Evidence map›Paper›PMID 33357248›Full record

ArticleEpidemiology and infection2020

Forecasting the final disease size: comparing calibrations of Bertalanffy-Pütter models.

Norbert Brunner, Manfred Kühleitner

Abstract read
In one paragraph

Article in Epidemiology and infection, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

2 authors.

Norbert BrunnerDepartment of Integrative Biology and Biodiversity Research (DIBB), University of Natural Resources and Life Sciences (BOKU), A-1180 Vienna, Austria.ORCID 0000-0001-6487-5752
Manfred KühleitnerDepartment of Integrative Biology and Biodiversity Research (DIBB), University of Natural Resources and Life Sciences (BOKU), A-1180 Vienna, Austria.ORCID 0000-0002-0217-7550

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Using monthly data from the Ebola-outbreak 2013-2016 in West Africa, we compared two calibrations for data fitting, least-squares (SSE) and weighted least-squares (SWSE) with weights reciprocal to the number of new infections. To compare (in hindsight) forecasts for the final disease size (the actual value was observed at month 28 of the outbreak) we fitted Bertalanffy-Pütter growth models to truncated initial data (first 11, 12, …, 28 months). The growth curves identified the epidemic peak at month 10 and the relative errors of the forecasts (asymptotic limits) were below 10%, if 16 or more month were used; for SWSE the relative errors were smaller than for SSE. However, the calibrations differed insofar as for SWSE there were good fitting models that forecasted reasonable upper and lower bounds, while SSE was biased, as the forecasts of good fitting models systematically underestimated the final disease size. Furthermore, for SSE the normal distribution hypothesis of the fit residuals was refuted, while the similar hypothesis for SWSE was not refuted. We therefore recommend considering SWSE for epidemic forecasts.

Indexed as

Disease OutbreaksModels, BiologicalModels, StatisticalAfrica, WesternForecastingHemorrhagic Fever, EbolaHumansBertalanffy–Pütter model (BP-model)epidemic trajectoryfinal disease sizeforecastweighted least-squares

Identifiers

PMID33357248
PMCPMC8057487

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.