Hepatitis Flashcards

1
Q

Hepatitis A

A
Acute
Fecal oral
Travellers
Vaccine is available 
IgM - infection
IgG - recoverinG
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2
Q

Hep E

A
Acute
Fecal oral
IgM infection 
IgG- recovering
Can become fulminant hepatitis
Avoid by boiling and purifying water, cooking meat
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3
Q

Hep C

A
Acute or chronic
Sex, needles and birth
No vaccine 
Drugs = sovaldi and harvoni
RNA / PCR
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4
Q

Hep D

A

Co-infection with Hep B
Co-infection at the same time
Superinfection is where Hep D comes after or during Hep B infection but not at same time

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5
Q

Hep B

A
Chronic
20% go on to become fulminant 
hepatocellular carcinoma and cirrhosis risks
Vaccines available
Sex, needles and childbirth
Antigens - surface, envelope, core, DNA
Antibodies - surface, core
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6
Q

What are the stages of Hep B infection?

A
  1. Surface antigen (supervillain) is detected
  2. Envelope and RNA is made, and core antigens (factory/ core workers)
  3. Window phase with IgM anti-Cag - all low - don’t know who will win
  4. Outcomes could be IgG anti-Sag, followed by IgM to IgG anti-cab
  5. Or chronic infection with IgM and high RNA and antigens
  6. Or latent infection with low IgG and low antigens
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7
Q

What blood tests for Hep B?

A

ALT>AST
Both high
bilirubin

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8
Q

What are the serotypes of hepatitis E? Which one is non-endemic?

A

1-4

3 is non-endemic

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9
Q

What are some complications of HEV?

A
Neurological:
– Guillain-Barre Syndrome
– Bell’s Palsy
– Acute transverse myelitis
– Meningioencephalitis
 Kidney Injury: Membranoprolefertaive and membranous
glomerulonephritis
 Pancreatitis mainly with HEV 1
 Haemolytic Disorders
– Thrombocytopenia
– Aplastic anaemia
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10
Q

What is some management for HEV?

A
Treatment:
– Reduction of immunosuppression – clearance in nearly one
third of patients
– Ribavirin
– Pegylated Interferon
 Prevention:
– Sanitation, clean water
– Avoiding eating undercooked meet
– Vaccines:
 VLP of E2 domain of HEV 1 capsid protein generated in
E Coli. Licensed for use in China
 VLP of E2 domain of HEV1 capsid protein generated in
insect cells. Phase 111 trial in Nepal
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11
Q

How many genotypes of HEV?

A

4

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12
Q

Who should have the HAV?

A

Travelling to or going to reside in areas of high or intermediate prevalence
– Patients with chronic liver disease
– Patients with haemophilia
– Men who have sex with men
– Injecting drug users
– Individuals at occupational risk i.e. laboratory workers, staff of some large
residential institutions, sewage workers, people who work with primates

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13
Q

Globally what are the main causes of death from liver disease?

A

 HBV 39%
 HCV 19% (fallen from 25% in 2000)
 alcohol 24%
 other causes 18%

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14
Q

Who is screened for HBV?

A
Blood and organ donors
• Healthcare workers
• Pregnant women
• Dialysis patients
• GUM clinic attendees
• IVDU/prisoners
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15
Q

How common is co-infection of HDV with HBV?

A

Co-infection in 10% chronic HBV infection in UK

 Migrants from high prevalence countries

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16
Q

What are the main treatments for HDV and HBV?

A

Interferons and nucleoside analogues:
Pegylated IFN alpha-2a
Entecavir
Tenofovir

17
Q

What type of virus is HDV?

A

Delta virus

18
Q

What is the natural history of HCV?

A
20% natural clearance, 
20% get chronic hepatitis at 20
50% get chronic hepatitis at 30
fulminant hepatitis 1%
hepatocellular carcinoma 
cirrhosis
19
Q

How was HCV treated?

A

Ribavirin and interferon

20
Q

How many serotypes are there of HCV?

A

6