CSL Innovations Pty Ltd, Victoria, Australia.
CSL Behring LLC, King of Prussia, PA, United States of America.
PLoS One. 2024 Sep 27;19(9):e0310883. doi: 10.1371/journal.pone.0310883. eCollection 2024.
The management of factor Xa (FXa) inhibitor-associated bleeding remains a clinical challenge. Massive bleeding is often associated with complex coagulopathy and, thus, the sole reversal of FXa inhibitors might not be sufficient to restore hemostasis, requiring instead a multimodal approach. Four-factor prothrombin complex concentrate (4F-PCC) is widely recognized as a viable treatment option for FXa inhibitor-associated bleeding. Here, we applied computational models to explore the effect 4F-PCC has on the coagulation cascade and restoration of thrombin generation in a system that simulates a patient that has received a FXa inhibitor. The coagulation model is largely based on a previously developed model with modifications incorporated from various other published sources. The model was calibrated and validated using data from a phase 3 clinical trial of vitamin K antagonist reversal with 4F-PCC. Using the parameters and initial conditions determined during the calibration and validation process, the prothrombin time (PT) test simulations predicted a PT of 11.4 seconds. The model successfully simulated the effects of rivaroxaban and apixaban on total thrombin concentration and showed that 4F-PCC increased thrombin generation in the presence of rivaroxaban or apixaban.
Xa 因子(FXa)抑制剂相关出血的管理仍然是一个临床挑战。大量出血通常与复杂的凝血功能障碍相关,因此,仅仅逆转 FXa 抑制剂可能不足以恢复止血,需要采用多模式方法。四种凝血因子浓缩物(4F-PCC)被广泛认为是治疗 FXa 抑制剂相关出血的可行选择。在这里,我们应用计算模型来探索 4F-PCC 对凝血级联反应的影响,并在模拟已接受 FXa 抑制剂的患者的系统中恢复凝血酶生成。该凝血模型主要基于先前开发的模型,并结合了来自其他各种已发表来源的修改。该模型使用来自 4F-PCC 逆转维生素 K 拮抗剂的 3 期临床试验的数据进行了校准和验证。使用在校准和验证过程中确定的参数和初始条件,对凝血酶原时间(PT)测试模拟预测 PT 为 11.4 秒。该模型成功模拟了利伐沙班和阿哌沙班对总凝血酶浓度的影响,并表明 4F-PCC 在存在利伐沙班或阿哌沙班的情况下增加了凝血酶生成。