Hepatitis Flashcards

1
Q

What are the positive serology markers for acute infection with Hepatitis?

A

HBsAg +
Anti-HBc (ab) IgM +
HBeAg +
HBV DNA +

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2
Q

What are the positive serology markers for prior hepatitis infection?

A

Anti-HBs +
Anti-HBc (ab) IgG +
Anti-HBe (ab) +/-

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3
Q

What is the serology for a chronic hepatitis carrier without active infection?

A

HBsAg+
Anti-HBc (ab) IgG +
Anti-HBe (ab) +
HBV DNA +

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4
Q

What is the serology for a chronic infection with active infection and replication?

A
HBsAg +
Anti-HBc IgM +/-
Anti-HBc IgG +
HBeAg+
HBV DNA +
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5
Q

What is the serology for immunization against hepatitis?

A

Anti-HBs +

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6
Q

What is the most common cause of Ascites?

A

Portal HTN from chronic liver disease.

Risk factors-> ETOH, transusions, tattoos, IVDU, Viral hep

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7
Q

What are the findings in NAFLD

A
  • Mild RUQ discomfort, HSM.
  • Normal to slightly elevated transaminases and ALKP
  • obesity, DM, hypertri, metabolic syn
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8
Q

What is the histology for NAFLD

A

Macrovesicular steatosis

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9
Q

What test do you do to check the ascitic fluid in a severely malnourished patient?

A

adenosine deaminase to R/O/I TB

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10
Q

What does a SAAG score tell you

A

Etiology of the ascites

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11
Q

What does a SAAG score >1.1 indicate

A

underlying portal HTN.

Less than 1.1 is non-portal HTN

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12
Q

How do you calculate SAAG score

A

Serum albumin- Ascitic fluid albumin

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13
Q

What must always be ruled out when a patient initially presents to the hospital with ascites

A

spontaneous bacteria peritonitis

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14
Q

What is a risk factor for developing HEV?

A

treatment with tacrolimus for immunosuppression

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15
Q

What causes very high tranaminiases

A

acetaminophen toxicity

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16
Q

What serology markers are positive in autoimmune hepatitis

A

+ANA and or smooth muscle ABs.

17
Q

What are patient with autoimmune hepatitis at risk for?

A

Cirrhosis and HCC

18
Q

What are some physical signs of CLD or Cirrhosis

A

Palmar erythema, spider angioma, gynecomastia, muscle wasting, jaundice, dupuytren’s contracture.

19
Q

What are some lab findings in cirrhotic patients?

A

Macrocytic anemia, dec WBCs, thrombocytopenia, prolonged PT time

20
Q

What lab do you need to calculate a patients child-pugh score?

A

CMP

21
Q

How does Primary Biliary Cirrhosis present

A
  • W>M
  • isolated elevated alkaline phosphatase
  • AMA
  • increased IgM

Associated with Sjogrens, scleroderma, Raynauds

22
Q

What are the risk factors for PBC?

A
  • h/o UTI
  • smoking
  • HRT
  • Hair dye
23
Q

Where is the increased iron absorption occurring in patients with Hemochromatosis?

A

Duodenum

24
Q

What is the etiology of hemochromatosis?

A

AR disorder, HFE mutation on chromosome 6 C282Y.

25
Q

What is the etiology of Wilson’s disease

A

AR disorder, chromosome 13, affects ATP7B

26
Q

What is Budd-Chiari syndrome?

A

Occulsion of flow to hepatic vein or IVC

Hypercoagulable state, that can be complicated by HCC.

27
Q

What is alpha-1 antitrypsin deficiency?

A

Defective alpha 1 antitrypsin which accumulates in the hepatocytes and causes liver damage and low serum levels of protease inhibitor.

  • panacinar emphysema also present
  • Lungs and Liver