Department of Pharmaceutical Services, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.
Department of Critical Care Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.
Ann Pharmacother. 2024 Apr;58(4):383-390. doi: 10.1177/10600280231183510. Epub 2023 Jul 3.
Only some studies have directly compared and analyzed the roles of activated partial thromboplastin time (aPTT) and activated clotting time (ACT) in coagulation monitoring during argatroban administration.
This study aims to assess the correlation of argatroban dose with ACT and aPTT values and to identify the optimal coagulation test for argatroban dose adjustment.
We evaluated 55 patients on extracorporeal membrane oxygenation (ECMO) who received argatroban for more than 72 hours. The correlation between argatroban dose and aPTT and ACT values was evaluated. To compare argatroban dose and bleeding events according to liver dysfunction, the patients were divided into 2 groups based on alanine aminotransferase and total bilirubin.
Among the 55 patients, a total of 459 doses and coagulation tests were evaluated. The aPTT and ACT values showed a weak correlation with argatroban dose, with the Pearson correlation coefficients of 0.261 ( < 0.001) and 0.194 ( = 0.001), respectively. The agreement between the target 150 to 180 seconds for ACT and 55 to 75 seconds for aPTT was observed in 140 patients (46.1%). Twenty-four patients (43.6%) had liver dysfunction when they started argatroban. The median argatroban dose was lower in the liver dysfunction group than in the control group (0.094 mcg/kg/min vs 0.169 mcg/kg/min, = 0.020). Difference was not observed between the 2 groups in the amount of red blood cell (0.47 vs 0.43 pack, = 0.909) and platelet (0.60 vs 0.08 pack, = 0.079) transfusion per day.
A weak correlation was observed between argatroban dose and the aPTT and ACT values. However, the agreement between aPTT and ACT was only 46.1% regarding the scope of target range. Further research is necessary to determine how to assess the optimal argatroban dose for patients administered argatroban while undergoing ECMO at the intensive care unit.
只有一些研究直接比较和分析了在阿加曲班给药期间,激活部分凝血活酶时间(aPTT)和激活凝血时间(ACT)在凝血监测中的作用。
本研究旨在评估阿加曲班剂量与 ACT 和 aPTT 值的相关性,并确定用于调整阿加曲班剂量的最佳凝血试验。
我们评估了 55 例接受 ECMO 超过 72 小时的患者,评估了阿加曲班剂量与 aPTT 和 ACT 值之间的相关性。为了根据肝功能障碍比较阿加曲班剂量和出血事件,根据丙氨酸氨基转移酶和总胆红素将患者分为 2 组。
在 55 例患者中,共评估了 459 个剂量和凝血试验。aPTT 和 ACT 值与阿加曲班剂量呈弱相关性,Pearson 相关系数分别为 0.261(<0.001)和 0.194(=0.001)。ACT 的目标值为 150 至 180 秒,aPTT 的目标值为 55 至 75 秒,在 140 例患者(46.1%)中观察到一致性。24 例(43.6%)患者在开始使用阿加曲班时存在肝功能障碍。肝功能障碍组的阿加曲班剂量中位数低于对照组(0.094 mcg/kg/min 比 0.169 mcg/kg/min,=0.020)。两组每日红细胞(0.47 比 0.43 袋,=0.909)和血小板(0.60 比 0.08 袋,=0.079)输注量无差异。
阿加曲班剂量与 aPTT 和 ACT 值之间存在弱相关性。然而,aPTT 和 ACT 在目标范围的范围内仅具有 46.1%的一致性。需要进一步研究如何评估 ICU 中接受 ECMO 的患者使用阿加曲班的最佳阿加曲班剂量。