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Intradermal Microdialysis: An Approach to Investigating Novel Mechanisms of Microvascular Dysfunction in Humans
Published on: July 21, 2023
Microvascular thrombosis and multiple organ dysfunction syndrome
1Division of Acute and Critical Care Medicine, Department of Anesthesiology and Critical Care Medicine, Hokkaido University Graduate School of Medicine, Kita-ku, Sapporo, Japan. gando@med.hokudai.ac.jp
Abstract:
This paper will review the involvement of disseminated intravascular coagulation-induced microvascular thrombosis in the pathogenesis of multiple organ dysfunction syndrome and the interaction between disseminated intravascular coagulation and systemic inflammatory response syndrome in critically ill patients. The published literature on clinical and experimental studies are the data sources of the study. Histologic evidence of microvascular thrombosis and tissue injury in disseminated intravascular coagulation has been reported in clinical, experimental, and autopsy findings. Proinflammatory cytokine-evoked neutrophil-endothelial activation and interplay between inflammation and coagulation through protease-activated receptors contribute to enhanced microvascular fibrin deposition in organs. In a clinical setting, systemic inflammatory response syndrome and disseminated intravascular coagulation synergistically play pivotal roles in the development of multiple organ dysfunction syndrome and in the poor prognosis of critical illness. Disseminated intravascular coagulation contributes to microvascular thrombosis and subsequent multiple organ dysfunction syndrome. Recent knowledge on the relationship between disseminated intravascular coagulation and systemic inflammatory response syndrome gives further insight into the pathogenic mechanisms of multiple organ dysfunction syndrome in critically ill patients.
Insights
Disseminated intravascular coagulation causes microvascular thrombosis, leading to multiple organ dysfunction syndrome. The interaction between this condition and systemic inflammatory response syndrome worsens outcomes in critically ill patients.
Area of Science:
- Critical Care Medicine
- Pathophysiology
- Hematology
Background:
- Disseminated intravascular coagulation (DIC) is a critical condition characterized by microvascular thrombosis.
- Systemic inflammatory response syndrome (SIRS) frequently co-occurs in critically ill patients.
- The interplay between DIC and SIRS is implicated in the pathogenesis of multiple organ dysfunction syndrome (MODS).
Purpose of the Study:
- To review the role of DIC-induced microvascular thrombosis in MODS.
- To examine the interaction between DIC and SIRS in critically ill patients.
- To elucidate the pathogenic mechanisms of MODS.
Main Methods:
- Literature review of published clinical and experimental studies.
- Analysis of histologic evidence from clinical, experimental, and autopsy findings.
- Examination of molecular pathways involving cytokines, neutrophils, endothelial cells, and protease-activated receptors.
Main Results:
- Histologic evidence confirms microvascular thrombosis and tissue injury in DIC.
- Proinflammatory cytokines and protease-activated receptors promote fibrin deposition in organs.
- DIC and SIRS synergistically contribute to MODS development and poor prognosis.
Conclusions:
- DIC-induced microvascular thrombosis is a key factor in MODS pathogenesis.
- The interaction between DIC and SIRS significantly impacts critical illness outcomes.
- Understanding these interactions provides insight into MODS mechanisms.
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