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September 13, 2018Journal of Magnetic Resonance Imaging3 citations

Assessing regional left ventricular thickening dysfunction and dyssynchrony via personalized modeling and 3D wall thickness measurements for acute myocardial infarction

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AKAmirah KhalidUniversity of MalayaELEinly LimUniversity of MalayaBCBee Ting ChanUniversity of Nottingham Malaysia Campus

Key Result

3D personalized left ventricular modeling revealed significantly higher dyssynchrony in AMI patients compared to healthy subjects (15.0% vs. 7.5%, P < 0.01).

Study Design

Type

Observational (n=44)

Structured PICO

Does a 3D personalized LV model and thickening assessment framework accurately assess regional wall thickening dysfunction and dyssynchrony compared to clinical evaluation in AMI patients?

P
Population
44 subjects consisting of 15 healthy subjects and 29 acute myocardial infarction (AMI) patients
I
Intervention
3D personalized left ventricular (LV) models and thickening assessment framework using 1.5T steady-state free precession cine MRI and LGE MRI scans
C
Comparator
Clinical evaluation of infarct transmurality by an experienced cardiac radiologist based on the American Heart Association (AHA) 17-segment model
O
Outcome
Correlation of quantitative thickening measurements across all cardiac phases with clinical evaluation of infarct transmuralitysurrogate

A novel 3D personalized LV modeling framework using MRI can accurately assess regional wall thickening dysfunction and dyssynchrony, correlating strongly with infarct severity in AMI patients.

Main Result

Absolute Event Rate: 15% vs 7.5%

p-value: p=<0.01

Abstract

BACKGROUND: Existing clinical diagnostic and assessment methods could be improved to facilitate early detection and treatment of cardiac dysfunction associated with acute myocardial infarction (AMI) to reduce morbidity and mortality. PURPOSE: To develop 3D personalized left ventricular (LV) models and thickening assessment framework for assessing regional wall thickening dysfunction and dyssynchrony in AMI patients. STUDY TYPE: Retrospective study, diagnostic accuracy. SUBJECTS: Forty-four subjects consisting of 15 healthy subjects and 29 AMI patients. FIELD STRENGTH/SEQUENCE: 1.5T/steady-state free precession cine MRI scans; LGE MRI scans. ASSESSMENT: Quantitative thickening measurements across all cardiac phases were correlated and validated against clinical evaluation of infarct transmurality by an experienced cardiac radiologist based on the American Heart Association (AHA) 17-segment model. STATISTICAL TEST: Nonparametric 2-k related sample-based Kruskal-Wallis test; Mann-Whitney U-test; Pearson's correlation coefficient. RESULTS: Healthy LV wall segments undergo significant wall thickening (P 50% transmurality) underwent remarkable wall thinning during contraction (thickening index TI = 1.46 ± 0.26 mm) as opposed to healthy myocardium (TI = 4.01 ± 1.04 mm). For AMI patients, LV that showed signs of thinning were found to be associated with a significantly higher percentage of dyssynchrony as compared with healthy subjects (dyssynchrony index DI = 15.0 ± 5.0% vs. 7.5 ± 2.0%, P < 0.01). Also, a strong correlation was found between our TI and left ventricular ejection fraction (LVEF) (r = 0.892, P < 0.01), and moderate correlation between DI and LVEF (r = 0.494, P < 0.01). DATA CONCLUSION: The extracted regional wall thickening and DIs are shown to be strongly correlated with infarct severity, therefore suggestive of possible practical clinical utility. LEVEL OF EVIDENCE: 2 Technical Efficacy: Stage 1 J. Magn. Reson. Imaging 2019;49:1006-1019.

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Cite This Study

Khalid et al. (2018) conducted an observational in Acute myocardial infarction (AMI) (n=44). 3D personalized left ventricular models and thickening assessment framework vs. Healthy subjects was evaluated on Dyssynchrony index (DI) (p=<0.01). 3D personalized left ventricular modeling revealed significantly higher dyssynchrony in AMI patients compared to healthy subjects (15.0% vs. 7.5%, P < 0.01).

synapsesocial.com/papers/6a1dbd9c984ea5c2d0ce39c4https://doi.org/10.1002/jmri.26302
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