Department of Pediatrics, Nara Medical University, 840 Shijo-cho, Kashihara, Nara, 634-8522, Japan.
Advanced Medical Science of Thrombosis and Hemostasis, Nara Medical University, Kashihara, Japan.
Int J Hematol. 2024 Nov;120(5):639-644. doi: 10.1007/s12185-024-03828-7. Epub 2024 Aug 7.
We describe a 67-year-old patient with hemophilia A and inhibitors (PwHA-I) receiving emicizumab prophylaxis who underwent surgical treatment for pseudoaneurysm. He was treated with a bolus infusion of recombinant factor VIIa (rFVIIa; 79 μg/kg) immediately before surgery, and a second dose of rFVIIa after an initial treatment on day 1. A third rFVIIa bolus was infused 17 h after the second dose on day 2, and the treatment was continued every 24 h on day 3 and day 4. Treatment with rFVIIa was discontinued on day 4. No perioperative bleeding or thrombotic events were observed. Coagulation potentials at 8 h after rFVIIa administration determined by clot waveform analysis (CWA) and thrombin generation assay (TGA) were within near-normal ranges, and results at 17 h after rFVIIa administration showed coagulation function comparable to that in the patient without rFVIIa. Our experimental data suggest that the coagulation potential in FVIII-deficient plasma spiked with both 0.28 µg/mL (11.2 μg/kg) rFVIIa and emicizumab was equivalent to or greater than that spiked with 2.2 µg/mL (90 μg/kg) rFVIIa alone. Thus, administration of rFVIIa every 8 h may be feasible for managing perioperative treatment in emicizumab-treated PwHA-I.
我们描述了一位 67 岁患有 A 型血友病和抑制剂(PwHA-I)的患者,他接受emicizumab 预防治疗,并接受了假性动脉瘤的手术治疗。他在手术前立即接受了重组因子 VIIa(rFVIIa;79μg/kg)的推注治疗,并在第 1 天的初始治疗后接受了第二剂 rFVIIa。在第 2 天的第 2 剂后 17 小时再次输注了第三剂 rFVIIa,并在第 3 天和第 4 天每天 24 小时继续治疗。第 4 天停止了 rFVIIa 的治疗。未观察到围手术期出血或血栓事件。通过凝血波形分析(CWA)和凝血酶生成试验(TGA)测定 rFVIIa 给药后 8 小时的凝血潜力在接近正常范围内,并且 rFVIIa 给药后 17 小时的结果表明凝血功能与未接受 rFVIIa 的患者相当。我们的实验数据表明,在添加了 0.28μg/mL(11.2μg/kg)rFVIIa 和 emicizumab 的 FVIII 缺乏血浆中添加的凝血潜力等同于或大于单独添加 2.2μg/mL(90μg/kg)rFVIIa 的凝血潜力。因此,每隔 8 小时给予 rFVIIa 可能适用于管理 emicizumab 治疗的 PwHA-I 的围手术期治疗。