Evidence map›Paper›PMID 21394629›Full record

ArticleIntensive care medicine2011

Early rise in circulating endothelial protein C receptor correlates with poor outcome in severe sepsis.

Christophe Guitton, Nathalie Gérard, Véronique Sébille, Cédric Bretonnière, Olivier Zambon, Daniel Villers, Béatrice Charreau

Open access · greenAbstract read
In one paragraph

Article in Intensive care medicine, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

12 citing papers in PubMed, 27 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Signaling pathways and intervention therapies in sepsis.Signal transduction and targeted therapy · 2021
    Review
  6. Article
  7. Review
  8. The coagulopathy of acute sepsis.Current opinion in anaesthesiology · 2015
    Review
  9. Article
  10. Article
  11. Article
  12. 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

7 authors at 3 institutions in 1 country.

Christophe GuittonINSERM UMR643, Institut de Transplantation et de Recherche en Transplantation, ITERT, CHU Nantes, 44000 Nantes, France. christophe.guitton@chu-nantes.fr
Nathalie Gérard
Véronique Sébille
Cédric Bretonnière
Olivier Zambon
Daniel Villers
Béatrice Charreau
Centre d'Investigation Clinique de Nantes · FRInserm · FRInstitut de Transplantation Urologie en Nephrologie · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThe endothelial protein C receptor (EPCR) negatively regulates the coagulopathy and inflammatory response in sepsis. Mechanisms controlling the expression of cell-bound and circulating soluble EPCR (sEPCR) are still unclear. Moreover, the clinical impact of EPCR shedding and its potential value to predict sepsis progression and outcome remain to be established.

methodsWe investigated the time course of plasma sEPCR over the 5 first days (D) of severe sepsis in 40 patients.

resultsNo significant difference was observed when comparing sEPCR at admission (D1) to healthy volunteers and to patients with vasculitis. We report that the kinetics profile of plasma sEPCR in patients was almost stable at the onset of sepsis with no change from D1 to D4 and then a significant decrease at D5. This pattern of release was consistently observed whatever the level of sEPCR at D1. Characteristics of patients or of infections (except Gram negative) had no or little critical influence on the sEPCR profile. However, we found that sEPCR kinetics was clearly associated with patient's outcome (D28 survival). We demonstrate that a significant but moderate (<15% of basal level) and transient increase in sEPCR level at D2 is associated with poor outcome at D28.

conclusionSevere sepsis, at the onset, only triggers moderate quantitative changes in plasma sEPCR levels. Our findings suggest that in severe sepsis, an early (at D2), transient but significant increase in circulating sEPCR may be detrimental suggesting that sEPCR could provide an early biological marker of sepsis outcome.

Indexed as

Outcome Assessment, Health CareSeverity of Illness IndexAdultAgedAntigens, CDEndothelial Protein C ReceptorFemaleFranceHumansIntensive Care UnitsMaleMiddle AgedReceptors, Cell SurfaceSepsisVasculitisAntigens, CDEndothelial Protein C ReceptorPROCR protein, humanReceptors, Cell Surface

Identifiers

PMID21394629
PMCPMC3529933
OpenAlexW2111507425

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.