Viral Hepatitis (A & E) Flashcards
Definition
Hepatitis caused by infection with the RNA viruses, hepatitis A or hepatitis E virus, that
follow an acute course without progression to chronic carriage
Aetiology
- 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
Histological features
o Inflammatory cell infiltration of portal tracts
o Zone 3 necrosis
o Bile duct proliferation
Epidemiology
- 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
Incubation period
Incubation period of HAV and HEV: 3-6 weeks
Presenting symptoms (prodromal period - period just after incubation)
o Malaise
o Anorexia
o Fever
o Nausea and vomiting
Presenting symptoms (hepatic)
o Dark urine
o Pale stools
o Jaundice lasting around 3 weeks
o Occasionally, itching and jaundice may last several weeks in HAV infection
Signs on physical examination
• Pyrexia • Jaundice • Tender hepatomegaly • Spleen may be palpable • ABSENCE of stigmata of chronic liver disease (although some spider naevi may appear transiently)
Investigations (bloods)
o LFTs - high AST, ALT, ALP and bilirubin
o High ESR
o Low albumin + high platelets (if severe)
Investigations (serology)
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
Investigations (urinalysis)
o Positive for bilirubin
o Raised urobilinogen
Management plan (symptomatic)
There is no specific management other than bed rest and symptomatic treatment (e.g. antipyretics, antiemetics or cholestyramine (for severe pruritus))
Management plan (prevention and control)
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
Possible complications
- 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
Prognosis
- 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%