Evidence map›Paper›PMID 42143270›Full record

ArticleBMC infectious diseases2026

Healthcare-associated COVID-19 in Ontario, Canada: case classification and relative mortality.

Natalie J Wilson, Alicia A Grima, Clara Eunyoung Lee, David N Fisman

Abstract read
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Article in BMC infectious diseases, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Natalie J WilsonDalla Lana School of Public Health, University of Toronto, Room 686, 155 College Street, Toronto, ON, M5T 3M7, Canada.
Alicia A GrimaDalla Lana School of Public Health, University of Toronto, Room 686, 155 College Street, Toronto, ON, M5T 3M7, Canada.
Clara Eunyoung LeeDalla Lana School of Public Health, University of Toronto, Room 686, 155 College Street, Toronto, ON, M5T 3M7, Canada.
David N FismanDalla Lana School of Public Health, University of Toronto, Room 686, 155 College Street, Toronto, ON, M5T 3M7, Canada. david.fisman@utoronto.ca.

Funding

CIHR #518192
6 · The paper itself

Abstract

backgroundThe COVID-19 pandemic placed immense strain on Canada's healthcare system and nosocomial infections increased risk for both healthcare workers and high-risk patients. Nosocomial COVID-19 surveillance typically relies on time-based case definitions that aim to balance sensitivity against specificity, yielding inconsistent estimates of relative mortality risk. We developed a latent class analysis approach to probabilistically classify healthcare-associated infections using multiple indicator variables and evaluated mortality risk in hospitalized COVID-19 patients.

methodsWe analyzed COVID-19 surveillance data from Ontario's Case Contact and Management System and COVaxON vaccine registry (March 17, 2020 to September 4, 2022). Latent class analysis (LCA) integrated five binary indicators (nosocomial flag, outbreak linkage, and three time intervals from admission to positive test) to classify 53,191 hospitalized cases by likelihood of healthcare-acquired infection. We estimated mortality odds and survival by classification using multivariable logistic regression and time-varying Cox models, adjusting for age, comorbidities, immunocompromised status, long-term care residence, vaccination, and pandemic wave.

resultsLCA identified three classes: unlikely (n = 46,819), moderately likely (n = 2,687), and likely (n = 3,685) healthcare-acquired infection. Compared to unlikely, moderately likely cases had elevated mortality (OR: 1.26, 95% CI: 1.14-1.40); likely cases showed no elevation in cumulative mortality (OR: 1.05, 95% CI: 0.96-1.15). Time-varying survival models revealed substantially higher mortality risk early in the period following infection: hazard ratios were 3.25 (95% CI: 2.99-3.52) for moderately likely and 4.88 (95% CI: 4.53-5.25) for likely healthcare-acquired infection. Single-indicator variable sensitivities ranged from 34% to 70%.

conclusionDefining nosocomial infections early in the COVID-19 pandemic was challenging due to the volume of cases and number of patients hospitalized. Several different characteristics can indicate a case's likelihood of being healthcare-acquired, and using a single variable to define a nosocomial case often presents trade-offs in terms of sensitivity or specificity. These findings underscore the limitations of single-indicator definitions and the risk of misclassifying cases in a way that would underestimate the relative severity of hospital-acquired infection by biasing effects toward the null. Latent class modeling addresses sensitivity-specificity trade-offs inherent in time-based nosocomial definitions and reveals elevated mortality risk that strict definitions miss.

Indexed as

COVID-19Cross InfectionAdultAgedFemaleHospitalizationHumansMaleMiddle AgedOntarioSARS-CoV-2COVID-19EpidemiologyNosocomial infectionPandemicsPublic healthSARS-CoV-2

Identifiers

PMID42143270
PMCPMC13360230

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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.