Hemocoagulation Disorders and Intoxication in Severe Acute Post-Manipulation Pancreatitis in the Experiment

M. I. Prudkov, M. Rantsev, P. Sarapultsev, O. Chupakhin
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Abstract

Introduction. Acute post-manipulation pancreatitis (APMP) is a frequent complication aſter interventions on the major duodenal papilla. The APMP incidence reaches 15 %, of which 5–10 % are severe. The goal of the research is to determine the possibility of correcting hemocoagulation disorders and reducing endogenous toxemia syndrome severity in APMP.Materials and methods. A comparative study was performed in 40 animals (nonlinear albino rats) with severe acute pancreatitis on APMP experimental model. L-17 compound from a new group of organic compounds substituted thiadiazines at a daily dose of 40 mg/kg was used.Results. The development of hemocoagulation disorders and severe toxemia in animals with an experimental model of APMP has been shown. The indicators of the severity of hemocoagulation disorders and toxemia were studied in experimental APMP against the background of the introduction of the compound L-17 from the group of substituted thiadiazines.Discussion. The course of APMP in the experiment is accompanied by the development of severe hemocoagulation disorders and severe toxemia. Effective indicators reflecting the severity of APLP are D-dimers (hemocoagulation) and albumin binding capacity (toxemia).Conclusion. The course of experimental severe APMP is accompanied by pronounced hemocoagulation disorders development involved in the pathogenesis and progression of multiple organ dysfunction, that is characterized by a high level of endogenous toxemia. The course of experimental APMP against the background of the introduction of the compound L-17 is marked by a decrease in the severity of hemocoagulation disorders and the level of endogenous toxemia.
实验中操纵后严重急性胰腺炎的血凝障碍和中毒现象
导言。操作后急性胰腺炎(APMP)是十二指肠大乳头手术后的常见并发症。APMP 发病率高达 15%,其中 5-10% 为重症。研究的目的是确定纠正血凝障碍和降低 APMP 内源性毒血症综合征严重程度的可能性。在 APMP 实验模型上对 40 只患有重症急性胰腺炎的动物(非线性白化大鼠)进行了比较研究。研究使用了一种新的有机化合物取代噻二嗪类的 L-17 化合物,每日剂量为 40 毫克/千克。结果表明,在 APMP 实验模型中,动物出现了血凝障碍和严重毒血症。在引入取代噻二嗪类化合物 L-17 的背景下,研究了实验性 APMP 中血凝障碍和毒血症严重程度的指标。在实验中,APMP的病程伴随着严重的凝血功能障碍和毒血症。反映APLP严重程度的有效指标是D-二聚体(血凝)和白蛋白结合能力(毒血症)。实验性重度APLP的病程伴随着明显的血凝障碍发展,参与了多器官功能障碍的发病和进展,其特点是高水平的内源性毒血症。在引入化合物L-17的背景下,实验性APMP的病程表现为血凝障碍的严重程度和内源性毒血症水平的降低。
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