Skip Navigation


Europace Advance Access first published online on November 12, 2008
This version published online on November 25, 2008

Europace, doi:10.1093/europace/eun307
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
11/3/316    most recent
eun307v2
eun307v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrowRequest Permissions
Right arrow Disclaimer
Google Scholar
Right arrow Articles by Berntsen, R. F.
Right arrow Articles by Berger, R. D.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Berntsen, R. F.
Right arrow Articles by Berger, R. D.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Published on behalf of the European Society of Cardiology. All rights reserved. © The Author 2008. For permissions please email: journals.permissions@oxfordjournals.org


CLINICAL RESEARCH

Evaluation of spatiotemporal organization of persistent atrial fibrillation with time- and frequency-domain measures in humans

Rolf Franck Berntsen1,*, Alan Cheng2, Hugh Calkins2 and Ronald D. Berger2

1 Department of Cardiology, Rikshospitalet University Hospital, Sognsvannsveien 20, 0027 Oslo, Norway; 2 Division of Cardiology, Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, MD, USA

Aims: Areas with complex fractionated electrograms are commonly targeted during ablation of persistent atrial fibrillation (AF). These signals are, however, found in most sampled areas of the left atrium (LA), implying the need for further differentiation.

Methods and results: Electrograms were recorded over 60 s at eight different LA endocardial sites in 10 patients with persistent AF, using a fully automated algorithm. These were analysed in sequential 2 s segments for activity, mean amplitude, continuous activity percentage, and dominant frequency (DF). All three time-domain measures differed significantly between the LA sites (P < 0.001), whereas DF did not. Activity, continuous activity percentage, and mean activity–amplitude were highest in the mid-coronary sinus and lowest on the posterior wall. In a pairwise analysis, there were significant differences in activity between all locations (P < 0.001–0.044). To visualize the spatiotemporal activity patterns, activity was plotted against amplitude. This revealed distinct activity patterns with large intra- and inter-individual differences.

Conclusion: There are significant activity gradients and distinct activity patterns within the LA in humans with persistent AF. Further work is required, however, to determine whether these findings signify areas with different roles and importance in AF maintenance.

Key Words: Atrial fibrillation, Mapping, Electrograms, Spectral analysis, Catheter ablation


* Corresponding author. Tel: +47 2307 2016, Fax: +47 2307 3917, Email: rfb123{at}hotmail.com

This paper has been versioned to correct an error in the legend to figure 3 part B.

Manuscript submitted 6 August 2008. Accepted after revision 21 October 2008.


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
EuropaceHome page
M. Duytschaever and R. Tavernier
What is needed for a good 'Decaf'?
Europace, March 1, 2009; 11(3): 278 - 279.
[Full Text] [PDF]



Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.