Viral Hepatitis Flashcards

1
Q

Types of Hep viruses and how common are they in the UK?

A

A - less common now due to vaccination for travellers and better housing

B - mostly in ethnic minorities, who may be chronic carriers of infection

C

D - rare

E - rising

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2
Q

Table of hepatitis types?

A

ADD TABLE

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3
Q

Clinical course of hep B infection?

A

Immune tolerance phase 1 Immune clearance phase 2 Immune control phase 3 Immune escape phase 4

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4
Q

Describe the general clinical course of Hep B infection

A

Patient’s relationship with infection is dynamic; people will move between stages

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5
Q

Potential steps in Hep A infection?

A
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6
Q

Potential steps in Hep B infection, if infected as an adult?

A
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7
Q

Potential steps in Hep C infection?

A
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8
Q

Management of acute viral hepatitis?

A

Symptomatic; no anti-virals are given

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9
Q

Monitoring in acute viral hepatitis?

A

Monitor for encephalopathy and resolution

Test for other infection, as they are at risk, and vaccinate against other infections, if they are at risk

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10
Q

Management of chronic viral hepatitis?

A

Anti-virals (there are six for HBV and eight for HCV)

Vaccination for other Hep viruses and, if cirrhotic, vaccinate against influenza and pneumococcal

Decrease alcohol intake

Infection control

Hepatocellular carcinoma awareness/screening

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11
Q

Which people are treated with anti-virals in hepatitis, e.g: adefovir and entecavir?

A

Chronic infection:

HCV RNA present and genotype known

HBsAg and Hep B DNA present

Risk of complications:

Evidence of inflammation / fibrosis sought

Non-invasive tests for fibrosis e.g. fibroscan or biopsy

Biochemical evidence of inflammation (↑ALT)

Fit for treatment:

Established cirrhosis more difficult to treat

Liver cancer is a contraindication

HIV co-infection more difficult to treat

Patient issues:

Consider risk of serious side effects of antivirals attitude to treatment, and lifestyle issues

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12
Q

How is HBV DNA load related to hepatocellular carcinoma?

A

Higher a chronic HBV patient’s starting HBV DNA load, the greater the risk of cancer on follow-up

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13
Q

What is interferon alfa?

A

A human protein that is part of the immune response to viral infection

It can be administered by infecting pegylated interferon (peginterferon), which has a complex mode of action but inc. action as an immune adjuvant

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14
Q

Common and severe side effects of peginterferon?

A

Common - flu-like illness with rigors, myalgia and malaise

Severe - thyroid disease, autoimmune disease (e.g: SLE), psychiatric disease (avoid in those with a PMH of depression)

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15
Q

2 options for hep B therapy?

A

Option 1 - peginterferon alone; try in HBsAg and HBeAg positive patients with compensated disease and a prediction of good chance of cure

Option 2 (more common) - suppressive anti-viral drug

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16
Q

Advantages and disadvantages of option 1?

A

Advantages: Sustained cure possible from a few months of therapy

Disadvantages:

Side effects injections

Only a minority gain benefit

17
Q

Advantages and disadvantages of option 2?

A

Advantage:

Safer

Increasing range available

Disadvantage:

Suppression, not cure

Resistance can develop

18
Q

Examples of Hep B anti-virals?

A

Entecavir

Tenofivir

19
Q

What is the aim, in terms of sustained virological response, in HCV therapy?

A

Responses of >90% SVR (sustained virological response) are now considered benchmark to aim for

20
Q

Which anti-virals, for Hep C, can be used for all genotypes?

A

Peginterferon alfa and ribavirin but these have serious side effects

21
Q

Use of telaprevir and boceprevir?

A

Only for genotype 1 and enhances peginterferon/ribavirin

Serious side effects

22
Q

What are the newer anti-virals and when are they used?

A

Simeprevir, Ledipasvir, Daclatasvir are used in certain genotypes in combination with other drugs; they are safe and well tolerated

Sofosbuvir can be used against all genotypes and is used in combination; it is safe and well tolerated