Department of Internal Medicine I, Jessenius Faculty of Medicine in Martin, Comenius University in Bratislava, Kollarova 2, 036 59, Martin, Slovakia.
National Centre of Hemostasis and Thrombosis, Department of Hematology and Blood Transfusion, Jessenius Faculty of Medicine in Martin, Comenius University in Bratislava, Martin, Slovakia.
J Thromb Thrombolysis. 2019 Jan;47(1):140-145. doi: 10.1007/s11239-018-1748-5.
Proton pump inhibition (PPI) reduces gastrointestinal bleeding on direct oral anticoagulants. However, PPI may affect dabigatran on-treatment levels; and there is no information regarding the effect of PPI on xabans on-treatment activity. Thus, the aim of this study was to determine the impact of PPI on therapeutic anti-Xa activity in rivaroxaban- and apixaban-treated patients with atrial fibrillation (AF). This single-centre pilot prospective study enrolled 77 consecutive xabans-treated patients (42 rivaroxaban-treated and 35 apixaban-treated patients) with AF. PPI was administrated in 44 patients. Trough and peak anti-Xa activity was assessed with factor Xa-calibrated anti-Xa chromogenic analysis. There were no significant differences in trough anti-Xa activity comparing PPI-treated patients and patients without PPI (80.5 ± 66.5 ng/mL in PPI group vs. 71.6 ± 64.1 ng/mL in non-PPI group, p = 0.57, Table 2). Similarly, there were no significant differences in peak anti-Xa activity between compared groups (175.2 ± 102.5 ng/mL in PPI group vs. 202.9 ± 84.1 ng/mL in non-PPI group, p = 0.21). This pilot study did not reveal significant changes in xabans on-treatment anti-Xa activity according the PPI status.
质子泵抑制剂(PPI)可减少直接口服抗凝剂引起的胃肠道出血。然而,PPI 可能会影响达比加群的治疗药物浓度;并且目前尚无关于 PPI 对新型口服抗凝药(Xa 因子抑制剂)治疗药物活性影响的信息。因此,本研究旨在评估质子泵抑制剂(PPI)对接受利伐沙班和阿哌沙班治疗的房颤(AF)患者的治疗性抗 Xa 活性的影响。这是一项单中心前瞻性研究,共纳入 77 例连续接受 Xa 因子抑制剂(利伐沙班或阿哌沙班)治疗的房颤患者(42 例接受利伐沙班治疗,35 例接受阿哌沙班治疗)。其中 44 例患者接受了 PPI 治疗。采用 Xa 因子校准的抗 Xa 显色分析检测药物谷浓度和药物峰浓度的抗 Xa 活性。PPI 治疗组和未使用 PPI 治疗组的药物谷浓度抗 Xa 活性无显著差异(PPI 组为 80.5 ± 66.5ng/mL,非 PPI 组为 71.6 ± 64.1ng/mL,p = 0.57,表 2)。同样,两组的药物峰浓度抗 Xa 活性也无显著差异(PPI 组为 175.2 ± 102.5ng/mL,非 PPI 组为 202.9 ± 84.1ng/mL,p = 0.21)。这项初步研究并未发现 PPI 使用情况与新型口服抗凝药治疗药物浓度抗 Xa 活性之间存在显著相关性。