High-Yield Concepts in Complications of Liver Cirrhosis (Gastrointestinal Diseases) Flashcards

1
Q

Portal Hypertension (HPN)

A

Elevation of hepatic venous pressure gradient (HVPG) to >5 mm Hg

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2
Q

Portal Hypertension (HPN)

A

Elevation of hepatic venous pressure gradient (HVPG) to >5 mm Hg

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3
Q

Most common cause of Portal HPN in the US

A

Cirrhosis

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4
Q

3 primary complications of Portal HPN

A

Gastroesophageal varices with hemorrhage
Ascites
Hypersplenism

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5
Q

First indication of Portal HPN in Liver Cirrhosis

A

Hypersplenism with thromboocytopenia

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6
Q

Palliative procedure for Portal HPN

A

Transjugular Intrahepatic Portosystemic Shunt (TIPS)

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7
Q

First-line treatment to control Acute Variceal Bleeding

A

Endoscopic intervention

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8
Q

Most common cause of ascites

A

Portal HPN related to cirrhosis

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9
Q

Laterality of Hepatic Hydrothorax

A

More common on the right side

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10
Q

Recommended Sodium Restriction for Small Amounts of Ascites

A
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11
Q

Most common organisms causing Spontaneous Bacterial Peritonitis (SBP)

A

Escherichia coli and other gut bacteria

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12
Q

Presumed mechanism for development of SBP

A

Bacterial translocation

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13
Q

Most common antibiotic for SBP

A

Cefotaxime

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14
Q

Hepatic Encephalopathy (Portosystemic Encephalopathy)

A

Alteration in mental status and cognitive function occuring in the presence of liver failure

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15
Q

Asterixis or Liver Flap

A

Sudden forward movement of the wrist after it is bent back on an extended arm; cannot be elicited if patient already comatose

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16
Q

Mainstay of treatment for Hepatic Encephalopathy

A

Lactulose, to promote 2-3 soft stools per day

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17
Q

Hepatorenal Syndrome (HRS)

A

Functional renal failure without renal pathology in patients with advanced cirrhosis or acute liver failure

18
Q

Type 1 HRS

A

Progressive impairment in renal function and significant reduction in creatinine clearance within 1-2 weeks

19
Q

Type 2 HRS

A

Reduction in GFR with an elevation of serum creatinine level, but fairly stable (better outcome than Type 1 HRS)

20
Q

Best Therapy for HRS

A

Liver transplantation

21
Q

Phenotype of A1AT Deficiency with Greatest Risk for Developing Chronic Liver Disease

A

ZZ phenotype

22
Q

Most common cause of Portal HPN in the US

A

Cirrhosis

23
Q

3 primary complications of Portal HPN

A

Gastroesophageal varices with hemorrhage
Ascites
Hypersplenism

24
Q

First indication of Portal HPN in Liver Cirrhosis

A

Hypersplenism with thromboocytopenia

25
Q

Palliative procedure for Portal HPN

A

Transjugular Intrahepatic Portosystemic Shunt (TIPS)

26
Q

First-line treatment to control Acute Variceal Bleeding

A

Endoscopic intervention

27
Q

Most common cause of ascites

A

Portal HPN related to cirrhosis

28
Q

Laterality of Hepatic Hydrothorax

A

More common on the right side

29
Q

Recommended Sodium Restriction for Small Amounts of Ascites

A
30
Q

Most common organisms causing Spontaneous Bacterial Peritonitis (SBP)

A

Escherichia coli and other gut bacteria

31
Q

Presumed mechanism for development of SBP

A

Bacterial translocation

32
Q

Most common antibiotic for SBP

A

Cefotaxime

33
Q

Hepatic Encephalopathy (Portosystemic Encephalopathy)

A

Alteration in mental status and cognitive function occuring in the presence of liver failure

34
Q

Asterixis or Liver Flap

A

Sudden forward movement of the wrist after it is bent back on an extended arm; cannot be elicited if patient already comatose

35
Q

Mainstay of treatment for Hepatic Encephalopathy

A

Lactulose, to promote 2-3 soft stools per day

36
Q

Hepatorenal Syndrome (HRS)

A

Functional renal failure without renal pathology in patients with advanced cirrhosis or acute liver failure

37
Q

Type 1 HRS

A

Progressive impairment in renal function and significant reduction in creatinine clearance within 1-2 weeks

38
Q

Type 2 HRS

A

Reduction in GFR with an elevation of serum creatinine level, but fairly stable (better outcome than Type 1 HRS)

39
Q

Best Therapy for HRS

A

Liver transplantation

40
Q

Phenotype of A1AT Deficiency with Greatest Risk for Developing Chronic Liver Disease

A

ZZ phenotype