Viral Hepatitis (particularly D and E)

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PatientPlus articles are written by UK doctors and are based on research evidence, UK and European Guidelines. They are designed for health professionals to use, so you may find the language more technical than the condition leaflets.

See also: Hepatitis B written for patients
This disease is notifiable in the UK, see NOIDs article for details.

Hepatitis is a general term that refers to inflammation of the liver. This condition may result from various infectious (viral, bacterial, fungal, and parasitic organisms) and non-infectious (medications, toxins, and autoimmune disorders) causes; however, this article considers hepatitis caused by viral infection. In the UK and the USA, viral hepatitis is most commonly caused by hepatitis A virus (HAV), hepatitis B virus (HBV), and hepatitis C virus (HCV). HAV, HBV and HCV are covered in separate articles detailed below under their individual headings.

HAV, HBV and HCV can all result in acute illness with symptoms of nausea, abdominal pain, fatigue, malaise, and jaundice. HBV and HCV can also lead to chronic infection. Patients who are chronically infected may go on to develop cirrhosis and hepatocellular carcinoma. Chronic hepatitis carriers remain infectious and may transmit the disease for many years.

The term viral hepatitis is generally used to refer to liver inflammation caused by the hepatropic viruses including: HAV, HBV, HCV, hepatitis D (HDV) and hepatitis E (HEV). Other viruses, which may cause hepatitis but which do not primarily infect the liver, include:

  • Cytomegalovirus (CMV)
  • Epstein-Barr virus
  • Adenovirus
  • Herpes simplex virus (rarely)

Despite their name, the hepatropic viruses (particularly B and C) can cause extrahepatic disease. Viral agents can cause acute, chronic and subclinical liver disease.

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The epidemiology of viral hepatitis has changed. Since the introduction of safe and effective vaccines for HAV and HBV in the 1980s, the incidence of acute infections caused by these viruses has been declining in the UK. At the same time, HEV has been recognised as an increasingly important cause of acute hepatitis.[1] 

Acute infection

  • Nausea and vomiting
  • Myalgia
  • Fatigue/malaise
  • Right upper quadrant pain
  • Change in sense of smell or taste
  • Coryza
  • Photophobia
  • Headache

Diarrhoea (with pale stools and dark urine) may also be present. However, often no signs are seen unless jaundice develops. Hepatomegaly, splenomegaly and lymphadenopathy may then be present. May present with liver failure.

Chronic infection

This is most commonly a consequence of infection with HBV, HCV or HDV. Presentation is very varied and may be asymptomatic. Subclinical infection causes only vague symptoms like fatigue and dyspepsia. Chronic infection may lead to chronic hepatitis, cirrhosis and hepatocellular carcinoma. Chronic hepatitis and cirrhosis can take months to decades to develop. Signs of chronic liver disease may be apparent.

  • FBC
  • U&Es
  • LFTs (see also the separate article Abnormal Liver Function Tests)
  • Clotting studies, including INR
  • Hepatitis serology
  • Imaging with ultrasound/CT/MRI scanning to assess for presence of cirrhosis or other causes of symptoms



HAV may occur in outbreaks in institutions. It is common in travellers. Most infections pass unnoticed in childhood. It is a small, unenveloped, symmetrical RNA virus (picornavirus). See the separate article Hepatitis A.

  • HBV is a double-stranded DNA virus which replicates by reverse transcription (Hepadnaviridae family).
  • It is endemic with more than 350 million people infected worldwide.[2] See the separate article Hepatitis B.

HCV is an enveloped RNA virus in the Flaviviridae family with a narrow host range (humans and chimpanzees). See the separate article Hepatitis C.

HDV is an unusual, defective, single-stranded RNA virus. It requires the presence of HBV to replicate. HDV infection develops only in patients who are positive for the hepatitis B surface antigen (HBsAg). Infection may be acquired along with HBV (co-infection) or after HBV infection (superinfection).


  • An estimated 15-20 million people infected with HBV worldwide are also infected with HDV.
  • It is an important cause of acute and severe chronic liver damage in some parts of the world (Mediterranean, parts of Eastern Europe, Middle East, Africa, and South America).

Route of transmission

It needs hepadnavirus to function and for its propagation in hepatocytes, and is therefore acquired as a co-infection with HBV, or as a superinfection in those with existing chronic HBV infection. Therefore transmission is, like HBV, by exposure to infected blood and blood products. It can be transmitted percutaneously and sexually. Perinatal transmission is rare.

Clinical features

HDV replicates only in liver cells and so the cellular damage associated with HDV infection involves mainly the liver. Immune-mediated liver damage is thought to be implicated in HDV infection. HDV co-infection with HBV may be associated with increased risk of severe clinical hepatitis, fulminant hepatic failure, chronic liver disease, cirrhosis and hepatocellular carcinoma.[4] 


Anti-HDV antibody. Other investigations as indicated for hepatitis, liver failure, cirrhosis and hepatocellular carcinoma.


Current treatments include pegylated interferon alfa and liver transplantation, which can be curative.[4] Management is otherwise supportive.


As for HBV.

HEV genotype 3 and 4 can cause liver disease in humans. The main reservoir is pigs. In humans, the infection may vary in severity from inapparent to fulminant. The mortality is between 1% and 4%, and can reach 25% in pregnant women.

In resource-limited countries, HEV infection is endemic and spreads mainly through contamination of water supplies.

Transmission of virus from domestic pigs to humans is common and higher rates of HEV seroprevalence are detected in slaughterhouse workers and vets. It is evaluated that one third of the worldwide population has been in contact with the virus.


  • In some areas it is the most common viral cause of hepatitis in adults and older children, causing major epidemics in the Indian subcontinent, Central and Southeast Asia, the Middle East, and parts of Africa.
  • Mortality is high in pregnancy. Intrauterine infection (± stillbirth) is common.

Route of transmission

  • This is by the faecal-oral route and similar to HAV.
  • Contaminated drinking water is the most common source of infection.
  • Person-to-person transmission is rare but maternal-neonatal transmission does occur.
  • Zoonotic spread may occur, as other animals (primates, cows, pigs, sheep, goats, and rodents) are susceptible to infection.

Clinical features

  • These are also similar to HAV with no apparent risk of chronic liver disease.
  • Incubation is 2-9 weeks.
  • It is usually a self-limiting illness.
  • There are no reports of chronic infection with HEV.
  • HEV usually causes an acute self-limiting illness like HAV. Fulminant disease occurs in about 10% of cases.
  • In pregnancy, the mortality rate may be as high as 15-20%.


Hepatitis serology.


This is mainly supportive, as HAV.


  • Good hygiene and sanitation.
  • Avoidance of tap water in high-risk areas (most outbreaks are associated with contaminated drinking water).
  • Gammaglobulin is ineffective.
  • No vaccine is currently available.

GB virus C (GBV-C), formerly known as hepatitis G virus (HGV), is a lymphotropic human virus that is related to HCV. To date, GBV-C has not been convincingly associated with any disease. However, it appears to be protective against HIV infection.

  • Two distinct viruses were identified initially when tamarind monkeys were inoculated with the serum of this patient (GBV-A and GBV-B).
  • The third virus, GBV-C, was later isolated from a human specimen (this was the new 'hepatitis G' virus separately identified in 1996).
  • All three are members of the Flaviviridae family of viruses and share significant homology with HCV.


GBV-C infection is common and is distributed worldwide. It may establish persistent infection without clinical symptoms or disease in either immunocompromised or healthy individuals. In developed countries, 1-5% of healthy blood donors are viraemic at the time of blood donation. The prevalence is higher in developing countries, with up to 20% of blood donors being viraemic in some studies.


Although GBV-C infection is common and may persist for decades, most healthy individuals clear viraemia within two years of infection.

Further reading & references

  1. Harvala H, Wong V, Simmonds P, et al; Acute viral hepatitis - Should the current screening strategy be modified? J Clin Virol. 2014 Mar;59(3):184-7. doi: 10.1016/j.jcv.2014.01.001. Epub 2014 Jan 13.
  2. Hepatitis B: the green book, chapter 18; Public Health England (December 2013)
  3. Abbas Z, Afzal R; Life cycle and pathogenesis of hepatitis D virus: A review. World J Hepatol. 2013 Dec 27;5(12):666-675.
  4. Alvarado-Mora MV, Locarnini S, Rizzetto M, et al; An update on HDV: virology, pathogenesis and treatment. Antivir Ther. 2013;18(3 Pt B):541-8. doi: 10.3851/IMP2598. Epub 2013 Jun 21.
  5. Berto A, Backer JA, Mesquita JR, et al; Prevalence and transmission of hepatitis E virus in domestic swine populations in different European countries. BMC Res Notes. 2012 Apr 25;5:190. doi: 10.1186/1756-0500-5-190.
  6. Bhattarai N, Stapleton JT; GB virus C: the good boy virus? Trends Microbiol. 2012 Mar;20(3):124-30. doi: 10.1016/j.tim.2012.01.004. Epub 2012 Feb 8.

Disclaimer: This article is for information only and should not be used for the diagnosis or treatment of medical conditions. EMIS has used all reasonable care in compiling the information but make no warranty as to its accuracy. Consult a doctor or other health care professional for diagnosis and treatment of medical conditions. For details see our conditions.

Original Author:
Dr Richard Draper
Current Version:
Peer Reviewer:
Dr Adrian Bonsall
Document ID:
2922 (v25)
Last Checked:
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