Viral Hepatitis (A & E) Flashcards

1
Q

Definition

A

Hepatitis caused by infection with the RNA viruses, hepatitis A or hepatitis E virus, that
follow an acute course without progression to chronic carriage

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2
Q

Aetiology

A
  • HAV = picornavirus
  • HEV = calicivirus
  • Transmission = faecal-oral route
  • Both viruses replicate within hepatocytes and are secreted into bile
  • Liver inflammation and hepatocyte necrosis is caused by the immune response
  • Infected cells are targeted by CD8+ T cells and NK cells
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3
Q

Histological features

A

o Inflammatory cell infiltration of portal tracts
o Zone 3 necrosis
o Bile duct proliferation

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4
Q

Epidemiology

A
  • HAV is endemic in the developing world
  • Infection often occurs sub-clinically
  • Better sanitation in the developed world means that it is less common, age of exposure is higher and, hence, patients are more likely to be symptomatic
  • HEV is endemic in Asia, Africa and Central America
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5
Q

Incubation period

A

Incubation period of HAV and HEV: 3-6 weeks

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6
Q

Presenting symptoms (prodromal period - period just after incubation)

A

o Malaise
o Anorexia
o Fever
o Nausea and vomiting

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7
Q

Presenting symptoms (hepatic)

A

o Dark urine
o Pale stools
o Jaundice lasting around 3 weeks
o Occasionally, itching and jaundice may last several weeks in HAV infection

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8
Q

Signs on physical examination

A
• Pyrexia
• Jaundice
• Tender hepatomegaly
• Spleen may be palpable
• ABSENCE of stigmata of chronic liver disease (although some spider naevi may appear
transiently)
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9
Q

Investigations (bloods)

A

o LFTs - high AST, ALT, ALP and bilirubin
o High ESR
o Low albumin + high platelets (if severe)

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10
Q

Investigations (serology)

A

o Hepatitis A:
• Anti-HAV IgM (during acute illness, disappears after 3-5 months)
• Anti- HAV IgG (recovery phase and lifelong persistence)

o Hepatitis E:
• Anti-HEV IgM (raised 1-4 weeks after onset)
• Anti-HEV IgG

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11
Q

Investigations (urinalysis)

A

o Positive for bilirubin

o Raised urobilinogen

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12
Q

Management plan (symptomatic)

A

There is no specific management other than bed rest and symptomatic treatment (e.g. antipyretics, antiemetics or cholestyramine (for severe pruritus))

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13
Q

Management plan (prevention and control)

A

o Public Health - safe water, sanitation and food hygiene

o These are notifiable diseases

o Immunisation is available for HAV
• Passive immunisation with IM human immunoglobulin (effective for a short
time)
• Active immunisation with attenuated HAV vaccine offers safe and effective
immunity for those travelling to endemic areas and high-risk individuals

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14
Q

Possible complications

A
  • Fulminant hepatic failure (in a very small proportion of patients but is more common in pregnant women)
  • Cholestatic hepatitis with prolonged jaundice and pruritus can develop after HAV infection
  • Post-hepatitis syndrome: continued malaise for weeks to months
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15
Q

Prognosis

A
  • Recovery is usually within 3-6 weeks
  • Occasionally patients may relapse during recovery
  • There is no chronic sequelae
  • Fulminant hepatic failure has a mortality of 80%
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