Very long-term outlook of acute coronary syndromes after percutaneous coronary intervention with implantation of polymer-free versus durable-polymer new-generation drug-eluting stents.


Journal

Minerva medica
ISSN: 1827-1669
Titre abrégé: Minerva Med
Pays: Italy
ID NLM: 0400732

Informations de publication

Date de publication:
Oct 2023
Historique:
pubmed: 9 6 2023
medline: 9 6 2023
entrez: 9 6 2023
Statut: ppublish

Résumé

Detailed long-term follow-up data on patients with acute coronary syndromes (ACS) in general, and those with ST-elevation myocardial infarction (STEMI) in particular, are limited. We aimed to appraise the long-term outlook of patients undergoing percutaneous coronary intervention (PCI) with state-of-the-art coronary stents for STEMI, other types of ACS and stable coronary artery disease (CAD), and also explore the potential beneficial impact of new-generation polymer-free drug-eluting stents (DES) in this setting. Baseline, procedural and very long-term outcome data on patients undergoing PCI and randomized to implantation of new-generation polymer-free vs. durable polymer DES were systematically collected, explicitly distinguishing subjects with admission diagnosis of STEMI, non-ST-elevation ACS (NSTEACS), and stable CAD. Outcomes of interest included death, myocardial infarction, revascularization (i.e. patient-oriented composite endpoints [POCE]), major adverse cardiac events (MACE), and device-oriented composite endpoints (DOCE). A total of 3002 patients were included, 1770 (59.0%) with stable CAD, 921 (30.7%) with NSTEACS, and 311 (10.4%) with STEMI. At long-term follow-up (7.5±3.1 years), all clinical events were significantly more common in the NSTEACS group and, to a lesser extent, in the stable CAD group (e.g. POCE occurred in, respectively, 637 [44.7%] vs. 964 [37.9%] vs. 133 [31.5%], P<0.001). While these differences were largely attributable to adverse coexisting features in patients with NSTEACS (e.g. advanced age, insulin-dependent diabetes, and extent of CAD), the unfavorable outlook of patients presenting with NSTEACS persisted even after multivariable adjustment including several prognostically relevant factors (hazard ratio [HR] of NSTEACS vs. stable CAD 1.19 [95% confidence interval 1.03-1.38], P=0.016). Notably, even after encompassing all prognostically impactful features, no difference between polymer-free and permanent polymer drug-eluting stents appeared (HR=0.96 [0.84-1.10], P=0.560). Unstable coronary artery disease, especially when presenting without ST-elevation, represents an informative marker of adverse long-term prognosis in current state-of-the-art invasive cardiology practice. Even considering admission diagnosis, and despite of using no polymer, polymer-free DES showed similar results with regards to safety and efficacy when compared with DES with permanent polymer.

Sections du résumé

BACKGROUND BACKGROUND
Detailed long-term follow-up data on patients with acute coronary syndromes (ACS) in general, and those with ST-elevation myocardial infarction (STEMI) in particular, are limited. We aimed to appraise the long-term outlook of patients undergoing percutaneous coronary intervention (PCI) with state-of-the-art coronary stents for STEMI, other types of ACS and stable coronary artery disease (CAD), and also explore the potential beneficial impact of new-generation polymer-free drug-eluting stents (DES) in this setting.
METHODS METHODS
Baseline, procedural and very long-term outcome data on patients undergoing PCI and randomized to implantation of new-generation polymer-free vs. durable polymer DES were systematically collected, explicitly distinguishing subjects with admission diagnosis of STEMI, non-ST-elevation ACS (NSTEACS), and stable CAD. Outcomes of interest included death, myocardial infarction, revascularization (i.e. patient-oriented composite endpoints [POCE]), major adverse cardiac events (MACE), and device-oriented composite endpoints (DOCE).
RESULTS RESULTS
A total of 3002 patients were included, 1770 (59.0%) with stable CAD, 921 (30.7%) with NSTEACS, and 311 (10.4%) with STEMI. At long-term follow-up (7.5±3.1 years), all clinical events were significantly more common in the NSTEACS group and, to a lesser extent, in the stable CAD group (e.g. POCE occurred in, respectively, 637 [44.7%] vs. 964 [37.9%] vs. 133 [31.5%], P<0.001). While these differences were largely attributable to adverse coexisting features in patients with NSTEACS (e.g. advanced age, insulin-dependent diabetes, and extent of CAD), the unfavorable outlook of patients presenting with NSTEACS persisted even after multivariable adjustment including several prognostically relevant factors (hazard ratio [HR] of NSTEACS vs. stable CAD 1.19 [95% confidence interval 1.03-1.38], P=0.016). Notably, even after encompassing all prognostically impactful features, no difference between polymer-free and permanent polymer drug-eluting stents appeared (HR=0.96 [0.84-1.10], P=0.560).
CONCLUSIONS CONCLUSIONS
Unstable coronary artery disease, especially when presenting without ST-elevation, represents an informative marker of adverse long-term prognosis in current state-of-the-art invasive cardiology practice. Even considering admission diagnosis, and despite of using no polymer, polymer-free DES showed similar results with regards to safety and efficacy when compared with DES with permanent polymer.

Identifiants

pubmed: 37293892
pii: S0026-4806.23.08684-6
doi: 10.23736/S0026-4806.23.08684-6
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

590-600

Auteurs

Francesco Versaci (F)

UOC UTIC Emodinamica e Cardiologia, Santa Maria Goretti Hospital, Latina, Italy.

Sebastian Kufner (S)

Deutsches Herzzentrum München, Technische Universität München (TUM), Munich, Germany.

Salvatore Cassese (S)

Deutsches Herzzentrum München, Technische Universität München (TUM), Munich, Germany.

Michael Joner (M)

Deutsches Herzzentrum München, Technische Universität München (TUM), Munich, Germany.
German Center for Cardiovascular Research, partner site Munich Heart Alliance, Munich, Germany.

Katharina Mayer (K)

Deutsches Herzzentrum München, Technische Universität München (TUM), Munich, Germany.

Erion Xhepa (E)

Deutsches Herzzentrum München, Technische Universität München (TUM), Munich, Germany.

Tobias Koch (T)

Deutsches Herzzentrum München, Technische Universität München (TUM), Munich, Germany.

Jens Wiebe (J)

Deutsches Herzzentrum München, Technische Universität München (TUM), Munich, Germany.

Tareq Ibrahim (T)

Klinik und Poliklinik Innere Medizin I (Kardiologie, Angiologie und Pneumologie), Rechts der Isar Hospital, Technische Universität München (TUM), Munich, Germany.

Karl-Ludwig Laugwitz (KL)

German Center for Cardiovascular Research, partner site Munich Heart Alliance, Munich, Germany.
Klinik und Poliklinik Innere Medizin I (Kardiologie, Angiologie und Pneumologie), Rechts der Isar Hospital, Technische Universität München (TUM), Munich, Germany.

Heribert Schunkert (H)

Deutsches Herzzentrum München, Technische Universität München (TUM), Munich, Germany.
German Center for Cardiovascular Research, partner site Munich Heart Alliance, Munich, Germany.

Adnan Kastrati (A)

Deutsches Herzzentrum München, Technische Universität München (TUM), Munich, Germany.
German Center for Cardiovascular Research, partner site Munich Heart Alliance, Munich, Germany.

Robert A Byrne (RA)

Dublin Cardiovascular Research Institute, Mater Private Hospital, Dublin, Ireland.
School of Pharmacy and Biomolecular Sciences, Royal College of Surgeons in Ireland, Dublin, Ireland.

Alessandra Spagnoli (A)

Section of BioMedical Statistics, Department of Public Health and Infectious Disease, Sapienza University, Rome, Italy.

Marco Bernardi (M)

Department of Clinical, Internal Medicine, Anesthesiology and Cardiovascular Sciences, Sapienza University, Rome, Italy.

Luigi Spadafora (L)

Department of Clinical, Internal Medicine, Anesthesiology and Cardiovascular Sciences, Sapienza University, Rome, Italy.

Giuseppe Biondi-Zoccai (G)

Department of Medical-Surgical Sciences and Biotechnologies, Sapienza University, Latina, Italy - giuseppe.biondizoccai@uniroma1.it.
Mediterranea Cardiocentro, Naples, Italy.

Classifications MeSH