Publications by authors named "T Fuderer"

In critically ill patients, compromised microcirculation causes tissue hypoxia, organ failure, and death. These pathophysiological processes occur particularly in patients with high illness severity, so reliable hypoxia biomarkers should reflect this in their occurrence. This secondary analysis of a prospective study categorized patients by their burden of organ dysfunction (BOD) using the cohort's median initial sequential organ failure assessment (SOFA) score of 8 as a cutoff.

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Article Synopsis
  • Trauma and infections trigger emergency granulopoiesis, which leads to an increase of immature granulocytes in the blood during severe conditions like sepsis, but their effectiveness as biomarkers is limited due to mixed disease severity responses.
  • * A study was conducted comparing sepsis patients to those with SIRS, using techniques like flow cytometry and gene expression assays to analyze granulocyte populations and their developmental stages.
  • * Results showed that immature granulocyte precursor counts were higher in sepsis but didn't correlate with disease severity, and that low-density granulocytes had a significantly greater number of precursors compared to high-density granulocytes.
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Tissue hypoxia is associated with the development of organ dysfunction and death in critically ill patients commonly captured using blood lactate. The kinetic parameters of serial lactate evaluations are superior at predicting mortality compared with single values. S-adenosylhomocysteine (SAH), which is also associated with hypoxia, was recently established as a useful predictor of septic organ dysfunction and death.

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Natural killer (NK) cells are innate cytokine-producing and cytolytic effector lymphocytes. Their function is responsive to environmental factors, e.g.

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Background: Pneumonia develops frequently after major surgery and polytrauma and thus in the presence of systemic inflammatory response syndrome (SIRS) and organ dysfunction. Immune checkpoints balance self-tolerance and immune activation. Altered checkpoint blood levels were reported for sepsis.

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