Key result
Andexanet alfa shows no benefit over 4F-PCC for mortality or thromboembolism in Factor Xa-related bleeding.
Why the study?
Limited studies have examined factors influencing the selection and time to administration of reversal agents for life-threatening hemorrhages associated with oral Factor Xa inhibitors.
Are sociodemographic factors associated with the selection of andexanet alfa vs 4F-PCC and time to administration in patients with life-threatening hemorrhage on Factor Xa inhibitors?
Cohort (n=144)
Yes
Are sociodemographic factors associated with the selection of andexanet alfa vs 4F-PCC and time to administration in patients with life-threatening hemorrhage on Factor Xa inhibitors?
While the choice of reversal agent for Factor Xa inhibitor-associated hemorrhage is not influenced by sociodemographic factors, significant racial disparities exist in time to administration.
No outcome differences or selection factors between agents support individualized use; leaves open comparative efficacy in randomized trials.
Andexanet alfa and 4‐factor prothrombin complex concentrate (4F‐PCC) are used for the reversal of life‐threatening hemorrhages associated with oral Factor Xa inhibitors. Limited studies have examined factors influencing reversal agent selection and time to administration. This retrospective, multicenter cohort study evaluated adult patients who presented with a life‐threatening hemorrhage associated with oral Factor Xa inhibitors (apixaban or rivaroxaban) and were administered either andexanet alfa or 4F‐PCC. The objectives of our study were to analyze whether sociodemographic factors were associated with reversal agent selection, time‐to‐treatment with the selected reversal agent, and patient outcomes. Among 144 patients (50% andexanet alfa and 50% 4F‐PCC), no differences were found in sociodemographic (age, sex, race and ethnicity, insurance, housing status, marital status) or logistical factors (time to reversal agent administration and type of arrival to site hospital) associated with reversal agent selection. There were no differences between andexanet alfa and 4F‐PCC for time to reversal agent administration, mortality, mechanical ventilation, length of stay, and thromboembolic events. Factors associated with a longer time to reversal agent administration included patients who were transferred from an outside hospital (RR: 1.27; 95% CI: 1.00, 1.61), patients who received blood products (RR: 1.30; 95% CI: 1.01, 1.68), and patients who were Black compared to non‐Hispanic White (RR: 1.34; 95% CI: 1.02, 1.76) after adjusting for age, sex, reversal agent selection (andexanet vs. 4F‐PCC), bleeding event type related to Factor Xa inhibitors, insurance, and marital status. In conclusion, there were no statistically significant disparities found in sociodemographic factors associated with the selection of andexanet alfa and 4F‐PCC.
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Galeano et al. (2026) conducted a cohort in Life-threatening hemorrhage associated with oral Factor Xa inhibitors (n=144). Andexanet alfa vs. 4-factor prothrombin complex concentrate (4F-PCC) was evaluated on Sociodemographic factors associated with reversal agent selection, time-to-treatment, and patient outcomes. In patients with Factor Xa inhibitor-associated hemorrhage, there were no differences between andexanet alfa and 4F-PCC in time to administration, mortality, or thromboembolic events.
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