Evidence map›Paper›PMID 37138790›Full record

ArticleResearch and practice in thrombosis and haemostasis2023

C-reactive protein and D-dimer in cerebral vein thrombosis: Relation to clinical and imaging characteristics as well as outcomes in a French cohort study.

Paul Billoir, Virginie Siguret, Elisabeth Masson Fron, Ludovic Drouet, Isabelle Crassard, Raphaël Marlu, Marianne Barbieux-Guillot, Pierre-Emmanuel Morange, Emmanuelle Robinet, Catherine Metzger and 35 more

Open access · goldAbstract read
In one paragraph

Article in Research and practice in thrombosis and haemostasis, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
2.1field-weighted citation impact, top 13% 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

8 citing papers in PubMed, 1 synthesis or guideline pooled it, 10 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Observational
  8. 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

45 authors at 20 institutions in 1 country.

Paul BilloirUniv Rouen Normandie, INSERM U1096, Department of Vascular Hemostasis Unit, CHU Rouen, Rouen, France.
Virginie SiguretDepartment of Biological Hematology, Lariboisière University Hospital, Université Paris Cité, Paris, France.
Elisabeth Masson FronDepartment of Biological Hematology, Lariboisière University Hospital, Université Paris Cité, Paris, France.
Ludovic DrouetDepartment of Biological Hematology, Lariboisière University Hospital, Université Paris Cité, Paris, France.
Isabelle CrassardDepartment of Neurology, Lariboisière University Hospital, Université Paris Cité, Paris, France.
Raphaël MarluDepartment of Biological Hematology, Grenoble University Hospital, Grenoble, France.
Marianne Barbieux-GuillotDepartment of Neurology, Grenoble University Hospital, Grenoble, France.
Pierre-Emmanuel MorangeDepartment of Biological Hematology, Marseille University Hospital, Marseille, France.
Emmanuelle RobinetDepartment of Neurology, Marseille University Hospital, Marseille, France.
Catherine MetzgerDepartment of Biological Hematology, Strasbourg University Hospital, Strasbourg, France.
Valérie WolffDepartment of Neurology, Strasbourg University Hospital, Strasbourg, France.
Elisabeth André-KerneisDepartment of Biological Hematology, Meaux Hospital, Meaux, France.
Frédéric KlapczynskiDepartment of Neurology, Meaux Hospital, Meaux, France.
Brigitte Martin-BastenaireDepartment of Biological Hematology, Versailles Hospital, Versailles, France.
Fernando PicoDepartment of Neurology, Versailles Hospital, Versailles, France.
Fanny MenardDepartment of Biological Hematology, Bayonne Hospital, Bayonne, France.
Emmanuel EllieDepartment of Neurology, Bayonne Hospital, Bayonne, France.
Geneviève FreyburgerDepartment of Biological Hematology, Bordeaux University Hospital, Bordeaux, France.
François RouanetDepartment of Neurology, Bordeaux University Hospital, Bordeaux, France.
Hong-An AllanoDepartment of Biological Hematology, La Rochelle Hospital, La Rochelle, France.
Gaëlle GodenècheDepartment of Neurology, La Rochelle Hospital, La Rochelle, France.
Guillaume MoureyDepartment of Biological Hematology, Besançon University Hospital, Besançon, France.
Thierry MoulinDepartment of Neurology, Besançon University Hospital, Besançon, France.
Micheline BerruyerDepartment of Biological Hematology, Lyon University Hospital, Lyon, France.
Laurent DerexDepartment of Neurology, Lyon University Hospital, Lyon, France.
Catherine TrichetDepartment of Biological Hematology, Argenteuil Hospital, Argenteuil, France.
Gwénaëlle RunavotDepartment of Neurology, Argenteuil Hospital, Argenteuil, France.
Agnès Le QuerrecDepartment of Biological Hematology, Caen University Hospital, Caen, France.
Fausto ViaderDepartment of Neurology, Caen University Hospital, Caen, France.
Sophie Cluet-DennetiereDepartment of Biological Hematology, Compiègne Hospital, Compiègne, France.
Thomas Tarek HuseinDepartment of Neurology, Compiègne Hospital, Compiègne, France.
Magali DonnardDepartment of Biological Hematology, Limoges University Hospital, Limoges, France.
Francisco Macian-MontoroDepartment of Neurology, Limoges University Hospital, Limoges, France.
Catherine TernisienDepartment of Biological Hematology, Nantes University Hospital, Nantes, France.
Benoît GuillonDepartment of Neurology, Nantes University Hospital, Nantes, France.
Sophie LaplancheDepartment of Biological Hematology, Saint Joseph Hospital, Paris, France.
Mathieu ZuberDepartment of Neurology, Saint Joseph Hospital, Paris, France.
Jean-Yves PeltierDepartment of Biological Hematology, Poissy Hospital, Poissy, France.
Philippe TassanDepartment of Neurology, Poissy Hospital, Poissy, France.
Bertrand RousselDepartment of Biological Hematology, Amiens university Hospital, Amiens, France.
Sandrine CanapleDepartment of Neurology, Amiens university Hospital, Amiens, France.
Emilie ScavazzaDepartment of Biological Hematology, Perpignan Hospital, Perpignan, France.
Nicolas GaillardDepartment of Neurology, Perpignan Hospital, Perpignan, France.
Aude Triquenot BaganDepartment of Neurology, CHU Rouen, Rouen, France.
Véronique Le Cam DuchezUniv Rouen Normandie, INSERM U1096, Department of Vascular Hemostasis Unit, CHU Rouen, Rouen, France.
Université Paris Cité · FRAssistance Publique Hôpitaux de Marseille · FRCentre Hospitalier Compiègne-Noyon · FRCentre Hospitalier de la Côte Basque · FRCentre Hospitalier de La Rochelle · FRCentre Hospitalier de Perpignan · FRCentre Hospitalier de Versailles · FRCentre Hospitalier Intercommunal de Poissy · FRCentre Hospitalier Universitaire Amiens-Picardie · FRCentre Hospitalier Universitaire de Besançon · FRCentre Hospitalier Universitaire de Caen Normandie · FRCentre Hospitalier Universitaire de Grenoble · FRCentre Hospitalier Universitaire de Nantes · FRCentre Hospitalier Victor Dupouy · FRHôpital Paris Saint-Joseph · FRHôpital Universitaire Dupuytren · FRInserm · FRUniversité de Bordeaux · FRCentre Hospitalier Universitaire de Rouen · FRHôpital de la Croix-Rousse · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Cerebral venous sinus thrombosis (CVST) is a rare disease with highly variable clinical presentation and outcomes. Clinical studies suggest a role of inflammation and coagulation in CVST outcomes. The aim of this study was to investigate the association of inflammation and hypercoagulability biomarkers with CVST clinical manifestations and prognosis. Methods: This prospective multicenter study was conducted from July 2011 to September 2016. Consecutive patients referred to 21 French stroke units and who had a diagnosis of symptomatic CVST were included. High-sensitivity C-reactive protein (hs-CRP), neutrophil-to-lymphocyte ratio (NLR), D-dimer, and thrombin generation using calibrated automated thrombogram system were measured at different time points until 1 month after anticoagulant therapy discontinuation. Results: Two hundred thirty-one patients were included. Eight patients died, of whom 5 during hospitalization. The day 0 hs-CRP levels, NLR, and D-dimer were higher in patients with initial consciousness disturbance than in those without (hs-CRP: 10.2 mg/L [3.6-25.5] vs 23.7 mg/L [4.8-60.0], respectively; NLR: 3.51 [2.15-5.88] vs 4.78 [3.10-9.59], respectively; D-dimer: 950 μg/L [520-2075] vs 1220 μg/L [950-2445], respectively). Patients with ischemic parenchymal lesions (n = 31) had a higher endogenous thrombin potential Conclusion: Two widely available biomarkers measured upon admission, especially hs-CRP, could help predict bad prognosis in CVST in addition to patient characteristics. These results need to be validated in other cohorts.

Indexed as

cerebral venous sinus thrombosisD-dimerhigh-sensitivity C-reactive proteinthrombin generation assay

Identifiers

PMID37138790
PMCPMC10149398
OpenAlexW4361212009

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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.