Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/13749
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dc.contributor.authorMaiden, MJ-
dc.contributor.authorOtto, S-
dc.contributor.authorBrealey, JK-
dc.contributor.authorFinnis, ME-
dc.contributor.authorChapman, MJ-
dc.contributor.authorKuchel, TR-
dc.contributor.authorNash, CH-
dc.contributor.authorEdwards, J-
dc.contributor.authorBellomo, Rinaldo-
dc.date2016-03-11-
dc.date.accessioned2016-03-22T22:12:27Z-
dc.date.accessioned2016-03-22T22:12:39Z-
dc.date.available2016-03-22T22:12:39Z-
dc.date.available2016-03-22T22:12:27Z-
dc.date.issued2016-
dc.identifier.citationAmerican Journal of Respiratory and Critical Care Medicine 2016, 11 March epuben_US
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/13749-
dc.description.abstractRATIONALE: It is unclear how septic shock causes acute kidney injury (AKI) and whether this is associated with histological change. OBJECTIVES: We aimed to determine the nature and extent of changes in renal structure and function over time in an ovine model of septic shock. METHODS: Fifteen sheep were instrumented with a renal artery flow probe and renal vein cannula. Ten were given intravenous E. coli to induce septic shock and five acted as controls. Animals were mechanically ventilated for 48 hours, while receiving protocol guided parenteral fluids and a norepinephrine infusion to maintain mean arterial pressure. Renal biopsies were taken every 24 hours or whenever animals were oliguric for two hours. A renal pathologist, blinded to tissue source, systematically quantified histological appearance under light and electron microscopy for 31 pre-specified structural changes. MEASUREMENTS AND MAIN RESULTS: Sheep given E. coli developed septic shock, oliguria, increased serum creatinine and reduced creatinine clearance (AKI) but there were no changes over time in renal blood flow between groups (P>0.30) or over time within groups (P>0.50). Renal oxygen consumption increased only in non-septic animals (P=0.01) but there was no between-group difference in renal lactate flux (P>0.50). There was little structural disturbance in all biopsies and, while some cellular appearances changed over time, the only difference between septic and non-septic animals was mesangial expansion on electron microscopy. CONCLUSIONS: In an intensive care supported model of Gram-negative septic shock, early AKI was not associated with changes in renal blood flow, oxygen delivery or histological appearance. Other mechanisms must contribute to septic AKIen_US
dc.subjectAcute Kidney Injuryen_US
dc.subjectShock, Septicen_US
dc.titleStructure and function of the kidney in septic shock: a prospective controlled experimental studyen_US
dc.typeJournal Articleen_US
dc.identifier.journaltitleAmerican Journal of Respiratory and Critical Care Medicineen_US
dc.identifier.affiliationSA Pathology, Department of Pathologyen_US
dc.identifier.affiliationRoyal Adelaide Hospital, Intensive Care Uniten_US
dc.identifier.affiliationUniversity of Adelaide, Discipline of Acute Care Medicineen_US
dc.identifier.affiliationRoyal Adelaide Hospital, Intensive Care Unit, Adelaideen_US
dc.identifier.affiliationAustin Health, Intensive Care Uniten_US
dc.identifier.pubmedurihttps://pubmed.ncbi.nlm.nih.gov/26967568en_US
dc.type.contentTexten_US
dc.type.austinJournal Articleen_US
local.name.researcherBellomo, Rinaldo
item.grantfulltextnone-
item.openairetypeJournal Article-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
crisitem.author.deptIntensive Care-
crisitem.author.deptData Analytics Research and Evaluation (DARE) Centre-
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