BACKGROUND: The need to deliver interventions targeting multiple diseases in a cost-effective manner calls for integrated disease control efforts. Consequently, maps are required that show where the risk of co-infection is particularly high. Co-infection risk is preferably estimated via Bayesian geostatistical multinomial modelling, using data from surveys screening for multiple infections simultaneously. However, only few surveys have collected this type of data. METHODS: Bayesian geostatistical shared component models (allowing for covariates, disease-specific and shared spatial and non-spatial random effects) are proposed to model the geographical distribution and burden of co-infection risk from single-disease surveys. The ability of the models to capture co-infection risk is assessed on simulated data sets based on multinomial distributions assuming light- and heavy-dependent diseases, and a real data set of Schistosoma mansoni-hookworm co-infection in the region of Man, Côte d'Ivoire. The data were restructured as if obtained from single-disease surveys. The estimated results of co-infection risk, together with independent and multinomial model results, were compared via different validation techniques. RESULTS: The results showed that shared component models result in more accurate estimates of co-infection risk than models assuming independence in settings of heavy-dependent diseases. The shared spatial random effects are similar to the spatial co-infection random effects of the multinomial model for heavy-dependent data. CONCLUSIONS: In the absence of true co-infection data geostatistical shared component models are able to estimate the spatial patterns and burden of co-infection risk from single-disease survey data, especially in settings of heavy-dependent diseases.
BACKGROUND: The need to deliver interventions targeting multiple diseases in a cost-effective manner calls for integrated disease control efforts. Consequently, maps are required that show where the risk of co-infection is particularly high. Co-infection risk is preferably estimated via Bayesian geostatistical multinomial modelling, using data from surveys screening for multiple infections simultaneously. However, only few surveys have collected this type of data. METHODS: Bayesian geostatistical shared component models (allowing for covariates, disease-specific and shared spatial and non-spatial random effects) are proposed to model the geographical distribution and burden of co-infection risk from single-disease surveys. The ability of the models to capture co-infection risk is assessed on simulated data sets based on multinomial distributions assuming light- and heavy-dependent diseases, and a real data set of Schistosoma mansoni-hookworm co-infection in the region of Man, Côte d'Ivoire. The data were restructured as if obtained from single-disease surveys. The estimated results of co-infection risk, together with independent and multinomial model results, were compared via different validation techniques. RESULTS: The results showed that shared component models result in more accurate estimates of co-infection risk than models assuming independence in settings of heavy-dependent diseases. The shared spatial random effects are similar to the spatial co-infection random effects of the multinomial model for heavy-dependent data. CONCLUSIONS: In the absence of true co-infection data geostatistical shared component models are able to estimate the spatial patterns and burden of co-infection risk from single-disease survey data, especially in settings of heavy-dependent diseases.
Authors: Simon J Brooker; Rachel L Pullan; Caroline W Gitonga; Ruth A Ashton; Jan H Kolaczinski; Narcis B Kabatereine; Robert W Snow Journal: J Infect Dis Date: 2012-01-18 Impact factor: 5.226