Abstract

To explore the epidemiology and clinical course of hepatitis A virus (HAV) infections at the Vienna General Hospital. We retrospectively identified patients who were tested positive for HAV-IgM at the Vienna General Hospital form Q1/2008 to Q3/2018. Our definition of severe HAV infection was AST and/or ALT > 5 × above the upper limit of normal (ULN); and liver dysfunction as (i) hepatic encephalopathy or ammonia > 100 μmol/L, (ii) coagulopathy with INR > 1.5, or (iii) jaundice with bilirubin > 5 mg/dL. A total of 578 HAV-IgM (+) were identified, including 31 (5.4%) and 38 (6.6%) without and with liver dysfunction, respectively. A proportional increase in severe HAV cases with and without liver dysfunction occurred in 2016/2017 with (21.5% (vs. 8.0% in the years before; p < 0.001). Thirty-seven (53.6%) patients with severe HAV were hospitalized, 6 (9%) required ICU support, and one patient received liver transplantation within 30 days. Patients with severe HAV and liver dysfunction were more often male (60.5 vs. 43.1%, p = 0.055) and younger (31.5 vs. 63 years, p < 0.001) as compared with other HAV-IgM (+) cases. The observed increase of severe HAV infections in Vienna in 2017 among young males, coincided with a multinational HAV outbreak among MSM. Our data suggests a higher likelihood of severe courses of hepatitis A in MSM. Vaccination against HAV should be recommended for risk groups.

Highlights

  • Hepatitis A virus (HAV) infection is usually a self-limiting viral disease with a reported case fatality of 0.1–0.3% [1, 2]

  • Of 178,940 persons included in this study, 178,095 (99.5%) were tested for anti-HAV-immunoglobulin G (IgG), and 112,200 (63.0%) were anti-HAV-IgG positive

  • The rate of HAV-RNA PCR positivity and the median quantitative HAV-IgM titer was lowest in patients with low transaminases and increased concurrently (s. supplemental Table S1)

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Summary

Introduction

Hepatitis A virus (HAV) infection is usually a self-limiting viral disease with a reported case fatality of 0.1–0.3% [1, 2]. According to estimations by the WHO, HAV caused 16,900 and 11,200 deaths worldwide in 2005 and 2015, respectively [3]. Persons aged 40 years and older are more susceptible to HAV-associated complications and mortality than younger persons [4]. Transmission usually occurs via the fecal-oral route as per contaminated food or water or person-to-person contact or smear transmission. While effective antiviral therapies are available for other types of viral infections, treatment options for acute HAV infection are limited to symptomatic measures [5, 6]. The HAV belongs to the family of Picornaviridae of the genus Hepatovirus and is a nonenveloped single-stranded RNA virus [7].

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