Department of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden.
Coagulation Unit, Department of Haematology, Karolinska University Hospital, Stockholm, Sweden.
Clin Appl Thromb Hemost. 2024 Jan-Dec;30:10760296241260053. doi: 10.1177/10760296241260053.
For patients with hemophilia A and high-titer inhibitors treated with bypassing agents there are no reliable methods to assess treatment effect. We investigated the utility of global hemostatic methods in assessing treatment with bypassing agents (rFVIIa or activated prothrombin complex [aPCC]). All patients with hemophilia A and inhibitors followed at the Coagulation Unit or the Pediatric Coagulation Unit at Karolinska University Hospital aged 6 years and above were eligible for this noninterventional study. Baseline plasma samples were spiked with bypassing agents in increasing concentrations (aPCC 50 U/kg, 100 U/kg, 150 U/kg, and rFVIIa 90 μg/kg and 270 μg/kg) in vitro. For patients treated with factor concentrates or bypassing agents follow-up samples were collected (in vivo tests). The samples were analyzed using overall hemostatic potential (OHP), and calibrated automated thrombogram, Calibrated Automated Thrombogram (CAT). Nine patients with hemophilia A with inhibitors were included. Spiking with rFVIIa normalized the coagulation potential in 6/8 samples, in 3 only with high dose. Only one sample did not improve adequately after spiking with aPCC. The improvement in hemostasis was reliably shown by both CAT and OHP. The baseline potential was, however, more often measurable by OHP compared to CAT. Factor concentrate had been administered to 5 patients normalizing the hemostatic potential in vivo in 2 (without spiking). The hemostatic improvement induced by spiking with rFVIIa or aPCC is shown by OHP and CAT, but the results have to be evaluated in larger cohorts.
对于接受旁路制剂(rFVIIa 或活化的凝血酶原复合物[aPCC])治疗的甲型血友病和高滴度抑制剂患者,目前尚无可靠的方法来评估治疗效果。我们研究了使用整体止血方法评估旁路制剂(rFVIIa 或活化的凝血酶原复合物[aPCC])治疗效果的效用。在卡罗林斯卡大学医院的凝血科或儿科凝血科接受治疗的所有甲型血友病和抑制剂患者均符合本非干预性研究的条件。在体外,将基线血浆样本用递增浓度的旁路制剂(aPCC 50 U/kg、100 U/kg、150 U/kg 和 rFVIIa 90 μg/kg 和 270 μg/kg)进行加标处理。对于接受因子浓缩物或旁路制剂治疗的患者,采集随访样本(体内试验)。使用整体止血潜能(OHP)和校准自动血栓图(CAT)对样本进行分析。纳入了 9 名甲型血友病伴抑制剂的患者。rFVIIa 加标可使 6/8 个样本的凝血潜能恢复正常,仅在高剂量时 3 个样本可恢复正常。只有 1 个样本在用 aPCC 加标后不能充分改善。CAT 和 OHP 均可靠地显示了止血的改善。然而,与 CAT 相比,OHP 更常可测量基线潜力。5 名患者接受了因子浓缩物治疗,其中 2 名(未加标)可使体内止血潜能恢复正常。rFVIIa 或 aPCC 加标诱导的止血改善可通过 OHP 和 CAT 显示,但需要在更大的队列中进行评估。