Abstract

Hepatitis B prevention in European Union/European Economic Area (EU/EEA) countries relies on vaccination programmes. We describe the epidemiology of acute hepatitis B virus (HBV) at country and EU/EEA level during 2006–2014. Using a multi-level mixed-effects Poisson regression model we assessed differences in the acute HBV infection notification rates between groups of countries that started universal HBV vaccination before/in vs after 1995; implemented or not a catch-up strategy; reached a vaccine coverage ≥ 95% vs < 95% and had a hepatitis B surface antigen prevalence ≥ 1% vs < 1%. Joinpoint regression analysis was used to assess trends by groups of countries, and additional Poisson regression models to evaluate the association between three-dose HBV vaccine coverage and acute HBV infection notification rates at country and EU/EEA level. The EU/EEA acute HBV infection notification rate decreased from 1.6 per 100,000 population in 2006 to 0.7 in 2014. No differences (p > 0.05) were found in the acute HBV infection notification rates between groups of countries, while as vaccine coverage increased, such rates decreased (p < 0.01). Countries with universal HBV vaccination before 1995, a catch-up strategy, and a vaccine coverage ≥ 95% had significant decreasing trends (p < 0.01). Ending HBV transmission in Europe by 2030 will require high vaccine coverage delivered through universal programmes, supported, where appropriate, by catch-up vaccination campaigns.

Highlights

  • Hepatitis B is caused by the hepatitis B virus (HBV), an enveloped DNA virus that infects the liver and causes cirrhosis and hepatocellular carcinoma [1]

  • We describe the epidemiology of acute hepatitis B virus (HBV) at country and EU/EEA level during 2006–2014

  • The aim of this study is to describe the epidemiological trend of the acute HBV infection notification rate at country and EU/EEA level during 2006–2014 and to assess the possible impact of the different HBV vaccination strategies implemented by the EU/EEA countries on these rates

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Summary

Introduction

Hepatitis B is caused by the hepatitis B virus (HBV), an enveloped DNA virus that infects the liver and causes cirrhosis and hepatocellular carcinoma [1]. HBV infection in susceptible individuals can be either symptomatic or asymptomatic, the latter being often the case. Hepatitis B surface antigen (HBsAg) is the www.eurosurveillance.org earliest marker of hepatitis B infection, and is widely used in seroprevalence surveys to estimate the number of infected people and as indicator of transmission risk [2]. Most primary acute infections are self-limiting, their case fatality rate is 0.5–1%. The risk of developing chronic HBV infection is dependent on age of infection, and for infants infected during the first year of life, it is estimated at 80–90% [1]. HBV is widely prevalent and it is estimated that approximately one third of the world’s population has been exposed to the virus, with 250 million people chronically infected [2]

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