Evidence map›Paper›PMID 28455780›Full record

ArticleEuropean journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology2017

Increase of circulating endocan over sepsis follow-up is associated with progression into organ dysfunction.

A Ioakeimidou, E Pagalou, M Kontogiorgi, E Antoniadou, K Kaziani, K Psaroulis, E J Giamarellos-Bourboulis, A Prekates, N Antonakos, P Lassale and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 1 pooled it
2.5field-weighted citation impact, top 11% 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

20 citing papers in PubMed, 1 synthesis or guideline pooled it, 38 citations in OpenAlex.

  1. Pooled it
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  15. Role of the extracellular matrix in the genesis of ventilator-induced lung injury.Medizinische Klinik, Intensivmedizin und Notfallmedizin · 2018
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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

12 authors at 4 institutions in 2 countries.

A IoakeimidouIntensive Care Unit, Korinthos General Hospital, Korinthos, Greece.
E PagalouIntensive Care Unit, Korgialeneion Benakeion General Hospital, Athens, Greece.
M Kontogiorgi2nd Department of Critical Care Medicine, National and Kapodistrian University of Athens, Medical School, Athens, Greece.
E AntoniadouIntensive Care Unit, "G. Gennimatas" General Hospital, Thessaloniki, Greece.
K Kaziani3rd Department of Internal Medicine, National and Kapodistrian University of Athens, Medical School, Athens, Greece.
K PsaroulisIntensive Care Unit, "Aghios Pavlos" General Hospital, Thessaloniki, Greece.
E J Giamarellos-Bourboulis4th Department of Internal Medicine, National and Kapodistrian University of Athens, Medical School, Athens, Greece. egiamarel@med.uoa.gr.ORCID http://orcid.org/0000-0003-4713-3911
A PrekatesIntensive Care Unit, Tzaneion General Hospital, Piraeus, Greece.
N Antonakos4th Department of Internal Medicine, National and Kapodistrian University of Athens, Medical School, Athens, Greece.
P LassaleINSERM U1019E13, Pasteur Institute of Lille, Lille, France.
C GogosDepartment of Internal Medicine, University of Patras, Medical School, Patras, Greece.
Hellenic Sepsis Study Group
National and Kapodistrian University of Athens · GRInserm · FRKAT General Hospital of Attica · GRUniversity of Patras · GR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

How circulating inflammatory mediators change upon sepsis progression has not been studied. We studied the follow-up changes of circulating vasoactive peptides and cytokines until the improvement or the worsening of a patient and progression into specific organ dysfunctions. In a prospective study, concentrations of tumor necrosis factor-alpha (TNFα), interleukin (IL)-6, IL-8, IL-10, interferon-gamma (IFNγ), endocan and angiopoietin-2 (Ang-2) were measured in serum by an enzyme immunoassay in 175 patients at baseline; this was repeated within 24 h upon progression into new organ dysfunction (n = 141) or improvement (n = 34). Endocan and Ang-2 were the only parameters that were significantly increased among patients who worsened. Any increase of endocan was associated with worsening with odds ratio 16.65 (p < 0.0001). This increase was independently associated with progression into acute respiratory distress syndrome (ARDS) as shown after logistic regression analysis (odds ratio 2.91, p: 0.002). Changes of circulating cytokines do not mediate worsening of the critically ill patients. Instead endocan and Ang2 are increased and this may be interpreted as a key-playing role in the pathogenesis of ARDS and septic shock. Any increase of endocan is a surrogate of worsening of the clinical course.

Indexed as

AdultAgedAged, 80 and overCytokinesDisease ProgressionEnzyme-Linked Immunosorbent AssayFemaleHumansLongitudinal StudiesMaleMiddle AgedNeoplasm ProteinsOrgan Dysfunction ScoresProspective StudiesProteoglycansRespiratory Distress SyndromeCytokinesESM1 protein, humanNeoplasm ProteinsProteoglycansVesicular Transport ProteinsVPS51 protein, humanAcute Kidney InjuryAcute Lung InjuryOrgan DysfunctionSeptic ShockSystemic Inflammatory Response Syndrome

Identifiers

PMID28455780
PMCPMC7101577
OpenAlexW2610130212

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.