Po-05-147 right on q: wide-complex tachycardia in setting of dextroposition

Dextroposition is a rare cardiac malformation defined as rightward cardiac displacement with leftward apex, vs. dextrocardia, which is rightward base-axis orientation. We report the second known case of dextroposition with accessory pathway, presenting as preexcited atrial tachycardia. Abnormal anatomy complicates ECG localization and pathway ablation. N/A N/A A 50-year-old woman was admitted with respiratory distress due to EBV infection. Chest X-ray showed right-sided heart. A month later, she presented in wide-complex tachycardia, rate 205 bpm. She was cardioverted after minimal response to procainamide/adenosine. Post-cardioversion ECG showed short PR interval and preexcitation, confirming presence of accessory pathway. However, the wide-complex tachycardia had morphology identical to baseline, supporting preexcited atrial tachycardia over AVRT. Despite X-ray findings and reverse R-wave progression in precordial leads, presence of left axis deviation and initial negative deflection in aVR argued against dextrocardia. Moreover, aVR had negative T- and P-waves, findings associated with levocardia. Thus, dextroposition was suspected. Millstein and Arruda criteria suggested posteroseptal accessory pathway, but no data on their applicability in right-sided heart exist. EP study was performed. Eccentric VA conduction was noted. Earliest activation was at proximal coronary sinus. During isoproterenol infusion, patient went into atrial tachycardia, cycle length 420ms. Multiple AT foci were identified, including at right atrial appendage and tricuspid annulus. During ablation, patient developed atrial fibrillation with preexcited RR <250ms, confirming high-risk accessory pathway. Given numerous AT foci and high risk, it was decided to focus on pathway over tachycardia sites. Pathway was successfully ablated at ostia of coronary sinus and middle cardiac vein. One prior case of accessory pathway ablation in dextroposition has been reported. This patient had left lateral pathway and multiple congenital abnormalities including lung hypoplasia. While our patient was found to have multifocal atrial tachycardia, she had no clinical or radiographic lung disease. ECG changes in dextroposition are less predictable than in dextrocardia; they vary with cardiac rotation, axis position, and lead position. Comorbid accessory pathway is rare; ECG-anatomy relationship is ill-defined. Structural abnormalities pose individual challenges during electrophysiologic procedures.