Skip to main content Accessibility help
×
Hostname: page-component-8448b6f56d-xtgtn Total loading time: 0 Render date: 2024-04-25T03:42:54.341Z Has data issue: false hasContentIssue false

43 - Acute viral hepatitis

from Part VII - Clinical syndromes: gastrointestinal tract, liver, and abdomen

Published online by Cambridge University Press:  05 April 2015

Kalyan Ram Bhamidimarri
Affiliation:
University of Miami Miller School of Medicine
Paul Martin
Affiliation:
University of Miami Miller School of Medicine
David Schlossberg
Affiliation:
Temple University, Philadelphia
HTML view is not available for this content. However, as you have access to this content, a full PDF is available via the 'Save PDF' action button.

Summary

Acute viral hepatitis is a systemic infection with predominant hepatic involvement and remains a significant cause of morbidity and mortality in the United States despite the availability of effective vaccines against the two major causes of acute viral hepatitis, namely A and B. There are five major hepatotropic viruses (A, B, C, D, and E) that cause acute hepatitis with acute hepatic inflammation and necrosis. Acute viral hepatitis typically runs its course in 6 months or less, in contrast to chronic hepatitis, which persists for longer. However, with modern serologic and molecular diagnostic testing, the time course is less important in distinguishing acute from chronic viral hepatitis. The clinical illness produced by these viruses can range from asymptomatic or clinically inapparent to a fulminant and fatal acute infection. A major distinction between hepatitis A and hepatitis B, C, D, and E is that the former causes acute hepatitis only, in contrast to the latter four which cause acute and chronic hepatitis. Other viral infections, such as herpes simplex, Epstein–Barr virus (EBV), cytomegalovirus (CMV), and parvovirus B19, can present with prominent hepatic dysfunction, although they are usually multisystem disorders. Hepatitis G, human herpesviruses, adenovirus, coronavirus, and TT virus (TTV) have also been implicated in causing hepatic dysfunction, but their clinical significance remains dubious.

Hepatitis A virus

The hepatitis A virus (HAV) is an RNA virus, identified in 1973, transmitted via the fecal–oral route and is a common cause of acute viral hepatitis in North America. Community outbreaks due to contaminated water or food are well recognized. Inhabitants in low-socioeconomic areas, international travelers, intravenous drug users, and homosexual men are at particular risk of HAV infection. In the United States, the incidence has decreased remarkably since the introduction (1995) of HAV vaccination and its administration to all children as part of the universal childhood vaccination policy since 2006. In underdeveloped countries, HAV infection typically occurs in childhood and is subclinical (age ≤6 years, 70% are asymptomatic), with most of the population infected before adulthood acquiring life-long immunity. HAV infection occurring in older children and adults is more likely to be symptomatic, with increased morbidity and even mortality (Figure 43.1).

Type
Chapter
Information
Publisher: Cambridge University Press
Print publication year: 2015

References

Bhamidimarri, KR, Park, J, Dieterich, D.Management of hepatitis B virus coinfection: HIV, hepatitis C virus, hepatitis D virus. Curr Hepatitis Rep. 2011;10(4):262–268.CrossRefGoogle Scholar
Bhattarai, N, Stapleton, JT. GB virus C: the good boy virus?Trends Microbiol. 2012;20(3):124–130.CrossRefGoogle ScholarPubMed
Deterding, K, Grüner, N, Buggish, P, et al. Delayed versus immediate treatment for patients with acute hepatitis C: a randomised controlled non-inferiority trial. Lancet Infect Dis. 2013;13(6):497–506.CrossRefGoogle ScholarPubMed
Hajarizadeh, B, Grebely, J, Dore, GJ. Epidemiology and natural history of HCV infection. NatRev Gastroenterol Hepatol. 2013;10(9):553–562.Google Scholar
Jeong, SH, Lee, HS. Hepatitis A: clinical manifestations and management. Intervirology. 2010;53(1):15–19.CrossRefGoogle ScholarPubMed
Jindal, A, Kumar, M, Sarin, SK. Management of acute hepatitis B and reactivation of hepatitis B. Liver Int. 2013;33(Suppl 1):164–175.CrossRefGoogle ScholarPubMed
Jung, YM, Park, SJ, Kim, JS, et al. Atypical manifestations of hepatitis A infection: a prospective, multicenter study in Korea. J Med Virol. 2010;82(8):1318–1326.CrossRefGoogle ScholarPubMed
Norvell, JP, Blei, AT, Jovanovic, BD, Levitsky, J. Herpes simplex virus hepatitis: an analysis of the published literature and institutional cases. Liver Transpl. 2007;13(10):1428–1434.CrossRefGoogle ScholarPubMed
Smedile, A, Rizzetto, M. HDV: thirty years later. Dig Liver Dis. 2011;43(Suppl 1):S15–S18.CrossRefGoogle ScholarPubMed
Young, NS, Brown, KE. Parvovirus B19. N Engl J Med. 2004;350(6):586–597.CrossRefGoogle ScholarPubMed

Save book to Kindle

To save this book to your Kindle, first ensure coreplatform@cambridge.org is added to your Approved Personal Document E-mail List under your Personal Document Settings on the Manage Your Content and Devices page of your Amazon account. Then enter the ‘name’ part of your Kindle email address below. Find out more about saving to your Kindle.

Note you can select to save to either the @free.kindle.com or @kindle.com variations. ‘@free.kindle.com’ emails are free but can only be saved to your device when it is connected to wi-fi. ‘@kindle.com’ emails can be delivered even when you are not connected to wi-fi, but note that service fees apply.

Find out more about the Kindle Personal Document Service.

Available formats
×

Save book to Dropbox

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Dropbox.

Available formats
×

Save book to Google Drive

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Google Drive.

Available formats
×