Department of Trauma, Hand and Reconstructive Surgery, Goethe University, Frankfurt, Germany.
Institute for Biostatistics and Mathematical Modeling, Goethe University, Frankfurt, Germany.
Shock. 2023 Sep 1;60(3):392-399. doi: 10.1097/SHK.0000000000002186. Epub 2023 Aug 4.
Background: Pneumonia is a frequent complication after polytrauma. This study aims to evaluate the ability of different serum markers to identify patients at risk of developing pneumonia after polytrauma. Methods: A retrospective analysis of prospectively collected data in polytraumatized patients with concomitant thoracic trauma (Injury Severity Score ≥16, Abbreviated Injury Scale Thorax ≥ 3) was performed. The study cohort was divided into patients with and without pneumonia during the clinical course. Serum levels of lung epithelial (CYFRA 21-1), endothelial (Ang-2), and inflammatory (PTX-3, sRAGE, IL-6, IL-10) markers were measured upon arrival in the trauma room and on days 2 and 5. Results: A total of 73 patients and 16 healthy controls were included in this study. Of these, 20 patients (27.4%) developed pneumonia. Polytraumatized patients showed significantly increased CYFRA 21-1 levels with a distinct peak after admission compared with healthy controls. Serum PTX-3 significantly increased on day 2 in polytraumatized patients compared with healthy controls. Injury Severity Score and demographic parameters were comparable between both groups (pneumonia vs. no pneumonia). No statistically significant difference could be observed for serum levels of CYFRA 21-1, Ang-2, PTX-3, sRAGE, IL-6, and IL-10 between the groups (pneumonia vs. no pneumonia) on all days. Logistic regression revealed a combination of IL-6, IL-10, sRAGE, and PTX-3 to be eventually helpful to identify patients at risk of developing pneumonia and our newly developed score was significantly higher on day 0 in patients developing pneumonia ( P < 0.05). Conclusion: The investigated serum markers alone are not helpful to identify polytraumatized patients at risk of developing pneumonia, while a combination of IL-6, IL-10, PTX-3, and sRAGE might be.
肺炎是多发创伤后的常见并发症。本研究旨在评估不同血清标志物识别多发创伤合并胸部创伤患者(创伤严重度评分≥16 分,胸部分值损伤量表≥3 分)发生肺炎风险的能力。
对多发创伤患者前瞻性采集的数据进行回顾性分析,患者伴有胸部创伤(创伤严重度评分≥16 分,胸部分值损伤量表≥3)。将研究队列分为临床病程中发生肺炎的患者和未发生肺炎的患者。在创伤室到达时和第 2 天及第 5 天,测定血清肺上皮(细胞角蛋白 19 片段 21-1,CYFRA 21-1)、内皮(血管生成素 2,Ang-2)和炎症(人三叶因子,PTX-3,可溶性晚期糖基化终产物受体,IL-6,IL-10)标志物的水平。
共纳入 73 例患者和 16 例健康对照者。其中,20 例(27.4%)患者发生肺炎。与健康对照组相比,多发创伤患者的 CYFRA 21-1 水平明显升高,入院后有明显峰值。与健康对照组相比,多发创伤患者在第 2 天 PTX-3 血清水平明显升高。两组的创伤严重度评分和人口统计学参数均无差异(肺炎组与非肺炎组)。在所有时间点,两组患者的 CYFRA 21-1、Ang-2、PTX-3、sRAGE、IL-6 和 IL-10 血清水平均无统计学差异(肺炎组与非肺炎组)。Logistic 回归显示,IL-6、IL-10、sRAGE 和 PTX-3 的组合最终有助于识别发生肺炎的风险患者,且在发生肺炎的患者中,在第 0 天新开发的评分明显更高(P<0.05)。
单独检测这些血清标志物无助于识别发生肺炎风险的多发创伤患者,而 IL-6、IL-10、PTX-3 和 sRAGE 的组合可能有助于识别。