From the Department of Surgery, University of Cincinnati, Cincinnati, Ohio.
J Trauma Acute Care Surg. 2022 Jan 1;92(1):12-20. doi: 10.1097/TA.0000000000003433.
The combined injury of traumatic brain injury and hemorrhagic shock has been shown to worsen coagulopathy and systemic inflammation, thereby increasing posttraumatic morbidity and mortality. Aeromedical evacuation to definitive care may exacerbate postinjury morbidity because of the inherent hypobaric hypoxic environment. We hypothesized that blood product resuscitation may mitigate the adverse physiologic effects of postinjury flight.
An established porcine model of controlled cortical injury was used to induce traumatic brain injury. Intracerebral monitors were placed to record intracranial pressure, brain tissue oxygenation, and cerebral perfusion. Each of the 42 pigs was hemorrhaged to a goal mean arterial pressure of 40 ± 5 mm Hg for 1 hour. Pigs were grouped according to resuscitation strategy used-Lactated Ringer's (LR) or shed whole blood (WB)-then placed in an altitude chamber for 2 hours at ground, 8,000 ft, or 22,000 ft, and then observed for 4 hours. Hourly blood samples were analyzed for proinflammatory cytokines and lactate. Internal jugular vein blood flow was monitored continuously for microbubble formation with altitude changes.
Cerebral perfusion, tissue oxygenation, and intracranial pressure were unchanged among the six study groups. Venous microbubbles were not observed even with differing altitude or resuscitation strategy. Serum lactate levels from hour 2 of flight to the end of observation were significantly elevated in 22,000 + LR compared with 8,000 + LR and 22,000 + WB. Serum IL-6 levels were significantly elevated in 22,000 + LR compared with 22,000 + WB, 8,000 + LR and ground+LR at hour 1 of observation. Serum tumor necrosis factor-α was significantly elevated at hour 2 of flight in 8,000 + LR versus ground+LR, and in 22,000 + LR vs. 22,000 + WB at hour 1 of observation. Serum IL-1β was significantly elevated hour 1 of flight between 8,000 + LR and ground+LR.
Crystalloid resuscitation during aeromedical transport may cause a prolonged lactic acidosis and proinflammatory response that can predispose multiple-injury patients to secondary cellular injury. This physiologic insult may be prevented by using blood product resuscitation strategies.
创伤性脑损伤和出血性休克的联合损伤已被证明会加重凝血障碍和全身炎症,从而增加创伤后的发病率和死亡率。航空医疗后送至确定性治疗可能会因固有低气压低氧环境而加重伤后发病率。我们假设血液制品复苏可能减轻受伤后飞行的不良生理影响。
使用已建立的猪控制性皮质损伤模型诱导创伤性脑损伤。放置颅内监测仪以记录颅内压、脑组织氧合和脑灌注。42 头猪中的每头猪均出血至目标平均动脉压 40±5mmHg 持续 1 小时。根据使用的复苏策略将猪分为乳酸林格氏液(LR)或输失血(WB)组,然后将其置于地面、8000 英尺和 22000 英尺的高原舱内 2 小时,然后观察 4 小时。每小时采集血样分析促炎细胞因子和乳酸。随着海拔变化连续监测颈内静脉血流以监测微泡形成。
在六个研究组中,脑灌注、组织氧合和颅内压均无变化。即使在不同的海拔或复苏策略下,也未观察到静脉微泡。与 8000+LR 和 22000+WB 相比,22000+LR 从飞行的第 2 小时到观察结束时的血清乳酸水平显著升高。与 22000+WB、8000+LR 和地面+LR 相比,22000+LR 在观察的第 1 小时时血清 IL-6 水平显著升高。与地面+LR 相比,8000+LR 在飞行的第 2 小时时血清肿瘤坏死因子-α水平显著升高,与 22000+WB 相比,在观察的第 1 小时时血清肿瘤坏死因子-α水平显著升高。与地面+LR 相比,8000+LR 在飞行的第 1 小时时血清 IL-1β水平显著升高。
航空医疗运输期间的晶体液复苏可能导致乳酸酸中毒和促炎反应延长,从而使多发伤患者易发生继发性细胞损伤。通过使用血液制品复苏策略可以预防这种生理损伤。