Variable clinical features and ablation of manifest nodofascicular/ventricular pathways.

BACKGROUND: Manifest nodofascicular/ventricular (NFV) pathways are rare. METHODS AND RESULTS: From 2008 to 2013, 4 cases were identified with manifest NFV pathways from 3 centers. The clinical findings and ablation sites are reported. All 4 cases presented with a wide complex tachycardia but with different QRS morphologies. Case 1 showed a left bundle branch block/superior axis, case 2 showed a right bundle branch block/inferior axis, case 3 showed a left bundle branch block/inferior axis, and case 4 showed a narrow QRS tachycardia and a wide complex tachycardia with a left bundle branch block/inferior axis. Three of the 4 tachycardias had atrioventricular dissociation ruling out extranodal accessory pathways, including atriofascicular pathways. Programmed extrastimuli showed evidence of a decremental accessory pathway in 3 of the 4 cases. Coexisting tachycardia mechanisms were seen in 3 of the 4 cases (atrioventricular nodal reentry tachycardia [2] and atrioventricular reentrant tachycardia [1]). Ablation in the slow pathway region eliminated the NFV pathway in 3 (transient in 1) with the other responding to surgical closure of a large atrial septal defect. The NFV pathway was a critical part of the tachycardia circuit in 1 and proved to be a bystander in the other 3 cases. CONCLUSIONS: Manifest NFV pathways presented with variable QRS expression dependent on the ventricular insertion site and often coexisted with other tachycardia mechanisms (atrioventricular nodal reentry tachycardia and atrioventricular reentrant tachycardia). In most cases, the atrial insertion of the pathway was in or near the slow pathway region. The NFV pathways were either critical to the tachycardia circuit or served as bystanders.

Right bundle-branch block ventricular tachycardias: septal versus lateral ventricular origin based on activation time to the right ventricular apex.

BACKGROUND: Identifying the septal versus lateral site of origin of ventricular tachycardia (VT) with a right bundle-branch block (RBBB)-type pattern and an R-S ratio >1 in lead V1 is difficult with the 12-lead ECG, especially in patients with prior apical infarction. METHODS AND RESULTS: We prospectively evaluated 58 patients with VT. Sixteen patients had apical infarcts (group 1), 29 had nonapical infarcts (group 2), and 13 had no heart disease (group 3). QRS complex onset to activation at the right ventricular apex (stim-RVA) was measured during left ventricular (LV) apical septal and lateral pacing, and 47 RBBB-type VTs (QRS-RVA) were localized to the septal or lateral apex by using entrainment techniques. Pacing and VT site of origin were confirmed by electroanatomic mapping. The stim-RVA time was 59+/-16 ms for septal versus 187+/-24 ms for lateral sites in group 1, P<0.001; 70+/-14 ms for septal versus 169+/-19 ms for lateral sites in group 2, P<0.001; and 42+/-15 ms for septal versus 86+/-16 ms for lateral sites in group 3, P<0.005. The QRS-RVA time was 50+/-13 ms for apical septal VTs versus 178+/-21 ms for lateral VTs in group 1, P<0.001; 71+/-17 ms for apical septal versus 157+/-20 ms for lateral VTs in group 2, P<0.001; and 32+/-12 ms for septal versus 71+/-16 ms for lateral VTs in group 3, P<0.01. CONCLUSIONS: The QRS-RVA differs for the VT site of origin from the LV septal versus lateral apex. These data prove useful in rapidly regionalizing the VT site of origin with a V1 R-S ratio >1, particularly in instances of an apical infarct, where surface ECG distinctions are less identifiable.

Change in distant atrial activation patterns during circumferential pacemapping of pulmonic vein ostium: implications for localizing triggers for atrial fibrillation.

INTRODUCTION: Unique intracardiac activation patterns recorded from multipolar catheters in the coronary sinus (CS) and posteromedial right atrium (RA) when pacing from ostium (os) of each pulmonic vein (PV) can serve as template for determining PV of origin of atrial premature complexes. Development of an accurate template requires knowledge of variations in activation pattern during pacing from different aspects of same PV. METHODS: In 25 patients undergoing catheter ablation for AF, a decapolar Lasso mapping catheter was placed at PV os of interest and multipolar catheters were placed in CS and RA-medial to crista terminalis (CT). For each PV, pacing was performed from Lasso catheter poles 1 through 10. For each bipole paced, activation sequence in CS (proximal to distal & vice-versa) was assessed, activation time (pacing stimulus to earliest electrogram recorded in catheters in CS/along CT) was measured and difference (CS - CT time) was determined. Significant interpolar variation was defined as the difference between the shortest and longest CS - CT activation time of >/=25 msec when pacing from different bipoles of same PV. RESULTS: In 59 PVs [19 right superior (RS), 20 left superior (LS), 8 right inferior (RI) and 12 left inferior (LI)], 259 bipoles were paced (median of 4 bipoles/PV). During circumferential PV pacing activation sequence in CS catheter was distal to proximal in 84.4% left-sided PVs (LSPV and LIPV) and proximal to distal in 92.6% right-sided PVs (RSPV and RIPV) with no change in activation sequence observed during pacing from different bipoles in same PV. Significant interpolar variation was observed with circumferential pacing in 1 of 19 RSPV (5.3%), 2 of 20 LSPV (10%), 1 of 12 LIPV (8.3%) and none of RIPV. CONCLUSION: Unique intracardiac activation patterns during ostial pacing from individual PV are not influenced by circumferential location of pacing site.