Hepatitis A virus: Difference between revisions
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*Rare transmission by blood transfusion |
*Rare transmission by blood transfusion |
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===Risk Factors=== |
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*Outbreak |
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*Close contact with a hepatitis A-infected person, including household, sexual, or other |
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*Travel to endemic country |
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*Men who have sex with men |
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*Homelessness |
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*Injection drug use |
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==Clinical Manifestations== |
==Clinical Manifestations== |
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**People who use recreational drugs |
**People who use recreational drugs |
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**People living in communities with outbreaks or endemic hepatitis A |
**People living in communities with outbreaks or endemic hepatitis A |
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**Close contacts of children adopted from endemic |
**Close contacts of children adopted from endemic countries |
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**Military personnel and humanitarian relief workers |
**Military personnel and humanitarian relief workers |
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**People receiving repeated doses of plasma-derived clotting factors |
**People receiving repeated doses of plasma-derived clotting factors |
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*Vaccination requires two doses spaced at least 6 months apart |
*Vaccination requires two doses spaced at least 6 months apart |
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*It provides immunity for decades, and possibly for life |
*It provides immunity for decades, and possibly for life |
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==== Coformulation with Hepatitis B Vaccine ==== |
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*Often given combined with [[hepatitis B vaccine]] (HAHB) |
*Often given combined with [[hepatitis B vaccine]] (HAHB) |
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*HAHB is given as three doses (for the hepatitis B component) |
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*The hepatitis A component contains a full dose of hepatitis A vaccine, so a HAHB series essentially contains an extra unnecessary dose of hepatitis A vaccine |
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==== High Risk Groups Who Cannot Receive Vaccine ==== |
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*In people with contraindications or who are expected to have suboptimal response to vaccination, consider using immunoglobulin as preexposure prophylaxis |
*In people with contraindications or who are expected to have suboptimal response to vaccination, consider using immunoglobulin as preexposure prophylaxis |
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*Groups include: |
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**Infants less than 6 months of age |
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**Immunocompromised people in whom the vaccine may not be as effective (though they should also still be vaccinated) |
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**Anaphylaxis after previous hepatitis A vaccination or component thereof |
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*Administering just before travel can confer immunity for up to 6 months of travel |
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*Dose is IMIg (GamaSTAN) 0.02 mL/kg for 3 months of protection, or 0.06 mL/kg every 6 months |
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**CDC recommends a dose of IMIg (GamaSTAN S/D) 0.2 mL/kg q2mo due to decreases in hepatitis A IgG among donors |
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==== Publicly Funded in Ontario ==== |
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* Only a subset of patients are publicly funded in Ontario: |
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** Intravenous drug use |
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** Chronic liver disease, including hepatitis B and C |
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** Men who have sex with men |
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===Post-Exposure Prophylaxis=== |
===Post-Exposure Prophylaxis=== |
Revision as of 20:30, 28 February 2021
Background
Microbiology
- Non-enveloped RNA virus within the Picornaviridae family
- Three genotypes, I through III
- Difficult to kill: needs higher temperatures and lower pH than other viruses, or bleach- or ammonium-based cleaners
Epidemiology
- Fecal-oral transmission with person-to-person spread (including sex)
- Can be transmitted by contaminated food and water, as well
- Most often linked to travel or to household contacts
- Rare transmission by blood transfusion
Risk Factors
- Outbreak
- Close contact with a hepatitis A-infected person, including household, sexual, or other
- Travel to endemic country
- Men who have sex with men
- Homelessness
- Injection drug use
Clinical Manifestations
- Incubation period is from 15 to 50 days, with an average of 28 days
- Children are usually asymptomatic
- Symptoms include non-specific influenza-like illness followed eventually by bilirubinuria, pale stools, jaundice, and scleral icterus
- May have hepatomegaly and splenomegaly, may have rash or arthralgia
- Self-limited, usually starting to resolve by the third week of illness with full recovery often taking several months
Diagnosis
Serology
IgM | IgG | Interpretation |
---|---|---|
– | – | No recent infection (unless in the incubation period). No prior infection or vaccination. |
– | + | No infection. Prior infection or vaccination. |
? | + | Cannot rule out active infection. Prior infection or vaccination. |
+ | +/– | Acute or recent infection. IgM positive from 2 weeks until 3-12 months. IgG positive from 8-12 weeks and remains positive for lifetime. |
Prevention
Vaccination
- Vaccination is indicated for people at increased risk of acquiring hepatitis A, or at increased risk of severe disease
- Travellers to endemic countries
- People with chronic liver disease
- Men who have sex with men
- People who use recreational drugs
- People living in communities with outbreaks or endemic hepatitis A
- Close contacts of children adopted from endemic countries
- Military personnel and humanitarian relief workers
- People receiving repeated doses of plasma-derived clotting factors
- Laboratory workers studying hepatitis A
- Zookeepers, veterinarians, and researchers who interact with non-human primates
- Vaccination requires two doses spaced at least 6 months apart
- It provides immunity for decades, and possibly for life
Coformulation with Hepatitis B Vaccine
- Often given combined with hepatitis B vaccine (HAHB)
- HAHB is given as three doses (for the hepatitis B component)
- The hepatitis A component contains a full dose of hepatitis A vaccine, so a HAHB series essentially contains an extra unnecessary dose of hepatitis A vaccine
High Risk Groups Who Cannot Receive Vaccine
- In people with contraindications or who are expected to have suboptimal response to vaccination, consider using immunoglobulin as preexposure prophylaxis
- Groups include:
- Infants less than 6 months of age
- Immunocompromised people in whom the vaccine may not be as effective (though they should also still be vaccinated)
- Anaphylaxis after previous hepatitis A vaccination or component thereof
- Administering just before travel can confer immunity for up to 6 months of travel
- Dose is IMIg (GamaSTAN) 0.02 mL/kg for 3 months of protection, or 0.06 mL/kg every 6 months
- CDC recommends a dose of IMIg (GamaSTAN S/D) 0.2 mL/kg q2mo due to decreases in hepatitis A IgG among donors
Publicly Funded in Ontario
- Only a subset of patients are publicly funded in Ontario:
- Intravenous drug use
- Chronic liver disease, including hepatitis B and C
- Men who have sex with men
Post-Exposure Prophylaxis
- Post-exposure prophylaxis is indicated for susceptible contacts including:
- Household members and close contacts of people infected with hepatitis A
- Contacts in group childcare centres and kindergartens
- Co-workers and clients of infected food handlers
- Prophylaxis is with monovalent hepatitis A vaccine
- In people with contraindications or who are expected to have suboptimal response to vaccination, immunogloulin should be given
- Groups include:
- Infants less than 6 months of age
- Immunocompromised people and people with liver disease, who should receive both vaccine and immunoglobulin
- If they have received IVIg ≥400 mg/kg within the 3 weeks before exposure, then they do not require further immunoglobulin
- Elderly susceptible adults age 60 years and older may also receive both
- It should be given as soon as possible, and can be given until 14 days after last exposure
- Dose is IMIg (GamaSTAN) 0.02 mL/kg body weight
- CDC recommends a dose of IMIg (GamaSTAN S/D) 0.1 mL/kg body weight due to decreases in hepatitis A IgG among donors
- Groups include:
References
- ^ J. T. Stapleton. Host Immune Response To Hepatitis A Virus. Journal of Infectious Diseases. 1995;171(Supplement 1):S9-S14. doi:10.1093/infdis/171.supplement_1.s9.