IRJET- Real Time QRS ECG Detection Method using Pan Tompkins Algorithm

International Research Journal of Engineering and Technology (IRJET)

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REAL TIME QRS ECG DETECTION METHOD USING PAN TOMPKINS ALGORITHM Amir Nazeer1, Dr Sukhvinder Kaur2, Dr Rahul Malhotra3 1, 2,3 ECE,

SDDIET, Panchkula Haryana. Place, INDIA -----------------------------------------------------------------------***--------------------------------------------------------------------

Abstract: Electrocardiogram (ECG) is one of the foremost important parameters for heart activity observing. The most objective of digital signal processing of ECG signal is to provide precise, fast and dependable estimation of clinically imperative parameters such as the term of the QRS complex, the R-R interval, the occurrence, amplitude and term of the P, R, and T waves. In this paper, I have measured all these parameters by utilizing pan- Tompkins’s calculation. It could be a genuine time QRS location algorithm. It gives the number of QRS peaks for recorded ECG signals. Results of simulations in MATLAB are presented.

Keywords: pan-Tompkins algorithm; ECG signal; band-pass filter; differentiator; integrator; moving-window.

INTRODUCTION Electrocardiogram (ECG) is the recording of electrical activity of the heart. Examination of ECG signal is very important to analyze a cardiac quiet. Amid the analysis of an ECG signal, different highlights are extracted, viz., the P wave, QRS complex, T wave, etc., that are delineated in Figure 1. In this figure, P wave, QRS complex and T wave demonstrate the depolarisation of atria, depolarisation of ventricles and repolarisation of ventricles, individually. Any alter in these components (i.e. plentifulness, term and shape) can indicate an arrhythmia. Length between onset focuses of two consecutive P waves is characterized as one heartbeat [1]. However, term of two sequential R-peak focuses is considered as one beat term (one cardiac cycle) because R-peak discovery is much less difficult than detection of P-peaks/waves.

Heart rate is the number of heart beats in one miniature. Discovery of R-wave is very important to degree the heart rate and discovery of other highlights [2], [3]. The heart rate between 60 and 100 is considered as normal heart rate.

Compression of ECG signal is required for transmitting and getting purposes in farther cardiac centre portable organize.

The most objective of compressing data is to diminish the estimate with holding the characteristic, valuable highlights required in signals. Heart illness is one of the most reasons for the deaths of the patients. An early conclusion of these heart diseases can maintain a strategic distance from the sudden passing of the patient.

Figure.1 This paper reports an effective ECG signal compression and transmission algorithm which employments direct change by implies of discrete wavelet change and Pan Tompkins Algorithm for further compression advancement [4]. The proposed algorithm offers comparatively high compression proportion and low percent root mean square difference. This paper incorporates four segments. Segment II centres on technique utilized by the proposed calculation. Segment III explains comes about and dialog portion after the execution of the proposed calculation over 48 records of ECG signals which are taken from MIT-BIH arrhythmia database [5].

Methodology In numerous applications for biomedical signal handling the useful signals are superposed by distinctive components. So, extraction and investigation of the information-bearing signal are complicated, caused by distortions from obstructions.

Using advanced signal handling this errand can be solved. Pan-Tompkins’s calculation could be a genuine time calculation which consists of band-pass channel, differentiator, integrator and moving-window [6]. The electrocardiogram (ECG) gives a physician with a diagnosis of the heart’s action through electrical signals created amid the cardiac cycle, and measured

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International Research Journal of Engineering and Technology (IRJET)

e-ISSN: 2395-0056

Volume: 07 Issue: 11 | Nov 2020

p-ISSN: 2395-0072

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with external terminals. Its clinical significance in cardiology is well set up, being utilized for illustration to decide heart rate, examine anomalous heart rhythms, and causes of chest pain.

Pan Tompkins Plan and Simulations The works of Pan Tompkins incredibly impact the QRS detection as compared to others. A study of literatures implies this approach as one of important algorithm in identifying QRS peak [7].Wherever The accuracy of any Electrocardiogram (ECG) waveform extraction plays a crucial part in making a difference a better diagnosis on any heart related sicknesses.

Ordinary ECG should comprise of a few parts incorporate P wave, QRS complex and T wave. These waves reflect the heart’s action such as P wave produced by muscle compression of Atria and its duration shows the atrial extension. Q wave gives the primary negative esteem and regularly gathered to be 25% less than the R wave esteem. The block diagram of Pan Tompkins Algorithm is shown in figure 1.2 below

Figure 1.2 Block Diagram of Pan and Tompkins Algorithm.

Low Pass Filter The transfer function of the second-order low-pass filter is H(Z) = (1-Z-6)2 / (1-Z-1)2 The amplitude response is H (ᴡ T) = Sin2 (3ᴡT) / (Sin2Wt/2) Where T is the sampling period the difference equation of the filter is Y (n T) = 2 y (n T-T) – y (nT-2T) + x (n T) – 2 x (nT6T) + x (nT-12T) Where the cut-off recurrence is around 11Hz and the gain is 36. The filter processing delay is six tests.

High Pass Filter The work of the high-pass filter is designed on subtracting the output of a first-order low-pass filter from an all-pass filter (i.e., the tests within the original signal). The transfer function for such a filter is H (Z) = -1 + 32 -16 + Z -32 / 1+Z-1 The amplitude response is H(ᴡ T)=|H (ᴡ T)| = [256+Sin2(16ᴡT) ]1/2 / (cos (Wt/2)) The difference equation is

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Y (n T) = 32 x (n T – 16T) – [y (n T – T) + x (n T) – x (n T –32T)] The low cut-off frequency of this filter is about 5Hz, the gain is32, and the delay is 16 samples.

Derivative After filtering, the signal is separated to supply the QRS complex slop data. We utilize a five-point subsidiary with the exchange function H (z) = (1/8T) ( Z-2 Z-1 - Z1 - Z2 ) The Amplitude response is H (w T) = (1/4T) [sin (2wT) + 2 sin (w T)].

The difference equation is Y (n T) = (1/8T) [-x (n T – 2T) – 2x (n T – T) +2 x (n T+T) + x (n T + 2T)].

Squaring After differentiation, the signal is squared point by point. The condition of this operation is Y (n T) = [X (n T)] This makes all information focuses positive and does nonlinear amplification of the yield of the subsidiary emphasizing the higher frequencies (i.e., overwhelmingly the ECG frequencies).

Moving Window Integration The purpose of moving-window integration is to get waveform feature data in expansion to the slant of the R wave. It is calculated from Y (n T) = (1/N) [x (n T – (N-1) T) + x (n T – (N – 2) T) +………. + x (n T)] Where N is the number of tests within the width of the integration window Graph 2 appears the relationship between the moving-window integration waveform and the QRS complex. The number of samples N within the moving window is vital.

By and large, the width of the window ought to be around the same as the widest conceivable QRS complex. on the off chance that the window is as well wide, the integration waveform will consolidate the QRS and T complexes together. In case it is too narrow, a few QRS complexes will produce a few crests within the integration waveform. These can cause trouble in ensuing QRS location forms. The width of the window is decided observationally. For our sample rate of 200 tests/s, the window is 30 tests wide (150 ms).

Algorithm Simulation Results Graph 1 shows the ECG signal after cancellation DC drift and normalization and The DC drift cancellation calculation decreases noise within the ECG signal by coordinating the range of the normal QRS complex. This attenuates noise due to muscle noise, control line interference, baseline wander, T wave interference.

Graph 1: ECG signal Volta Vs Second

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Graph 2 and graph 3 shows The band pass filter for the QRS detection algorithm reduces noise within the ECG signal by matching the spectrum of the normal QRS complex attenuates noise due to muscle noise, control line interference, baseline wander, T wave interference. The pass band that maximizes the QRS vitality is in the 5Hz-35Hz extend. The channel actualized in this algorithm is composed of cascaded high pass and low pass ECG signal after low pass filter (LPF) Graph 2 and High pass filter (HPF) Graph 3.

Graph 2: ECG signal Volta Vs Second

Graph 3: ECG signal Volta Vs Second Graph 4 describes the ECG signal after derivative and it prevents high frequency noise amplification also used to give data approximately the slant of the QRS.

Graph 4: ECG signal after Derivative The filtered signal is squared to improve the overwhelming peaks of (QRSs) [7] so that we can decrease the possibility of wrongly recognizing a T wave as an R peak. In this signal is being squared that means the negative part of the signal is also converted into positive part as seen in below figure.

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Graph: 5 ECG signal after squaring Signal is averaged with a moving window to get rid of noise (0.150 seconds length)

Graph: 6 Signal after averaging Interval

Reason For Generation Atrial Depolarisation

P Wave

wave

Amplitude

Time Interval

Normal amplitude is 1-1.5 mm

˂0.12 sec

QRS Complex

Atrial Depolarisation

Normal amplitude of R wave is 8-12 mm

˂0.04 to 0.10sec (QRS Interval

T Wave

Ventricular Repolarisation

Normal amplitude of T wave is 2-5 mm

˂0.04 to 0.10sec (QRS Interval

U Wave

Purkinje fibber Repolarisation

Not Measured

˂0.01 sec

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Characteristics Small, rounded and upright The first negative wave in the complex is the Q wave, the first positive wave in the complex is the R-wave and the first negative wave following the R-wave is the S-wave Same polarity as QRS complex usually correlates with polarity of R wave Usually of low voltage and same polarity as T wave when present

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Volume: 07 Issue: 11 | Nov 2020

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In the below figure we have also calculated peak point detection, HRV [7] and POINT CARE PLOT from the raw ECG Data between Time and Amplitude.

Filtered ECG signal

Raw ECG Data plotting 400 amplitude

amplitude

1400 1200 1000 800

0

2000 time

200 0 -200

4000

0

5 time

10

amplitude

PEAK POINT DETECTED IN ECG SIGNAL 400 200 0 -200

0

5 time

DISPLAY HRV

10

RR(n)

80

75

0.8

0.75 0.75 70

0

5

10

15

POINCARE PLOT

0.85

0.8 RR(n+1)

0.85

Fig 2. Peak point detection, HRV Display and Point Care Plot CONCLUSION In this paper we have proposed Mat lab software for the Pan Tompkins Algorithm QRS detection algorithm for detection of QRS complexes, R-R intervals, occurrence, Amplitude and also the calculation of P, R, T waves. Above thesis also provides the number of QRS Peaks for the recorded ECG signals. The above thesis proposed the HRV and Point Care Plot of recorded ECG signal REFRENCES [1] JIAPU PAN and WILLS J. TOMPKINS “REAL TIME QRS DETECTION METHOD”, IEEE Transactions on Bio Medical Engineering, vol. BME-32 NO 3 MARCH 1985 [2] M. M. BENOSMAN, F. BEREKSI-REGUIG, and E. G. SALEURD, "Strong Real-Time QRS Complex Detection," Journal of Mechanics in Medicine and Biology, vol. 17, no.8, pp. 1-15, 2017

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[3] R. HARIKUMMAR, and S. N. SHIVAPPRIYA, "Analysis of QRS Detection Algorithm for Cardiac Abnormalities-A Review," International Journal of Soft Computing and Engineering, vol. 1, no. 5, pp. 80-88, 2011.

[4] Li CW, Zheng CX, Tai CF. “Detection of ECG Characteristic Points Using Wavelet Transforms”. IEEE T Bio-Med Eng. 1995; 42(1):21–8. Pmid: WOS: A1995QA31700003.

[5] G. MOODY, R. MARK “The impact of the MIT-BIH Arrhythmia Database” Eng. Med. Biol. Mag. IEEE, 20 (2001), pp. 45-50.

[6]. SACHIN SINGH ET AL. “ Pattern analysis of different ECG signal using Pan-Tompkins’s algorithm” (IJCSE) International Journal on Computer Science and Engineering Vol. 02, No. 07, 2010, 2502-2505.

[7] RAMI, J.O. and BASIM, O.A. “QRS Detection and Heart Rate Variability Analysis” A Survey. Biomedical Science and Engineering, vol 2, no. 1, 2014, pp. 13-34.

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