Evidence map›Paper›PMID 40753103›Full record

ArticleScientific reports2025

Validation of the age, neutrophil to lymphocyte ratio, C reactive protein score on 28 day mortality in the National COVID cohort collaborative.

Benjamin J Sines, Kunal K Jakharia, Chih-Huan Lu, Leslie Appleton, Colleen Rice, William A Fischer, Shannon M Wallet, G Stephen DeCherney, Jason R Mock, M Bradley Drummond

Abstract readMulticenter StudyValidation Study
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. 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

10 authors.

Benjamin J SinesDivision of Pulmonary Diseases and Critical Care Medicine, Department of Medicine, University of North Carolina Chapel Hill, 4th Floor Bioinformatics Bldg 130 Mason Farm Road, Chapel Hill, NC, 27599, USA. Benjamin.sines@unchealth.unc.edu.
Kunal K JakhariaDivision of Pulmonary Diseases and Critical Care Medicine, Department of Medicine, University of North Carolina Chapel Hill, 4th Floor Bioinformatics Bldg 130 Mason Farm Road, Chapel Hill, NC, 27599, USA.
Chih-Huan LuDepartment of Internal Medicine, University of North Carolina Chapel Hill, Chapel Hill, NC, USA.
Leslie AppletonDepartment of Internal Medicine, University of North Carolina Chapel Hill, Chapel Hill, NC, USA.
Colleen RiceDivision of Pulmonary Diseases and Critical Care Medicine, Department of Medicine, University of North Carolina Chapel Hill, 4th Floor Bioinformatics Bldg 130 Mason Farm Road, Chapel Hill, NC, 27599, USA.
William A FischerDivision of Pulmonary Diseases and Critical Care Medicine, Department of Medicine, University of North Carolina Chapel Hill, 4th Floor Bioinformatics Bldg 130 Mason Farm Road, Chapel Hill, NC, 27599, USA.
Shannon M WalletDepartment of Oral Biology, College of Dentistry, University of Florida, Gainesville, USA.
G Stephen DeCherneyDivision of Endocrinology and Metabolism, University of North Carolina Chapel Hill, Chapel Hill, NC, USA.
Jason R MockDivision of Pulmonary Diseases and Critical Care Medicine, Department of Medicine, University of North Carolina Chapel Hill, 4th Floor Bioinformatics Bldg 130 Mason Farm Road, Chapel Hill, NC, 27599, USA.
M Bradley DrummondDivision of Pulmonary Diseases and Critical Care Medicine, Department of Medicine, University of North Carolina Chapel Hill, 4th Floor Bioinformatics Bldg 130 Mason Farm Road, Chapel Hill, NC, 27599, USA.

Funding

NIH HHS 5T32HL007106-45
6 · The paper itself

Abstract

Identifying patients at high mortality risk can improve outcomes in SARS-CoV-2 pneumonia (COVID-19). We validate a prognostic model for mortality in patients hospitalized with COVID-19 receiving dexamethasone using a retrospective multi-centered study. This is a retrospective cohort study using the National COVID Cohort Collaborative (NC3) including 9,708 adult patients admitted for COVID-19 who received dexamethasone within 24 h of admission and remained hospitalized for 72 h. Previous work from a single-center cohort informed selection of prognostic variables including Age, day 3 neutrophil-lymphocyte Ratio, and day 3 C-reactive protein level (ARC Score). Variables from the development cohort were analyzed in a training cohort, and the resulting model was tested in a validation cohort. Age and day 3 measures of the neutrophil-lymphocyte ratio and C-reactive protein level were included in a logistic regression model to predict 28-day mortality. The 28-day mortality in this patient population was 15.4%. The area under the curve for the ARC model was 0.77 (95% confidence interval, 0.74-0.79). The Age, neutrophil-lymphocyte Ratio, and C-reactive protein (ARC) score identifies COVID-19 patients with a high risk of mortality within 28 days of hospitalization using clinical information on day 3 of hospitalization. ARC scores perform well across all variants of concern.

Indexed as

COVID-19C-Reactive ProteinLymphocytesNeutrophilsAdultAgedAged, 80 and overAge FactorsCOVID-19 Drug TreatmentDexamethasoneFemaleHospitalizationHumansMaleMiddle AgedPrognosisC-Reactive ProteinDexamethasoneAcute respiratory distress syndromeCOVID-19Critical careSARS-CoV-2Viral pneumonia

Identifiers

PMID40753103
PMCPMC12318015

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.