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Europace Advance Access originally published online on May 31, 2007
Europace 2007 9(7):466-470; doi:10.1093/europace/eum096
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© The European Society of Cardiology 2007. All rights reserved. For Permissions, please e-mail: journals.permissions@oxfordjournals.org


ELECTROPHYSIOLOGY

Abrupt changes in fibrillatory wave characteristics at the termination of paroxysmal atrial fibrillation in humans

Simona Petrutiu1,3, Alan V. Sahakian1,2,3 and Steven Swiryn1,3,4,*

1 Department of Electrical Engineering and Computer Science, Northwestern University, Evanston, IL, USA; 2 Department of Biomedical Engineering, Northwestern University, Evanston, IL, USA; 3 Evanston Northwestern Healthcare, Evanston, IL, USA; 4 HeartCare Midwest, 5405 N. Knoxville Avenue, Peoria, IL 61614, USA

Manuscript submitted 19 January 2007. Accepted after revision 17 April 2007.

* Corresponding author. Tel: +1 309 691 4410; fax: +1 309 692 4730. E-mail address: s-swiryn{at}northwestern.edu


    Abstract
 Top
 Abstract
 Introduction
 Methods
 Results
 Discussion
 Acknowledgements
 References
 
Aims We investigated the process of spontaneous termination of atrial fibrillation (AF) to determine its time course from the surface ECG.

Methods and results We studied fibrillatory waves in Holter recordings of paroxysmal and sustained AF. Following QRS-T cancellation dominant frequencies (DFs) were computed and the relationship of DF to termination was scrutinized. For 57 episodes of paroxysmal AF (PAF) in 24 patients, DF ranged from 4.4 to 6.5 Hz (5.2 ± 0.4 Hz) compared to 5.8 to 7.4 Hz (6.6 ± 0.6 Hz) for sustained AF recordings. Comparison of the atrial frequency of the ultimate to the penultimate second demonstrated a drop in frequency in 51 of 57 episodes, P < 0.00001. No comparable change was seen at longer time periods. Moments of comparably low frequency without termination were only occasionally seen in patients with PAF but not in patients with sustained AF.

Conclusion Low frequency fibrillation was found to be much more likely to terminate. Frequency changes preceding spontaneous termination were abrupt, in contrast to the gradual frequency drop reported with drug-induced termination. The analysis of fibrillatory wave characteristics and their change over time might be used to target specific moments for pacing therapy in patients with AF.

Key Words: Atrial fibrillation, Cancellation, Spectral analysis, Termination


    Introduction
 Top
 Abstract
 Introduction
 Methods
 Results
 Discussion
 Acknowledgements
 References
 
The mechanisms of maintenance and termination of atrial fibrillation (AF) are not completely understood. It is not known why AF is self-terminating in certain individuals but not in others although electrophysiological and structural remodeling during AF are believed to play a part in the transition from paroxysmal (PAF) to permanent AF.1Go,2Go The duration of episodes of spontaneously terminating AF varies from patient to patient and from episode to episode and it is not known why PAF self-terminates at a particular moment in time.

Pacemakers have had limited success in the prevention and termination of PAF.3Go–5Go Understanding the mechanisms of spontaneous termination of AF may lead to improvements in treatment by identifying conditions to be promoted or avoided, or moments during PAF that are promising or ill-timed for intervention. The fibrillatory wave characteristics and their change over time might be used in determining a window of opportunity to pace-terminate AF.

The atrial activity during AF can be characterized through the study of the fibrillatory waves from the surface electrocardiogram (ECG).6Go–8Go Spontaneous termination during PAF episodes is rarely encountered in the electrophysiology laboratory and therefore long-term surface ECG recordings provide the best way to document these events in humans. There is a good correlation between surface ECG characteristics and simultaneously recorded endocardial signals.9Go

Although termination of AF with anti-arrhythmic drugs10Go–13Go has been well studied and seems to depend on such factors as cycle length, organization, refractory periods and wavefront curvature, the spontaneous termination of AF remains poorly understood. In the multiple circulating wavelet model, termination probability relates to a decrease in the number of wavelets present, which is in turn a function of critical mass14Go and wavelength.15Go With models of AF based on focal firing,16Go slowing or complete cessation of the firing foci would lead to termination, but the mechanisms involved are unknown. With models based on rotors,17Go a change in wavefront curvature should result in termination. The time course of these events and whether they are registered in the surface ECG is unknown.

In this study, we evaluated 24-h Holter ECG recordings during episodes of PAF to determine if fibrillatory wave changes can be detected during the spontaneous termination of AF episodes. We investigated the process of termination to determine its time course from the surface ECG. We also investigated whether self-terminating AF episodes can be differentiated from sustained AF.


    Methods
 Top
 Abstract
 Introduction
 Methods
 Results
 Discussion
 Acknowledgements
 References
 
We retrieved analog 24-h ECG Holter recordings from 44 consecutive patients with AF. Patients were divided into those with PAF and those where AF persisted throughout the 24 h, which will be referred to as sustained AF. Though the exact duration in patients with AF throughout the 24 h is unknown, most of these patients had permanent AF. From the PAF recordings, we analysed all episodes lasting longer than 1 min, and where termination was documented during the 24-h Holter recording.

Signal processing and data analysis
All analog data were digitized at a sampling rate of 128 Hz with a resolution of 16 bits. Digital signal processing was performed using MATLAB (The Mathworks Inc., Natick, MA). The signals were first band-pass filtered with cutoff frequencies of 1 and 50 Hz to avoid baseline wander and power line interference. To isolate fibrillatory waves, we used a template-matching QRS-T cancellation algorithm similar to the one previously described by Slocum et al.18Go and validated by Xi et al.19Go We performed QRS-T detection on the channel with a higher ratio of ventricular to atrial activity. QRS-T complexes were identified, and the point of maximum negative slope was chosen as the fiducial point. An adaptive median beat was then computed for the channel with a lower ratio of ventricular to atrial activity, and a template of median beats was generated and subtracted from the original signal. PVC and aberrant beat detection was performed by comparing the morphology of the median beat with all detected QRS-T complexes. The abnormal beats were zeroed out before template subtraction.

Following QRS-T cancellation, the power spectrum of each ‘remainder’ ECG was calculated using the Fast Fourier Transform. We analysed 1-min segments as well as shorter segments of 10-s, 2-s and 1-s duration. When the length of the signal was short, the signal was zero-padded to keep the frequency resolution at < 0.1 Hz. Dominant frequency (DF) was defined as the peak of highest power in the 3–9 Hz band. Peak power was also recorded as a way to look at the amplitude change and organization of the signal. For patients with sustained AF, we analysed a sample minute selected from the middle of the 24-h recording. Figure 1 shows an example of a 10-s segment from a Holter lead, the remainder ECG obtained after QRS-T cancellation and the power spectrum of the remainder ECG.


Figure 1
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Figure 1 Example of a 10-s Holter lead, the remainder ECG obtained after QRS-T subtraction, and the power spectrum of the remainder ECG.

 
We compared our measurements between groups of patients and within patients using Student's t-test for unpaired or paired data, respectively. A P-value < 0.05 was considered statistically significant.

All activities for this research were reviewed and approved by the Institutional Review Board of Evanston/Northwestern Healthcare.


    Results
 Top
 Abstract
 Introduction
 Methods
 Results
 Discussion
 Acknowledgements
 References
 
A total of 44 patients were included in this study, 24 with PAF and a control group of 20 patients with sustained AF. Patients with PAF ranged in age from 43 to 89 years (mean ± SD, 67 ± 11 years). There were 12 men and 12 women. Patients with sustained AF ranged in age from 39 to 87 years (66 ± 12 years). There were 15 men and 5 women. Twenty-six patients (pts) were not taking any cardioactive drugs. Eighteen patients were taking cardioactive medications including beta-blockers (10 pts), calcium channel blockers (6 pts), digoxin (1 pt) and amiodorone (1 pt).

Fifty-five episodes of PAF whose initiation and termination were documented lasted from 1 to 530 min (mean 87 ± 146 min, median 18 min). One episode was preceded by atrial flutter. Two additional episodes with only the termination but not the onset documented lasted longer than 470 and 550 min, respectively. Ten patients had only one episode, 14 patients had two or more episodes documented during 24 h. DF ranged from 4.4 to 6.5 Hz (5.2 ± 0.4 Hz) for PAF episodes compared to 5.8 to 7.4 Hz (6.6 ± 0.6 Hz) for sustained AF recordings (P < 0.00001).

Pre-termination characteristics for PAF
We investigated the process of termination in all 57 episodes of PAF. To study the time course of termination, we analysed different length segments (1-min, 10-s, 2-s and 1-s). No significant difference was found between the penultimate and ultimate 1-min segments or between the penultimate and the ultimate 10-s segments (NS). The penultimate 2-s segment DF ranged from 3.0 to 6.9 Hz (5.3 ± 0.7 Hz) compared to the ultimate 2-s segments that ranged from 3.0 to 6.6 Hz (4.9 ± 0.8 Hz). Thus, there was a significant decrease in DF only from the penultimate to the ultimate 2-s segment (P < 0.0001).

To determine if there was a decrease in frequency within the last 2-s segment, we further scrutinized the difference between the penultimate and the ultimate seconds. DF in the penultimate second of PAF ranged from 3.9 to 6.6 Hz (5.3 ± 0.7 Hz). DF in the ultimate second of PAF ranged from 3.0 to 5.8 Hz (last-second-mean-dominant-frequency, 4.4 ± 0.7 Hz). Comparison of the atrial frequency of the ultimate to the penultimate second demonstrated a drop in frequency in 51 of 57 episodes with a mean drop of 0.8 Hz, (P < 0.00001) which is illustrated in Figure 2. Figure 3 shows a comparison of the mean DF for the entire episodes of sustained vs. PAF as well as the means of the penultimate and ultimate 2-s segments and the penultimate and ultimate seconds of PAF.


Figure 2
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Figure 2 Penultimate second vs. ultimate second dominant frequency for all 57 episodes of atrial fibrillation. Each line represents the penultimate and ultimate second of one episode of atrial fibrillation. Fifty-one out of 57 episodes showed a decrease in dominant frequency from the penultimate to the ultimate second.

 


Figure 3
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Figure 3 Comparison of the mean dominant frequency for the entire episodes of sustained vs. paroxysmal atrial fibrillation patients as well as the means of the penultimate and ultimate 2-s and 1-s segments of paroxysmal atrial fibrillation (mean ± SD). It can be observed that the mean for the ultimate 2-s segment is much lower than the mean for the penultimate 2-s segment and lower than the overall mean for paroxysmal atrial fibrillation episodes. Most of this is attributable to slowing during the ultimate second.

 
Peak power was compared between the penultimate and ultimate 1-s segments to determine whether the amplitude and organization of the signal changed in the moments preceding termination. Peak power ranged from 0.2 to 16.2 mV2 (5.1 ± 4.8 mV2) in the penultimate and from 0.2 to 13.2 mV2 (5.2 ± 4.6 mV2) in the ultimate 1-s segments and no significant difference was found between the two (NS).

Does low frequency AF always lead to termination?
Because moments of termination of fibrillation were almost invariably preceded by low fibrillation frequency, we scrutinized the last minute of each paroxysmal episode lasting longer than 4 min for other 1-s segments with comparably low frequency to that of the final second. The number of segments per patient with equal or lower frequency ranged from 0 to 23 segments (mean 8 ± 6 segments, median 6) of the 59 possible for each episode. The duration of the frequency drop was on the order of 1 to 2 s. Only in three instances, we found consecutive segments with a comparable low frequency lasting 4 s.

For patients with sustained AF, we compared the frequency of each of the 1-s segments of the selected sample minute to the last-second-mean-dominant-frequency of the PAF patients (4.4 Hz). The number of seconds of sustained AF with frequency less than the last- second- mean- dominant-frequency for patients with PAF was only 36 out of 1200 possible seconds of AF (60 s for each of 20 patients with sustained AF). Figure 4 shows a histogram distribution of the percentage of 1-s segments over the entire range of frequencies for AF and illustrates the difference between paroxysmal and sustained AF with PAF segments clustered at a lower frequency compared to sustained AF segments and terminating segments clustered at an even lower frequency compared to non-terminating segments.


Figure 4
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Figure 4 Histogram of the percentage of 1-s segments of sustained atrial fibrillation, non-terminating 1-s segments of paroxysmal atrial fibrillation and terminating 1-s segments of paroxysmal atrial fibrillation. Paroxysmal atrial fibrillation 1-s segments are mostly at lower frequencies than sustained atrial fibrillation. Terminating 1-s segments are clustered at even lower frequencies than non-terminating segments of paroxysmal atrial fibrillation.

 

    Discussion
 Top
 Abstract
 Introduction
 Methods
 Results
 Discussion
 Acknowledgements
 References
 
Main findings
Our study confirmed that episodes of PAF have a lower overall DF than episodes of sustained AF.20Go We found that frequency changes preceding spontaneous termination are abrupt, in marked contrast to the time course of such changes reported for anti-arrhythmic drug-induced termination. We observed a significant decrease in DF only in the last second or two of each episode, but no change in the organization of the signal. This abrupt change was nearly universal, being observed as a drop from the penultimate to the ultimate second in 51 of 57 episodes. Moments of comparably low frequency without termination were occasionally seen in patients with PAF. It was rare to find such moments of comparable low frequency in patients with sustained AF.

Pre-termination changes reflected in the surface ECG
It is known that termination of AF by anti-fibrillatory drugs is preceded by gradual slowing of fibrillatory frequency.9Go–12Go Asano et al. studied the termination of induced AF in humans and demonstrated that the mean FF intervals prolonged before termination when compared to initial values.21Go Capucci et al. determined in a pacing induced AF study in humans that the mean of 100 AF intervals prolonged before termination in episodes lasting less than 5 min.22Go Sih et al. reported that termination in three out of seven episodes of induced AF in humans was accompanied by a slight increase in atrial rate.23Go These studies reported observations before termination of induced AF in comparison to onset, but the actual time course of changes produced by the spontaneous termination of PAF episodes was not investigated.

Unlike the process at onset and the slowing during drug-induced termination, which are progressive over a few minutes, the process of spontaneous termination of AF in our study occurred abruptly with changes in frequency only in the last few seconds before termination. The presence of other moments of comparably low frequency without termination suggests that low fibrillatory frequency reflects a necessary, but perhaps not a sufficient condition for termination.

Clinical studies have shown conflicting results about the effectiveness of AF pacing prevention and termination algorithms.24Go,25Go The ADOPT trial demonstrated that overdrive atrial pacing with the AF Suppression Algorithm decreased symptomatic AF burden significantly in patients with sick sinus syndrome and AF.3Go One limitation of this study was that only symptomatic AF was used as an end point. The ATTEST trial determined that atrial prevention and termination therapies combined did not reduce burden, total frequency, or symptomatic frequency of AF.4Go Anti-tachycardia pacing (ATP) only achieves local capture in AF26Go,27Go and although it has been successful in pace-terminating other atrial tachyarrhythmias,5Go it has had limited success in terminating AF.28Go There may be specific moments during AF, detectable by frequency characteristics that would be optimal times either to intervene by pacing or perhaps to avoid pacing interventions, since spontaneous termination may occur.

Limitations
Although a list of medications was available for each patient, we do not know the timing of administration of different medications. We have previously reported in a larger group of patients the effect of medication on these parameters, as well as the relationship between the DF and the type and duration of AF.20Go The time course we have described in the present study seems much too short to be a direct effect of medications or meals.

Although the atrial activity during AF can be characterized directly from the surface ECG, it may be important to investigate the process of termination from intra-cardiac recordings to allow for the detection of more local events for example, in the pulmonary veins. However, spontaneous termination during PAF is rarely encountered in the electrophysiology laboratory and therefore long-term surface ECG recordings provide the best way to document these events.

Summary and clinical implications
Short-term changes that occur during the spontaneous termination of PAF are reflected in, and can be quantified from the surface ECG. Low frequency fibrillation was found to be much more likely to terminate. The process of spontaneous termination has a quite different time course than anti-arrhythmic drug-induced termination, and is reflected in an abrupt decrease in frequency just before termination. The analysis of fibrillatory wave characteristics and their change over time might be used in determining specific moments to target pacing therapy in patients with AF.


    Acknowledgements
 Top
 Abstract
 Introduction
 Methods
 Results
 Discussion
 Acknowledgements
 References
 
The authors would like to thank George Moody and Sonia Weinberger for their technical assistance with this study.

This work was supported in part by a grant from The Dr. Scholl Foundation.

Conflict of interest: none declared.


    References
 Top
 Abstract
 Introduction
 Methods
 Results
 Discussion
 Acknowledgements
 References
 
[1] Wijffels MC, Kirchhof CJ, Dorland R, Allessie MA. Atrial fibrillation begets atrial fibrillation. A study in awake chronically instrumented goats. Circulation (1995) 92:1954–68.[Abstract/Free Full Text]

[2] Ausuma J, Wijffels M, Thone F, Wouters L, Allessie M, Borgers M. Structural changes of atrial myocardium due to sustained atrial fibrillation in the goat. Circulation (1997) 96:3157–63.[Abstract/Free Full Text]

[3] Lee MA, Weachter R, Pollak S, Kremers MS, Naik AM, Silverman R, et al. The effect of atrial pacing therapies on atrial tachyarrhythmia burden and frequency: results of a randomized trial in patients with bradycardia and atrial tachyarrhythmias. J Am Coll Cardiol (2003) 41:1926–32.[Abstract/Free Full Text]

[4] Carlson MD, Ip J, Messenger J, Beau S, Kalbfleisch S, Gervais P, et al. A new pacemaker algorithm for the treatment of atrial fibrillation: results of the atrial dynamic overdrive pacing trial (ADOPT). J Am Coll Cardiol (2003) 42:627–33.[Abstract/Free Full Text]

[5] Israel CW, Hugl B, Unterberg C, Lawo T, Kennis I, Hettrick D, et al. Pace-termination and pacing for prevention of atrial tachyarrhythmias: results from a multicenter study with an implantable device for atrial therapy. J Cardiovasc Electrophysiol (2001) 12:1121–8.[CrossRef][Web of Science][Medline]

[6] Holm M, Pehrson S, Ingemansson M, Sornmo L, Johansson R, Sandhall L, et al. Non-invasive assessment of the atrial cycle length during atrial fibrillation in man: introducing, validating and illustrating a new ECG method. Cardiovasc Res (1998) 38:69–81.[Abstract/Free Full Text]

[7] Bollmann A, Sonne K, Esperer HD, Toepffer I, Langberg JJ, Klein HU. Non-invasive assessment of fibrillatory activity in patients with paroxysmal and persistent atrial fibrillation using the Holter ECG. Cardiovasc Res (1999) 44:60–6.[Abstract/Free Full Text]

[8] Xi Q, Sahakian AV, Ng J, Swiryn S. Atrial fibrillatory wave characteristics on surface electrocardiogram: ECG to ECG repeatability over twenty-four hours in clinically stable patients. J Cardiovasc Electrophysiol (2004) 15:911–7.[Web of Science][Medline]

[9] Slocum SE, Ropella KM. Correspondence between the frequency domain characteristics of simultaneous surface and intra-atrial recordings of atrial fibrillation. Computers in Cardiology (1994) 21:781–84.

[10] Ropella KM, Sahakian AV, Baerman JM, Swiryn S. Effects of procainamide on intra-atrial electrograms during atrial fibrillation: implications for detection algorithms. Circulation (1988) 77:1047–54.[Abstract/Free Full Text]

[11] Bollmann A, Kanuru NK, McTeague KK, Walter PF, DeLurgio DB, Langberg JJ. Frequency analysis of human atrial fibrillation using the surface electrocardiogram and its response to ibutilide. Am J Cardiol (1998) 81:1439–45.[CrossRef][Web of Science][Medline]

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[13] Biffi M, Boriani G, Bronzetti G, Cappuci A, Branzi A, Magnani B. Electrophysiological effects of flecainide and propafenone on atrial fibrillation cycle length and relation with arrhythmia termination. Heart (1999) 82:176–82.[Abstract/Free Full Text]

[14] Byrd GD, Sandip MP, Ripplinger CM, Cassilly TR, Schuessler RB, Boineau JP, et al. Importance of geometry and refractory period in sustaining atrial fibrillation: testing the critical mass hypothesis. Circulation (2005) 112:I7–13.[CrossRef][Web of Science][Medline]

[15] Moe GK. On the multiple wavelet hypothesis of atrial fibrillation. Arch Int Pharmacodyn Ther (1962) 140:183–8.[Web of Science]

[16] Haissaguerre M, Jais P, Shah DC, Takahashi A, Hocini M, Quiniou G, et al. Spontaneous initiation of atrial fibrillation by ectopic beats originating in the pulmonary veins. N Engl J Med (1998) 339:659–66.[Abstract/Free Full Text]

[17] Jalife J, Berenfeld O, Mansour M. Mother rotors and fibrillatory conduction: a mechanism of atrial fibrillation. Cardiovasc Res (2002) 54:204–16.[Abstract/Free Full Text]

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[19] Xi Q, Sahakian AV, Swiryn S. The effect of QRS cancellation on atrial fibrillatory wave signal characteristics in the surface electrocardiogram. J Electrocardiol (2003) 36:243–9.[CrossRef][Web of Science][Medline]

[20] Xi Q, Sahakian AV, Frohlich TG, Ng J, Swiryn S. Relationship between pattern of occurrence of atrial fibrillation and surface electrocardiographic fibrillatory wave characteristics. Heart Rhythm (2004) 1:656–63.[CrossRef][Web of Science][Medline]

[21] Asano Y, Saito J, Matsumoto K, Kaneko K, Yamamoto T, Uchida M. On the mechanism of termination and perpetuation of atrial fibrillation. Am J Cardiol (1992) 69:1033–8.[CrossRef][Web of Science][Medline]

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[23] Sih HJ, Ropella KM, Swiryn S, Gerstenfeld EP, Sahakian AV. Observations from intraatrial recordings on the termination of electrically induced atrial fibrillation in humans. Pacing Clin Electrophysiol (1994) 17:1231–42.[CrossRef][Medline]

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[27] Kirchhof C, Chorro F, Scheffer GJ, Brugada J, Konings K, Zetelaki Z, et al. Regional entrainment of atrial fibrillation studied by high-resolution mapping in open-chest dogs. Circulation (1993) 88:736–49.[Abstract/Free Full Text]

[28] Paladino W, Baju M, Knight PB, Weiss R, Sousa J, Zivin A, et al. Failure of single and multisite high-frequency atrial pacing to terminate atrial fibrillation. Am J Cardiol (1997) 80:226–7.[CrossRef][Web of Science][Medline]


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L. Sornmo, M. Stridh, D. Husser, A. Bollmann, and S. B. Olsson
Analysis of atrial fibrillation: from electrocardiogram signal processing to clinical management
Phil Trans R Soc A, January 28, 2009; 367(1887): 235 - 253.
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