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Published on: August 14, 2019
Vaccine Effectiveness Against Laboratory-confirmed Influenza in Healthy Young Children: A Case-Control Study
Heath Kelly1, Peter Jacoby, Gabriela A Dixon
1School of Computer Science and Software Engineering, University of Western Australia, Perth, Western Australia, Australia.
Insights
Inactivated influenza vaccination showed significant effectiveness in young children. Testing for other respiratory viruses improved vaccine effectiveness estimates in this study.
Area of Science:
- Pediatric infectious diseases
- Vaccinology
- Epidemiology
Background:
- The Western Australian Influenza Vaccine Effectiveness study began in 2008.
- The study evaluated a program offering free influenza vaccine to children aged 6-59 months.
Purpose of the Study:
- To assess the protective effect of inactivated influenza vaccination in children aged 6 to 59 months.
- To determine influenza vaccine effectiveness (VE) against laboratory-confirmed influenza.
Main Methods:
- A prospective case-control study was conducted in general practices and a hospital emergency department.
- Children with influenza-like illness were tested for influenza and other respiratory viruses.
- VE was calculated using adjusted odds ratios from multivariate logistic regression.
Main Results:
- A total of 289 children were enrolled; 48 had laboratory-confirmed influenza.
- Adjusted VE was 58% (95% CI, 9-81) using all influenza-negative controls.
- Adjusted VE was 68% (95% CI, 26-86) when controls had another detected respiratory virus.
Conclusions:
- Influenza vaccine effectiveness estimates were higher when the control group included children with other detected respiratory viruses.
- Testing for other respiratory viruses can refine control group selection for improved VE studies.
Background:
the Western Australian Influenza Vaccine Effectiveness study commenced in 2008 to evaluate a new program to provide free influenza vaccine to all children aged 6 to 59 months. We aimed to assess the protective effect of inactivated influenza vaccination in these children.
Methods:
We conducted a prospective case-control study in general practices and a hospital emergency department, testing all eligible patients for influenza and a range of other common respiratory viruses. Influenza vaccine effectiveness (VE) against laboratory-confirmed influenza was estimated with cases defined as children with an influenza-like illness who tested positive and controls as those with an influenza-like illness who tested negative for influenza virus. We calculated VE using the adjusted odds ratio from multivariate logistic regression. As a surrogate marker for adequate specimen collection, we explored the difference in VE point estimates defining controls as children in whom another respiratory virus was detected.
Results:
a total of 75 children were enrolled from general practices and 214 through the emergency department, with 12 (27%) and 36 (17%), respectively, having laboratory-confirmed influenza. Using all the influenza-negative controls, the adjusted VE was 58% (95% confidence interval, 9-81). When controls were limited to those with another virus present, the adjusted VE was 68% (95% confidence interval, 26-86).
Conclusions:
VE estimates were higher when controls included only those children with another respiratory virus detected. Testing for other common respiratory viruses enables the control group to be restricted to those for whom an adequate sample is likely.
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