From the University of Wisconsin School of Medicine & Public Health, Madison, WI (Savage, Zarzaur, Carney, Do).
University of Texas Health Science Center at Houston, Houston, TX (Fox, Wade).
J Am Coll Surg. 2023 Aug 1;237(2):259-269. doi: 10.1097/XCS.0000000000000678. Epub 2023 Mar 15.
Acute traumatic coagulopathy (ATC) has many phenotypes and varying morbidity and mortality. The MA-R ratio, calculated from the admission thromboelastogram, serves as a biomarker to identify 1 phenotype of ATC and has previously been associated with significant derangements in the inflammatory response. This study evaluates outcomes related to abnormal MA-R ratios, including inflammatory responses, in a heterogeneous patient population.
Patients from the Pragmatic, Randomized Optimal Platelet and Plasma Ratios (PROPPR) dataset were included. The MA-R ratio was calculated from admission thromboelastography, with a CRITICAL ratio defined as 11 or less. Key inflammatory mediators were identified as a priori. Cytokine expression was assessed during 24 hours using multivariable logistic regression.
Significant elevations in the proinflammatory cytokines IL-1b, IL-6, and IL-8, as well as in the chemokines eotaxin, IFN-γ-induced protein 10, monocyte chemoattractant protein-1, and macrophage inflammatory protein-1β, persisted during the first 24 hours. CRITICAL patients had significantly lower survival at 1, 3, 6, 12, and 18 hours and demonstrated significantly increased ARDS (odds ratio [OR] 1.817, 95% CI 1.082 to 3.051, p = 0.0239). CRITICAL patients had fewer ICU-free days (CRITICAL, 10 days, interquartile range [IQR] 0 to 25; vs NORMAL, 22 days, IQR 4 to 26, p < 0.0001) and fewer ventilator-free days (CRITICAL, 15 days, IQR 0 to 28; vs NORMAL, 26 days, IQR 9 to 28, p < 0.0001). CRITICAL patients were protected against systemic inflammatory response (OR 0.521, 95% CI 0.322 to 0.816, p = 0.0044).
The subtype of ATC identified by the low MA-R ratio is associated with significant elevations in multiple proinflammatory cytokines at admission. Early mortality remains elevated in the CRITICAL group, in part due to coagulopathy. The MA-R ratio at admission is associated with a particularly morbid type of coagulopathy, associated with significant alterations in the inflammatory response after severe injury in heterogeneous patient populations.
急性创伤性凝血病(ATC)有多种表型,发病率和死亡率也各不相同。入院时血栓弹性图计算出的 MA-R 比值可作为一种生物标志物,用于识别 ATC 的一种表型,并且之前与炎症反应的显著失调有关。本研究评估了与异常 MA-R 比值相关的结局,包括炎症反应,这些结局在异质患者群体中存在。
纳入 Pragmatic,Randomized Optimal Platelet and Plasma Ratios(PROPPR)数据集的患者。入院时通过血栓弹性图计算 MA-R 比值,临界比值定义为 11 或更低。关键的炎症介质作为先验确定。使用多变量逻辑回归在 24 小时内评估细胞因子表达。
在最初的 24 小时内,促炎细胞因子 IL-1b、IL-6 和 IL-8,以及趋化因子 eotaxin、IFN-γ诱导蛋白 10、单核细胞趋化蛋白-1 和巨噬细胞炎症蛋白-1β 的表达显著升高。临界值患者在 1、3、6、12 和 18 小时的生存率显著降低,并表现出显著增加的急性呼吸窘迫综合征(OR 1.817,95%CI 1.082 至 3.051,p = 0.0239)。临界值患者 ICU 无天数(临界值,10 天,四分位距[IQR] 0 至 25;与正常,22 天,IQR 4 至 26,p < 0.0001)和无呼吸机天数(临界值,15 天,IQR 0 至 28;与正常,26 天,IQR 9 至 28,p < 0.0001)较少。临界值患者对全身炎症反应有保护作用(OR 0.521,95%CI 0.322 至 0.816,p = 0.0044)。
低 MA-R 比值确定的 ATC 亚类与入院时多种促炎细胞因子的显著升高有关。在临界组中,早期死亡率仍然较高,部分原因是凝血障碍。入院时的 MA-R 比值与严重创伤后异质患者群体中凝血障碍的一种特别严重的类型有关,与炎症反应的显著改变有关。