Evidence map›Paper›PMID 32728438›Full record

ArticleClinical & translational immunology2020

Safety and potential efficacy of cyclooxygenase-2 inhibitors in coronavirus disease 2019.

Sean Wei Xiang Ong, Wilnard Yeong Tze Tan, Yi-Hao Chan, Siew-Wai Fong, Laurent Renia, Lisa Fp Ng, Yee-Sin Leo, David Chien Lye, Barnaby Edward Young

Open access · goldAbstract read
In one paragraph

Article in Clinical & translational immunology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed, 1 pooled it
0.6field-weighted citation impact, top 20% 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

21 citing papers in PubMed, 1 synthesis or guideline pooled it, 30 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Observational
  5. Article
  6. Imrecoxib: Advances in Pharmacology and Therapeutics.Drug design, development and therapy · 2024
    Review
  7. Article
  8. Review
  9. Review
  10. Article
  11. Article
  12. Review
  13. Dipyridamole and adenosinergic pathway in Covid-19: a juice or holy grail.The Egyptian journal of medical human genetics · 2022
    Review
  14. Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Testosterone in COVID-19: An Adversary Bane or Comrade Boon.Frontiers in cellular and infection microbiology · 2021
    Review
  20. 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

9 authors at 4 institutions in 2 countries.

Sean Wei Xiang OngNational Centre for Infectious Diseases Singapore.ORCID https://orcid.org/0000-0002-8570-436X
Wilnard Yeong Tze TanNational Centre for Infectious Diseases Singapore.
Yi-Hao ChanSingapore Immunology Network Agency for Science, Technology and Research Singapore.ORCID https://orcid.org/0000-0003-0329-238X
Siew-Wai FongSingapore Immunology Network Agency for Science, Technology and Research Singapore.
Laurent ReniaSingapore Immunology Network Agency for Science, Technology and Research Singapore.ORCID https://orcid.org/0000-0003-0349-1557
Lisa Fp NgSingapore Immunology Network Agency for Science, Technology and Research Singapore.ORCID https://orcid.org/0000-0003-4071-5222
Yee-Sin LeoNational Centre for Infectious Diseases Singapore.ORCID https://orcid.org/0000-0003-4978-5825
David Chien LyeNational Centre for Infectious Diseases Singapore.ORCID https://orcid.org/0000-0003-0324-0205
Barnaby Edward YoungNational Centre for Infectious Diseases Singapore.ORCID https://orcid.org/0000-0003-1010-2230
Agency for Science, Technology and Research · SGNational University of Singapore · SGTan Tock Seng Hospital · SGNanyang Technological University · SG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesWhile the safety of non-steroidal anti-inflammatory drugs in COVID-19 has been questioned, they may be beneficial given the hyper-inflammatory immune response associated with severe disease. We aimed to assess the safety and potential efficacy of cyclooxygenase-2 (COX-2) selective inhibitors in high-risk patients.

methodsRetrospective study of patients with COVID-19 pneumonia and aged ≥ 50 years who were admitted to hospital. Adverse outcomes analysed included supplemental oxygen use, intensive care unit admission, mechanical ventilation and mortality, with the primary endpoint a composite of any of these. Plasma levels of inflammatory cytokines and chemokines were measured in a subset.

resultsTwenty-two of 168 (13.1%) in the cohort received COX-2 inhibitors [median duration 3 days, interquartile range (IQR) 3-4.25]. Median age was 61 (IQR 55-67.75), 44.6% were female, and 72.6% had at least one comorbidity. A lower proportion of patients receiving COX-2 inhibitors met the primary endpoint: 4 (18.2%) versus 57 (39.0%),

conclusionTreatment with COX-2 inhibitors was not associated with an increase in adverse outcomes. Its potential for therapeutic use as an immune modulator warrants further evaluation in a large randomised controlled trial.

Indexed as

COVID‐19COX‐2 inhibitorsinterleukin‐6SARS‐CoV‐2

Identifiers

PMID32728438
PMCPMC7382954
OpenAlexW3044938555

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.