Department of Clinical Science and Education, Södersjukhuset, Stockholm, Sweden.
Department of Neuroscience, Karolinska Institutet, Stockholm, Sweden.
Exp Lung Res. 2020 May-Jun;46(5):117-127. doi: 10.1080/01902148.2020.1742252. Epub 2020 Mar 17.
Severe thoracic trauma affects 55% of patients with multiple traumatic injuries and may lead to acute lung injury or acute respiratory distress syndrome. Pulmonary trauma differs clinically and biologically from lung injury of other origins and carries a mortality rate of 10%. Treatment options are limited, and it is not possible to monitor the progression of lung injury with specific biomarkers. Microdialysis of pleural fluid may offer a viable entry to monitor the lung directly and specifically. Bronchial microdialysis has been described, but not pleural microdialysis. We therefore investigated the feasibility of microdialysis of pleural fluid, and its ability to detect pulmonary injury and inflammation in the pleural cavity after traumatic acute lung injury. 16 pigs (mean weight 64 kg) were randomized to groups "exposed with MD", receiving a focally severe pulmonary contusion and microdialysis (n = 7), "control with MD", receiving only microdialysis and no pulmonary contusion (n = 5), "normal no MD" receiving only anesthesia (n = 2) and "naïve no MD" (no instrumentation) (n = 2). Microdialysate from the pleura and the perilesional subcutis, plasma and bronchoalveolar lavage were collected for 5 hours. Pleura lactate, plasma lactate and pleura lactate/pyruvate ratio increased in injured lungs ( < 0.05). Subcutis and plasma glucose increased after trauma ( < 0.05). Pleura glycerol increased although not reaching statistical significance. IL-6 and IL-8 were dissimilar in plasma, bronchoalveolar lavage and pleural fluid, while IL-1 did not differ. Neutrophils increased in bronchoalveolar lavage ( < 0.001) after trauma, and in pleural fluid, although not when the microdialysis catheter was omitted. Pleural microdialysis was technically feasible and detected signs of cellular injury and anaerobic metabolism after focally severe pulmonary contusion and may be of interest for future clinical applications. The microdialysis catheter triggered a recruitment of neutrophils to the pleura which needs to be elucidated further before taking the technique into clinical practice.
严重的胸部创伤影响 55%的多发创伤患者,可能导致急性肺损伤或急性呼吸窘迫综合征。肺部创伤在临床上和生物学上与其他来源的肺损伤不同,死亡率为 10%。治疗选择有限,并且无法使用特定的生物标志物监测肺损伤的进展。胸腔液的微透析可能提供了一种可行的途径,可以直接和特异性地监测肺部。支气管微透析已经被描述过,但胸腔液微透析还没有。因此,我们研究了胸腔液微透析的可行性,以及其在创伤性急性肺损伤后检测胸腔内肺损伤和炎症的能力。16 头猪(平均体重 64 公斤)随机分为“暴露于 MD 组”(接受局灶性严重肺挫伤和微透析,n=7)、“MD 对照组”(仅接受微透析而不接受肺挫伤,n=5)、“正常无 MD 组”(仅接受麻醉,n=2)和“未处理无 MD 组”(无仪器)(n=2)。采集胸膜和胸膜旁皮下组织、血浆和支气管肺泡灌洗液 5 小时。损伤肺中的胸膜乳酸、血浆乳酸和胸膜乳酸/丙酮酸比值增加( < 0.05)。创伤后皮下组织和血浆葡萄糖增加( < 0.05)。胸膜甘油增加,但无统计学意义。IL-6 和 IL-8 在血浆、支气管肺泡灌洗液和胸膜液中的水平不同,而 IL-1 则无差异。创伤后支气管肺泡灌洗液中的中性粒细胞增加( < 0.001),而在胸膜液中增加,但当微透析导管被省略时则没有增加。胸膜微透析技术上是可行的,可检测局灶性严重肺挫伤后细胞损伤和无氧代谢的迹象,可能对未来的临床应用有兴趣。微透析导管引发中性粒细胞向胸膜募集,这需要进一步阐明,然后才能将该技术应用于临床实践。