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感染性休克期间高迁移率族蛋白B1的血浆浓度

High-mobility group box 1 protein plasma concentrations during septic shock.

作者信息

Gibot Sébastien, Massin Frédéric, Cravoisy Aurélie, Barraud Damien, Nace Lionel, Levy Brune, Bollaert Pierre-Edouard

机构信息

Hôpital Central, Service de Réanimation Médicale, 29 avenue du Maréchal de Lattre de Tassigny, 54000, Nancy, France.

出版信息

Intensive Care Med. 2007 Aug;33(8):1347-53. doi: 10.1007/s00134-007-0691-2. Epub 2007 May 25.

Abstract

OBJECTIVE

To investigate plasma high-mobility group box 1 protein (HMGB1) concentration and its relationship with organ dysfunction and outcome in septic shock patients.

DESIGN AND SETTING

Prospective, noninterventional study. Medical adult intensive care unit at a university hospital in France.

PATIENTS

42 critically ill patients with septic shock.

METHODS

Arterial blood was drawn within 12 h of admission for the measurement of plasma HMGB1 concentration by ELISA. Repeated sampling was performed on days 3, 7, and 14.

RESULTS

Median HMGB1 concentration was 4.4 ng/ml (IQR 1.2-12.5) at admission, with no difference between survivors and nonsurvivors. A positive correlation was observed between HMGB1 and SOFA score and lactate, and procalcitonin concentrations. There was a progressive but statistically nonsignificant decline in HMGB1 concentration among the survivors, while nonsurvivors showed an increase in HMGB1 level between days 1 and 3. SOFA score and lactate and procalcitonin concentrations did not vary significantly between days 1 and 3. When measured on day 3, HMGB1 discriminated survivors from nonsurvivors with 66% sensitivity and 67% specificity, and concentration greater than 4 ng/ml was associated with an odds ratio of death of 5.5 (95% CI 1.3-23.6).

摘要

目的

探讨脓毒性休克患者血浆高迁移率族蛋白B1(HMGB1)浓度及其与器官功能障碍和预后的关系。

设计与背景

前瞻性、非干预性研究。法国一家大学医院的内科成人重症监护病房。

患者

42例脓毒性休克重症患者。

方法

入院后12小时内采集动脉血,采用酶联免疫吸附测定法(ELISA)检测血浆HMGB1浓度。在第3、7和14天进行重复采样。

结果

入院时HMGB1浓度中位数为4.4 ng/ml(四分位间距1.2 - 12.5),存活者与非存活者之间无差异。观察到HMGB1与序贯器官衰竭评估(SOFA)评分、乳酸及降钙素原浓度呈正相关。存活者中HMGB1浓度呈逐渐下降趋势,但无统计学意义,而非存活者在第1天至第3天HMGB1水平升高。第1天至第3天SOFA评分、乳酸及降钙素原浓度无显著变化。在第3天测量时,HMGB1区分存活者与非存活者的敏感度为66%,特异度为67%,浓度大于4 ng/ml时死亡比值比为5.5(95%可信区间1.3 - 23.6)。

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