Evidence map›Paper›PMID 36073083›Full record

Observational studyPharmacotherapy2022

Reversal of apixaban and rivaroxaban with andexanet alfa prior to invasive or surgical procedures.

Paige Garber Bradshaw, Shaun Patrick Keegan, Molly Elizabeth Droege, Nicole Jade Harger Dykes, Neil Edward Ernst, Madeline Jane Foertsch, Amy Teres Makley, Eric William Mueller, Carolyn Dosen Philpott, Vasisht Srinivasan and 3 more

Open access · hybridAbstract readObservational Study
In one paragraph

Observational study in Pharmacotherapy, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
3.8field-weighted citation impact, top 6% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

15 citing papers in PubMed, 18 citations in OpenAlex.

  1. Observational
  2. Article
  3. Andexanet alfa for the reversal of anticoagulation: Dutch practice data.Research and practice in thrombosis and haemostasis · 2026
    Observational
  4. Review
  5. Article
  6. Review
  7. Article
  8. DOACs: role of anti-Xa and drug level monitoring.Hematology. American Society of Hematology. Education Program · 2024
    Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Observational
  15. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors at 2 institutions in 1 country.

Paige Garber BradshawDepartment of Pharmacy, UC Health - University of Cincinnati Medical Center, Cincinnati, Ohio, USA.ORCID 0000-0002-8030-7269
Shaun Patrick KeeganDepartment of Pharmacy, UC Health - University of Cincinnati Medical Center, Cincinnati, Ohio, USA.
Molly Elizabeth DroegeDepartment of Pharmacy, UC Health - University of Cincinnati Medical Center, Cincinnati, Ohio, USA.ORCID 0000-0002-4338-1021
Nicole Jade Harger DykesDepartment of Pharmacy, UC Health - University of Cincinnati Medical Center, Cincinnati, Ohio, USA.
Neil Edward ErnstDepartment of Pharmacy, UC Health - University of Cincinnati Medical Center, Cincinnati, Ohio, USA.
Madeline Jane FoertschDepartment of Pharmacy, UC Health - University of Cincinnati Medical Center, Cincinnati, Ohio, USA.
Amy Teres MakleyDepartment of Surgery, Division of Trauma, University of Cincinnati, Cincinnati, Ohio, USA.
Eric William MuellerDepartment of Pharmacy, UC Health - University of Cincinnati Medical Center, Cincinnati, Ohio, USA.
Carolyn Dosen PhilpottDepartment of Pharmacy, UC Health - University of Cincinnati Medical Center, Cincinnati, Ohio, USA.ORCID 0000-0002-0962-1001
Vasisht SrinivasanDepartment of Emergency Medicine, University of Washington School of Medicine, Seattle, Washington, USA.
Jessica Brooke WinterDepartment of Pharmacy, UC Health - University of Cincinnati Medical Center, Cincinnati, Ohio, USA.
Michael D GoodmanDepartment of Surgery, Division of Trauma, University of Cincinnati, Cincinnati, Ohio, USA.
Christopher Allen DroegeDepartment of Pharmacy, UC Health - University of Cincinnati Medical Center, Cincinnati, Ohio, USA.
University of Cincinnati · USUniversity of Washington · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundOutcomes following andexanet alfa reversal of factor Xa inhibitors in patients requiring urgent or emergent invasive procedures are lacking. This study aimed to describe efficacy and safety outcomes following andexanet alfa administration within 24 h of an invasive procedure.

methodsThis single-center, observational, retrospective study included patients who received andexanet alfa within 24 h of an invasive or surgical procedure. The primary outcome was hemostatic efficacy graded as excellent, good, or poor using similar definitions to the ANNEXA-4 criteria. 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.

resultsForty-four patients met inclusion criteria; of these, 27 (62.8%) received apixaban and 16 (37.2%) were treated with rivaroxaban prior to admission. The indications for reversal were categorized as intracranial (n = 20 [45.5%]) or extracranial (n = 24 [54.5%]) sites. Majority of patients required emergent operative procedures (18 [40.9%]), followed by invasive device placement (10 [22.7%]) or arterial embolization (9 [20.5%]). Thirty-eight (86.4%) patients were able to be adequately graded for hemostatic efficacy. Overall, 30 (78.9%) patients achieved excellent or good hemostasis within 24 h after periprocedural administration of andexanet alfa (19 [82.6%] apixaban vs. 11 [78.6%] rivaroxaban; 12 [80.0%] intracranial events vs. 18 [78.3%] extracranial events). Discharge disposition was most often to a short- or long-term care facilities (27 [61.4%]). Thirty-day mortality and thromboischemic complications occurred in 15 (34.1%) and 12 (27.3%) patients, respectively. 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.

conclusionAndexanet alfa may be used for urgent or emergent reversal of apixaban and rivaroxaban peri-procedurally with promising hemostatic outcomes. Further prospective, comparative clinical research is warranted.

Indexed as

Factor XaHemostaticsFactor Xa InhibitorsHemorrhageHumansPyrazolesPyridonesRecombinant ProteinsRetrospective StudiesRivaroxabanapixabanFactor XaFactor Xa InhibitorsHemostaticsPRT064445PyrazolesPyridonesRecombinant ProteinsRivaroxabananticoagulation reversalanticoagulation reversal agentsfactor Xafactor Xa inhibitorsgeneral surgeryrecombinant proteins

Identifiers

PMID36073083
PMCPMC9826450
OpenAlexW4294991942

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.