Evidence map›Paper›PMID 32881304›Full record

ArticleJournal of thrombosis and haemostasis : JTH2020

Coagulation biomarkers are independent predictors of increased oxygen requirements in COVID-19.

Antoine Rauch, Julien Labreuche, Fanny Lassalle, Julien Goutay, Morgan Caplan, Leslie Charbonnier, Aurelien Rohn, Emmanuelle Jeanpierre, Annabelle Dupont, Alain Duhamel and 7 more

Open access · bronzeAbstract read
In one paragraph

Article in Journal of thrombosis and haemostasis : JTH, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers, 6 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed, 6 pooled it
2.1field-weighted citation impact, top 7% 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

49 citing papers in PubMed, 6 syntheses or guidelines pooled it, 88 citations in OpenAlex.

  1. Endotheliopathy in Acute COVID-19 and Long COVID.International journal of molecular sciences · 2023
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  4. Endotheliopathy marked by high von Willebrand factor (vWF) antigen in COVID-19 is associated with poor outcome: a systematic review and meta-analysis.International journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases · 2022
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  13. Prognostic markers in patients with COVID-19 requiring intensive care support.Journal of Taibah University Medical Sciences · 2023
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

17 authors at 4 institutions in 1 country.

Antoine RauchDepartment of Hematology and Transfusion, Pôle de Biologie Pathologie Génétique, Institut Pasteur de Lille, UMR1011-EGID, Univ. Lille, Inserm, CHU Lille, Lille, France.ORCID 0000-0002-1182-4131
Julien LabreucheULR 2694 - METRICS: Évaluation des technologies de santé et des pratiques médicales, Univ. Lille, CHU Lille, Lille, France.
Fanny LassalleDepartment of Hematology and Transfusion, Pôle de Biologie Pathologie Génétique, Institut Pasteur de Lille, UMR1011-EGID, Univ. Lille, Inserm, CHU Lille, Lille, France.ORCID 0000-0003-0494-823X
Julien GoutayIntensive Care Department, Pôle de Réanimation, Centre Hospitalier Universitaire Lille, Lille, France.
Morgan CaplanIntensive Care Department, Pôle de Réanimation, Centre Hospitalier Universitaire Lille, Lille, France.
Leslie CharbonnierEmergency Department, Pôle de l'Urgence, Centre Hospitalier Universitaire Lille, Lille, France.
Aurelien RohnEmergency Department, Pôle de l'Urgence, Centre Hospitalier Universitaire Lille, Lille, France.
Emmanuelle JeanpierreDepartment of Hematology and Transfusion, Pôle de Biologie Pathologie Génétique, Institut Pasteur de Lille, UMR1011-EGID, Univ. Lille, Inserm, CHU Lille, Lille, France.
Annabelle DupontDepartment of Hematology and Transfusion, Pôle de Biologie Pathologie Génétique, Institut Pasteur de Lille, UMR1011-EGID, Univ. Lille, Inserm, CHU Lille, Lille, France.
Alain DuhamelULR 2694 - METRICS: Évaluation des technologies de santé et des pratiques médicales, Univ. Lille, CHU Lille, Lille, France.
Karine FaureDepartment of Infectious Diseases, Institut Pasteur de Lille, UMR1019-CIIL, Univ. Lille, Inserm, CHU Lille, Lille, France.
Marc LambertDepartment of Internal Medicine, INSERM U 1167, Institut Pasteur, Univ. Lille, Inserm, CHU Lille, Lille, France.
Eric KipnisSurgical Critical Care, Department of Anesthesiology and Critical Care, Institut Pasteur de Lille, U1019 - UMR 9017 - CIIL - Center for Infection and Immunity of Lille, Univ. Lille, CNRS, Inserm, CHU Lille, Lille, France.
Delphine GarrigueEmergency Department, Pôle de l'Urgence, Centre Hospitalier Universitaire Lille, Lille, France.
Peter J LentingUMR_1176, Inserm, Université Paris-Saclay, Le Kremlin-Bicêtre, France.ORCID 0000-0002-7937-3429
Julien PoissyPôle de Réanimation, CNRS, UMR 8576 - UGSF - Unité de Glycobiologie Structurale et Fonctionnelle, Univ. Lille, Inserm U1285, CHU Lille, Lille, France.
Sophie SusenDepartment of Hematology and Transfusion, Pôle de Biologie Pathologie Génétique, Institut Pasteur de Lille, UMR1011-EGID, Univ. Lille, Inserm, CHU Lille, Lille, France.ORCID 0000-0001-5953-163X
Inserm · FRCentre Hospitalier Universitaire de Lille · FRCentre National de la Recherche Scientifique · FRUniversité de Lille · FR

Funding

Agence Nationale de la Recherche I-SITE ULNE / ANR-16-IDEX-0004 ULNE
6 · The paper itself

Abstract

backgroundHypercoagulability seems to contribute to SARS-CoV-2 pneumonia pathogenesis. However, age and metabolic syndrome are potential confounders when assessing the value of coagulation biomarkers' prediction of COVID-19 outcomes. We assessed whether coagulation biomarkers, including factor VIII (FVIII) and von Willebrand factor (VWF) levels, measured at time of admission, were predictive of COVID-19 adverse outcomes irrespective of age and major comorbidities associated with metabolic syndrome.

methodsBlood was sampled at admission in 243 adult COVID-19 patients for analysis of coagulation biomarkers including FVIII and VWF on platelet-poor plasma. The association between baseline C-reactive protein (CRP), activated partial thromboplastin time ratio, prothrombin time ratio, D-dimers, fibrinogen, FVIII, VWF antigen (VWF:Ag), and FVIII/VWF:Ag ratio levels and adverse outcomes (increased oxygen requirements, thrombosis, and death at day 30) was assessed by regression analysis after adjustment on age, sex, body mass index (BMI), diabetes, and hypertension.

resultsIn univariable regression analysis increased CRP (subdistribution hazard ratio [SHR], 1.68; 95% confidence interval [CI], 1.26-2.23), increased fibrinogen (SHR, 1.32; 95% CI, 1.04-1.68), and decreased FVIII/VWF:Ag ratio (SHR, 0.70; 95% CI, 0.52-0.96) levels at admission were significantly associated with the risk of increased oxygen requirement during follow-up. Leucocytes (SHR, 1.36; 95% CI, 1.04-1.76), platelets (SHR,1.71; 95% CI, 1.11-2.62), D-dimers (SHR, 2.48; 95% CI, 1.66-3.78), and FVIII (SHR, 1.78; 95% CI, 1.17-2.68) were associated with early onset of thrombosis after admission. After adjustment for age, sex, BMI, hypertension, and diabetes, these associations were not modified.

conclusionCoagulation biomarkers are early and independent predictors of increased oxygen requirement in COVID-19 patients.

Indexed as

Blood CoagulationOxygen Inhalation TherapyAge FactorsAnticoagulantsBiomarkersComorbidityCOVID-19Factor VIIIFemaleFranceHumansMaleMiddle AgedPatient AdmissionPrevalenceProspective StudiesAnticoagulantsBiomarkersF8 protein, humanFactor VIIIvon Willebrand Factorbody mass indexfactor VIIIoxygenSARS-CoV2von Willebrand factor

Identifiers

PMID32881304
PMCPMC7461161
OpenAlexW3049307290

What OpenQuestion holds

Textmetadata
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.