Chronic Liver Disease Flashcards

1
Q

What are the potential causes of chronic liver disease?

A
Alcoholic liver disease
NAFLD
Autoimmune hepatitis
Primary biliary cholangitis
Primary sclerosis cholangitis
Glycogen storage disease
Alpha 1 antitrypsin deficiency
Haemochromatosis
Wilson's disease
Viral hepatitis (B/C, cytomegalovirus, EBV)
Drugs - methotrexate, amiodarone
Budd chiari syndrome
Veno-occulsive disease
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2
Q

What is the treatment for ascites?

A

Sodium restriction

Diuretics

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3
Q

Describe the management of chronic liver disease?

A

Treat the underlying cause
Manage complications
Consider liver transplant / TIPS

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4
Q

What are the potential complications of chronic liver disease?

A
Portal hypertension -> ascite -> SBP
Portal hypertension -> oesophageal varices -> haemorrhage
Portal hypertension -> splenomegaly
Hepatorenal syndrome
Heptopulmonary syndrome
Coagulopathy - > bleeding / bruising
Acute decompensation
Encephalopathy
Heptocellular carcinoma 
Hypogonadism
Hepatic oesteodystrophy
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5
Q

What antibodies are present in autoimmune hepatitis?

A
Type 1 (common in females) - ANA, SNA
Type 2 (common in children) - anti-LKM1
Type 3 (rare) - p-ANCA
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6
Q

What is the treatment for autoimmune hepatitis?

A

Corticosteroids +/- immunosuppressants

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7
Q

What are the risk factors for NAFLD?

A
Insulin resistance / diabetes
Obesity
Dyslipidaemia
Total parenteral nutrition
History of recent weight loss
Medications
Hypertension 
Metabolic syndrome
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8
Q

What is the management of NAFLD?

A

Weight loss - diet, exercise, pharmacotherapy, roux-en-y gastric bypass
Statins if dyslipidaemia
Glycemic control if diabetic

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9
Q

Which other autoimmune diseases are associated with primary biliary cholangitis?

A

Sjogren’s
Scleroderma
Coeliac disease

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10
Q

How is primary biliary cholangitis managed?

A

Corticosteroids to reduce inflammation
Replace of bile acids - ursodeoxycholic acid
Anti-puritics
Liver transplant for end-stage disease

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11
Q

How is primary sclerosing cholangitis managed?

A

Antipuritics
Immunosuppressants if there is overlapping AI hepatitis
Calcium and Vitamin D if there is associated osteopenia
Bisphosphonates +/- HRT is there is associated osteoporosis
Liver transplant for end-stage disease

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12
Q

Which malignancies are there increased risk of in primary sclerosing cholangitis?

A

Cholangiocarcinoma

Hepatocellular carcinoma

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13
Q

What are the potential complications of primary sclerosing cholangitis?

A
  • Osteoporosis
  • Cholangiocarcinoma
  • Hepatocellular carcinoma
  • Cirrhosis and its complications
  • Bacterial cholangitis
  • Fat soluble vitamin deficiencies
  • Choledocholithiasis
  • Gallbladder carcinoma
  • Colon cancer
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14
Q

What is the inheritance pattern of hereditary haemochromatosis?

A

AR

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15
Q

How can hereditary haemochromatosis present?

A
Fatigue
Arthralhia
Lethargy
Loss of libido
Skin bronzing
Complication - cirrhosis, cardiomyopathy, diabetes, arthritis
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16
Q

In addition to phlebotomy, what is important in the management of haemochromatosis?

A

Vaccination against hepatitis A and B

17
Q

What is the inheritance pattern of Wilson’s disease?

18
Q

What is the typical presentation of Wilson’s disease?

A

Patient aged 10-40 years presenting with either hepatic disease of neurological disease (movement disorder, psychiatric)

19
Q

What investigations can be conducted for Wilson’s disease?

A

24 hour urine copper
Serum ceruloplasmin
Opthalmological slit lamp examination for Kayer- Fleischer rings
Liver biopsy looking for accumulation of copper

20
Q

How is Wilson’s disease treated?

A

For hepatic disease - Trientine and zinc

For neurological disease - zinc

21
Q

Other than cirrhosis, what are the potential causes of ascites?

A
Congestive heart failure
Congestive pericarditis
Nephrotic syndrome
Budd chiari syndrome
Alcoholic liver disease
Massive liver mets
22
Q

Describe the four clinical stages of hepatic encephalopathy?

A

1) slurred speech, sleep disturbances, mild confusion, altered behaviour
2) lethargy, moderate confusion
3) stupor, in cohort speech, sleeping
4) coma

23
Q

What factors can precipitate hepatic encephalopathy in chronic liver disease?

A
Constipation
Use of sedatives
GI bleeding
Hypokalaemia
Infection
Alkalosis
24
Q

How is hepatic encephalopathy treated?

A

Supportive measures e.g. preventing aspiration
Tx underlying / precipitants
Reduce GI ammonia production

25
Hepatitis A is usually asymptomatic in children and symptomatic in adults. T/F?
True
26
Hepatitis B is usually symptomatic in children and asymptomatic but chronic in adults. T/F?
False - the opposite is true: | Hep B is usually asymptomatic but chronic in children and symptomatic but acute in adults
27
What is the treatment for hepatitis B?
Interferon | Tenofevir / entecavir
28
What is the treatment of hepatitis C?
Direct acting antivirals
29
What is the treatment of hepatitis D?
Interferon only
30
Describe how antibody/antigen testing in hepatitis B can tell the difference between current infection, previous infection and previous vaccination?
Surface antibody is positive if previously vaccinated Core antigen is positive if previously infected but not if previously vaccinated Surface antigen indicates current infection
31
How can hepatitis B be transmitted?
Mother to child IVDU / needle sharing / needle stick injury Infected blood products Transplant
32
In what group of patients can hepatitis E infection be severe?
Pregnant women
33
What are the potential neurological sequelae of hepatitis E?
Guillain-barre syndrome Ataxia Encephalitis Myopathy
34
Other than the hepatitis viruses, what are the other potential infectious causes of hepatitis?
- EBV - CMV - Toxoplasmosis - Yellow fever - Leptospirosis - Q fever - Syphilis - Malaria - Viral haemorrhagic fevers