可溶性纤维蛋白单体复合物和d -二聚体作为急性胰腺炎严重程度的指标

S. Chooklin, B. Pidhirnyi, R. Barylyak
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To study the dynamics of D-dimers, soluble fibrin-monomeric complexes in the blood of patients with acute pancreatitis, depending on the severity of the disease. Materials and methods. A prospective examination of 206 patients with AP was carried out. According to the criteria of the International Classification, mild pancreatitis was verified in 51 patients, moderate – in 98, severe – in 57. The concentration of SFMK, D-dimers was determined in 66 patients with AP on the first, third, seventh and fourteenth days of conservative treatment. The reference values were estimated in 11 healthy individuals. Results. The enhansed concentration of SFMK and D-dimers were detected in the blood of all patients under examination. 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引用次数: 0

摘要

介绍。局部和全身性炎症、止血系统紊乱是急性胰腺炎(AP)发病机制的关键组成部分,已经处于早期阶段,并在未来发展为血栓出血性并发症。AP患者的全身性止血障碍程度不一,从亚临床凝血激活(只能通过凝血因子激活的敏感标志物检测)到暴发性弥散性血管内凝血综合征(以多发全身微血管血栓形成和不同部位大量出血为特征)。已经证明,d -二聚体和可溶性纤维蛋白单体复合物(SFMK)是凝血和纤维蛋白溶解激活的有价值的标志物。研究的目的。研究d -二聚体,可溶性纤维蛋白单体复合物在急性胰腺炎患者血液中的动力学,这取决于疾病的严重程度。材料和方法。对206例AP患者进行前瞻性检查。根据国际分类标准,51例确诊为轻度胰腺炎,98例确诊为中度胰腺炎,57例确诊为重度胰腺炎。测定66例AP患者保守治疗第1、3、7、14天的SFMK、d -二聚体浓度。在11名健康个体中估计参考值。结果。所有接受检查的患者血液中均检测到SFMK和d -二聚体浓度升高。它们的含量与Ranson和BISAP评分确定的AP病程严重程度、APACHE II评分确定的患者病情严重程度、SOFA评分确定的器官功能障碍程度以及Balthazar标准确定的胰腺损害程度直接相关。SFMK和d -二聚体的浓度随着呼吸、心血管、肾脏和代谢功能障碍的发生而显著升高。确定SFMK的量与AP患者血肌酐、葡萄糖浓度有可靠的直接相关关系。d -二聚体水平升高与血清肌酐浓度有显著的直接相关关系。SFMK检测(cut-of value 137.50 ng/L)预测肺功能障碍的敏感性为86.20%,特异性为83.80%,阳性预测值为80.65%,阴性预测值为88.57%。结论。急性胰腺炎病程伴局部或全身性炎症、止血系统改变,其严重程度与疾病的严重程度相关。重症急性胰腺炎患者的特征是全身性炎症与促凝剂改变的结合。急性胰腺炎的严重程度、患者病情和器官功能障碍的严重程度、胰腺病变的严重程度与纤维蛋白降解产物的增加有关。可溶性纤维蛋白单体复合物的浓度可用于预测急性胰腺炎患者的肺功能障碍。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Soluble Fibrin-monomeric Complexes and D-dimers as Indicators of Acute Pancreatitis Severity
Introduction. Local and systemic inflammation, disorders in the hemostatic system are among the key components of acute pancreatitis (AP) pathogenesis already in its early stages, and in future development of thrombohemorrhagic complications. The degree of systemic hemostatic disorders in AP varies from subclinical activation of coagulation, which can only be detected using sensitive markers of activation of coagulation factors, to fulminant disseminated intravascular coagulation syndrome, characterized by multiple systemic microvascular thrombosis and profuse bleeding from different sites. It has been proven that D-dimers and soluble fibrin-monomeric complexes (SFMK) are valuable markers of coagulation and fibrinolysis activation. The aim of the study. To study the dynamics of D-dimers, soluble fibrin-monomeric complexes in the blood of patients with acute pancreatitis, depending on the severity of the disease. Materials and methods. A prospective examination of 206 patients with AP was carried out. According to the criteria of the International Classification, mild pancreatitis was verified in 51 patients, moderate – in 98, severe – in 57. The concentration of SFMK, D-dimers was determined in 66 patients with AP on the first, third, seventh and fourteenth days of conservative treatment. The reference values were estimated in 11 healthy individuals. Results. The enhansed concentration of SFMK and D-dimers were detected in the blood of all patients under examination. Their content directly correlated with the severity of AP course as determined by the Ranson and BISAP score, the severity of the patient’s condition by the APACHE II score and organ dysfunction by the SOFA score, and the degree of damage to the pancreas by the Balthazar criteria. The concentration of SFMK and D-dimers significantly increased with the occurrence of respiratory, cardiovascular, renal, and metabolic dysfunction. A reliable direct correlation was determined between the amount of SFMK and the concentration of creatinine and glucose in the blood of patients with AP. The increase in the level of D-dimers significantly directly correlated with the concentration of creatinine in the blood serum. The sensitivity of SFMK determination (cut-of value 137.50 ng/L) for predicting pulmonary dysfunction was 86.20 %, and the specificity was 83.80 %, with positive and negative predictive values of 80.65 and 88.57 % respectively. Conclusions. The course of acute pancreatitis is accompanied by local or systemic inflammation, changes in the hemostatic system, severity of which correlating with the severity of the disease. Characteristic feature for patients with severe acute pancreatitis is the combination of systemic inflammation with procoagulant changes. The severity of acute pancreatitis, the severity of patient’s condition and organ dysfunction, the severity of pancreatic lesions are associated with an increase of fibrin degradation products. The concentration of soluble fibrin-monomeric complexes can be used to predict pulmonary dysfunction in patients with acute pancreatitis.
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