Sanne Engkilde-Pedersen
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Research Subjects
Sanne Engkilde-Pedersen has a total of 32 co-authors. Here are the top co-authors by number of shared publications:
- John F. Fraser
Institute for Molecular Bioscience, The University of Queensland Brisbane Queensland Australia
3 shared publications - John-Paul Tung
Critical Care Research Group, The Prince Charles Hospital, Brisbane, QLD, Australia
3 shared publications - Ai-Ching Boon
Critical Care Research Group, Prince Charles Hospital, Brisbane, Australia; University of Queensland, Brisbane, Australia
2 shared publications - Arlanna Esguerra-Lallen
Strategic Transformation and Readiness, Australian Red Cross Lifeblood, PO Box 41, Everton Park, QLD, Australia, 4053; Critical Care Research Group (CCRG), The Prince Charles Hospital, 627 Rode Rd, Chermside, QLD, Australia, 4032; Adult Intensive Care Services, The Prince Charles Hospital, 627 Rode Rd, Chermside, QLD, Australia, 4032
2 shared publications - Chris Anstey
Department of Intensive Care, Sunshine Coast Hospital, Nambour, QLD, 4560, Australia
2 shared publications - Gabriela Simonova
Critical Care Research Group, University of Queensland and the Prince Charles Hospital, Brisbane, Australia
2 shared publications
Latest Publications
- Open Access
- 16 May 2026
- Published by Elsevier in Immunology Letters
- Vol. 280, 107187
Cardiac surgery modulates leucocyte subsets and inflammatory mediators
- 16 May 2026
- Published by Elsevier in Immunology Letters
- Vol. 280, 107187
Open AccessCardiac surgery modulates leucocyte subsets and inflammatory mediators
- Open Access
- 12 February 2019
- Published by Elsevier in Thrombosis Research
- Vol. 176, 39-45
Fluid resuscitation with 0.9% saline alters haemostasis in an ovine model of endotoxemic shock
- 12 February 2019
- Published by Elsevier in Thrombosis Research
- Vol. 176, 39-45
Open AccessFluid resuscitation with 0.9% saline alters haemostasis in an ovine model of endotoxemic shock
- Open Access
- 22 November 2018
- Published by Springer Nature in Respiratory Research
- Vol. 19 (1) , 231
Inflammation and lung injury in an ovine model of fluid resuscitated endotoxemic shock
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. 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. 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. 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.
- 22 November 2018
- Published by Springer Nature in Respiratory Research
- Vol. 19 (1) , 231
Open AccessInflammation and lung injury in an ovine model of fluid resuscitated endotoxemic shock
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. 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. 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. 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.