Abstract

Within I-MOVE (European programme to monitor seasonal and pandemic influenza vaccine effectiveness (IVE)) five countries conducted IVE pilot case-control studies in 2008-9. One hundred and sixty sentinel general practitioners (GP) swabbed all elderly consulting for influenza-like illness (ILI). Influenza confirmed cases were compared to influenza negative controls. We conducted a pooled analysis to obtain a summary IVE in the age group of >or=65 years. We measured IVE in each study and assessed heterogeneity between studies qualitatively and using the I2 index. We used a one-stage pooled model with study as a fixed effect. We adjusted estimates for age-group, sex, chronic diseases, smoking, functional status, previous influenza vaccinations and previous hospitalisations. The pooled analysis included 138 cases and 189 test-negative controls. There was no statistical heterogeneity (I2=0) between studies but ILI case definition, previous hospitalisations and functional status were slightly different. The adjusted IVE was 59.1% (95% CI: 15.3-80.3%). IVE was 65.4% (95% CI: 15.6-85.8%) in the 65-74, 59.6% (95% CI: -72.6 -90.6%) in the age group of >or=75 and 56.4% (95% CI: -0.2-81.3%) for A(H3). Pooled analysis is feasible among European studies. The variables definitions need further standardisation. Larger sample sizes are needed to achieve greater precision for subgroup analysis. For 2009-10, I-MOVE will extend the study to obtain early IVE estimates in groups targeted for pandemic H1N1 influenza vaccination.

Highlights

  • The influenza virus has a high genetic mutation rate that frequently determines antigenic drifts and occasionally antigenic shifts

  • To control for health seeking behaviour, recent studies suggested comparing individuals who consult for influenza-like illness (ILI) and are influenza positive to individuals consulting for ILI who test negative for influenza [3,4,5;9]

  • Our results suggest that general practitioners (GP) based casecontrol studies using test-negative controls to estimate seasonal IVE against laboratory-confirmed medically- attended influenza, are feasible in Europe

Read more

Summary

Introduction

The influenza virus has a high genetic mutation rate that frequently determines antigenic drifts and occasionally antigenic shifts. IVE is underestimated when individuals at higher risk of acquiring influenza are more likely to be vaccinated than individuals at lower risk (negative confounding by indication) [6,7]. IVE is overestimated if individuals more cautious about their health and at lower risk of acquiring influenza are more likely to be vaccinated (positive confounding due to healthy vaccinee effect) [7,8]. Vaccinated individuals with influenza symptoms will have a higher probability of being included in the study than vaccinated individuals with no influenza symptoms. The assumption is that test-negative controls have the same vaccination coverage as the source population giving rise to the influenza cases detected at the GP practice

Methods
Results
Discussion
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call