Liver disease Flashcards

(45 cards)

1
Q

What indicates hepatitis?

A

Raised AST and ALT

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2
Q

What is cholestasis?

A

Bile not reaching duodenum

Obstructive/metabolic

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3
Q

Signs of obstructive cholestasis:

A

Raised alkaline phosphatase

Raised GGT

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4
Q

What is blocked in large duct obstruction?

A

Extrahepatic bile duct

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5
Q

What is blocked in primary sclerosis cholangitis?

A

Large and/or small bile duct

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6
Q

What is blocked in primary biliary cirrhosis?

A

Small interlobular bile duct

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7
Q

What is haemochromatosis?

A

Autosomal recessive (HFE gene) disorder of iron metabolism that results in iron accumulation - causes abnormal liver enzymes, cirrhosis, hepatomegaly, joint pain and bronze skin

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8
Q

Important liver virology:

A

Hep B surface antigen

Hep C antibody

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9
Q

Features of hepatitis A:

A

Faeco-oral route
No chronicity
Hep A IgM = acute
Hep A IgG = previous exposure

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10
Q

Features of acute hepatitis B:

A

Initially Hep B surface antigen and core-IgM are present
Once virus is cleared these two go away and core-IgG develops
Later still Hep B surface antibody develops (implies immunity)

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11
Q

Features of chronic hepatitis B:

A

Hep B surface antigen and core-IgG stay risen (IgM falls)

Do not develop Hep B surface antibody

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12
Q

What does Hep B core-IgM indicate?

A

Acute infection

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13
Q

What does Hep B core-IgG indicate?

A

Hep B exposure

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14
Q

What should you do if you detect Hep B surface antigen?

A

Refer

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15
Q

What does Hep B surface antibody (>100) indicate?

A

Immunity

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16
Q

What are the different phases of Hep B infection?

A

Phase I = Viral load is high and inflammation is low; immune tolerant (0-18 years)
Phase II = Immune active hepatitis; liver problems (18-51 years)
Phase III = Cirrhosis, non-replicative (51-69 years)

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17
Q

When should you treat Hep B?

A

High viral load + elevated ALT

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18
Q

Hepatitis C curable treatments:

A

Ledipasvir/Sofosbuvir combined oral pill - 99% clear rate
OMV/PTV/RTV+DSV+RBV - 100% clear rate
Sofosbuvir/Velpatasvir >95% clear rate

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19
Q

Features of haemochromatosis (end organ failure):

A
Cirrhosis
Skin pigmentation
Diabetes
Cardiomyopathy
Arthritis
Pituitary failure
20
Q

How do you diagnose haemochromatosis?

A
Raised ferritin (women >200, men >300) and HFE genotype homozygote
Biopsy and hepatic iron index if ferritin is raised but HFE negative
21
Q

What does abnormal LFTs and ferritin >1000 indicate in haemochromatosis?

A

Cirrhosis

Liver should be biopsied

22
Q

Diagnosis of primary biliary cholangitis:

A

+ve anti-Mt Ab
Cholestatic LFTs
Raised IgG
Liver biopsy showing BD damage and granulomatous cholangitis

23
Q

Signs and symptoms of primary biliary cholangitis:

A
Asymp/fatigue/pruritis
Itching and tiredness
Cholestatic jaundice
Hyperpigmentation esp over pressure points
Xanthelasmas, xanthomata
Clubbing, hepatosplenomegaly
24
Q

Complications of primary biliary cholangitis:

A

Malabsorption causing osteomalacia or coagulopathy
Sicca syndrome
Portal hypertension causing ascites and vatical haemorrhage
Hepatocellular cancer

25
Treatment for primary biliary cholangitis:
Ursodeoxycholic acid | Obeticholic acid
26
How do you diagnose AI hepatitis?
Raised IgG +ve anti-nuclear antibody +ve smooth muscle antibody +ve liver-kidney microsomal antibody
27
Treatment of AI hepatitis:
Prednisolone | Azathioprine
28
How do you diagnose primary sclerosis cholangitis?
Liver biopsy for "onion skin" fibrosis + angiography imaging (ERCP or MRCP) Treat with ursodeoxycholic acid Males > females 75% association with IBD
29
Features of alpha 1-antitrypsin deficiency:
Autosomal recessive co-dominant - PiZZ genotype SOB from panacinar emphysema Cirrhosis and hepatocellular carcinoma in adults Cholestasis in children
30
Diagnosis of alpha 1-antitrypsin deficiency:
Alpha-1-antitrypsin level <25% | Liver biopsy = PAS +ve globules
31
What is Wilson's disease?
High urinary copper excretion Low serum caeruloplasmin Reduced biliary copper excretion
32
Features of Wilson's disease:
Liver cirrhosis Acute liver failure Neuropsychological disorders Kayser-Fleischer rings
33
Diagnosis of Wilson's disease:
Biopsy - liver copper >250 ug/g liver dry weight | Genetic tests
34
Treatment of Wilson's disease:
Penicillamine | Transplant
35
What is the difference between non-alcoholic fatty liver disease and non-alcoholic streatohepatitis?
NASH is more dangerous as it is inflammation and fibrosis whereas NAFLD is just fat
36
What do cirrhotic patients need to be screened for?
HCC
37
What causes ALT to go up?
Liver cell death
38
What is spider nave a sign of?
Chronic liver disease | Abnormal oestrogen metabolism
39
INR in poor liver function?
Raised
40
What is acutely decompensated cirrhosis?
Long-standing cirrhosis with a recent change
41
What forms the chronic liver disease screen?
``` Abdominal ultrasound AI screen Caeruloplasimn Alpha-1-antitrypsin Transferrin saturation Hepatitis ```
42
What does a transjugular biopsy of alcoholic hepatitis reveal?
Ballooning of hepatocytes | Neutrophil infiltration
43
Complication of alcoholic hepatitis (cirrhosis):
Hydrothorax - ascites fill lungs with fluid from the abdomen
44
Management of cirrhosis:
Give prednisone to bring bilirubin down Oesophageal vatical banding Transplant only if abstinent for 4-6 months
45
Association of liver disease?
Impaired oestrogen metabolism causing gynaecomastia