Cirrhosis Flashcards

1
Q

What is cirrhosis?

A

End-stage of chronic liver damage with replacement of normal liver architecture with diffuse fibrosis + nodules of regenerating hepatocytes.

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2
Q

When is cirrhosis considered decompensated?

A
Once it becomes complicated by: 
Ascites  
Jaundice 
Encephalopathy 
GI bleed
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3
Q

List 8 causes of cirrhosis

A

Chronic alcohol misuse (most common in UK)
Chronic viral hepatitis (hep B/C: most common worldwide)
AI hepatitis
Drugs (e.g. methotrexate, hepatotoxic drugs)
Inherited
Vascular: Budd-Chiari Syndrome, Hepatic Venous Congestion
Chronic Biliary Diseases: PBC, PSC, Biliary atresia
Unknown: 5-10%
Non-Alcoholic Steatohepatitis (NASH)

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4
Q

What things may precipitate decompensation?

A
Infection
GI bleeding
Constipation
High-protein meal
Electrolyte imbalances
Alcohol + drugs
Tumour development
Portal vein thrombosis
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5
Q

Describe the epidemiology of cirrhosis

A

In top 10 causes of death worldwide

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6
Q

List 5 early non-specific symptoms in cirrhosis

A
Anorexia 
Weight loss
Nausea  
Fatigue  
Weakness
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7
Q

List 3 symptoms caused by reduced liver synthetic function

A

Easy bruising
Abnormal swelling
Ankle oedema

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8
Q

List 5 symptoms caused by reduced detoxification function

A
Jaundice  
Personality change  
Altered sleep pattern  
Amenorrhoea 
Galactorrhoea
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9
Q

List 3 symptoms caused by portal HTN

A

Abdominal swelling
Haematemesis
PR bleeding or melaena

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10
Q

What are the ABCDE signs in cirrhosis?

A
Asterixis 
Bruises  
Clubbing  
Dupuytren's contracture 
Palmar erythema
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11
Q

List 11 signs of cirrhosis

A
Jaundice  
Gynaecomastia  
Leukonychia  
Parotid enlargement  
Spider naevi 
Scratch mark (from cholestatic pruritis)  
Ascites (shifting dullness)
Enlarged liver (shrunken in later stages)  
Testicular atrophy 
Caput medusae  
Splenomegaly
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12
Q

What bloods should be investigated in cirrhosis?

A

FBC: low platelets + Hb = because of hypersplenism due to portal HTN
LFTs: some normal, but often get:
High AST, ALT, ALP, GGT + BR
Low albumin
Clotting: prolonged PT (decreased synth of clotting factors)
Serum AFP (tumour marker for liver cancer):
Raised in chronic liver disease but high levels may suggest hepatocellular carcinoma

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13
Q

Why should an Ascitic Tap be performed in cirrhosis?

A

MC+S : check for infection
Biochemistry (protein, albumin, glucose, amylase)
Cytology
If neutrophils > 250/mm3 = spontaneous bacterial peritonitis (SBP)

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14
Q

Which method of liver biopsy is used in cirrhosis? What are the histopathological features?

A
Percutaneously 
Transjugular (if clotting deranged or ascitic) 
Periportal fibrosis  
Loss of normal liver architecture  
Nodular appearance  
Grade: degree of inflammation  
Stage: degree of architectural distortion (from mild portal fibrosis to cirrhosis)
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15
Q

What imaging should be performed in cirrhosis?

A

US, CT or MRI: to detect Ascites, HCC, Hepatic or portal vein thrombosis + Exclude biliary obstruction
MRCP (if PSC suspected)

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16
Q

What may be found on endoscopy in cirrhosis?

A

Varices

Portal hypertensive gastropathy

17
Q

What grading system is used to estimate prognosis in cirrhosis?

A
Child-Pugh Grading A-C: based on 5 factors: 
Albumin  
BR
PT 
Ascites  
Encephalopathy
18
Q

How is cirrhosis managed?

A
Treat the CAUSE if possible  
Avoid alcohol, sedatives, opiates, NSAIDs + drugs that affect the liver  
Nutrition is important  
Enteral supplements should be given  
NG feeding may be indicated
19
Q

How is encephalopathy treated?

A

Treat infections
Exclude GI bleed
Use lactulose + phosphate enemas
Avoid sedation

20
Q

How is ascites treated?

A

Diuretics (spironolactone +/- furosemide)
Dietary sodium restriction
Therapeutic paracentesis (with human albumin replacement)
Monitor weight
Fluid restrict if plasma Na+ < 120 mmol/L
Avoid alcohol + NSAIDs

21
Q

How is SBP treated?

A

Abx (e.g. cefuroxime + metronidazole)

Prophylaxis against recurrent SBP with ciprofloxacin

22
Q

What surgical intervention may be used in cirrhosis to reduce portal HTN? What is the issue with this?

A

TIPS (transjugular intrahepatic portosystemic shunt) to reduce portal HTN
May precipitate encephalopathy as provides a route for blood from GIT to bypass the liver

23
Q

List 7 complications of cirrhosis

A
Portal HTN with ascites  
Hepatic encephalopathy 
Variceal haemorrhage  
SBP 
HCC 
Renal failure (hepatorenal syndrome)  
Pulmonary HTN (hepatopulmonary syndrome)
24
Q

What is the prognosis in cirrhosis?

A

Depends on aetiology + complications
Generally poor prognosis
Overall 5 year survival = 50%
If ascites, 2 year survival = 50%

25
Q

List 5 inherited diseases that can lead to cirrhosis

A
a1-antitrypsin deficiency
Haemochromatosis
Wilson's disease
Galactosaemia
Cystic Fibrosis
26
Q

List 6 risk factors for NASH

A
Obesity
Diabetes
Total parenteral nutrition
Short bowel syndromes
Hyperlipidaemia
Drugs (e.g. amiodarone, tamoxifen)
27
Q

What investigations can be used to determine the cause of cirrhosis?

A
Viral serology (hep B + C)
a1-antitrypsin  
Caeruloplasmin (LOW in Wilson's)  
Iron studies: serum ferritin, iron, total iron binding capacity (TIBC): for haemochromatosis 
Anti-mitochondrial antibody (PBC) 
ANA
SMA (AI hepatitis)
28
Q

How does encephalopathy arise in cirrhosis? How does lactulose treat this?

A

Normal liver breaks down ammonia absorbed in GIT
In Cirrhosis, ammonia goes through liver without being broken down + exerts toxic effects on the brain
Lactulose reduces absorption of ammonia from gut
Helps prevent encephalopathy caused by ammonia reaching the brain

29
Q

What is the only curative method for cirrhosis?

A

Liver transplant