P ost-infarct reentrant ventricular tachycardia (VT) is dependent on channels of surviving myocardium within the infarct scar.1 Substrate-based ablation that eliminates all abnormal electrograms, including fractionated and late potentials within scar, can reduce long-term VT recurrence. However, detailed mapping studies of local electrograms can identify paths of activation within the scar, forming channels that are considered a more specific target for substrate ablation. 3,4 Ripple mapping (RM) is a method of 3-dimensional activation visualization that displays each electrogram component as a dynamic bar that protrudes from its 3-dimensional location on the surface geometry. 5 The height of each bar correlates with the voltage amplitude of the electrogram at that time point. When multiple points are collected, activation is visually apparent from the direction of propagation of bar movement on the map. This is achieved without the need for manual annotation or setting a window of interest. Ripple activation maps can be superimposed on a conventional bipolar voltage map, thereby displaying the surface geometry with both voltage and activation simultaneously.6,7 RM is incorporated into CARTO3v4 (Biosense Webster) and has been © 2016 American Heart Association, Inc. Original ArticleBackground-Post-infarct ventricular tachycardia is associated with channels of surviving myocardium within scar characterized by fractionated and low-amplitude signals usually occurring late during sinus rhythm. Conventional automated algorithms for 3-dimensional electro-anatomic mapping cannot differentiate the delayed local signal of conduction within the scar from the initial far-field signal generated by surrounding healthy tissue. Ripple mapping displays every deflection of an electrogram, thereby providing fully informative activation sequences. We prospectively used CARTO-based ripple maps to identify conducting channels as a target for ablation. Methods and Results-High-density bipolar left ventricular endocardial electrograms were collected using CARTO3v4 in sinus rhythm or ventricular pacing and reviewed for ripple mapping conducting channel identification. Fifteen consecutive patients (median age 68 years, left ventricular ejection fraction 30%) were studied (6 month preprocedural implantable cardioverter defibrillator therapies: median 19 ATP events [Q1-Q3=4-93] and 1 shock [Q1-Q3=0-3]). Scar (<1.5 mV) occupied a median 29% of the total surface area (median 540 points collected within scar). A median of 2 ripple mapping conducting channels were seen within each scar (length 60 mm; initial component 0.44 mV; delayed component 0.20 mV; conduction 55 cm/s). Ablation was performed along all identified ripple mapping conducting channels (median 18 lesions) and any presumed interconnected late-activating sites (median 6 lesions; Q1-Q3=2-12). The diastolic isthmus in ventricular tachycardia was mapped in 3 patients and colocated within the ripple mapping conducting channels identified. Ventricular tachycardia was noninducible in 8...