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监测低达比加群浓度:在临床相关决策阈值下的诊断性能。

Monitoring of low dabigatran concentrations: diagnostic performance at clinically relevant decision thresholds.

机构信息

Department of Neurology & Stroke, and Hertie Institute for Clinical Brain Research, University of Tübingen, Hoppe-Seyler-Str. 3, Tübingen, 72076, Germany.

Department of Internal Medicine and Cardiology, Charité University Medicine Berlin - Campus Virchow Klinikum, Berlin, Germany.

出版信息

J Thromb Thrombolysis. 2020 Apr;49(3):457-467. doi: 10.1007/s11239-019-01981-z.

Abstract

The direct oral anticoagulant dabigatran does not require therapeutic drug monitoring, however emergency measurements are gaining importance. Current assays feature good performance at intermediate and high dabigatran concentrations but show limited accuracy at low concentrations. This area requires more attention as clinical decision threshold values currently lie at 30 and 50 ng/ml. The objective of the study was to evaluate and compare diagnostic performance of dabigatran assays at these thresholds. Dabigatran concentrations of 293 plasma samples taken from 50 patients were measured with the INNOVANCE direct thrombin inhibitor assay (DTI) from Siemens, the Biophen direct thrombin inhibitor assay (BDTI), the BDTI using a low range calibrator (BDTI-low), the Hemoclot direct thrombin inhibitor assay (HTI) and an ecarin clotting time assay (ECT). Assay results were compared to ultra-performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS), and test characteristics were calculated for thresholds of 30 and 50 ng/ml. DTI, BDTI-low and ECT showed very strong correlation and high agreement with UPLC-MS/MS and an improved determination of low dabigatran concentrations. ROC curve analyses revealed very high accuracy at the 30/50 ng/ml thresholds for DTI (AUC = 0.989/0.995), BDTI-low (AUC = 0.980/0.991) and ECT (AUC = 0.990/0.996) measurements. Sensitivity and specificity in detecting were calculated for DTI (98/92%), BDTI-low (87/95%), ECT (97/96%), BDTI (99/82%) and HTI (86/89%) measurements. Compared to the previously available HTI and BDTI, both novel assays, DTI and BDTI-low, reliably determine low dabigatran plasma concentrations around the clinical decision thresholds with very high sensitivity and specificity.

摘要

直接口服抗凝剂达比加群无需进行治疗药物监测,但紧急检测正变得越来越重要。目前的检测方法在中高浓度达比加群时具有良好的性能,但在低浓度时准确性有限。由于目前的临床决策阈值为 30 和 50ng/ml,因此该领域需要更多关注。研究的目的是评估和比较这些阈值下达比加群检测方法的诊断性能。使用西门子的 INNOVANCE 直接凝血酶抑制剂检测(DTI)、Biophen 直接凝血酶抑制剂检测(BDTI)、使用低范围校准器的 BDTI(BDTI-low)、Hemoclot 直接凝血酶抑制剂检测(HTI)和蝰蛇凝血时间检测(ECT)对 50 名患者的 293 份血浆样本的达比加群浓度进行了测量。将检测结果与超高效液相色谱-串联质谱法(UPLC-MS/MS)进行比较,并计算了 30 和 50ng/ml 阈值下的检测特征。DTI、BDTI-low 和 ECT 与 UPLC-MS/MS 具有非常强的相关性和高度一致性,并能更好地确定低浓度的达比加群。ROC 曲线分析显示,DTI(AUC=0.989/0.995)、BDTI-low(AUC=0.980/0.991)和 ECT(AUC=0.990/0.996)在 30/50ng/ml 阈值下具有非常高的准确性。计算了 DTI(98/92%)、BDTI-low(87/95%)、ECT(97/96%)、BDTI(99/82%)和 HTI(86/89%)检测的敏感性和特异性。与之前可用的 HTI 和 BDTI 相比,新型 DTI 和 BDTI-low 两种检测方法都能可靠地确定接近临床决策阈值的低达比加群血浆浓度,具有非常高的灵敏度和特异性。

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