Evidence map›Paper›PMID 30527203›Full record

Observational studyThe Kaohsiung journal of medical sciences2018

Can endocan be a new biomarker in ventilator-associated pneumonia?

Ilke Kupeli, Sara Salcan, Mehmet Kuzucu, Ufuk Kuyrukluyıldız

Registry-linked trialOpen access · goldAbstract readObservational Study
In one paragraph

Observational study in The Kaohsiung journal of medical sciences, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02916277 (Endocan; Can be a New Biomarker in Ventilator-associated Pneumonia?), which is not on this map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.4field-weighted citation impact, top 40% 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.

NCT02916277 unknown statusnot on this map

Endocan; Can be a New Biomarker in Ventilator-associated Pneumonia?

Typeobservational_patient_registrySponsorErzincan UniversityRan2016 to 2017Enrolled60ConditionsSerial Endocan MeasurementsArmsendocan
3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 10 citations in OpenAlex.

  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

4 authors at 1 institution in 1 country.

Ilke KupeliDepartment of Anesthesiology and Reanimation, Faculty of Medicine, Erzincan University, Erzincan, Turkey. Electronic address: ilkeser2004@gmail.com.
Sara SalcanDepartment of Public Health, Faculty of Medicine, Erzincan University, Erzincan, Turkey.
Mehmet KuzucuMolecular Biology Division, Faculty of Sciences and Arts, Erzincan Universıty, Erzincan, Turkey.
Ufuk KuyrukluyıldızDepartment of Anesthesiology and Reanimation, Faculty of Medicine, Erzincan University, Erzincan, Turkey.
Erzincan Binali Yıldırım University · TR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ventilator-Associated Pneumonia (VAP) is a hospital-acquired bacterial infection with high incidence and mortality rate. The aim of this study is to investigate the correlation between the Endocan level and development of VAP and whether or not this correlation was correlated with the clinical findings. Demographic data, white blood cell (WBC) count, procalcitonin (PCT), c-reactive protein (CRP), and fever levels of 60 patients were recorded in serial measurements for 5 days. When there was the presence of fever or elevated Endocan, alveolar lavage culture was taken and chest radiographies were taken. Correlations of the Endocan levels with the culture results and laboratory values were examined. The rate of VAP was found as 10.4/1000 mechanical ventilator days. Endocan levels were significantly higher in patients with VAP (p < 0.05). However, there was no significant difference among PCT, WBC, CRP measurements (p > 0.05). No correlation was found between Endocan levels and PCT, WBC and CRP levels in those with VAP (p > 0.05). A significant correlation was found between the Endocan level and the elevated fever 24 h later (p:0.001). The serum Endocan level on the day 3 had a specificity of 73.3%, a sensitivity of 68.9%, positive predictive value of 44%, and negative predictive value of 88.5% at the cut off level of 9.17 ng/mL. In this study, it was determined that high Endocan levels were associated with the development of VAP. The present study suggested that Endocan can be used as a screening tool for the development of VAP. CLINICAL TRIALS.GOV ID: NCT02916277.

Indexed as

AgedAge FactorsBiomarkersFemaleHumansMaleNeoplasm ProteinsPneumonia, Ventilator-AssociatedProteoglycansBiomarkersESM1 protein, humanNeoplasm ProteinsProteoglycansBiomarkerEndocanVentilator-associated pneumonia

Identifiers

PMID30527203
PMCPMC11915590
OpenAlexW2887445565

What OpenQuestion holds

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LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

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.