P Wave Detection in Pathological ECG Signals

Důležitou součástí hodnocení elektrokardiogramu (EKG) a následné detekce srdečních patologií, zejména v dlouhodobém monitorování, je detekce vln P. Výsledky detekce vln P umožňují získat ze záznamu EKG více informací o srdeční činnosti. Podle správně detekovaných pozic vln P je možné detekovat a odlišit patologie, které současné programy používané v medicínské praxi identifikovat neumožňují (např. atrioventrikulární blok 1., 2. a 3. stupně, cestující pacemaker, Wolffův-Parkinsonův-Whiteův syndrom). Tato dizertační práce představuje novou metodu detekce vln P v záznamech EKG během fyziologické a zejména patologické srdeční činnosti. Metoda je založena na fázorové transformaci, inovativních pravidlech detekce a identifikaci možných patologií zpřesňující detekci vln P. Dalším důležitým výsledkem práce je vytvoření dvou veřejně dostupných databází záznamů EKG s obsahem patologií a anotovanými vlnami P. Dizertační práce je rozdělena na teoretickou část a soubor publikací představující příspěvek autora v oblasti detekce vlny P.Accurate software for the P wave detection, mainly in long-term monitoring, is an important part of electrocardiogram (ECG) evaluation and subsequent cardiac pathological events detection. The results of P wave detection allow us to obtain more information from the ECG records. According to the correct P wave detection, it is possible to detect and distinguish cardiac pathologies which are nowadays automatically undetectable by commonly used software in medical practice (events e.g. atrioventricular block 1st, 2nd and 3rd degree, WPW syndrome, wandering pacemaker, etc.). This thesis introduces a new method for P wave detection in ECG signals during both physiological and pathological heart function. This novel method is based on a phasor transform, innovative rules, and identification of possible pathologies that improve P wave detection. An equally important part of the work is the creation of two publicly available databases of physiological and pathological ECG records with annotated P waves. The dissertation is divided into theoretical analysis and a set of publications representing the contribution of the author in the area of P wave detection.

Serum potassium concentration monitoring by ECG time warping analysis on the T wave

This doctoral thesis was developed within the joint Ph.D. program in biomedical engineering at Universitat Politècnica de Catalunya (Barcelona, Spain) and University of Zaragoza (Zaragoza, Spain) in the framework of Doctorats Industrials program co-financed by Laboratorios Rubió S.A. (Castellbisbal, Spain) and Agència de Gestió d’Ajuts Universitaris i de Recerca, Generalitat de Catalunya (Spain). This thesis was performed in partnership with the Nephrology ward from Hospital Clínico Universitario Lozano Blesa (Zaragoza, Spain) and in collaboration with Dr J. Ramírez from the William Harvey Research Institute, Queen Mary University of London (London, UK).End-stage renal disease (ESRD) patients demonstrate an increased incidence of sudden cardiac death (SCD) with declining kidney functioning as a consequence of blood potassium ([K+]) homeostasis impairment, which is restored by hemodialysis (HD) therapy. The clinically established method for the diagnosis of [K+] imbalance is blood tests, an invasive and costly procedure that limits continuous monitoring of ESRD patients. A non-invasive ambulatory index, able to quantify changes in [K+] level is an open issue. In this context, the electrocardiogram (ECG) and in particular, the T wave (TW) morphology, has been shown to be strongly correlated with [K+] imbalance. Therefore, the aim of this dissertation is to investigate and to propose TW-derived markers able to monitor changes in [K+] levels in ESRD patients undergoing HD. For that purpose, the time warping analysis, a technique that allows the comparison and quantification of differences between two different TW shapes, was investigated. The application of TW time warping based markers in monitoring [K+ ] variations (Δ [K+]) and the derivation of a heart-rate corrected marker is proposed and compared with respect to two well-established Δ [K+]-related TW-based indexes. All the markers are evaluated in a single lead approach and after having emphasised the TW energy content through spatial transformation by Principal Component Analysis (PCA). Results demonstrate that the proposed biomarkers outperform the already proposed indexes, also proving that the use of PCA transformed lead generates markers with a higher correlation with Δ [K+] than the single lead approach. The possibility to improve markers robustness in the case of low signal-to-noise ratio ECGs, by spatially transforming the signal maximising the beat-to-beat TW periodicity criteria through the so-called Periodic Component Analysis (pCA), is then explored. pCA-based markers show superior performance during and after the HD than those obtained by PCA suggesting improved stability for continuous Δ [K+] tracking. The thesis studies also the application of regressions models to quantify Δ [K+] from pCA-based time warping markers. The accuracy of the regression models is evaluated by correlation and estimation error between the actual and the corresponding model-estimated Δ [K+] values, and the smallest estimation error is found for quadratic regression models. Being the time warping derived markers sensitive to TW boundary delineation errors, which may endanger their prognostic power, the advantages of using a weighting stage is investigated for their robust computation. The performance of two weighting functions (WF)s is tested and compared with respect to the control no weighting case, in simulated scenarios and in real scenarios (i.e. for [K+] monitoring and SCD risk stratification). No improvements in [K+] monitoring are found, probably due to the considerable marked [K+]-induced TW morphological changes. On the contrary, both simulation tests and SCD risk stratification analysis show that the proposed WFs can enhance the robustness of TW time warping analysis against TW delineation errors. In conclusion, this Doctoral Thesis confirms the hypothesis that enhanced perforce in Δ [K+] tracking and quantification can be achieved by analysing the overall TW morphology by time warping analysis. The simplicity of the technology, together with its low cost and ease of acquisition, should provide a new opportunity for TW analysis to reach standard clinical practice. Moreover, the use of WFs to minimise the undesired effects of TW delineation errors on the computation of time warping markers revealed a noticeable improvement of the SCD risk stratification power of time warping derived indexes.Los pacientes con enfermedad renal en etapa terminal (ESRD) demuestran una mayor incidencia de muerte cardíaca súbita (SCD) tras el deterioro del funcionamiento renal como consecuencia del desequilibrio del potasio ([K+]) en sangre. Este último se restablece mediante la terapia de hemodiálisis (HD). El desequilibrio de [K+] se diagnostica a través del análisis de sangre, un procedimiento invasivo y costoso que limita la monitorización de los pacientes con ESRD. Se necesita un índice ambulatorio no invasivo, capaz de cuantificar los cambios en el nivel de [K+] (Δ [K+]). En este contexto, se ha demostrado que el electrocardiograma (ECG) y en particular la onda T (TW), están correlacionados con Δ [K+]. El objetivo de esta tesis es evaluar marcadores derivados de la TW capaces de monitorizar ¿[K+] en pacientes con ESRD sometidos a HD. Para ello, se aplicó el análisis time warping, una técnica que permite la comparación de dos formas diferentes de TW. En primer lugar, se evalúa la aplicación de marcadores basados en el time warping para el seguimiento de Δ [K+] así como la derivación de un marcador corregido por la frecuencia cardíaca, comparando los marcadores con respecto a dos índices basados en TW bien establecidos y relacionados con Δ [K+]. Todos los marcadores se evalúan en las derivaciones independientes y después de haber enfatizado el contenido de energía de TW a través del Análisis de Componentes Principales (PCA). Los resultados demuestran mejores prestaciones de los marcadores time warping respecto a los ya propuestos y que el uso de PCA genera marcadores con una correlación más alta con Δ [K+] respecto a las derivaciones independientes. A continuación, se explora la posibilidad de mejorar la robustez de los marcadores en el caso de ECG con una relación señal/ruido baja, maximizando la periodicidad de TW latido a latido mediante el Análisisde Componentes Periódicos (pCA). Los marcadores basados en pCA muestran un rendimiento superior durante y después de la HD que los obtenidos por PCA, lo que sugiere una estabilidad mejorada para el seguimiento continuo de Δ [K+]. Luego, se evalúan modelos de regresión para cuantificar [K+] a partir de marcadores basados en pCA. La precisión de los modelos de regresión se evalúa mediante el error de estimación entre valores reales de Δ [K+] y los correspondientes estimados por el modelo. Con el error de estimación más pequeño, el modelo cuadrático es el más adecuado para la cuantificación de [K+].Siendo el análisis time warping sensible a los errores de delineación de los límites de TW, lo que supone un riesgo para su poder pronóstico, se investigan las ventajas de usar una etapa de ponderación para el cálculo de marcadores time warping. El rendimiento de dos funciones de ponderación (WF) se prueba y se compara con respecto al caso de control sin ponderación, en escenarios simulados y en escenarios reales (para el seguimiento de [K+] y la estratificación del riesgo de SCD). No se encontraron mejoras en la monitorización de [K+] debido a los considerables cambios morfológicos de TW inducidos por Δ [K+]. Por otro lado, tanto las pruebas de simulación como el análisis de estratificación de riesgo de SCD muestran que los WF propuestos pueden mejorar la robustez del análisis time warping de TW contra los errores dedelineación de TW. En conclusión, esta tesis doctoral confirma la hipótesis de que se puede lograr un mejor seguimiento y cuantificación de Δ [K+] mediante el análisis de la morfología de TW mediante el análisis time warping. La simplicidad de la tecnología, junto con su bajo costo y facilidad de adquisición del ECG, debería brindar una nueva oportunidad para que el análisis de TW en la práctica clínica rutinaria. Además, el uso de WF para minimizar los efectos no deseados de errores de delineación de TW en el cálculo de los marcadores time warping reveló una mejora del poder de estratificación del riesgoEnginyeria biomèdic

Serum potassium concentration monitoring by ECG time warping analysis on the T wave

This doctoral thesis was developed within the joint Ph.D. program in biomedical engineering at Universitat Politècnica de Catalunya (Barcelona, Spain) and University of Zaragoza (Zaragoza, Spain) in the framework of Doctorats Industrials program co-financed by Laboratorios Rubió S.A. (Castellbisbal, Spain) and Agència de Gestió d’Ajuts Universitaris i de Recerca, Generalitat de Catalunya (Spain). This thesis was performed in partnership with the Nephrology ward from Hospital Clínico Universitario Lozano Blesa (Zaragoza, Spain) and in collaboration with Dr J. Ramírez from the William Harvey Research Institute, Queen Mary University of London (London, UK).End-stage renal disease (ESRD) patients demonstrate an increased incidence of sudden cardiac death (SCD) with declining kidney functioning as a consequence of blood potassium ([K+]) homeostasis impairment, which is restored by hemodialysis (HD) therapy. The clinically established method for the diagnosis of [K+] imbalance is blood tests, an invasive and costly procedure that limits continuous monitoring of ESRD patients. A non-invasive ambulatory index, able to quantify changes in [K+] level is an open issue. In this context, the electrocardiogram (ECG) and in particular, the T wave (TW) morphology, has been shown to be strongly correlated with [K+] imbalance. Therefore, the aim of this dissertation is to investigate and to propose TW-derived markers able to monitor changes in [K+] levels in ESRD patients undergoing HD. For that purpose, the time warping analysis, a technique that allows the comparison and quantification of differences between two different TW shapes, was investigated. The application of TW time warping based markers in monitoring [K+ ] variations (Δ [K+]) and the derivation of a heart-rate corrected marker is proposed and compared with respect to two well-established Δ [K+]-related TW-based indexes. All the markers are evaluated in a single lead approach and after having emphasised the TW energy content through spatial transformation by Principal Component Analysis (PCA). Results demonstrate that the proposed biomarkers outperform the already proposed indexes, also proving that the use of PCA transformed lead generates markers with a higher correlation with Δ [K+] than the single lead approach. The possibility to improve markers robustness in the case of low signal-to-noise ratio ECGs, by spatially transforming the signal maximising the beat-to-beat TW periodicity criteria through the so-called Periodic Component Analysis (pCA), is then explored. pCA-based markers show superior performance during and after the HD than those obtained by PCA suggesting improved stability for continuous Δ [K+] tracking. The thesis studies also the application of regressions models to quantify Δ [K+] from pCA-based time warping markers. The accuracy of the regression models is evaluated by correlation and estimation error between the actual and the corresponding model-estimated Δ [K+] values, and the smallest estimation error is found for quadratic regression models. Being the time warping derived markers sensitive to TW boundary delineation errors, which may endanger their prognostic power, the advantages of using a weighting stage is investigated for their robust computation. The performance of two weighting functions (WF)s is tested and compared with respect to the control no weighting case, in simulated scenarios and in real scenarios (i.e. for [K+] monitoring and SCD risk stratification). No improvements in [K+] monitoring are found, probably due to the considerable marked [K+]-induced TW morphological changes. On the contrary, both simulation tests and SCD risk stratification analysis show that the proposed WFs can enhance the robustness of TW time warping analysis against TW delineation errors. In conclusion, this Doctoral Thesis confirms the hypothesis that enhanced perforce in Δ [K+] tracking and quantification can be achieved by analysing the overall TW morphology by time warping analysis. The simplicity of the technology, together with its low cost and ease of acquisition, should provide a new opportunity for TW analysis to reach standard clinical practice. Moreover, the use of WFs to minimise the undesired effects of TW delineation errors on the computation of time warping markers revealed a noticeable improvement of the SCD risk stratification power of time warping derived indexes.Los pacientes con enfermedad renal en etapa terminal (ESRD) demuestran una mayor incidencia de muerte cardíaca súbita (SCD) tras el deterioro del funcionamiento renal como consecuencia del desequilibrio del potasio ([K+]) en sangre. Este último se restablece mediante la terapia de hemodiálisis (HD). El desequilibrio de [K+] se diagnostica a través del análisis de sangre, un procedimiento invasivo y costoso que limita la monitorización de los pacientes con ESRD. Se necesita un índice ambulatorio no invasivo, capaz de cuantificar los cambios en el nivel de [K+] (Δ [K+]). En este contexto, se ha demostrado que el electrocardiograma (ECG) y en particular la onda T (TW), están correlacionados con Δ [K+]. El objetivo de esta tesis es evaluar marcadores derivados de la TW capaces de monitorizar ¿[K+] en pacientes con ESRD sometidos a HD. Para ello, se aplicó el análisis time warping, una técnica que permite la comparación de dos formas diferentes de TW. En primer lugar, se evalúa la aplicación de marcadores basados en el time warping para el seguimiento de Δ [K+] así como la derivación de un marcador corregido por la frecuencia cardíaca, comparando los marcadores con respecto a dos índices basados en TW bien establecidos y relacionados con Δ [K+]. Todos los marcadores se evalúan en las derivaciones independientes y después de haber enfatizado el contenido de energía de TW a través del Análisis de Componentes Principales (PCA). Los resultados demuestran mejores prestaciones de los marcadores time warping respecto a los ya propuestos y que el uso de PCA genera marcadores con una correlación más alta con Δ [K+] respecto a las derivaciones independientes. A continuación, se explora la posibilidad de mejorar la robustez de los marcadores en el caso de ECG con una relación señal/ruido baja, maximizando la periodicidad de TW latido a latido mediante el Análisisde Componentes Periódicos (pCA). Los marcadores basados en pCA muestran un rendimiento superior durante y después de la HD que los obtenidos por PCA, lo que sugiere una estabilidad mejorada para el seguimiento continuo de Δ [K+]. Luego, se evalúan modelos de regresión para cuantificar [K+] a partir de marcadores basados en pCA. La precisión de los modelos de regresión se evalúa mediante el error de estimación entre valores reales de Δ [K+] y los correspondientes estimados por el modelo. Con el error de estimación más pequeño, el modelo cuadrático es el más adecuado para la cuantificación de [K+].Siendo el análisis time warping sensible a los errores de delineación de los límites de TW, lo que supone un riesgo para su poder pronóstico, se investigan las ventajas de usar una etapa de ponderación para el cálculo de marcadores time warping. El rendimiento de dos funciones de ponderación (WF) se prueba y se compara con respecto al caso de control sin ponderación, en escenarios simulados y en escenarios reales (para el seguimiento de [K+] y la estratificación del riesgo de SCD). No se encontraron mejoras en la monitorización de [K+] debido a los considerables cambios morfológicos de TW inducidos por Δ [K+]. Por otro lado, tanto las pruebas de simulación como el análisis de estratificación de riesgo de SCD muestran que los WF propuestos pueden mejorar la robustez del análisis time warping de TW contra los errores dedelineación de TW. En conclusión, esta tesis doctoral confirma la hipótesis de que se puede lograr un mejor seguimiento y cuantificación de Δ [K+] mediante el análisis de la morfología de TW mediante el análisis time warping. La simplicidad de la tecnología, junto con su bajo costo y facilidad de adquisición del ECG, debería brindar una nueva oportunidad para que el análisis de TW en la práctica clínica rutinaria. Además, el uso de WF para minimizar los efectos no deseados de errores de delineación de TW en el cálculo de los marcadores time warping reveló una mejora del poder de estratificación del riesgoPostprint (published version

Prognosis of symptomatic patients with Brugada Syndrome through electrocardiogram biomarkers and machine learning

La Síndrome de Brugada (BrS) és un trastorn cardiovascular poc comú però greu que pot causar batecs perillosament ràpids i es caracteritza per presentar un conjunt particular de patrons d'electrocardiograma (ECG) als seus pacients. És una condició molt impredictible. Moltes persones no presenten cap símptoma, mentre que per altres, lamentablement, el primer símptoma és la mort. Per a pacients d'alt risc es recomana col•locar un desfibril•lador cardioversor implantable. Desafortunadament, això té greus riscos associats, com infeccions i descàrregues inadequades, per la qual cosa és clau identificar aquests pacients d'alt risc correctament. L'objectiu d'aquest projecte ha estat desenvolupar eines basades en aprenentatge automàtic que poguessin diferenciar els pacients amb Síndrome de Brugada simptomàtics dels quals no ho són. Es van considerar pacients simptomàtics aquells que s'havien recuperat de mort cardíaca, van patir un síncope arritmogènic o taquicàrdia sostinguda. Per fer-ho, després d'una investigació de l'estat de l'art dels temes pertinents, es van extreure diversos biomarcadors relacionats amb els patrons d'ECG de Brugada a partir de registres d'ECG de 24 hores de 45 pacients diferents, després d'haver estat processats per mitjà de promediat de senyal per reduir el soroll. Aquests biomarcadors, juntament amb algunes dades clíniques, es van separar de diferents maneres per entrenar i provar diferents models de classificació automatitzats basats en aprenentatge automàtic. Els resultats obtinguts dels models han estat molt pobres. Cap d'ells no ha pogut classificar de manera fiable els pacients amb BrS com es desitjava. Això no obstant, d'aquesta primera aproximació es poden extreure conclusions valuoses per assolir l'objectiu del projecte, i s’han desenvolupat eines útils que poden permetre un processament més ràpid de la base de dades utilitzada.El Síndrome de Brugada (BrS) es un trastorno cardiovascular poco común pero grave que puede causar latidos peligrosamente rápidos y se caracteriza por presentar un conjunto particular de patrones de electrocardiograma (ECG) en sus pacientes. Es una condición muy impredecible. Muchas personas no presentan ningún síntoma, mientras que para otras, lamentablemente, el primer síntoma es la muerte. Para pacientes de alto riesgo se recomienda la colocación de un desfibrilador cardioversor implantable. Desafortunadamente, eso tiene graves riesgos asociados, como infecciones y descargas inapropiadas, por lo que es clave identificar a esos pacientes de alto riesgo correctamente. El objetivo de este proyecto era desarrollar herramientas basadas en aprendizaje automático que puedan diferenciar a los pacientes con Síndrome de Brugada sintomáticos de aquellos que no lo son. Se consideraron pacientes sintomáticos aquellos que se habían recuperado de muerte cardiaca, sufrieron un síncope arritmogénico o una taquicardia sostenida. Para ello, tras una investigación del estado del arte de los temas relevantes, se extrajeron varios biomarcadores relacionados con los patrones de ECG de Brugada a partir de registros de ECG de 24h de 45 pacientes diferentes, después de haber sido procesados mediante promedio de señal para reducir su ruido. Estos biomarcadores, junto con algunos datos clínicos, se separaron de diferentes maneras para entrenar y probar diferentes modelos de clasificación automatizados basados en aprendizaje automático. Los resultados de los modelos obtenidos han sido muy pobres. Ninguno de ellos pudo clasificar de manera confiable a los pacientes con BrS como se deseaba. No obstante, de esta primera aproximación se pueden extraer valiosas conclusiones para continuar avanzando hacia el objetivo perseguido, y se desarrollaron herramientas útiles que permitirán un procesamiento más rápido de la base de datos utilizada.The Brugada Syndrome (BrS) is a rare but serious cardiovascular disorder that can cause dangerously fast heartbeats and is characterized by a particular set of electrocardiogram (ECG) patterns. It’s a very unpredictable condition. Many people don’t present symptoms at all, while for others, unfortunately, the first symptom is death. For high risk patients, having an implantable cardioverter-defibrillator placed is recommended. Unfortunately, that has severe risks associated, like infections and inappropriate shocks, so it’s key to identify those high risk patients. The objective of this project was to develop machine learning based tools that are able to tell symptomatic Brugada Syndrome patients apart from those who are not. Symptomatic patients were considered those who had recovered from cardiac death, suffered an arrhythmogenic syncope or sustained tachycardia. In order to do so, after an investigation of the state of the art of the relevant subjects, several biomarkers related with Brugada ECG patterns were extracted from 24h ECG recordings of 45 different patients, after having been processed by signal averaging in order to reduce their noise. Those biomarkers, alongside some clinical data, were then separated in different ways in order to train and test different machine learning based automated classifier models. The performances of those models were very poor. None of them was able to reliably classify BrS patients as desired. Nevertheless, valuable conclusions can be extracted from this first approach to pursue the intended goal further, and useful tools were developed that would allow for a faster processing of the database used

ADAPTIVE MODELS-BASED CARDIAC SIGNALS ANALYSIS AND FEATURE EXTRACTION

Signal modeling and feature extraction are among the most crucial and important steps for stochastic signal processing. In this thesis, a general framework that employs adaptive model-based recursive Bayesian state estimation for signal processing and feature extraction is described. As a case study, the proposed framework is studied for the problem of cardiac signal analysis. The main objective is to improve the signal processing aspects of cardiac signals by developing new techniques based on adaptive modelling of electrocardiogram (ECG) wave-forms. Specially several novel and improved approaches to model-based ECG decomposition, waveform characterization and feature extraction are proposed and studied in detail. In the concept of ECG decomposition and wave-forms characterization, the main idea is to extend and improve the signal dynamical models (i.e. reducing the non-linearity of the state model with respect to previous solutions) while combining with Kalman smoother to increase the accuracy of the model in order to split the ECG signal into its waveform components, as it is proved that Kalman filter/smoother is an optimal estimator in minimum mean square error (MMSE) for linear dynamical systems. The framework is used for many real applications, such as: ECG components extraction, ST segment analysis (estimation of a possible marker of ventricular repolarization known as T/QRS ratio) and T-wave Alternans (TWA) detection, and its extension to many other applications is straightforward. Based on the proposed framework, a novel model to characterization of Atrial Fibrillation (AF) is presented which is more effective when compared with other methods proposed with the same aims. In this model, ventricular activity (VA) is represented by a sum of Gaussian kernels, while a sinusoidal model is employed for atrial activity (AA). This new model is able to track AA, VA and fibrillatory frequency simultaneously against other methods which try to analyze the atrial fibrillatory waves (f-waves) after VA cancellation. Furthermore we study a new ECG processing method for assessing the spatial dispersion of ventricular repolarization (SHVR) using V-index and a novel algorithm to estimate the index is presented, leading to more accurate estimates. The proposed algorithm was used to study the diagnostic and prognostic value of the V-index in patients with symptoms suggestive of Acute Myocardial Infraction (AMI)

Reliable Detection of Myocardial Ischemia Using Machine Learning Based on Temporal-Spatial Characteristics of Electrocardiogram and Vectorcardiogram

Background: Myocardial ischemia is a common early symptom of cardiovascular disease (CVD). Reliable detection of myocardial ischemia using computer-aided analysis of electrocardiograms (ECG) provides an important reference for early diagnosis of CVD. The vectorcardiogram (VCG) could improve the performance of ECG-based myocardial ischemia detection by affording temporal-spatial characteristics related to myocardial ischemia and capturing subtle changes in ST-T segment in continuous cardiac cycles. We aim to investigate if the combination of ECG and VCG could improve the performance of machine learning algorithms in automatic myocardial ischemia detection. Methods: The ST-T segments of 20-second, 12-lead ECGs, and VCGs were extracted from 377 patients with myocardial ischemia and 52 healthy controls. Then, sample entropy (SampEn, of 12 ECG leads and of three VCG leads), spatial heterogeneity index (SHI, of VCG) and temporal heterogeneity index (THI, of VCG) are calculated. Using a grid search, four SampEn and two features are selected as input signal features for ECG-only and VCG-only models based on support vector machine (SVM), respectively. Similarly, three features (S ( I ), THI, and SHI, where S ( I ) is the SampEn of lead I) are further selected for the ECG + VCG model. 5-fold cross validation was used to assess the performance of ECG-only, VCG-only, and ECG + VCG models. To fully evaluate the algorithmic generalization ability, the model with the best performance was selected and tested on a third independent dataset of 148 patients with myocardial ischemia and 52 healthy controls. Results: The ECG + VCG model with three features (S ( I ),THI, and SHI) yields better classifying results than ECG-only and VCG-only models with the average accuracy of 0.903, sensitivity of 0.903, specificity of 0.905, F1 score of 0.942, and AUC of 0.904, which shows better performance with fewer features compared with existing works. On the third independent dataset, the testing showed an AUC of 0.814. Conclusion: The SVM algorithm based on the ECG + VCG model could reliably detect myocardial ischemia, providing a potential tool to assist cardiologists in the early diagnosis of CVD in routine screening during primary care services

Individual identification via electrocardiogram analysis

Background: During last decade the use of ECG recordings in biometric recognition studies has increased. ECG characteristics made it suitable for subject identification: it is unique, present in all living individuals, and hard to forge. However, in spite of the great number of approaches found in literature, no agreement exists on the most appropriate methodology. This study aimed at providing a survey of the techniques used so far in ECG-based human identification. Specifically, a pattern recognition perspective is here proposed providing a unifying framework to appreciate previous studies and, hopefully, guide future research. Methods: We searched for papers on the subject from the earliest available date using relevant electronic databases (Medline, IEEEXplore, Scopus, and Web of Knowledge). The following terms were used in different combinations: electrocardiogram, ECG, human identification, biometric, authentication and individual variability. The electronic sources were last searched on 1st March 2015. In our selection we included published research on peer-reviewed journals, books chapters and conferences proceedings. The search was performed for English language documents. Results: 100 pertinent papers were found. Number of subjects involved in the journal studies ranges from 10 to 502, age from 16 to 86, male and female subjects are generally present. Number of analysed leads varies as well as the recording conditions. Identification performance differs widely as well as verification rate. Many studies refer to publicly available databases (Physionet ECG databases repository) while others rely on proprietary recordings making difficult them to compare. As a measure of overall accuracy we computed a weighted average of the identification rate and equal error rate in authentication scenarios. Identification rate resulted equal to 94.95 % while the equal error rate equal to 0.92 %. Conclusions: Biometric recognition is a mature field of research. Nevertheless, the use of physiological signals features, such as the ECG traits, needs further improvements. ECG features have the potential to be used in daily activities such as access control and patient handling as well as in wearable electronics applications. However, some barriers still limit its growth. Further analysis should be addressed on the use of single lead recordings and the study of features which are not dependent on the recording sites (e.g. fingers, hand palms). Moreover, it is expected that new techniques will be developed using fiducials and non-fiducial based features in order to catch the best of both approaches. ECG recognition in pathological subjects is also worth of additional investigations

A HARDWARE-SOFTWARE CO-DESIGNED WEARABLE FOR REAL-TIME PHYSIOLOGICAL DATA COLLECTION AND SIGNAL QUALITY ASSESSMENT

In the future, Smart and Connected Communities (S&CC) will use distributed wireless sensors and embedded computing platforms to produce meaningful data that can help individuals, and communities. Here, we presented a scanner, a data reliability estimation algorithm and Electrocardiogram (ECG) beat classification algorithm which contributes to the S&CC framework .In part 1, we report the design, prototyping, and functional validation of a low-power, small, and portable signal acquisition device for these sensors. The scanner was fully tested, characterized, and validated in the lab, as well as through deployment to users homes. As a test case, we show results of the scanner measuring WRAP temperature sensors with relative error within the 0.01% range. The scanner measurement shows distinguish temperature of 1F difference and excellent linear dependence between actual and measured resistance (R2 = 0.998). This device hasdemonstrated the possibility of a small, low-power portable scanner for WRAP sensors.Additionally, we explored the statistical data reliability metric (DReM) to explain the quality of bio-signal quantitatively on a scale between 0.0 -1.0. As proof of concept, we analyzed the ECG signal. Our DReM prediction algorithm measures the reliability of the ECG signals effectively with low Root mean square error = 0.010 and Mean absolute error = 0.008 and coefficient of determination R2 value of 0.990. Finally, we tested our model against the opinions of three independent judges and presented R2 value to determine the agreement between judgments vs our prediction model.We concluded our contribution to the S&CC framework by analyzing ECG beat classification with a pipeline of classifiers that focuses on improving the models performance on identifying minority classes (ventricular ectopic beat, supraventricular ectopic beat). Moreover, we intended to minimize morphological distortion introduced due to indiscriminate use of filtering techniques on ECG signals. Our approach shows an average positive predictive value 95.21%, sensitivity of95.28%, and F-1 score 95.76% respectively

P and T wave analysis in ECG signals using Bayesian methods

Cette thèse a pour objet l’étude de méthodes Bayésiennes pour l’analyse des ondes P et T des signaux ECG. Différents modèles statistiques et des méthodes Bayésiennes associées sont proposés afin de réaliser la détection des ondes P et T et leur caractérisation (détermination du sommet et des limites des ondes ainsi que l’estimation des formes d’onde). Ces modèles prennent en compte des lois a priori pour les paramètres inconnus (les positions des ondes, les amplitudes et les coefficients de ces formes d'onde) associés aux signaux ECG. Ces lois a priori sont ensuite combinées avec la vraisemblance des données observées pour fournir les lois a posteriori des paramètres inconnus. En raison de la complexité des lois a posteriori obtenues, des méthodes de Monte Carlo par Chaînes de Markov sont proposées pour générer des échantillons distribués asymptotiquement suivant les lois d’intérêt. Ces échantillons sont ensuite utilisés pour approcher les estimateurs Bayésiens classiques (MAP ou MMSE). D'autre part, pour profiter de la nature séquentielle du signal ECG, un modèle dynamique est proposé. Une méthode d'inférence Bayésienne similaire à celle développée précédemment et des méthodes de Monte Carlo séquentielles (SMC) sont ensuite étudiées pour ce modèle dynamique. Dans la dernière partie de ce travail, deux modèles Bayésiens introduits dans cette thèse sont adaptés pour répondre à un sujet de recherche clinique spécifique appelé détection de l'alternance des ondes T. Une des approches proposées a servi comme outil d'analyse dans un projet en collaboration avec St. Jude Medical, Inc et l'hôpital de Rangueil à Toulouse, qui vise à évaluer prospectivement la faisabilité de la détection des alternances des ondes T dans les signaux intracardiaques. ABSTRACT : This thesis studies Bayesian estimation/detection algorithms for P and T wave analysis in ECG signals. In this work, different statistical models and associated Bayesian methods are proposed to solve simultaneously the P and T wave delineation task (determination of the positions of the peaks and boundaries of the individual waves) and the waveform-estimation problem. These models take into account appropriate prior distributions for the unknown parameters (wave locations and amplitudes, and waveform coefficients). These prior distributions are combined with the likelihood of the observed data to provide the posterior distribution of the unknown parameters. Due to the complexity of the resulting posterior distributions, Markov chain Monte Carlo algorithms are proposed for (sample-based) detection/estimation. On the other hand, to take full advantage of the sequential nature of the ECG, a dynamic model is proposed under a similar Bayesian framework. Sequential Monte Carlo methods (SMC) are also considered for delineation and waveform estimation. In the last part of the thesis, two Bayesian models introduced in this thesis are adapted to address a specific clinical research problem referred to as T wave alternans (TWA) detection. One of the proposed approaches has served as an efficient analysis tool in the Endocardial T wave Alternans Study (ETWAS) project in collaboration with St. Jude Medical, Inc and Toulouse Rangueil Hospital. This project was devoted to prospectively assess the feasibility of TWA detection in repolarisation on EGM stored in ICD memories

Analyse des ondes P et T des signaux ECG à l'aide de méthodes Bayésienne

Cette thèse a pour objet l étude de méthodes Bayésiennes pour l analyse des ondes P et T des signaux ECG. Différents modèles statistiques et des méthodes Bayésiennes associées sont proposés afin de réaliser la détection des ondes P et T et leur caractérisation (détermination du sommet et des limites des ondes ainsi que l estimation des formes d onde). Ces modèles prennent en compte des lois a priori pour les paramètres inconnus (les positions des ondes, les amplitudes et les coefficients de ces formes d'onde) associés aux signaux ECG. Ces lois a priori sont ensuite combinées avec la vraisemblance des données observées pour fournir les lois a posteriori des paramètres inconnus. En raison de la complexité des lois a posteriori obtenues, des méthodes de Monte Carlo par Chaînes de Markov sont proposées pour générer des échantillons distribués asymptotiquement suivant les lois d intérêt. Ces échantillons sont ensuite utilisés pour approcher les estimateurs Bayésiens classiques (MAP ou MMSE). D'autre part, pour profiter de la nature séquentielle du signal ECG, un modèle dynamique est proposé. Une méthode d'inférence Bayésienne similaire à celle développée précédemment et des méthodes de Monte Carlo séquentielles (SMC) sont ensuite étudiées pour ce modèle dynamique. Dans la dernière partie de ce travail, deux modèles Bayésiens introduits dans cette thèse sont adaptés pour répondre à un sujet de recherche clinique spécifique appelé détection de l'alternance des ondes T. Une des approches proposées a servi comme outil d'analyse dans un projet en collaboration avec St. Jude Medical, Inc et l'hôpital de Rangueil à Toulouse, qui vise à évaluer prospectivement la faisabilité de la détection des alternances des ondes T dans les signaux intracardiaques.This thesis studies Bayesian estimation/detection algorithms for P and T wave analysis in ECG signals. In this work, different statistical models and associated Bayesian methods are proposed to solve simultaneously the P and T wave delineation task (determination of the positions of the peaks and boundaries of the individual waves) and the waveform-estimation problem. These models take into account appropriate prior distributions for the unknown parameters (wave locations and amplitudes, and waveform coefficients). These prior distributions are combined with the likelihood of the observed data to provide the posterior distribution of the unknown parameters. Due to the complexity of the resulting posterior distributions, Markov chain Monte Carlo algorithms are proposed for (sample-based) detection/estimation. On the other hand, to take full advantage of the sequential nature of the ECG, a dynamic model is proposed under a similar Bayesian framework. Sequential Monte Carlo methods (SMC) are also considered for delineation and waveform estimation. In the last part of the thesis, two Bayesian models introduced in this thesis are adapted to address a specific clinical research problem referred to as T wave alternans (TWA) detection. One of the proposed approaches has served as an efficient analysis tool in the Endocardial T wave Alternans Study (ETWAS) project in collaboration with St. Jude Medical, Inc and Toulouse Rangueil Hospital. This project was devoted to prospectively assess the feasibility of TWA detection in repolarisation on EGM stored in ICD memories.TOULOUSE-INP (315552154) / SudocSudocFranceF