From the Institute of Cardiology, Jagiellonian University Medical College and John Paul II Hospital, Kraków, Poland (Ząbczyk, Natorska, Kopytek, Undas).
Faculty of Health Sciences, Jagiellonian University Medical College, Kraków, Poland (Malinowski).
Arch Pathol Lab Med. 2021 Jan 1;145(1):99-104. doi: 10.5858/arpa.2020-0021-OA.
CONTEXT.—: Direct oral anticoagulants (DOACs) may cause false negative results of antithrombin (AT) deficiency screening.
OBJECTIVE.—: To evaluate the impact of DOAC-Stop, an agent reversing in vitro effects of DOACs, on AT testing in anticoagulated patients.
DESIGN.—: We assessed 130 venous thromboembolism patients aged 46.7 ± 13.5 years. Blood samples were collected 2 to 27 hours after DOAC intake from 49 patients on rivaroxaban, 54 on apixaban, and 27 on dabigatran. Antithrombin activity was assessed using the activated factor X (FXa)-based and the activated factor II (FIIa)-based method twice, before and after DOAC-Stop treatment, together with plasma DOAC levels using coagulometric assays.
RESULTS.—: The use of DOAC-Stop did not influence AT activity measured using the FIIa-based assay, whereas there was a marked decrease in AT activity determined using the FXa-based assay (ΔAT = 16.9%; 95% CI, 12.9%-19.1%). The AT-FIIa assay revealed decreased AT level (<79%) in all 10 (7.7%) genetically confirmed AT-deficient patients treated with rivaroxaban or apixaban (n = 5 each), whereas the AT-FXa assay showed decreased AT activity (<83%) in 2 subjects on rivaroxaban and 1 on apixaban with low plasma DOAC concentrations (<90 ng/mL). After DOAC-Stop median AT-FXa activity lowered from 83.5% (interquartile range, 66%-143%) to 65.5% (interquartile range, 57%-75%; P = .005; ΔAT = 18%) in AT-deficient patients, without any false negative results. The ΔAT in the FXa-based assay correlated with rivaroxaban and apixaban concentrations in the AT-deficient patients (r = 0.99, P < .001).
CONCLUSIONS.—: Application of DOAC-Stop enables reliable evaluation of AT deficiency screening in patients taking rivaroxaban or apixaban and tested using the FXa-based method.
直接口服抗凝剂(DOAC)可能导致抗凝血酶(AT)缺乏筛查出现假阴性结果。
评估 DOAC-Stop(一种逆转 DOAC 体外作用的药物)对接受抗凝治疗的患者 AT 检测的影响。
我们评估了 130 名年龄为 46.7±13.5 岁的静脉血栓栓塞患者。从接受利伐沙班治疗的 49 名患者、接受阿哌沙班治疗的 54 名患者和接受达比加群治疗的 27 名患者中采集 DOAC 给药后 2 至 27 小时的静脉血样本。使用基于活化因子 X(FXa)和基于活化因子 II(FIIa)的方法两次评估抗凝血酶活性,在使用 DOAC-Stop 治疗前后进行,并使用凝固法检测血浆 DOAC 水平。
使用 DOAC-Stop 不影响基于 FIIa 的检测法测定的 AT 活性,而基于 FXa 的检测法测定的 AT 活性明显降低(ΔAT=16.9%;95%置信区间,12.9%-19.1%)。AT-FIIa 检测法显示,所有 10 名(7.7%)经基因确认为 AT 缺乏的患者(接受利伐沙班或阿哌沙班治疗的患者各 5 名)的 AT 水平降低(<79%),而 AT-FXa 检测法显示,在 2 名接受利伐沙班治疗和 1 名接受阿哌沙班治疗且血浆 DOAC 浓度较低(<90ng/mL)的患者中,AT 活性降低(<83%)。在 AT 缺乏的患者中,DOAC-Stop 中位 AT-FXa 活性从 83.5%(四分位距,66%-143%)降至 65.5%(四分位距,57%-75%;P=0.005;ΔAT=18%),无假阴性结果。在 AT 缺乏的患者中,基于 FXa 的检测法中的ΔAT 与利伐沙班和阿哌沙班的浓度相关(r=0.99,P<0.001)。
应用 DOAC-Stop 可在使用 FXa 基于方法进行检测的情况下,可靠地评估接受利伐沙班或阿哌沙班治疗的患者的 AT 缺乏筛查。