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Updated: Aug 19, 2026

In Vivo Quantitative Assessment of Myocardial Structure, Function, Perfusion and Viability Using Cardiac Micro-computed Tomography
Published on: February 16, 2016
Computed Tomography-Derived Abrupt Wall-Thickness Transitions as Complementary Markers of Ventricular Tachycardia
Haruka Matsuura1, Tsukasa Kamakura2, Takashi Ikee2
1Department of Cardiovascular Medicine, National Cerebral and Cardiovascular Center, Osaka, Japan; Department of Advanced Cardiovascular Medicine, Graduate School of Medical Sciences, Kumamoto University, Kumamoto, Japan.
Background:
Functional substrate mapping for ventricular tachycardia (VT) is activation dependent and may incompletely delineate critical substrate.
Objectives:
This study sought to determine whether abrupt wall-thickness transitions on computed tomography angiography (CTA)-derived maps colocalize with mappable VT isthmus boundaries in patients with ischemic cardiomyopathy (ICM). Associations with deceleration zones (DZs) and VT-related sites in unmappable VTs were also assessed.
Methods:
Color-coded left ventricular wall-thickness maps were generated from preprocedural CTA in 21 patients with ICM (median age: 67.0 years) using commercially available software. Abrupt wall-thickness transitions were defined as ≥3 millimeter change within a local 1-cm region based on closely spaced color transitions. Their spatial relationships with DZs during baseline rhythm mapping, mappable VT isthmus boundaries, and pace map-defined exit sites in unmappable VTs were evaluated.
Results:
Among 32 substrate maps, 25 DZs were identified, with 92% colocalizing with abrupt wall-thickness transitions. Of 40 VTs, activation mapping was feasible in 20. In these mappable VTs, VT isthmus boundaries colocalized with DZs in 10 (50.0%) and with abrupt wall-thickness transitions in 14 (70.0%). Among the unmappable VTs, good pace maps consistent with VT exit sites were identified in areas of abrupt wall-thickness transition in 17 of 20 VTs (85.0%). On segment-level analysis, the positive predictive value of abrupt wall-thickness transitions for identifying DZs and VT isthmus boundaries was modest (28.3% and 18.9%, respectively).
Conclusions:
Abrupt wall-thickness transitions on CTA-derived maps frequently colocalized with mappable VT isthmus boundaries and DZs in patients with ICM, supporting their role as complementary markers.
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