Evidence map›Paper›PMID 41859898›Full record

Trial reportJournal of the American Heart Association2026

Ex Vivo Effect of Apixaban on Hemostatic Biomarkers in Children With Heart Disease: A SAXOPHONE Trial Substudy.

Ghada A Aborkhees, Amy J Barr, Kevin Dietrich, Christoph Male, Zhaoqing Wang, Chen Yao, R Mark Payne, Andrew C Glatz, Paul Monagle, Kristin M Burns and 5 more

Abstract readRandomized Controlled TrialMulticenter Study
In one paragraph

Trial report in Journal of the American Heart Association, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

15 authors.

Ghada A AborkheesUniversity of Alberta Edmonton Alberta Canada.
Amy J BarrUniversity of Alberta Edmonton Alberta Canada.ORCID 0000-0002-2514-2238
Kevin DietrichUniversity of Alberta Edmonton Alberta Canada.
Christoph MaleMedical University of Vienna Department of Paediatrics Vienna Austria.ORCID 0000-0002-4989-6421
Zhaoqing WangBristol Myers Squibb Lawrenceville NJ USA.ORCID 0000-0003-1515-4945
Chen YaoBristol Myers Squibb Lawrenceville NJ USA.
R Mark PayneIndiana University School of Medicine Indianapolis IN USA.ORCID 0000-0002-6232-3628
Andrew C GlatzWashington University School of Medicine St. Louis MO USA.ORCID 0000-0003-3791-8280
Paul MonagleRoyal Children's Hospital, Murdoch Children's Research Institute University of Melbourne Melbourne Australia.
Kristin M BurnsNational Heart, Lung and Blood Institute Bethesda MD USA.ORCID 0000-0001-8665-1303
Alison M ReedyBristol Myers Squibb Lawrenceville NJ USA.
Joshua L DymeBristol Myers Squibb Lawrenceville NJ USA.
Peter H SchaferBristol Myers Squibb Lawrenceville NJ USA.ORCID 0000-0002-3880-0850
Antoinette Ajavon-HartmannBristol Myers Squibb Lawrenceville NJ USA.
Lesley G MitchellUniversity of Alberta Edmonton Alberta Canada.ORCID 0009-0006-5455-8028

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe SAXOPHONE (Safety of Apixaban on Pediatric Heart Disease on the Prevention of Embolism) trial demonstrated the safety of apixaban for thromboprophylaxis in children with heart disease. Included a priori in the trial design was an exploratory biomarker substudy to evaluate the effects of apixaban on surrogate biomarkers of efficacy, thrombin generation capacity, and hemostatic proteins. The study assessed changes in d-dimer, thrombin generation assay parameters, factor VIII, fibrinogen, protein C, and protein S in children receiving apixaban compared with standard-of-care vitamin K antagonists (VKAs) or low-molecular-weight heparin.

methodsSAXOPHONE participants aged >1 year (n=182) had blood samples for biomarkers collected at baseline, week 2, or month 6. Participants were randomized to apixaban (n=123) or standard of care (VKA or low-molecular-weight heparin; n=59). Subgroup analyses accounted for prior VKA exposure.

resultsd-dimer levels decreased at month 6 in all treatment groups and remained stable during VKA-to-apixaban bridging. Apixaban significantly prolonged thrombin generation assay lag time and time to peak compared with VKAs and decreased peak thrombin similarly to VKAs in anticoagulant-naïve participants. Apixaban was associated with decreased fibrinogen and factor VIII at month 6, with no effect on protein C or S. Prior VKA exposure produced carryover effects, suppressing baseline d-dimer, thrombin generation assay parameters, and proteins C and S.

conclusionsApixaban reduced hypercoagulability, as shown by decreased d-dimer levels and prolonged lag time, and preserved endogenous thrombin potential in thrombin generation assay, changes consistent with adult data. These findings align with SAXOPHONE's primary outcomes, supporting apixaban's favorable risk-benefit profile as a thromboprophylaxis option in children with heart disease.

Indexed as

Factor Xa InhibitorsHeart DiseasesHemostasisPyrazolesPyridonesAdolescentAnticoagulantsBiomarkersChildChild, PreschoolFactor VIIIFemaleFibrin Fibrinogen Degradation ProductsFibrinogenHeparin, Low-Molecular-WeightHumansAnticoagulantsapixabanBiomarkersFactor VIIIFactor Xa InhibitorsFibrin Fibrinogen Degradation Productsfibrin fragment DFibrinogenHeparin, Low-Molecular-WeightPyrazolesPyridonesThrombinVitamin Kapixabanhemostatic biomarkershypercoagulabilitylow‐molecular‐weight heparinpediatric heart diseasethromboprophylaxisvitamin K antagonist

Identifiers

PMID41859898
PMCPMC13279061

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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.