Evidence map›Paper›PMID 32685265›Full record

ArticleAmerican journal of cardiovascular disease2020

Early thrombogenicity of coronary stents: comparison of bioresorbable polymer sirolimus-eluting and bare metal stents in an aortic rat model.

Carole Verhaegen, Shakeel Kautbally, Diego Castanares Zapareto, Davide Brusa, Guillaume Courtoy, Selda Aydin, Caroline Bouzin, Cecile Oury, Luc Bertrand, Pascal J Jacques and 3 more

Open access · greenAbstract read
In one paragraph

Article in American journal of cardiovascular disease, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.6field-weighted citation impact, top 29% of its field
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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Observational
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

13 authors at 2 institutions in 1 country.

Carole VerhaegenPole de Recherche Cardiovasculaire, Institut de Recherche Experimentale et Clinique (IREC), Universite Catholique de Louvain (UCLouvain) Brussels, Belgium.
Shakeel KautballyPole de Recherche Cardiovasculaire, Institut de Recherche Experimentale et Clinique (IREC), Universite Catholique de Louvain (UCLouvain) Brussels, Belgium.
Diego Castanares ZaparetoPole de Recherche Cardiovasculaire, Institut de Recherche Experimentale et Clinique (IREC), Universite Catholique de Louvain (UCLouvain) Brussels, Belgium.
Davide BrusaPlateforme de Cytometrie de Flux, Institut de Recherche Experimentale et Clinique (IREC), Universite Catholique de Louvain (UCLouvain) Brussels, Belgium.
Guillaume CourtoyIREC Imaging Platform (2IP), Universite Catholique de Louvain (UCLouvain) Brussels, Belgium.
Selda AydinDivision of Anatomical Pathology, Cliniques Universitaires Saint-Luc, Universite Catholique de Louvain (UCLouvain) Brussels, Belgium.
Caroline BouzinIREC Imaging Platform (2IP), Universite Catholique de Louvain (UCLouvain) Brussels, Belgium.
Cecile OuryGIGA Cardiovascular Sciences, University of Liege Liege, Belgium.
Luc BertrandPole de Recherche Cardiovasculaire, Institut de Recherche Experimentale et Clinique (IREC), Universite Catholique de Louvain (UCLouvain) Brussels, Belgium.
Pascal J JacquesInstitute of Mechanics, Materials and Civil Engineering, IMAP, Universite Catholique de Louvain (UCLouvain) Louvain-la-Neuve, Belgium.
Christophe BeauloyePole de Recherche Cardiovasculaire, Institut de Recherche Experimentale et Clinique (IREC), Universite Catholique de Louvain (UCLouvain) Brussels, Belgium.
Sandrine HormanPole de Recherche Cardiovasculaire, Institut de Recherche Experimentale et Clinique (IREC), Universite Catholique de Louvain (UCLouvain) Brussels, Belgium.
Joelle KeferPole de Recherche Cardiovasculaire, Institut de Recherche Experimentale et Clinique (IREC), Universite Catholique de Louvain (UCLouvain) Brussels, Belgium.
UCLouvain · BEUniversity of Liège · BE

Funding

HSRD VA IIR 20-066
6 · The paper itself

Abstract

backgroundAlthough 1-month dual antiplatelet therapy (DAPT) in patients treated with bare metal stents (BMS) is well established, the optimal duration of DAPT after implantation of a drug-eluting stent (DES) is still a matter of debate. The safety of shortened DAPT is under investigation due to concern about the risk of stent thrombosis. Data on platelet activation and prothrombotic response in vivo following bioresorbable polymer sirolimus-eluting stent (BP-SES) implantation are scarce.

objectivesThe aim of our study was to compare the early thrombogenicity of BP-SES with that of BMS in an aortic rat model. METHODS AND

resultsOverall, 30 rats underwent stent implantation in the abdominal aorta: BMS (Pro-Kinetic Energy; N=15) and BP-SES (Ultimaster Tansei; N=15) were compared in terms of their early thrombogenicity. CD62P exposure at the platelet surface and fibrinogen binding at the integrin receptor were not different between BMS and BP-SES over time. The thrombus coverage of the scaffold (0 vs. 0.1%, P=0.84) was similarly low in both groups at Day 28; thrombotic deposits had totally disappeared at Day 84. The endothelial strut coverage was similarly high at 1 month (90 vs. 95%, P=0.64) and 3 months (87 vs. 97%, P=0.99) following BMS and BP-SES implantation, respectively.

conclusionsThis study demonstrates the low early thrombogenicity of a BP-SES implanted in an aortic rat model, which did not differ from a BMS. These data could be helpful to support the safety of a shortened 1-month DAPT duration following BP-SES implantation in the human coronary artery.

Indexed as

animal modelplateletStentthrombus

Identifiers

PMID32685265
PMCPMC7364276
OpenAlexW3044109507

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.