Evidence map›Paper›PMID 41665905›Full record

ArticleJAMA network open2026

Invasive Group A Streptococcal Disease in Persons Experiencing Postpandemic Homelessness in Canada.

Caroline Kassee, Halima Dabaja-Younis, Lucie Richard, Alyssa R Golden, Zoe Zhong, Vanessa Allen, Huda Almohri, Irene Armstrong, Mahin Baqi, Kevin R Barker and 22 more

Abstract read
In one paragraph

Article in JAMA network open, 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

32 authors.

Caroline KasseeDepartment of Microbiology, Sinai Health, Toronto, Ontario, Canada.
Halima Dabaja-YounisInfection Prevention and Control Unit, Rambam Health Care Campus, Haifa, Israel.
Lucie RichardMAP Centre for Urban Health Solutions, Unity Health Toronto, Toronto, Ontario, Canada.
Alyssa R GoldenNational Microbiology Laboratory, Public Health Agency of Canada, Winnipeg, Manitoba, Canada.
Zoe ZhongDepartment of Microbiology, Sinai Health, Toronto, Ontario, Canada.
Vanessa AllenDepartment of Microbiology, Sinai Health, Toronto, Ontario, Canada.
Huda AlmohriLifelabs, Toronto, Ontario, Canada.
Irene ArmstrongToronto Public Health, Toronto, Ontario, Canada.
Mahin BaqiWilliam Osler Health System, Brampton, Ontario, Canada.
Kevin R BarkerTrillium Health Partners, Mississauga, Ontario, Canada.
Sergio BorgiaWilliam Osler Health System, Brampton, Ontario, Canada.
Aaron CampigottoThe Hospital for Sick Children, Toronto, Ontario, Canada.
Sumon ChakrabartiTrillium Health Partners, Mississauga, Ontario, Canada.
Wayne L GoldUniversity Health Network, Toronto, Ontario, Canada.
Rachel K HinkNational Microbiology Laboratory, Public Health Agency of Canada, Winnipeg, Manitoba, Canada.
Christopher KandelMichael Garron Hospital, Toronto East Health Network, Toronto, Ontario, Canada.
Ian KitaiThe Hospital for Sick Children, Toronto, Ontario, Canada.
Julianne KusPublic Health Ontario, Toronto, Ontario, Canada.
Liane MacdonaldPublic Health Ontario, Toronto, Ontario, Canada.
Matthew P MullerUnity Health, Toronto, Ontario, Canada.
Jeya NadarajahOak Valley Health, Markham, Ontario, Canada.
Krystyna OstrowskaTrillium Health Partners, Mississauga, Ontario, Canada.
Daniel RicciutoLakeridge Health, Oshawa, Ontario, Canada.
David RichardsonWilliam Osler Health System, Brampton, Ontario, Canada.
Medina SaffieJoseph Brant Hospital, Burlington, Ontario, Canada.
Michael SilvermanSchulich School of Medicine and Dentistry, Western University, London, Ontario, Canada.
Manal TadrosThe Hospital for Sick Children, Toronto, Ontario, Canada.
Monali VariaRegion of Peel-Public Health, Brampton, Ontario, Canada.
Stephen W HwangMAP Centre for Urban Health Solutions, Unity Health Toronto, Toronto, Ontario, Canada.
Irene MartinNational Microbiology Laboratory, Public Health Agency of Canada, Winnipeg, Manitoba, Canada.
Allison McGeerDepartment of Microbiology, Sinai Health, Toronto, Ontario, Canada.
Toronto Invasive Bacterial Diseases Network

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Importance: Both invasive group A streptococcal (iGAS) infections and the number of persons experiencing homelessness (PEH) are increasing. Protection of PEH from the burden of iGAS infections requires understanding of its epidemiology. Objective: To assess whether the resurgence of iGAS infections after the COVID-19 pandemic included PEH. Design, Setting, and Participants: This cross-sectional study of population-based iGAS surveillance used Canada's National Microbiology Laboratory for emm typing and Statistics Canada and point-in-time counts to identify denominators. Participants included 503 persons with iGAS infections from January 1, 2022, to December 31, 2023, in the Toronto and Peel Region, Canada (population, 4.5 million). Main Outcomes and Measures: The main outcome was disease incidence among PEH over time and compared with housed persons. Secondary outcomes were differences in risk factors, presentation, disease severity, and infecting emm types between PEH and housed persons. Results: Ninety iGAS cases occurred among PEH (median age, 47.0 years [IQR, 37.7-59.5 years]; 66 men [73.3%]) and 413 occurred among housed adults (median age, 58.9 years [IQR, 42.1-73.3 years]; 259 men [62.7%]). iGAS incidence among PEH increased from 270.4 (95% CI, 184.5-383.2) per 100 000 per year in 2022 to 451.2 (95% CI, 348.2-575.7) per 100 000 per year in 2023 (incidence rate ratio [IRR], 1.67; 95% CI, 1.06-2.69), not significantly different than the increase from 3.4 to 7.0 per 100 000 per year among housed persons (IRR, 2.05; 95% CI, 1.67-2.52). iGAS incidence overall was 70.7-fold higher (95% CI, 56.3-fold to 88.7-fold) among PEH than housed persons. Compared with housed adults, PEH were less likely to be immunocompromised (adjusted odds ratio [AOR], 0.29; 95% CI, 0.11-0.73) and were more likely to be persons who inject drugs (AOR, 5.06; 95% CI, 2.79-9.19), to have nonintact skin (AOR, 4.16; 95% CI, 2.45-7.04), and to have iGAS presenting as soft tissue infection (AOR, 1.64; 95% CI, 1.02-2.64). PEH were less likely to die of iGAS than housed adults (AOR, 0.33; 95% CI, 0.12-0.95). Overall, emm1 and emm12 caused 33.7% of iGAS cases (137 of 406) among housed persons, but only 2.2% (2 of 90) among PEH; in contrast, isolates with emm types 49, 74, 80, 82, and 92 caused 77.8% of iGAS cases (70 of 90) among PEH, but only 34.2% (139 of 406) among housed persons (P < .001). The emm types frequently causing iGAS infections among PEH also caused iGAS infections among housed persons and were too highly clonal to assess transmission risk. Conclusions and Relevance: In this cross-sectional study, the post-COVID-19 pandemic resurgence of iGAS infections occurred among both PEH and housed adults, although the incidence among PEH was 70.7-fold greater. Risk factors, clinical presentations, outcomes, and infecting strains were very different. Improved iGAS protection for PEH, such as vaccines, is needed.

Indexed as

COVID-19Ill-Housed PersonsStreptococcal InfectionsStreptococcus pyogenesAdultCanadaCross-Sectional StudiesFemaleHumansIncidenceMaleMiddle AgedRisk FactorsSARS-CoV-2

Identifiers

PMID41665905
PMCPMC12892144

What OpenQuestion holds

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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.