Huebner Benjamin R, Dorlac Warren C, Cribari Chris
Department of Surgery, University of Cincinnati, Cincinnati, OH (Dr Huebner).
University of Colorado Health, Loveland, CO and Volunteer Clinical Faculty, Department of Surgery, University of Cincinnati, Cincinnati, OH (Dr Dorlac).
Wilderness Environ Med. 2017 Jun;28(2S):S50-S60. doi: 10.1016/j.wem.2016.12.006.
The use of tranexamic acid (TXA) in the treatment of trauma patients was relatively unexplored until the landmark Clinical Randomisation of an Antifibrinolytic in Significant Haemorrhage-2 (CRASH-2) trial in 2010 demonstrated a reduction in mortality with the use of TXA. Although this trial was a randomized, double-blinded, placebo-controlled study incorporating >20,000 patients, numerous limitations and weaknesses have been described. As a result, additional studies have followed, delineating the potential risks and benefits of TXA administration. A systematic review of the literature to date reveals a mortality benefit of early (ideally <1 hour and no later than 3 hours after injury) TXA administration in the treatment of severely injured trauma patients (systolic blood pressure <90 mm Hg, heart rate >110). Combined with abundant literature showing a reduction in bleeding in elective surgery, the most significant benefit may be administration of TXA before the patient goes into shock. Those trials that failed to show a mortality benefit of TXA in the treatment of hemorrhagic shock acknowledged that most patients received blood products before TXA administration, thus confounding the results. Although the use of prehospital TXA in the severely injured trauma patient will become more clear with the trauma studies currently underway, the current literature supports the use of prehospital TXA in this high-risk population. We recommend considering a 1 g TXA bolus en route to definitive care in high-risk patients and withholding subsequent doses until hyperfibrinolysis is confirmed by thromboelastography.
直到2010年具有里程碑意义的“重大出血中抗纤溶药物的临床随机试验-2(CRASH-2)”试验证明使用氨甲环酸(TXA)可降低死亡率,TXA在创伤患者治疗中的应用才相对未被充分探索。尽管该试验是一项纳入了超过20000名患者的随机、双盲、安慰剂对照研究,但已被描述存在众多局限性和弱点。因此,后续又开展了其他研究,以阐明TXA给药的潜在风险和益处。对迄今为止的文献进行系统回顾发现,早期(理想情况下在受伤后<1小时且不迟于3小时)给予TXA治疗严重受伤的创伤患者(收缩压<90 mmHg,心率>110)可带来死亡率益处。结合大量显示择期手术中出血减少的文献,最显著的益处可能是在患者休克前给予TXA。那些未能显示TXA在治疗失血性休克中有死亡率益处的试验承认,大多数患者在给予TXA之前接受了血液制品,从而混淆了结果。尽管随着目前正在进行的创伤研究,院前使用TXA治疗严重受伤的创伤患者的情况将变得更加清晰,但当前文献支持在这一高风险人群中使用院前TXA。我们建议在将高危患者送往确定性治疗的途中考虑给予1 g TXA推注,并在通过血栓弹力图确认存在高纤溶状态之前暂停后续剂量。