Evidence map›Paper›PMID 39467897›Full record

ArticleJournal of thrombosis and thrombolysis2025

3-Factor prothrombin complex concentrate versus 4-factor prothrombin complex concentrate for the reversal of oral factor Xa inhibitors.

William Blake Hays, Kelsey Billups, Jessica Nicholson, Abby M Bailey, Haili Gregory, Erin R Weeda, Kyle A Weant

Abstract readMulticenter StudyComparative Study
In one paragraph

Article in Journal of thrombosis and thrombolysis, 2025. 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

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

1 citing paper in PubMed.

  1. Review
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

7 authors.

William Blake HaysDepartment of Pharmacy, Indiana University Health West Hospital, Avon, IN, USA.
Kelsey BillupsDepartment of Pharmacy Services, Medical University of South Carolina, Charleston, SC, USA.
Jessica NicholsonDepartment of Pharmacy, Indiana University Health Adult Academic Medical Center, Indianapolis, IN, USA.
Abby M BaileyDepartment of Pharmacy Services, University of Kentucky HealthCare, Lexington, KY, USA.
Haili GregoryDepartment of Pharmacy, University of North Carolina Health, Chapel Hill, NC, USA.
Erin R WeedaDepartment of Biomedical Sciences, University of South Carolina School of Medicine Greenville, Greenville, SC, USA.
Kyle A WeantDepartment of Clinical Pharmacy and Outcomes Sciences, College of Pharmacy, University of South Carolina, 715 Sumter Street-CLS 316A, Columbia, SC, 29208, USA. kweant@mailbox.sc.edu.ORCID http://orcid.org/0000-0003-0835-7955

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Multiple agents exist for the reversal of oral Factor Xa inhibitor (FXa) associated bleeding, including Coagulation FXa Recombinant, Inactivated zhzo (andexanet alfa) and 4-factor prothrombin complex concentrate (4F-PCC). While classified as a 3F-PCC product, Profilnine contains up to 35 IU of Factor VII (per 100 IU of Factor IX) in addition to therapeutic levels of Factors II, IX, and X, and has demonstrated a similar impact on prothrombin time and blood product usage in non-warfarin related bleeding. This was a retrospective, multicenter study at four medical centers of adult patients who presented with major bleeding associated with oral FXa inhibitors and received either 4F-PCC (n = 64) or 3F-PCC (n = 61). The primary outcome was hemostatic effectiveness. Secondary outcomes included the incidence of thromboembolism, in-hospital mortality, and length of stay. The most common indication for reversal was intracranial bleeding. For the primary outcome, 84% of all patients were rated as effective with no difference noted between the groups (p = 0.81). No significant difference between groups was found in the multivariable analysis adjusting for baseline differences between groups including race, total body weight, type of bleeding, and the use of antiplatelet therapy. There was no difference in the length of stay, in-hospital mortality, or the incidence of thromboembolism between the groups. Overall, no significant differences were found in the effectiveness or safety of 4F-PCC and 3F-PCC use in the management of oral FXa inhibitor-associated bleeding. Further investigations are warranted to explore the use of 3F-PCC for this indication and its safety and effectiveness.

Indexed as

Blood Coagulation FactorsFactor Xa InhibitorsHemorrhageAdministration, OralAdultAgedAged, 80 and overFemaleHumansMaleMiddle AgedRetrospective StudiesThromboembolismBlood Coagulation FactorsFactor Xa Inhibitorsprothrombin complex concentratesFactor IXFactor VIIFactor Xa inhibitorsHemorrhageHemostaticsPlatelet aggregation inhibitorsProthrombin complex concentrationsThromboembolism

Identifiers

PMID39467897
PMCPMC11885330

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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.