Evidence map›Paper›PMID 41091813›Full record

ArticlePLoS computational biology2025

Transmission thresholds for the spread of infections in healthcare facilities.

Damon J A Toth, Karim Khader, Christopher Mitchell, Matthew H Samore

Abstract read
In one paragraph

Article in PLoS computational 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

4 authors.

Damon J A TothDivision of Epidemiology, Department of Internal Medicine, University of Utah School of Medicine, Salt Lake City, Utah, United States of America.ORCID 0000-0001-7393-4814
Karim KhaderDivision of Epidemiology, Department of Internal Medicine, University of Utah School of Medicine, Salt Lake City, Utah, United States of America.
Christopher MitchellDepartment of Quantitative and Qualitative Health Sciences, University of Texas School of Public Health San Antonio, San Antonio, Texas, United States of America.ORCID 0000-0001-8792-9370
Matthew H SamoreDivision of Epidemiology, Department of Internal Medicine, University of Utah School of Medicine, Salt Lake City, Utah, United States of America.

Funding

NCEZID CDC HHS U01 CK000585
6 · The paper itself

Abstract

Some infections may be sustained in the human population by persistent transmission among patients in healthcare facilities, including patients colonized with multi-drug-resistant organisms posing a major health threat. A nuanced understanding of facility characteristics that contribute to crossing a threshold for self-sustaining outbreak potential may be crucial to designing efficient interventions for lowering regional disease burden and preventing high-risk infections. Using a mathematical model, we define the facility basic reproduction number R0, where a single facility can sustain an outbreak without ongoing importation under the threshold condition R0 > 1. We define R0 for a general model with heterogeneous patient susceptibility and transmissibility and with generic length-of-stay assumptions, and we provide a software package for numerical calculation of user-defined examples. We estimate R0 using published data for carbapenemase-producing Enterobacteriaceae (CPE) in long-term acute-care hospitals (LTACHs) and the effects of interventions on R0, including surveillance, pathogen reduction treatments, and length-of-stay reduction. In a simple model, R0 is directly proportional to the sum of the mean and variance-to-mean ratio of the length-of-stay distribution. In intervention models, R0 depends on the moment-generating function of the length-of-stay distribution. From the CPE data, we estimated R0 = 1.24 (95% CI: 1.04, 1.45) prior to intervention. Weekly surveillance with 50% transmission reduction of detected patients alone could have reduced R0 to 0.85 (0.72, 0.98), with additional reduction if detected patients could be decolonized. Reducing the mean length of stay does not necessarily reduce R0 if the variance-to-mean ratio is not also reduced. We conclude that R0 > 1 conditions plausibly exist in LTACHs, where CPE outbreaks could be sustained by patients who acquire colonization and subsequently transmit to other patients during the same hospital stay. Our findings illuminate epidemiological mechanisms producing those conditions and their relationship to interventions that could efficiently improve population health.

Indexed as

Cross InfectionEnterobacteriaceae InfectionsHealth FacilitiesBasic Reproduction NumberComputational BiologyDisease OutbreaksHumansModels, Biological

Identifiers

PMID41091813
PMCPMC12539749

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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.