Please use this identifier to cite or link to this item: http://hdl.handle.net/11452/23315
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dc.contributor.authorFailing, Klaus H.-
dc.contributor.authorMoritz, Andreas-
dc.contributor.authorBauer, Natali B.-
dc.date.accessioned2021-12-16T08:15:32Z-
dc.date.available2021-12-16T08:15:32Z-
dc.date.issued2011-
dc.identifier.citationEralp, O. vd. (2011). "Effect of experimental endotoxemia on thrombelastography parameters, secondary and tertiary hemostasis in dogs". Journal of Veterinary Internal Medicine, 25(3), 524-531.en_US
dc.identifier.issn0891-6640-
dc.identifier.urihttps://doi.org/10.1111/j.1939-1676.2011.0698.x-
dc.identifier.urihttps://onlinelibrary.wiley.com/doi/10.1111/j.1939-1676.2011.0698.x-
dc.identifier.urihttp://hdl.handle.net/11452/23315-
dc.description.abstractBackground Thrombelastography (TEG) and indicators of secondary and tertiary hemostasis might be altered in dogs with endotoxemia. Hypothesis Endotoxemia influences measures of coagulation in dogs. Animals Ten healthy cross-bred dogs. Material and Methods Prospective laboratory study between controls (n = 5) receiving 0.9% saline IV and the study group (n = 5) treated with low-dose lipopolysaccharide (0.02 mg/kg IV). Physical examination and sampling for measurement of leukocytes, platelets, and coagulation variables were performed at time points 0, 1, 4, and 24 hours. Coagulation variables included kaolin-activated TEG, 1-stage prothrombin time (OSPT), activated partial thromboplastin time (aPTT), fibrinogen, factor VIII, antithrombin, protein C, protein S, activated protein C (APC)-ratio calculated from aPTT with and without presence of APC), and D-Dimers. Results Endotoxemia-induced clinical signs included lethargy (n = 5/5), diarrhea (n = 4/5), emesis (n = 4/5), and abdominal pain (2/5). After 1 hour there was severe leukopenia (2.5 +/- 0.7 x 109/L; mean +/- SD, P < .0001) and a 2.2-fold increase in D-Dimers (0.81 +/- 0.64 mg/L, P < .0001). After 4 hours there was hyperthermia (40.3 +/- 0.4 degrees C, P < .0001) and increases in OSPT (10.5 +/- 2.7 seconds, P < .0001), aPTT (16.7 +/- 5.2 seconds, P = 0.002). A significant decrease in fibrinogen (1.5 +/- 1.0 g/L, P = 0.001), protein C (31 +/- 33%, P <.0001), protein S (63 +/- 47%, P < .0001), TEG alpha (58 +/- 19, P = .007), and TEG maximal amplitude (50 +/- 19 mm, P = .003) was seen compared with the controls. APC-ratio rose significantly (2.5 +/- 0.2, P < .0001) without exceeding the reference interval (n = 4/5). Conclusion and Clinical Importance D-Dimers are the earliest indicator for endotoxemia-associated coagulation abnormalities followed by decreased protein C concentration. APC-ratio and TEG were not good screening variables.en_US
dc.description.sponsorshipRobert Siranovicen_US
dc.description.sponsorshipRoche Diagnostics GmbH, Mannheim, Germanyen_US
dc.description.sponsorshipDirk Rohmann, Dahlhausen Company, Cologne, Germanyen_US
dc.description.sponsorshipEberhard Hock, Scil Animal Care Company, Viernheim, Germanyen_US
dc.language.isoenen_US
dc.publisherWileyen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.rightsAtıf Gayri Ticari Türetilemez 4.0 Uluslararasıtr_TR
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectVeterinary sciencesen_US
dc.subjectAcute phase reactionen_US
dc.subjectCoagulationen_US
dc.subjectDisseminated intravascular coagulationen_US
dc.subjectProtein Cen_US
dc.subjectProtein Sen_US
dc.subjectSystemic inflammatory response syndromeen_US
dc.subjectThromboembolismen_US
dc.subjectDisseminated intravascular coagulationen_US
dc.subjectActivated protein-Cen_US
dc.subjectSeptic shocken_US
dc.subjectReference intervalsen_US
dc.subjectSevere sepsisen_US
dc.subjectResistanceen_US
dc.subjectFibrinolysisen_US
dc.subjectHypercoagulabilityen_US
dc.subjectAntithrombinen_US
dc.subjectInflammationen_US
dc.subjectAnimaliaen_US
dc.subjectCanis familiarisen_US
dc.subject.meshAnimalsen_US
dc.subject.meshDog diseasesen_US
dc.subject.meshDogsen_US
dc.subject.meshEndotoxemiaen_US
dc.subject.meshFemaleen_US
dc.subject.meshHemostasisen_US
dc.subject.meshLipopolysaccharidesen_US
dc.subject.meshMaleen_US
dc.subject.meshThrombelastographyen_US
dc.titleEffect of experimental endotoxemia on thrombelastography parameters, secondary and tertiary hemostasis in dogsen_US
dc.typeArticleen_US
dc.identifier.wos000290179100017tr_TR
dc.identifier.scopus2-s2.0-79955523932tr_TR
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergitr_TR
dc.contributor.departmentUludağ Üniversitesi/Veterinerlik Fakültesi/Dahiliye Anabilim Dalı.tr_TR
dc.contributor.orcid0000-0002-4242-8609tr_TR
dc.contributor.orcid0000-0001-9836-0749tr_TR
dc.identifier.startpage524tr_TR
dc.identifier.endpage531tr_TR
dc.identifier.volume25tr_TR
dc.identifier.issue3tr_TR
dc.relation.journalJournal of Veterinary Internal Medicineen_US
dc.contributor.buuauthorEralp, Oya-
dc.contributor.buuauthorYılmaz, Zeki-
dc.contributor.researcheridAAG-2943-2020tr_TR
dc.relation.collaborationYurt dışıtr_TR
dc.identifier.pubmed21418317tr_TR
dc.subject.wosVeterinary sciencesen_US
dc.indexed.wosSCIEen_US
dc.indexed.scopusScopusen_US
dc.indexed.pubmedPubmeden_US
dc.wos.quartileQ1en_US
dc.contributor.scopusid24472964600tr_TR
dc.contributor.scopusid35944810500tr_TR
dc.subject.scopusThromboelastography; Partial Thromboplastin Time; Cushing Syndromeen_US
dc.subject.emtreeLipopolysaccharideen_US
dc.subject.emtreeAnimalen_US
dc.subject.emtreeAnimal diseaseen_US
dc.subject.emtreeArticleen_US
dc.subject.emtreeBlooden_US
dc.subject.emtreeChemically induced disorderen_US
dc.subject.emtreeDogen_US
dc.subject.emtreeDog diseaseen_US
dc.subject.emtreeEndotoxemiaen_US
dc.subject.emtreeFemaleen_US
dc.subject.emtreeHomeostasisen_US
dc.subject.emtreeMaleen_US
dc.subject.emtreePsychologyen_US
dc.subject.emtreeThromboelastographyen_US
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