Please use this identifier to cite or link to this item: https://open.uns.ac.rs/handle/123456789/7719
DC FieldValueLanguage
dc.contributor.authorDunja Mihajlovićen_US
dc.contributor.authorDajana Lendaken_US
dc.contributor.authorSnežana Brkićen_US
dc.contributor.authorBiljana Draškovićen_US
dc.contributor.authorGorana Mitićen_US
dc.contributor.authorAleksandra Novakov Mikićen_US
dc.contributor.authorTatjana Ćebovićen_US
dc.date.accessioned2019-09-30T09:03:54Z-
dc.date.available2019-09-30T09:03:54Z-
dc.date.issued2014-01-01-
dc.identifier.issn262862en_US
dc.identifier.urihttps://open.uns.ac.rs/handle/123456789/7719-
dc.description.abstractIntroduction: Coagulation abnormalities which occur as a consequence of endothelial changes are recognized as diagnostic criteria for sepsis, but significance of these changes in the outcome prognosis and prediction of the course of sepsis is still not accurately defined. Materials and methods: 60 patients who fulfilled the criteria for diagnosis of sepsis were included in our study. Patients were categorized in two groups according to sepsis severity and organ failure and MODS development was assessed in the first 48. h from ICU admission. Prothrombin time (PT), activated partial thromboplastin time (aPTT) and endothelial cell specific molecule-1(endocan) levels, as well as procalcitonin (PCT) and C-reactive protein (CRP) were determined within the first 24. h of the onset of the disease. Predictive APACHE II (Acute Physiology and Chronic Health Evaluation II) and SOFA (Sequential Organ Failure Assessment) scores were calculated on the day of ICU admission. Data were used to determine an association between day 1 biomarker levels, organ dysfunction score values and the development of organ failure, multiple organ dysfunction syndrome (MODS), and mortality during 28. days. These connections were determined by plotting of receiver operating characteristic (ROC) curves. Differences between groups were assessed by Mann-Whitney U test. Categorical variables were compared using chi-square test. Results: Concentration of endocan was significantly higher in the group of patients with sepsis induced organ failure, MODS development and in the group of non- survivors in contrast to group with less severe form of the disease, without multiorgan failure, and in contrast to group of survivors (p. <. 0.05). Values of areas under the ROC curves showed that endocan levels had good discriminative power for more severe course of sepsis, MODS development and possible discriminative power for mortality prediction (AUC: 0.81, 0.67, 0.71 retrospectively), better than PCT for fatality (AUC:053) and better than APACHE II (AUC:0.55) and SOFA (AUC: 0.57) scores for organ failure. Conclusions: Results of our study show that endocan can be used as strong and significant predictor of sepsis severity and outcome, perhaps even better than SOFA and APACHE II scores. © 2014 Elsevier Inc.en_US
dc.language.isoenen_US
dc.relation.ispartofMicrovascular Researchen_US
dc.subjectSepsisen_US
dc.subjectEndotheliumen_US
dc.subjectHemostasisen_US
dc.subjectCoagulationen_US
dc.subjectPrognosisen_US
dc.subjectAPACHEen_US
dc.subjectEndocanen_US
dc.subjectShocken_US
dc.subjectMODSen_US
dc.titleEndocan is useful biomarker of survival and severity in sepsisen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.doi10.1016/j.mvr.2014.04.004-
dc.identifier.pmid93-
dc.identifier.scopus2-s2.0-84901233765-
dc.identifier.urlhttps://api.elsevier.com/content/abstract/scopus_id/84901233765-
dc.description.versionPublisheden_US
dc.relation.lastpage97en_US
dc.relation.firstpage92en_US
dc.relation.volume93en_US
item.grantfulltextnone-
item.fulltextNo Fulltext-
crisitem.author.deptMedicinski fakultet, Katedra za anesteziju i perioperativnu medicinu-
crisitem.author.deptMedicinski fakultet, Katedra za infektivne bolesti-
crisitem.author.deptMedicinski fakultet, Katedra za infektivne bolesti-
crisitem.author.deptMedicinski fakultet, Katedra za anesteziju i perioperativnu medicinu-
crisitem.author.deptMedicinski fakultet, Katedra za patološku fiziologiju i laboratorijsku medicinu-
crisitem.author.deptMedicinski fakultet, Katedra za biohemiju-
crisitem.author.parentorgMedicinski fakultet-
crisitem.author.parentorgMedicinski fakultet-
crisitem.author.parentorgMedicinski fakultet-
crisitem.author.parentorgMedicinski fakultet-
crisitem.author.parentorgMedicinski fakultet-
crisitem.author.parentorgMedicinski fakultet-
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