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J Am Coll Cardiol, 2002; 39:896-906 © 2002 by the American College of Cardiology Foundation |
a Department of Cardiology, The Royal Melbourne Hospital and University of Melbourne, Melbourne, Australia
Manuscript received September 11, 2001; revised manuscript received December 3, 2001, accepted December 14, 2001.
* Reprint requests and correspondence: Prof. Jonathan M. Kalman, Department of Cardiology, The Royal Melbourne Hospital, Grattan Street, Parkville 3050, Melbourne, Australia
jon.kalman{at}mh.org.au
OBJECTIVES
This study was designed to determine the sensitivity and specificity of concealed entrainment (CE) for the identification of a critical isthmus in the atrium.
BACKGROUND
Isthmus identification during entrainment mapping of macro-reentrant atrial tachycardia (MRAT) relies on the demonstration of CE.
METHODS
Using the model of typical atrial flutter, entrainment was performed in 10 patients at four rates (flutter cycle length [FCL] minus 10/20/30/40 ms) from seven sites: isthmus entrance/exit, low lateral/high lateral/high septal right atrium and proximal/distal coronary sinus. Surface 12-lead electrocardiogram fusion was evaluated by three observers blind to patient status. The extent of antidromic penetration (AP) was measured off the pacing catheter positioned around the tricuspid annulus.
RESULTS
The sensitivity for CE identifying any isthmus site was greatest at FCL10 (100%), but the specificity was poor (54%). Conversely, specificity was greatest at FCL40 (98%), but the sensitivity was poor (65%), with manifest entrainment (ME) observed from the isthmus entrance in 70% of episodes. At FCL30, sensitivity (85%) and specificity (90%) were "balanced," but CE still resulted during entrainment from a non-isthmus site in five of 10 patients. Antidromic penetration increased with pacing CL shortening (p < 0.001) and correlated with the development of ME (p < 0.001). Antidromic penetration was significantly blunted from the isthmus exit compared to all other sites (p = 0.003).
CONCLUSIONS
The sensitivity and specificity of CE for identifying an isthmus in the atrium are critically dependent on the pacing rate and the precise anatomic pacing site within the isthmus. These findings may have implications for the use of entrainment in the mapping of unknown MRAT circuits.
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