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      Optimizing Provider Recruitment for Influenza Surveillance Networks

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          Abstract

          The increasingly complex and rapid transmission dynamics of many infectious diseases necessitates the use of new, more advanced methods for surveillance, early detection, and decision-making. Here, we demonstrate that a new method for optimizing surveillance networks can improve the quality of epidemiological information produced by typical provider-based networks. Using past surveillance and Internet search data, it determines the precise locations where providers should be enrolled. When applied to redesigning the provider-based, influenza-like-illness surveillance network (ILINet) for the state of Texas, the method identifies networks that are expected to significantly outperform the existing network with far fewer providers. This optimized network avoids informational redundancies and is thereby more effective than networks designed by conventional methods and a recently published algorithm based on maximizing population coverage. We show further that Google Flu Trends data, when incorporated into a network as a virtual provider, can enhance but not replace traditional surveillance methods.

          Author Summary

          Public health agencies use surveillance systems to detect and monitor chronic and infectious diseases. These systems often rely on data sources that are chosen based on loose guidelines or out of convenience. In this paper, we introduce a new, data-driven method for designing and improving surveillance systems. Our approach is a geographic optimization of data sources designed to achieve specific surveillance goals. We tested our method by re-designing Texas' provider-based influenza surveillance system (ILINet). The resulting networks better predicted influenza associated hospitalizations and contained fewer providers than the existing ILINet. Furthermore, our study demonstrates that the integration of Internet source data, like Google Flu Trends, into surveillance systems can enhance traditional, provider-based networks.

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          Most cited references27

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            Surveillance Sans Frontières: Internet-Based Emerging Infectious Disease Intelligence and the HealthMap Project

            John Brownstein and colleagues discuss HealthMap, an automated real-time system that monitors and disseminates online information about emerging infectious diseases.
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              Methods for monitoring influenza surveillance data.

              A variety of Serfling-type statistical algorithms requiring long series of historical data, exclusively from temperate climate zones, have been proposed for automated monitoring of influenza sentinel surveillance data. We evaluated three alternative statistical approaches where alert thresholds are based on recent data in both temperate and subtropical regions. We compared time series, regression, and cumulative sum (CUSUM) models on empirical data from Hong Kong and the US using a composite index (range = 0-1) consisting of the key outcomes of sensitivity, specificity, and time to detection (lag). The index was calculated based on alarms generated within the first 2 or 4 weeks of the peak season. We found that the time series model was optimal in the Hong Kong setting, while both the time series and CUSUM models worked equally well on US data. For alarms generated within the first 2 weeks (4 weeks) of the peak season in Hong Kong, the maximum values of the index were: time series 0.77 (0.86); regression 0.75 (0.82); CUSUM 0.56 (0.75). In the US data the maximum values of the index were: time series 0.81 (0.95); regression 0.81 (0.91); CUSUM 0.90 (0.94). Automated influenza surveillance methods based on short-term data, including time series and CUSUM models, can generate sensitive, specific, and timely alerts, and can offer a useful alternative to Serfling-like methods that rely on long-term, historically based thresholds.
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                Author and article information

                Contributors
                Role: Editor
                Journal
                PLoS Comput Biol
                PLoS Comput. Biol
                plos
                ploscomp
                PLoS Computational Biology
                Public Library of Science (San Francisco, USA )
                1553-734X
                1553-7358
                April 2012
                April 2012
                12 April 2012
                : 8
                : 4
                : e1002472
                Affiliations
                [1 ]The University of Texas at Austin, Section of Integrative Biology, Austin, Texas, United States of America
                [2 ]Naval Postgraduate School, Operations Research Department, Monterey, California, United States of America
                [3 ]The Santa Fe Institute, Santa Fe, New Mexico, United States of America
                University of New South Wales, Australia
                Author notes

                Conceived and designed the experiments: SVS NBD LAM. Performed the experiments: SVS NBD. Analyzed the data: SVS NBD. Contributed reagents/materials/analysis tools: SVS NBD. Wrote the paper: SVS NBD LAM.

                Article
                PCOMPBIOL-D-11-01185
                10.1371/journal.pcbi.1002472
                3325176
                22511860
                54229ef7-21ab-4409-bd20-a14b999fc9c3
                Scarpino et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
                History
                : 9 August 2011
                : 29 February 2012
                Page count
                Pages: 12
                Categories
                Research Article
                Medicine
                Epidemiology
                Disease Informatics
                Epidemiological Methods
                Infectious Disease Epidemiology
                Infectious Diseases
                Viral Diseases
                Influenza

                Quantitative & Systems biology
                Quantitative & Systems biology

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