Suppr超能文献

脓毒症中组织因子生成未被组织因子途径抑制物平衡,会导致预后不良。

Tissue factor production not balanced by tissue factor pathway inhibitor in sepsis promotes poor prognosis.

作者信息

Gando Satoshi, Kameue Takashi, Morimoto Yuji, Matsuda Naoyuki, Hayakawa Mineji, Kemmotsu Osamu

机构信息

Department of Anesthesiology and Critical Care Medicine, Hokkaido University Graduate School of Medicine, Kita-ku, Sapporo, Japan.

出版信息

Crit Care Med. 2002 Aug;30(8):1729-34. doi: 10.1097/00003246-200208000-00009.

Abstract

OBJECTIVE

To determine the precise relationship among tissue factor, tissue factor pathway inhibitor (TFPI), and neutrophil elastase in sepsis, as well as to test the hypothesis that low TFPI concentrations are not sufficient to prevent tissue factor-dependent intravascular coagulation, leading to multiple organ dysfunction syndrome and death.

DESIGN

Prospective, cohort study.

SETTING

General intensive care unit of tertiary care emergency department.

PATIENTS

Thirty-one consecutive patients with sepsis, classified as 15 survivors and 16 nonsurvivors. Ten normal, healthy volunteers served as controls.

INTERVENTIONS

None.

MEASUREMENTS AND MAIN RESULTS

Tissue factor antigen concentration (tissue factor), TFPI, neutrophil elastase, and global variables of coagulation and fibrinolysis were measured on the day of diagnosis of sepsis, severe sepsis, and septic shock and days on 1-4 after diagnosis. The number of systemic inflammatory response syndrome criteria that patients met and the disseminated intravascular coagulation score were determined simultaneously. The results of these measurements were compared between the survivors and the nonsurvivors. In the nonsurvivors, significantly higher concentrations of tissue factor and neutrophil elastase were found compared with the survivors and control subjects. However, the TFPI values showed no difference between the two groups. No correlation was found between the peak concentrations of tissue factor and TFPI. Disseminated intravascular coagulation scores and numbers of the SIRS criteria met by the survivors significantly decreased from day 0 to day 4, but those of the nonsurvivors did not improve during the study period. The nonsurvivors showed thrombocytopenia and higher numbers of dysfunctioning organs than did the survivors.

CONCLUSIONS

We systematically elucidated the relationship between tissue factor and TFPI in patients with sepsis, severe sepsis, and septic shock. Activation of tissue factor-dependent coagulation pathway not adequately balanced by TFPI has important roles in sustaining DIC and systemic inflammatory response syndrome, and it contributes to multiple organ dysfunction syndrome and death. High concentrations of neutrophil elastase released from activated neutrophils may explain, in part, the imbalance of tissue factor and TFPI in sepsis.

摘要

目的

确定脓毒症中组织因子、组织因子途径抑制剂(TFPI)和中性粒细胞弹性蛋白酶之间的确切关系,并验证低TFPI浓度不足以预防组织因子依赖性血管内凝血,进而导致多器官功能障碍综合征和死亡这一假说。

设计

前瞻性队列研究。

地点

三级护理急诊科的综合重症监护病房。

患者

31例连续的脓毒症患者,分为15例幸存者和16例非幸存者。10名正常健康志愿者作为对照。

干预措施

无。

测量指标及主要结果

在脓毒症、严重脓毒症和感染性休克诊断当天以及诊断后1 - 4天,测量组织因子抗原浓度(组织因子)、TFPI、中性粒细胞弹性蛋白酶以及凝血和纤溶的整体变量。同时确定患者符合的全身炎症反应综合征标准数量和弥散性血管内凝血评分。比较幸存者和非幸存者的这些测量结果。在非幸存者中,与幸存者和对照受试者相比,发现组织因子和中性粒细胞弹性蛋白酶浓度显著更高。然而,两组间TFPI值无差异。组织因子和TFPI的峰值浓度之间未发现相关性。幸存者的弥散性血管内凝血评分和符合的SIRS标准数量从第0天到第4天显著下降,但非幸存者在研究期间未改善。非幸存者比幸存者表现出血小板减少和更多功能障碍的器官。

结论

我们系统地阐明了脓毒症、严重脓毒症和感染性休克患者中组织因子与TFPI之间的关系。TFPI未能充分平衡组织因子依赖性凝血途径的激活在维持弥散性血管内凝血和全身炎症反应综合征中起重要作用,并导致多器官功能障碍综合征和死亡。活化的中性粒细胞释放的高浓度中性粒细胞弹性蛋白酶可能部分解释了脓毒症中组织因子和TFPI的失衡。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验