(Circulation. 2001;104:957.)
© 2001 American Heart Association, Inc.
Basic Science Reports |
From the Department of Physiology, Maastricht University, Maastricht, the Netherlands.
Correspondence to Prof M.A. Allessie, Department of Physiology, Maastricht University, PO Box 616, 6200 MD Maastricht, the Netherlands.
Background Recently, the temporal excitable gap during atrial fibrillation (AF) has been identified as a vulnerable parameter for cardioversion of AF. In this study, we evaluated 5 methods to measure the refractory period (RPAF) and the excitable period (EPAF) during persistent AF.
Methods and Results In 11 goats instrumented with 83 epicardial atrial electrodes, persistent AF (43±34 days) was induced with a median AF cycle length (CL) of 98±14 ms. To measure RPAF, premature stimuli were applied to the center of the electrode array on the right or left atrium. The RPAF measured by mapping of premature stimuli was 70±12 ms ("gold standard"). The RPAF determined during entrainment of AF was 77±17 ms (R2=0.88, P<0.01). Statistical analysis of the effects of synchronized stimuli (each coupling interval x100) on the AFCL histogram yielded an RPAF of 70±13 ms (R2=0.94, P<0.01). A further simplification was to apply slow fixed-rate pacing (1 Hz) during AF. For each stimulus (n=250 to 500), the paced AFCL was plotted against its coupling interval, and capture was determined by statistical shortening of the AFCL (RPAF 71±17 ms, R2=0.84, P<0.01). The 5th percentile of the AFCL histogram as an index of RPAF was 77±12 ms (R2=0.90, P<0.01).
Conclusions During persistent AF with an AFCL of 98±14 ms, the RPAF determined by mapping of synchronized premature stimuli (gold standard) was 70±12 ms, with an excitable period of 28±8 ms. Although the indirect methods to measure RPAF all correlated well with the gold standard, slow fixed-rate pacing seems to be the most attractive technique because of the ease of acquiring the data and the clear graphic result.
Key Words: fibrillation electrophysiology excitation
This article has been cited by other articles:
![]() |
H.-R. Neuberger, U. Schotten, Y. Blaauw, D. Vollmann, S. Eijsbouts, A. van Hunnik, and M. Allessie Chronic Atrial Dilation, Electrical Remodeling, and Atrial Fibrillation in the Goat J. Am. Coll. Cardiol., February 7, 2006; 47(3): 644 - 653. [Abstract] [Full Text] [PDF] |
||||
![]() |
V. Jacquemet, N. Virag, and L. Kappenberger Wavelength and vulnerability to atrial fibrillation: Insights from a computer model of human atria Europace, January 1, 2005; 7(s2): S83 - S92. [Abstract] [Full Text] [PDF] |
||||
![]() |
Y. Blaauw, H. Gogelein, R.G. Tieleman, A. van Hunnik, U. Schotten, and M.A. Allessie "Early" Class III Drugs for the Treatment of Atrial Fibrillation: Efficacy and Atrial Selectivity of AVE0118 in Remodeled Atria of the Goat Circulation, September 28, 2004; 110(13): 1717 - 1724. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. G. KLEBER and Y. RUDY Basic Mechanisms of Cardiac Impulse Propagation and Associated Arrhythmias Physiol Rev, April 1, 2004; 84(2): 431 - 488. [Abstract] [Full Text] [PDF] |
||||
![]() |
T. Ashihara, T. Namba, T. Ikeda, M. Ito, K. Nakazawa, and N. Trayanova Mechanisms of Myocardial Capture and Temporal Excitable Gap During Spiral Wave Reentry in a Bidomain Model Circulation, February 24, 2004; 109(7): 920 - 925. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. G. Akar, T. H. Everett, R. Ho, J. Craft, D. E. Haines, A. P. Somlyo, and A. V. Somlyo Intracellular Chloride Accumulation and Subcellular Elemental Distribution During Atrial Fibrillation Circulation, April 8, 2003; 107(13): 1810 - 1815. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. Kawase, T. Ikeda, K. Nakazawa, T. Ashihara, T. Namba, T. Kubota, K. Sugi, and H. Hirai Widening of the Excitable Gap and Enlargement of the Core of Reentry During Atrial Fibrillation With a Pure Sodium Channel Blocker in Canine Atria Circulation, February 18, 2003; 107(6): 905 - 910. [Abstract] [Full Text] [PDF] |
||||
|
Circulation Home | Subscriptions | Archives | Feedback | Authors | Help | AHA Journals Home | Search Copyright © 2001 American Heart Association, Inc. All rights reserved. Unauthorized use prohibited. |