Evidence map›Paper›PMID 35570298›Full record

ArticleVirology journal2022

NSAID use and clinical outcomes in COVID-19 patients: a 38-center retrospective cohort study.

Justin T Reese, Ben Coleman, Lauren Chan, Hannah Blau, Tiffany J Callahan, Luca Cappelletti, Tommaso Fontana, Katie R Bradwell, Nomi L Harris, Elena Casiraghi and 13 more

Open access · goldAbstract readMulticenter Study
In one paragraph

Article in Virology journal, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 2 pooled it
4.5field-weighted citation impact, top 4% of its field
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

17 citing papers in PubMed, 2 syntheses or guidelines pooled it, 31 citations in OpenAlex.

  1. Pooled it
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  6. Article
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  9. KG-Hub-building and exchanging biological knowledge graphs.Bioinformatics (Oxford, England) · 2023
    Article
  10. Article
  11. Review
  12. Article
  13. Effect of the Duration of NSAID Use on COVID-19.Medicina (Kaunas, Lithuania) · 2022
    Observational
  14. Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

23 authors at 12 institutions in 3 countries.

Justin T ReeseEnvironmental Genomics and Systems Biology Division, Lawrence Berkeley National Laboratory, Berkeley, CA, USA. justin.reese@lbl.gov.
Ben ColemanThe Jackson Laboratory for Genomic Medicine, Farmington, CT, USA.
Lauren ChanTranslational and Integrative Sciences Center, Oregon State University, Corvallis, OR, USA.
Hannah BlauThe Jackson Laboratory for Genomic Medicine, Farmington, CT, USA.
Tiffany J CallahanComputational Bioscience, University of Colorado Anschutz Medical Campus, Boulder, CO, USA.
Luca CappellettiAnacletoLab, Dipartimento Di Informatica, Università Degli Studi Di Milano, Milan, Italy.
Tommaso FontanaAnacletoLab, Dipartimento Di Informatica, Università Degli Studi Di Milano, Milan, Italy.
Katie R BradwellPalantir Technologies, Denver, CO, USA.
Nomi L HarrisEnvironmental Genomics and Systems Biology Division, Lawrence Berkeley National Laboratory, Berkeley, CA, USA.
Elena CasiraghiAnacletoLab, Dipartimento Di Informatica, Università Degli Studi Di Milano, Milan, Italy.
Giorgio ValentiniAnacletoLab, Dipartimento Di Informatica, Università Degli Studi Di Milano, Milan, Italy.
Guy KarlebachThe Jackson Laboratory for Genomic Medicine, Farmington, CT, USA.
Rachel DeerUniversity of Texas Medical Branch, Galveston, TX, USA.
Julie A McMurryCenter for Health AI, University of Colorado Anschutz Medical Campus, Aurora, CO, USA.
Melissa A HaendelCenter for Health AI, University of Colorado Anschutz Medical Campus, Aurora, CO, USA.
Christopher G ChuteSchools of Medicine, Public Health, and Nursing, Johns Hopkins University, Baltimore, MD, USA.
Emily PfaffNorth Carolina Translational and Clinical Sciences Institute (NC TraCS), University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
Richard MoffittDepartment of Biomedical Informatics, Stony Brook University, Stony Brook, NY, USA.
Heidi SprattUniversity of Texas Medical Branch, Galveston, TX, USA.
Jasvinder A SinghUniversity of Alabama at Birmingham, Birmingham, AL, USA.
Christopher J MungallEnvironmental Genomics and Systems Biology Division, Lawrence Berkeley National Laboratory, Berkeley, CA, USA.
Andrew E WilliamsTufts Medical Center Clinical and Translational Science Institute, Tufts Medical Center, Boston, MA, USA.
Peter N RobinsonThe Jackson Laboratory for Genomic Medicine, Farmington, CT, USA. Peter.Robinson@jax.org.ORCID 0000-0002-0736-9199
University of Milan · ITLawrence Berkeley National Laboratory · USUniversity of Colorado Anschutz Medical Campus · USJackson Laboratory · USThe University of Texas Medical Branch at Galveston · USUniversity of Connecticut · USBoston University · USJohns Hopkins University · USOregon State University · USStony Brook University · USUniversity of Alabama at Birmingham · USUniversity of North Carolina at Chapel Hill · US

Funding

Vanderbilt Institute for Clinical and Translational Research (VICTR) -Identifying correlates of functional immunity in SARS-CoV-2 convalescent plasmaUL1TR002243 · NCATS · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Paul A. Harris, Wesley H Self · 2017 to 2026
$130.7M
Transform Dissemination and Implementation Science in CTSA ProgramsUL1TR002319 · NCATS · UNIVERSITY OF WASHINGTON · PI John K. Amory · 2017 to 2026
$100.0M
Clinical and Translational Science AwardUL1TR001873 · NCATS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI REILLY, MUREDACH P · 2016 to 2025
$99.0M
WU INSTITUTE OF CLINICAL AND TRANSLATIONAL SCIENCESUL1TR002345 · NCATS · WASHINGTON UNIVERSITY · PI William G. Powderly · 2017 to 2026
$97.8M
Southern California Clinical and Translational Science InstituteUL1TR001855 · NCATS · UNIVERSITY OF SOUTHERN CALIFORNIA · PI Thomas A Buchanan, Michele D. Kipke · 2016 to 2026
$81.3M
West Virginia IDEA-CTRU54GM104942 · NIGMS · WEST VIRGINIA UNIVERSITY · PI Laura F. Gibson · 2012 to 2026
$81.0M
Mayo Clinic Center for Clinical and Translational Science (CCaTS UL1 Supplement - Dr. Timothy Curry)UL1TR002377 · NCATS · MAYO CLINIC ROCHESTER · PI VESNA D GAROVIC · 2017 to 2026
$78.4M
Oregon Clinical and Translational Research Institute - The National COVID Cohort Collaborative (N3C)UL1TR002369 · NCATS · OREGON HEALTH & SCIENCE UNIVERSITY · PI Cynthia D Morris, Christopher G. Slatore · 2017 to 2026
$78.4M
University of Wisconsin Institute for Clinical and Translational ResearchUL1TR002373 · NCATS · UNIVERSITY OF WISCONSIN-MADISON · PI ELIZABETH S BURNSIDE, Allan R. Brasier · 2017 to 2026
$75.9M
The Institute for Translational MedicineUL1TR002389 · NCATS · UNIVERSITY OF CHICAGO · PI Joshua J Jacobs, DAVID O MELTZER · 2017 to 2026
$71.6M
Tracking & Evaluation CoreU54GM104940 · NIGMS · LSU PENNINGTON BIOMEDICAL RESEARCH CTR · PI JUDD E SHELLITO · 2012 to 2026
$69.1M
Tracking and Evaluation CoreU54GM104938 · NIGMS · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI TIMOTHY M VANWAGONER · 2013 to 2026
$68.2M
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6 · The paper itself

Abstract

backgroundNon-steroidal anti-inflammatory drugs (NSAIDs) are commonly used to reduce pain, fever, and inflammation but have been associated with complications in community-acquired pneumonia. Observations shortly after the start of the COVID-19 pandemic in 2020 suggested that ibuprofen was associated with an increased risk of adverse events in COVID-19 patients, but subsequent observational studies failed to demonstrate increased risk and in one case showed reduced risk associated with NSAID use.

methodsA 38-center retrospective cohort study was performed that leveraged the harmonized, high-granularity electronic health record data of the National COVID Cohort Collaborative. A propensity-matched cohort of 19,746 COVID-19 inpatients was constructed by matching cases (treated with NSAIDs at the time of admission) and 19,746 controls (not treated) from 857,061 patients with COVID-19 available for analysis. The primary outcome of interest was COVID-19 severity in hospitalized patients, which was classified as: moderate, severe, or mortality/hospice. Secondary outcomes were acute kidney injury (AKI), extracorporeal membrane oxygenation (ECMO), invasive ventilation, and all-cause mortality at any time following COVID-19 diagnosis.

resultsLogistic regression showed that NSAID use was not associated with increased COVID-19 severity (OR: 0.57 95% CI: 0.53-0.61). Analysis of secondary outcomes using logistic regression showed that NSAID use was not associated with increased risk of all-cause mortality (OR 0.51 95% CI: 0.47-0.56), invasive ventilation (OR: 0.59 95% CI: 0.55-0.64), AKI (OR: 0.67 95% CI: 0.63-0.72), or ECMO (OR: 0.51 95% CI: 0.36-0.7). In contrast, the odds ratios indicate reduced risk of these outcomes, but our quantitative bias analysis showed E-values of between 1.9 and 3.3 for these associations, indicating that comparatively weak or moderate confounder associations could explain away the observed associations.

conclusionsStudy interpretation is limited by the observational design. Recording of NSAID use may have been incomplete. Our study demonstrates that NSAID use is not associated with increased COVID-19 severity, all-cause mortality, invasive ventilation, AKI, or ECMO in COVID-19 inpatients. A conservative interpretation in light of the quantitative bias analysis is that there is no evidence that NSAID use is associated with risk of increased severity or the other measured outcomes. Our results confirm and extend analogous findings in previous observational studies using a large cohort of patients drawn from 38 centers in a nationally representative multicenter database.

Indexed as

Acute Kidney InjuryCOVID-19Anti-Inflammatory Agents, Non-SteroidalCohort StudiesCOVID-19 TestingHumansPandemicsRetrospective StudiesAnti-Inflammatory Agents, Non-SteroidalCOVID-19Cyclooxygenase inhibitorsNSAIDsObservational study

Identifiers

PMID35570298
PMCPMC9107579
OpenAlexW4280531656

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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.