Evidence map›Paper›PMID 40815367›Full record

ArticleJournal of cardiovascular translational research2025

Preclinical Assessment of a Novel Polymer-Free Hybrid Drug Eluting Stent.

Léa Wild, Alicia Beele, Masaru Seguchi, Tobias Lenz, Philipp Nicol, Emina Sabic-Halilcevic, Grace R Klosterman, Adnan Kastrati, Michael Joner

Abstract read
In one paragraph

Article in Journal of cardiovascular translational research, 2025. 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

9 authors.

Léa Wild *Department of Cardiovascular Diseases, German Heart Center Munich, Technical University Munich University Hospital, Lazarettstraße 36, 80636, Munich, Germany.
Alicia Beele *Department of Cardiovascular Diseases, German Heart Center Munich, Technical University Munich University Hospital, Lazarettstraße 36, 80636, Munich, Germany.
Masaru SeguchiDepartment of Cardiovascular Diseases, German Heart Center Munich, Technical University Munich University Hospital, Lazarettstraße 36, 80636, Munich, Germany.
Tobias LenzDepartment of Cardiovascular Diseases, German Heart Center Munich, Technical University Munich University Hospital, Lazarettstraße 36, 80636, Munich, Germany.
Philipp NicolDepartment of Cardiovascular Diseases, German Heart Center Munich, Technical University Munich University Hospital, Lazarettstraße 36, 80636, Munich, Germany.
Emina Sabic-HalilcevicDepartment of Cardiovascular Diseases, German Heart Center Munich, Technical University Munich University Hospital, Lazarettstraße 36, 80636, Munich, Germany.
Grace R KlostermanDepartment of Cardiovascular Diseases, German Heart Center Munich, Technical University Munich University Hospital, Lazarettstraße 36, 80636, Munich, Germany.
Adnan KastratiDepartment of Cardiovascular Diseases, German Heart Center Munich, Technical University Munich University Hospital, Lazarettstraße 36, 80636, Munich, Germany.
Michael JonerDepartment of Cardiovascular Diseases, German Heart Center Munich, Technical University Munich University Hospital, Lazarettstraße 36, 80636, Munich, Germany. michaeljoner@me.com.ORCID 0000-0002-2971-8310

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We aimed to evaluate a novel polymer-free hybrid drug eluting stent (DES) relative to benchmark devices and specific controls addressing singular components of the test device in a juvenile pig model of coronary stenting. 80 stents were implanted in 28 juvenile pigs and evaluated at 28 and 90 days using quantitative coronary angiography and histopathology (n = 10 per group). Scanning electron microscopy was used at 14 days to assess early re-endothelialization (n = 3 per group). The test device featured a cobalt-chromium (CoCr) backbone with a polymer-free probucol matrix releasing everolimus. The polymer-free test stent showed improved strut coverage at 28 days compared to the polymer-coated control, with significantly lower neointimal growth at 90 days and near complete endothelialization at 14 days. This preclinical study supports the favorable vascular healing profile of a polymer-free hybrid DES, warranting further clinical investigation.

Indexed as

Cardiovascular AgentsCoronary VesselsDrug-Eluting StentsEverolimusPercutaneous Coronary InterventionAnimalsChromium AlloysCoronary AngiographyMaterials TestingModels, AnimalNeointimaProsthesis DesignSus scrofaSwineTime FactorsCardiovascular AgentsChromium AlloysEverolimusDrug-eluting stentPercutaneous coronary interventionPorcine modelVascular healing

Identifiers

PMID40815367
PMCPMC12630216

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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.