throbber
See discussions, stats, and author profiles for this publication at: https://www.researchgate.net/publication/222110888
`
`Classification of cardiac arrhythmia with respect to ECG and HRV signal by
`genetic programming
`
`Article · January 2012
`
`CITATIONS
`12
`
`3 authors, including:
`
`Mohammad Mehdi Ebadzadeh
`Amirkabir University of Technology
`
`111 PUBLICATIONS   1,380 CITATIONS   
`
`SEE PROFILE
`
`READS
`885
`
`Some of the authors of this publication are also working on these related projects:
`
`Evolutionary Computing View project
`
`Fuzzy Neural Networks View project
`
`All content following this page was uploaded by Mohammad Mehdi Ebadzadeh on 01 June 2014.
`
`The user has requested enhancement of the downloaded file.
`
`APPLE 1038
`
`1
`
`

`

`Canadian Journal on Artificial Intelligence, Machine Learning and Pattern Recognition Vol. 3 No. 1, January 2012
`
`
`Classification of cardiac arrhythmia with respect to
`ECG and HRV signal by genetic programming
`
`Masih Tavassoli, Mohammad Mehdi Ebadzadeh, Hamed Malek
`
`
`
`
`
`Abstract — Consistent or periodical heart rhythm disorders may
`result cardiac arrhythmias. In this article, heart rate variability
`(HRV) signals are analyzed and various features including time
`domain, frequency domain and nonlinear parameters are extracted.
`Moreover, additional nonlinear features are extracted from
`electrocardiogram (ECG) signals. These features are helpful in
`classifying cardiac arrhythmias. In this paper, genetic programming
`is applied to classify heart arrhythmias using both HRV and ECG
`features. Genetic programming selects effective features, and then
`finds the most suitable trees to distinguish between different types
`of arrhythmia. By considering the variety of extracted parameters
`from ECG and HRV signals, genetic programming can precisely
`differentiate various arrhythmias. The performance of proposed
`algorithm is evaluated on MIT–BIH Database. The results show
`that seven different types of arrhythmia classes including normal
`beat , left bundle branch block beat, right bundle branch beat,
`premature ventricular contraction, fusion of ventricular and normal
`beat, atrial premature contraction and paced beat are classified
`with an accuracy of 98.75%, 98.93% , 99.10%, 99.46%, 99.82%,
`99.46% and 99.82% respectively..
`
`
`
`Key Words — Arrhythmia, Electrocardiogram (ECG),
`Heart Rate Variability (HRV), Genetic Programming (GP),
`Feature Selection
`
`I. INTRODUCTION
`
`Heart is a muscular organ which is responsible to pump
`oxygenated blood throughout blood vessels by rhythmic
`contractions. Any disturbance in the heart rhythm can be
`very dangerous. Although cardiac arrhythmia is one of the
`leading causes of death, it can be treated if detected on time.
`Heart arrhythmia can cause too slow or too fast performance
`of the heart. To detect it, ECG and HRV signals are widely
`used. ECG signal records electrical performance of the heart.
`It contains a lot of important information related to the
`condition of the heart and one of the most important tools in
`detecting heart diseases. A typical ECG signal consists of
`the P-wave, QRS complex, and T-waves. The P wave is the
`result of slow-moving depolarization of the atria. QRS
`complex which is made of Q, R and S waves shows
`ventricular depolarization. The T wave
`represents
`repolarization of the ventricles, and is longer in duration
`than depolarization. HRV signal describes the variations
`between consecutive heartbeats. It
`is a non-offensive
`evaluation method of the nervous system which controls
`cardiovascular system and
`is a measurement of
`the
`interaction between sympathetic and parasympathetic
`activity in autonomic nervous system. HRV signal is a non-
`stationary signal and its changes can be interpreted as a
`current or upcoming disease.
`
`and
`detection
`automatic
`for
`Several methods
`classification of cardiac arrhythmias have been proposed in
`literature, including: artificial immune recognition system
`with fuzzy weighted [1], threshold-crossing intervals [2],
`neural networks [3], fuzzy neural networks [8], fuzzy
`equivalence relations [12], Bayesian classifiers [16], support
`vector machines [17,22], wavelet
`transforms [18-20],
`combined wavelet transformation and radial basis neural
`networks [21], fuzzy logic combined with the Markov
`models [23] and the rule-based algorithms [24]. Some papers
`used
`techniques which are based on ECG segment
`[2,9,11,21,22,23,25]. In these papers, the various features of
`the ECG signal including the morphological features are
`extracted and used for classification of
`the cardiac
`arrhythmias. This is a time consuming procedure and the
`results are very sensitive to the amount of noise. An
`alternative approach would be to extract the HRV signal
`from the ECG signal [12-18,26,29] first by recording the R-
`R time intervals and then processing the HRV signal instead.
`This is a more robust method since the R-R time intervals
`are less affected by noise. One drawback of the proposed
`HRV-based algorithm is that some of the arrhythmia types
`such as the left bundle branch block and the right bundle
`branch block beats cannot be detected using only the heart
`rate variability features.
`In this paper a new arrhythmia classification algorithm is
`proposed which is able to effectively classify seven types of
`arrhythmia. These arrhythmias are namely the normal beat
`(NB), left bundle branch block beat (LBBB), right bundle
`branch beat (RBBB), premature ventricular contraction
`(PVC), fusion of ventricular and normal beat (FUSION),
`atrial premature contraction (APC) and paced beat (PACE).
`In this article, various features from both ECG and HRV
`signal are extracted and given to a genetic programming to
`produce the suitable solution trees to distinguish between
`different types of arrhythmia. From the various identified
`features the proposed method selects the effective ones and
`categorizes the seven classes of heart arrhythmia highly
`precisely.
`The reminder of this paper is formatted as follows:
`section 2 provides the overall block diagram of the proposed
`algorithm. In section 3, the database which is being utilized
`in this paper is introduced. Extracted features from HRV and
`ECG signal are explained in section 4. Genetic programming
`algorithm is introduced in the fifth section. The results are
`shown in section 6. Section 7 discusses about the result
`.Finally, Section 8 concludes the paper.
`
`
`
`1
`
`2
`
`

`

`Canadian Journal on Artificial Intelligence, Machine Learning and Pattern Recognition Vol. 3 No. 1, January 2012
`
`II. THE PROPOSED ALGORITHM
`
`IV. FEATURE EXTRACTION
`
`The block diagram of
`is
`the proposed algorithm
`demonstrated in Fig. 1. As seen, it consists of four steps:
`pre-processing on ECG signals to divide ECG signals to
`eight consecutive RR intervals and extract HRV signal,
`feature extraction from ECG and HRV signal, creating
`seven optimal trees to detect each arrhythmia by a genetic
`programming
`algorithm
`and
`finally
`arrhythmia
`classification. The following sections describe each block of
`this algorithm in more details.
`
`Input Data
`
`•
`
`Extract eight consecutive RR intervals
`from ECG signals
`
`• HRV signal extraction
`
`Extract features from HRV and ECG signals
`
`Create seven trees to distinguish
`between different types of arrhythmia
`genetic programming
`
`Arrhythmia classification
`
`Fig. 1. Block diagram of the proposed arrhythmia classification
`algorithm.
`
`III. DATABASE
`
`In this paper, the proposed approach is tested using the
`MIT-BIH arrhythmia database. This database contains 48
`ECG records. Each record is approximately 30 minutes long
`and
`it
`includes 109000 R-R
`intervals with sampling
`frequency of 360 Hz. Each beat has been annotated
`independently by two cardiologists. Their annotations were
`compared, consensus on disagreements was obtained, and
`the reference annotation files were prepared [27]. In most
`records, the upper signal is a modified limb lead II (ML II)
`and the lower signal is a modified lead V1 (VI). All of the
`ECG records of this article are chosen from lead II and
`include 8 sequential R-R intervals. Extracted records of this
`database include all seven classes of heart beat.
`After dividing the ECG signals into 8 sequential RR
`intervals, HRV signal is extracted from calculating the time
`intervals between every two consequential R-wave in an
`ECG signal (R-wave is located in the maximum absolute
`value of the signal within the time window).
`
`As seen in Fig. 1, features are extracted from both HRV
`and ECG signals. In the following subsections extracted
`features are explained.
`
`A. Extracted features from HRV signal
`
`Since the behavior of HRV signal includes both linear
`and non-linear behavior, a combination of these features is
`considered. These features include time domain, frequency
`domain and nonlinear parameters. Each ECG signal is
`divided into 8 consequential R-R intervals and each segment
`of HRV signal includes time distances between every two
`consequential R-wave in ECG signal.
`1) Time domain features
`Time-domain parameters of HRV are the easiest as they
`are based on common statistical methods. In this paper,
`seven commonly used time domain features are as follows:
`[28]:
`
`•
`
`•
`
`The mean value of the eight R-R intervals within
`each segment (Mean).
`The root mean square successive difference of the
`eight R-R intervals in each segment (RMSSD).
`The standard deviation of the 8 R-R intervals
`within each segment (SDNN).
`The standard deviation of differences between the
`adjacent R-R
`intervals within each segment
`(SDSD).
`The number of successive difference of intervals
`which differ by more than 50, 10 and 5 ms,
`respectively, divided by 8, the total number of the
`R-R
`Intervals within each segment
`(pNN50,
`pNN10, pNN5).
`2) Frequency domain features
`LF/HF: Although time domain features are important in
`classifying arrhythmia, they are not capable of distinction of
`sympathetic and parasympathetic content of the HRV signal
`[29]. For this purpose, HRV signal is transformed into
`frequency domain and the ratio of spectral power in lower
`bound (0.04-0.15Hz) to spectral power in upper bound
`(0.15-0.5Hz) is calculated. The lower bound frequency
`power
`is
`related
`to
`controlling
`temperature
`and
`cardiovascular mechanism and the upper frequency is related
`to the cardiac vagal activity.
`3) Nonlinear features
`The nonlinear properties of HRV can be analyzed using
`such as follow measures:
`
`•
`
`•
`
`•
`
`ApEn: Approximate entropy measures the complexity or
`irregularity of the signal. Large values of ApEn indicate high
`irregularity and smaller values of ApEn implies higher
`regularity [30]. The ApEn is computed as follows.
`For each segment in HRV signal with length N, uj is
`defined as follow:
`
`6
`
`3
`
`

`

`Canadian Journal on Artificial Intelligence, Machine Learning and Pattern Recognition Vol. 3 No. 1, January 2012
`
`u
`
`j
`
`=
`
`,RR(
`j
`
`...
`
`RR,
`
`−+
`1
`mj
`
`j,)
`
`=
`
`1
`,
`
`...
`
`+−
`1
`,mN,
`
`(1)
`
`RRj(ms)
`
`RRj+1(ms)
`
`=
`
`RR(
`
`,...,
`
`=
`
`where m is called the embedding dimension and N is the
`number of measured RR intervals. The distance between
`these vectors is defined as the maximum absolute difference
`between the corresponding elements. For each uj the relative
`number of vectors uk for which d(uj , uk) ≤ r is calculated by
`Eqs. (2) and (3)
`=
`max
`)u,u(d
`j
`k
`
`RR{|
`
`+
`nj
`
`−
`
`RR
`
`+
`nk
`
`n|
`
`=
`
`0
`
`−
`1
`,}m,...,
`
`
`
`
`
`(2)
`
`.
`
`
`
`
`
`(3)
`
`{|
`u
`
`k
`
`|
`
`,
`(
`uud
`j
`
`k
`
`)
`
`≤
`
`|}
`r
`
`−
`mN
`
`+
`
`1
`
`=
`
`m j
`
`)(
`rC
`
`Due to the normalization, the value of
`
`is always
`
`)(rC m
`j
`smaller or equal to 1. Afterward, the mean of natural
`)(rC m
`j
`
`logarithm of each
`
` over j is taken to yield:
`
`
`
`(4)
`
`)5(
`
`
`
`+−
`1
`mN
`.)r(Cln
`
`∑
`
`mj
`
`m
`

`
`)r(
`
`=
`
`1
`+−
`mN
`
`1
`
`=
`1
`j
` Finally approximate entropy calculated by Eq. (5)
`1+Φ−
`m
`m
`
`
`
`
`
` )N,r,m(ApEn
`
`Φ=
`
`)r(
`
`).r(
`
`For calculating ApEn for each HRV segment, the value of
`m and r are chosen as m = 2 and r = 0.2SDNN.
`
`Fig. 2. Poincar´e plot analysis with the ellipse fitting procedure. SD1
`and SD2 are the standard deviations in the directions x1 and x2, where
`x2 is the line-of-identity for which RRj = RRj+1.
`Correlation Dimension: This parameter is an index of
`system complexity and indicates the number of independent
`variabilities to describe the behaviour of the system [33].
`Correlation Dimension of chaotic system is always a
`fraction, but it can be either a fraction or an integer number
`for a random system. By considering HRV signal as a time
`series, the correlation dimension can be calculated as
`follows:
`For each segment in HRV signal with length N, uj is defined
`as follow:
`u
`
`j
`
`j
`
`RR
`
`−+
`1
`mj
`
`j),
`
`−
`+
`1
`1
`,mN,...,
`
`
`
` (7)
`
`afterward by calculating d(uj,uk) distances, the number of
`vectors shorter than r is calculated, as in Eqs. (8) and (9).
`
`
`
`(8)
`
`(9)
`
`−
`))l(u)l(u(
`j
`k
`
`2
`
`,
`
`m
`
`∑ =
`
`l
`
`1
`
`
`
`)u,u(d
`j
`k
`
`=
`
`)u,u(d|u{|
`k
`j
`k
`
`≤
`
`|}r
`
`−
`mN
`
`+
`
`1
`
` .k
`∀
`
`=
`
`mj
`
`)r(C
`
`Then the mean value of
`
`)r(Cm
`j
`
` is calculated:
`
`
`
`
`
`(10)
`
`+−
`1
`mN
`.)r(C
`
`∑
`
`mj
`
`m
`)r(C
`
`=
`
`1
`+−
`mN
`
`1
`
`=
`1
`j
`The correlation dimension is calculated by Eq. (11)
`m
`)r(Clog
`
`lim
`
`r
`
`lim
`
`∞
`
`0
`
`N
`
`=
`)m(D
`
`2 A
`
`.
`
`
`
`
`
`)11(
`
`log
`r
`s shown in Fig. 3, in practice, this limit value is
`)r(Clog m
`
`approximated by slope of
`
` versus
`
`
`
`rlog when m
`
`is increased.
`
`7
`
`the HRV signal
`SpEn: Spectral entropy evaluates
`complexity in frequency domain [31]. Shanon channel
`entropy estimates HRV entropy as
`
`H
`
`f∑−=
`
`P
`
`log(
`
`,)P
`f
`
`
`
`(6)
`
`f
`where Pf is the value of the probability density function
`(PDF) of the process at frequency f.
`
`Poincare´ plot: This plot is another technique for analysis
`of HRV signal [32]. It is a graphical representation of the
`correlation between
`successive R-R
`intervals. By
`considering Poincare´plot as a time series of RRi, if each
`interval RRn + 1 is plotted as a function of the previous
`interval RRn, then the resulting plot is known as the
`Poincare´ plot. This plot shows the heart problem and some
`information about short term and long term oscillations. The
`Poincare´plot is derived by calculating SD1 and SD2
`parameters which are standard deviations of RRi distances
`from y=x and y=-x+2(RRm) lines respectively. RRm is the
`relation between
`mean of RRi. SD1/SD2 describes
`parameters. A common approach to parameterize the shape
`is to fit an ellipse to the plot as shown in Fig. 2.
`
`4
`
`

`

`Canadian Journal on Artificial Intelligence, Machine Learning and Pattern Recognition Vol. 3 No. 1, January 2012
`
`
`dc1 to dcn-2 are calculated. LE is approximately calculated by
`Eq. (13).
`
`1
`t
`
`.
`
`
`
`
`
`)13(
`
`t
`
`dd
`
`log
`
`∑−
`
`1
`
`n
`
`=
`
`1
`−
`
`1
`
`n
`

`
`=
`
`0
`t
`Hurst Exponent: The Hurst exponent is based on Hurst
`investigations to detect the incoming water flow in dam that
`he built on the Nile River. The incoming water flow in dams
`was assumed to be random but Hurst found out a non-
`periodic cycles in incoming flows based on the previous
`data. Hurst test was over generalized to other phenomena
`which seem to be random but may have an organized
`pattern. The Hurst exponent is a measure of the smoothness
`of a fractal time-series based on the asymptotic behavior of
`the rescaled range of the process. The test procedure is as
`follows [34]:
`time series of
`By considering ECG signal as a
`U=u0,u1,…,uT-1, divide this series to a consequential time
`series of length n into a contiguous subperiods. Each
`=
`−
`10
`1
`j
`,
`a,...,
`subperiod Ij is labeled with
` and each element
`
`
`Fig. 3. Approximation of the correlation dimension D2 from the log r,
`m
`
` (r) plot.
`log C
`B. Extracted features from ECG signal
`In this section, ECG signal is divided into 8 consequential
`RR intervals and by employing fractal dimension, lyapunov
`exponent and Hurst exponent, follow nonlinear features are
`extracted.
`
`Fractal Dimension: The concept of fractal dimension that
`refers to a non-integer or fractional dimension originates
`from fractal geometry. This feature has been used in the
`analysis of ECG and EEG to identify and distinguish
`specific states of physiologic function [35]. Box-counting
`
`
`dimension method is used to calculate the fractal dimension.
`The fractal dimension of an ECG signal is based on chaos
`theory and is a quantitative measurement of the roughness of
`that signal. It can be used as an effective parameter in
`categorizing heart arrhythmias. To calculate
`fractal
`dimension, each dimension of the signal is divided to S
`segments and the box which contain ECG signals are
`counted. N is the number of such boxes.
`Nlog
`
`in Ij is labeled N[j][k] such that k = 0, 1,..., n-1. For each
`subperiod Ij, the mean value is calculated and data scale is
`normalized by Eqs. (14) and (15):
`
`
`E
`
`=
`
`j ∑
`
`1
`
`n
`
`n
`
`−
`1
`
`k
`
`=
`
`0
`
` ,]k][j[N
`
` ) 14(
`
`]k][j[X
`
`k
`
`=∑
`
`−
`k),E]k][j[N(
`j
`
`=
`
`−
` .n,...,
`210
`1
`,,
`
`)15(
`
`−
`
`k][j[Xmin(
`
`]).
`
`
`
`) 16(
`
`
`
`
`
`=
`)S(
`
`.
`
`=
`0
`i
`The sample standard deviation calculated for each
`subperiod Ij is:
`=
`R
`max(
`])k][j[X
`jI
`−≤≤
`1
`0
`k
`n
`For each subperiod Ij, the value of R vector is calculated
`by Eq. (17).
`−
`1
`n
`
`1 ∑
`
`−
`)E]k][j[N(
`j
`
`2
`
`21
`)
`
`.
`
`
`
`
`
`
`
`) 17(
`
`0
`k
`The RIj is normalized with respect to a particular length n
`with Eq. (18).
`a
`
`=
`0
`j
`As a result amplitude Rij is always non-negative. By
`increasing n such that T/n is always an integer, this
`procedure is repeated until n=T/2. Hurst offered these
`equations by using the half rule in statistics.
`
`
`
`log(
`
`=
`
`log(
`
`+
`H)c
`
`log(
`
` ),n
`
`)S/R
`n
`in which R is the rescaled amplitude. S is the standard
`deviation of the time series, c is a constant, n is the length of
`the subperiod and the slope of the equation is the estimate of
`the Hurst exponent, H. According to Hurst results, if the
`
`(19)
`
`−
`1
`
`j∑
`
`SR
`
`II
`
` .
`
`)18(
`
`j
`
`
`
`S
`
`I j
`
`=
`
`(
`
`n
`
`
`
`)SR(
`n
`
`=
`
`=
`
`1
`
`a
`
`dim
`box
`
`lim
`
`
`
`
`
`)12(
`
`log
`S
`0
`S
`In practice, this limit value is approximated by slope of
`
`Slog when m is decreased.
`Nlog
` versus
`
`
`
`
`the
`system,
`In a dynamic
`Lyapunov Exponent:
`dependence on initial condition is described by Lyapunov
`Exponent (LE), and calculates the rate of deviating from
`roots. A positive LE shows that the distance of two points is
`increasing exponentially. This means that system tends to
`chaos. A negative LE indicates stable behaviour and a zero
`LE means that two close points on a root, keep their
`distance. By considering ECG signal as a time series of
`X=x0, x1,…,xn-1, it can be calculated as follows [34]:
`The procedure is started at t0 with x0, next the point in the
`time series which is closest to x0 is found and is called xi.
`Then d0 the absolute difference of these two points is
`calculated. dc0 is the absolute difference of the two
`consecutive points of x0 and xi, namely x1 and xi+1. The same
`procedure is repeated for points x1 to xn-1 and d1 to dn-2 and
`
`
`
`8
`
`5
`
`

`

`Canadian Journal on Artificial Intelligence, Machine Learning and Pattern Recognition Vol. 3 No. 1, January 2012
`
`value of Hurst exponent is equal to 0.5 it indicates an
`independent time series. It means that there is no correlation
`between any of the current element and a future element. If
`the Hurst exponent is between 0.5 and 1, it indicates a
`persistent behaviour. It means that if the time series has been
`increasing for a while, it is likely to increase for another
`period, and if the time series has been decreasing, it
`probably continue decreasing. Finally, if the value of the
`Hurst exponent is positive but less than 0.5, it indicates an
`anti-persistent behaviour. It means that if the time-series
`increases, it is more likely to decrease in future, and vice-
`versa.
`
` Fig. 4. Schematical overview of GP.
`
`
`
`
`accuracy of output of genetic programming with respect to
`ideal output.
`
`
`B. Generating new population
`To generate a new population, some processes should be
`repeated until the number of new population becomes equal
`to number of old population.
`
`
`C. Genetic operators
`After defining the fitness function, genetic operators
`should also be defined in order to improve the population.
`Common genetic operators are reproduction, crossover and
`mutation. In reproduction, 10% of population in each
`generation is transmitted to the new population without any
`changes. The procedure of choosing individuals to transmit
`to the new population depends on selecting strategy. In
`crossover, random nodes are chosen from both parent trees,
`and the subtrees starting at these two nodes are swapped
`resulting in two offspring. There is no bias in choosing
`internal or terminal nodes as the crossing sites. In tree
`mutation, a random node is chosen from the parent tree and
`the subtree starting by a randomly generated tree. This new
`random tree is created with the Grow initialization method
`and obeys the size/depth restrictions imposed on the trees
`created for the initial generation.
`
`
`D. Selection strategy
`A genetic programming without a suitable selection
`strategy is not different than random search [36]. Some
`
`TABLE I
` THE RATIO OF TRAINING DATA TO DISTINGUISH EACH ARRHYTHMIA
`FROM OTHERS.
`
`Arrhythmia
` NB
`LBBB
`
`Type
`
`
`RBBB
`
`PVC
`
`
`FUSION
`
`APC
`
`
`PACE
`
`
`
`9
`
`NB
`
`LBBB
`
`RBBB
`PVC
`
`FUSION
`APC
`PACE
`
`
`300
`
`60
`
`30
`35
`
`35
`
`10
`20
`20
`
`
`120
`35
`
`35
`
`10
`20
`20
`
`60
`
`30
`200
`
`
`35
`
`10
`20
`20
`
`60
`
`30
`35
`
`
`
`200
`
`10
`20
`20
`
`22
`
`22
`22
`
`22
`
`30
`20
`20
`
`50
`
`30
`35
`
`35
`
`50
`
`30
`35
`
`35
`
`10
`120
`
`20
`
`10
`20
`120
`
`
`
`
`correctly
`classified
`
`(%)
`
`
`
`99.00
`
`
`
`
`95.86
`95.34
`
`
`
`98.21
`
`
`98.36
`
`98.47
`
`100
`
`V. GENETIC PROGRAMMING
`
`Several evolutionary algorithms have already been
`offered by different researchers. The difference between
`these algorithms is in process of representing chromosomes,
`fitness function and the way that it works. In this article, we
`offer a genetic programming to classify arrhythmias. Genetic
`programming was first introduced by Koza using tree
`representation [36]. A member in a genetic programming has
`tree structure and as a result two types of genes, called
`functions and terminals are defined in this method. In fact,
`intermediate nodes act as functions and the leaves act as
`terminals. In our method, extracted features and some
`random numbers are used as terminals of the tree. The
`initialization of population is random and each tree is
`evaluated by fitness function. Different genetic operators
`like crossover and mutation are used to make new trees and
`the new generation is generated. As shown in Fig. 4, this
`procedure continues until the ending requirements are met.
`The procedure is explained in details in the following sub
`section.
`A. Create an initial population:
`The initial population is created by ramped half-and-half
`method. In this method, both Grow and Full methods are
`used to produce the initial population [36]. For each depth
`level of trees considered, half of the individuals are
`initialized using the Full method, and the other half using the
`Grow method. The population of trees resulting from this
`initialization method is very diverse with balanced and
`unbalanced
`trees of
`several different depths. The
`individual`s terminals are selected from extracted features
`and a set of random numbers. In this paper, we use the
`following operators as function set: add, subtract, times,
`divide, sin, cos and if-then-else structures. While calculating
`X1/X2, if X2 is zero, X1 is returned as the response. The if-
`then-else structure is defined as follows:
`
`
` (21)
`
`<
`0
`a
`Otherwise
`
`
`
`c
`b
`
`)c,b,a(myif
`
`=
`
`
`
`
`When the initial population is created, each individual`s
`fitness is measured. The value of each individual reflects the
`
`
`
`6
`
`

`

`Canadian Journal on Artificial Intelligence, Machine Learning and Pattern Recognition Vol. 3 No. 1, January 2012
`
`common approaches for selecting suitable parents are fitness
`proportionate selection, Greedy selection and Tournament
`selection. In this paper Lexicographic Parsimony Pressure
`Tournament strategy is chosen for selecting parents. In this
`strategy, like the Tournament selection, a random number of
`individuals are selected from the population and the best of
`them is determined. The main difference is that if two
`individuals are equally fit, the tree with fewer nodes is
`chosen as the best. This technique has shown to effectively
`control bloat in different types of problems [37].
`
`VI. RESULT
`
`To classify arrhythmia of Normal beat (NB), Left Bundle
`Branch Block beat (LBBB), Right Bundle Branch Block
`beat (RBBB), Premature Ventricular Contraction (PVC),
`fusion of ventricular and normal beat (FUSION), Atrial
`Premature Contraction (APC) and paced beat (PACE),
`genetic programming produce
`the appropriate
`tree
`to
`distinguish any arrhythmia from others. For avoiding bias,
`the number of training data of each specific arrhythmia type
`has about the same size of the summation of other classes.
`Table I shows the ratio of training data and the percentage of
`correctly classified training data in each class.
`Table II shows the results of test data for each class. Seven
`optimum trees were derived to distinguish each class from
`other classes by genetic programming. The four commonly
`used measures of
`sensitivity,
`specificity, positive
`predictivity, and accuracy are derived for the proposed
`algorithm [6,19]. As seen, the proposed method can
`discriminate the NB with an accuracy of 98.75%, the LBBB
`with 98.93%, RBBB with 99.10%, PVC with 99.46%,
`FUSION with 99.82%, APC with 99.46% and PACE
`99.82%. These results demonstrate the effectiveness of the
`proposed
`arrhythmia
`classification
`algorithm
`in
`discriminating the seven types of arrhythmias.
`
`7. Discussion
`
`In this study, an automatic procedure for detection of
`arrhythmias using ECG and HRV signals has been
`developed. For classification of arrhythmias, a genetic
`programming algorithm proposed which can select effective
`
`ApEn
`
`yes
`
`SpEn
`
`yes
`
`TABLE II
` THE CLASSIFICATION RESULT OF CARDIAC ARRHYTHMIAS.
`Correlation
`yes
`Dimension
`
`Poincare´
`plot
`
`features to detect each type of arrhythmia. Table III shows
`the effective
`features
`that are selected by genetic
`programming to distinguish each arrhythmia from others. As
`it can be seen in Table III, each optimum tree use features
`from time domain, frequency domain and nonlinear feature
`for arrhythmia detection. All of features are used to create
`optimum trees.
`the arrhythmia
`Several researchers have addressed
`detection and classification problem using the ECG or HRV
`signals. A summary of different methods together with their
`reported results in terms of the four commonly used
`measures of sensitivity, specificity, positive predictivity, and
`accuracy is showed in Table IV. Most papers have focused
`on the detection of a single arrhythmia type (mostly the VF
`and AF) within normal sinus rhythms. In [2] the authors
`have detected ventricular fibrillation with four techniques.
`The author of [11] has classified the ECG signals into the
`normal or arrhythmic classes via Adaptive Neuro-Fuzzy
`Inference System (ANFIS) and feature reduction by Linear
`Discriminate Analysis (LDA). In another attempt, different
`heart rhythms were detected and classified into the three
`arrhythmia types using short-time multifractality and fuzzy
`Kohonen network [9]. In another study, arrhythmias are
`classified into 6 classes using feature dimensions reduction
`
`TABLE III
` EFFECTIVE FEATURES THAT ARE SELECTED TO DISTINGUISH EACH
`ARRHYTHMIA FROM OTHERS.
`
`Features NB LBBB RBBB PVC FUSION APC PACE
`
`Mean
`
`Yes
`
`RMSSD
`
`SDNN
`
`SDSD
`
`pNN50
`
`pNN10
`
`yes
`
`yes
`
`yes
`
`yes
`
`yes
`
`yes
`
`yes
`
`yes
`
`yes
`
`yes
`
`yes
`
`yes
`
`yes
`
`yes
`
`yes
`
`pNN5
`
`Frequency
` domain
`
`yes
`
`yes
`
`yes
`
`yes
`
`yes
`
`yes
`
`yes
`
`
`Arrhythmia type
`
`
`Number of segment
`
`LBBB NB
`
`RBBB
`
`
`
` FUSION PVC
`
`Fractal
`PACE APC
`Dimension
`
`NB
`LBBB
`RBBB
`PVC
`
`FUSION
`APC
`PACE
`
`Average
`
`251
`52
`56
`90
`24
`30
`56
`
`-
`
`247
`3
`49 1
`0 1
`0 1
`0 0
`0 0
`0 0
`
`1
`0
`2
`0
`54
`1
`88 0
`0
`0
`0
`0
`0
`0
`
`-
`
`-
`
`-
`
`-
`
`0
`0
`0
`0
`23
`0
`0
`
`-
`
`0 0
`Lyapunov
`0 0
` Exponent
`0 0
`Hurst
`0 1
` Exponent
`0 1
`29
`1
`56 0
`
`10
`
`
`
`Sensitivity*
`
`yes
`(%)
`98.41
`
`yes
`94.23
`96.43
`97.78
`yes
`95.84
`96.67
`100
`
`
`
`Specificity*
`yes
`
`(%)
`99.03
`yes
`99.41
`99.40
`99.79
`yes
`100
`99.62
`99.80
`
`yes
`
`Positive*
`
`Predictivity
`(%)
`98.80
`
`94.23
`94.74
`98.88
`
`100
`93.55
`98.25
`
`*Sensitivity= TP/ (TP+ FN), Specificity= TN/ (TN +FP), Positive Predictivity= TP/ (TP+FP), Accuracy= (TP +TN)/ (TP+ FN+TN+FP), where TP true
`positive, FN false negative, TN true negative, and FP false positive.
`
`-
`
`-
`
`97.05
`
`99.58
`
`96.92
`
`99.33
`
`yes
`
`yes
`
`yes
`
`yes
`
`yes
`
`yes
`
`yes
`
`Accuracy*
`yes
`yes
`(%)
`
`
`98.75
`yes
`98.93
`99.10
`99.46
`yes
`
`99.82
`99.46
`99.82
`
`7
`
`

`

`Canadian Journal on Artificial Intelligence, Machine Learning and Pattern Recognition Vol. 3 No. 1, January 2012
`
`by LDA and support vector machine [22]. In [21] a classifier
`is developed based on wavelet transforms for extracting
`features and then using a Radial Basis Function Neural
`Network (RBFNN) to classify the arrhythmias. The authors
`of [13] have classified the ECG signal segments into the
`normal or arrhythmic classes. It is based on time analysis
`and time-frequency analysis features via neural networks. In
`a recent paper [17] six different types of arrhythmia classes
`are differentiated. It is based on the LDA and Generalized
`Discriminate Analysis (GDA) feature reduction scheme and
`
`the SVM classifier. The effective ECG and HRV based
`algorithm which is proposed in the current work provides a
`better accuracy over a wider range of different types of
`cardiac arrhythmia, comparing
`to other studies. The
`proposed method can select the effective features to create
`each type of arrhythmia. The only signals used in this
`method are selected from lead II. Since the features are
`extracted from both HRV and ECG signals, the proposed
`method is not sensitive to noise and has the ability to classify
`different types of arrhythmias.
`
`11
`
`8
`
`

`

`Positive
`Specificity
`Method
`Dataset
`Arrhythmia type
`Sensitivity
`Author
`(%)
`Predictivity
`
`
`Canadian Journal on Artificial Intelligence, Machine Learning and Pattern Recognition Vol. 3 No. 1, January 2012
`(%)
`
`(%)
`
`
`Accuracy
`(%)
`
`TABLE IV
` SUMMARY OF PERVIOUS WORK.
`
`Clayton et al. [2]
`
`Threshold crossing intervals
`Autocorrelation function
`VF filter leakage
`Signal spectrum shape
`
`ECG
`
`Ventricular fibrillation
`
`Sengur [11]
`
`ANFIS+ feature reduction
`by LDA
`
`ECG
`
`Wang et al. Error!
`Reference source
`not found.
`
`Short-Time Multifractal
`
`ECG
`
`Song et al.[22]
`
`Support Vector
`Machine+feature reduction
`by LDA
`
`ECG
`
`AlFahoum et al. [21]
`
`wavelet transformation and
`radial basis neural networks
`
`ECG
`
`Tsipouras et al.[13]
`
`Time analysis
`t-f analysis
`
`HRV
`
`Mohammadzadeh Asl
`et al.[17]
`
`SVM+linear and nonlinear
`analysis
`
`HRV
`
`Mohammadzadeh Asl
`et al.[17]
`
`SVM+feature reduction by
`GDA
`
`HRV
`
`Proposed method
`
`Genetic programming HRV+ECG
`
`Normal
`Abnormal
`Ventricular Tachycardia
`Ventricular fibrillation
`Atrial fibrillation
`
`Normal sinus rhythm
`APC
` supraventricular
`tachycardia
`PVC
`ventricular tachycardia
`ventricular fibrillation
`
`Normal
`Atrial fibrillation
`Ventricular tachycardia
`Ventricular fibrillation
`
` Normal
`arrhythmatic
`
`Normal sinus rhythm
`PVC
`Atrial fibrillation
`Ventricular fibrillation
`sick sinus syndrome
`2° heart block
`
`Normal sinus rhythm
`PVC
`Atrial fibrillation
`Ventricular fibrillation
`sick sinus syndrome
`2° heart block
`
`NB
`LBBB
`RBBB
`PVC
`FUSION
`APC
`PACE
`
`46
`67
`77
`53
`
`95.9
`
`95.0
`98.3
`98.3
`
`99.657
`88.294
`82.821
`92.157
`91.695
`99.751
`
`92.51
`95.2
`100
`100
`
`87.53
`89.95
`
`97.86
`100
`92.59
`65
`100
`100
`
`99.25
`94.74
`94.63
`86
`100
`100
`
`
`98.41
`
`94.23
`
`96.43
`
`97.78
`
`95.84
`
`96.67
`
`100
`
`72
`38
`55
`93
`
`94
`
`99.2
`96.7
`100
`
`96.215
`99.951
`100
`98.937
`99.632
`99.993
`
`97.5
`85.7
`100
`100
`
`89.48
`92.91
`
`96.72
`98.65
`99.72
`98.19
`100
`100
`
`98.47
`99.14
`99.72
`99.07
`100
`100
`
`
`98.80
`
`94.23
`
`94.74
`
`98.88
`
`
`100
`93.55
`
`98.25
`
`
`97.8
`97.2
`99.4
`
`99.307
`99.274
`99.854
`98.344
`99.441
`99.883
`
`97.41
`98.70
`98.06
`96.76
`100
`100
`
`98.94
`98.96
`98.53
`98.51
`100
`100
`
`
`98.41
`
`94.23
`
`96.43
`
`97.78
`
`95.84
`
`96.67
`100
`
`
`97.86
`76.00
`99.01
`68.42
`100
`100
`
`99.00
`82.57
`99.03
`80.75
`100
`100
`
`
`99.03
`
`99.41
`
`99.40
`
`99.79
`100
`
`
`99.62
`
`99.80
`
`
`8. Conclusion
`
`In closing, for classification of cardiac arrhythmia, each
`ECG signals divi

This document is available on Docket Alarm but you must sign up to view it.


Or .

Accessing this document will incur an additional charge of $.

After purchase, you can access this document again without charge.

Accept $ Charge
throbber

Still Working On It

This document is taking longer than usual to download. This can happen if we need to contact the court directly to obtain the document and their servers are running slowly.

Give it another minute or two to complete, and then try the refresh button.

throbber

A few More Minutes ... Still Working

It can take up to 5 minutes for us to download a document if the court servers are running slowly.

Thank you for your continued patience.

This document could not be displayed.

We could not find this document within its docket. Please go back to the docket page and check the link. If that does not work, go back to the docket and refresh it to pull the newest information.

Your account does not support viewing this document.

You need a Paid Account to view this document. Click here to change your account type.

Your account does not support viewing this document.

Set your membership status to view this document.

With a Docket Alarm membership, you'll get a whole lot more, including:

  • Up-to-date information for this case.
  • Email alerts whenever there is an update.
  • Full text search for other cases.
  • Get email alerts whenever a new case matches your search.

Become a Member

One Moment Please

The filing “” is large (MB) and is being downloaded.

Please refresh this page in a few minutes to see if the filing has been downloaded. The filing will also be emailed to you when the download completes.

Your document is on its way!

If you do not receive the document in five minutes, contact support at support@docketalarm.com.

Sealed Document

We are unable to display this document, it may be under a court ordered seal.

If you have proper credentials to access the file, you may proceed directly to the court's system using your government issued username and password.


Access Government Site

We are redirecting you
to a mobile optimized page.





Document Unreadable or Corrupt

Refresh this Document
Go to the Docket

We are unable to display this document.

Refresh this Document
Go to the Docket