Newman Zachary C, McKinley W Ian, Nordgren Rachel K, Deshpande David V, Barbosa Claire E, Pramuka Pierce E, Benjamin Andrew J, Schreiber Martin A, Rowell Susan E
From The University of Chicago Pritzker School of Medicine, Chicago, IL (Newman, Deshpande).
Departments of Surgery (McKinley, Pramuka), The University of Chicago, Chicago, IL.
J Am Coll Surg. 2025 Jul 1;241(1):7-15. doi: 10.1097/XCS.0000000000001401. Epub 2025 Jun 13.
Tranexamic acid (TXA) is an antifibrinolytic drug known to reduce mortality in bleeding trauma patients, yet the evidence of TXAs impact on blood product use within this population is conflicting. In patients with traumatic brain injury (TBI), the impact of TXA on transfusion remains unclear.
This is a secondary analysis of the prehospital TXA for TBI trial that enrolled patients in the prehospital setting with a Glasgow Coma Scale score of 3 to 12 and not in shock (systolic blood pressure < 90 mmHg) before enrollment within 2 hours of injury. Subjects with isolated TBI (iTBI; Abbreviated Injury Scale Head score 3 or greater and Abbreviated Injury Scale 2 or less in any other category) were included. Factors associated with transfusion were characterized using logistic regression.
Of 966 patients enrolled in the primary trial, 306 subjects met the definition of iTBI and were included (101 in the 2-g prehospital TXA bolus arm, 97 in the 1-g prehospital TXA bolus or 1-g in-hospital TXA infusion arm, and 108 in the placebo arm). In multivariable regression analysis, receipt of a 1-g TXA bolus or 1-g TXA infusion (odds ratio 0.27, p = 0.03) and receipt of TXA after combining TXA treatment arms (odds ratio 0.32, p = 0.02) were associated with decreased odds of red cell transfusion.
In subjects with iTBI, prehospital TXA may be associated with lower odds of red cell transfusion compared with placebo. This effect was likely mediated by treatment group imbalances in the percentage of subjects with a penetrating mechanism of injury, as well as the need for emergent neurosurgical intervention.
氨甲环酸(TXA)是一种抗纤溶药物,已知可降低出血性创伤患者的死亡率,但TXA对该人群血液制品使用影响的证据存在矛盾。在创伤性脑损伤(TBI)患者中,TXA对输血的影响仍不清楚。
这是对院前TXA治疗TBI试验的二次分析,该试验纳入了院前环境中格拉斯哥昏迷量表评分为3至12且在受伤后2小时内入组前未休克(收缩压<90 mmHg)的患者。纳入了孤立性TBI(iTBI;简明损伤定级标准头部评分3或更高且任何其他类别简明损伤定级标准2或更低)的受试者。使用逻辑回归对与输血相关的因素进行了特征分析。
在初级试验纳入的966例患者中,306例受试者符合iTBI的定义并被纳入(院前TXA大剂量2 g组101例,院前TXA大剂量1 g或院内TXA输注1 g组97例,安慰剂组108例)。在多变量回归分析中,接受1 g TXA大剂量或1 g TXA输注(比值比0.27,p = 0.03)以及合并TXA治疗组后接受TXA(比值比0.32,p = 0.02)与红细胞输血几率降低相关。
在iTBI受试者中,与安慰剂相比,院前TXA可能与较低的红细胞输血几率相关。这种效应可能是由损伤机制为穿透性的受试者百分比的治疗组不平衡以及紧急神经外科干预的需求所介导的。