Hepatitis A
- Overview
- Theory
- Diagnosis
- Management
- Follow up
- Resources
Treatment algorithm
Please note that formulations/routes and doses may differ between drug names and brands, drug formularies, or locations. Treatment recommendations are specific to patient groups: see disclaimer
unvaccinated people with recent exposure to hepatitis A (<2 weeks)
hepatitis A vaccine and/or immunoglobulin
Active or passive immunisation is available for protection following exposure to hepatitis A virus (HAV) infection.
The Centers for Disease Control and Prevention (CDC) recommends a single dose of hepatitis A vaccine as soon as possible post-exposure (<2 weeks) for immunocompetent people (aged ≥12 months) who have not completed the two-dose hepatitis A vaccine series:[21]Nelson NP, Weng MK, Hofmeister MG, et al. Prevention of hepatitis A virus infection in the United States: recommendations of the Advisory Committee on Immunization Practices, 2020. MMWR Recomm Rep. 2020 Jul 3;69(5):1-38. https://www.cdc.gov/mmwr/volumes/69/rr/rr6905a1.htm http://www.ncbi.nlm.nih.gov/pubmed/32614811?tool=bestpractice.com CDC: hepatitis A FAQs for health professionals Opens in new window Co-administration of immunolobulin (at a discrete anatomical site) may be considered for people aged >40 years with risk factors for HAV infection or its complications.
For immunocompromised people, or those with chronic liver disease, who have not completed the two-dose hepatitis A vaccine series, the CDC recommends immunoglobulin and a single dose of hepatitis A vaccine simultaneously (at a discrete anatomical site), as soon as possible (<2 weeks since exposure).
Infants aged <12 months and those with a history of life-threatening allergy following administration of hepatitis A vaccine (or severe allergy to any component of the vaccine) should receive immunoglobulin as soon as possible (<2 weeks since exposure).[21]Nelson NP, Weng MK, Hofmeister MG, et al. Prevention of hepatitis A virus infection in the United States: recommendations of the Advisory Committee on Immunization Practices, 2020. MMWR Recomm Rep. 2020 Jul 3;69(5):1-38. https://www.cdc.gov/mmwr/volumes/69/rr/rr6905a1.htm http://www.ncbi.nlm.nih.gov/pubmed/32614811?tool=bestpractice.com CDC: hepatitis A FAQs for health professionals Opens in new window
Recommendations concerning post-exposure prophylaxis may differ geographically, so specific national guidelines should be consulted.[21]Nelson NP, Weng MK, Hofmeister MG, et al. Prevention of hepatitis A virus infection in the United States: recommendations of the Advisory Committee on Immunization Practices, 2020. MMWR Recomm Rep. 2020 Jul 3;69(5):1-38. https://www.cdc.gov/mmwr/volumes/69/rr/rr6905a1.htm http://www.ncbi.nlm.nih.gov/pubmed/32614811?tool=bestpractice.com [31]World Health Organization. WHO position paper on hepatitis A vaccines – October 2022. Oct 2022 [internet publication]. https://www.who.int/publications/i/item/who-wer9740-493-512 [32]UK Health Security Agency. Hepatitis A: guidance, data and analysis. Jun 2021 [internet publication]. https://www.gov.uk/government/collections/hepatitis-a-guidance-data-and-analysis [43]Centers for Disease Control and Prevention. Morbidity and mortality weekly report: update: recommendations of the Advisory Committee on Immunization Practices for use of hepatitis A vaccine for postexposure prophylaxis and for preexposure prophylaxis for international travel. Mar 2019 [internet publication]. https://www.cdc.gov/mmwr/volumes/67/wr/mm6743a5.htm [44]Public Health England. Public health control and management of hepatitis A. Jun 2017 [internet publication]. https://www.gov.uk/government/uploads/system/uploads/attachment_data/file/623036/Public_health_control_and_management_of_hepatitis_A_2017.pdf
Intramuscular immunoglobulin may need to be obtained from a specialist centre; it is not widely commercially available.
Primary options
hepatitis A vaccine: administer according to current recommended schedule
and/or
normal immunoglobulin human: consult specialist for guidance on intramuscular dose
confirmed hepatitis A
supportive care
Treatment for infection is primarily supportive, including appropriate rest when necessary.[19]Cuthbert JA. Hepatitis A: old and new. Clin Microbiol Rev. 2001 Jan;14(1):38-58. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC88961 http://www.ncbi.nlm.nih.gov/pubmed/11148002?tool=bestpractice.com No specific antiviral therapy is available.
Excess paracetamol and alcohol should be avoided.[2]Brundage SC, Fitzpatrick AN. Hepatitis A. Am Fam Physician. 2006 Jun 15;73(12):2162-8. http://www.aafp.org/afp/20060615/2162.html http://www.ncbi.nlm.nih.gov/pubmed/16848078?tool=bestpractice.com [18]Kemmer NM, Miskovsky EP. Hepatitis A. Infect Dis Clin North Am. 2000 Sep;14(3):605-15. http://www.ncbi.nlm.nih.gov/pubmed/10987112?tool=bestpractice.com
Rarely, hospitalisation may become necessary for volume depletion, coagulopathy, encephalopathy, or severe prostration.[18]Kemmer NM, Miskovsky EP. Hepatitis A. Infect Dis Clin North Am. 2000 Sep;14(3):605-15. http://www.ncbi.nlm.nih.gov/pubmed/10987112?tool=bestpractice.com This is particularly important in patients with co-infection with hepatitis B virus, hepatitis C virus, or cirrhosis of any cause, as acute hepatitis A virus (HAV) infection in these conditions has a higher risk for severe disease.
liver transplant
Treatment recommended for ALL patients in selected patient group
In <1% of patients, acute liver failure occurs characterised by worsening jaundice, coagulopathy, and encephalopathy.[35]Taylor RM, Davern T, Munoz S, et al. Fulminant hepatitis A virus infection in the United States: incidence, prognosis, and outcomes. Hepatology. 2006 Dec;44(6):1589-97. http://www.ncbi.nlm.nih.gov/pubmed/17133489?tool=bestpractice.com [36]Ajmera V, Xia G, Vaughan G, et al; the Acute Liver Failure Study Group. What factors determine the severity of hepatitis A-related acute liver failure? J Viral Hepat. 2011 Jul;18(7):e167-74. http://www.ncbi.nlm.nih.gov/pubmed/21143345?tool=bestpractice.com Prompt referral to centres experienced in liver transplantation is warranted in such cases. This is of particular significance in patients with coexisting hepatitis C or hepatitis B virus infections, or cirrhosis of any cause. Hepatitis A virus (HAV) infection in these conditions has a higher risk for acute liver failure.
A prognostic index consisting of four clinical and laboratory features (serum alanine aminotransferase [ALT] <2600 units/L, creatinine >177 micromoles/L [>2 mg/dL], intubation, pressors) predicts the likelihood of transplantation/death significantly better than other published models.[35]Taylor RM, Davern T, Munoz S, et al. Fulminant hepatitis A virus infection in the United States: incidence, prognosis, and outcomes. Hepatology. 2006 Dec;44(6):1589-97. http://www.ncbi.nlm.nih.gov/pubmed/17133489?tool=bestpractice.com The lower ALT levels that were found to be one of the indicators of poor prognosis were thought to be due to extensive necrosis at presentation.[35]Taylor RM, Davern T, Munoz S, et al. Fulminant hepatitis A virus infection in the United States: incidence, prognosis, and outcomes. Hepatology. 2006 Dec;44(6):1589-97. http://www.ncbi.nlm.nih.gov/pubmed/17133489?tool=bestpractice.com
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Please note that formulations/routes and doses may differ between drug names and brands, drug formularies, or locations. Treatment recommendations are specific to patient groups. See disclaimer
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