Evidence map›Paper›PMID 42607064›Full record

ArticlePloS one2026

Factors associated with severe COVID-19 outcomes among adults with at least a primary vaccination schedule: A retrospective cohort study from Alberta, Canada.

Sylvia Aponte-Hao, Huong Luu, Karen J B Martins, Jason R Randall, Lynora Saxinger, Elissa Rennert-May, Jenine Leal, Tyler Williamson, Amanda Wilson, Michelle Blake and 6 more

Abstract read
In one paragraph

Article in PloS one, 2026. 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

16 authors.

Sylvia Aponte-HaoData and Research Services, Alberta SPOR SUPPORT Unit Data Platform, Calgary, Alberta, Canada.
Huong LuuReal World Evidence Unit, Faculty of Medicine and Dentistry, University of Alberta, Edmonton, Alberta, Canada.
Karen J B MartinsReal World Evidence Unit, Faculty of Medicine and Dentistry, University of Alberta, Edmonton, Alberta, Canada.ORCID https://orcid.org/0000-0002-3400-7214
Jason R RandallReal World Evidence Unit, Faculty of Medicine and Dentistry, University of Alberta, Edmonton, Alberta, Canada.
Lynora SaxingerDepartment of Medicine, University of Alberta, Edmonton, Alberta, Canada.
Elissa Rennert-MayDepartment of Community Health Sciences, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada.
Jenine LealDepartment of Community Health Sciences, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada.
Tyler WilliamsonDepartment of Community Health Sciences, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada.ORCID https://orcid.org/0000-0001-5029-2345
Amanda WilsonModerna, Cambridge, Massachusetts, United States of America.
Michelle BlakeModerna, Cambridge, Massachusetts, United States of America.
Tianyi LuModerna, Cambridge, Massachusetts, United States of America.
Shehzad M IqbalModerna, Cambridge, Massachusetts, United States of America.
James A MansiModerna, Cambridge, Massachusetts, United States of America.
Andre B AraujoModerna, Cambridge, Massachusetts, United States of America.
David MartinModerna, Cambridge, Massachusetts, United States of America.
Scott W KlarenbachReal World Evidence Unit, Faculty of Medicine and Dentistry, University of Alberta, Edmonton, Alberta, Canada.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundWith a large proportion of adults in Canada vaccinated against SARS-CoV-2, it is important to identify who remain at risk for severe COVID-19 outcomes after primary vaccination and additional (booster) doses.

methodsAdults (≥18 years) who received at least a primary vaccination schedule between December 2020 and March 2023 in Alberta, Canada were identified through population-level administrative data. Factors associated with severe COVID-19 outcomes (COVID-19 related hospitalization or death) were examined using univariable and multivariable Cox proportional hazard models.

resultsAmong those who received a primary vaccination schedule (n = 2,639,731), 0.2% (n = 5,475) had ≥ 1 severe COVID-19 outcome. Factors associated with a greater risk of a severe COVID-19 outcome included older age (≥65 versus <65 years; unadjusted hazard ratio [95% confidence interval]: 8.83 [8.33-9.35]), and living with a higher comorbid burden (severe versus no burden; 32.56 [29.78-35.60]) or health condition of interest (1.33 [1.25-1.42] to 29.25 [23.14-36.99]) such as the relatively common condition of cardiovascular disease (7.01 [6.62-7.42]; present in 10.5% of the cohort) and less common condition of dementia (13.96 [12.76-15.28]; present in 1.5% of the cohort); male sex was also associated with risk (versus female; 1.07 [1.01-1.13]). Results remained significant in fully adjusted analysis, and among those with ≥1 additional vaccination dose (n = 1,580,110).

conclusionAlthough primary vaccination and additional doses have dramatically reduced the occurrence of severe COVID-19 outcomes, results showed that continued risk remained for specific groups. Findings can be used to inform decision making, public health strategies, and policy development to protect those who remain at risk of severe COVID-19 outcomes after receipt of a primary vaccination schedule or additional doses, and support Canada's National Advisory Committee on Immunisation recommendations for specific groups to stay up to date with COVID-19 vaccination to protect against severe COVID-19 outcomes.

Indexed as

COVID-19COVID-19 VaccinesImmunization ScheduleAdolescentAdultAgedAlbertaFemaleHospitalizationHumansMaleMiddle AgedRetrospective StudiesRisk FactorsSARS-CoV-2VaccinationCOVID-19 Vaccines

Identifiers

PMID42607064
PMCPMC13480603

What Socratic holds

Textmetadata
Read underepoch 390

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 Socratic graph.