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评估andexanet alfa和四因子凝血酶原复合物浓缩剂(4F-PCC)对利伐沙班和阿哌沙班相关颅内出血的逆转作用。

Evaluation of andexanet alfa and four-factor prothrombin complex concentrate (4F-PCC) for reversal of rivaroxaban- and apixaban-associated intracranial hemorrhages.

作者信息

Barra Megan E, Das Alvin S, Hayes Bryan D, Rosenthal Eric S, Rosovsky Rachel P, Fuh Lanting, Patel Aman B, Goldstein Joshua N, Roberts Russel J

机构信息

Department of Pharmacy, Massachusetts General Hospital, Boston, MA, USA.

Department of Neurology, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA.

出版信息

J Thromb Haemost. 2020 Jul;18(7):1637-1647. doi: 10.1111/jth.14838. Epub 2020 May 12.

Abstract

BACKGROUND/OBJECTIVE: Before approval of andexanet alfa, off-label treatment with 4-factor prothrombin complex concentrate (4F-PCC) was often utilized for the management of life-threatening hemorrhages associated with oral factor Xa inhibitors. We evaluated the operational processes and outcomes of patients with oral factor Xa inhibitor-associated intracranial hemorrhages (ICH) treated with andexanet alfa or 4F-PCC.

METHODS

We performed a retrospective, single-center case series of rivaroxaban or apixaban-associated ICH between 2016-2019 treated with andexanet alfa or 4F-PCC. Good or excellent hemostatic effectiveness, good functional outcome (Glasgow Outcome Score [GOS]> 3) at hospital discharge, and incidence of thrombosis within 30 days were reported.

RESULTS

Eighteen patients were included in the andexanet alfa cohort and 11 in the 4F-PCC cohort. Excellent or good hemostasis occurred in 88.9% of andexanet alfa-treated patients and 60% of 4F-PCC-treated patients. Good functional outcome on discharge occurred in 55.6% of andexanet alfa-treated patients and 9.1% of 4F-PCC-treated patients. Thrombotic complications occurred in 16.7% of andexanet alfa-treated patients and 9.1% of 4F-PCC-treated patients. Median order-to-administration time was 1.1 hours [0.8-1.4] versus 0.5 hours [0.1-0.8] in the andexanet alfa and 4F-PCC group, respectively. The median cost of therapy was $29970/patient versus $6925/patient in the andexanet alfa and 4F-PCC group, respectively.

CONCLUSIONS

We observed higher rates of occurrence of good or excellent hemostasis and GOS > 3 on hospital discharge and increased incidence of thrombosis in patients who received andexanet alfa compared to 4F-PCC for oral factor Xa inhibitor reversal. However, patients receiving 4F-PCC had lower pre-reversal Glasgow Coma Scale (GCS)score and larger pre-reversal ICH volume.

摘要

背景/目的:在andexanet alfa获批之前,常使用4因子凝血酶原复合物浓缩剂(4F-PCC)进行非标签治疗,以管理与口服Xa因子抑制剂相关的危及生命的出血。我们评估了接受andexanet alfa或4F-PCC治疗的口服Xa因子抑制剂相关颅内出血(ICH)患者的治疗过程和结果。

方法

我们对2016年至2019年间接受andexanet alfa或4F-PCC治疗的利伐沙班或阿哌沙班相关ICH进行了一项回顾性单中心病例系列研究。报告了良好或优异的止血效果、出院时良好的功能结局(格拉斯哥结局评分[GOS]>3)以及30天内血栓形成的发生率。

结果

andexanet alfa队列纳入18例患者,4F-PCC队列纳入11例患者。接受andexanet alfa治疗的患者中88.9%实现了优异或良好的止血,接受4F-PCC治疗的患者中这一比例为60%。接受andexanet alfa治疗的患者中55.6%出院时功能结局良好,接受4F-PCC治疗的患者中这一比例为9.1%。接受andexanet alfa治疗的患者中16.7%出现血栓并发症,接受4F-PCC治疗的患者中这一比例为9.1%。andexanet alfa组和4F-PCC组的中位医嘱到用药时间分别为1.1小时[0.8 - 1.4]和0.5小时[0.1 - 0.8]。治疗的中位费用分别为每位患者29970美元和每位患者6925美元,分别在andexanet alfa组和4F-PCC组。

结论

我们观察到,与4F-PCC相比,接受andexanet alfa进行口服Xa因子抑制剂逆转的患者,实现良好或优异止血以及出院时GOS>3的发生率更高,血栓形成的发生率也增加。然而,接受4F-PCC治疗的患者在逆转前格拉斯哥昏迷量表(GCS)评分较低,逆转前ICH体积较大。

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