Cirrhosis Flashcards

1
Q

Cirrhosis

Pathophysiology

A
  • Stellate cells activated by the cytokines from the kuppfer cells, hepatocytes
  • Stellate cells produce collagen, pro inflm cytokines which damage the hepatocytes and cause fibrosis
  • Overtime the liver architecture changes and from nodules and shrink
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2
Q

Cirrhosis

Two anatomical subtypes

A
  • Macronodular - viral hep
  • Micronodular- alcoholic, biliary disease
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3
Q

Cirrhosis

Etiology

A
  • Alcohol
  • NAFLD
  • Infections- Hep B/D, C
  • Immune- auto immune hep
  • Biliary- primary biliary cirrhosis, IIry biliary cirrhosis, sclerosing cholangitis
  • Genetic- wilson disease, Alpha 1 AT deficiency
  • Veno- occlusive- budd- chiari Sx
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4
Q

Cirrhosis

Peripheral stigmata

A
  • Icterus
  • Parotid swelling ( alcoholic Cirrhosis)
  • Gynecomastia
  • Spider nevi
  • Loss of body hair/ axillary hair
  • Clubbing
  • Palmar erythema
  • Dupuytren’s Contracture
  • Hepatic flaps
  • Dilated abdominal Vein/ caput medusae
  • Ascites
  • Edema of legs
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5
Q

Cirrhosis

Complications

A
  • Portal HTN&raquo_space;»> Variceal bleeding
  • Ascites, Spontaneous bacterial peritonitis
  • Hepatic encephalopathy
  • Hepatorenal syndrome
  • Coagulopathy
  • HCC
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6
Q

Cirrhosis

Sx seen in alcoholic Cirrhosis specifically

A
  • Parotid swelling
  • Dupuytren’s contracture
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7
Q

Cirrhosis

Decompensated Cirrhosis

A
  • HE
  • Ascites
  • Bleeding
  • Portal HTN
  • New- onset Jaundice
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8
Q

Cirrhosis

Hepatic flap?

A

Asterixis

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9
Q

Cirrhosis

Ix done to

A
  • Confirm the Dx
  • Find the etiology
  • Assess the complications
  • Estimate the prognosis
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10
Q

Cirrhosis

Ix done to confirm the Dx

A
  • USS Abd- architecture, splenomegaly, ascites
  • FBC- thrombocyto»» pancyto
  • LFT- AST> ALT
  • Sr. Bilirubin reduced
  • Sr. Albumin reduced
  • PT/INR- Increased
  • Renal Function test ( Hepatorenal Xd) - Low Na
  • Sr. AFP- >=200 is HCC
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11
Q

Cirrhosis

LFT

A
  • AST> ALT ( norm ALT>AST)
  • Sr. Bilirubin
  • Sr. Albumin
  • PT/INR
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12
Q

Cirrhosis

Best Ix for HCC

A

Triphasic CT before Now Fourphasic CT

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13
Q

Cirrhosis

Why is albumin only seen during chronic liver cell disease

A

Long t 1/2.

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14
Q

Cirrhosis

Why is PT/INR elevated in acute and chronic liver cell disease

A

Short t1/2

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15
Q

Cirrhosis

Ix to look for etiology - Infective

A

Viral Hep- Hep B, C serology

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16
Q

Cirrhosis

Ix to look for the etiology- Autoimmune

A

Autoimmune Hep - ANA, Anti smooth muscle Ab , IgG increased

17
Q

Cirrhosis

Ix to look for the etiology - Metabolic

A
  • Wilsons’ disease- Sr. ceruloplasmin reduced, 24h urine Cu excretion increased
  • Hemochromatosis- Sr Fe studies
18
Q

Cirrhosis

Ix to look for the etiology- Biliary cirrhosis

A

Iry- Anti mitochondrial AB, Increased IgM

19
Q

Cirrhosis

If tests are inconclusive and cannot find the etiology

A

Do a biopsy

20
Q

Cirrhosis

Why are Bx not usually done

A

prone to bleeding

21
Q

Cirrhosis

if the cause cannot be confirmed even w a Bx

A

Cryptogenic Cirrhosis

22
Q

Cirrhosis

Assess the prognosis

A
  • Child- Pugh score
  • MELD score
23
Q

Cirrhosis

Child- Pugh score

A
  • PT/INR
  • HE
  • Bilirubin
  • Albumin
24
Q

Cirrhosis

MELD score

A
  • PT/INR
  • Bilirubin
  • Creatinine
25
# Cirrhosis General Mx
* Remove the causative agent * Adequate diet of vegetable proteins * Avoid physical exertion * Vaccines- HBV, HAV, Pneumococcal, flu * Avoid precipitating factors of HE
26
# Cirrhosis Diet intake
* Correct deficiencies of protein, calorie, vitamin, minerals * Vegetable protein- 1g/kg/d * Adequate calorie intake to prevent proteolysis - 25- 35kcal/d