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[Systemic coagulopathic distress syndrome in surgery: concept, pathogenesis, prophylaxis]
A P Vlasov1, V V Trofimov1, T I Vlasova1
1N.P. Ogarev Mordovsky National State Medical University, Saransk, Russia.
Khirurgiia
|September 19, 2019
Summary
Urgent surgical diseases disrupt hemostasis and lipid metabolism, leading to systemic coagulopathic distress syndrome. This new syndrome highlights the role of membrane destabilization and supports targeted therapies like Remaxol.
Area of Science:
- Surgical pathology
- Hemostasis and thrombosis
- Lipid metabolism
Background:
- Urgent surgical diseases significantly impact hemostasis and lipid metabolism.
- Understanding these interactions is crucial for managing thrombohemorrhagic complications.
Purpose of the Study:
- To correlate changes in hemostasis (humoral and tissue) with lipid metabolism in urgent surgical diseases.
- To establish a scientific basis for defining a new syndrome: systemic coagulopathic distress syndrome.
Main Methods:
- Experimental studies in dogs with induced pancreatitis, peritonitis, and intestinal obstruction.
- Clinical analysis of 55 patients with various acute abdominal conditions.
- Evaluation of hemostasis components and lipid metabolism indicators.
- Assessment of Remaxol's therapeutic effect in a subgroup.
Main Results:
- Early, pronounced changes in humoral and tissue hemostasis were observed in all studied conditions.
- Coagulation system modifications occurred in both affected and target organs.
- Membrane destabilization, driven by phospholipid changes and lipid peroxidation, triggers the hemostatic cascade.
- A new syndrome, systemic coagulopathic distress syndrome, was defined based on these findings.
Conclusions:
- Systemic coagulopathic distress syndrome involves phospholipid bilayer disruption due to oxidative and phospholipase activity, leading to coagulopathy.
- This understanding shifts prevention strategies for thrombohemorrhagic complications.
- Complex therapy, including membrane-stabilizing agents like Remaxol, is effective.