Evidence-Based Medicine

Hepatitis E Virus (HEV) Infection

Hepatitis E Virus (HEV) Infection

Background

  • Hepatitis E virus (HEV) is a cause of viral hepatitis worldwide and is endemic in many parts of the developing world, particularly Africa and Asia.
  • HEV is transmitted mainly by the fecal-oral route, and outbreaks have been associated with the consumption of raw or undercooked meat of HEV-infected animals.
  • Acute infection typically causes self-limiting hepatitis. Symptoms arise about 2-8 weeks after infection, and are similar to other forms of viral hepatitis, including fever, nausea/vomiting, abdominal pain, and anorexia.
  • Fulminant hepatitis due to HEV is uncommon, but most often occurs in pregnant women, solid organ transplant recipients, or other immunocompromised patients.
  • A progression to chronic infection and cirrhosis is rare but has been reported in immunocompromised patients.
  • Mortality ranges from 0% to 20%, with the highest rate in pregnant women.

Evaluation

  • Consider the diagnosis of HEV in any patient with abnormal liver function tests, particularly immunocompromised patients or pregnant women with severe hepatitis.
    • Aminotransferase levels peak, usually around 1,000-2,000 units/L, near symptom onset.
    • Bilirubin levels rise later in the course.
  • A diagnosis of acute HEV infection can be confirmed by either serology or reverse transcriptase-polymerase chain reaction (RT-PCR).
    • Immunoglobulin M (IgM) and immunoglobulin G (IgG) appear around the time of the start of symptoms.
      • IgM remains detectable for about 3-12 months.
      • IgG remains detectable for years.
    • RT-PCR can be performed on serum or stool, though sensitivity and specificity vary by viral genotype.
      • Viremia is present about 1 week prior to the onset of clinical symptoms, and for a few weeks thereafter.
      • The virus can be detected in a stool for about 2-3 months after an acute infection.

Management

  • The treatment is supportive care.
  • Ribavirin may be effective but supportive data is limited to case series.
  • The reduction of immunosuppression may aid in clearance in organ transplant recipients.

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

References

  1. Hoofnagle JH, Nelson KE, Purcell RH. Hepatitis E. N Engl J Med. 2012 Sep 27;367(13):1237-44
  2. Kamar N, Abravanel F, Lhomme S, Rostaing L, Izopet J. Hepatitis E virus: Chronic infection, extra-hepatic manifestations, and treatment. Clin Res Hepatol Gastroenterol. 2015 Feb;39(1):20-7
  3. Nelson KE, Heaney CD, Labrique AB, Kmush BL, Krain LJ. Hepatitis E: prevention and treatment. Curr Opin Infect Dis. 2016 Oct;29(5):478-85
  4. Hakim MS, Wang W, Bramer WM, et al. The global burden of hepatitis E outbreaks: a systematic review. Liver Int 2017 Jan;37(1):19

Related Topics