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Ten-Year Outcome of Recanalization or Medical Therapy for Concomitant Chronic Total Occlusion After Myocardial Infarction.
van Veelen, Anna; Coerkamp, Casper F; Somsen, Yvemarie B O; Råmunddal, Truls; Ioanes, Dan; Laanmets, Peep; van der Schaaf, René J; Eriksen, Erlend; Bax, Matthijs; Suttorp, Maarten Jan; Strauss, Bradley H; Barbato, Emanuele; Marques, Koen M; Meuwissen, Martijn; Bertrand, Olivier; van der Ent, Martin; Knaapen, Paul; Tijssen, Jan G P; Claessen, Bimmer E P M; Hoebers, Loes P C; Elias, Joëlle; Henriques, José P S.
Afiliación
  • van Veelen A; Department of Cardiology, Heart Center, Amsterdam UMC, Location AMC Amsterdam Cardiovascular Sciences Amsterdam the Netherlands.
  • Coerkamp CF; Department of Cardiology, Heart Center, Amsterdam UMC, Location AMC Amsterdam Cardiovascular Sciences Amsterdam the Netherlands.
  • Somsen YBO; Department of Cardiology, Heart Center, Amsterdam UMC, Location VUMC Amsterdam Cardiovascular Sciences Amsterdam the Netherlands.
  • Råmunddal T; Department of Cardiology Sahlgrenska University Hospital Gothenburg Sweden.
  • Ioanes D; Department of Cardiology Sahlgrenska University Hospital Gothenburg Sweden.
  • Laanmets P; Department of Cardiology North-Estonia Medical Center Tallinn Estonia.
  • van der Schaaf RJ; Department of Cardiology OLVG Hospital Amsterdam the Netherlands.
  • Eriksen E; Department of Cardiology Haukeland University Hospital Bergen Norway.
  • Bax M; Department of Cardiology Haga Teaching Hospital The Hague the Netherlands.
  • Suttorp MJ; Department of Cardiology St. Antonius Hospital Nieuwegein the Netherlands.
  • Strauss BH; Department of Cardiology Sunnybrook Health Sciences Centre Toronto Canada.
  • Barbato E; Department of Clinical and Molecular Medicine Sapienza University of Rome Rome Italy.
  • Marques KM; Department of Cardiology, Heart Center, Amsterdam UMC, Location VUMC Amsterdam Cardiovascular Sciences Amsterdam the Netherlands.
  • Meuwissen M; Department of Cardiology Amphia Hospital Breda the Netherlands.
  • Bertrand O; Department of Cardiology Quebec Heart-Lung Institute Quebec Canada.
  • van der Ent M; Department of Cardiology Maasstad Hospital Rotterdam the Netherlands.
  • Knaapen P; Department of Cardiology, Heart Center, Amsterdam UMC, Location VUMC Amsterdam Cardiovascular Sciences Amsterdam the Netherlands.
  • Tijssen JGP; Department of Cardiology, Heart Center, Amsterdam UMC, Location AMC Amsterdam Cardiovascular Sciences Amsterdam the Netherlands.
  • Claessen BEPM; Department of Cardiology, Heart Center, Amsterdam UMC, Location AMC Amsterdam Cardiovascular Sciences Amsterdam the Netherlands.
  • Hoebers LPC; Department of Cardiology, Heart Center, Amsterdam UMC, Location AMC Amsterdam Cardiovascular Sciences Amsterdam the Netherlands.
  • Elias J; Department of Cardiology Maastricht UMC+ Maastricht the Netherlands.
  • Henriques JPS; Department of Cardiology, Heart Center, Amsterdam UMC, Location AMC Amsterdam Cardiovascular Sciences Amsterdam the Netherlands.
J Am Heart Assoc ; 13(10): e033556, 2024 May 21.
Article en En | MEDLINE | ID: mdl-38726918
ABSTRACT

BACKGROUND:

The EXPLORE (Evaluating Xience and Left Ventricular Function in PCI on Occlusions After STEMI) trial was the first and only randomized trial investigating chronic total occlusion (CTO) percutaneous coronary intervention (PCI) early after primary PCI for ST-segment-elevation myocardial infarction, compared with medical therapy for the CTO. We performed a 10-year follow-up of EXPLORE to investigate long-term safety and clinical impact of CTO PCI after ST-segment-elevation myocardial infarction, compared with no-CTO PCI. METHODS AND

RESULTS:

In EXPLORE, 302 patients post-ST-segment-elevation myocardial infarction with concurrent CTO were randomized to CTO PCI within ≈1 week or no-CTO PCI. We performed an extended clinical follow-up for the primary end point of major adverse cardiac events, consisting of cardiovascular death, coronary artery bypass grafting, or myocardial infarction. Secondary end points included all-cause death, angina, and dyspnea. Median follow-up was 10 years (interquartile range, 8-11 years). The primary end point occurred in 25% of patients with CTO PCI and in 24% of patients with no-CTO PCI (hazard ratio [HR], 1.11 [95% CI, 0.70-1.76]). Cardiovascular mortality was higher in the CTO PCI group (HR, 2.09 [95% CI, 1.10-2.50]), but all-cause death was similar (HR, 1.53 [95% CI, 0.93-2.50]). Dyspnea relief was more frequent after CTO PCI (83% versus 65%, P=0.005), with no significant difference in angina.

CONCLUSIONS:

This 10-year follow-up of patients post-ST-segment-elevation myocardial infarction randomized to CTO PCI or no-CTO PCI demonstrated no clinical benefit of CTO PCI in major adverse cardiac events or overall mortality. However, CTO PCI was associated with a higher cardiovascular mortality compared with no-CTO PCI. Our long-term data support a careful weighing of effective symptom relief against an elevated cardiovascular mortality risk in CTO PCI decisions. REGISTRATION URL https//www.trialregister.nl; Unique identifier NTR1108.
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Oclusión Coronaria / Intervención Coronaria Percutánea / Infarto del Miocardio con Elevación del ST Límite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: J Am Heart Assoc Año: 2024 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Oclusión Coronaria / Intervención Coronaria Percutánea / Infarto del Miocardio con Elevación del ST Límite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: J Am Heart Assoc Año: 2024 Tipo del documento: Article