Hepatitis A and E Flashcards
Define:
- Hepatitis caused by infection with the RNA viruses, hepatitis A or hepatitis E virus, that follow an acute course without progression to chronic carriage
- Acute infection only
Aetiology/risk factors:
These are both transmitted by faecal oral route.
Hep A - uncooked poultry (usually picked up by travellers)
Hep E - uncooked seafood
• Both viruses are small non-enveloped single-stranded linear RNA viruses.
They replicate in hepatocytes and then are excreted in the bile leading to inflammation and tissue necrosis
Epidemiology:
- HAV is endemic in the developing world
- Infection often occurs sub-clinically (no clinical findings)
- 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
- Annual UK incidence: 5000
- HEV is endemic in Asia, Africa and Central America
Symptoms:
There is an incubation period of a couple of weeks.
- Malaise
- Fever
- Weight loss - smokers often no longer want cigarettes
- nausea and vomiting
Signs of jaundice: Yellow sclera Dark urine Pale stools itching
Signs:
- Pyrexia
- Jaundice
- Tender hepatomegaly
- Spleen may be palpable
- ABSENCE of stigmata of chronic liver disease (although some spider naevi may appear transiently)
Investigations:
Bloods:
- LFT’s - AST, ALT, ALP up and albumin down
- ESR
- platelets
Serology:
anti -Hep A antibody IG M = acute where IG G = CHRONIC
anti - Hep E antibody
urinanalysis:
- High urobilinogen
- positive for bilirubin
Management:
These are acute and the management is often symptomatic - anti-emetics, anti-pyretics and cholestyramine ( for itchiness)
There can be control and prevention such as sanitsation and vaccination in hep A.
complications:
fulminant hepatitis (usually in pregnant women, massive necrosis of liver parenchyma and a decrease in liver size) • Cholestatic hepatitis with prolonged jaundice and pruritus can develop after HAV infection • Post-hepatitis syndrome: continued malaise for weeks to months
prognosis:
usually recover in 3-6 weeks.
- Occasionally patients may relapse during recovery
- There are no chronic sequelae
- Fulminant hepatic failure has a mortality of 80%