Institute for Anaesthesiology, Heart and Diabetes Centre North Rhine-Westphalia, Ruhr-University Bochum, Georgstr. 11, D-32545 Bad Oeynhausen, Germany.
Br J Anaesth. 2013 Jan;110(1):34-40. doi: 10.1093/bja/aes310. Epub 2012 Sep 17.
Convulsive seizures (CS) occur in ∼1% of the patients after cardiac surgery with cardiopulmonary bypass. Recent investigations indicate an up to seven-fold increase in CS in cardiac surgical patients receiving high doses (≥60 mg kg(-1) body weight) of tranexamic acid (TA).
In a retrospective data analysis of 4883 cardiac surgical patients, we investigated the incidence of CS in patients receiving a moderate dose of TA (24 mg kg(-1) body weight) compared with a reference group not receiving TA as a primary endpoint. Secondary endpoints were intensive care unit stay and in-hospital mortality. We performed propensity score (PS)-adjusted logistic regression analysis to test the association between TA use/non-use and clinical outcomes.
Compared with the reference group, the PS-adjusted odds ratio (OR) for CS in the TA group was 1.703 [95% confidence interval (CI): 1.01-2.87; P=0.045; incidence 2.5% vs 1.2%]. Log-ICU-stay was significantly longer (P=0.004) and PS-adjusted relative in-hospital mortality risk was significantly higher for the TA group compared with the reference group (OR=1.89; 95% CI: 1.21-2.96; P=0.005). Both the TA-associated CS incidence and the in-hospital mortality risk were only significant in patients undergoing open-heart surgery (OR=2.034, 95% CI: 1.07-3.87; P=0.034 and OR=2.20, 95% CI: 1.32-3.69; P=0.003, respectively) but not in patients undergoing coronary artery bypass grafting (OR=1.21, 95% CI: 0.49-3.03; P=0.678 and OR=1.13, 95% CI: 0.42-3.02; P=0.809, respectively).
In open-heart surgery, even moderate TA doses are associated with a doubled rate of CS and in-hospital mortality. Prospective trials are needed to further evaluate the safety profile of TA in cardiac surgery.
心脏体外循环手术后约有 1%的患者会出现惊厥性癫痫发作(CS)。最近的研究表明,接受高剂量(≥60mg/kg 体重)氨甲环酸(TA)的心脏外科患者 CS 的发生率增加了七倍以上。
在对 4883 例心脏外科患者的回顾性数据分析中,我们将接受中等剂量 TA(24mg/kg 体重)的患者的 CS 发生率与未接受 TA 的参考组作为主要终点进行比较。次要终点是重症监护病房(ICU)入住时间和院内死亡率。我们进行了倾向评分(PS)调整的逻辑回归分析,以检验 TA 使用/不使用与临床结果之间的关联。
与参考组相比,TA 组 CS 的 PS 调整后的优势比(OR)为 1.703(95%置信区间(CI):1.01-2.87;P=0.045;发生率为 2.5% vs. 1.2%)。TA 组的 ICU 住院时间明显延长(P=0.004),且 PS 调整后的相对院内死亡率风险也明显高于参考组(OR=1.89;95%CI:1.21-2.96;P=0.005)。TA 相关 CS 发生率和院内死亡率风险仅在接受心脏直视手术的患者中具有统计学意义(OR=2.034,95%CI:1.07-3.87;P=0.034 和 OR=2.20,95%CI:1.32-3.69;P=0.003),而在接受冠状动脉旁路移植术的患者中则无统计学意义(OR=1.21,95%CI:0.49-3.03;P=0.678 和 OR=1.13,95%CI:0.42-3.02;P=0.809)。
在心脏直视手术中,即使是中等剂量的 TA 也与 CS 和院内死亡率的增加呈两倍相关。需要前瞻性试验进一步评估 TA 在心脏手术中的安全性。