From the Institute of Anesthesiology, University and University Hospital Zurich, Zurich, Switzerland; Division of Biostatistics, Institute of Social and Preventive Medicine, University of Zurich, Zurich, Switzerland; and Schutz und Rettung Stadt Zürich, Zurich, Switzerland.
Anesth Analg. 2015 Mar;120(3):627-635. doi: 10.1213/ANE.0000000000000561.
When trauma patients arrive in the emergency department (ED), coagulopathy frequently is present. The time course, however, in which this coagulopathy develops is poorly understood. No study has fully evaluated the coagulation status, including thromboelastometry on-scene and at hospital arrival. We hypothesized that measured coagulation variables might change when measured at the scene of injury and upon arrival to the ED.
We performed a prospective, single-center, observational study investigating coagulation status in 50 trauma patients on-scene and at arrival in the ED. Measurements included arterial blood gases, ROTEM®, protein S100, protein C activity, protein S, Quick value, international normalized ratio, activated partial thromboplastin time, D-dimer, coagulation factor V (FV), coagulation factor XIII (FXIII), fibrinogen, hemoglobin, hematocrit, platelets, and volume and blood products being administered during the first 24 hours.
Significant changes between on-scene and the ED were observed for the following values: partial venous oxygen pressure increased and sodium, glucose, and lactate decreased. For EXTEM, INTEM, and APTEM, clotting time and clot formation time increased significantly, whereas maximal clot firmness and angle α decreased significantly (all P ≤ 0.004). For FIBTEM, clotting time increased significantly and maximal clot firmness decreased significantly. In the laboratory, significant reductions in hemoglobin, hematocrit, platelets, activated partial thromboplastin time, fibrinogen, FV, FXIII, protein C activity, protein S, and protein S100 were observed (all P ≤ 0.001).
Although most all laboratory and rotational thromboelastometry coagulation tests worsened over time when measured on-scene and in the ED, monitoring coagulation at the scene of trauma does not provide clinically important information in a majority of trauma patients. One hour after injury, significant activation and consumption of fibrinogen, FV, FXIII, protein C activity, and protein S were observed.
当创伤患者到达急诊科 (ED) 时,通常会出现凝血功能障碍。然而,这种凝血功能障碍的发展过程尚不清楚。没有研究充分评估过包括血栓弹性描记术在内的凝血状态,无论是在现场还是在到达 ED 时。我们假设,在受伤现场和到达 ED 时测量的凝血变量可能会发生变化。
我们进行了一项前瞻性、单中心、观察性研究,调查了 50 例创伤患者在现场和到达 ED 时的凝血状态。测量包括动脉血气、ROTEM®、S100 蛋白、蛋白 C 活性、蛋白 S、Quick 值、国际标准化比值、活化部分凝血活酶时间、D-二聚体、凝血因子 V (FV)、凝血因子 XIII (FXIII)、纤维蛋白原、血红蛋白、血细胞比容、血小板以及在最初 24 小时内给予的容量和血液制品。
现场和 ED 之间的以下值存在显著变化:部分静脉血氧分压升高,钠、葡萄糖和乳酸降低。对于 EXTEM、INTEM 和 APTEM,凝血时间和凝块形成时间显著增加,而最大凝块硬度和α角显著降低(所有 P ≤ 0.004)。对于 FIBTEM,凝血时间显著增加,最大凝块硬度显著降低。在实验室中,血红蛋白、血细胞比容、血小板、活化部分凝血活酶时间、纤维蛋白原、FV、FXIII、蛋白 C 活性、蛋白 S 和 S100 蛋白显著减少(所有 P ≤ 0.001)。
尽管大多数实验室和旋转血栓弹性描记术凝血试验在现场和 ED 测量时随时间恶化,但在大多数创伤患者中,在创伤现场监测凝血并不能提供临床重要信息。在受伤后 1 小时,观察到纤维蛋白原、FV、FXIII、蛋白 C 活性和蛋白 S 的显著激活和消耗。