Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2013 Dec 31;8(12):e83622.
doi: 10.1371/journal.pone.0083622. eCollection 2013.

An IDEA for short term outbreak projection: nearcasting using the basic reproduction number

Affiliations

An IDEA for short term outbreak projection: nearcasting using the basic reproduction number

David N Fisman et al. PLoS One. .

Abstract

Background: Communicable disease outbreaks of novel or existing pathogens threaten human health around the globe. It would be desirable to rapidly characterize such outbreaks and develop accurate projections of their duration and cumulative size even when limited preliminary data are available. Here we develop a mathematical model to aid public health authorities in tracking the expansion and contraction of outbreaks with explicit representation of factors (other than population immunity) that may slow epidemic growth.

Methodology: The Incidence Decay and Exponential Adjustment (IDEA) model is a parsimonious function that uses the basic reproduction number R0, along with a discounting factor to project the growth of outbreaks using only basic epidemiological information (e.g., daily incidence counts).

Principal findings: Compared to simulated data, IDEA provides highly accurate estimates of total size and duration for a given outbreak when R0 is low or moderate, and also identifies turning points or new waves. When tested with an outbreak of pandemic influenza A (H1N1), the model generates estimated incidence at the i+1(th) serial interval using data from the i(th) serial interval within an average of 20% of actual incidence.

Conclusions and significance: This model for communicable disease outbreaks provides rapid assessments of outbreak growth and public health interventions. Further evaluation in the context of real-world outbreaks will establish the utility of IDEA as a tool for front-line epidemiologists.

PubMed Disclaimer

Conflict of interest statement

Competing Interests: The authors have declared that no competing interests exist.

Figures

Figure 1
Figure 1. Model fits and “order of control”.
Relationship between final-size-normalized root-mean squared differences (RMSD, Y-axis) between SIR model outputs and IDEA model fits, for R0 ranging from 1.5 to 7 (legend), with variation in order of control in SIR models (X-axis). It can be seen that for all R0 best-fits are achieved with first order control. Model fits were however better with low R0 simulations than with higher R0 simulations.
Figure 2
Figure 2. IDEA model fits for low R0 epidemics.
Comparison of prevalent infections and cumulative infections from data generated using the SIR difference equation model described in the text (gray curves), and an IDEA model fitted to the first four generations of the simulated SIR epidemic (dashed curves). The true R0 used in the SIR model was 3.0. It can be seen that the IDEA model projections reproduce future case counts in the SIR model almost perfectly.
Figure 3
Figure 3. IDEA model fits for higher R0 epidemics.
Concordance between simulated data from an SIR difference model for a higher-R0 system (R0 = 6) (solid gray curves) and IDEA fits based on early (T < = 10) generations (gray dashed curves), and based on fits from generation 15 onwards (black dashed curves). Prevalent infections are shown in the left hand panel while cumulative infections are shown on the right. Fits from generations prior to the epidemic peak (T< = 10) reproduce the initial growth of the epidemic well, and also provide accurate estimates of the true R0 (R0∼6.34, d = 0.054); however, these parameters result in IDEA projections of far larger epidemics than actually occur. Once IDEA models are fit using generations that include and follow the epidemic peak (i.e., T> = 15) projections of both prevalent and cumulative infections become fairly accurate (black dashed curves); however, estimated R0 is much larger than the true value (R0∼7.56) and the best-fit value for d increases as well (from 0.054 to 0.069).
Figure 4
Figure 4. Model behaviour.
The overall behaviour of the IDEA model based on a range of possible Ro and d values (a) the variation of tmax or outbreak duration as a function of Ro and d (b) the variation of Itotal or the final cumulative incidence as a function of R0 and d.
Figure 5
Figure 5. Pandemic H1N1 case counts modeled with the IDEA Model.
The IDEA model applied to an outbreak of influenza A (H1N1) in Nunavut, Canada, with the model parameters R0, d, tmax, Itotal and Δd. (a) the early stages of the outbreak, with largely exponential growth, (b) dampened growth with reduced projected tmax values by serial interval 7, (c) a second wave in the outbreak and (d) the fit of the model at 24 out of 27 generations.
Figure 6
Figure 6. Utility of the IDEA model in evaluating the impact of public health and social or environmental factors on outbreak behaviour.
(a) The utility of the IDEA model in evaluating the level of control over the outbreak. Each projection is based on the outbreak up to i intervals, projected to the i+1th interval. With the exception of serial intervals 6 and 7 illustrated in the figure, the projected case counts were less than the actual case counts implying that at each serial interval the outbreak grew more than would be expected by its previous course. During this outbreak, the model underestimated the actual number of cases except during two serial intervals. (b) Percent error between the projection for the next generation and actual case counts according to generation.

References

    1. Lipsitch M, Cohen T, Cooper B, Robins JM, Ma S, et al. (2003) Transmission dynamics and control of severe acute respiratory syndrome. Science 300: 1966–1970. - PMC - PubMed
    1. Peiris JSM, Guan Y, Yuen KY (2004) Severe acute respiratory syndrome. Nature Medicine 10. - PMC - PubMed
    1. Bautista E, Chotpitayasunondh T, Gao Z, Harper SA, Shaw M, et al.. (2010) Clinical aspects of pandemic 2009 influenza a (H1N1) virus infection. New England Journal of Medicine 362. - PubMed
    1. Chang LY, Shih SR, Shao PL, Huang DTN, Huang LM (2009) Novel Swine-origin Influenza Virus A (H1N1): The First Pandemic of the 21st Century. Journal of the Formosan Medical Association 108: 526–532. - PubMed
    1. Arguin PM, Marano N, Freedman DO (2009) Globally mobile populations and the spread of emerging pathogens. Emerging Infectious Diseases 15: 1713–1714. - PMC - PubMed

MeSH terms