Evidence map›Paper›PMID 39323753›Full record

ArticleFrontiers in cardiovascular medicine2024

Ten-year clinical outcomes of everolimus- and biolimus-eluting coronary stents vs. everolimus-eluting bioresorbable vascular scaffolds-insights from the EVERBIO-2 trial.

Samir Bengueddache, Malica Cook, Sonja Lehmann, Diego Arroyo, Mario Togni, Serban Puricel, Stephane Cook

Registry-linked trialAbstract read
In one paragraph

Article in Frontiers in cardiovascular medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01711931 (Comparison of Everolimus- and Biolimus-Eluting Stents With Everolimus-Eluting Bioresorbable Vascular Scaffold Stents), which is not on this map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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.

NCT01711931 phase4completednot on this map

Comparison of Everolimus- and Biolimus-Eluting Stents With Everolimus-Eluting Bioresorbable Vascular Scaffold Stents

TypeinterventionalSponsorUniversity of FreiburgRan2012 to 2013Enrolled240ConditionsCoronary Artery DiseaseArmsImplantation of everolimus-eluting bioresorbable vascular scaffold stent, Implantation of everolimus-eluting stents, Implantation of biolimus-eluting stents
3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Article
  2. Review
  3. 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.

Samir Bengueddache *Department of Cardiology, Fribourg University and Hospital, Fribourg, Switzerland.
Malica Cook *Department of Cardiology, Fribourg University and Hospital, Fribourg, Switzerland.
Sonja LehmannDepartment of Cardiology, Fribourg University and Hospital, Fribourg, Switzerland.
Diego ArroyoDepartment of Cardiology, Fribourg University and Hospital, Fribourg, Switzerland.
Mario TogniDepartment of Cardiology, Fribourg University and Hospital, Fribourg, Switzerland.
Serban PuricelDepartment of Cardiology, Fribourg University and Hospital, Fribourg, Switzerland.
Stephane CookDepartment of Cardiology, Fribourg University and Hospital, Fribourg, Switzerland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Bioresorbable vascular scaffolds (BVSs) have been developed as a potential solution to mitigate late complications associated with drug-eluting metallic stents (DESs) in percutaneous coronary intervention for coronary artery disease. While numerous studies have compared BVSs to DESs, none have assessed clinical outcomes beyond 5 years. Objectives: This study aimed to compare the 10-year clinical outcomes of patients treated with BVSs vs. DESs. Methods: The EverBio-2 trial (Comparison of Everolimus- and Biolimus-Eluting Coronary Stents with Everolimus-Eluting Bioresorbable Vascular Scaffold) is a single-center, assessor-blinded, randomized controlled trial that enrolled 240 patients allocated in a 1:1:1 ratio to receive BVSs, everolimus-eluting stents, or biolimus-eluting stents (BESs). Clinical follow-up was scheduled for 10 years. Results: Clinical follow-up was completed in 222 patients (93%) at the 10-year mark. The rate of device-oriented composite events (DOCE) was 28% in the DES group and 29% in the BVS group ( Conclusions: Over 10 years, the rates of clinical DOCE and POCE were similar between the BVS and DES groups but individual outcomes of stent thrombosis were higher (3%) in the BVS group compared to the DES group. Clinical Trial Registration: ClinicalTrials.gov, identifier (NCT01711931).

Indexed as

bioresorbable vascular scaffold (BVS)coronary artery diseasedrug-eluting stent (DES)percutaneous coronary intervention (PCI)randomized clinical trial

Identifiers

PMID39323753
PMCPMC11423422

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Registered trials

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.