15503University of Colorado Skaggs School of Pharmacy and Pharmaceutical Sciences, 22095Aurora, CO, USA.
Clin Appl Thromb Hemost. 2021 Jan-Dec;27:10760296211039020. doi: 10.1177/10760296211039020.
The aim of this retrospective study was to compare andexanet alfa and 4-factor prothrombin complex (4F-PCC) for reversal of factor Xa (FXa)-inhibitor bleeding. Patients that received andexanet alfa for reversal were included. An equivalent number of patients administered 4F-PCC for FXa-inhibitor bleeding were randomly selected as historical controls. The primary outcome was effective hemostasis achievement within 12 h, defined using ANNEXA-4 criteria. Thromboembolic events and mortality within 30 days were also evaluated. A total of 32 patients were included. Baseline characteristics were not statistically different between andexanet alfa (n = 16) and 4F-PCC (n = 16). Intracranial bleeding was the primary reversal indication in 43.8% versus 62.5% of patients, respectively. Effective hemostasis was reached in 75.0% of andexanet alfa patients compared to 62.5% of 4F-PCC patients ( = .70). Thromboembolic events occurred in 4 (25.0%) patients and 3 (18.8%) patients, respectively ( = .99). Mortality incidence was 12.5% and 31.3%, respectively ( = .39). Andexanet alfa and 4F-PCC attained hemostasis in a majority of patients. A high, but a similar rate of thromboembolic events was seen with both treatments. Prospective studies are needed to elucidate comparative risks and benefits of the 2 agents.
本回顾性研究旨在比较andexanet alfa 和 4 因子凝血酶原复合物(4F-PCC)在逆转因子 Xa(FXa)抑制剂出血方面的疗效。纳入接受 andexanet alfa 逆转治疗的患者。随机选择等量接受 4F-PCC 治疗 FXa 抑制剂出血的患者作为历史对照。主要结局是根据 ANNEXA-4 标准在 12 小时内达到有效止血。还评估了 30 天内血栓栓塞事件和死亡率。共纳入 32 例患者。andexanet alfa 组(n=16)和 4F-PCC 组(n=16)之间的基线特征无统计学差异。颅内出血分别是主要逆转指征的 43.8%和 62.5%。andexanet alfa 组的有效止血率为 75.0%,4F-PCC 组为 62.5%( = .70)。血栓栓塞事件分别发生在 4 例(25.0%)和 3 例(18.8%)患者中( = .99)。死亡率分别为 12.5%和 31.3%( = .39)。andexanet alfa 和 4F-PCC 使大多数患者达到止血。两种治疗方法均有较高的血栓栓塞事件发生率,但相似。需要前瞻性研究阐明这两种药物的相对风险和获益。