A new transform for the analysis of complex fractionated atrial electrograms
© Ciaccio et al; licensee BioMed Central Ltd. 2011
Received: 10 January 2011
Accepted: 12 May 2011
Published: 12 May 2011
Representation of independent biophysical sources using Fourier analysis can be inefficient because the basis is sinusoidal and general. When complex fractionated atrial electrograms (CFAE) are acquired during atrial fibrillation (AF), the electrogram morphology depends on the mix of distinct nonsinusoidal generators. Identification of these generators using efficient methods of representation and comparison would be useful for targeting catheter ablation sites to prevent arrhythmia reinduction.
A data-driven basis and transform is described which utilizes the ensemble average of signal segments to identify and distinguish CFAE morphologic components and frequencies. Calculation of the dominant frequency (DF) of actual CFAE, and identification of simulated independent generator frequencies and morphologies embedded in CFAE, is done using a total of 216 recordings from 10 paroxysmal and 10 persistent AF patients. The transform is tested versus Fourier analysis to detect spectral components in the presence of phase noise and interference. Correspondence is shown between ensemble basis vectors of highest power and corresponding synthetic drivers embedded in CFAE.
The ensemble basis is orthogonal, and efficient for representation of CFAE components as compared with Fourier analysis (p ≤ 0.002). When three synthetic drivers with additive phase noise and interference were decomposed, the top three peaks in the ensemble power spectrum corresponded to the driver frequencies more closely as compared with top Fourier power spectrum peaks (p ≤ 0.005). The synthesized drivers with phase noise and interference were extractable from their corresponding ensemble basis with a mean error of less than 10%.
The new transform is able to efficiently identify CFAE features using DF calculation and by discerning morphologic differences. Unlike the Fourier transform method, it does not distort CFAE signals prior to analysis, and is relatively robust to jitter in periodic events. Thus the ensemble method can provide a useful alternative for quantitative characterization of CFAE during clinical study.
Keywordsdecomposition ensemble average Fourier transform reconstruction spectral analysis
Transforms that use a general basis like Fourier analysis are not efficient for representation of independent biophysical sources, or drivers, unless these happen to be generated by sinusoidal functions. In contrast, transforms that use data-driven bases can be efficacious for distinguishing uncorrelated signal components generated by independent drivers, if the morphology is reproduced in the basis. For example the Fukunaga-Koontz transform has been found useful to discern two independent sources in cardiac electrogram data by separating correlated versus uncorrelated components of the variance (second central moment) . Development of a data-driven basis and transform that utilizes the ensemble average (first central moment) would be desirable to detect the actual signal morphologic components originating from distinct sources. This would be useful for example in the analysis of complex fractionated atrial electrograms (CFAE)  which are likely formed by multiple independent generators (focal areas of high frequency and/or reentrant circuits) [3–6]. Currently, CFAE are often quantified using the dominant frequency (DF), defined as the largest spectral component within the physiologic range of electrical activation rate (~2-10Hz) . The DF is typically calculated by bandpass filtering the CFAE, rectification, and low pass filtering of the result, followed by Fourier power spectral analysis [8, 9]. However, the filtering process distorts important signal components and the method is not robust to phase noise [10–13]. Moreover, signal morphologic components arising from each generator are not readily apparent in the sinusoidal basis. Development of an improved estimate of independent generator frequency and of morphologic characteristics would potentially be useful to target abnormal atrial tissue for catheter ablation , particularly for persistent AF cases [15, 16].
In this study we describe a new transform which does not distort analyzed signals and is robust to phase noise, for calculation of the DF and identification of independent generator frequency and morphology in CFAE. In previous analyses of CFAE, the DF has been calculated by ensemble averaging [17, 18], and this prior work was used as a foundation for development of the transform. In the current study, the transform equations are first derived. Then the transform is tested versus Fourier analysis to measure the DF of CFAE, and to determine the robustness of each method of DF measurement when random noise is added to the signal. Additionally, the frequencies of simulated drivers embedded in CFAE in the presence of phase noise and interference are detected with each method. Correspondence is shown between basis vectors of highest power derived from the new transform, versus actual CFAE morphology and synthesized drivers. Finally, DF measurement error is compared when the short-time Fourier transform and the short-time ensemble averaging transform are used to improve spectral time resolution.
A. Transform Equations
which reduces to 1/w when the sample rate is 1 kHz and the time units are milliseconds. The peak in the autocorrelation function over a frequency range f1 to f2 (i.e., 1/w1 to 1/w2) that is physiologic for electrical activation rate has been used to estimate the DF in atrial electrograms [19–21].
where Eq. 9b and 9c are formed by substituting Eq.'s 7 and 8 into Eq. 9a, and i and j are segment numbers from 1 to n. Eq. 9c is similar to Eq. 3, except that instead of computing the autocorrelation between successive signal segment pairs s wi, s wi+1 only (lag w), it is computed between all signal segments s wi, s wj. Therefore Pw is equivalent to computing the mean autocorrelation coefficient from n points in the autocorrelation function separated by lag w, i.e., to averaging the autocorrelation coefficients at lags w, 2w, 3w, ... nw. However, to generate Pw in this way rather than by using Eq. 9c would require a sequence length 2N to convolve the signal with itself along its entire length, halving the time resolution and doubling the sequence length needed for analysis.
The ensemble average calculation was repeated for all segments w in the frequency range of interest, as given by Eq. 6, with a sampling rate of 977Hz. The RMS power in the ensemble average was then plotted using Eq. 11 and is shown in Figure 1D. The DF occurs at 7.52 Hz, corresponding to w = 130 sample points (panel B). In contrast, the location marked NF (noise floor) coincides with frequency f = 5.92 Hz, i.e., w = 165 sample points (panel C). The ensemble average spectrum thus displays correlated components as spectral peaks with higher power. These spectra also have more detail at the lower end of the range due to the w = 1/f relationship (Eq. 6), and DF subharmonics are pronounced.
where S is the power spectral density, dφ is the phase lag w, i is the segment number, and substitution using Eq.'s 1 and 3 were utilized to form Eq.'s 12b and 12c. The Fourier power spectral density calculation decomposes the autocorrelation function into its native sinusoids. Therefore, in contrast to autocorrelation spectral analysis (Eq. 3), both ensemble and Fourier spectral analyses account for periodicity at all autocorrelation lags - ensemble by averaging (Eq. 9) and Fourier by fitting sinusoids (Eq. 12c).
where the middle and RHS in Eq. 15 are obtained by substitution and rearrangement using Eq.'s 9 and 13-14. Eq. 15 states that if each signal segment of length w is correlated with the ensemble average at w (LHS), the resulting correlation coefficient equals the ensemble average power (RHS).
The magnitudes are greatest along the main diagonal and equal Σ 1/ni, where n is given by Eq. 5. This matrix is also not invertible (Matlab ver. 7.7, R2008b, The MathWorks, Natick MA). In general, as with the individual transform matrices, the total transform matrix will not be invertible.
Consider how acts to transform signal x. Let a subset γ of highest basis vectors, when ranked in descending order of power, be summed using (Eq. 17). In this case transfers the most correlated periodic components of the signal to form estimate v. The relative amplitude relationships of these components, each extracted by a different T i embedded in , are maintained by scale factor 1/ni during transformation (Eq. 16). However, when the components are independent (i.e., no harmonic relationships), their combination causes the 'noise' power in v to increase by √γ. To maintain the same power for best match with x, the estimate can either be scaled by 1/√γ, or alternatively v and x can be scaled to the same power. Any unique signal structure that is not periodic is also transformed by , but it is via the main diagonal, not by the off-diagonal elements which sum and reinforce correlated content. As γ is increased, the magnitude of the main diagonal elements increases so that acts in part as an N × N identity matrix I N to directly transfer the unique uncorrelated detail during formation of v. So long as a i and a j are approximately orthogonal, the unique detail as well as correlated components maintain their correct amplitude relationships in v, since they are added in tandem and scaled by 1/ni.
B. Clinical data
Atrial electrograms were recorded in a series of 20 patients, 10 with paroxysmal and 10 with longstanding persistent atrial fibrillation, referred to the Columbia University Medical Center cardiac electrophysiology (EP) laboratory for catheter ablation. Two bipolar recordings, each greater than 16 seconds in duration, were obtained from six anatomical regions: the ostia of the left superior and inferior pulmonary veins (LSPV, LIPV), the ostia of the right superior and inferior pulmonary veins (RSPV, RIPV), and the anterior and posterior left atrial free wall (ANT, POS). The recordings were obtained from these regions via the distal bipolar catheter ablation electrode during sustained AF prior to any ablation. Using standard settings, all signals were filtered in hardware at acquisition to remove baseline drift and high frequency noise (digitization rate = 977Hz; first order filter passband: 30-500 Hz). In each patient, a CFAE sequence 8192 sample points long (~8.4 seconds) as determined visually by two cardiac electrophysiologists was retrospectively selected for analysis from two sites at each of the six locations. CFAE were defined as atrial electrograms with three or more deflections on both sides of the isoelectric line, or continuous electrical activity with no well-defined isoelectric line . In all, 216 of 240 recordings met these criteria, as determined by the two cardiac electrophysiologists, and were used for further analysis. No ventricular component, corresponding to the QRS deflection of the electrocardiogram, was visually evident in the CFAE. In these bipolar recordings it is uncommon for QRS artifact to be evident in CFAE obtained from the pulmonary veins and free wall. The signals were stored in both raw form, and following normalization to mean zero and unity variance.
C. Tests of Fourier versus ensemble methods
The following six tests were developed to determine the effectiveness of the new transform versus Fourier analysis for representation of frequency and morphologic components of CFAE. The Fourier DF method is optimized when CFAE recordings are bipolar and approximately 8s in length [11, 22, 23]. We therefore used these parameters for most measurements in our study. The 8s sequences were readily available from retrospective data. During electroanatomic mapping, recordings with relatively short sequence length are commonly acquired from each site to minimize the procedure time.
C.1. Orthogonality of the ensemble basis
for all pairs i, j from w = 500 to w = 20 (f = 2-50Hz) for one paroxysmal and one persistent CFAE signal. The dp's were graphed for i versus j. The ensemble averaging basis was considered to be orthogonal if dp = 1.0, i = j, and dp ≈ 0, i ≠ j, except for small integer (i.e., harmonic) relationships in i/j. For comparison, dp was also calculated with the Fourier basis using the same paroxysmal CFAE signal.
C.2. Spectral analysis of synthetic drivers with phase noise and interference
Phase noise was created by randomly and independently shifting the timing of each driver pulse (each 229, 177, or 123 sample point interval) using a mean-zero random number generator with standard deviation of ± 16 ms. Interference was added by summing the combined synthetic signal D1+D2+D3 with one of the 216 scaled CFAE signals (i.e., the CFAE signals themselves acted as interference during measurement of synthetic driver characteristics). The following combinations of gains for the phase noise random vector (p) and interference (i) were used for assessment: (p = 1 ×,i = 1 ×), (p = 0.5 ×,i = 2 ×), (p = 0.3 ×,i = 3 ×), and (p = 0 ×,i = ± 1 ×... ± 10 ×). Fourier and ensemble power spectra were constructed in the range 2-10Hz from the resulting signals. The spectral peaks were ranked by amplitude, and the sum of ranks for peaks having frequencies of 4.26Hz, 5.52Hz, and 7.94Hz, with a tolerance of ± 0.2Hz, was tabulated. The best (minimum) sum of ranks is 6 which occurs when the driver frequencies at 4.26Hz, 5.52Hz, and 7.94Hz are ranked 1st, 2nd, and 3rd in amplitude, in some combination, among all spectral peaks.
C.3. Identification of synthetic driver morphology
As the ensemble method but not the Fourier transform has a data-driven basis, only ensemble was used in this test. The synthetic drivers with additive phase noise and interference described in Test 2 were corrupted using two noise gain sets: p = 0.3 ×,i = 3 ×, and p = 0 ×,i = 5 ×, where the interferences consisted of the 216 CFAE signals (thus 216 comparisons for each of the two noise gain sets). The mean squared error difference between each original synthetic driver (Figure 2), and the corresponding ensemble basis vector of the corrupted signal at segment lengths of 123, 177, and 229 sample points, the periods of the drivers, when both were normalized to unity power, was tabulated in mV2/ms.
C.4. Degradation of DF in CFAE with additive random noise
This test was used to determined the efficacy of each transform to detect the DF of CFAE in the presence of random noise (no added synthetic drivers). For each of 20 selected CFAE having a prominent DF (sharp peak with its base dropping to a low noise floor), random white noise was added with a standard deviation of 0.16 mV, approximately half that of the raw CFAE signals. The absolute differences in the DF before versus after random noise addition were tabulated. This was repeated for 10 different random noise vectors. The mean and standard deviation of these values was calculated for ensemble versus Fourier spectral analysis and the significance was determined. The entire process was then repeated for random white noise with a standard deviation of 0.32 mV, approximately equal to the standard deviation of the raw CFAE signals.
C.5. CFAE reconstruction
where a w1 to a w12 were the top 12 basis vectors ranked in descending order of power. The average error was determined for Fourier versus ensemble reconstruction.
C.6. Single driver test
The CFAE signals were then altered by adding a low-power transient component at 200 sample point intervals (977 samples per second/200 samples ~5Hz). The transient itself consisted of a 42 sample point long biphasic component extracted from a CFAE acquired from the LSPV ostia during persistent AF. This transient had properties of mean = 0.13 mV, standard deviation = 0.54 mV, and peak-peak values of ~ ± 1 mV. CFAEs after addition of the low-power transient were analyzed using Fourier and ensemble spectral analysis to determine whether the component could be readily identified. Identification was defined to be presence of a distinct power spectral peak, with the base of the peak reaching the surrounding noise floor.
The Fourier power spectrum was computed using MATLAB (ver. 5.1, 1997, The MathWorks, Natick MA) by applying a Hann window to the 8192 discrete point signal. To prevent signal distortion, the traditional Fourier preprocessing method of bandpass filtering, rectification, and low pass filtering was not used (see Background). A fast Fourier transform (FFT) was then computed from the windowed signal, and the power spectrum was graphed.
C.7. Short-time Fourier and Ensemble Transformation
where the nonstationarity and measurement error are uncorrelated so that there is no divide by √n in Eq. 22. If the ensemble average and Fourier transform generate the same mean DF, then the technique with greatest standard deviation σ, regardless of whether or not the real DF is stationary, will have the largest measurement error. The means and standard deviations in 2s DF for all 216 CFAE sequences were averaged and tabulated to make this comparison.
The statistical t-test and F-test were used for detecting differences in means and variances, respectively, with significance at the p < 0.05 level (SigmaPlot ver. 9.0, Systat Software, 2004, and MedCalc ver. 9.5, MedCalc Statistical Software 2008).
This section is arranged according to the seven tests that were described in the Methods.
A.1. Orthogonality of the ensemble basis
A.2. Spectral analysis of synthetic drivers with phase noise and interference
Sum of Ranks of Three Driver Frequencies
7.12 ± 1.41
6.71 ± 1.08
7.03 ± 0.48
6.31 ± 0.10
7.88 ± 0.30
6.73 ± 0.08
10.24 ± 3.37
8.82 ± 3.08
A.3. Identification of synthetic driver morphology
A.4. Degradation of DF in CFAE with additive random noise
A.5. CFAE reconstruction
A.6. Single driver test
A.7. Short-time Fourier and ensemble transformation
Comparison of Short-Time Transform Frequency Measurements
Paroxysmal, DF (Hz)
Persistent, DF (Hz)
p < 0.001
p < 0.001
In this study a data-driven transform was described for application to CFAE signals. The basis is constructed from the ensemble averages of signal segments and was found to be orthogonal except for small integer-multiple (i.e. harmonic) relationships. The power in each ensemble average is equivalent to the projection of the signal onto the corresponding basis (Eq. 15). The relationship of the ensemble average spectrum to the autocorrelation spectrum and to the Fourier power spectrum was described. While the autocorrelation spectrum is based on correlation at a single lag w, the ensemble and Fourier power spectra are based on correlation at multiple lags w, 2w, ..., nw. During construction of the ensemble spectrum, the autocorrelation function at lags are averaged, as compared to the Fourier power spectrum which is a sinusoidal curve-fitting of the autocorrelation function. Several tests were used to compare the efficacy of the Fourier transform, versus transformation using ensemble averaging, for representation of CFAE signal components. At several levels of additive noise and interference, the highest peaks in the ensemble spectrum corresponded to the frequencies of three synthetic drivers with greater accuracy as compared to Fourier spectral analysis (p ≤ 0.005; Table 1). Similarly, when random white noise corrupted actual CFAE signals, the ensemble spectrum was more accurate than Fourier in representation of the DF (p ≤ 0.01). The ensemble basis was found to be useful for representation of the signal morphology of three independent synthetic drivers. When only interference was added to the combined driver signal, the three top-ranked basis vectors in order of greatest power corresponded to the independent driver morphology almost exactly. When phase noise (jitter) was added, the three top-ranked basis vectors corresponded to driver morphology but with some smoothing. When a single low-power, short duration component was added, as would simulate presence of a distant driver, it was evident as a distinct peak in all 216/216 ensemble average spectra but in only 82/216 Fourier spectra. During reconstruction of actual CFAE signals, the ordered ensemble average basis from 1-12 vectors was more accurate for representation as compared with Fourier (p ≤ 0.002). Finally, DF measurement error as estimated by the standard deviation in DF was reduced in ensemble as compared with Fourier spectral analysis when short-time transformation was used to improve time resolution. Thus it was found that the new transform is efficacious for representation and measurement of morphologic and frequency components in real CFAE, and in synthetically-derived independent generators, as compared with the Fourier transform.
B. Computational and mathematical considerations
Although ensemble average analysis is relatively robust to noise and jitter, to further reduce their affect on signal analysis, the inner product between the spectrum and a model can be used for gradual, adaptive update  or alternatively, finite differences can be used for adaptation . When computing the DF of atrial fibrillation signals, variation by as much as 2.5Hz can occur over a time interval of a few seconds; hence tracking with time-frequency methods may be required for accurate analysis [27, 28]. Since ensemble averaging is a form of autocorrelation, a minimum sequence length of two cycles of the periodic signal is needed for construction of the frequency spectrum (which would result in a very course estimation). To include low frequency activity to a lower limit of 2Hz, as was done in this study, a window of at least 1000ms (1s) should thus be used. Any such measurement could be updated by shifting the analysis window, for example by 100-150ms steps, to describe the time-frequency evolution of the signal . To reduce error when short sequences are utilized for analysis, a model-based approach for update of the spectral profile can be implemented .
In a study by another group, the DF computed by Fourier analysis was compared with the mean, median, and mode activation rate, as obtained by electrogram marking, to determine efficacy . However, as stated in that study, DF does not specifically reflect activation rate and therefore is only an approximate measure, with a level of uncertainty. For this reason, we chose to add artificial drivers at specific frequencies, as well as to analyze the degradation of actual DFs in CFAE when random noise is introduced, as tests to compare the Fourier versus ensemble averaging methods. In each of our tests of DF measurement, the highest peak in the spectral range was selected as the DF. The more accurate selection of DF in presence of noise and interference by ensemble average analysis may in part be due to increased spectral power in the fundamental frequency versus the superharmonics as compared with the standard Fourier method .
C. Clinical applications and future directions
Knowledge of the mechanisms for onset and maintenance of atrial fibrillation is scant due in part to the difficulty in quantitative assessment of the CFAE signal with the standard Fourier method of DF calculation, which distorts the signal during preprocessing and suffers from phase noise degradation of the estimate . By devising a data-driven frequency transform, independent synthetic drivers were successfully extracted and characterized using both frequency and morphologic measurements in our study. It is anticipated that independent drivers can similarly be discerned in real clinical data. For example, when a simulated mother rotor located in a uniformly conducting medium drives AF, around which is a boundary leading to nonuniformly conducting regions, then the rotor's frequency components will still be prominent in nonuniform region spectra, although the noise floor increases . At such conduction boundaries, jitter and additive random noise caused by wavelet formation likely act to increase the noise floor. Based upon the results of this study, ensemble spectral analysis is more robust to jitter and random noise in CFAE as compared with Fourier, and thus is probably more likely to identify distant drivers even in nonuniformly conducting regions where secondary wavelets form. Such uniform/nonuniform boundaries can be quite common in arrhythmogenic atrial tissue, and include interfaces between electrically remodeled versus nonremodeled tissue, and between areas with fibrosis versus no fibrosis.
The transform can be further developed for clinical use by activation mapping of the substrate during clinical electrophysiologic study, identification during AF of independent focal or reentrant sources in the maps, and determining the correspondence of these to the most important ensemble average basis vectors and frequency components. It is expected that ablation lesions at these sources will prevent AF [5, 6], although this must be verified. Simulations have suggested that sinusoidal electric fields may be important for excitation of cardiac tissue . If such sinusoidal generators exist in nature, they will be efficiently represented by the Fourier transform, which is based upon sinusoidal components, but also by the ensemble averaging basis, from which any such components are also readily reconstructed.
where P and P' denote power spectra of two different CFAE. Suppose for example that many CFAE recordings are obtained simultaneously from the left atrium. The ensemble spectrum of each can be compared with its nearest-neighbors by averaging the Euclidean distance between nearest-neighbor spectra. If this is repeated for nearest-neighbors throughout the mapping region, then areas with smallest Euclidean distance would suggest presence of a nearby driver or substrate homogeneity, while areas with large spectral difference would suggest either locally heterogeneous properties of electrical conduction, or a boundary area where multiple independent drivers compete. Another method of classification would be to sum all CFAE in a neighborhood region, compute the ensemble average basis, project each CFAE onto the ensemble average space resulting from this basis, and cluster and classify according to the position of each point in the space.
Our study was limited to the measurement of retrospectively-obtained CFAE. According to our results, under certain conditions, ensemble averaging is more robust to phase noise and interference as compared with Fourier analysis. However, to show that the new method is efficacious for clinical electrophysiologic study, CFAEs of AF patients should be classified prospectively into ablative and non-ablative groups, followed by catheter ablation at the areas designated for ablation. The efficacy would then be determined by any reduction in procedural time, and in the need for follow-up study, as compared with not using the technique.
The importance of the ensemble averaging method will also depend upon other practical applications. In recent work, DF maps at early onset of ventricular tachyarrhythmia in postinfarction canine border zone were constructed with ensemble averaging . Using DF gradients, it was possible to predict the arrhythmia type that would be manifested (monomorphic ventricular tachycardia, polymorphic ventricular tachycardia, or ventricular fibrillation). This technique could be useful for arrhythmia detection from an ICD at a time sufficiently early in onset so that low voltage shock would prevent ventricular fibrillation , the subject of future study. In another recent study, videocapsule endoscopy images were assessed with ensemble averaging for estimation of the dominant period over many image frames . This dominant period was found to be correlated to small bowel motility, which can be altered in celiac disease and in patients with other diseases causing small intestinal lesions. Furthermore, ensemble average spectra have been used to show differences at the pulmonary vein ostia and the left atrial free wall in paroxysmal as compared with longstanding persistent AF patients . Using ensemble spectra, the study showed that there is greater spatial uniformity of left atrial DF in longstanding persistent as compared with paroxysmal AF patients. The DF also tended to approach a common upper bound value of ~6.0 - 6.5Hz in persistent AF patients . Thus the new transform may have wider application for prospective clinical data analysis.
The frequency decompositions used in this study are strictly applicable only to stationary signals. Thus caution must be exercised in interpreting the spectra as being representative of the entire measured interval. When nonstationarity is present, other transforms such as Wavelet decomposition can provide additional information. For some comparative tests, three synthetic drivers were constructed by extracting sequences from one CFAE. In another test, a short low-power transient was synthetically added to CFAE to simulate a far-field driver. To confirm the utility of the new transform, tests with synthesized data should be repeated using real AF drivers as determined by activation mapping (noncontact or sequential contact mapping). Confirmation of the reduction in error in the decomposition and reconstruction of CFAE signals by ensemble averaging as compared with other transformations, and in its robustness to noise, may require proving optimality, the subject of future research. The frequency resolution of the ensemble average spectrum can be made homogeneous by using appropriate fractional values of w and interpolating between sample points of the signal, although for simplicity it was not done in this study.
We have described a new transform that can be used for evaluation of CFAE signals. The ensemble average of signal segments was utilized to construct a data-driven basis, and it was shown to have significant advantages over Fourier analysis for correct prediction of the DF of independent synthetic drivers in the presence of phase noise and interference, identification of the distinctive morphologic components associated with each driver, as well as for representation of CFAE signals in general. The transform therefore may have application to prospectively target atrial fibrillation drivers during clinical catheter ablation to prevent arrhythmia recurrence, as well as for improved understanding of the mechanisms by which paroxysmal and persistent AF are initiated and maintained.
The following tested Fortran code is useful to compute ensemble average power spectra from multiple CFAEs. The code runs in ~1 second on a PC-type laptop computer and can be implemented in real time.
parameter (n0 = 50, n1 = 500, n2 = 8192, n3 = 216, rate =.977)
real en(n1, n1), f(n1), inp(n2, n3), s(n1, n3)
do 1 i = 1, n3
do 2 j = n1/2+1, n1
en(j, 1:j) = 0.
do 2 k = 1, n2/j
en(j, 1:j) = en(j, 1:j) + inp((k-1)*j+1:(k-1)*j+j, i)
do 3 j = n1/2, n0, -1
en(j, 1:j) = en(2*j, 1:j) + en(2*j, j+1:2*j)
do 1 j = n0, n1
s(j, i) = sqrt(sum(en(j, 1:j)**2)/n2); if(i.eq.1) f(j) = rate/j
en = ensemble vector, rate = digital sampling rate, s = spectral magnitude, f = frequency
inp = input matrix consisting of CFAEs normalized to mean zero and standard deviation = 1.
n0, n1 = range of segment widths = (50, 500). Frequency f = 977/50 - 977/500 = 19.54Hz - 1.95Hz.
n2 = number of sample points in each CFAE = 8192.
n3 = number of CFAE from which to calculate spectra = 216.
Loop 1 (inner) computes the RMS power spectrum s(j, i) based upon Eq. 11, with frequencies given by f.
Loop 2 zeros the ensemble matrix and computes ensemble averages from (n1)/2 + 1 to n1.
Loop 3 computes ensemble averages from w = n0 to (n1)/2 by averaging the two half segments of the ensemble average with width 2w (see Eq. 21).
No outside funding was received for this study. Map3d was used for creation of Figure 4. Its development was funded by the NIH/NCRR Center for Integrative Biomedical Computing, P41-RR12553-10.
- Ciaccio EJ, Dunn SM, Akay M, Wit AL, Coromilas J, Costeas CA: Localized spatial discrimination of epicardial conduction paths after linear transformation of variant information. Ann Biomed Eng 1994, 22: 480–492. 10.1007/BF02367084View ArticleGoogle Scholar
- Nademanee K, McKenzie J, Kosar E, Schwab M, Sunsaneewitayakul B, Vasavakul T, Khunnawat C, Ngarmukos T: A new approach for catheter ablation of atrial fibrillation: Mapping of the electrophysiologic substrate. J Am Coll Cardiol 2004, 43: 2044–2053. 10.1016/j.jacc.2003.12.054View ArticleGoogle Scholar
- Mandapati R, Skanes A, Chen J, Berenfeld O, Jalife J: Stable microreentrant sources as a mechanism of atrial fibrillation in the isolated sheep heart. Circulation 2000, 101: 194–199.View ArticleGoogle Scholar
- Oral H, Chugh A, Good E, Sankaran S, Reich SS, Igic P, Elmouchi D, Tschopp D, Crawford T, Dey S, Wimmer A, Lemola K, Jongnarangsin K, Bogun F, Pelosi F Jr, Morady F: A tailored approach to catheter ablation of paroxysmal atrial fibrillation. Circulation 2006, 113: 1824–1831. 10.1161/CIRCULATIONAHA.105.601898View ArticleGoogle Scholar
- Niu G, Scherlag B, Lu Z, Ghias M, Zhang Y, Patterson E, Dasari T, Zacharias S, Lazzara R, Jackman WM, Po SS: An acute experimental model demonstrating two different forms of sustained atrial tachyarrhythmias. Circ Arrhythmia Electrophysiol 2009, 2: 384–392. 10.1161/CIRCEP.108.810689View ArticleGoogle Scholar
- Kapa S, Asirvatham SJ: Atrial Fibrillation: Focal or Reentrant or Both? Circulation: Arrhythmia and Electrophysiology 2009, 2: 345–348. 10.1161/CIRCEP.109.888081Google Scholar
- Sanders P, Berenfeld O, Hocini M, Jais P, Vaidyanathan R, Hsu LF, Garrigue S, Takahashi Y, Rotter M, Sacher F, Scavee C, Ploutz-Snyder R, Jalife J, Haïssaguerre M: Spectral analysis identifies sites of high-frequency activity maintaining atrial fibrillation in humans. Circulation 2005, 112: 789–797. 10.1161/CIRCULATIONAHA.104.517011View ArticleGoogle Scholar
- Botteron GW, Smith JM: A technique for measurement of the extent of spatial organization of atrial activation during atrial fibrillation in the intact human heart. IEEE Trans Biomed Eng 1995, 42: 579–586. 10.1109/10.387197View ArticleGoogle Scholar
- Botteron GW, Smith JM: Quantitative assessment of the spatial organization of atrial fibrillation in the intact human heart. Circulation 1996, 93: 513–518.View ArticleGoogle Scholar
- Ng J, Kadish AH, Goldberger JJ: Effect of electrogram characteristics on the relationship of dominant frequency to atrial activation rate in atrial fibrillation. Heart Rhythm 2006, 3: 1295–1305. 10.1016/j.hrthm.2006.07.027View ArticleGoogle Scholar
- Ng J, Kadish AH, Goldberger JJ: Technical considerations for dominant frequency analysis. J Cardiovasc Electrophysiol 2007, 18: 757–764. 10.1111/j.1540-8167.2007.00810.xView ArticleGoogle Scholar
- Ng J, Goldberger JJ: Understanding and interpreting dominant frequency analysis of af electrograms. J Cardiovasc Electrophysiol 2007, 18: 680–685. 10.1111/j.1540-8167.2007.00832.xView ArticleGoogle Scholar
- Fischer G, Stühlinger MC, Nowak CN, Wieser L, Tilg B, Hintringer F: On computing dominant frequency from bipolar intracardiac electrograms. IEEE Trans Biomed Eng 2007, 54: 165–169.View ArticleGoogle Scholar
- Verma A, Patel D, Famey T, Martin DO, Burkhardt JD, Elayi SC, Lakkireddy D, Wazni O, Cummings J, Schweikert RA, Saliba W, Tchou PJ, Natale A: Efficacy of adjuvant anterior left atrial ablation during intracardiac echocardiography-guided pulmonary vein antrum isolation for atrial fibrillation. J Cardiovasc Electrophysiol 2007, 18: 151–156. 10.1111/j.1540-8167.2006.00673.xView ArticleGoogle Scholar
- Brooks AG, Stiles MK, Laborderie J, Lau DH, Kuklik P, Shipp NJ, Hsu LF, Sanders P: Outcomes of long-standing persistent atrial fibrillation ablation: A systematic review. Heart Rhythm 2010, 7: 835–846. 10.1016/j.hrthm.2010.01.017View ArticleGoogle Scholar
- Ciaccio EJ: Ablation of longstanding persistent atrial fibrillation. J Atrial Fibrillation 2010, 2: 806–809.View ArticleGoogle Scholar
- Ciaccio EJ, Biviano AB, Whang W, Wit AL, Garan H, Coromilas J: New methods for estimating local electrical activation rate during atrial fibrillation. Heart Rhythm 2009, 6: 21–32. 10.1016/j.hrthm.2008.10.016View ArticleGoogle Scholar
- Ciaccio EJ, Biviano AB, Whang W, Wit AL, Coromilas J, Garan H: Optimized measurement of activation rate at left atrial sites with complex fractionated electrograms during atrial fibrillation. J Cardiovasc Electrophysiol 2010, 21: 133–143. 10.1111/j.1540-8167.2009.01595.xView ArticleGoogle Scholar
- Narayan SM, Krummen DE, Kahn AM, Karasik PL, Franz MR: Evaluating fluctuations in human atrial fibrillatory cycle length using monophasic action potentials. PACE 2006, 29: 1209–1218.View ArticleGoogle Scholar
- Brown JP, Krummen DE, Feld GK, Narayan SM: Using electrocardiographic activation time and diastolic intervals to separate focal from macro-re-entrant atrial tachycardias. J Am Coll Cardiol 2007, 49: 1965–1973. 10.1016/j.jacc.2006.10.080View ArticleGoogle Scholar
- Narayan SM, Franz MR: Quantifying fractionation and rate in human atrial fibrillation using monophasic action potentials: Implications for substrate mapping. Europace 2007, 9: vi89-vi95. 10.1093/europace/eum212View ArticleGoogle Scholar
- Stiles MK, Brooks AG, John B, Shashidhar , Wilson L, Kuklik P, Dimitri H, Lau DH, Roberts-Thomson RL, Mackenzie L, Willoughby S, Young GD, Sanders P: The effect of electrogram duration on quantification of complex fractionated atrial electrograms and dominant frequency. J Cardiovasc Electrophysiol 2008, 19: 252–258. 10.1111/j.1540-8167.2007.01034.xView ArticleGoogle Scholar
- Biviano AB, Coromilas J, Ciaccio EJ, Whang W, Hickey K, Garan H: Frequency domain and time complex analyses manifest low correlation and temporal variability when calculating activation rates in atrial fibrillation patients. Pacing Clin Electrophysiol 2011, in press.Google Scholar
- MacLeod RS, Johnson CR: Map3d: Interactive scientific visualization for bioengineering data. IEEE Engineering Medicine Biology Society 15th Ann Int Conference 1993, 30–31.View ArticleGoogle Scholar
- Stridh M, Sörnmo L, Meurling CJ, Olsson SB: Sequential characterization of atrial tachyarrhythmias based on ECG time-frequency analysis. IEEE Trans Biomed Eng 2004, 51: 100–114. 10.1109/TBME.2003.820331View ArticleGoogle Scholar
- Ciaccio EJ, Drzewiecki GM: Tonometric arterial pulse sensor with noise cancellation. IEEE Trans Biomed Eng 2008, 55: 2388–2396.View ArticleGoogle Scholar
- Stridh M, Bollmann A, Olsson B, Sörnmo L: Detection and feature extraction of atrial tachyarrhythmias. A three stage method of time-frequency analysis. IEEE Engineering Medicine Biology Magazine 2006, 25: 31–39.View ArticleGoogle Scholar
- Sandberg F, Stridh M, Sörnmo L: Frequency tracking of atrial fibrillation using hidden markov models. IEEE Trans Biomed Eng 2008, 55: 502–511.View ArticleGoogle Scholar
- Ciaccio EJ, Coromilas J, Wit AL, Garan H: Onset dynamics of ventricular tachyarrhythmias as measured by dominant frequency. Heart Rhythm 2011, 8: 615–622. 10.1016/j.hrthm.2010.11.028View ArticleGoogle Scholar
- Corino VDA, Mainardi LT, Stridh M, Sörnmo L: Improved time-frequency analysis of atrial fibrillation signals using spectral modeling. IEEE Trans Biomed Eng 2008, 55: 2723–2730.View ArticleGoogle Scholar
- Elvan A, Linnenbank AC, van Bemmel MW, Ramdat Misier AR, Delnoy PPHM, Beukema WP, de Bakker JMT: Dominant frequency of atrial fibrillation correlates poorly with atrial fibrillation cycle length. Circ Arrhythm Electrophysiol 2009, 2: 634–644. 10.1161/CIRCEP.108.843284View ArticleGoogle Scholar
- Zlochiver S, Yamazaki M, Kalifa J, Berenfeld O: Rotor meandering contributes to irregularity in electrograms during atrial fibrillation. Heart Rhythm 2008, 5: 846–854. 10.1016/j.hrthm.2008.03.010View ArticleGoogle Scholar
- Gray RA, Mornev OA, Jalife J, Aslanidi OV, Pertsov AM: Standing excitation waves in the heart induced by strong alternating electric fields. Phys Rev Lett 2001, 87: 168104–1-168104–4.View ArticleGoogle Scholar
- Ciaccio EJ, Tennyson CA, Lewis SK, Bhagat G, Green PH: Distinguishing patients with celiac disease by quantitative analysis of videocapsule endoscopy images. Comput Methods Programs Biomed 2010, 100: 39–48. 10.1016/j.cmpb.2010.02.005View ArticleGoogle Scholar
- Ciaccio EJ, Biviano AB, Whang W, Vest JA, Gambhir A, Einstein AJ, Garan H: Differences in repeating patterns of complex fractionated left atrial electrograms in longstanding persistent as compared with paroxysmal atrial fibrillation. Circulation: Arrhythmia and Electrophysiology 2011. [Epub ahead of print] 10.1161/circep.110.960153Google Scholar
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