Evidence map›Paper›PMID 40600602›Full record

ArticleCatheterization and cardiovascular interventions : official journal of the Society for Cardiac Angiography & Interventions2025

Enhanced Hemocompatibility via Bivalirudin and Bicarbonate as Alternative to Heparin in a Catheter-Based Axial-Flow System.

Kaitlyn R Ammann, Christine E Outridge, Tiana Silver, Sami Muslmani, Jun Ding, Vladimir Gilman, Scott Corbett, Marvin J Slepian

Abstract readComparative Study
In one paragraph

Article in Catheterization and cardiovascular interventions : official journal of the Society for Cardiac Angiography & Interventions, 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. 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

8 authors.

Kaitlyn R AmmannArizona Center for Accelerated Biomedical Innovation, Sarver Heart Center, University of Arizona Health Sciences, The University of Arizona, Tucson, Arizona, USA.ORCID 0000-0002-8245-3796
Christine E OutridgeArizona Center for Accelerated Biomedical Innovation, Sarver Heart Center, University of Arizona Health Sciences, The University of Arizona, Tucson, Arizona, USA.
Tiana SilverArizona Center for Accelerated Biomedical Innovation, Sarver Heart Center, University of Arizona Health Sciences, The University of Arizona, Tucson, Arizona, USA.
Sami MuslmaniArizona Center for Accelerated Biomedical Innovation, Sarver Heart Center, University of Arizona Health Sciences, The University of Arizona, Tucson, Arizona, USA.
Jun DingAbiomed Inc., Danvers, Massachusetts, USA.
Vladimir GilmanAbiomed Inc., Danvers, Massachusetts, USA.
Scott CorbettAbiomed Inc., Danvers, Massachusetts, USA.
Marvin J SlepianDepartment of Medicine, Department of Biomedical Engineering, Arizona Center for Accelerated Biomedical Innovation, Sarver Heart Center, The University of Arizona, Tucson, Arizona, USA.

Funding

This work was supported by an unrestricted educational grant from Johnson and Johnson/Abiomed Inc as well as from a grant from the Arizona Center for Accelerated Biomedical Innovation-ACABI of the University of Arizona.
6 · The paper itself

Abstract

backgroundCardiovascular therapeutic devices typically require systemic heparin due to underlying thrombotic risk. The Impella axial flow system further relies on internal perfusion with either a heparin-containing or sodium bicarbonate purge solution during operation. The combination of systemic and device-mediated heparin often contributes to varying levels of overall anticoagulation, raising the possibility of increased bleeding risk and complications due to heparin sensitivity. To reduce adverse events, efforts have been ongoing to eliminate heparin, both systemically and via the device. Here, we investigate bivalirudin as an alternative to systemic heparin and sodium bicarbonate as an alternative to local device heparin in the purge solution.

methodsWe examined hemocompatibility in a mock loop environment with circulating whole porcine blood to determine feasibility of heparin-free Impella system. Anticoagulated (heparin or bivalirudin) blood was loaded into a circulatory loop with a contained Impella 5.5 and run for 4 h with either heparin or sodium bicarbonate-containing purge solution. Blood samples were collected serially and analyzed for metrics of hemocompatibility: hemolysis, platelet activation, and vWF degradation.

resultsBivalirudin and sodium bicarbonate adjunctive environment led to similar or improved hemocompatibility as compared to heparin-containing environment-notably, decreased hemolysis (40 ± 20.8 mg/dL average decrease) and preserved platelet activity measured by P-selectin exposure (8.0 ± 5.6% average increase).

conclusionsOur data supports the potential to create an overall heparin-free approach simplifying anticoagulation management, offering potential for overall reduced bleeding risk and heparin-related complications.

Indexed as

AnticoagulantsAntithrombinsCardiac CatheterizationHeart-Assist DevicesHeparinHirudinsPeptide FragmentsSodium BicarbonateAnimalsFeasibility StudiesHemolysisMaterials TestingModels, AnimalPlatelet ActivationRecombinant ProteinsSwineAnticoagulantsAntithrombinsbivalirudinHeparinHirudinsPeptide FragmentsRecombinant ProteinsSodium Bicarbonatebicarbonatebivalirudinhemocompatibilityheparinmechanical circulatory support

Identifiers

PMID40600602
PMCPMC12412434

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LicenceCC BY-NC-ND
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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.