Rosengart Matthew R, Nathens Avery B, Arbabi Saman, Neff Margaret J, Garcia Iris, Martin Thomas R, Maier Ronald V
Department of Surgery, University of Washington, Seattle, USA.
Ann Surg. 2003 Jan;237(1):94-100. doi: 10.1097/00000658-200301000-00013.
To evaluate the prognostic significance of the activational status of p38, specifically progression to multiple organ dysfunction syndrome (MODS), in a group of severely injured trauma patients.
To date, therapeutic manipulation of the host immunoinflammatory response has not affected the outcome of patients with MODS. A major concern is the inability to identify the patient most at risk so as to enable early intervention.
Nineteen trauma patients underwent bronchoalveolar lavage (BAL). Cells obtained were plated, stimulated with lipopolysaccharide (LPS), and then harvested at varying time points after stimulation. p38 was evaluated by Western blot.
Nineteen patients were categorized into two groups according to baseline and LPS-stimulated p38 activation in cells obtained by BAL. Group 1 demonstrated a 10-fold increase in p38 activation with LPS treatment over unstimulated controls. Group 2 had high baseline levels of p38 that were unresponsive to subsequent LPS stimulation. Both groups were similar with respect to age, gender, shock (systolic blood pressure < 90), Injury Severity Score, APACHE II, lactate levels, base deficit, blood transfusions, and the cell differential of BAL fluid. However, patients in group 2 had a greater incidence of progression to MODS as defined by the Marshall MOD score, a longer duration of mechanical ventilation, a longer stay in the intensive care unit, and a longer overall hospital stay than group 1.
These results demonstrate the prognostic significance of p38 activation in predicting outcome in critically ill trauma patients. Furthermore, these results demonstrate that trauma populations identical by current scoring systems contain a mixture of patients with markedly different outcomes as identified by p38 activation. Measurement of p38 may enable early identification of a subgroup of patients at increased risk for MODS to permit effective therapeutic intervention.
评估p38激活状态,特别是进展为多器官功能障碍综合征(MODS),在一组严重创伤患者中的预后意义。
迄今为止,对宿主免疫炎症反应的治疗性干预尚未影响MODS患者的预后。一个主要问题是无法识别风险最高的患者以便进行早期干预。
19例创伤患者接受了支气管肺泡灌洗(BAL)。获取的细胞进行接种,用脂多糖(LPS)刺激,然后在刺激后的不同时间点收获。通过蛋白质印迹法评估p38。
根据BAL获取的细胞中基线和LPS刺激后的p38激活情况,将19例患者分为两组。第1组显示LPS处理后p38激活比未刺激的对照组增加了10倍。第2组p38基线水平高,对随后的LPS刺激无反应。两组在年龄、性别、休克(收缩压<90)、损伤严重度评分、急性生理与慢性健康状况评分系统II(APACHE II)、乳酸水平、碱缺失、输血以及BAL液细胞分类方面相似。然而,根据马歇尔MOD评分定义,第2组患者进展为MODS的发生率更高,机械通气时间更长,在重症监护病房停留时间更长,总体住院时间比第1组长。
这些结果证明了p38激活在预测重症创伤患者预后方面的预后意义。此外,这些结果表明,目前评分系统相同的创伤人群包含了通过p38激活识别出的结局明显不同的患者混合群体。测量p38可能有助于早期识别MODS风险增加的患者亚组,以便进行有效的治疗干预。