Metabolic Scar Assessment with 18F-FDG -PET: Correlation to Ischemic VT Substrate and Successful Ablation Sites.

Background: Functional/molecular imaging characteristics of ischemic ventricular tachycardia (VT) substrate are incompletely understood. Objective: Compare regional 18F-FDG - PET tracer uptake with detailed electroanatomic maps (EAM) in a more extensive series of post-infarction VT patients to define metabolic properties of the VT substrate/successful ablation sites. \n\nMethods: 3D metabolic left ventricular (LV) reconstructions were created from perfusion-normalized 18F-FDG images in consecutive patients undergoing VT ablation. Metabolic defects were defined as severe (\u003c50% uptake) or moderate (50-70% uptake) referenced to the maximal 17-segmental uptake. Color-coded PET scars reconstructions were co-registered with corresponding high-resolution 3D EAM. \n\nResults: All 56 patients had ischemic cardiomyopathy (EF=29±12%). Severe PET defect ( 70% (n = 7,782, 3.2±1.3mV, p 70%). Metabolic channels (n = 26) existed in 45% (n = 25) of patients with average length/width of 17.6±12.5mm/10.3±4.2mm. Metabolic channels were oriented apex/base (86%) predominantly, harboring VT channel/exit sites in 31%. Metabolic Rapid Transition Areas (RTA: \u003e50% change of 18F-FDG tracer uptake/15mm) were detected in 59% (n = 33) co-localizing to VT channels/exit sites (15%) or its proximity (85%, 12.8±8.5mm). Metabolism-voltage mismatches (MVM) with PET 1.5mV) were seen in 21% (n = 12) harboring VT channel/exit sites in 41% of patients. \n\nConclusion: Abnormal 18F-FDG uptake categories can be detected using incremental 3D step-up reconstructions. They predicted decreasing bipolar voltages and VT channel/exit sites in ~90%. Additionally, functional imaging allowed detecting novel molecular tissue characteristics within the ischemic VT substrate such as metabolic channels, RTA, and MVM demonstrating intra-substrate heterogeneity and providing possible targets for imaging-guided ablation.