Evidence map›Paper›PMID 37808526›Full record

ReviewEuropean heart journal open2023

In-stent restenosis after percutaneous coronary intervention: emerging knowledge on biological pathways.

Francesco Pelliccia, Marco Zimarino, Giampaolo Niccoli, Doralisa Morrone, Giuseppe De Luca, Fabio Miraldi, Raffaele De Caterina

Open access · goldAbstract readReview
In one paragraph

Review in European heart journal open, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed, 2 pooled it
20.3field-weighted citation impact, top 1% 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

42 citing papers in PubMed, 2 syntheses or guidelines pooled it, 64 citations in OpenAlex.

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  17. Observational
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  19. Diabetes-related ten-year outcomes after percutaneous coronary intervention of in-stent restenosis.Clinical research in cardiology : official journal of the German Cardiac Society · 2026
    Observational
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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 at 5 institutions in 1 country.

Francesco PellicciaDepartment of Cardiovascular Sciences, University Sapienza, Viale del Policlinico 155, 00161 Rome, Italy.ORCID https://orcid.org/0000-0003-1260-1308
Marco ZimarinoDepartment of Neuroscience, Imaging and Clinical Sciences, "G. d'Annunzio" University, Viale Abruzzo, 332, 66100 Chieti, Italy.ORCID https://orcid.org/0000-0001-5455-6010
Giampaolo NiccoliDepartment of Cardiology, University of Parma, Piazzale S. Francesco, 3, 43121 Parma, Italy.
Doralisa MorroneDepartment of Surgical, Medical and Molecular Pathology and of Critical Sciences, University of Pisa, Lungarno Antonio Pacinotti 43, 56126 Pisa, Italy.
Giuseppe De LucaDivision of Cardiology, AOU "Policlinico G. Martino", Department of Clinical and Experimental Medicine, University of Messina, Via Consolare Valeria 1, 98124 Messina, Italy.
Fabio MiraldiDepartment of Cardiovascular Sciences, University Sapienza, Viale del Policlinico 155, 00161 Rome, Italy.
Raffaele De CaterinaDepartment of Surgical, Medical and Molecular Pathology and of Critical Sciences, University of Pisa, Lungarno Antonio Pacinotti 43, 56126 Pisa, Italy.ORCID https://orcid.org/0000-0003-1637-574X
Policlinico Umberto I · ITUniversity of Pisa · ITUniversity of Chieti-Pescara · ITUniversity of Messina · ITUniversity of Parma · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Percutaneous coronary intervention (PCI) has evolved significantly over the past four decades. Since its inception, in-stent restenosis (ISR)-the progressive reduction in vessel lumen diameter after PCI-has emerged as the main complication of the procedure. Although the incidence of ISR has reduced from 30% at 6 months with bare-metal stents to 7% at 4 years with drug-eluting stents (DESs), its occurrence is relevant in absolute terms because of the dimensions of the population treated with PCI. The aim of this review is to summarize the emerging understanding of the biological pathways that underlie ISR. In-stent restenosis is associated with several factors, including patient-related, genetic, anatomic, stent, lesion, and procedural characteristics. Regardless of associated factors, there are common pathophysiological pathways involving molecular phenomena triggered by the mechanical trauma caused by PCI. Such biological pathways are responses to the denudation of the intima during balloon angioplasty and involve inflammation, hypersensitivity reactions, and stem cell mobilization particularly of endothelial progenitor cells (EPCs). The results of these processes are either vessel wall healing or neointimal hyperplasia and/or neo-atherosclerosis. Unravelling the key molecular and signal pathways involved in ISR is crucial to identify appropriate therapeutic strategies aimed at abolishing the 'Achille's heel' of PCI. In this regard, we discuss novel approaches to prevent DES restenosis. Indeed, available evidence suggests that EPC-capturing stents promote rapid stent re-endothelization, which, in turn, has the potential to decrease the risk of stent thrombosis and allow the use of a shorter-duration dual antiplatelet therapy.

Indexed as

Bare-metal stentsDrug-eluting stentsEndothelial progenitor cellsHypersensitivityInflammationIn-stent restenosisPercutaneous coronary intervention

Identifiers

PMID37808526
PMCPMC10558044
OpenAlexW4386173276

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.