Evidence map›Paper›PMID 39626643›Full record

ArticleJournal of innate immunity2024

Complex Thrombo-Inflammatory Responses versus Outcomes of Non-COVID-19 Community-Acquired Pneumonia and COVID-19.

Greg Haljan, Terry Lee, Anne McCarthy, Juthaporn Cowan, Jennifer Tsang, Francois Lelouche, Alexis F Turgeon, Patrick Archambault, Francois Lamontagne, Robert Fowler and 16 more

Abstract read
In one paragraph

Article in Journal of innate immunity, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

26 authors.

Greg HaljanDepartment of Medicine, Surrey Memorial Hospital, Surrey, British Columbia, Canada.
Terry LeeCentre for Advancing Health Outcomes St. Paul's Hospital, University of British Columbia, Vancouver, British Columbia, Canada.
Anne McCarthyThe Ottawa Hospital, Ottawa Research Institute, University of Ottawa, Ottawa, Ontario, Canada.
Juthaporn CowanThe Ottawa Hospital, Ottawa Research Institute, University of Ottawa, Ottawa, Ontario, Canada.
Jennifer TsangNiagara Health Knowledge Institute, Niagara Health, St. Catharines, Ontario, Canada.
Francois LeloucheDepartment of Medicine, Institut Universitaire de Cardiologie et de Pneumologie de Québec, Université Laval, Québec, Québec, Canada.
Alexis F TurgeonCHU de Québec-Université Laval Research Center, Population Health and Optimal Health Practices Unit, Trauma-Emergency-Critical Care Medicine, Québec, Québec, Canada.
Patrick ArchambaultDepartment of Family Medicine and Emergency Medicine, Université Laval, Québec, Québec, Canada.
Francois LamontagneUniversity of Sherbrooke, Sherbrooke, Québec, Canada.
Robert FowlerSunnybrook Health Sciences Centre, Toronto, Ontario, Canada.
Jennifer YoonHumber River Hospital, Toronto, Ontario, Canada.
Peter DaleyMemorial University of Newfoundland, St. John's, Newfoundland, Canada.
Matthew P ChengDivision of Infectious Diseases, Department of Medicine, McGill University Health Centre, Montreal, Québec, Canada.
Donald C VinhDivision of Infectious Diseases, Department of Medicine, McGill University Health Centre, Montreal, Québec, Canada.
Todd C LeeDivision of Infectious Diseases, Department of Medicine, McGill University Health Centre, Montreal, Québec, Canada.
Karen C TranDivision of General Internal Medicine, Department of Medicine, Vancouver General Hospital, Vancouver, British Columbia, Canada.
Brent W WinstonDepartments of Critical Care Medicine, Medicine and Biochemistry and Molecular Biology, Foothills Medical Centre, Calgary, Alberta, Canada.
Hyejin Julia KongCentre for Heart Lung Innovation, St. Paul's Hospital, University of British Columbia, Vancouver, British Columbia, Canada.
John H BoydCentre for Heart Lung Innovation, St. Paul's Hospital, University of British Columbia, Vancouver, British Columbia, Canada.
Keith R WalleyCentre for Heart Lung Innovation, St. Paul's Hospital, University of British Columbia, Vancouver, British Columbia, Canada.
Allison McGeerMt. Sinai Hospital, Toronto, Ontario, Canada.
David M MasloveDepartment of Critical Care, Kingston General Hospital, Queen's University, Kingston, Ontario, Canada.
John C MarshallDepartment of Surgery, St. Michael's Hospital, Toronto, Ontario, Canada.
Joel SingerCentre for Advancing Health Outcomes St. Paul's Hospital, University of British Columbia, Vancouver, British Columbia, Canada.
Fagun JainBlack Tusk Research Group, Vancouver, British Columbia, Canada.
James A RussellCentre for Heart Lung Innovation, St. Paul's Hospital, University of British Columbia, Vancouver, British Columbia, Canada.

Funding

CIHR
6 · The paper itself

Abstract

introductionThe thrombo-inflammatory response and outcomes of community-acquired pneumonia (CAP) due to various organisms (non-COVID-19 CAP) versus CAP due to a single virus, SARS-CoV-2 (i.e., COVID-19) may differ.

methodsAdults hospitalized with non-COVID-19 CAP (December 1, 2021-June 15, 2023) or COVID-19 (March 2, 2020-June 15, 2023) in Canada. We compared non-COVID-19 CAP and COVID-19 baseline, thrombo-inflammatory response, and mortality. We measured plasma cytokine and coagulation factor levels in a sample of patients, did hierarchical clustering, and compared cytokine and coagulation factor levels.

resultsIn 2,485 patients (non-COVID-19 CAP, n = 719; COVID-19 patients, n = 2,157), non-COVID-19 CAP patients had significantly lower 28-day mortality (CAP vs. COVID-19 waves 1 and 2; 10% vs. 18% and 16%, respectively), intensive care unit admission (CAP vs. all waves; 15% vs. 39%, 37%, 33%, and 24%, respectively), invasive ventilation (CAP vs. waves 1, 2, and 3 patients; 11% vs. 25%, 20%, and 16%), vasopressor use (CAP 12% vs. 23%, 21%, and 18%), and renal replacement therapy use (CAP 3% vs. Omicron 7%). Complexity of hierarchical clustering aligned directly with mortality: COVID-19 wave 1 and 2 patients had six clusters at admission and higher mortality than non-COVID-19 CAP and Omicron that had three clusters at admission. Pooling all COVID-19 waves increased complexity with seven clusters on admission.

conclusionComplex thrombo-inflammatory responses aligned with mortality of CAP. At a fundamental level, the human thrombo-inflammatory response to a brand new virus was "confused" whereas humans had eons of time to develop a more concise efficient thrombo-inflammatory host response to CAP.

Indexed as

Community-Acquired InfectionsCOVID-19SARS-CoV-2AdultAgedAged, 80 and overCanadaCytokinesFemaleHospitalizationHumansMaleMiddle AgedPneumoniaPneumonia, ViralThromboinflammationCytokinesCoagulation factorsCommunity-acquired pneumoniaCOVID-19CytokinesHierarchical clusteringMortality

Identifiers

PMID39626643
PMCPMC11614459

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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 OpenQuestion graph.