Evidence map›Paper›PMID 41460848›Full record

ArticlePloS one2025

Long-term outcomes following drug-coated balloons versus thin-strut drug-eluting stents for treatment of in-stent restenosis in Chronic Kidney Disease (CKD Dragon-Registry).

Rafał Januszek, Marta Chamera, Sylwia Iwańczyk, Fabrizio D'Ascenzo, Łukasz Kuźma, Brunon Tomasiewicz, Piotr Niezgoda, Rafał Wolny, Mariusz Kowalewski, Maciej Wybraniec and 17 more

Abstract readComparative Study
In one paragraph

Article in PloS one, 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. 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

27 authors.

Rafał JanuszekFaculty of Medicine and Health Sciences, Andrzej Frycz Modrzewski Cracow University, Kraków, Poland.ORCID https://orcid.org/0000-0002-6591-1919
Marta ChameraDepartment of Cardiology and Structural Heart Diseases, Medical University of Silesia, Katowice, Poland.
Sylwia IwańczykDCB Academy, Milano, Italy.
Fabrizio D'AscenzoDivision of Cardiology, Department of Internal Medicine, Città della Salute e della Scienza, University of Turin, Turin, Italy.
Łukasz KuźmaDepartment of Invasive Cardiology, Medical University of Bialystok, Bialystok, Poland.
Brunon TomasiewiczCentre for Heart Disease, University Hospital Wroclaw Department of Heart Disease, Wroclaw Medical University, Wrocław, Poland.
Piotr NiezgodaDepartment of Cardiology and Internal Medicine, Collegium Medicum, Nicolaus Copernicus University, Bydgoszcz, Poland.
Rafał WolnyDepartment of Interventional Cardiology and Angiology, National Institute of Cardiology, Warsaw, Poland.
Mariusz KowalewskiClinical Department of Cardiac Surgery and Transplantology, National Medical Institute of the Ministry of Interior and Administration, Warsaw, Poland.
Maciej Wybraniec1st Department of Cardiology, School of Medicine in Katowice, Medical University of Silesia, Katowice, Poland.
Krzysztof ReczuchCentre for Heart Disease, University Hospital Wroclaw Department of Heart Disease, Wroclaw Medical University, Wrocław, Poland.ORCID https://orcid.org/0000-0002-1699-739X
Sławomir DobrzyckiDepartment of Invasive Cardiology, Medical University of Bialystok, Bialystok, Poland.
Ovidio De FilippoDivision of Cardiology, Department of Internal Medicine, Città della Salute e della Scienza, University of Turin, Turin, Italy.
Artur PawlikJagiellonian University Medical College, Kraków, Poland.
Karol KasprzyckiJagiellonian University Medical College, Kraków, Poland.
Kamil SkowronJagiellonian University Medical College, Kraków, Poland.
Stanisław BartuśJagiellonian University Medical College, Kraków, Poland.
Maciej Lesiak1st Department of Cardiology, Poznan University of Medical Sciences, Poznan, Poland.ORCID https://orcid.org/0000-0003-2630-5016
Mariusz GąsiorThird Department of Cardiology, Medical University of Silesia, Zabrze, Poland.
Jacek KubicaDepartment of Cardiology and Internal Medicine, Collegium Medicum, Nicolaus Copernicus University, Bydgoszcz, Poland.
Tomasz PawłowskiDepartment of Cardiology, National Medical Institute of the Ministry of Interior and Administration, Warsaw, Poland.
Robert J GilDepartment of Cardiology, National Medical Institute of the Ministry of Interior and Administration, Warsaw, Poland.
Piotr WacińskiClinical Department of Interventional Cardiology, Medical University of Lublin, Lublin, Poland.
Francesco BrunoDivision of Cardiology, Department of Internal Medicine, Città della Salute e della Scienza, University of Turin, Turin, Italy.
Bernardo CorteseDCB Academy, Milano, Italy.ORCID https://orcid.org/0000-0002-5808-7810
Wojciech WojakowskiDepartment of Cardiology and Structural Heart Diseases, Medical University of Silesia, Katowice, Poland.ORCID https://orcid.org/0000-0002-3681-5207
Wojciech WańhaDepartment of Cardiology and Structural Heart Diseases, Medical University of Silesia, Katowice, Poland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We sought to investigated the outcomes of patients with chronic kidney disease (CKD) and drug-eluting stent (DES)-in-stent restenosis (ISR) undergoing percutaneous coronary intervention (PCI) with a drug-coated balloon (DCB) or thin strut drug-eluting stent (thin-DES). Consecutive patients with DES-ISR who underwent PCI with a thin-DES or a paclitaxel-coated DCB for DES-ISR were enrolled. The primary outcome was target lesion revascularization (TLR), while the secondary was target vessel revascularization (TVR) and device-oriented composite endpoint (DOCE). The pooled analysis included 1,317 patients, with 585 (44.42%) treated using a thin-DES and 732 (55.58%) by DCB. In the crude analysis of CKD patients (n = 286) undergoing PCI for ISR, thin-DES vs. DCB showed similar outcomes for TLR (hazard ratio [HR]=0.94, 95% confidence interval [CI]=0.44-2.00; p = 0.873), TVR (HR = 0.82, 95% CI = 0.44-1.55; p = 0.542), MI (HR = 0.71, 95% CI = 0.34-1.46; p = 0.348) and DOCE (HR = 0.71, 95% CI = 0.36-1.40; p = 0.325). After propensity score matching (n = 184), the HRs remained non-significant for TLR (0.52, 95% CI = 0.21-1.29; p = 0.159), TVR (0.54, 95% CI = 0.24-1.01; p = 0.134), MI (0.56, 95% CI = 0.24-1.32; p = 0.183), TV-MI (0.56, 95% CI = 0.09-3.39; p = 0.528), cardiac death (0.63, 95% CI = 0.10-3.81; p = 0.615), and DOCE (0.45, 95% CI = 0.19-1.04; p = 0.062). In conclusion, in CKD patients undergoing PCI for ISR, thin-DES treatment was associated with a numerical reduction in TLR, TVR, and DOCE compared with DCB. However, these differences did not achieve statistical significance in the crude or propensity score-matched analyses.

Indexed as

Coronary RestenosisDrug-Eluting StentsPercutaneous Coronary InterventionRenal Insufficiency, ChronicAgedFemaleHumansMaleMiddle AgedPaclitaxelRegistriesTreatment OutcomePaclitaxel

Identifiers

PMID41460848
PMCPMC12747340

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