Reversal of Factor Xa Inhibitor-Related Intracranial Hemorrhage: A Multicenter, Retrospective, Observational Study Comparing the Efficacy and Safety of Andexanet and Prothrombin Complex Concentrates

被引:0
作者
Panos, Nicholas G. [1 ]
Jones, G. Morgan [2 ]
Cook, Aaron M. [3 ]
Peksa, Gary D. [1 ]
John, Sayona [4 ]
Demott, Joshua M. [1 ]
Tobias, Philip [1 ]
Da Silva, Ivan [5 ]
机构
[1] Rush Univ, Med Ctr, Dept Pharm, Chicago, IL 60612 USA
[2] Univ Tennessee, Hlth Sci Ctr, Dept Clin Pharm & Translat Sci, Memphis, TN USA
[3] Univ Kentucky, Coll Pharm, Dept Pharm Practice & Sci, Lexington, KY USA
[4] Rush Univ, Med Ctr, Dept Neurol Sci, Chicago, IL USA
[5] Univ Florida, Coll Med, Div Neurocrit Care, Gainesville, FL USA
基金
美国国家卫生研究院;
关键词
andexanet; anticoagulation reversal; factor Xa inhibitors; intracranial hemorrhage; prothrombin complex concentrates; INTRACEREBRAL HEMORRHAGE; MANAGEMENT; ALPHA; ANTICOAGULATION; RIVAROXABAN; APIXABAN;
D O I
10.1097/CCM.0000000000006656
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
OBJECTIVE:To determine the effectiveness and safety of andexanet and prothrombin complex concentrates (PCCs) when administered after intracranial hemorrhage (ICrH) associated with direct oral anticoagulants, specifically apixaban or rivaroxaban.DESIGN:A multicenter, retrospective, observational study of patients with apixaban or rivaroxaban-related ICrH who received andexanet or PCCs between January 1, 2015, and March 31, 2023. A predefined sensitivity analysis excluding patients with an admission Glasgow Coma Scale score of less than 7 was also performed.SETTING:Forty-two stroke centers in the United States.PATIENTS:A total of 1133 patients.INTERVENTIONS:None.MEASUREMENTS AND MAIN RESULTS:The primary efficacy outcome was the percentage of patients with excellent or good hemostasis as defined by the modified Sarode criteria. The primary safety outcome was the occurrence of a thrombotic event (TE) during their hospital stay. Of the 1133 patients evaluated, 1096 were included. In the full hemostatic efficacy analysis, patients receiving andexanet (87.8%) had higher odds of achieving excellent or good hemostasis (odds ratio [OR] 1.60; 95% CI, 1.00-2.56; p = 0.048) compared with PCCs (81.8%). Patients treated with andexanet (7.9%) had higher odds of a TE (OR 1.91; 95% CI, 1.13-3.20; p = 0.014) compared to those treated with PCCs (4.2%). No differences in hemostatic or thrombotic outcomes were observed when the sensitivity analysis was applied.CONCLUSIONS:Despite statistically higher odds of achieving hemostatic efficacy with andexanet, we also observed higher odds of a TE with no difference in discharge outcomes observed between groups. When those with more severe neurologic injuries were excluded, efficacy and safety outcomes were similar between treatments.
引用
收藏
页码:e1202 / e1213
页数:12
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