Week 10 - Hepatobiliary and Pancreatic Disease Flashcards

(59 cards)

1
Q

How can you differentiate acute v chronic liver disease?

A
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2
Q

What are the acute causes of liver disease?

A

Drugs (paracetamol, herbal, penicillins, thiopurines)
Alcohol
Viruses (Hep A, B & E, CMV, Covid, EBV)
Vascular (hepatic vein thrombosis)
Ischaemic liver disease
Wilsons’s disease

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3
Q

What are the chronic causes of liver disease?

A

Alcohol
Fatty liver disease
AI disease - (AI hepatitis, Primary biliary cirrhosis)
PSC
Viruses - Hep B&C
Congenital - Haemochromatosis, Wilsons, A1AT deficiency

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4
Q

If the liver is damages - what synthetic functions are limited causing Sx?

A

Failure to clear bilirubin -> Jaundice

Failure to produce clotting factors (2,7, 9 & 10) -> coagulopathy & raised INR

Failure to produce protein -> hypoalbuminaemia

Failure to get rid of toxins -> encephalopathy

Ascites

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5
Q

Which viruses that cause hepatitis tend to be self limiting?

A

Hep A, B & E,
CMV
EBV
Covid

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6
Q

Which viruses that cause hepatitis need treatment?

A

B, C & E

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7
Q

In viral hepatitis - what level will ALT usually be?

A

Usually >1000

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8
Q

Which is the only DNA hepatitis virus?

A

Hep B

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9
Q

What is the transmission of Hep E?

A

4 types (1-4)

3 & 4 = zoonotic
Rest = faecal-oral or blood

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10
Q

Which hepatitis is the most common cause of liver failure in pregnancy?

A

Hep E

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11
Q

How can Ps with Hep E present?

A

Mostly asymptomatic
S&S = jaundice, fever, myalgia, vomiting and abdo pain

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12
Q

Which serology can screen for Hep E infection?

A

anti-HEV IgM

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13
Q

What is the trouble of catching Hep E in the immunosuppressed?

A

Can cause chronic hepatitis (cirrhosis does not occur)

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14
Q

What is the most common method of transmission of Hep B?

A

Mother to baby

Also - sex, IVDU

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15
Q

What are the consequences of Hep B infection if untreated?

A

Can cause cirrhosis and hepatocellular cancer

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16
Q

What is the definition of chronic Hep B infection?

A

Hep B +ve for > 6 months

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17
Q

What are the 4 states of hepatitis B infection?

A

Born - and contract Hep B during delivery - have the virus until 25-30 - high viral load but liver doesn’t care = immunotolerant phase. Really high viral load but liver handles it ok.

Liver decides it doesn’t like it and tries to get rid of it - attacks the E antigen which makes it from positive to negative - viral load drops, liver function tests get raised and then normalise = inactive state - low viral load and normal LFTs. Around 30.

Cycle of viral load starts creeping up - liver gets angry - LFTs go up, viral load goes down again - cycle of inflammation and calming causes liver scarring - 10-30 years - develops into cirrhosis. 4 phases.

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18
Q

What are the S&S of acute Hep B infection?

A

Mostly asymptomatic
Many get jaundice and fever
Acute liver failure rare

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19
Q

How can you identify Hep B infection from serology?

A

ALT >1000 in acute
In chronic - ALT may be normal or slightly elevated

Can also look for
Hep B sAg (surface antigen) and sAb (surface antibody)
Hep B eAg (envelope antigen)
Hep B cAb (core AB)

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20
Q

When should you Rx Ps with drugs with Hep B?

A

When they are fibrotic, or HBV DNA >2000 or they have elevated ALT on more than 2 occasion

OR

In 3rd trimester to prevent transmission

OR If immunosuppressed

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21
Q

What does Hep D to a Hep B infection?

A

Makes it more aggressive and increases the risk of liver failure

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21
Q

How is Hep C transmitted?

A

Blood, sex or IVDU.
Vertical transmission low.

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22
Q

How can you confirm active Hep C infection?

A

Presence of Hep C IgC

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23
Q

Without Rx, what is the prognosis of a Hep C infection?

A

30% will progress to cirrhosis in 10-20 years, another 20% over 20-30 years and a further 30% over 30 years. So 90% will develop cirrhosis within 30 years

23
How can you test for EBV?
Positive monospot test
24
What is the Rx for CMV?
Ganciclovir if severe
25
What is the Rx for HSV 1 & 2?
Aciclovir
26
Which drugs can cause hepatitis?
27
Which drugs can cause cholestasis?
28
Which drugs can cause mixed hepatitis and cholestasis?
29
How does alcoholic hepatitis present histologically?
Steatohepatitis Mallory denk bodies Ballooning degeneration of hepatocytes Neutrophillic inflammation
30
What is the Rx for alcoholic hepatitis?
Steriods Nutrition Abstinence
31
What does histology showing lymphoplasmacytic interface hepatitis with rosettes of hepatocytes indicate?
AI Hepatitis
32
Which ABs are liked to AI hepatitis?
Smooth muscle AB - anti-SMA Liver kidney microsomal - anti-LKM1 Also - AMA and immunoglobulins which indicate PBC and AI hepatitis
33
What is Rx for AI hepatitis?
Steriods Azathioprine
34
How will Ps with hyperacute, acute and subacute liver failure present?
Depends on time from jaundice to hepatic encephalopathy. Hyperacute = happens less than 1w Severe coagulopathy (+++), not so much jaundice (+) and raised intracranial HTN - Paracetamol, Hep A &E Acute = happens within 1 month (1-4w), less severe coagulopathy (++), more jaundice (++) and same levels of raised intracranial HTN - Hep B Subacute - happens over up to 3m (4w-12w), much less severe coagulopathy (+), but severe jaundice (+++), and may or may not have raised intracranial HTN - Hep D
35
What causes ascites?
Leakage of fluid from portal vessels into the peritoneal cavity.
36
Which criteria is used to differentiate between transudate and exudate? What is used to determine this?
Light's criteria Uses protein and LDH levels in fluid and blood
37
What type of fluid is found in ascites?
Transudate
38
Ascitic fluid can also be found where?
It can cross the diaphragm -> pleural effusions
39
What are the clinical signs of decompensated cirrhosis?
Ascites Encephalopathy Jaundice GI Bleeding Renal failure
40
What is the mean survival for 2 years after decompensated cirrhosis?
2 years
41
What can cause decompensated cirrhosis?
Infection - SBP Hepatocellular carcinoma Electrolyte abnormalities GI bleeding Natural progression of liver disease - e.g. cont drinking
42
What do raised ferritin and transferritin saturations indicate?
High iron levels - Hereditary haemochromatosis
43
What do raised caeruloplasmin and copper indicate?
Wilson's disease
44
What does low levels of α 1 antitrypsin possibly indicate?
α 1 antitrypsin deficiency
45
What protein do we test for to exclude hepatocellular carcinoma?
AFP - alphafetoprotein Typically most high in HCC - can get very elevated levels. Can get less high increases with liver disease, pregnancy, pancreatic or GI cancers.
46
How can you determine whether a disease is causing hepatitis or cholestasis using serology?
Look at the ALP and ALT Disease that causes hepatitis - typically raises ALT Cholestasis - typically raises ALP Look at R value R value = ALT / ULN : ALP / ULN If >5 = hepatocellular If <2 = cholestatic If 2-5 = mixed cause
47
What is transaminitis?
Raised ALT levels
48
What percentage of Ps are antibody negative but still have AI hepatitis?
20%
49
How is acute liver failure defined?
Acute liver injury - so no underlying chronic liver disease - Damage - ALT 2-3x ULN - Impaired function -> jaundice or coagulopathy and Hepatic Encephalopathy
50
What normally causes - Hyperacute liver failure - Acute liver failure - Subacute liver failure?
Hyperactive = Paracetamol, Hep A & E Acute = Hep B Subacute = Hep D
51
What does SBP stand for?
Spontaneous bacterial peritonitis
52
Which score is used to assess the progress of chronic liver disease?
Child Pugh Score
53
What are the endocrine and exocrine functions of the pancreas?
Endocrine = produce insulin and glucagon Exocrine = produce faecal elastase
54
What are the causes of acute pancreatitis?
55
Which drugs can cause acute pancreatitis?
Azathioprine Mesalazines Thiazide diuretics
56
What can necrotising pancreatitis form?
Pseudocysts A pseudocyst is a fluid-filled sac that forms in the abdomen, typically following an episode of acute pancreatitis or as a complication of chronic pancreatitis. Unlike true cysts, pseudocysts do not have an epithelial lining; instead, they are surrounded by a fibrous or granulation tissue.
57
Why does CF cause pancreatitis?
Ducts get block due to thicker fluid in the pancreas (due to Cl channel impairment due to CFTR gene problems). -> Inflammation = pancreatitis -> Fibrosis and atrophy Can cause failure to thrive, steatorrhoea