Borgman Matthew A, Nishijima Daniel K
From the Brooke Army Medical Center (M.A.B.), Uniformed Services University, Ft. Sam Houston, Texas; and UC Davis Medical Center (D.K.N.), University of California, Sacramento, California.
J Trauma Acute Care Surg. 2023 Jan 1;94(1S Suppl 1):S36-S40. doi: 10.1097/TA.0000000000003775. Epub 2022 Aug 31.
There is strong evidence in adult literature that tranexamic acid (TXA) given within 3 hours from injury is associated with improved outcomes. The evidence for TXA use in injured children is limited to retrospective studies and one prospective observational trial. Two studies in combat settings and one prospective civilian US study have found association with improved mortality. These studies indicate the need for a randomized controlled trial to evaluate the efficacy of TXA in injured children and to clarify appropriate timing, dose and patient selection. Additional research is also necessary to evaluate trauma-induced coagulopathy in children. Recent studies have identified three distinct fibrinolytic phenotypes following trauma (hyperfibrinolysis, physiologic fibrinolysis, and fibrinolytic shutdown), which can be identified with viscohemostatic assays. Whether viscohemostatic assays can appropriately identify children who may benefit or be harmed by TXA is also unknown.
成人文献中有强有力的证据表明,在受伤后3小时内给予氨甲环酸(TXA)与改善预后相关。TXA用于受伤儿童的证据仅限于回顾性研究和一项前瞻性观察性试验。两项在战斗环境中的研究和一项美国平民前瞻性研究发现,TXA与死亡率改善相关。这些研究表明,需要进行一项随机对照试验,以评估TXA在受伤儿童中的疗效,并明确合适的给药时间、剂量和患者选择。还需要进行额外的研究来评估儿童创伤性凝血病。最近的研究已经确定了创伤后三种不同的纤维蛋白溶解表型(高纤维蛋白溶解、生理性纤维蛋白溶解和纤维蛋白溶解停止),这可以通过粘弹性止血试验来识别。粘弹性止血试验能否适当地识别可能从TXA中获益或受到伤害的儿童也尚不清楚。