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Andexanet alfa
Andexanet alfa




andexanet alfa

Current trends in the duration of anticoagulant therapy for venous thromboembolism: a systematic review.

andexanet alfa

1 Alexander P, Visagan S, Issa R, et al.Further prospective, comparative clinical research is warranted.

andexanet alfa

ConclusionĪndexanet alfa may be used for urgent or emergent reversal of apixaban and rivaroxaban peri-procedurally with promising hemostatic outcomes. Prothrombin time and antifactor Xa assay results were significantly decreased after andexanet alfa administration ( p < 0.05) while thromboelastogram assay values (reaction time, kinetic time, and activated clotting time) showed nonsignificant changes pre- versus postreversal. Thirty-day mortality and thromboischemic complications occurred in 15 (34.1%) and 12 (27.3%) patients, respectively. Discharge disposition was most often to a short- or long-term care facilities (27 ). 11 rivaroxaban 12 intracranial events vs. Overall, 30 (78.9%) patients achieved excellent or good hemostasis within 24 h after periprocedural administration of andexanet alfa (19 apixaban vs. Thirty-eight (86.4%) patients were able to be adequately graded for hemostatic efficacy. Majority of patients required emergent operative procedures (18 ), followed by invasive device placement (10 ) or arterial embolization (9 ). The indications for reversal were categorized as intracranial ( n = 20 ) or extracranial ( n = 24 ) sites. Resultsįorty-four patients met inclusion criteria of these, 27 (62.8%) received apixaban and 16 (37.2%) were treated with rivaroxaban prior to admission. Secondary outcomes included hospital discharge disposition, intensive care unit (ICU) and hospital length of stay, 30-day mortality, 30-day thromboischemic event rates, and serum coagulation assay changes pre- and postreversal. The primary outcome was hemostatic efficacy graded as excellent, good, or poor using similar definitions to the ANNEXA-4 criteria. This single-center, observational, retrospective study included patients who received andexanet alfa within 24 h of an invasive or surgical procedure. This study aimed to describe efficacy and safety outcomes following andexanet alfa administration within 24 h of an invasive procedure. Outcomes following andexanet alfa reversal of factor Xa inhibitors in patients requiring urgent or emergent invasive procedures are lacking.






Andexanet alfa