Please use this identifier to cite or link to this item: https://www.um.edu.mt/library/oar/handle/123456789/97544
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dc.contributor.authorVught, Lonneke A. van-
dc.contributor.authorWiewel, Maryse A.-
dc.contributor.authorKlein Klouwenberg, Peter M.C.-
dc.contributor.authorHoogendijk, Arie J.-
dc.contributor.authorScicluna, Brendon P.-
dc.contributor.authorOng, David S.Y.-
dc.contributor.authorCremer, Olaf L.-
dc.contributor.authorHorn, Janneke-
dc.contributor.authorBonten, Marc M.J.-
dc.contributor.authorSchultz, Marcus J.-
dc.contributor.authorPoll, Tom van der-
dc.date.accessioned2022-06-11T08:25:17Z-
dc.date.available2022-06-11T08:25:17Z-
dc.date.issued2016-
dc.identifier.citationvan Vught, L. A., Wiewel, M. A., Klein Klouwenberg, P., Hoogendijk, A. J., Scicluna, B. P., Ong, D. S., ... & van der Poll, T. (2016). Admission hyperglycemia in critically ill sepsis patients: association with outcome and host response. Critical Care Medicine, 44(7), 1338-1346.en_GB
dc.identifier.urihttps://www.um.edu.mt/library/oar/handle/123456789/97544-
dc.description.abstractObjectives: To investigate whether admission hyperglycemia is associated with the presentation and/or outcome of sepsis, what the influence of hyperglycemia is on key host responses to sepsis, and whether hyperglycemia differentially affects patients with diabetes mellitus.en_GB
dc.description.abstractDesign and setting: A substudy of a prospective observational cohort study was conducted in the intensive care of two tertiary hospitals between January 2011 and July 2013.en_GB
dc.description.abstractPatients: Of all consecutive critically ill sepsis patients, admission glucose was used to stratify patients in euglycemia (71-140 mg/dL), mild hyperglycemia (141-199 mg/dL), and severe hyperglycemia (≥ 200 mg/dL), and patients with hypoglycemia were excluded. Fifteen plasma biomarkers providing insight in key host responses implicated in sepsis pathogenesis were measured on admission.en_GB
dc.description.abstractMeasurements and main results: Of 987 sepsis patients with admission glucose levels greater than 70 mg/dL, 519 (52.6%) had normal glucose levels, 267 (27.1%) had mild, and 201 (20.4%) severe hyperglycemia. Admission hyperglycemia was accompanied by mitigated alterations in plasma host response biomarker levels indicative of activation of the cytokine network, the vascular endothelium, and the coagulation system in patients without a history of diabetes. Severe, but not mild, admission hyperglycemia was associated with increased 30-day mortality (adjusted hazard ratio, 1.66 [95% CI, 1.24-2.23]), in both patients without diabetes (adjusted hazard ratio, 1.65 [95% CI, 1.12-2.42]) and with diabetes (adjusted hazard ratio, 1.91 [95% CI, 1.01-3.62]).en_GB
dc.description.abstractConclusion: Admission hyperglycemia is associated with adverse outcome of sepsis irrespective of the presence or absence of preexisting diabetes by a mechanism unrelated to exaggerated inflammation or coagulation.en_GB
dc.language.isoenen_GB
dc.publisherLippincott Williams & Wilkinsen_GB
dc.rightsinfo:eu-repo/semantics/restrictedAccessen_GB
dc.subjectBiochemical markers -- Diagnostic useen_GB
dc.subjectCritically illen_GB
dc.subjectHost-virus relationshipsen_GB
dc.subjectHyperglycemiaen_GB
dc.subjectIntensive care unitsen_GB
dc.subjectSepticemia -- Diagnosisen_GB
dc.titleAdmission hyperglycemia in critically ill sepsis patients : association with outcome and host responseen_GB
dc.typearticleen_GB
dc.rights.holderThe copyright of this work belongs to the author(s)/publisher. The rights of this work are as defined by the appropriate Copyright Legislation or as modified by any successive legislation. Users may access this work and can make use of the information contained in accordance with the Copyright Legislation provided that the author must be properly acknowledged. Further distribution or reproduction in any format is prohibited without the prior permission of the copyright holderen_GB
dc.contributor.corpauthorMolecular Diagnosis and Risk Stratification of Sepsis (MARS) Consortiumen_GB
dc.description.reviewedpeer-revieweden_GB
dc.identifier.doi10.1097/CCM.0000000000001650-
dc.publication.titleCritical Care Medicineen_GB
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