Incidence, prognosis and predictors of post-discharge heart failure in ST-elevation myocardial infarction (STEMI) patients with preserved left ventricular function: - A Study of the Collaborative Registry on Cardiovascular Magnetic Resonance in STEMI

Anno
2017
Proponente Luciano Agati - Professore Associato
Sottosettore ERC del proponente del progetto
Componenti gruppo di ricerca
Componente Categoria
Carlo Iacoboni Componenti il gruppo di ricerca
Giulia Benedetti Componenti il gruppo di ricerca
Componente Qualifica Struttura Categoria
Lorenzo Belli Student SCIENZE CARDIOVASCOLARI, RESPIRATORIE, NEFROLOGICHE, ANESTESIOLOGICHE E GERIATRICHE Altro personale Sapienza o esterni
Domenico Filomena Medical Doctor SCIENZE CARDIOVASCOLARI, RESPIRATORIE, NEFROLOGICHE, ANESTESIOLOGICHE E GERIATRICHE Altro personale Sapienza o esterni
Abstract

Aim of this study will be to analyze incidence, predictors and prognosis of de-novo heart failure occurring at 12 months follow-up in the subset of patients with left ventricular ejection fraction >50% after ST-elevation acute myocardial infarction (STEMI) and without history of previous heart failure (HF). The large database of "Acute Myocardial Infarction Cardiac Imaging" (AMICI) trial will be analyzed. This is a multicentre, prospective, longitudinal study conducted in a cohort of acute STEMI patients studied with cardiac magnetic resonance (CMR). Between May 2005 and May 2014, 512 acute STEMI patients from three tertiary referral centres [244 at University Hospitals Leuven, Leuven, Belgium (Centre A), 157 at La Sapienza University Hospital, Rome, Italy (Centre B), and 111 at Fondazione G. Monasterio, Pisa, Italy (Centre C)] were screened for study enrolment
Inclusion Criteria: All patients consecutively admitted to the cardiology departments of our tertiary hospitals, undergoing primary PCI for ST-segment elevation myocardial infarction, in which cardiac MR was performed within 5 days from admission. Only patients with LVEF > 50% after STEMI and without history of previous HF will be included in this study.
Exclusion Criteria:Patients died in hospital and those with no data on vital status and/or on HF status during follow-up, patients with history of HF, Killip III at admission, in-hospital HF, LVEF Clinical Endpoints:
- Primary endpoint:
Incidence and determinants of de novo HF at 1 year follow-up
- Secondary endpoints:
- Major adverse coronary events at 1 year follow-up in patients with normal LVEF after STEMI
- Incidence and determinants of LV remodeling at 1 year follow up in these subset of patients

ERC
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