Department of Anesthesiology and Intensive Care Medicine, University Hospital "Carl Gustav Carus," Technische Universität Dresden, Dresden, Germany.
Institute of Clinical Pharmacology, Faculty of Medicine, University Hospital "Carl Gustav Carus," Technische Universität Dresden, Dresden, Germany.
Anesthesiology. 2024 Feb 1;140(2):261-271. doi: 10.1097/ALN.0000000000004787.
The direct thrombin inhibitor argatroban is indicated for the treatment of heparin-induced thrombocytopenia II, but it is also used off-label to treat critically ill patients presenting with heparin resistance, severe antithrombin deficiency, or hypercoagulability. Direct drug monitoring is not routinely available, and argatroban dosing is mainly based on global coagulation assays such as activated partial thromboplastin time (PTT) or diluted thrombin time (TT), both of which have limitations in patients with hypercoagulability.
Blood samples were obtained from critically ill patients treated with argatroban. Activated PTT and diluted TT were measured with a STA R Max3 analyzer (STAGO Deutschland GmbH, Germany) using an argatroban-calibrated kit. Ecarin clotting time was measured using a point-of-care viscoelastic test device. Liquid chromatography with tandem mass spectrometry was performed using a reversed-phase column, a solvent gradient, and an API4000 mass spectrometer with electrospray. Correlation was described using Pearson correlation coefficient r and Bayesian multilevel regression to estimate relationships between outcomes and covariates.
From June 2021 to March 2022, 205 blood samples from 22 patients were analyzed, allowing for 195 activated PTT-liquid chromatography with tandem mass spectrometry comparisons, 153 ecarin clotting time-liquid chromatography with tandem mass spectrometry comparison, and 105 diluted TT-liquid chromatography with tandem mass spectrometry comparisons. Compared to liquid chromatography with tandem mass spectrometry, performance of argatroban quantification was best for diluted TT (r = 0.91), followed by ecarin clotting time (r = 0.58) and activated PTT (r = 0.48). Regression analysis revealed that patients with sepsis were more prone to argatroban overdosing (coefficient, 4.194; 95% credible interval, 2.220 to 6.792).
Although activated PTT monitoring of argatroban is the most commonly used test, in critically ill patients, diluted TT provides more precise measurements. Alternately, point-of-care viscoelastic ecarin clotting time also provides guidance for argatroban dosing to identify overdosing if available. The data also suggested that patients with sepsis are at greater risk for argatroban overdosing.
直接凝血酶抑制剂阿加曲班被批准用于治疗肝素诱导的血小板减少症 II 型,但也被超说明书用于治疗出现肝素抵抗、严重抗凝血酶缺乏或高凝状态的重症患者。直接药物监测并不常规进行,阿加曲班的剂量主要基于活化部分凝血活酶时间(activated partial thromboplastin time,APTT)或稀释凝血酶时间(diluted thrombin time,TT)等全球凝血检测,而这些检测在高凝患者中均存在局限性。
从接受阿加曲班治疗的重症患者中采集血样。使用 STA R Max3 分析仪(德国 STAGO 公司)和阿加曲班校准试剂盒,分别测量 APTT 和 TT。使用即时检测(point-of-care,POC)的粘弹性测试设备测量蝰蛇凝血酶时间(e-car in clotting time,ECT)。采用反相柱、溶剂梯度和 API4000 质谱仪,进行液相色谱-串联质谱分析。使用 Pearson 相关系数 r 描述相关性,并采用贝叶斯多层回归来估计结果与协变量之间的关系。
2021 年 6 月至 2022 年 3 月,分析了 22 例患者的 205 份血样,共进行了 195 次 APTT-液相色谱-串联质谱、153 次 ECT-液相色谱-串联质谱和 105 次 TT-液相色谱-串联质谱比较。与液相色谱-串联质谱相比,阿加曲班定量检测的性能在稀释 TT 中最佳(r = 0.91),其次是 ECT(r = 0.58)和 APTT(r = 0.48)。回归分析显示,脓毒症患者更易发生阿加曲班超剂量用药(系数为 4.194,95%可信区间为 2.220 至 6.792)。
虽然阿加曲班监测中最常用的检测是 APTT,但在重症患者中,稀释 TT 可提供更精确的测量。如果可以使用 POC 粘弹性 ECT,也可提供指导阿加曲班剂量的信息,以识别超剂量用药。数据还提示,脓毒症患者更易发生阿加曲班超剂量用药。