of esophageal varices

A
  1. Size larger than 5mm
  2. Red wale markings
  3. Severity of liver disease
  4. Active alcohol abuse
30
Q

Esophageal varices prevention drug

A

No selective beta-adrenergic blockers

31
Q

Major treatment for esophageal varices

A

Band ligation

32
Q

Treatment for hepatic encephalopathy + how it works

A

Lactulose -> colonic acidification and diarrhea