Key result
Functional conduction abnormalities predominantly localized within thinned myocardium, with slow conduction zones demonstrating a mean wall thickness of 3.6 mm compared to 6.3 mm in remote myocardium.
Why the study?
Anatomical correlates of functional mapping tools within CT-derived myocardial wall-thickness maps during VT ablation are incompletely defined.
Does CT-derived wall-thickness mapping accurately identify functional slow conduction zones and critical isthmuses during VT ablation in patients with ischemic cardiomyopathy?
Observational (n=7)
No
Does CT-derived wall-thickness mapping accurately identify functional slow conduction zones and critical isthmuses during VT ablation in patients with ischemic cardiomyopathy?
CT-derived wall-thickness mapping identifies thinned myocardium that hosts slow conduction zones, but functional mapping remains essential as anatomical channels only colocalize with true functional isthmuses in 50% of cases.
Should not yet alter VT ablation practice; leaves open CT-WT utility to guide functional substrate mapping in trials.
Functional mapping tools such as Coherent Mapping (CM) and Isochronal Late Activation Mapping (ILAM) allow visualization of conduction slowing and block during ventricular tachycardia (VT) ablation; however, their anatomical correlates within computed tomography (CT)–derived myocardial wall-thickness (WT) maps are incompletely defined. We aimed to evaluate the spatial relationship between CT-derived WT characteristics and functional electroanatomical markers and to assess the predictive value of WT-derived conduction channels (WTC) for identifying critical VT isthmuses. Seven consecutive patients with ischemic cardiomyopathy undergoing VT ablation and pre-procedural contrast-enhanced CT were analyzed. WT maps and WTCs were reconstructed using the inHeart™ platform and integrated with CARTO 3 electroanatomical maps. CM-SCZs, ILAM-DZs, and lines of blocks (LOBs) were identified using predefined criteria and projected onto WT models. Local WT values, overlap with WT ≤ 5 mm regions, and Dice similarity coefficients were calculated to quantify anatomical–functional concordance. Eighteen CM-SCZs, 15 ILAM-DZs, and 12 LOBs were identified. Functional regions predominantly localized within thinned myocardium (WT ≤ 5 mm). Mean WT was 3.6 ± 0.8 mm for SCZs, 3.8 ± 0.9 mm for DZs, and 4.2 ± 1.1 mm for LOBs, compared with 6.3 ± 1.3 mm in remote myocardium (p < 0.01). SCZs overlapped with WT ≤ 5 mm areas by 74 ± 12% (Dice 0.67 ± 0.10), while DZs showed 70 ± 15% overlap (Dice 0.63 ± 0.11). Direct correspondence between WTCs and SCZs occurred in 50% of cases. Although CT-derived WTCs identify regions at risk, functional mapping remains essential for precise substrate delineation. Integrated CT and CM/ILAM analysis may enhance targeting efficiency during VT ablation.
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Yalin et al. (2026) conducted an observational in Ischemic cardiomyopathy with scar-related ventricular tachycardia (n=7). CT-derived wall-thickness mapping integrated with Coherent Mapping and ILAM vs. Remote myocardium was evaluated on Mean wall thickness in Coherent Mapping slow conduction zones (CM-SCZs) (p=<0.01). Functional conduction abnormalities predominantly localized within thinned myocardium, with slow conduction zones demonstrating a mean wall thickness of 3.6 mm compared to 6.3 mm in remote myocardium.
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