Andexanet alfa for reversal of rivaroxaban in a child with intracranial hemorrhage

2021 ◽  
Author(s):  
Kaoru Takasaki ◽  
David Hehir ◽  
Leslie Raffini ◽  
Benjamin J. Samelson‐Jones ◽  
Evelyn Shih ◽  
...  
2020 ◽  
Vol 49 (1) ◽  
pp. 375-375
Author(s):  
Paige Bradshaw ◽  
Shaun Keegan ◽  
Madeline Foertsch

Author(s):  
Joseph Friedli

<p>A critical appraisal and clinical application of Connolly SJ, Milling TJ, Eikelboom JW, et al. Andexanet alfa for acute major bleeding associated with factor Xa inhibitors. <em>N Engl J Med</em>. 2016;375(12):1131-1141. doi: <a href="https://doi.org/10.1056/NEJMoa1607887">10.1056/NEJMoa1607887</a>.</p>


Stroke ◽  
2021 ◽  
Author(s):  
Andrew M. Demchuk ◽  
Patrick Yue ◽  
Elena Zotova ◽  
Juliet Nakamya ◽  
Lizhen Xu ◽  
...  

Background and Purpose: Andexanet alfa is a recombinant modified human FXa (factor Xa) developed to reverse FXa inhibition from anticoagulants. Hemostatic efficacy and reversal of anti-FXa activity with andexanet were assessed in patients from the ANNEXA-4 study (Andexanet Alfa, a Novel Antidote to the Anticoagulation Effects of FXa Inhibitors) with intracranial hemorrhage (ICrH). Methods: ANNEXA-4 was a single-arm study evaluating andexanet in patients presenting with major bleeding ≤18 hours after taking an FXa inhibitor. Patients received a bolus plus 2-hour infusion of andexanet. Brain imaging in patients with ICrH was performed at baseline and at 1 and 12 hours postandexanet infusion. Coprimary efficacy outcomes were change in anti-FXa activity and hemostatic efficacy at 12 hours (excellent/good efficacy defined as ≤35% increase in hemorrhage volume/thickness). Safety outcomes included occurrence of thrombotic events and death at 30 days. Results: A total of 227 patients with ICrH were included in the safety population (51.5% male; mean age 79.3 years) and 171 in the efficacy population (99 spontaneous and 72 traumatic bleeds). In efficacy evaluable patients, excellent/good hemostasis 12 hours postandexanet occurred in 77 out of 98 (78.6%) and in 58 out of 70 (82.9%) patients with spontaneous and traumatic bleeding, respectively. In the subanalysis by FXa inhibitor treatment group in the efficacy population, median of percent change in anti-FXa from baseline to nadir showed a decrease of 93.8% for apixaban-treated patients (n=99) and by 92.6% for rivaroxaban-treated patients (n=59). Within 30 days, death occurred in 34 out of 227 (15.0%) patients and thrombotic events occurred in 21 out of 227 (9.3%) patients (safety population). Conclusions: Andexanet reduced anti-FXa activity in FXa inhibitor-treated patients with ICrH, with a high rate of hemostatic efficacy. Andexanet may substantially benefit patients with ICrH, the most serious complication of anticoagulation. REGISTRATION: URL: https://www.clinicaltrials.gov ; Unique identifier: NCT02329327.


2020 ◽  
Vol 49 (1) ◽  
pp. 301-301
Author(s):  
Gregory Semon ◽  
Angela Straughn ◽  
Claire Hardman ◽  
Barbara Steel ◽  
Akpofure Ekeh

2019 ◽  
Vol 74 (4) ◽  
pp. S78-S79
Author(s):  
T.J. Milling ◽  
P. Yue ◽  
E. Zotova ◽  
J. Nakamya ◽  
J.T. Curnutte ◽  
...  

2021 ◽  
pp. 194187442110480
Author(s):  
Sarah Elizabeth B. Davis ◽  
Kelly A. Dehne ◽  
Clio A. Rubinos ◽  
Winnie K. Lau ◽  
Kalynn A. Northam

Coagulation factor Xa (recombinant), inactivated-zhzo (andexanet alfa) is approved for reversal of life-threatening bleeding with rivaroxaban and apixaban use. Clinical decision-making to initiate reversal is reliant on dose taken and timing of last dose. In practice, timing of last dose may be unknown, and the turnaround time for drug-specific anti-factor Xa levels at some institutions may be prolonged, leaving clinicians balancing a difficult decision with limited tools. This report includes a series of 3 patients who presented to our institution with an intracranial hemorrhage and received andexanet alfa for apixaban reversal. These cases highlight the challenges clinicians are facing when using andexanet alfa for emergent rivaroxaban or apixaban reversal when the timing of last dose is unknown, or patients fall outside of the recommended timeframe for use and clinically relevant drug levels are still suspected. Based on our experiences, we encourage other institutions to evaluate their abilities to rapidly and accurately detect the presence of clinically relevant rivaroxaban and apixaban levels when utilizing andexanet alfa.


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