Abstract
Vectorcardiography (VCG) is another useful method that provides us with useful spatial information about the electrical activity of the heart. The use of vectorcardiography in clinical practice is not common nowadays, mainly due to the well-established 12-lead ECG system. However, VCG leads can be derived from standard 12-lead ECG systems using mathematical transformations. These derived or directly measured VCG records have proven to be a useful tool for diagnosing various heart diseases such as myocardial infarction, ventricular hypertrophy, myocardial scars, long QT syndrome, etc., where standard ECG does not achieve reliable accuracy within automated detection. With the development of computer technology in recent years, vectorcardiography is beginning to come to the forefront again. In this review we highlight the analysis of VCG records within the extraction of functional parameters for the detection of heart disease. We focus on methods of processing VCG functionalities and their use in given pathologies. Improving or combining current or developing new advanced signal processing methods can contribute to better and earlier detection of heart disease. We also focus on the most commonly used methods to derive a VCG from 12-lead ECG.
1 Introduction
Measuring the electrical activity of the heart using electrocardiography and vectorcardiography is well established, as these methods have been used for more than a hundred years , . The cells that create the myocardium are joined together by gap junctions, which have very low resistance to a normal healthy heart. As a result, activity in one cell easily spreads to neighboring cells. However, this muscle cannot be controlled by the will. published a study which shows that activation wavefronts progress relatively evenly, from endocardium to epicardium and from apex to base. Electrical activation of the heart begins in the sinus node (SA), and it spreads along the atrial walls. Then depolarization reach the atrioventricular (AV) node. Propagation of AV junction is very slow and results in delays during activation, which is a desirable, because it allows completion of ventricular filling. Once the activation reaches the chambers, the excitement continues along the Purkinje fibers. Furthermore, depolarization waves occur from left to right of the septum. Then, the depolarization spread through the left and right ventricular wall. Because the left ventricular wall is thicker, depolarization of the left ventricle continues even after depolarization of a large portion of the right ventricle. The left ventricle is depolarized mainly in parallel through the left anterior and posterior fascicles and the left the lateral basal part is the last to be activated. Ventricular repolarization begins on the outside of the ventricles and “spreads” inward. Although the epicardium is depolarized last, its action potential duration is short and it is the first to recover. Although single cell recovery does not propagate to neighboring cells, it can be noted that recovery generally moves from the epicardium to the endocardium. Inward repolarization generates a signal with the same sign as outward depolarization. Due to the diffuse form of repolarization, the amplitude of the signal is much smaller than the amplitude of the depolarization wave and lasts longer . These changes in depolarization and repolarization are then measured from the patient’s body surface, most often in the form of a 12-lead ECG.
The method of vectorcardiography dates back to 1887, when in the first article concerning the human electrocardiogram, Augustus D. Waller pointed out the dipolar nature of the cardiac electric generator. Thus, it is possible to describe an electric generator of the heart with reasonable accuracy by an equivalent dipole. This dipole can be described as an electric heart vector (EHV) and it is possible to display it in vector form Waller (1887). In 1920s Mann first introduced the concept of a “loop” representing a continuous series of vectors for depicting electrical depolarization and repolarization magnitudes. Mann derived these loops manually from three Einthoven leads . From 1936 to 1940 the technique of vector representation of the electric field of the heart was actively developed in Germany . For direct measurement of orthogonal leads, Schellong et al. (1937) introduced the first uncorrected orthogonal system in 1937. Their work was further developed by other authors who defined new lead systems , , , Milnor et al. (1953). These lead systems differ by placing the electrodes on the hull and are represented by signals that are orthogonal to each other. However, they do not take into account the different torso geometry or intrinsic tissue inhomogeneity. The first corrected lead system was derived by Frank based on a mathematical model . This system, which uses seven measuring electrodes, is today one of the most widely used vectorcardiographic leads. Other published but less commonly used vectorcardiographic leads include McFee and Parungao (1961), SVEC III Schmitt and Simonson (1955), and hybrid lead systems .
Like the ECG, VCG is a diagnostic method which is considered as a very useful method for measuring the electrical activity of the heart. It is more sensitive than a standard 12-lead ECG and provides the cardiologist with important additional information such as a clearer indication of the phase relationships between leads Rubel et al. (1991), . Today, the QRS-T angle is the most commonly analyzed of the VCG, while current ECG markers of repolarization abnormalities mainly include ST depression, T wave inversion, and QT prolongation , Voulgari and Tentolouris (2009). The VCG is projected into three mutually perpendicular planes: sagittal, transversal and frontal, see Figure 1 (left), where placement of the electrodes are shown in Figure 1 (right). The individual planes are most often located as: frontal plane between X and Y leads, transversal plane between X and Z leads and sagittal plane between Y and Z leads. Cardiac activity is then described by three loops, which represent the individual phases of the cardiac cycle. The first loop corresponds to wave P, the second loop which is the largest corresponds to QRS complex and the third loop corresponds to wave T. The loops can be seen in three 2-D projections or in one 3-D image in a demonstrative physiological record from the PTB database, see Figure 2. The records contained in this database are sampled by sampling frequency of 1 kHz with a 16-bit resolution in the range of ±16,384 mV. Based on the recommendation Merri et al. (1990), the sampling frequency for measuring electrical activity of the heart should be at least 128 Hz. However, setting parameters in the PTB database is suitable for subsequent and detailed analysis of the electrical activity of the heart. However, along with the required signal, interfering components that need to be removed from the records can also be measured. When designing filters, it is necessary to take into account the frequency range of the desired signal and the frequency characteristics of individual filters.
FIGURE 1
FIGURE 2

Demonstration display of individual VCG planes for randomly selected physiological record: (A) Transverse plane of X and Y leads, (B) Sagittal plane of X and Z leads, (C) Frontal plane of Y and Z leads, (D) 3-D image of X, Y and Z leads. The record s0503rem from the PhysioNet PTB database was used as a randomly selected physiological record. The individual planes are related to the basic principle of VCG measurement on ideal uniform lead fields from Figure 2.
The benefits of a 12-lead ECG for diagnostic evaluation of electrical activity of the heart has been a standard in clinical practice over a hundred of years. However, there are certain cases where the vectorcardiogram is superior to the electrocardiogram. In some publications, a higher sensitivity of VCG compared to conventional ECG has been reported in the diagnosis of atrial enlargement and right ventricular hypertrophy. It has been proposed to re-evaluate the frequency of 12-lead ECG usage to increase vectorcardiography measurements in clinical practice van Bemmel et al. (1992),
Vectorcardiography, which represents a slightly different approach, is used less commonly in practice and VCG leads are often derived
In recent years, vectorcardiographic recordings have been increasingly used for the analysis and detection of heart disease. If directly measured records using Frank lead system are not used, they are often transformed by various methods from a 12-lead ECG. In the following chapter, this paper provides an overview of the most commonly used transformation methods. In addition, it reviews the processing and extraction of important diagnostic parameters, the most promising techniques and current challenges for the detection of various heart diseases.
2 Review Strategy
This work presents a comprehensive overview of the multidisciplinary area of vectorcardiographic record processing and methods of possible transformation from 12-lead ECG to obtain derived VCG leads. The individual methods and steps for the implementation of this overview are presented here. These are mainly: selection of suitable databases, selection of search terms, and evaluation of results. This review was conducted using full papers, including publications in journals, conference papers, books, and academic papers. The search was performed without a time limit to provide a historical background. The search for relevant works was carried out in English.
2.1 Database Selection
Four basic databases were selected for the classification of suitable literature. These include the Scopus database and the Web of Science, which are among the largest databases, including peer-reviewed citation sources. PubMed and ProQuest databases, which focus on the selection of medical and medical literature, were also used. The combination of medical and technical literature should be the basis for comprehensive information, both medical and especially technical in the field of vectorcardiographic processing.
2.2 Indexed Terms
In this section, we list the individual indexed terms that have been used for this overview. In the case of processing vectorcardiographic records, the terminology is inconsistent. Therefore, several combinations of indexed terms have been used to include the widest possible range of articles that are relevant to this review. A summary of the individual indexed terms used can be seen in Table 1.
TABLE 1
| Index terms | |
|---|---|
| 1. | Vectorcardiography OR Vector Cardiography OR Vector Electrocardiography |
| 2. | VCG OR ECG |
| 3. | Transformation methods OR Derivation methods OR Linear transformation methods OR Quasi-orthogonal transformation OR Frank lead system |
| 4. | VCG features OR ECG features |
| 5. | P-loop OR QRS-loop OR T-loop |
| 6. | Medical signal processing OR Biomedical signal processing |
Indexed terms and their combinations.
3 Transformation Methods
The first consideration on the transformation of individual lead systems was presented by
Many of the transformation methods were derived only for the QRS complex of the heart cycle. There are also transformation matrices that are focused on other parts of the heart cycle. For example,
Transformation methods for the derivation of ECG and VCG leads are an integral part of obtaining further beneficial information from the measurement of electrical activity of the heart. Most of the published articles use databases with already measured ECG and VCG records. However, simultaneously measured orthogonal data with a 12-lead ECG is not always available. Therefore, this chapter is devoted to the most commonly used transformation methods used in publications and scientific works.
3.1 Quasi—Orthogonal Transformation
Any ECG lead system can be converted into vectorcardiographic loops. However, these derived VCG loops will not be orthogonal. Certain leads from a 12-lead ECG show a high correlation with orthogonal leads. These leads are called as quasi-orthogonal. Such derived lead systems correspond approximately to uncorrected VCG leads. Correction can be achieved using geometry based on the torso model derived by
3.2 Transformation Methods Based on Linear Approach
The standard 12-lead ECG does not provide much information about the sagittal plane, so it is necessary to use all the information contained in the ECG to derive the VCG. It is the VCG that provides us information of cardiac activity in all three planes. The simplest conversion to a VCG is to use quasi-orthogonal conversions, where one ECG lead corresponds to one VCG lead. A more reliable variant is the use of linear transformation methods, where each ECG lead (I, II, V1, V2, … , V6) contributes to a certain extent to a specific orthogonal lead. The individual weight coefficients then form the resulting transformation matrix M. This approach was first introduced by
For the conversion, the IDT has become one of the most widely used transformations. The coefficients can therefore be applied to individual ECG leads in the form of (Eq. 3).
The Y and Z leads can be derived similarly. The difference between a quasi-orthogonal systems and a linear transformation can be noticed here. Individual VCG leads in a quasi-orthogonal system correspond to exactly one ECG lead, while in the case of a linear transformation matrix the VCG leads is formed by the weight coefficients of the individual ECG leads. The mathematical transformation is then realized as a multiplication of two matrices (Eq. 4).where M is the transformation matrix, E is matrix whose rows are formed by independent ECG leads and V is matrix whose rows correspond to the derived VCG.
The coefficients of the transformation matrices are also derived on the basis of the torso model described by
3.3 Kors Regression Transformation
The transformation matrix introduced by
TABLE 2
| Lead | I | II | V1 | V2 | V3 | V4 | V5 | V6 |
|---|---|---|---|---|---|---|---|---|
| X | 0.38 | −0.07 | −0.13 | 0.05 | −0.01 | 0.14 | 0.06 | 0.54 |
| Y | −0.07 | 0.93 | 0.06 | −0.02 | −0.05 | 0.06 | −0.17 | 0.13 |
| Z | 0.11 | −0.23 | −0.43 | −0.06 | −0.14 | −0.20 | −0.11 | 0.31 |
Transformation coefficients of Kors regression method.
In this way, Kors derived several transformation matrices for different complex segments. He also stated that the differences between individual transformation matrices are small. Given that the QRS complex is most often analyzed, the resulting matrix is based only on the regression of the QRS complex.
Several publications have studied the transformation method introduced by Kors. The authors in
3.4 Inverse Dower Transformation (IDT)
In 1980,
TABLE 3
| Lead | I | II | III | aVR | aVL | aVF | V1 | V2 | V3 | V4 | V5 | V6 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| X | 0.632 | 0.235 | −0.397 | −0.434 | 0.515 | −0.081 | −0.515 | 0.044 | 0.882 | 1.213 | 2.125 | 0.831 |
| Y | −0.235 | 1.066 | 1.301 | −0.415 | −0.768 | 1.184 | 0.157 | 0.164 | 0.098 | 0.127 | 0.127 | 0.076 |
| Z | 0.059 | −0.132 | −0.191 | 0.037 | 0.125 | −0.162 | −0.917 | −1.387 | −1.277 | −0.604 | −0.086 | 0.230 |
Leading vectors for deriving a 12-lead electrocardiogram from the Frank XYZ signal.
Using this knowledge,
TABLE 4
| Lead | I | II | V1 | V2 | V3 | V4 | V5 | V6 |
|---|---|---|---|---|---|---|---|---|
| X | 0.156 | −0.010 | −0.172 | −0.074 | 0.122 | 0.231 | 0.239 | 0.194 |
| Y | −0.227 | 0.887 | 0.057 | −0.019 | −0.106 | −0.022 | 0.041 | 0.048 |
| Z | 0.022 | 0.102 | −0.229 | −0.310 | −0.246 | −0.063 | 0.055 | 0.108 |
Transformation matrix for Inverse Dower transformation (IDT).
The Inverse Dower Transformation was used by Panagiotou et al. (2013) and
3.5 P Least Square Value (PLSV) and Q Least Square Value (QLSV) Transformations
Transformation matrices derived from the regression approach mainly focus only on the QRS complex of the heart cycle. The accuracy of P and T waves is usually considered sufficient in transformations and the differences in transformation matrices are minimal. VCG loops can be used to detect arrhythmias with high accuracy, emphasis is also placed on the accuracy of P and T wave transformation
TABLE 5
| Lead | I | II | V1 | V2 | V3 | V4 | V5 | V6 |
|---|---|---|---|---|---|---|---|---|
| X | 0.370 | −0.154 | −0.266 | 0.027 | 0.065 | 0.131 | 0.203 | 0.220 |
| Y | −0.131 | 0.717 | 0.088 | −0.088 | 0.003 | 0.042 | 0.048 | 0.067 |
| Z | 0.184 | −0.114 | −0.319 | −0.198 | −0.167 | −0.099 | −0.009 | 0.060 |
PLSV transformation matrix.
TABLE 6
| Lead | I | II | V1 | V2 | V3 | V4 | V5 | V6 |
|---|---|---|---|---|---|---|---|---|
| X | 0.199 | −0.018 | −0.147 | −0.058 | 0.037 | 0.139 | 0.232 | 0.226 |
| Y | −0.164 | 0.503 | 0.023 | −0.085 | −0.003 | 0.033 | 0.060 | 0.104 |
| Z | 0.085 | −0.130 | −0.184 | −0.163 | −0.193 | −0.119 | −0.023 | 0.043 |
QLSV transformation matrix.
3.6 Transformation From Mason-Likar (ML) ECG Leads
During stress tests, measuring a 12-lead ECG is not appropriate due to limb movement. Therefore, Mason and Likar have published their recommendations on how to limit the movement of electrodes when measuring ECG in stress tests Mason and Likar (1966). Interfering components that are created by movement are eliminated by moving the measuring electrodes to the chest. The resulting differences in signals should always be taken into account Papouchado et al. (1987). For these reasons, standard linear transformation methods cannot be used.
TABLE 7
| Lead | I | II | V1 | V2 | V3 | V4 | V5 | V6 |
|---|---|---|---|---|---|---|---|---|
| X | 0.5169 | −0.0722 | −0.0753 | 0.0162 | 0.0384 | 0.0545 | 0.1384 | 0.4606 |
| Y | −0.2406 | 0.6344 | 0.1707 | −0.0833 | 0.1182 | 0.0237 | −0.1649 | 0.2100 |
| Z | −0.0715 | −0.1962 | −0.4987 | −0.0319 | −0.2362 | −0.0507 | −0.2007 | 0.4122 |
Mason–Likar transformation matrix.
3.7 Singular Value Decomposition of 12-Lead ECG
Another possibility of deriving vector cardiographic leads is by reducing the dimension of data using Singular Value Decomposition (SVD). This is an orthogonal matrix reduction of the data dimension defined by
where columns of U are referred to as the left singular vectors, columns of V are referred to as the right singular vectors and M is 8 x n matrix of individual ECG lead of n samples
The orthogonal leads obtained in this way do not correspond directly to the Frank VCG, and the indications obtained from these leads do not correspond to the indications derived from the VCG leads, as stated by
3.8 Summary of Transformation Methods
Transformation methods were derived to obtain orthogonal lead leads from a 12-lead ECG. There are many linear transformation methods that are used in various branches of VCG processing. However, each method has its advantages and disadvantages, especially in the processing of pathological records, where different pathologies affect different parts of the heart cycle. In such a case, knowledge of the effect of pathology on the ECG would be required to select the correct transformation method. If a transformation method is selected that is not suitable for a particular part of the ECG recordings, diagnostic information may be lost by signal distortion. The following Table 8 summarizes the key features of each linear transformation method. The Accuracy column shows the accuracy of the transformation method according to the evaluation parameter of correlation in individual leads. This is one of the most frequently used parameters in the evaluation of transformation methods. The stated quantitative values are defined as average values of all leads from publications
TABLE 8
| Transformation method | Derivation of transformation methods | Primary use | Accuracy |
|---|---|---|---|
| Kors regression transformation | Minimizing the mean error between the measured VCG and the transformed VCG | All types of ECG | 98% |
| Inverse Dower transformation (IDT) | Pseudo-inverse matrix to a system based on a torso model | Pathology affecting the QRS section | 97.2% |
| PLSV transformation | Derivation by least squares method | P wave of ECG | 96.8% |
| QLSV transformation | Derivation by least squares method | QRS complex of ECG | 97% |
| Quasi-orthogonal transformation | Approximation to VCG leads from ECG leads | All types of ECG | 90% |
| Mason-Likar (ML) | Designed using the regression method | Exercise and movement ECG | 95% |
Overview of transformation methods.
One of the most frequently used transformation method is the IDT followed by the Kors regression method. There are more and more studies that point to the fact that Kors regression method achieves higher accuracy than other transformations
If we assume a pathology that will affect more parts of the ECG, a combination of two or more transformation methods could be used to obtain a more accurately derived VCG. A graphic comparison of the individual transformation methods can be seen in Figure 3. From the first point of view, it can be seen that the Kors regression method copies the shape of the directly measured curve most accurately. However, various statistical tests are needed to verify the accuracy of the individual methods. Nevertheless, in the case of greater use of Frank’s lead system in clinical practice to obtain the original VCG, it would not be necessary to address the possibilities of transformation and their accuracy in the preservation of diagnostic information.
FIGURE 3

An exemplary comparison of transformation methods, where the blue curve is measured by the Frank lead system and the red curves are the transformed one.
The following chapter describes the possibilities of detecting individual heart diseases from VCG records. Because VCG is not commonly obtained in clinical practice, transformation methods are being approached. These transformation methods are also listed in the individual publications when used.
4 Heart Disease Analysis From Vectorcardiography
Since the 19th century, it has been known that the heart muscle emits quasi-periodic electrical signals during its activity. Although it is very important, there are no standardized methods for detecting pathologies from electrical heart activity measured in three mutually perpendicular planes. This is mainly due to the poor use of VCG in clinical practice and the scientific work that does not provide the necessary evaluation from cardiologists. Greater cooperation between authors and relevant doctors and mutual openness to new procedures could address this shortcoming.
Using various methods, it is possible to find a pattern of healthy cardiac rhythms and different patterns for each type of hearth disease. Published contributions and studies evaluate patient records using various methods. It is important to use the right criteria for an objective comparison of the new methods. This section presents the different methods and techniques used for the subsequent evaluation of the most frequently analyzed pathologies.
4.1 Acute Cardiac Ischemia
Acute cardiac ischemia can be characterized as an imbalance between myocardial oxygen supply and demand. The reduction in blood circulation is progressive and by delivering insufficient blood to the myocardium are myocardial cells deprived of the blood combinations necessary for their survival Tomey and Gidwani (2016). The authors approached to the detection of these life-threatening conditions by various methods of processing VCG records, where the most common cases were mainly myocardial ischemia and myocardial infarction.
4.1.1 Myocardial Ischemia
In recent years, several publications have promoted different methods for detecting and classifying electrical cardiac activity in patients with myocardial ischemia Persson et al. (2006),
Schuepbach et al. (2008) used cardiogoniometric leads (VCGC) and classifies healthy (HC) and ischemic (IHD) patients. Coronary angiography (CA) was used as a reference method. They describe VCG as a set of parameters including: time scale, size and direction of vectors, ratios of R/T vectors and ST/T segments, and the percentage location of QRS and T loops in space. A follow-up article by Seeck et al. (2009) already uses Linear Discriminant Functional Analysis (LDA) and the Machine Learning Method for classification.
4.1.2 Myocardial Infarction
Myocardial infarction (MI), also known as a heart attack, is a consequence of coronary artery occlusion and insufficient blood supply to the myocardium and may occur in different parts of the heart. MI triad: ischemia, injury and necrosis or any of the three may appear alone or in combination
VCG loops contain almost periodic activities of P, QRS and T waves in three-dimensional space. This space can be divided into eight octants, defined by
FIGURE 4

(A) Acquiring VCG signals; (B) Locations of the eight octants Yang et al. (2012).
In a previous study Yang (2010) examined the quantification of VCG signals to identify cardiac disorders using the discrete wavelet transform (DWT). A total of three classification models were used to separate healthy and MI records: linear, quadratic, and nearest neighbor (KNN). The linear discriminant analysis (LDA) is based on Eq. 9 and assumes that the linear plane serves as a boundary separating the points HC and MI.where αi are model coefficients and Si represents input properties. The residual error ϵ of the difference between the actual value and the model output determines whether VCG is HC or MI. Quadratic Discriminant Analysis (QDA), based on Eq. 10, assumes that the hyperplane serves as a boundary separating the HC and MI points in the element space.where αi, βij are coefficients, Si represents input properties and ϵ are residual errors. In the KNN classification model, the authors proceeded to use the Euclidean metric to measure proximity. From all the three analyzed classification models it was LDA that has reached the highest accuracy with sensitivity 96.5% and specificity 75%. The LDA classification technique was also used by
Similarly,
In other publications, the authors dealt with the extraction of VCG MI features affected at various sites in the heart
By evaluating certain sections of the heart cycle, such as PR
In recent years, there has been an increasing move to process VCG features to improve pathology detection. Therefore,
Romero et al. (2010) assess depolarization changes during AMI using analysis of the QRS loop represented by principal component analysis (PCA). In addition to the classical method based on the analysis of the ST-T section of ECG leads, it thus provides a new vector approach to the detection of AMI. The method includes signal preprocessing, which includes QRS detection, detection of normal cardiac cycles, isolation of the isoelectric line by cubic spline interpolation (CSI), delineation using wavelet (WT) techniques, and normalization. The result is an improvement in the sensitivity of the ST-segment inclination parameters by 103%, respectively 46% for the VCG method compared to the ECG for AMI detection.
The processing of vectorcardiographic features has become a reliable and recently expanded tool for the analysis of the VCG curve. The creation of new features or improvements in analysis techniques can contribute to better processing of VCG data and achieve early detection of heart disease. The new VCG feature was also proposed by Sadhukhan et al. (2017), which consists of a combination of the volume ratio of the 3-D QRS and the ST-T loop. From a statistical analysis, they found that this new feature provide high sensitivity (98.8%) between the MI and HC groups.
There are also papers that point to a significant impact of a combination of QRS complex and ST segment analysis Treskes et al. (2015), van Hellemond et al. (2013). Treskes et al. (2015) analyzed ST vector at J-point (J-point is automatically localized when the heart vector between QRS and T wave reaches its minimum value) and ventricular gradient vector (VG) from modified VCG by Kors regression method. According to their findings, the authors report that ST and VG analysis for the detection of acute myocardial ischemia is feasible and has either the same or even better performance than the conventional method. Also, van Hellemond et al. (2013) based on their QRS and ST parameter evaluation study, the myocardial risk area (MaR) estimation was more accurate that both ST and QRS abnormalities were taken into account than using individual components alone. The morphology of QRS-T for MI identification was also addressed by
4.2 Myocardial Scar
Fatal arrhythmias (ventricular tachycardia, fibrillation, etc.), most commonly caused by conduction defect from injured cardiac tissue known as scar, are a major cause of sudden cardiac death. Myocardial scar is the result of myocardial infarction (MI), which is caused by insufficient blood supply to the heart. This results in the death of part of the heart cells (scar tissue) and affects the contractile properties of the myocardium. Methods for accurate localization and scar size determination are different imaging techniques such as magnetic resonance imaging (MRI). However, this presents a number of disadvantages such as limited availability, high costs and mobility. Therefore, new methods for early identification of scar tissue in patients suffering from MI are being approached.
In 1971, Selvester et al. (1971) described detailed ECG and VCG criteria developed from simulations for localization and quantification of MI size. From these simulations, it was found that in a lead at right angles to the epicardium of the respective area, the degree of QRS change was proportional to the size of the infarct. Wickline and McNamara (1978) confirmed this finding based on autopsy results performed on baboons and Selvester et al. (1979, 1982) correlated the ECG/VCG QRS MI size scores with biplane ventriculograms that of the LV. The VCG score was calculated based on the deformations in the amplitude and length of the QRS applied to the nomogram developed in the set-learning test mode to predict the size of the MI. The 12-lead ECG MI size score involved 57 criteria (Q- and R-wave duration, R- and S-wave amplitudes, R/Q ratios, R/S ratios, and QRS slurs or notches) in 10 of the 12 standard leads except aVR and III. The maximum number of points was 32, and each point corresponded to 3% of the LV mass (representing 96% of the LV) Strauss and Selvester (2009).
VCG features are typically used for automatic classification using machine learning algorithms. For example, Panagiotou et al. (2013) used 27 spatial features to detect the presence or absence of a scar in myocardial tissue. For processing they used modified VCG by using IDT. For a total of 46 records, they developed a classification scheme based on SVM for scar detection. The proposed method achieves an accuracy of 82.36% (sensitivity 84.31% and specificity 77.36%). Another method for scar detection using a complex model based on the SVM was presented by
Nguyên et al. (2018) investigated the relationship between VCG parameters and myocardial scar (focal and diffuse) on CMR in patients with heart failure with ventricular dysfunction and whether the combination of VCG with scar parameters obtained by CMR improves the prediction of CRT response. They extracted QRSarea, Tarea and QRSTarea from the derived leads using the Kors regression method. Based on their findings, it follows that focal scar CMR parameters and QRSarea are independent predictors for CRT response and are inversely associated with each other. The highest percentage of CRT response was observed in patients with low focal scar CMR values and high QRSarea, indicating that combined CMR-VCG parameters may improve prediction to CRT response. The issue dealing with QRSarea and CMR was also dealt by Okafor et al. (2020). The purpose of their study was to determine in patients with ideally deployed quadripolar left ventricular lead whether a reduction QRSarea leads to an acute hemodynamic response (AHR) and whether the scar affects this interaction. In their study, they found that lowering the QRSarea improved AHR to CRT, myocardial scar adversely affects QRSarea and AHR.
Approximately 80% of the causes of SCD are associated with coronary heart disease Myerburg and Junttila (2012). The possibility of finding a suitable marker for SCD identification was analyzed by Waks et al. (2015). They analyzed beat-to-beat spatiotemporal variability in the T vector as the mean angle between consecutive T-wave vectors. They applied IDT transformation to derive VCG leads to the measured ECG recordings. Based on their findings in a large study, the increased risk of SCD is associated with higher variability in temporal and spatial variability between beats in the spatial T vector. In a previous study Tereshchenko et al. (2010) also looked at beat-to-beat analysis of VCG records now to predict ventricular arrhythmia (AV) as a possible predisposition to SCD. From their analysis, the authors state that T peaks are predictors associated with an increased risk of ventricular arrhythmias.
4.3 Left Bundle Branch Block
Left Bundle Branch Block (LBBB) is a disorder of cardiac conduction in the myocardium. Rather than heart disease, it is an abnormality of intraventricular conduction where the left ventricle is abnormally activated from the right bundle branch which starts branching in the apical region. The entire left ventricle is depolarized from the right bundle branching in the apical region, thereby expanding and morphologically changing the QRS complex. The main feature of LBBB is the mismatch between the main axes of the QRS complex and the T-wave, which is consistent with very wide QRS-T angles. Frank lead system can be considered the gold standard for precisely defining the mean spatial and vertex angles of QRS-T Schreurs et al. (2010). In patients with LBBB and heart failure, the goal is to achieve a more synchronous model of electrical ventricular activation and contraction by left ventricular-based stimulation (LV), thereby improving LV systolic function. Therefore, van Deursen et al. (2015a) and van Deursen et al. (2015b) utilized vectorcardiography knowledge to more accurately select patients for cardiac resynchronization therapy (CRT). They evaluated the QRS region from vectorcardiography against the commonly used QRS duration and left bundle branching morphology. Their findings suggest that the QRS area is a stronger predictor of CRT compared to the QRS time or conventionally defined LBBB morphology. A more precise selection of candidates for CRT was also dealt by Rad et al. (2016), where the main parameter of the study was also the QRS area. They used a total of 51 VCGs derived by Kors regression method. They compared the QRS area with QRS length and, based on their analysis, conclude that the QRS area is a non-invasive alternative to intracardiac measurement of electrical activation that identifies delayed left ventricular lateral wall activation better than QRS duration and LBBB morphology.
Shvilkin et al. (2010) in their study they distinguished the criteria to differentiate new and old LBBB. IDT were applied to the measured ECG recordings to obtain derived VCG leads. They analyzed QRS and T-wave amplitudes, directions, and durations and found that the QRS/T vector magnitude ratio and the deepest S to largest T wave ratio allow accurate discrimination between the new and old LBBBs with 100% sensitivity and 96–68% specificity. This finding may help management of patients with chest pain and LBBB. In another study, Villongco et al. (2014) described a method for simulating LBBB branches and RV-stimulated ventricular activation profiles in three dimensions from non-invasive routine clinical measurements. They used IDT and Kors regression transformation to derive VCG. They developed an activation pattern predicted by optimal parameters that correlates with invasive endocardial activation time measurements. The aim of this approach is to improve non-invasive electrocardiographic imaging techniques.
4.4 Hypertrophic Cardiomyopathy
Hypertrophic cardiomyopathy (HCM) is a cardiac disorder with heterogeneous expression, specific pathophysiology and a diverse clinical course. Several disease-causing mutations have been reported in genes encoding sarcomere proteins. Due to its characteristic clinical, morphological and genetic diversity, hypertrophic cardiomyopathy has maintained the curiosity of physicians and scientists for almost 40 years
One of the first studies at HCM was conducted by
Current ECG criteria have low accuracy in the diagnosis of left ventricular hypertrophy (LVH). However, the magnitude of QRS vectors and the direction of T loops can be considered useful parameters for the diagnosis of LVH from VCG MURATA et al. (1964).
HCM is a genetic heart disease with unexplained left ventricular hypertrophy and is one of the most common causes of sudden cardiac death in young people. The issue of HCM was also studied by
The HCM study in children was also studied by
4.5 Long QT Syndrome
Long Q-T syndrome (LQTS) is an inherited and life-threatening condition whose initial symptoms develop in childhood or adolescence. Ion channel dysfunction in myocytes causes delayed repolarization. The characteristic prolonged Q-T interval is associated with torsade de pointes and sudden cardiac death
Important finding was presented by
4.6 Atrial Fibrillation
Atrial fibrillation (AF) is one of the most common heart diseases occurring in 1–2% of the population. Although AF itself is not a life-threatening condition, it increases the risk of stroke fivefold, and every fifth stroke is attributed to this arrhythmia. Ischemic strokes associated with AF are often fatal, and patients who survive are more affected by stroke and are more likely to relapse than patients with other causes of stroke
New methods for correct AF detection were sought.
The problem of early detection of AF was also addressed by
Transformation methods have also found application in the analysis of spatial characteristics of AF from derived VCG using IDT
However, AF can also be reliably detected on a standard ECG, but there may be some problems when using one or a few leads. In this respect, VCG could provide support in applications where fewer leads are used in a 12-lead ECG, such as patient monitors or smartphones or watches. The use of a lower number of leads can also be used in VCG, where it is necessary to focus on the direction of propagation of the potential P wave vector.
5 Current Problems
The identification of heart disease from diagnostic methods is a frequently discussed topic in recent years. For decades, 12-lead ECG has been considered as the gold standard for electrical heart activity diagnostics. However, there are cases where a standard ECG does not achieve the necessary success rate of detecting various ischemia using automated detection. Therefore, VCG is approached as a method that can provide additional information
For the processing of pathological data, there may be a problem in selecting the most suitable transformation method. The reliability of the methods is also conditioned by different and inconsistent evaluation parameters. Linear transformation methods have proven to be a useful and frequently used tool for converting 12-lead ECGs to VCGs. The most commonly used transformation methods include the IDT, the Kors regression, the PLSV and QLSV methods, and in some cases also the Quasi-orthogonal approach. IDT is the most commonly used transformation method for further processing. This transformation method is mainly focused on the QRS complex, but also achieve reliable accuracy in other parts of the ECG signal. Methods that have been derived to improve accuracy only for some parts of the cardiac cycle (QLSV, PLSV) achieve the same accuracy as the regression approach. However, the accuracy of transformation methods also needs to be evaluated with a cardiologist. The problem with transformation methods and their transformation accuracy, in which the preservation of diagnostic information is addressed, would be solved by more frequent use of Frank lead system in clinical practice.
As additional information for the detection of heart disease are used VCG features. Studies have shown that VCG features extracted from pathological records such as myocardial infarction, myocardial ischemia, myocardial scar or atrial fibrillation can reliably distinguish test groups from healthy controls. Current studies have confirmed that the VCG features analysis especially of the QRS complex in particular provides reliable detection results
TABLE 9
| Author | Year | Purpose | VCG features | Data collection | Transformation method |
|---|---|---|---|---|---|
| 2003 | QRS, ST-T parameters study | 2 features QRS vector difference, ST vector magnitude | VCG measured by authors | none | |
| 2011 | MI detection | 64 features, QRS, T vector magnitudes R-T peak angle | PhysioNet PTB | none | |
| Yang et al. (2012) | 2012 | MI detection | 48 features Q, R, T—vector magnitude, R, T—vector angle, Angle between R and T-vector | PhysioNet PTB | none |
| 2012 | QRS, ST-T parameters study | 8 features QRS—Volume, Planar Area, Ratio between Area and Perimeter, Perimeter, ST Vector Magnitude, ST segment Level, T-wave amplitude | PhysioNet PTB | Kors regress | |
| 2013 | Cardiac ischemia detection | 8 features | PhysioNet PTB | Kors regress | |
| Panagiotou et al. (2013) | 2013 | Myocardial scar detection | 27 features R-width, T-width magnitude, R-peak, T-peak | PhysioNet PTB, Cardiology Department (UHS-NHS) | Dower’s inverse |
| 2013 | Myocardial scar detection | 25 features | PhysioNet PTB, Cardiology Department (UHS-NHS) | Dower’s inverse | |
| Treskes et al. (2015) | 2015 | Myocardial ischemia detection | 2 features ST vector, Ventricular gradient vector | ECG measured by authors | Kors regress |
| 2015 | MI detection | 98 features | PhysioNet PTB | Dower’s inverse | |
| 2016 | MI detection | 9 features QRS—Volume, Planar Area, Perimeter, Vector difference in ST segment and T-wave, ST-T Vector Magnitude Difference | PhysioNet PTB | none | |
| Sedaghat et al. (2016) | 2016 | QRS parameters Study | 5 features QRS loop roundness, planarity, thickness, rotational angle, dihedral angle | ECG and VCG measured by authors | Dower’s inverse |
| Sun et al. (2017) | 2017 | Myocardial ischemia screening | 17 features | PhysioNet PTB, STAFF III | Dower’s inverse |
| Tripathy and Dandapat (2017) | 2017 | MI detection | 15 features | PhysioNet PTB | none |
| Sharma and Sunkaria (2018) | 2018 | MI detection | 10 features | PhysioNet PTB | none |
| 2020 | Myocardial scar detection | 6 features | Derived whole-torso computational model with simulations | none | |
| 2021 | MI detection | 48 features | PhysioNet PTB | none |
An overview of important comparative studies.
Paramount is to evaluate the diagnostic significance of individual features, which may be different for different pathologies. Most studies only deal with the individualization of VCG features to a particular dataset. Thus, their results do not have to correspond to another database. It would be useful to compare the effectiveness of different features between the databases because each dataset is obtained by different measurement parameters. This fact is also correlated to the small number of available VCG datasets, where only a few authors use their own measured records for their study. The lack of records could be reduced by providing records by the authors or creating new datasets using modern devices. There are VCG features that are used in most publications and achieve high detection accuracy in terms of statistical evaluation. However, these features are not standardized for certain arrhythmias despite their possible diagnostic benefit, caused mainly by not consulting the results with cardiologists. The derivation and extraction of additional VCG features could further contribute to obtaining additional information necessary for the early diagnosis of heart disease.
6 Conclusion
Vectorcardiography, which in recent years is more often analyzed mainly in the research field, and which represents a different approach in the representation of electrical activity of the heart, can help us to obtain information that can help in the early diagnosis of heart disease. The main problem is that this method is not measured in clinical practice and the authors approach this method using transformation methods. The most important condition for the transformations is that diagnostic information must not be lost. Only an experienced cardiologist can evaluate the effect of transformation. If we only need a certain part of the heart revolution for processing, it is more appropriate to use specialized methods, which are focused on that part. The most accurate current methods are the IDT and the Kors regression transform but they lag slightly behind the accuracy of the P and T waves. This gap in the imperfection of linear transformation methods needs to be further addressed, due to the consequent better accuracy of transformation and preservation of diagnostic information. The new transformation method could refine VCG findings and provide physicians additional information for the early treatment of heart disease. Complications of applying transformation methods could be reduced by more frequent use of Frank lead system in clinical practice.
In most cases processing of VCG is performed on already measured datasets and is performed so-called offline. Future intentions may lead to the creation of devices that will process data using already proven techniques in real time or on newly created data or datasets. To detect different pathologies, the authors use different VCG features applied to derived or directly measured VCGs. Certain features are often pointed out that achieve reliable pathological detection. The authors analyze various parts of the cardiac revolution, such as the QRS complex, where they achieve relatively high detection accuracy (sensitivity and specificity is often 90%) or the S-T region with sensitivity and specificity around 80%. However, different processing methods for each access are often used. To complete the knowledge, it would be appropriate to focus on a certain type of processing. Few authors also consult their results with cardiologists to confirm their importance. They merely point out differences in morphological properties to assess the new method. The assessment of certain features by cardiologists could help standardize the features for certain pathologies. Combinations of VCG features for different loops of cardiac cycle achieve promising results but this approach is rarely used. By combining the QRS complex and the ST segment features, greater differences can be achieved between groups HC and the pathology. It would be advisable to consider using multiple VCG parts (QRS loop, ST segment, T wave) for analysis rather than just one.
Combining the above suggestions and discussing the results with cardiologists could help with visualization and gain new insights into the electrical activity of the heart. It would also be beneficial to increase the frequency of use of Frank lead system in clinical practice because as has been shown by more accessible and improving computer technology, the VCG method is suitable for the analysis of various heart diseases.
Statements
Author contributions
JV: Conceptualization, Investigation, Methodology, and Writing—review and editing. MP: Funding acquisition, Supervision, and Project administration.
Funding
The work and the contributions were supported by the project SV450021/2101, SP 2021/112 “Biomedical Engineering systems XVII.”
Conflict of interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Publisher’s note
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.
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Summary
Keywords
vectorcardiography, heart disease, VCG features, transformation methods, electrocardiography
Citation
Vondrak J and Penhaker M (2022) Review of Processing Pathological Vectorcardiographic Records for the Detection of Heart Disease. Front. Physiol. 13:856590. doi: 10.3389/fphys.2022.856590
Received
17 January 2022
Accepted
04 March 2022
Published
21 March 2022
Volume
13 - 2022
Edited by
Sebastian Clauss, Ludwig Maximilian University of Munich, Germany
Reviewed by
Lennart Bergfeldt, University of Gothenburg, Sweden
Mathias Baumert, University of Adelaide, Australia
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© 2022 Vondrak and Penhaker.
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*Correspondence: Jaroslav Vondrak, jaroslav.vondrak@vsb.cz
This article was submitted to Cardiac Electrophysiology, a section of the journal Frontiers in Physiology
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