Liver Symposium Flashcards

1
Q

Define enteric vs parenteral?

A

Enteric - Occuring within the intestines

Parenteral - Occuring outwith the mouth & Alimentary canal

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2
Q

How many hepatitis viruses are there and are they enteric or parenteral?

A

A&E are enteric (normally self-limiting)

B,C,D are parenteral (often cause chronic disease)

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3
Q

How is HEP A transmitted?

A

By Faecal-Oral
Blood
Or Sexually

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4
Q

How do we diagnose HEP A?

A

With an IgM antibody test in the acute stage and IgG detectable for life

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5
Q

Who gets a HEP A immunisation?

A
  • Travellers
  • Chronic Liver Disease Patients
  • Hemophiliacs
  • Those with occupational exposure (E.g. lab workers)
  • Men who have Sex with Men (MSM)
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6
Q

What are the symptoms of hepatitis?

A

Short term hepatitis is often aymptomatic but can lead to:

  • Arthralgia
  • Fever
  • Nausea/Vomiting
  • Fatigue
  • Malaise
  • loss of appetite
  • abdominal pain
  • Pruritis
  • Jaundice
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7
Q

Describe the antigens associated with hepatitis B?

A

Hep Surface antigen - HBsAg - Indicates presence of virus

Hep e antigen - HBeAg - Virus Actively Replicating (found in blood)

Hep Core Antigen - HBcAg - Active Replication (found in liver biopsy)

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8
Q

Describe the antibodies associated with Hep B

A

IgM anti-HBc = Shows acute illness
IgG anti-HBc = Shows chronic or past infection
Anti-HBe = Shows up as virus is being inactivated by treatment
Anti-HBs = Shows infection or immunisation induced immunity (fights HBsAg)

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9
Q

When do people normally clear a HEP B infection and how do we tell if they’re beyond this period?

A

Around 6 months

If they are ill and IgM -ve it means theryre past the acute stage and unlikely to kick it themselves.

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10
Q

Consequence of chronic HEP B?

A

Cirrhosis -> End stage liver disease

Some develop liver cancer

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11
Q

How do we treat HEP B?

A

Antivirals

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12
Q

How does HEP C present differently?

A

Most people have no symptoms acutely but will develop chronic infection.
They dont usually show symptoms until they’re cirrhotic

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13
Q

How do we test for HEP C?

A

Chronic Anti-HCV antibodies

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14
Q

What special about Hepatitis D?

A

Its a small RNA virus and doesnt code for its own protien coat.
So it attaches itself to HEP B and acts as a co-infection.

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15
Q

What do we know about HEP E?

A

Its self limiting
Its the most common acute hepatitis in grampian
We have no treatment or vaccine

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16
Q

Name some other viruses that can cause hepatitis?

A
EBV or CMV in the immunocompromised
Herpes Simplex (rarely)
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17
Q

What is non-alcoholic fatty liver disease?

A

An umbrella term for:

  • Simple Steatosis (large but harmless fat in liver cells)
  • Non-alcoholic Steatohepatitis (Causing liver inflammation)
  • Fibrosis & Cirrhosis (result after years of NAFLD)

Occuring due to a build up of fat in the liver

18
Q

What are the risk factors or associations with NAFLD?

A
Diabetes Mellitus
Obesity
Hypertension
Hypercholesterolaemia
Hypertriglyceridemia
Age
Smoking
Ethnicity (hispanics)
Genetic Factors
19
Q

How do we test for NAFLD?

A

Often picked up during a LFT (reduced AST/ALT ratio) or ultrasound.

Follow up with CT/MRI

20
Q

How do we assess a NAFLD patient?

A

With a NAFLD score
Created from a set of criteria based on the patients test results and health/environmental factors to determine whether they are low or high risk

21
Q

What are the treatments for NAFLD?

A
  • Diet & Weight Reduction
  • Weight reduction Surgeries
  • Glucagon-like peptide-1 (GLP-1) analogues for chronic weight management.
  • Control of risk factors (e.g. diabetes, hypertension etc)
  • Vitamin E
  • Insulin Sensitisers for the diabetes.
22
Q

What are the commonest autoimmune liver diseasees?

A
  • Autoimmune hepatitis
  • Primary Biliary Cholangitis (PBC)
  • Primary Sclerosing Cholangitis (PSC)
  • Overlap Syndromes
  • Autoimmune Cholangiopathy
  • IgG 4 Disease
23
Q

How do we classify autoimmune hepatitis?

A

By the type of auto-antibody, split into:

  • Type 1
  • Type 2
  • Type 3
24
Q

How do we diagnose and treat autoimmune hepatitis?

A
  • Liver Biopsy -> Histological
  • Elevated IgG
  • Autoantibodies

Treat with immunosupressants:

  • Steroids (prednisalone)
  • Azathioprine
25
What is primary biliary cholangitis
Chronic granulomatous inflammation of the bile ducts - > Loss of the intra-hepatic bile ducts - > Eventually Cirrhosis May be down to an environmental trigger + genetic predisposition leading to immune intolerance to self-mitochondirla proteins
26
How do we test for Primary Biliary Cirrhosis? (PBC)
- Elevated Serum Alkaline Phosphatase (ALP) | - Test for antimitochondrial antibodies
27
Which gender is more likely to get Primary Biliary Cholangitis?
Women Whereas Primary Sclerosing Cholangitis is male predominant
28
What are the symptoms of PBC?
Fatigue & Pruritis Eventually Jaundice from backup of bilirubin Eventually cirrhosis and liver failure
29
How do we treat Primary BIliary Cholangitis?
UDCA (Urodeoxycholic acid) - a secondary bile acid - reduces cholestasis & improves LFTs Otherwise treat symptoms and eventually need a liver transplant.
30
What is primary sclerosing cholangitis? (PSC)
Progressive cholestasis with bile duct inflammation & fibrose stricture formation
31
What other conditions are associated with PSC?
Associated with IBD | Also increases risk of cholangiocarcinoma
32
Define cholangiocarcinoma?
Bile duct cancer (cancer of the epithelial lining of the biliary system). Usually adenocarcinoma
33
How do we test for Primary Sclerosing Cholangitis?
pANCA test. (neutrophil antibodies) | Magnetic Resonance Cholangiopancreatography (MRCP)
34
How does PSC present?
Reccurent Cholangitis & Jaundice | Also pruritis & fatigue
35
How do we treat PSC?
Liver transplant | Biliary Stents
36
What criteria deserve a liver transplant?
- Chronic liver disease with poor survival prediction - Chronic liver disease with poor quality of life - Hepatocellular Carcinoma - Acute Liver Failure - Genetic Diseases e.g. tyrosenimia, primary oxaluria
37
Tyrosenimia? Primary Oxaluria?
Tyrosenimia is an inbuilt error of metabolism where you cant break down tyrosine Primary Oxaluria, inherited condition causing excess oxalate in urine
38
Contraindications of a liver transplant?
- Active extrahepatic malignancy - Hepatic malignancy with macrovascular or diffuse invasion - Active substance abuse - Uncontrolled infection outside hepatobiliary system - Severe cardiopulmonary or other cormobid conditions - Psychosocial factors that preclude recovery - brain death - Technical/anatomical barriers
39
We have different protocol for deciding transplants in those with acute liver failure and chronic cirrhosis. How do we assess someone with chronic cirrhosis for a tansplant?
MELD Score - Model for End-Stage Liver Disease UKELD score The higher these scores the more likely you are to die without a transplant
40
Liver TRansplant is an orthotopic transplant, what does this mean?
It means it occurs at the same spot. | I.e. the original liver must be removed and the new one implanted in its place
41
What post op care is there for a liver transplant?
ICU care with a MDT Prophylactic antibiotics & antifungals Anti-rejection meds for life: - Steroids - Azathioprine (steroid-sparing immunosuppresant) - Tacrolimus/Cyclosporin
42
LFT results of NAFLD?
- RAised ALT, AST, ALKP, GGT | - Low AST/ALT ratio