Bridging anatomy and function in ischemic VT: CT wall-thickness and coherent mapping insights
| dc.contributor.author | Yalin, Kivanc | |
| dc.contributor.author | Yalman, Hakan | |
| dc.contributor.author | Soysal, Ali Ugur | |
| dc.contributor.author | Durmaz, Sebnem | |
| dc.contributor.author | Altuntas, Ilayda Bilgili | |
| dc.contributor.author | Ikitimur, Baris | |
| dc.contributor.author | Bilge, Ahmet Kaya | |
| dc.contributor.author | Ozcan, Kazim Serhan | |
| dc.contributor.author | Huang, Henry D. | |
| dc.contributor.author | Aksu, Tolga | |
| dc.date.accessioned | 2026-11-05T11:07:13Z | |
| dc.date.issued | 2026 | |
| dc.description.abstract | Background 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. Methods 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 (TM) 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. Results 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. Conclusions 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. | |
| dc.description.sponsorship | Open access funding provided by the Scientific and Technological Research Council of Turkiye (TUB & Idot;TAK). | |
| dc.identifier.doi | 10.1007/s10840-026-02333-7 | |
| dc.identifier.issn | 1383-875X | |
| dc.identifier.issn | 1572-8595 | |
| dc.identifier.uri | https://doi.org/10.1007/s10840-026-02333-7 | |
| dc.identifier.uri | https://openaccess.acibadem.edu.tr/handle/11443/11431 | |
| dc.identifier.wos | WOS:001746146200001 | |
| dc.language.iso | en | |
| dc.publisher | SPRINGER | |
| dc.relation.funding | Istanbul Aydimath | |
| dc.relation.funding | n University | |
| dc.relation.hasversion | 10.1007/s10840-026-02333-7 | |
| dc.relation.ispartof | JOURNAL OF INTERVENTIONAL CARDIAC ELECTROPHYSIOLOGY | |
| dc.subject | Ventricular tachycardia | |
| dc.subject | Ischemic cardiomyopathy | |
| dc.subject | Coherent mapping | |
| dc.subject | Isochronal mapping | |
| dc.subject | Computed tomography | |
| dc.subject | VENTRICULAR-TACHYCARDIA | |
| dc.subject | SUBSTRATE | |
| dc.subject | ABLATION | |
| dc.subject | Cardiac & Cardiovascular Systems | |
| dc.subject | Cardiovascular System & Cardiology | |
| dc.title | Bridging anatomy and function in ischemic VT: CT wall-thickness and coherent mapping insights | |
| dc.type | Article | |
| oaire.citation.edition | Science Citation Index Expanded (SCI-EXPANDED) | |
| person.identifier.rid | GXF-5001-2022 | |
| person.identifier.rid | C-1801-2015 | |
| person.identifier.rid | AAE-6929-2020 | |
| person.identifier.rid | O-1466-2013 | |
| person.identifier.rid | M-7118-2013 | |
| person.identifier.rid | PSK-7229-2026 |
