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Original Articles

Estimating Vaccine Efficacy from Outbreak Size Household Data in the Presence of Heterogeneous Transmission Probabilities

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Pages 499-516 | Received 13 Mar 2006, Accepted 13 Mar 2006, Published online: 03 Sep 2006
 

Abstract

We develop a Bayesian approach for estimating vaccine efficacy for susceptibility ( VE S ) and infectiousness ( VE I ) using outbreak size household data. Our method allows for heterogeneity in transmission probabilities due to factors that are related to individual' characteristics, such as age, in addition to vaccination status. It also allows for between-household heterogeneity in transmission probabilities due to random effects associated with households, such as genetic or environmental effects. Using age as a potential covariate causing heterogeneity in individual' transmission probabilities in households consisting of adults and children, we present the results of a simulation study designed to evaluate the performance of the proposed estimators of VE S and VE I . We found that estimates of VE I have larger bias and variance compared to those of VE S . We also use the approach to compare two vaccination designs: one vaccinating both adults and children, the other only children. Simulations reveal that the design that vaccinates both adults and children provides better estimates of V E S . There is no obvious difference between the two designs in the performance of the estimates of V E I . In regard to random effects between households and the scenarios considered, models that do not account for between-households heterogeneity produce fairly robust estimates even when household-level random effects are present.

ACKNOWLEDGMENT

The authors wish to thank John Hanfelt and two reviewers for helpful comments and suggestions.

Notes

Model 1 – no age effect without intercepts; Model 2 – no age effect with intercepts; Model 3 − β age effect; Model 4 − γ age effect; Model 5 − β and γ age related.

⋆ any values.

Model 1 – no age effect without intercepts; Model 2 – no age effect with intercepts; Model 3 − β age effect; Model 4 − γ age effect; Model 5 − β and γ age related.

Model 1 – no age effect without intercepts; model 2 – no age effect with intercepts; model 3 − β age effect; model 4 − γ age effect; model 5 − β and γ age related.

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