Baidwan Navneet K, Schauer Steven G, Dixon Julia M, Bhaumik Smitha, April Michael D, April Michael D, Dengler Bradley A, Mould-Millman Nee-Kofi
Department of Emergency Medicine, School of Medicine, University of Colorado, Aurora, CO.
US Army Institute of Surgical Research, JBSA Fort Sam Houston, TX; Brooke Army Medical Center, JBSA Fort Sam Houston, TX; and Uniformed Services University of the Health Sciences, Bethesda, MD.
Med J (Ft Sam Houst Tex). 2023 Jan-Mar(Per 23-1/2/3):34-40.
Approximately 1.7 million people sustain traumatic brain injuries (TBI) annually in the US. To reduce morbidity and mortality, management strategies aim to control progressive intracranial bleeding. This study analyzes the association between Tranexamic Acid (TXA) administration and mortality among casualties within the Department of Defense Trauma Registry, specifically focusing on subsets of patients with varying degree of head injury severities.
Besides descriptive statistics, we used inverse probability weighted (for age, military service category, mechanism of injury, total units of blood units administered), and injury severity (ISS) and Abbreviated Injury Scale (AIS) head score adjusted generalized linear models to analyze the association between TXA and mortality. Specific subgroups of interest were increasing severities of head injury and further stratifying these by Glasgow Coma Score of 3-8 and severe overall bodily injuries (ISS>=15).
25,866 patients were included in the analysis. 2,352 (9.1%) received TXA and 23,514 (90.9%) did not receive TXA. Among those with ISS>=15 (n=6,420), 21.2% received TXA. Among those with any head injury (AIS head injury severity score>=1; n=9,153), 7.2% received TXA. The median ISS scores were greater in the TXA versus no-TXA group (17 versus 6). Weighted and adjusted models showed overall, there was 25% lower mortality risk between those who received TXA at any point and those who did not (OR:0.75, 95% CI: 0.59, 0.95). Further, as the AIS severity score increased from >=1 (1.08; 0.80, 1.47) to >=5 (0.56; 0.33, 0.97), the odds of mortality decreased.
TXA may potentially be beneficial in patients with severe head injuries, especially those with severe overall injury profiles. There is a need of definitive studies to confirm this association.
在美国,每年约有170万人遭受创伤性脑损伤(TBI)。为降低发病率和死亡率,管理策略旨在控制进行性颅内出血。本研究分析了氨甲环酸(TXA)给药与国防部创伤登记处伤亡人员死亡率之间的关联,特别关注不同程度颅脑损伤严重程度的患者亚组。
除描述性统计外,我们使用逆概率加权法(针对年龄、兵役类别、损伤机制、输注的总血单位数),以及损伤严重程度评分(ISS)和简明损伤定级标准(AIS)头部评分调整后的广义线性模型来分析TXA与死亡率之间的关联。感兴趣的特定亚组包括颅脑损伤严重程度增加,并按格拉斯哥昏迷评分为3 - 8分以及严重全身损伤(ISS>=15)进一步分层。
25866名患者纳入分析。2352名(9.1%)接受了TXA,23514名(90.9%)未接受TXA。在ISS>=15的患者中(n = 6420),21.2%接受了TXA。在有任何颅脑损伤的患者中(AIS颅脑损伤严重程度评分>=1;n = 9153),7.2%接受了TXA。TXA组的ISS中位数得分高于未接受TXA组(17对6)。加权和调整后的模型显示,总体而言,在任何时间点接受TXA的患者与未接受TXA的患者相比,死亡风险降低了25%(OR:0.75,95% CI:0.59,0.95)。此外,随着AIS严重程度评分从>=1(1.08;0.80,1.47)增加到>=5(0.56;0.33,0.97),死亡几率降低。
TXA可能对重度颅脑损伤患者有益,尤其是那些具有严重全身损伤情况的患者。需要确定性研究来证实这种关联。