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      Inflammation and lung injury in an ovine model of fluid resuscitated endotoxemic shock

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          Abstract

          Background

          Sepsis is a multi-system syndrome that remains the leading cause of mortality and critical illness worldwide, with hemodynamic support being one of the cornerstones of the acute management of sepsis. We used an ovine model of endotoxemic shock to determine if 0.9% saline resuscitation contributes to lung inflammation and injury in acute respiratory distress syndrome, which is a common complication of sepsis, and investigated the potential role of matrix metalloproteinases in this process.

          Methods

          Endotoxemic shock was induced in sheep by administration of an escalating dose of lipopolysaccharide, after which they subsequently received either no fluid bolus resuscitation or a 0.9% saline bolus. Lung tissue, bronchoalveolar fluid (BAL) and plasma were analysed by real-time PCR, ELISA, flow cytometry and immunohistochemical staining to assess inflammatory cells, cytokines, hyaluronan and matrix metalloproteinases.

          Results

          Endotoxemia was associated with decreased serum albumin and total protein levels, with activated neutrophils, while the glycocalyx glycosaminoglycan hyaluronan was significantly increased in BAL. Quantitative real-time PCR studies showed higher expression of IL-6 and IL-8 with saline resuscitation but no difference in matrix metalloproteinase expression. BAL and tissue homogenate levels of IL-6, IL-8 and IL-1β were elevated.

          Conclusions

          This data shows that the inflammatory response is enhanced when a host with endotoxemia is resuscitated with saline, with a comparatively higher release of inflammatory cytokines and endothelial/glycocalyx damage, but no change in matrix metalloproteinase levels.

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          Most cited references36

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          The IL-1 family: regulators of immunity.

          Over recent years it has become increasingly clear that innate immune responses can shape the adaptive immune response. Among the most potent molecules of the innate immune system are the interleukin-1 (IL-1) family members. These evolutionarily ancient cytokines are made by and act on innate immune cells to influence their survival and function. In addition, they act directly on lymphocytes to reinforce certain adaptive immune responses. This Review provides an overview of both the long-established and more recently characterized members of the IL-1 family. In addition to their effects on immune cells, their involvement in human disease and disease models is discussed.
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            Effectiveness of treatments for severe sepsis: a prospective, multicenter, observational study.

            Several Surviving Sepsis Campaign Guidelines recommendations are reevaluated. To analyze the effectiveness of treatments recommended in the sepsis guidelines. In a prospective observational study, we studied all adult patients with severe sepsis from 77 intensive care units. We recorded compliance with four therapeutic goals (central venous pressure 8 mm Hg or greater for persistent hypotension despite fluid resuscitation and/or lactate greater than 36 mg/dl, central venous oxygen saturation 70% or greater for persistent hypotension despite fluid resuscitation and/or lactate greater than 36 mg/dl, blood glucose greater than or equal to the lower limit of normal but less than 150 mg/dl, and inspiratory plateau pressure less than 30 cm H(2)O for mechanically ventilated patients) and four treatments (early broad-spectrum antibiotics, fluid challenge in the event of hypotension and/or lactate greater than 36 mg/dl, low-dose steroids for septic shock, drotrecogin alfa [activated] for multiorgan failure). The primary outcome measure was hospital mortality. The effectiveness of each treatment was estimated using propensity scores. Of 2,796 patients, 41.6% died before hospital discharge. Treatments associated with lower hospital mortality were early broad-spectrum antibiotic treatment (treatment within 1 hour vs. no treatment within first 6 hours of diagnosis; odds ratio, 0.67; 95% confidence interval, 0.50-0.90; P = 0.008) and drotrecogin alfa (activated) (odds ratio, 0.59; 95% confidence interval, 0.41-0.84; P = 0.004). Fluid challenge and low-dose steroids showed no benefits. In severe sepsis, early administration of broad-spectrum antibiotics in all patients and administration of drotrecogin alfa (activated) in the most severe patients reduce mortality.
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              Review of a large clinical series: association of cumulative fluid balance on outcome in acute lung injury: a retrospective review of the ARDSnet tidal volume study cohort.

              To evaluate the independent influence of fluid balance on outcomes for patients with acute lung injury. Secondary analysis of a prospective cohort study conducted between March 1996 and March 1999. The study involved 10 academic clinical centers (with 24 hospitals and 75 Intensive Care Units). All patients for whom fluid balance data existed (844) from the 902 patients enrolled in the National Heart Lung Blood Institute's ARDS Network ventilator-tidal volume trial. The study had no interventions. On the first day of study enrollment, 683 patients were, on average, more than 3.5 L in positive fluid balance compared to 161 patients in negative fluid balance (P < .001). Cumulative negative fluid balance on day 4 of the study was associated with an independently lower hospital mortality (OR, 0.50; 95% CI, 0.28-0.89; P < .001) more ventilator and intensive care unit-free days. Negative cumulative fluid balance at day 4 of acute lung injury is associated with significantly lower mortality, independent of other measures of severity of illness.
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                Author and article information

                Contributors
                M.Passmore@uq.edu.au
                liambyrne.syd@gmail.com
                gnchafatso@gmail.com
                l.seehoe@uq.edu.au
                c.boon0207@gmail.com
                sara_diab5@hotmail.com
                Kimble.Dunster@health.qld.gov.au
                Kavita.Bisht@mater.uq.edu.au
                JTung@redcrossblood.org.au
                hashairi@usm.my
                monica.narula@live.com.au
                sanne.pedersen.work@gmail.com
                lanna.ross@gmail.com
                GSimonova@redcrossblood.org.au
                annette.sultana@live.com.au
                Chris.Anstey@health.qld.gov.au
                kiran.shekar@health.qld.gov.au
                kathryn.maitland@gmail.com
                j.suen1@uq.edu.au
                j.fraser@uq.edu.au
                Journal
                Respir Res
                Respir. Res
                Respiratory Research
                BioMed Central (London )
                1465-9921
                1465-993X
                22 November 2018
                22 November 2018
                2018
                : 19
                : 231
                Affiliations
                [1 ]ISNI 0000 0004 0614 0266, GRID grid.415184.d, Critical Care Research Group, Level 3, Clinical Sciences Building, The Prince Charles Hospital, ; Rode Rd, Brisbane, Australia
                [2 ]ISNI 0000 0000 9320 7537, GRID grid.1003.2, University of Queensland, ; Brisbane, Australia
                [3 ]ISNI 0000 0001 2180 7477, GRID grid.1001.0, Australian National University, ; Canberra, Australia
                [4 ]ISNI 0000 0001 0155 5938, GRID grid.33058.3d, KEMRI-Wellcome Trust Research Programme, ; Kilifi, Kenya
                [5 ]ISNI 0000000089150953, GRID grid.1024.7, Queensland University of Technology, ; Brisbane, Australia
                [6 ]ISNI 0000 0000 8831 6915, GRID grid.420118.e, Research and Development, Australian Red Cross Blood Service, ; Brisbane, Australia
                [7 ]ISNI 0000 0001 2294 3534, GRID grid.11875.3a, Department of Emergency Medicine, , Universiti Sains Malaysia Health Campus, ; Kubang Kerian, Kelantan Malaysia
                [8 ]Sunshine Coast University Hospital Intensive Care, Birtinya, Australia
                [9 ]ISNI 0000 0001 2113 8111, GRID grid.7445.2, Wellcome Trust Centre for Clinical Tropical Medicine and Department of Paediatrics, Faculty of Medicine, Imperial College, ; London, UK
                Author information
                http://orcid.org/0000-0002-0859-8882
                Article
                935
                10.1186/s12931-018-0935-4
                6249903
                30466423
                b38bc4d9-982a-403d-95e7-2d0c41f3e4b5
                © The Author(s). 2018

                Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

                History
                : 22 August 2018
                : 12 November 2018
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/501100000925, National Health and Medical Research Council;
                Award ID: APP1061382
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/501100001078, Queensland Emergency Medicine Research Foundation;
                Award ID: EMPJ-358R25-2016
                Award Recipient :
                Categories
                Research
                Custom metadata
                © The Author(s) 2018

                Respiratory medicine
                endotoxemic shock,inflammation,lung injury,matrix metalloproteinases
                Respiratory medicine
                endotoxemic shock, inflammation, lung injury, matrix metalloproteinases

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