Evidence map›Paper›PMID 41165884›Full record

ArticleJournal of mathematical biology2025

Mapping Incidence and Prevalence Peak Data for SIR Modeling Applications.

Alexander C Murph, G Casey Gibson, Lauren J Beesley, Nishant Panda, Lauren A Castro, Sara Y Del Valle, Carrie A Manore, Dave A Osthus

Abstract read
In one paragraph

Article in Journal of mathematical biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

8 authors.

Alexander C MurphStatistics (CAI-4), Computing and Artificial Intelligence Division, Los Alamos National Lab, Los Alamos, 87545, New Mexico, USA. murph@lanl.gov.ORCID 0000-0001-7170-867X
G Casey GibsonStatistics (CAI-4), Computing and Artificial Intelligence Division, Los Alamos National Lab, Los Alamos, 87545, New Mexico, USA.
Lauren J BeesleyStatistics (CAI-4), Computing and Artificial Intelligence Division, Los Alamos National Lab, Los Alamos, 87545, New Mexico, USA.
Nishant PandaInformation Systems & Modeling Group (A-1), Analytics, Intelligence, & Technology Division, Los Alamos National Laboratory, Los Alamos, 87545, New Mexico, USA.
Lauren A CastroInformation Systems & Modeling Group (A-1), Analytics, Intelligence, & Technology Division, Los Alamos National Laboratory, Los Alamos, 87545, New Mexico, USA.
Sara Y Del ValleInformation Systems & Modeling Group (A-1), Analytics, Intelligence, & Technology Division, Los Alamos National Laboratory, Los Alamos, 87545, New Mexico, USA.
Carrie A ManoreTheoretical Biology & Biophysics (T-6), Theoretical Division, Los Alamos National Laboratory, Los Alamos, 87545, New Mexico, USA.
Dave A OsthusStatistics (CAI-4), Computing and Artificial Intelligence Division, Los Alamos National Lab, Los Alamos, 87545, New Mexico, USA.

Funding

Development of an Open-Source and Data-Driven Modeling Platform to Monitor and Forecast Disease ActivityR01GM130668 · NIGMS · NORTHEASTERN UNIVERSITY · PI SANTILLANA, MAURICIO · 2018 to 2022
$1.9M
Los Alamos National Laboratory 20240066DRNational Institute of Health (US) R01GM130668-01NIGMS NIH HHS R01 GM130668
6 · The paper itself

Abstract

Infectious disease modeling and forecasting have played a key role in helping assess and respond to epidemics and pandemics. Recent work has leveraged data on disease peak infection and peak hospital incidence to fit compartmental models for the purpose of forecasting and describing the dynamics of a disease outbreak. Incorporating these data can greatly stabilize a compartmental model fit on early observations, where slight perturbations in the data may lead to model fits that forecast wildly unrealistic peak infection. We introduce a new method for incorporating historic data on the value and time of peak incidence of hospitalization into the fit for a Susceptible-Infectious-Recovered (SIR) model by formulating the relationship between an SIR model's starting parameters and peak incidence as a system of two equations that can be solved computationally. We demonstrate how to calculate SIR parameter estimates - which describe disease dynamics such as transmission and recovery rates - using this method, and determine that there is a noticeable loss in accuracy whenever prevalence data is misspecified as incidence data. To exhibit the modeling potential, we update the Dirichlet-Beta State Space modeling framework to use hospital incidence data, as this framework was previously formulated to incorporate only data on total infections. This approach is assessed for practicality in terms of accuracy and speed of computation via simulation.

Indexed as

Communicable DiseasesEpidemiological ModelsModels, BiologicalComputer SimulationCOVID-19Disease OutbreaksDisease SusceptibilityEpidemicsForecastingHospitalizationHumansIncidenceMathematical ConceptsPrevalenceCompartmental ModelsDisease ForecastingHospital IncidencePrevalence

Identifiers

PMID41165884
PMCPMC12575469

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LicenceCC BY
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Registered trials

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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.