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. 2017 Oct;145(13):2666-2677.
doi: 10.1017/S0950268817001546. Epub 2017 Aug 22.

A systematic review of varicella seroprevalence in European countries before universal childhood immunization: deriving incidence from seroprevalence data

Affiliations

A systematic review of varicella seroprevalence in European countries before universal childhood immunization: deriving incidence from seroprevalence data

K Bollaerts et al. Epidemiol Infect. 2017 Oct.

Abstract

Surveillance systems for varicella in Europe are highly heterogeneous or completely absent. We estimated the varicella incidence based on seroprevalence data, as these data are largely available and not biased by under-reporting or underascertainment. We conducted a systematic literature search for varicella serological data in Europe prior to introduction of universal varicella immunization. Age-specific serological data were pooled by country and serological profiles estimated using the catalytic model with piecewise constant force of infection. From the estimated profiles, we derived the annual incidence of varicella infection (/100·000) for six age groups (<5, 5-9, 10-14, 15-19, 20-39 and 40-65 years). In total, 43 studies from 16 countries were identified. By the age of 15 years, over 90% of the population has been infected by varicella in all countries except for Greece (86·6%) and Italy (85·3%). Substantial variability across countries exists in the age-specific annual incidence of varicella primary infection among the <5 years old (from 7052 to 16 122 per 100 000) and 5-9 years old (from 3292 to 11 798 per 100 000). The apparent validity and robustness of our estimates highlight the importance of serological data for the characterization of varicella epidemiology, even in the absence of sampling or assay standardization.

Keywords: Chickenpox; Europe; immunization; incidence; seroepidemiology; varicella zoster virus.

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Conflict of interest statement

KB, MR-M and TV received consulting fees from SPMSD for this work. SH was a SPMSD employee at the time of the conduct of the work; AS was mandated by SPMSD. No honoraria were paid to UH and NH for this work. UH and NH have no conflicts to declare.

Figures

Fig. 1.
Fig. 1.
Study selection (PRISMA flow diagram).
Fig. 2.
Fig. 2.
Observed age-specific VZV seroprevalence (circles with the area reflecting the sample size) and age-specific seroprevalence profiles as estimated by the catalytic model with piecewise constant force of infection (solid line) and the isotonic splines model (dashed line) before universal childhood immunization, by country.
Fig. 3.
Fig. 3.
Age-specific annual incidence (/100·000) of VZV in sixteen European countries* before the introduction of universal childhood immunization programs by age group.

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