State-of-the-Art Review
Sudden Cardiac Death in Ischemic Heart Disease: From Imaging Arrhythmogenic Substrate to Guiding Therapies

https://doi.org/10.1016/j.jcmg.2019.10.021Get rights and content
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Highlights

  • Sudden cardiac death remains a leading cause of cardiovascular deaths in patients with ischemic heart disease, and current risk stratification is limited.

  • Further studies are needed for a better risk stratification in these patients.

  • Fibrosis is an arrhythmogenic substrate in patients with ischemic heart disease, and cardiac magnetic resonance is the modality of choice to display scar and diffuse fibrosis.

  • Cardiac magnetic resonance is a promising tool to improve risk stratification in patients with ischemic heart disease.

Abstract

Despite substantial medical advances over the past decades, sudden cardiac death (SCD) remains a leading cause of cardiovascular deaths in patients with ischemic heart disease. The presence of structural heart disease with left ventricular ejection fraction <35% is the current criteria for implantable cardioverter-defibrillator therapy as a primary prevention to SCD. However, more than 80% of patients who suffer SCD have a left ventricular ejection fraction >35%, whereas few patients who received an implantable cardioverter-defibrillator required appropriate defibrillation. Cardiac magnetic resonance enables the visualization of the arrhythmogenic myocardial substrate including the presence and pattern of scar and fibrosis. The most promising of these features, besides left ventricular function, strain analysis, and morphology, include tissue characterization using late-gadolinium enhancement, T1 mapping, and extracellular volume fraction calculation. We review the current evidence of SCD relating to ischemic heart disease, provide insights into imaging of the arrhythmogenic substrate that produces lethal ventricular arrhythmia, and discuss how imaging may guide therapies toward SCD prevention.

Key Words

arrhythmia
cardiac magnetic resonance
computed tomography
coronary artery disease
extracellular volume fraction
ischemic heart disease
late gadolinium enhancement
positron emission tomography
substrate
sudden cardiac death
ventricular tachycardia

Abbreviations and Acronyms

ACE
angiotensin-converting enzyme
ARB
angiotensin receptor blocker
CFR
coronary flow reserve
CMR
cardiac magnetic resonance
CT
computed tomography
ECV
extracellular volume fraction
GDMT
guideline-directed medical therapy
ICD
implantable cardioverter-defibrillator
IHD
ischemic heart disease
LGE
late gadolinium enhancement
LVEF
left ventricular ejection fraction
MDE
myocardial delayed enhancement
PET
positron emission tomography
SCD
sudden cardiac death
SPECT
single-photon emission tomography
VT
ventricular tachycardia

Cited by (0)

Dr. Gräni has received funding support from the Novartis Foundation for Medical-Biological Research, Bangerter-Rhyner Foundation, Swiss Sports Medicine Society, and Kreislauf Kardiologie Foundation. Dr. Benz has received research grant from Theodor und Ida Herzog-Egli-Foundation. Dr. Windecker has received research grants to the institution from Amgen, Abbott, Bayer, Boston Scientific, Biotronik, Medtronic, Edwards Lifesciences, St. Jude Medical, and Terumo. Dr. Kwong has received research funding from the National Institutes of Health, Society for Cardiovascular Magnetic Resonance, and Myokardia Pharmaceuticals. All other authors have reported that they have no relationships relevant to the contents of this paper to disclose. Dudley Pennell, MD, was Guest Editor on this paper.

The authors attest they are in compliance with human studies committees and animal welfare regulations of the authors’ institutions and Food and Drug Administration guidelines, including patient consent where appropriate. For more information, visit the JACC: Cardiovascular Imaging author instructions page.