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Circulation. 1996;94:1357-1363

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(Circulation. 1996;94:1357-1363.)
© 1996 American Heart Association, Inc.


Articles

Spatial Resolution of Atrial Pace Mapping as Determined by Unipolar Atrial Pacing at Adjacent Sites

K. Ching Man, DO; K.K. Chan, MD; Paul Kovack, DO; Rajiva Goyal, MD; Frank Bogun, MD; Mark Harvey, MD; Emile Daoud, MD; S. Adam Strickberger, MD; Fred Morady, MD

the Division of Cardiology, Department of Internal Medicine, University of Michigan Medical Center, Ann Arbor.


*    Abstract
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*Abstract
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Background The purpose of this study was to examine the spatial resolution of unipolar atrial pace mapping by pacing at adjacent sites within the coronary sinus and the right atrium.

Methods and Results Unipolar pacing from each pole of a quadripolar catheter was performed in the coronary sinus (n=29) and in the right atrium (n=10). Pacing from the distal electrode was used to simulate the site of origin of an atrial tachycardia. These P waves were compared with the P waves generated by unipolar pacing from each of the three proximal electrodes. The P waves were analyzed for changes in amplitude, duration, and configuration. Pacing within the coronary sinus resulted in significant changes in amplitude and duration at distances of 17 and 21 mm from the distal pole, respectively. Similarly, pacing in the right atrium resulted in significant changes in amplitude and duration at distances of 17 and 32 mm from the distal pole, respectively. No significant changes in configuration were noted in the coronary sinus in any lead at pacing sites <=32 mm from the distal pole. Configurational changes were noted in the right atrium at pacing sites 17 mm from the distal pole.

Conclusions The spatial resolution of unipolar atrial pace mapping is {approx}17 mm. These findings indicate that mapping techniques that depend on the accurate discrimination of P-wave morphology, such as pace mapping or concealed entrainment, are likely to be imprecise when used in the atria.


Key Words: tachycardia • mapping • pacing


*    Introduction
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*Introduction
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Mapping techniques for selection of target sites for ablation of atrial tachycardias include atrial pacing in the setting of sinus rhythm (pace mapping) and during tachycardia (concealed entrainment).1 2 3 4 5 The successful application of these techniques depends on the accurate discrimination of P-wave morphology during pacing. However, no prior studies have quantified the spatial resolution of changes in P-wave size or configuration. Therefore, the goal of this study was to quantify the differences in P-wave size and morphology during unipolar pacing within the coronary sinus and the right atrium from the four poles of a quadripolar catheter at known interelectrode distances.


*    Methods
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Study Population
The subjects of this study consisted of 39 patients without structural heart disease who underwent an electrophysiology procedure for the purpose of radiofrequency catheter ablation of supraventricular tachycardia. There were 21 patients with AV nodal reentrant tachycardia, 11 with a concealed accessory pathway, 3 with atrial flutter, and 4 without inducible supraventricular tachycardia. There were 16 men and 23 women, and their mean age was 48±16 years (±SD). The 12-lead ECG did not demonstrate an atrial abnormality in any patient. Inclusion criteria for this study were (1) sinus rate <100 bpm, (2) the ability to perform unipolar cathodal atrial pacing within the coronary sinus and right atrium from each pole of a quadripolar electrode catheter, and (3) catheter stability during cathodal unipolar pacing and recording. Catheter stability was defined by the absence of catheter movement under fluoroscopic inspection.

Study Protocol
Informed consent under a protocol approved by the Human Research Committee of the University of Michigan was obtained from all patients. Electrophysiology tests were performed after discontinuation of all antiarrhythmic agents for at least 5 half-lives. The study protocol was performed after completion of the clinically indicated portion of the electrophysiology procedure. Twelve-lead ECGs were recorded during unipolar pacing at a cycle length of 500 ms from each pole of a quadripolar catheter within the coronary sinus or the right atrium. Initially, patients were randomly assigned to undergo the study protocol in the coronary sinus with quadripolar catheters with 5-mm (n=18) or 10-mm (n=11) interelectrode spacing. In 10 additional patients, the study protocol was performed in the right atrium with quadripolar catheters with 5-mm (n=5) or 10-mm (n=5) interelectrode spacing. Via a femoral vein approach, the quadripolar catheter was placed in the coronary sinus with the distal electrode in the region of the posterolateral mitral annulus {approx}3 to 4 cm from the coronary sinus ostium or in the right atrium with the distal electrode against the low lateral wall and the proximal electrode against the high right atrium. Pacing from the distal pole was used to simulate the site of origin of atrial tachycardia. Pacing was also performed at poles 2, 3, and 4. The width of the electrodes at poles 2, 3, and 4 of the quadripolar catheter was 1 mm. Relative to the catheter tip, the pacing sites were at distances of 5, 11, and 17 mm with the 5-mm interelectrode quadripolar catheter and 10, 21, and 32 mm with the 10-mm interelectrode quadripolar catheter. The spatial resolution of pace mapping was determined by comparison of the surface ECGs obtained from the distal pole with those obtained from pacing at poles 2, 3, and 4 at diastolic threshold and twice diastolic threshold in the coronary sinus and twice diastolic threshold in the right atrium.

The late diastolic stimulation threshold was determined in incremental steps of 0.1 mA. Unipolar cathodal pacing was performed with a pulse duration of 2 ms with a programmable stimulator (Bloom Associates, Ltd). An electrode catheter placed at the junction of the inferior vena cava and the right atrium was used as the indifferent electrode.6 The mean unipolar atrial pacing threshold at electrodes 1, 2, 3, and 4 were not significantly different with either the 5- or the 10-mm interelectrode spacing catheters, ranging from 1.1±0.3 to 1.8±1.6 and 0.9±0.3 to 1.4±1.0 mV, respectively, in the coronary sinus and from 0.8±0.5 to 2.3±1.9 and 0.6±0.5 to 1.2±1.4 mV, respectively, in the right atrium. Twelve-lead ECGs were recorded at a paper speed of 50 mm/s and at a gain setting of 2 cm/mV on a Mingograph 7 recorder (Siemens-Elema, Inc).

Analysis of P Waves
In each ECG lead, three consecutive P waves were examined for amplitude, duration, and configuration differences according to the following criteria.

Amplitude
The amplitude of P waves was measured to the nearest 0.025 mV (0.5 mm). The isoelectric portion of the PR interval served as the baseline for the measurement of amplitude. The TP interval could not be used as the baseline because the pacing stimulus often obscured the terminal portion of the preceding T wave.

Duration
The P-wave duration was measured at a paper speed of 50 mm/s. The first 20 ms after the pacing stimulus was deleted to exclude the pacing artifact from the measurement. Onset of P wave was defined as the first rapid deflection from the isoelectric line.

Configuration
Changes in P-wave configuration were defined as specific morphological variations, eg, axis shift and notching, from the P wave generated by pacing at the distal electrode.

Intraobserver Variability
All ECGs were analyzed by one of the authors. The measurements then were repeated by two other authors to assess for intraobserver variability. A total of 9792 P waves were analyzed. The intraobserver agreement was within 0.05 mV and 2 ms in 65% of the P waves and within 0.1 mV and 5 ms in 95% of the P waves. There was 80% intraobserver agreement in the determination of configurational changes in the P waves. Differences were resolved by consensus.

Data Analysis
Data are expressed as mean±SD. Amplitude and duration comparisons were performed by ANOVA with repeated measures. A value of P<.05 was considered significant.


*    Results
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P-Wave Amplitude
Pacing at threshold from the coronary sinus did not result in P-wave amplitude differences in any of the ECG leads at pacing distances that were <11 mm apart. When the pacing sites were 17 mm apart, a significant difference in mean amplitude of 0.014±0.015 mV was present in only lead I (P<.05, Fig 1Down). At pacing sites 21 mm apart, 6 of 12 leads demonstrated a significant amplitude difference, ranging from 0.006±0.056 mV in lead V4 to 0.059±0.038 mV in lead aVL (mean, 0.037±0.037 mV; P<.05). At pacing sites 32 mm apart, 9 of 12 leads demonstrated a significant amplitude difference, ranging from 0.009±0.056 mV in lead V5 to 0.072±0.042 mV in lead aVL (mean, 0.032±0.041 mV; P<.05) (Table 1Down).



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Figure 1. Recordings from lead I of P waves resulting from unipolar pacing in the coronary sinus from the tip electrode and at electrodes 5, 11, and 17 mm from the tip. In this patient, a difference in P-wave amplitude of 0.05 mV was observed between the tip electrode and the electrode 17 mm away from the tip. ECGs were recorded at 2 cm/mV and 50 mm/s.


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Table 1. P-Wave Amplitudes During Atrial Pacing at Threshold in the Coronary Sinus

Pacing in the coronary sinus at a current strength of twice threshold did not change the proximity at which the amplitude differences were detected. A mean amplitude difference of 0.022±0.029 mV (P<.05) was noted only in lead aVL at pacing sites 17 mm apart. At pacing sites 21 mm apart, 9 of 12 leads demonstrated a significant amplitude difference, ranging from 0.008±0.011 mV in lead V6 to 0.044±0.027 mV in lead III (mean, 0.021±0.024 mV; P<.05). At pacing sites 32 mm apart, 8 of 12 leads demonstrated a significant amplitude difference, ranging from 0.009±0.010 mV in lead V6 to 0.058±0.040 mV in lead III (mean, 0.021±0.023 mV; P<.05) (Table 2Down).


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Table 2. P-Wave Amplitudes During Atrial Pacing at Twice Threshold in the Coronary Sinus

Similarly, P-wave amplitude differences were not observed in any of the ECG leads at pacing distances <11 mm apart when performed at a current strength of twice threshold in the right atrium. At pacing sites 17 mm apart, a significant difference in mean amplitude of 0.045±0.078 mV was present in only lead V3 (P<.05) (Fig 2Down). At pacing sites 21 mm apart, 2 of 12 leads demonstrated a significant amplitude difference, ranging from 0.065±0.068 mV in lead aVF to 0.110±0.076 mV in lead II (mean, 0.034±0.072 mV; P<.05). At pacing sites 32 mm apart, 5 of 12 leads demonstrated a significant amplitude difference, ranging from 0.001±0.102 mV in lead V1 to 0.090±0.058 mV in lead V5 (mean, 0.056±0.076 mV; P<.05) (Table 3Down).



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Figure 2. Recordings from lead V3 of P waves resulting from unipolar pacing in the lateral right atrium from the tip electrode and at electrodes 5, 11, and 17 mm from the tip. In this patient, a difference in P-wave amplitude of 0.1 mV was observed between the tip electrode and the electrode 17 mm away from the tip. ECGs were recorded at 2 cm/mV and 50 mm/s.


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Table 3. P-Wave Amplitudes During Atrial Pacing at Twice Threshold in the Right Atrium

P-Wave Duration
The number of leads demonstrating a significant difference in P-wave duration increased as the distance from the pacing site increased. Pacing at threshold in the coronary sinus did not result in any significant changes in P-wave duration in any surface ECG lead at pacing distances <17 mm. At pacing sites 21 mm apart, 2 of 12 leads demonstrated a significant change in duration: 9 ms in lead aVR and 13 ms in lead I (mean, 11 ms; P<.05) (Fig 3Down). At pacing sites 32 mm apart, 3 of 12 leads demonstrated a significant change in duration, ranging from 12 ms in lead II to 15 ms in lead I (mean, 14 ms; P<.05) (Table 4Down).



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Figure 3. Recordings of duration and amplitude difference in leads I and aVR of P waves resulting from unipolar pacing in the coronary sinus from the tip electrode and at electrodes 10, 21, and 32 mm from the tip. In this patient, a difference of 0.07 mV and 13 ms was noted in lead I and 0.05 mV and 13 ms in lead aVR at pacing sites 21 mm apart. Changes in the configuration of the QRS complex in lead I were attributable to respiratory variation. However, no respiratory changes in the P waves were noted. ECGs were recorded at 2 cm/mV and 50 mm/s.


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Table 4. P-Wave Duration During Atrial Pacing at Threshold in the Coronary Sinus

Pacing at a current strength of twice threshold in the coronary sinus did not change the proximity at which significant duration changes were detected. At a pacing distance of 21 mm apart, 5 of 12 leads demonstrated a significant duration difference, ranging from 4 ms in lead V2 to 11 ms in lead V4 (mean, 8 ms; P<.05). At a pacing distance of 32 mm, 11 of 12 leads demonstrated a significant duration difference, ranging from 5 ms in lead aVL to 14 ms in lead V4 (mean, 8 ms; P<.05) (Table 5Down).


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Table 5. P-Wave Duration During Atrial Pacing at Twice Threshold in the Coronary Sinus

No significant duration changes were detected at a current strength of twice threshold in the right atrium at pacing distances <21 mm apart. At a pacing distance of 32 mm apart, a significant difference in duration was noted in only lead aVL (P<.05) (Fig 4Down, Table 6Down).



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Figure 4. Duration difference in P wave noted in lead aVL at a pacing site 32 mm from the tip electrode in the lateral right atrium. In this patient, a difference of 20 ms was noted in lead aVL at pacing sites 32 mm apart. ECGs were recorded at 2 cm/mV and 50 mm/s.


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Table 6. P-Wave Duration During Atrial Pacing at Twice Threshold in the Right Atrium

P-Wave Configuration
Only minor and infrequent differences in P-wave configuration were noted in the coronary sinus among the 12 ECG leads as distance between the pacing sites increased (Figs 5Down and 6).Down Pacing at twice the current strength in the coronary sinus had no effect on P-wave configuration.



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Figure 5. Surface ECG demonstrating that no or only minor configurational changes in P waves were observed at pacing distances as far as 32 mm from the tip electrode in the coronary sinus. ECGs were recorded at 2 cm/mV and 50 mm/s.



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Figure 6. Recordings of lead aVR demonstrating configurational changes in the P wave at different pacing distances in the coronary sinus. Notching is noted on the downslope of the P waves at the tip electrode and at 10-mm pacing distance (arrows). This is absent during pacing at a distance of 21 or 32 mm from the tip. ECGs were recorded at 2 cm/mV and 50 mm/s.

When pacing was performed at twice threshold in the right atrium, there was a progressive increase in configurational changes as the distance between the pacing sites increased. When the catheter with 5-mm interelectrode spacing was used, pacing sites of 5, 11, and 17 mm from the tip demonstrated a change in configuration in a mean of 0.2±1.2, 0.8±3.6, and 1.2±3.6 leads per ECG, respectively (Fig 7Down). When the catheter with 10-mm interelectrode spacing was used, pacing sites of 10, 21, and 32 mm from the tip demonstrated a change in configuration in a mean of 1.0±3.6, 4.8±6.0, and 4.8±6.0 leads per ECG, respectively (Fig 8Down).



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Figure 7. Surface ECG demonstrating configurational changes in P waves during pacing from the lateral right atrium. In this patient, minor changes were observed in two leads (*) at a pacing distance of 11 mm from the tip electrode. ECGs were recorded at 2 cm/mV and 50 mm/s.



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Figure 8. Surface ECG demonstrating configurational changes in P waves during pacing from the lateral right atrium. In this patient, minor changes were observed in three leads (*) at a pacing distance of 10 mm from the tip electrode. ECGs were recorded at 2 cm/mV and 50 mm/s.


*    Discussion
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*Discussion
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Main Findings
The results of this study demonstrate that pacing sites as far apart as 32 mm in the coronary sinus and 17 mm in the right atrium can result in P waves that are very similar or identical in appearance. Although changes in P-wave amplitude and/or duration may be detected at pacing sites 17 mm apart, these changes are minor in magnitude and not apparent by visual inspection. These findings indicate that atrial mapping techniques that rely on discrimination of changes in P-wave configuration, such as pace mapping or concealed entrainment, are likely to be inaccurate by at least 17 mm and therefore not clinically useful for identifying potential target sites for catheter ablation of atrial tachycardia or atrial flutter.

Effect of Current Strength
Unipolar pacing from the distal electrode was used to simulate an atrial tachycardia. An increase in current strength might increase the amount of myocardial tissue captured by the pacing stimulus, thereby decreasing the ability to discriminate changes in P-wave morphology. Traditionally, pacing has been performed at twice the diastolic threshold. In this study, pacing also was performed at threshold in the coronary sinus, the minimal energy required for cellular depolarization, to determine whether the resolution of atrial pace mapping could be improved. However, pacing at threshold did not improve the proximity at which amplitude or duration differences were detected, nor did it have an effect on P-wave configuration. The spatial resolution of atrial pace mapping remains poor even when the smallest possible area of atrial myocardium is captured.

Prior Studies
Prior studies demonstrated that P-wave morphology may be used only as a rough guide in localizing a region of the atrium.7 8 9 In the present study, the results indicate that within certain regions of the atrium, eg, the posterolateral portion of the left atrium and the lateral wall of the right atrium, inspection of the P wave provides no useful information regarding site of origin. Although the spatial resolution in the right atrium is improved on the basis of configurational changes, no significant changes could be observed within 1.7 cm.

Previous studies have compared differences in QRS configuration during unipolar pacing from adjacent sites in the ventricle to determine the resolution of ventricular pace mapping.10 11 When analysis of the QRS complexes was based on major configurational changes, pacing sites as far apart as 15 mm were similar. However, when minor differences in configuration and amplitude were considered, pacing sites 5 mm apart usually could be distinguished. Therefore, the spatial resolution of unipolar ventricular pace mapping was within 5 mm. The lower resolution power of atrial pace mapping compared with ventricular pace mapping may be attributable to the smaller amplitude of the P wave compared with the QRS complex, to obscuration of the P wave by the preceding T wave,12 and to possible differences in activation patterns between the atrium and ventricle.

Concealed Entrainment
Concealed entrainment has been described as being useful in identifying appropriate sites for ablation of atrial tachycardia and atrial flutter.1 2 3 4 5 During classic entrainment, which is not helpful in identifying specific target sites for ablation, there is fusion of the paced P-wave morphology with the P wave generated by the atrial tachycardia or flutter. In contrast, during concealed entrainment, there is no fusion of the P wave, and the P wave during pacing maintains the same configuration as during atrial tachycardia or flutter. Therefore, the differentiation of classic from concealed entrainment depends on the ability to discriminate whether or not there is P-wave fusion during pacing.

In the present study, P waves generated at sites that were up to 32 mm apart in the coronary sinus and 17 mm apart in the right atrium usually could not be distinguished by visual inspection. This implies that the phenomenon of classic entrainment at sites up to {approx}1.7 cm away from where concealed entrainment occurs could easily be mistaken to be concealed entrainment. Therefore, although concealed entrainment may be a sensitive indicator of critical sites within the reentry circuit of atrial tachycardia or flutter, limitations in the ability to identify P-wave fusion indicate that in practice, its specificity in identifying appropriate target sites will be low.

Study Limitations
A limitation of this study is that the pacing sites were limited to the coronary sinus and the lateral wall of the right atrium. Therefore, the possibility that different results might be obtained in other parts of the atria cannot be ruled out. This study was limited to the coronary sinus and the right atrium because these were convenient, stable, and reproducible locations for pacing.

A second possible limitation is that the analysis of P waves was performed only at a pacing cycle length of 500 ms. This may not accurately reflect the rate-related changes that might occur during atrial tachycardias with a cycle length <500 ms. However, when pacing was performed at shorter cycle lengths, the P waves often were obscured by the preceding T wave.

Clinical Implications
This study demonstrates that only subtle changes in P-wave morphology occur when atrial pacing sites are between 11 and 17 mm apart. Although significant changes in P-wave amplitude and duration can be detected, the magnitude of the differences are small and usually indiscernible by visual inspection. Even at pacing sites 17 mm apart, the P waves generated by pacing may be virtually indistinguishable. Therefore, mapping techniques that depend on the accurate detection of changes in P-wave morphology, ie, pace mapping and concealed entrainment, are unlikely to be clinically useful in patients with atrial tachycardia or atrial flutter.


*    Footnotes
 
Reprint requests to K. Ching Man, DO, University of Michigan Medical Center, 1500 E Medical Center Dr, Ann Arbor, MI 48109-0022.

Received January 22, 1996; revision received March 13, 1996; accepted March 26, 1996.


*    References
up arrowTop
up arrowAbstract
up arrowIntroduction
up arrowMethods
up arrowResults
up arrowDiscussion
*References
 
1. Triedman JK, Saul P, Weindling SN, Walsh EP. Radiofrequency ablation of intra-atrial reentrant tachycardia after surgical palliation of congenital heart disease. Circulation. 1995;91:707-714.[Abstract/Free Full Text]

2. Feld GK, Fleck RP, Chen P, Boyce K, Bahnson TD, Stein JB, Calisi CM, Ibarra M. Radiofrequency catheter ablation for the treatment of human type 1 atrial flutter: identification of a critical zone in the reentrant circuit by endocardial mapping techniques. Circulation. 1992;86:1233-1240.[Abstract/Free Full Text]

3. Lesh MD. Radiofrequency catheter ablation of atrial tachycardia and flutter. In: Zipes DP, Jalife J, eds. Cardiac Electrophysiology: From Cell to Bedside. 2nd ed. Philadelphia, Pa: WB Saunders Co; 1995:1461-1471.

4. Chen S, Chiang C, Yang C, Cheng C, Wu T, Wang S, Chiang BN, Chang M. Radiofrequency catheter ablation of sustained intra-atrial reentrant tachycardia in adult patients: identification of electrophysiological characteristics and endocardial mapping techniques. Circulation. 1993;88:578-587.[Abstract/Free Full Text]

5. Stevenson WG, Sager PT, Friedman PL. Entrainment techniques for mapping atrial and ventricular tachycardias. J Cardiovasc Electrophysiol. 1995;6:201-216.[Medline] [Order article via Infotrieve]

6. Kadish AH, Morady F, Rosenbeck S, Summitt J, Schmaltz S. The effect of electrode configuration on unipolar His bundle electrogram. Pacing Clin Electrophysiol. 1989;12:1445-1450.[Medline] [Order article via Infotrieve]

7. Waldo AL, Vitikainen KJ, Kaiser GA, Malm JR, Hoffman BF. The P wave and P-R interval: effects of the site of origin of atrial depolarization. Circulation. 1970;42:653-671.[Abstract/Free Full Text]

8. Tang CW, Scheinman MM, VanHare GF, Epstein LM, Fitzpatrick AP, Lee RJ, Lesh MD. Use of P wave configuration during atrial tachycardia to predict site of origin. J Am Coll Cardiol. 1995;26:1315-1324.[Abstract]

9. Maclean WA, Karp RB, Kouchoukos NT, James TN, Waldo AL. P waves during ectopic atrial rhythms in man. Circulation. 1975;52:426-434.[Abstract/Free Full Text]

10. Kadish AH, Childs K, Schmaltz S, Morady F. Differences in QRS configuration during unipolar pacing from adjacent sites: implications for the spatial resolution of pace-mapping. J Am Coll Cardiol. 1991;17:143-151.[Abstract]

11. Kadish AH, Schmaltz S, Morady F. A comparison of QRS complexes resulting from unipolar and bipolar pacing: implications for pace-mapping. Pacing Clin Electrophysiol. 1991;14:823-832.[Medline] [Order article via Infotrieve]

12. Tracy CM, Swartz JF, Fletcher RD, Hoops HG, Solomon AJ, Karasik PE, Mukherjee D. Radiofrequency catheter ablation of ectopic atrial tachycardia using paced activation sequence mapping. J Am Coll Cardiol. 1993;21:910-917.[Abstract]




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