Pritzker School of Medicine, University of Chicago, Chicago, Illinois.
Department of Surgery, University of Chicago, Chicago, Illinois.
J Surg Res. 2024 Sep;301:359-364. doi: 10.1016/j.jss.2024.06.035. Epub 2024 Jul 17.
Tranexamic acid (TXA) administered within 2 h of injury reduces mortality in traumatic brain injury (TBI) with intracranial hemorrhage. TXA also reduces the seizure threshold in a dose-dependent manner. We examined whether a 2-g bolus of prehospital TXA administered in moderate or severe TBI is associated with seizure activity within 72 h of injury.
Patients from the prehospital TXA for TBI trial with Glasgow Coma Scale < 13, blunt head injury, and time-of-seizure data were included in this analysis. The original trial randomized patients with suspected TBI to placebo, 1-g TXA bolus + 1-g 8-h TXA infusion, or 2-g TXA bolus within 2 h of injury. In this secondary analysis, multivariable logistic regression was performed to examine the association of treatment group with seizure incidence. The model controlled for age, Glasgow Coma Scale, Injury Severity Score, intracranial hemorrhage, Abbreviated Injury Scale-head, and home antiseizure medication use.
Of the 786 patients who met the inclusion criteria, 19 had seizures within 72 h (five in placebo, two in 1-g bolus/1-g infusion, and 12 in 2-g bolus). The 2-g TXA bolus was not associated with increased seizures compared to placebo (odds ratio 0.41, 95% confidence interval 0.12-1.18, P = 0.12). Home antiseizure medication use was associated with increased seizures (odds ratio 15.95, 95% confidence interval 3.79-60.57, P < 0.001).
A prehospital 2-g TXA bolus in moderate or severe TBI was not associated with increased seizure activity during the first 72 h after injury; however, limited power, limited use of continuous electroencephalography, and unavailable seizure prophylaxis data highlight the need for further study.
在创伤性脑损伤(TBI)伴颅内出血的情况下,伤后 2 小时内给予氨甲环酸(TXA)可降低死亡率。TXA 还以剂量依赖性方式降低癫痫发作阈值。我们研究了在中度或重度 TBI 中院前给予 2 克 TXA 弹丸是否与伤后 72 小时内的癫痫发作活动有关。
本分析纳入了来自院前 TXA 治疗 TBI 试验的格拉斯哥昏迷量表(GCS)<13、钝性头部损伤和癫痫发作时间数据的患者。原始试验将疑似 TBI 患者随机分配至安慰剂组、1 克 TXA 弹丸+1 克 8 小时 TXA 输注组或伤后 2 小时内 2 克 TXA 弹丸组。在这项二次分析中,采用多变量逻辑回归来检查治疗组与癫痫发作发生率的关联。该模型控制了年龄、GCS、损伤严重程度评分、颅内出血、简明损伤量表-头部和家庭抗癫痫药物使用。
在符合纳入标准的 786 例患者中,19 例在 72 小时内发生癫痫发作(安慰剂组 5 例,1 克弹丸/1 克输注组 2 例,2 克弹丸组 12 例)。与安慰剂相比,2 克 TXA 弹丸并未增加癫痫发作(比值比 0.41,95%置信区间 0.12-1.18,P=0.12)。家庭抗癫痫药物使用与癫痫发作增加相关(比值比 15.95,95%置信区间 3.79-60.57,P<0.001)。
在中度或重度 TBI 中,院前给予 2 克 TXA 弹丸与伤后前 72 小时内的癫痫活动增加无关;然而,有限的效能、有限的连续脑电图使用和无法获得的癫痫预防数据突出表明需要进一步研究。