Late gadolinium enhancement and the risk of ventricular arrhythmias and sudden death in NYHA class I patients with non‐ischaemic cardiomyopathy

Author:

Di Marco Andrea123,Brown Pamela4,Mateus Gemma1,Faga Valentina12,Nucifora Gaetano4,Claver Eduard12,Viedma Jisela1,Galvan Francisco1,Bradley Joshua4,Dallaglio Paolo D.12,de Frutos Fernando12,Miller Christopher A.356,Comín‐Colet Josep127,Anguera Ignasi12,Schmitt Matthias34

Affiliation:

1. Department of Cardiology Hospital Universitari de Bellvitge Barcelona Spain

2. Bioheart‐Cardiovascular Diseases Group, Cardiovascular, Respiratory and Systemic Diseases and Cellular Aging Program Institut d'Investigació Biomèdica de Bellvitge–IDIBELL Barcelona Spain

3. Division of Cardiovascular Sciences, School of Medical Sciences, Faculty of Biology, Medicine and Health University of Manchester, Manchester Academic Health Science Centre Manchester UK

4. Department of Cardiology, North West Heart Centre Manchester University NHS Foundation Trust Manchester UK

5. Manchester University NHS Foundation Trust Manchester Academic Health Science Centre Manchester UK

6. Wellcome Centre for Cell‐Matrix Research, Division of Cell‐Matrix Biology & Regenerative Medicine, School of Biology, Faculty of Biology, Medicine and Health University of Manchester, Manchester Academic Health Science Centre Manchester UK

7. Department of Clinical Sciences, School of Medicine University of Barcelona Barcelona Spain

Abstract

AimTo compare the risk of ventricular arrhythmias (VA) and sudden death (SD) between New York Heart Association (NYHA) class I and NYHA class II–III patients with non‐ischaemic cardiomyopathy (NICM).Methods and resultsObservational retrospective cohort study including patients with NICM who underwent cardiac magnetic resonance at two hospitals. The primary endpoint included appropriate implantable cardioverter defibrillator (ICD) therapies, sustained ventricular tachycardia, resuscitated cardiac arrest and SD. The secondary endpoint included heart failure (HF) hospitalizations, heart transplant, left ventricular assist device implant or HF death. Overall, 698 patients were included, 33% in NYHA class I. During a median follow‐up of 31 months, the primary endpoint occurred in 57 patients (8%), with no differences between NYHA class I and NYHA class II–III cases (7% vs. 9%, p = 0.62). Late gadolinium enhancement (LGE) was the only independent predictor of the primary outcome both in NYHA class I and NYHA class II–III patients. LGE+ NYHA class I patients had a similar cumulative incidence of the primary endpoint as compared to LGE+ NYHA class II–III (p = 0.92) and a significantly higher risk as compared to LGE– NYHA class II–III cases (p < 0.001). The risk of the secondary endpoint was significantly higher in patients in NYHA class II–III as compared to those in NYHA class I (hazard ratio 3.2, p = 0.001).ConclusionsPatients with NICM in NYHA class I are not necessarily at low risk of VA and SD. Actually, LGE+ NYHA class I patients have a high risk. NYHA class I patients with high‐risk factors, such as LGE, could benefit from primary prevention ICD at least as much as those in NYHA class II–III with the same risk factors.

Publisher

Wiley

Subject

Cardiology and Cardiovascular Medicine

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