Hepatitis B vaccination targeted at behavioural risk groups in the Netherlands: Does it work?
Introduction
Hepatitis B virus (HBV) infections and the consequent increased risk for chronic infection with its sequelae cirrhosis and hepatocellular carcinoma can be prevented by a safe and effective vaccine. The WHO has advised worldwide universal vaccination since 1992, not only in countries where HBV is highly endemic but also in low-endemic countries [1].
The Netherlands is a low-endemic country with an estimated HBsAg prevalence of 0.3–0.5% [2], where HBV transmission is restricted mainly to risk groups. Therefore, the Netherlands, like Britain, and the Scandinavian countries, has adopted a policy of vaccination targeted at behavioural risk groups, rather than universal vaccination [3]. This targeted program was implemented in November 2002, after a pilot of 2 years that was conducted in several regions of the Netherlands to investigate its feasibility [4], [5]. Within the program, commercial sex workers (CSWs), hard drug users (DUs), and men having sex with men (MSM) are vaccinated free of charge at their local Public Health Service and at clinics that treat sexually transmitted infections (STI). Furthermore, various outreach strategies are tailored to these risk groups. Until October 2007, heterosexuals with an indication for an STI exam were also considered a risk group and therefore vaccinated.
Before implementation of this targeted vaccination program, HBV prevention in the Netherlands consisted mainly of prenatal screening and vaccination of newborns with a chronically infected mother, vaccination of certain patient groups (e.g. hemophiliacs), and healthcare workers. These preventive measures are still ongoing and were extended with the targeted vaccination program and with the vaccination of newborns with at least one parent born in a country with a HBV prevalence over 2%, as of 2003.
Since the Netherlands did not implement universal HBV vaccination, it is important to monitor the effect of our current strategy targeted at behavioural risk groups. Such an evaluation may have implications for countries with a comparable vaccination strategy and even for countries with a universal vaccination program, since they have the same risk groups.
The pilot study preceding nationwide implementation of the vaccination program targeted at behavioural risk groups reached only a small number of people, most of whom were vaccinated in Amsterdam [4], [5]. As Amsterdam is not representative for the rest of the Netherlands, we have evaluated the current risk group vaccination program 5 years after implementation, using nationwide epidemiological data of reported HBV cases and national vaccination data. Only acute cases were included in this study, because they give insight in the evolution of HBV transmission in the Netherlands. Molecular epidemiology was used to obtain insight into the impact of this targeted vaccination program, and on the dynamics of HBV transmission between and amongst behavioural risk groups and the general population.
Section snippets
Patients
In the Netherlands, all cases of HBV infection have to be reported to the local Public Health Service and subsequently to the National Centre of Infectious Diseases Control. The reporting criteria for acute HBV are: clinical signs and symptoms of acute hepatitis in combination with the presence of HBsAg in the serum. Reported patients are approached by public health nurses for source and contact tracing and for information about the most likely mode of infection. These data are stored in the
General characterization of acute HBV cases
From January 2003 through December 2007, 1386 patients acutely infected with HBV were reported in the Netherlands. Of these, 78% were men. The annual number of reported cases declined from 326 in 2003 to 220 in 2007, equivalent to a decline in reported incidence from 2.0 to 1.4 per 100,000 inhabitants. Based on interviews with public health nurses, patients were classified according to the most probable mode of transmission (Table 1). For both men and women sexual intercourse was the most
Discussion
In November 2002, the Netherlands adopted a HBV vaccination program targeted at behavioural risk groups, instead of implementing a universal vaccination program. Five years after its implementation, the total number of reported patients acutely infected with HBV has declined from 326 in 2003 to 220 in 2007 and has returned to the level of the 1990s. This decline could be observed in all risk groups. The largest decline was seen among MSM, although it was not significantly larger than in other
Acknowledgements
The authors thank J.A.R. van den Hoek, B.A. Wolters, C.J.P.A. Hoebe, A. Gadiot, S. Esman, H.M. Götz, S. Feenstra-van Gols, J. Sleven, P.B.G. ten Ham, M. Hosseinnia, P.H.A. Jacobs, A. van Heukelum, H. van den Kerkhof, J.T. Versteegen, M.F. Siebbeles, R. van Kessel, M. Besselse, A.G. Kraaijeveld, R.P.M. Koene, D. van der Werf, E. Lodder, R. ter Schegget, E. van Dijk, M.G.E. Hottinga, J.J. Tiessen, E.J.M. de Coster, J.M.C. de Vries, B. Hoendermis, E. Rood, S.L. Lie, R. van Essen, L. Helmhout, G.
References (23)
- et al.
Results of an enhanced-outreach program of hepatitis B vaccination in the Netherlands (1998–2000) among men who have sex with men, hard drug users, sex workers, and heterosexual persons with multiple partners
J Hepatol
(2002) - et al.
Impact of a targeted hepatitis B vaccination program in Amsterdam, The Netherlands
Vaccine
(2007) - et al.
Molecular epidemiology of hepatitis B virus infections in Denmark
J Clin Virol
(2004) - et al.
Incidence and routes of transmission of hepatitis B virus in England and Wales 1995–2000: implications for immunisation policy
J Clin Virol
(2004) - et al.
Acute hepatitis B virus infection by genotype F despite successful vaccination in an immune competent German patient
J Clin Virol
(2007) - et al.
Social-cognitive determinants of vaccination behaviour against hepatitis B: an assessment among men who have sex with men
Prevent Med
(2005) - et al.
Immunogenicity, reactogenicity, and safety of two-dose versus three-dose (standard care) hepatitis B immunization of healthy adolescents ages 11-15 years: a randomized control trial
Vaccine
(2007) - et al.
Model based analysis of hepatitis B vaccination strategies in the Netherlands
Vaccine
(2009) - WHO. Hepatitis B fact sheet 204. http://www.who.int/mediacentre/factsheets/fs204/en/index.html [accessed February, 11,...
- et al.
High impact of migration on the prevalence of chronic hepatitis B in the Netherlands
Eur J Gastroenterol Hepatol
(2008)
Hepatitis B control in Europe by universal vaccination programs: the situation in 2001
J Med Virol
Cited by (30)
A cohesive European policy for hepatitis B vaccination, are we there yet?
2014, Clinical Microbiology and InfectionTargeted vaccination programme successful in reducing acute hepatitis B in men having sex with men in Amsterdam, the Netherlands
2013, Journal of HepatologyCitation Excerpt :Our findings have important policy implications. Previous evaluations of this programme up to 2006 (incidence trend analysis, mathematical modelling and molecular sequence models) could prove no impact [22–24]. Concern also exists about the effectiveness of such programmes when the uptake or coverage remains low [25,26], and in the past the programme aimed at including as many MSM possible.
Hepatitis B vaccination: Europe goes universal!
2013, VacunasPreparing for the next public debate: Universal vaccination against hepatitis B
2011, VaccineCitation Excerpt :An important finding of evaluation studies is that these intensive vaccination campaigns nevertheless failed to reach a large part of the behavioural high-risk groups [4]. Estimates of the vaccination coverage among MSM varied from 12% in Amsterdam to about half that percentage for the rest of the country [6,10]. Allowing for the fact that a substantial number of those in the high-risk groups is already infected and therefore would no longer benefit from vaccination, it was estimated that more than half of the members of behavioural high-risk groups still run the risk of contracting hepatitis B [6].