Evidence-Based Medicine

Acute Hepatitis B Virus (HBV) Infection

Acute Hepatitis B Virus (HBV) Infection

Background

  • HBV is an enveloped, double-stranded DNA virus of the Hepadnaviridae family that may cause an acute self-limited infection, fulminant hepatic failure, or may develop into a chronic disease.
  • Globally, approximately 240 million patients are infected with hepatitis B, with prevalence ranging from < 2% in the United States and other western countries to over 5% in some parts of East Asia, Southeast Asia, and sub-Saharan Africa.
  • In the United States, the overall incidence is lower due to preventive strategies such as vaccination and about 800,000 to 1.4 million people have chronic HBV infection.
  • HBV is transmitted via infected body fluids, as with sexual contact, needle sharing, needlestick injury, or perinatally.
  • Acute infection is often asymptomatic, when present, symptoms of acute infection are often nonspecific and include fever, fatigue, nausea, vomiting, right upper quadrant tenderness, and jaundice.
  • Fulminant hepatitis occurs in < 1% of patients and is the most common cause of death.
  • The risk of developing chronic infection is inversely related to age at the time of the initial infection; about 90% of infant infections, 25%-50% of infections in children aged 1-5 years, and < 5% of infections in older children and adults result in chronic disease.
  • Extrahepatic manifestations can occur with acute infection and include serum sickness-like reaction and Guillain-Barre syndrome.

Evaluation

  • Consider the diagnosis of hepatitis B virus infection in any patient presenting with right upper quadrant tenderness and abnormal liver function tests.
  • Confirm the diagnosis using serologic testing and HBV viral load testing. The hepatitis B viral serologic panel includes the following:
    • hepatitis B surface antigen (HBsAg)
    • hepatitis B surface antibody (HBsAb)
    • hepatitis B core immunoglobulin M (HBcIgM)
    • hepatitis B core antibody
    • hepatitis B "e" antigen (HBeAg)
    • hepatitis B "e" antibody (HBeAb)
  • Acute infection is defined by a positive HBsAg with a positive HBcIgM.
  • Additional testing that may help determine the disease severity, the disease stage, and the need for treatment includes:
    • hepatitis B viral load
    • liver function tests
  • Screen patients diagnosed with hepatitis B infection for coinfections including hepatitis C virus, hepatitis D virus, and HIV.

Management

  • Acute HBV infection resolves spontaneously in > 95% of patients and treatment is typically not needed.
  • Consider treatment for patients with fulminant hepatitis or protracted severe acute hepatitis B (increase in INR, severe jaundice > 4 weeks) (AASLD Grade III) with
    • lamivudine or telbivudine if anticipated duration of treatment is short.
    • entecavir or tenofovir preferred for all other situations.
  • For patients with fulminant hepatitis also consider referral to a transplant center.
  • Vaccination is recommended for all children aged 0-18 years, and in United States vaccination should be offered to all unvaccinated individuals, particularly those at high risk for infection.
  • Recommendations for postexposure prophylaxis vary with the host immune status and the type of exposure and may include the use of hepatitis B immunoglobulin, vaccination, or both.

Published: 27-06-2023 Updeted: 27-06-2023

References

  1. Song JE, Kim DY. Diagnosis of hepatitis B. Ann Transl Med. 2016 Sep;4(18):338
  2. Trépo C, Chan HL, Lok A. Hepatitis B virus infection. Lancet. 2014 Dec 6;384(9959):2053-63
  3. Lok AS, McMahon BJ. American Association for the Study of Liver Diseases (AASLD) Practice Guideline Update. Chronic hepatitis B: update 2009. Hepatology. 2009 Sep;50(3):661-2, commentary can be found in Hepatology 2010 Mar;51(3):1087
  4. Schillie S, Vellozzi C, Reingold A, Harris A, Haber P, Ward JW, Nelson NP. Prevention of Hepatitis B Virus Infection in the United States: Recommendations of the Advisory Committee on Immunization Practices. MMWR Recomm Rep. 2018 Jan 12;67(1):1-31

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