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      Electrophysiological predictors of propafenone efficacy in prevention of atrioventricular nodal re-entrant and atrioventricular re-entrant tachycardia

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          Abstract

          Aim

          To assess the efficacy of propafenone in prevention of atrioventricular nodal reentrant tachycardia (AVNRT) and orthodromic atrioventricular tachycardia (AVRT) based on the clinical results of arrhythmia recurrence and find the electrophysiological predictor of propafenone effectiveness.

          Methods

          This retrospective study included 44 participants in a 12-month period, who were divided in two groups: group A – in which propafenone caused complete ventriculo-atrial block and group B – in which propafenone did not cause complete ventriculo-atrial block.

          Results

          Group A had significantly lower incidence of tachycardia than group B (95% vs 70.8%, P = 0.038), and complete ventriculo-atrial block predicted the efficacy of propafenone oral therapy in the prevention of tachycardia (sensitivity 87.5%, specificity 52.8%, positive predictive value 95%, negative predictive value 29.2%). Patients with AVNRT in group B who did not experience the recurrences of tachycardia had significantly shorter echo zone before intravenous administration of propafenone than the patients who experienced episodes of sustained tachycardia (median 40 ms [range 15-60 ms] vs 79 ms [range 50-180 ms], P = 0.008).

          Conclusion

          In patients with non-inducible tachycardia, complete ventriculo-atrial block can be used as an electrophysiological predictor of the efficacy of propafenone oral therapy in the prevention of tachycardia. In patients with non-inducible AVNRT, but without complete ventriculo-atrial block, propafenone was more effective in patients with shorter echo zone of tachycardia.

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          Most cited references25

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          ACC/AHA/ESC guidelines for the management of patients with supraventricular arrhythmias--executive summary: a report of the American College of Cardiology/American Heart Association Task Force on Practice Guidelines and the European Society of Cardiology Committee for Practice Guidelines (Writing Committee to Develop Guidelines for the Management of Patients With Supraventricular Arrhythmias).

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            Paroxysmal supraventricular tachycardia in the general population.

            We sought to determine the epidemiology and clinical significance of paroxysmal supraventricular tachycardia (PSVT) in the general population. Current knowledge of PSVT has been derived primarily from otherwise healthy patients referred to specialized centers. We used the resources of the Marshfield Epidemiologic Study Area, a region covering practically all medical care received by its 50,000 residents. A review of 1,763 records identified prevalent cases as of July 1, 1991 and all new cases of PSVT diagnosed from that day until June 30, 1993. A mean follow-up period of 2 years was completed in all incident patients. Patients without other cardiovascular disease were labeled as having "lone PSVT." The prevalence was 2.25/1,000 persons and the incidence was 35/100,000 person-years (95% confidence interval, 23 to 47/100,000). Other cardiovascular disease was present in 90% of males and 48% of females (p = 0.0495). Compared with patients with other cardiovascular disease, those with lone PSVT were younger (mean 37 vs. 69 years, p = 0.0002), had a faster PSVT heart rate (mean 186 vs. 155 beats/min, p = 0.0006) and were more likely to have their condition first documented in the emergency room (69% vs. 30%, p = 0.0377). The onset of symptoms occurred during the childbearing years in 58% of females with lone PSVT versus 9% of females with other cardiovascular disease (p = 0.0272). There are approximately 89,000 new cases/year and 570,000 persons with PSVT in the United States. In the general population, there are two distinct subsets of patients with PSVT: those with other cardiovascular disease and those with lone PSVT. Our data suggest etiologic heterogeneity in the pathogenesis of PSVT and the need for more population-based research on this common condition.
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              Direct visualization of the slow pathway using voltage gradient mapping: a novel approach for successful ablation of atrioventricular nodal reentry tachycardia.

              Ablation of atrioventricular nodal reentry tachycardia (AVNRT) has become treatment of choice because of a high success and low complication rate. Most ablations are successful in utilizing an anatomic approach, but anatomic variance, unusual pathway locations, or multiple pathways may complicate the procedure. Visualization of the slow pathway could expedite ablation success and enhance safety. Our purpose is to determine whether voltage gradient mapping can directly image the slow pathway and aid successful ablation of AVNRT. Three-dimensional voltage maps of the right atrial septum were constructed from intracardiac recordings obtained by contact mapping. Voltage values were adjusted until low-voltage bridging was observed within the Triangle of Koch. Forty-eight consecutive patients undergoing ablation for inducible AVNRT, underwent voltage gradient mapping. The slow pathway was identified in all 48 patients via its corresponding low-voltage bridge. Ablation of the slow pathway associated low-voltage bridges in 48 patients was successful in preventing reinduction following the first lesion in 43 of 48 patients. Five patients had multiple slow pathways and >1 lesion was required to prevent reinduction. Repeat mapping confirmed the absence of low-voltage connections previously observed in all 48 patients. Voltage gradient mapping can assist in visualization of the slow pathway. Ablation of the associated low-voltage bridge results in loss of slow pathway function and significant changes in the post-ablation voltage map. We conclude that voltage gradient mapping offers the ability to target the slow pathway for successful ablation.
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                Author and article information

                Journal
                Croat Med J
                Croat. Med. J
                CMJ
                Croatian Medical Journal
                Croatian Medical Schools
                0353-9504
                1332-8166
                December 2012
                : 53
                : 6
                : 605-611
                Affiliations
                [1 ]Department of Internal Medicine, Sestre milosrdnice University Hospital Center, Zagreb, Croatia
                [2 ]School of Dental Medicine, University of Zagreb, Zagreb, Croatia
                [3 ]University of Zagreb School of Medicine, Zagreb, Croatia
                Author notes
                Correspondence to: 
Hrvoje Pintarić 
Department of Internal Medicine
Sestre milosrdnice University Hospital Centre 
Vinogradska cesta 29
10 000 Zagreb, Croatia
 hrvojepintaric@ 123456yahoo.com
                Article
                CroatMedJ_53_0605
                10.3325/cmj.2012.53.605
                3541586
                23275326
                1051f1d3-dee5-48c5-85de-bcc0a04ee907
                Copyright © 2012 by the Croatian Medical Journal. All rights reserved.

                This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 02 May 2012
                : 01 December 2012
                Categories
                Clinical Science

                Medicine
                Medicine

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