Department of Traumatology and Acute Critical Medicine, Osaka University Graduate School of Medicine, Suita, Osaka, 565-0871, Japan.
Division of Trauma and Surgical Critical Care, Osaka General Medical Center, 3-1-56 Bandai-Higashi, Sumiyoshi, Osaka, 558-8558, Japan.
Crit Care. 2021 Nov 1;25(1):380. doi: 10.1186/s13054-021-03799-9.
Tranexamic acid (TXA) reduces surgical bleeding and reduces death from bleeding after trauma and childbirth. However, its effects on thrombotic events and seizures are less clear. We conducted a systematic review and meta-analysis to examine the safety of TXA in bleeding patients.
For this systematic review and meta-analysis, we searched MEDLINE, EMBASE and the Cochrane Central Register of Controlled trials from inception until June 1, 2020. We included randomized trials comparing intravenous tranexamic acid and placebo or no intervention in bleeding patients. The primary outcomes were thrombotic events, venous thromboembolism, acute coronary syndrome, stroke and seizures. A meta-analysis was performed using a random effects model and meta-regression analysis was performed to evaluate how effects vary by dose. We assessed the certainty of evidence using the grading of recommendations, assessment, development and evaluations (GRADE) approach.
A total of 234 studies with 102,681 patients were included in the meta-analysis. In bleeding patients, there was no evidence that TXA increased the risk of thrombotic events (RR = 1.00 [95% CI 0.93-1.08]), seizures (1.18 [0.91-1.53]), venous thromboembolism (1.04 [0.92-1.17]), acute coronary syndrome (0.88 [0.78-1.00]) or stroke (1.12 [0.98-1.27]). In a dose-by-dose sensitivity analysis, seizures were increased in patients receiving more than 2 g/day of TXA (3.05 [1.01-9.20]). Meta-regression showed an increased risk of seizures with increased dose of TXA (p = 0.011).
Tranexamic acid did not appear to increase the risk of thrombotic events in bleeding patients. However, because there may be dose-dependent increase in the risk of seizures, very high doses should be avoided.
氨甲环酸(TXA)可减少创伤和分娩后出血以及因出血导致的死亡。然而,其对血栓形成事件和癫痫发作的影响尚不清楚。我们进行了系统评价和荟萃分析,以检查 TXA 在出血患者中的安全性。
在这项系统评价和荟萃分析中,我们从开始到 2020 年 6 月 1 日,在 MEDLINE、EMBASE 和 Cochrane 对照试验中心注册库中进行了检索。我们纳入了比较静脉注射氨甲环酸与安慰剂或无干预措施治疗出血患者的随机试验。主要结局为血栓形成事件、静脉血栓栓塞、急性冠脉综合征、卒中和癫痫发作。使用随机效应模型进行荟萃分析,并进行荟萃回归分析以评估剂量如何影响效果。我们使用推荐评估、制定与评价分级(GRADE)方法评估证据的确定性。
共有 234 项研究,纳入了 102681 例患者,纳入荟萃分析。在出血患者中,TXA 并未增加血栓形成事件(RR=1.00 [95%CI 0.93-1.08])、癫痫发作(1.18 [0.91-1.53])、静脉血栓栓塞(1.04 [0.92-1.17])、急性冠脉综合征(0.88 [0.78-1.00])或卒中等风险。在按剂量的敏感性分析中,接受 TXA 剂量超过 2 g/天的患者癫痫发作风险增加(3.05 [1.01-9.20])。荟萃回归显示,TXA 剂量增加与癫痫发作风险增加相关(p=0.011)。
氨甲环酸似乎不会增加出血患者的血栓形成事件风险。然而,由于癫痫发作的风险可能与剂量有关,因此应避免使用非常高的剂量。