Relationship Between the Current Definitions of Periprocedural Myocardial Infarction and Clinical Outcomes Following Percutaneous Coronary Revascularization

Since the beginning of the percutaneous coronary intervention (PCI) era, periprocedural myocardial infarction (PMI) has been recognized as a potential source of impaired outcomes in patients undergoing revascularization. Subsequently, several different definitions of PMI have been provided, coming from trial research groups or international consensus. Despite these efforts, the debate over the prognostic value or PMI in terms of mortality risk, as well as its role in defining composite ischemic endpoints in clinical investigations, has been extremely active. Currently, three international definitions of PMI are available: the Universal Definition of Myocardial Infarction (UDMI), the Academic Research Consortium (ARC)-2 definition, and the definition by the Society for Cardiovascular Angiography and Interventions (SCAI). These definitions differ significantly in terms of sensitivity and prognostic relevance, which has led to heterogeneous findings in clinical studies investigating this topic. Thus, this review aims to provide an overview of the main features of these definitions, their association with the risk of mortality, and how different definitions can influence the results of major investigations in the research setting.

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Journal
Reviews in Cardiovascular Medicine
Published
2025-11-11
DOI
https://doi.org/10.31083/rcm43839
Citations
1
Primary Topic
Coronary Interventions and Diagnostics
Type
article
Field-Weighted Citation Impact
2.01
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article

Relationship Between the Current Definitions of Periprocedural Myocardial Infarction and Clinical Outcomes Following Percutaneous Coronary Revascularization

Giulia Nardi, Iginio Colaiori, Giovanni Occhipinti, Fabio Mangiacapra et al.
1 citations
Reviews in Cardiovascular Medicine
Coronary Interventions and Diagnostics
2.01
article

Relationship Between the Current Definitions of Periprocedural Myocardial Infarction and Clinical Outcomes Following Percutaneous Coronary Revascularization

Giulia Nardi, Iginio Colaiori, Giovanni Occhipinti, Fabio Mangiacapra, Francesco De Felice, Domenico Gabrielli, Rocco Vergallo, Carlo Briguori, Marco Lombardi, Carmine Musto, Luca Paolucci
article en
1 citations

Abstract

Since the beginning of the percutaneous coronary intervention (PCI) era, periprocedural myocardial infarction (PMI) has been recognized as a potential source of impaired outcomes in patients undergoing revascularization. Subsequently, several different definitions of PMI have been provided, coming from trial research groups or international consensus. Despite these efforts, the debate over the prognostic value or PMI in terms of mortality risk, as well as its role in defining composite ischemic endpoints in clinical investigations, has been extremely active. Currently, three international definitions of PMI are available: the Universal Definition of Myocardial Infarction (UDMI), the Academic Research Consortium (ARC)-2 definition, and the definition by the Society for Cardiovascular Angiography and Interventions (SCAI). These definitions differ significantly in terms of sensitivity and prognostic relevance, which has led to heterogeneous findings in clinical studies investigating this topic. Thus, this review aims to provide an overview of the main features of these definitions, their association with the risk of mortality, and how different definitions can influence the results of major investigations in the research setting.

Reviews in Cardiovascular MedicineVol. 26(11)
Università Campus Bio-Medico (IT), Azienda Ospedaliero Universitaria San Giovanni Battista (IT), Hospital Clínic de Barcelona (ES), Azienda Ospedaliero-Universitaria Careggi (IT), Clinica Mediterranea (IT), Ospedale Santa Maria Goretti (IT), Ospedale Policlinico San Martino (IT), Carlo Forlanini Hospital (IT), Consorci Institut D'Investigacions Biomediques August Pi I Sunyer (ES), University of Genoa (IT)
Openalex Percentile: Top 10%
Coronary Interventions and Diagnostics
2.01
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