Evidence map›Paper›PMID 40481640›Full record

ArticleAmerican journal of epidemiology2025

Inferring temporal trends of multiple pathogens, variants, subtypes or serotypes from routine surveillance data.

Oliver Eales, Saras M Windecker, James M McCaw, Freya M Shearer

Abstract read
In one paragraph

Article in American journal of epidemiology, 2025. 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

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Oliver EalesInfectious Disease Dynamics Unit, Centre for Epidemiology and Biostatistics, Melbourne School of Population and Global Health, The University of Melbourne, Parkville, Australia.ORCID 0000-0002-8086-4495
Saras M WindeckerInfectious Disease Ecology and Modelling, The Kids Research Institute, Perth, Australia.ORCID 0000-0002-4870-8353
James M McCawInfectious Disease Dynamics Unit, Centre for Epidemiology and Biostatistics, Melbourne School of Population and Global Health, The University of Melbourne, Parkville, Australia.ORCID 0000-0002-2452-3098
Freya M ShearerInfectious Disease Dynamics Unit, Centre for Epidemiology and Biostatistics, Melbourne School of Population and Global Health, The University of Melbourne, Parkville, Australia.ORCID 0000-0001-9600-3473

Funding

Australian Consortium of Epidemic Forecasting and Analytics (ACEFA), a National Health and Medical Research Council of Australia Centre of Research Excellence 2035303Australian Research Council Discovery Project Grant DP240102286Australian Research Council through the Laureate Fellowship Scheme FL240100126National Health and Medical Research Council of Australia through the Investigator Grant Scheme 2021/GNT2010051University of Melbourne McKenzie fellowship
6 · The paper itself

Abstract

Estimating the temporal trends in infectious disease activity is crucial for monitoring disease spread and the impact of interventions. Surveillance indicators routinely collected to monitor these trends are often a composite of multiple pathogens. For example, "influenza-like illness"-routinely monitored as a proxy for influenza infections-is a symptom definition that could be caused by a wide range of pathogens, including multiple subtypes of influenza, SARS-CoV-2, and RSV. Inferred trends from such composite time series may not reflect the trends of any one of the component pathogens, each of which can exhibit distinct dynamics. Although many surveillance systems routinely test a subset of individuals contributing to a surveillance indicator-providing information on the relative contribution of the component pathogens-trends may be obscured by time-varying testing rates or substantial noise in the observation process. Here we develop a general statistical framework for inferring temporal trends of multiple pathogens from routinely collected surveillance data. We demonstrate its application to three different surveillance systems covering multiple pathogens (influenza, SARS-CoV-2, dengue), locations (Australia, Singapore, USA, Taiwan, UK), scenarios (seasonal epidemics, non-seasonal epidemics, pandemic emergence), and temporal reporting resolutions (weekly, daily). This methodology is applicable to a wide range of pathogens and surveillance systems.

Indexed as

COVID-19DengueInfluenza, HumanPopulation SurveillanceAustraliaEpidemiological MonitoringHumansSARS-CoV-2SerogroupSingaporeBayesian time-series analysisdengue serotypesinfluenza subtypespathogen dynamicsSARS-CoV-2 variantsstatistical modeling

Identifiers

PMID40481640
PMCPMC12799599

What OpenQuestion holds

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LicenceCC BY-NC
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Registered trials

None linked

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.