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Updated: Aug 10, 2026

In Vivo Quantitative Assessment of Myocardial Structure, Function, Perfusion and Viability Using Cardiac Micro-computed Tomography
Published on: February 16, 2016
Assessing myocardial viability to help select patients for revascularization to improve left ventricular dysfunction
1Carlyle Fraser Heart Center, Emory, GA, USA.
Insights
Identifying viable myocardium is crucial for improving left ventricular dysfunction after coronary artery disease revascularization. Positron emission tomography (PET) myocardial imaging is the gold standard for detecting this viable heart muscle.
Area of Science:
- Cardiology
- Nuclear Cardiology
- Cardiovascular Imaging
Background:
- Left ventricular dysfunction, often caused by coronary artery disease (CAD), leads to significant mortality, morbidity, and healthcare costs.
- Successful revascularization can improve left ventricular dysfunction, but patient outcomes depend on the presence of viable myocardium.
- Distinguishing viable myocardium from scar tissue is critical for selecting appropriate patients for revascularization.
Observation:
- Traditional methods like clinical history, ECG, and standard cardiac imaging often fail to accurately identify viable myocardium.
- Thallium-201 myocardial imaging with reinjection shows improvement but can still miss viable tissue.
- Positron emission tomography (PET) myocardial imaging, comparing perfusion and metabolic tracers (e.g., 18FDG), is recognized as the gold standard.
Findings:
- PET imaging, by assessing both blood flow and metabolic activity (18FDG uptake), reliably identifies myocardial viability.
- Other promising techniques include PET imaging of rubidium-82 (assessing tracer washout) and gated magnetic resonance imaging (MRI).
Implications:
- Accurate identification of viable myocardium using advanced imaging techniques like PET can optimize patient selection for revascularization.
- Improved patient selection can lead to better functional recovery, reduced disability, and potentially lower healthcare costs associated with left ventricular dysfunction.
- Further validation and integration of these advanced imaging modalities can enhance therapeutic decision-making in patients with coronary artery disease.
Abstract:
Left ventricular dysfunction has become one of the most common causes of death, disability, and health care costs. Left ventricular dysfunction is usually due to coronary artery disease (CAD) and can be improved considerably by successful revascularization in many, but not all, patients. The key issue determining whether revascularization will relieve left ventricular dysfunction is whether the patient has enough viable myocardium to improve after revascularization. Viable myocardium is located anatomically in the subepicardial layers of the left ventricular wall, above the infarct in the subendocardial layers in the distribution of a stenotic coronary artery. Clinical history, physical examination, resting or exercise ECG, and imaging studies of left ventricular function often fail to distinguish patients with viable myocardium. Thallium-201 myocardial imaging at stress and rest is better if performed with reinjection of thallium-201 at rest, but this method still misses many patients with viable myocardium. Positron emission tomographic (PET) myocardial imaging to compare distributions of a perfusion tracer versus a metabolic tracer (fluorine-18-fluoro-deoxyglucose, 18FDG) has been cited as the "gold standard" method to identify viable myocardium by position papers from several professional organizations. PET imaging of rubidium-82, a potassium analogue ("washout" from "early" [first 1.5 minutes] to "late" [next 5 minutes] images) and gated magnetic resonance imaging (MRI) also show promise.
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