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The Ideal Reporting Interval for an Epidemic to Objectively Interpret the Epidemiological Time Course

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Date 2009 Jul 3
PMID 19570792
Citations 32
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Abstract

The reporting interval of infectious diseases is often determined as a time unit in the calendar regardless of the epidemiological characteristics of the disease. No guidelines have been proposed to choose the reporting interval of infectious diseases. The present study aims at translating coarsely reported epidemic data into the reproduction number and clarifying the ideal reporting interval to offer detailed insights into the time course of an epidemic. We briefly revisit the dispersibility ratio, i.e. ratio of cases in successive reporting intervals, proposed by Clare Oswald Stallybrass, detecting technical flaws in the historical studies. We derive a corrected expression for this quantity and propose simple algorithms to estimate the effective reproduction number as a function of time, adjusting the reporting interval to the generation time of a disease and demonstrating a clear relationship among the generation-time distribution, reporting interval and growth rate of an epidemic. Our exercise suggests that an ideal reporting interval is the mean generation time, so that the ratio of cases in successive intervals can yield the reproduction number. When it is impractical to report observations every mean generation time, we also present an alternative method that enables us to obtain straightforward estimates of the reproduction number for any reporting interval that suits the practical purpose of infection control.

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References
1.
Roberts M, Heesterbeek J . Model-consistent estimation of the basic reproduction number from the incidence of an emerging infection. J Math Biol. 2007; 55(5-6):803-16. PMC: 2782110. DOI: 10.1007/s00285-007-0112-8. View

2.
Ferguson N, Donnelly C, Anderson R . Transmission intensity and impact of control policies on the foot and mouth epidemic in Great Britain. Nature. 2001; 413(6855):542-8. DOI: 10.1038/35097116. View

3.
Wallinga J, Teunis P . Different epidemic curves for severe acute respiratory syndrome reveal similar impacts of control measures. Am J Epidemiol. 2004; 160(6):509-16. PMC: 7110200. DOI: 10.1093/aje/kwh255. View

4.
Fraser C . Estimating individual and household reproduction numbers in an emerging epidemic. PLoS One. 2007; 2(8):e758. PMC: 1950082. DOI: 10.1371/journal.pone.0000758. View

5.
Cauchemez S, Boelle P, Donnelly C, Ferguson N, Thomas G, Leung G . Real-time estimates in early detection of SARS. Emerg Infect Dis. 2006; 12(1):110-3. PMC: 3293464. DOI: 10.3201/eid1201.050593. View