Evidence map›Paper›PMID 42293737›Full record

ArticleResearch and practice in thrombosis and haemostasis2026

A UK-wide analysis of the use of reversal agents in 198 patients on direct oral anticoagulants prior to urgent procedures.

HaemSTAR Collaborators

Abstract read
In one paragraph

Article in Research and practice in thrombosis and haemostasis, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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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

1 citing paper in PubMed.

  1. 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

1 author.

HaemSTAR Collaborators

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Direct oral anticoagulants (DOACs) are widely prescribed but present challenges when patients require urgent invasive procedures. While idarucizumab is licensed for preprocedural reversal of dabigatran, 4-factor prothrombin complex concentrates (4F-PCCs) are often used off-label for oral factor (F)Xa inhibitors. Objectives: We aimed to describe real-world UK use of reversal agents prior to urgent procedures. Methods: We conducted a UK-wide audit of adults receiving andexanet alfa, idarucizumab, or 4F-PCC to reverse apixaban, dabigatran, edoxaban, or rivaroxaban, before urgent procedures between October 2020 and June 2023. Data were collected by members of HaemSTAR, a UK-wide network led by hematology resident doctors. Primary outcomes were (1) receipt of reversal ≤24 hours before procedure and (2) adherence to recommended dosing. Secondary outcomes included procedural bleeding risk, 90-day mortality, and 30-day thrombosis rate. Results: Data were collected on 198 patients, with 48% undergoing high-risk procedures. Median time from reversal to procedure was 1.6 hours and 76% took place within 24 hours. 4F-PCC was used in 87%, idarucizumab in 8%, and andexanet alfa in 5%. Tranexamic acid was administered in 20%, 90-day mortality was 24%, and thromboembolic events occurred in 3%, all following 4F-PCC. Conclusion: Reversal agents are frequently used prior to urgent procedures in direct oral anticoagulant-treated patients, including for low-risk interventions. There is limited evidence to support the off-label use of 4F-PCC; the risks, benefits, and cost effectiveness are uncertain. Delays to intervention, low use of tranexamic acid, and infrequent drug-level testing highlight opportunities to improve clinical workflows and inform future trials.

Indexed as

AnticoagulantsAnticoagulation ReversalBlood Coagulation FactorsFactor Xa InhibitorsHemorrhageAdministration, OralAgedAged, 80 and overAntibodies, Monoclonal, HumanizedFactor XaFemaleHumansMaleMiddle AgedRecombinant ProteinsUnited KingdomAntibodies, Monoclonal, HumanizedAnticoagulantsBlood Coagulation FactorsFactor XaFactor Xa Inhibitorsidarucizumabprothrombin complex concentratesPRT064445Recombinant Proteinsanticoagulantsfactor Xa inhibitorsprothrombin complex concentratesradiology, interventionalsurgical procedures, operative

Identifiers

PMID42293737
PMCPMC13264241

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Registered trials

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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.