Thrombosis Center, Service d'Hématologie Biologique Hôpital Tenon, Hôpitaux Universitaires de l'Est Parisien, Assistance Publique Hôpitaux de Paris, Faculté de Médecine Sorbonne Université, Paris, France.
Sorbonne University, INSERM UMRS-938, Team "Cancer Vessels, Biology and Therapeutics," Group "Cancer - Angiogenesis - Thrombosis," Institut Universitaire de Cancérologie, Centre de Recherche Saint Antoine, Hôpital Saint Antoine, Assistance Publique - Hôpitaux de Paris, Paris, France.
Clin Appl Thromb Hemost. 2023 Jan-Dec;29:10760296231179684. doi: 10.1177/10760296231179684.
Identifying adherence to direct oral anticoagulants (DOACs) plays a major role in treatment efficacy and safety. The DOAC Dipstick can detect DOACs in urine samples of acutely diseased patients at plasma thresholds of about 30 ng/mL. A prospective observational consecutive cohort study was performed on outpatients taking DOACs. The presence of direct oral factor Xa inhibitors (DXIs) in patient urine samples were independently evaluated by visual interpretation of the DOAC Dipstick pad colors. DOAC plasma concentration was assessed using STA®-Liquid Anti-Xa and STA®-Liquid Anti-IIa chromogenic substrate assays. Positive DOAC Dipstick results were compared with a threshold plasma of DOAC concentration ≥30 ng/mL. Of 120 patients (age 55.4 + 16.1 years, female n = 63), 77 were on rivaroxaban and 43 on apixaban. Plasma concentrations were 129 ± 118 ng/mL for rivaroxaban, and 163 ± 130 ng/mL for apixaban, DOAC Dipstick test has a sensitivity of 97.2% and a positive predictive value of 89.5% at 30 ng/mL. No differences occurred between DXIs. Specificity and negative predictive value could not be determined due to the low number of true negative values. There were no differences in the interpretation of rivaroxaban and apixaban pad colors between observers (Kappa 1.0). Results show that DOAC Dipstick may be a useful tool for identifying DXIs in urine samples in an outpatient setting at a plasma threshold ≥ 30 ng/mL. Further studies should include patients treated with dabigatran, vitamin K antagonists, or other anticoagulants.
确定直接口服抗凝剂(DOACs)的依从性在治疗效果和安全性方面起着重要作用。DOAC 尿试纸可在血浆阈值约为 30ng/mL 时检测出急性疾病患者尿液样本中的 DOACs。对服用 DOAC 的门诊患者进行了前瞻性观察连续队列研究。通过视觉解读 DOAC 尿试纸垫的颜色,独立评估患者尿液样本中直接口服因子 Xa 抑制剂(DXIs)的存在情况。使用 STA®-Liquid Anti-Xa 和 STA®-Liquid Anti-IIa 显色基质测定法评估 DOAC 血浆浓度。将阳性 DOAC 尿试纸结果与 DOAC 浓度≥30ng/mL 的血浆阈值进行比较。在 120 名患者(年龄 55.4 + 16.1 岁,女性 n = 63)中,77 名服用利伐沙班,43 名服用阿哌沙班。利伐沙班的血浆浓度为 129 ± 118ng/mL,阿哌沙班的血浆浓度为 163 ± 130ng/mL。DOAC 尿试纸试验在 30ng/mL 时具有 97.2%的灵敏度和 89.5%的阳性预测值。DXIs 之间没有差异。由于真阴性值数量较少,特异性和阴性预测值无法确定。观察者之间对利伐沙班和阿哌沙班尿试纸垫颜色的解读没有差异(Kappa 1.0)。结果表明,DOAC 尿试纸在血浆阈值≥30ng/mL 的门诊环境中可能是一种识别尿液样本中 DXIs 的有用工具。进一步的研究应包括接受达比加群、维生素 K 拮抗剂或其他抗凝剂治疗的患者。