Complex and High-Risk Coronary Interventional Procedures

A special issue of Journal of Personalized Medicine (ISSN 2075-4426). This special issue belongs to the section "Clinical Medicine, Cell, and Organism Physiology".

Deadline for manuscript submissions: 10 February 2026 | Viewed by 1254

Special Issue Editors


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Guest Editor
Department of Internal Medicine, Invasive Cardiology Division, University of Szeged, 6720 Szeged, Hungary
Interests: vascular medicine; cardiovascular system; stents; angiography; carotid arteries; coronary angioplasty; vascular diseases
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Guest Editor
Department of Cardiology, Medical University of Graz, 8010 Graz, Austria
Interests: cardiovascular system; stents; angiography; coronary angioplasty; fractional flow reserve
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Guest Editor
Department of Cardiology, “Niculae Stancioiu” Heart Institute, University of Medicine and Pharmacy, 400001 Cluj-Napoca, Romania
Interests: vascular medicine; cardiovascular system; stents; angiography; coronary angioplasty; vascular diseases
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Special Issue Information

Dear Colleagues,

Background & history of this topic: Advanced percutaneous coronary intervention (PCI) techniques used during complex high-risk intervention (CHIP) include rotational, orbital, and laser, specialized antegrade and retrograde coronary artery chronic total occlusion (CTO) approaches, and complex bifurcation stenting. After receiving CHIP, patients often experience dramatic improvement in symptoms, improved quality of life, and less re-admissions to the hospital. We also include clinical subsets such as CHIP intervention in severe heart failure (HFrEF) and valve disease (aortic stenosis and mitral regurgitation).

Aim and scope of the special issue:

The goal of this Research Topic is the following:
1) To show long-term results of CHIP interventions such as CTO, bifurcation, multivessel, and left main PCI.
2) To highlight the importance of LVAD use in complex CHIP cases.
3) To update the current knowledge of technical aspect of complex CHIP PCI.
4) To gain exposure to CHIP-related complications and their management.

Cutting-edge research:

  1. Long-term results of CHIP (CTO, bifurcation) procedures.
  2. Short-term results of coronary CTO recanalization (CTO, bifurcation) interventions.
  3. CHIP procedures in ACS.
  4. New devices and approaches during CHIP procedures.
  5. New access sites to perform CHIP procedures.

The kind of papers that we are soliciting are as follows:

Potential topics include, but are not limited to, the following: left main intervention, bifurcation intervention, chronic total occlusion recanalization, and multivessel disease intervention.

Dr. Zoltan Ruzsa
Dr. Toth-Gayor Gabor
Dr. Alexandru Achim
Guest Editors

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Keywords

  • complex high-risk intervention (CHIP)
  • coronary bifurcation
  • coronary chronic total occlusion
  • severe coronary calcification
  • protected PCI
  • access site I during CHIP procedures

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Published Papers (1 paper)

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9 pages, 762 KiB  
Protocol
The Design and Feasibility of Optimal Treatment for Coronary Drug-Eluting Stent In-Stent Restenosis (OPEN-ISR)—A Prospective, Randomised, Multicentre Clinical Trial
by Péter Márton Kulyassa, Balázs Tamás Németh, István Hizoh, Laura Krisztina Jankó, Zoltán Ruzsa, Zoltán Jambrik, Brúnó Bánk Balázs, Dávid Becker, Béla Merkely and István Ferenc Édes
J. Pers. Med. 2025, 15(2), 60; https://doi.org/10.3390/jpm15020060 - 2 Feb 2025
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Abstract
Introduction: Percutaneous coronary intervention (PCI) with drug-eluting stents (DES) is a cornerstone of the management of ischemic heart disease. However, in-stent restenosis (ISR) remains a significant clinical challenge, occurring in approximately 5–10% of patients undergoing PCI. This study is designed to compare the [...] Read more.
Introduction: Percutaneous coronary intervention (PCI) with drug-eluting stents (DES) is a cornerstone of the management of ischemic heart disease. However, in-stent restenosis (ISR) remains a significant clinical challenge, occurring in approximately 5–10% of patients undergoing PCI. This study is designed to compare the efficacy and safety of the primary therapeutic approaches for DES-ISR, specifically drug-coated balloons (DCBs)—paclitaxel-coated balloons (PCBs) and sirolimus-coated balloons (SCBs)—with a new-generation everolimus-eluting stent (EES), contributing to the evolving field of personalized medicine. Methods and Analysis: This prospective, multicentre, randomised, non-inferiority trial aims to enroll 150 patients with DES-ISR, who will be randomised into one of the following: SCB, PCB, or EES. The primary endpoint comparing DCB and EES is late lumen loss (LLL) at 6 months, as measured by quantitative coronary angiography (QCA). Secondary endpoints comparing the three arms include a device-oriented composite endpoint, intraluminal gain, optical coherence tomography (OCT) measured LLL, and correlations between LLL and quantitative flow ratio (QFR). The primary endpoint will be analysed using a non-inferiority design, with a margin set at 0.25 mm, for which the sample size was calculated. Statistical analysis of the primary endpoint will be conducted on an intention-to-treat basis with a one-tailed Mann–Whitney U test with a significance level of 95. Secondary endpoints will be analysed via superiority testing using ANOVA, the Kruskal–Wallis test, logistic regression, or Fisher’s exact test, as appropriate. Ethics and Dissemination: The study protocol has been approved by the Medical Devices Department of the Hungarian National Institute of Pharmacy and Nutrition, ensuring compliance with ethical standards as outlined in the Declaration of Helsinki. All investigators declare no conflicts of interest related to this study. The trial is registered in ClinicalTrials.gov under the ID: NCT04862052. Full article
(This article belongs to the Special Issue Complex and High-Risk Coronary Interventional Procedures)
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