Evidence map›Paper›PMID 41044785›Full record

ArticleInternational journal of health geographics2025

Assessing spatial variability in observed infectious disease spread in a prospective time-space series.

Chih-Chieh Wu, Chien-Hsiun Chen, Shann-Rong Wang, Sanjay Shete

Abstract read
In one paragraph

Article in International journal of health geographics, 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

4 authors.

Chih-Chieh WuDepartment of Environmental and Occupational Health, College of Medicine, National Cheng Kung University, 1 University Road, Tainan, 701, Taiwan. cc_wu@mail.ncku.edu.tw.
Chien-Hsiun ChenInstitute of Biomedical Sciences, Academia Sinica, Taipei, Taiwan.
Shann-Rong WangDepartment of Environmental and Occupational Health, College of Medicine, National Cheng Kung University, 1 University Road, Tainan, 701, Taiwan.
Sanjay SheteDepartment of Biostatistics, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Fabien Delerue · 1985 to 2026
$290.8M
Molecular Epidemiology of Neuropathic Pain in Head and Neck CancerR01DE022891 · NIDCR · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI REYES-GIBBY, CIELITO C, SHETE, SANJAY · 2012 to 2016
$3.0M
Genome Wide Association Study of Head and Neck CancerR01CA131324 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI SHETE, SANJAY · 2009 to 2013
$2.8M
National Science and Technology Council MOST 111-2118-M-006-006, NSTC 112-2314- B-006-078NCI NIH HHS P30 CA016672NCI NIH HHS R01 CA131324NIDCR NIH HHS R01 DE022891NIH HHS 1R01CA131324, R01DE022891, P30CA016672
6 · The paper itself

Abstract

Most of the growing prospective analytic methods in space-time disease surveillance and intended functions of disease surveillance systems focus on earlier detection of disease outbreaks, disease clusters, or increased incidence. The spread of the virus such as SARS-CoV-2 has not been spatially and temporally uniform in an outbreak. With the identification of an infectious disease outbreak, recognizing and evaluating anomalies (excess and decline) of disease incidence spread at the time of occurrence during the course of an outbreak is a logical next step. We propose and formulate a hypergeometric probability model that investigates anomalies of infectious disease incidence spread at the time of occurrence in the timeline for many geographically described populations (e.g., hospitals, towns, counties) in an ongoing daily monitoring process. It is structured to determine whether the incidence grows or declines more rapidly in a region on the single current day or the most recent few days compared to the occurrence of the incidence during the previous few days relative to elsewhere in the surveillance period. The new method uses a time-varying baseline risk model, accounting for regularly (e.g., daily) updated information on disease incidence at the time of occurrence, and evaluates the probability of the deviation of particular frequencies to be attributed to sampling fluctuations, accounting for the unequal variances of the rates due to different population bases in geographical units. We attempt to present and illustrate a new model to advance the investigation of anomalies of infectious disease incidence spread by analyzing subsamples of spatiotemporal disease surveillance data from Taiwan on dengue and COVID-19 incidence which are mosquito-borne and contagious infectious diseases, respectively. Efficient R packages for computation are available to implement the two approximate formulae of the hypergeometric probability model for large numbers of events.

Indexed as

Communicable DiseasesCOVID-19Disease OutbreaksPopulation SurveillanceSpatio-Temporal AnalysisHumansIncidenceProspective StudiesSARS-CoV-2

Identifiers

PMID41044785
PMCPMC12495847

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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.