“…6 Mapping PVC from MB could be an issue, therefore some strategies should be considered to increase the chance of success as medication drips used during mapping a PVC as isoproterenol or dobutamine iv, pacing during mapping to induce PVC, pace mapping approaches, even using multipolar catheters as Pentaray (Biosense Webster, Diamond Bar, California), to collect as many activation points as you can on one touch. 17 The moderator band contains Purkinje system cells is consider a potentially arrhythmogenic structure, PVC from this structure can lead to a ventricular fibrillation; ablation can be a real challenge to a electrophysiologist; 18 even though, there are several aspects to consider: first the best target is difficult to achieve described as the identification of preceding Purkinje potential, pre ventricular activation, concordant morphology with pace mapping; second: stability is difficult to achieve in this structure, some strategies are been proposed: www.medigraphic.org.mx using a tridimensional mapping, intracardiac echocardiogram, even cryo catheters to freeze de area, 19 or a strategy who includes: a 3D mapping, ICE, radiofrequency and 23 mm balloon to cryoablation (freezing up to 4 minutes up to -47 o C) has been reported in the setting of a patient with already two failed procedures with successful results, 20 at last but not less the ablation with RF or Cryo could be trigger VF or VT, as a destruction of conduction cells during applications. 19 The percentages of the patients who might need a second procedure have been reported up to 60%; and the possible reasons to explain failed procedures or turn an early successful ablation into a fail therapy with increasing of PVC burden are: poor tissue contact with ablation catheter, lack of stability, insufficient deep lesions during ablation, and change of PVC exit (as a result of ablation points); though, a failed procedure can be dangerous to the patient if the clinic is syncope or even ventricular tachycardia or ventricular fibrillation.…”