Adenosine-induced atrial tachycardia and multiple foci initiating atrial fibrillation eliminated by catheter ablation using a non-contact mapping system

2011 ◽  
Vol 27 (2) ◽  
pp. 221-226 ◽  
Author(s):  
Mika Hioki ◽  
Seiichiro Matsuo ◽  
Teiichi Yamane ◽  
Ken-ichi Tokutake ◽  
Keiichi Ito ◽  
...  
ESC CardioMed ◽  
2018 ◽  
pp. 2070-2075
Author(s):  
Pierre Jaïs ◽  
Nicolas Derval

Atrial tachycardia (AT) is increasingly observed in patients, particularly in the context of atrial fibrillation ablation. The exact electrophysiological mechanisms are not easy to establish but a practical approach consists in distinguishing macroreentries from focal ATs as this is crucial for the ablation strategy. In centrifugal arrhythmias (such as focal AT and localized reentry), the activation originates from a source and spreads centrifugally to the rest of the atria, while in macroreentries, it follows a large path around a central obstacle and reenters. The analysis of the surface electrocardiogram is of limited value to predict the macroreentrant or focal nature of the arrhythmia. Antiarrhythmic drugs are usually tried first and in case of failure, catheter ablation is considered, with or without the support of a localization/mapping system. The most challenging cases are those with multifocal AT as they are poorly responsive to drugs, difficult to ablate, and arise in patients in poor medical conditions. New technologies such as high-density mapping and non-invasive mapping may facilitate the identification of mechanisms and target(s) for catheter ablation.


2013 ◽  
Vol 43 (1) ◽  
pp. 29 ◽  
Author(s):  
Yae Min Park ◽  
Hyungdon Kook ◽  
Woohyeon Kim ◽  
Son Ki Lee ◽  
Jong-Il Choi ◽  
...  

Circulation ◽  
2015 ◽  
Vol 132 (suppl_3) ◽  
Author(s):  
Hiroshige Yamabe ◽  
Hisanori Kanazawa ◽  
Tadashi Hoshiyama ◽  
Miwa Ito ◽  
Shozo Kaneko ◽  
...  

Background: It has been suggested rotor which is located within the pulmonary vein (PV) acted as the driving sources of atrial fibrillation (AF). However, it has never been confirmed whether or not the rotor exists within PV in human. Objectives: We analyzed the activation sequence within the PV during AF and examined how the PV acted as the driving sources of AF. Methods: Selective endocardial mapping of left superior PV (LSPV) was performed during AF in 11 paroxysmal AF patients using a non-contact mapping system (EnSite 3000). Presence of rotor activation was defined when the circular activation around the functional block line once completed its whole reentrant activation. We analyzed the relation between the pivoting activation and the rotor activation. To define the preferable site of rotor and pivoting activation, we also analyzed the relation between the location of rotor and pivoting activation and region of the complex fractionated electrogram (CFE) recording site. Results: Rotor activation was observed with a mean number of 4.6±3.6 times/sec. CFE was observed at the roof (n=5), ridge (n=11) and carina (n=7) of the proximal half of LSPV with a mean area of 9.1±3.4 cm2. The number of rotor activation observed at the CFE area was significantly higher than that at the non-CFE area (4.1±3.9 vs. 0.7±1.2 times/sec, p=0.025). Total frequency of pivoting activation was 37.0±14.7 times/sec. Pivoting activation involved in the rotor activation was significantly lower than that not involved in the rotor activation (8.8±8.1 vs. 27.7±15.8 times/sec, p=0.0116). Regarding the CFE area, pivoting activation involved in the rotor activation was also significantly lower than that not involved in the rotor activation (8.4±8.2 vs. 24.1±12.0 times/sec, p=0.0105). However, there was no difference between the frequencies of pivoting activation with and without rotor activation in the non-CFE area (1.0±2.0 vs. 3.6±6.1 times/sec, p=NS). Conclusions: Rotor activation was observed at the proximal portion of the LSPV coincided with the location of CFE area. However, most of pivoting activation was not involved in the rotor activation. These suggest that AF was driven by the other meandering propagation associated with frequent non-stable pivoting activation over the CFE area.


ESC CardioMed ◽  
2018 ◽  
pp. 2049-2050
Author(s):  
Carina Blomström-Lundqvist

Supraventricular arrhythmias encompass atrial premature beats, supraventricular tachycardias (SVTs), and atrial fibrillation. SVT is used to describe tachycardias in which the mechanism involves tissue from the His bundle or above, thus including atrial tachycardias, atrioventricular nodal reentrant tachycardia, and atrioventricular reentrant tachycardia due to accessory pathways. Atrial fibrillation is not included among the SVTs and is described elsewhere. The term tachycardia refers to atrial and/or ventricular rates greater than 100 beats per minute at rest. Atrial premature beats, the most common supraventricular arrhythmia, can be seen in Holter recordings in the majority of healthy individuals, and increase in frequency with age and presence of structural heart disease. Paroxysmal SVTs that can be terminated by vagal manoeuvres are usually reentrant tachycardias involving the atrioventricular node, such as atrioventricular nodal reentrant tachycardia or atrioventricular reentrant tachycardia. Symptoms may result in a poor quality of life. Rarely, patients with the Wolff–Parkinson–White syndrome develop atrial fibrillation that may degenerate into ventricular fibrillation in case the anterograde refractory period of the accessory pathway is very short and permanent forms of SVTs result in tachycardiomyopathy with left ventricular dysfunction. Paroxysmal SVT can be terminated by vagal manoeuvres, adenosine, overdrive pacing, and DC cardioversion. Atrial flutter, the most common atrial tachycardia, is a macro-reentrant atrial tachycardia that can be terminated by drugs, overdrive atrial pacing, and DC cardioversion. Most SVTs can be successfully treated by catheter ablation facilitated by modern electroanatomical mapping systems. Long-term antiarrhythmic drug therapy may be required for patients who are not suitable for or cured by catheter ablation.


2011 ◽  
Vol 41 (8) ◽  
pp. 447 ◽  
Author(s):  
Sung-Won Jang ◽  
Woo-Seung Shin ◽  
Ji-Hoon Kim ◽  
Min-Seok Choi ◽  
Yun Seok Choi ◽  
...  

2009 ◽  
Vol 18 ◽  
pp. S139
Author(s):  
Andrew W. Teh ◽  
Caroline Medi ◽  
Raphael Rosso ◽  
Geoffrey Lee ◽  
Paul B. Sparks ◽  
...  

2010 ◽  
Vol 51 (1) ◽  
pp. 72-74 ◽  
Author(s):  
Kenta Tsutsui ◽  
Kohsuke Ajiki ◽  
Katsuhito Fujiu ◽  
Yasushi Imai ◽  
Noriyuki Hayami ◽  
...  

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