Grant: Discovery Grants Program - Individual
Toronto Metropolitan University
$28,000.00
Adaptive Data Processing, Modeling, and Quantification Methods for Analyzing Cardiac Fibrillation
EF 2022-23
Résumé
Heart is a vital organ that beats (i.e. expands and contracts) nonstop to maintain blood circulation to keep us alive. The rhythmic contractions and expansion of the heart transports nutrients and oxygen via blood to all parts of the body to sustain life. When this rhythmic functioning of the heart gets disturbed because of various pathophysiological reasons, arrhythmic contractions result in compromising the normal functioning of the heart. Depending on the origin of these arrhythmic contractions, it may lead to lethal conditions. The most lethal of the arrhythmias is Ventricular Fibrillation (VF) which originates from the lower chambers of the heart (i.e. ventricles). VF can lead to sudden cardiac death (SCD) if no medical attention is provided within minutes of onset. About 300,000 SCDs are reported every year in North America (45,000 in Canada) most of which are VF related. Atrial fibrillation (AF) originating from atria, although not as lethal as VF, can seriously impact quality of life and increases the risk of stroke. Despite research efforts over many decades, there is still a significant knowledge gap in understanding the mechanistic basis of cardiac fibrillation which is preventing effective means to reduce the mortality rates associated with cardiac fibrillation (especially for VF). This strongly motivates the need for developing new engineering methods in understanding mechanisms behind these arrhythmias and translating them to realizable practical solutions to reduce the mortality associated with the arrhythmias. Major bottle necks in decoding the mechanisms behind lethal VF is that SCD occurs within minutes and that in most cases [especially in out-of-the-hospital cardiac arrests (OHCA)] the only immediately available information on the electrical state of the heart is through surface electrocardiograms. In addressing the above knowledge gap, the proposed research program will develop new ways of analyzing and extracting information from multi-channel electrograms and electrocardiograms during arrhythmia and build computer simulation models to decipher the mechanistic insights of cardiac fibrillation. Specifically, the research, in collaboration with Toronto General and St. Michael's Hospitals, will develop advanced data processing and modeling techniques to characterize and regionally locate the sources that initiate and sustain cardiac arrhythmias. The informative clues on these fibrillatory sources will be appropriately translated into electrograms and multi-channel electrocardiogram signal morphologies. These discriminative signal morphologies along with the evolution of the arrhythmia over time will then be used to develop intelligent ablation and defibrillation strategies. The mechanistic knowledge gained through the proposed research program and the developed analysis strategies will significantly augment long-term focused (in-hospital) medical strategies for arrhythmias as well as improve survival rates in OHCA.
Programme
Discovery Grants Program - Individual
Bénéficiaire
Emplacement
Ontario, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
NSERC's Awards Data
Tel que publié
Application id
RGPIN-2020-04933
Name nom
Umapathy, Karthikeyan
Department département
Electrical, Computer and Biomedical Engineering - Electrical, Computer and Biomedical Engineering
Organization id
43
Institution établissement
Toronto Metropolitan University
Province en
Ontario
Province fr
Ontario
Country en
CANADA
Country fr
CANADA
Fiscal year exercice financier
2022
Competition year année de concours
2020
Award amount
28000
Program id
RGPIN
Program name en
Discovery Grants Program - Individual
Program name fr
Programme de subventions à la découverte - individuelles
Group en
DISCOVERY RESEARCH
Group fr
RECHERCHE AXÉE SUR LA DÉCOUVERTE
Committee code
1510
Committee name en
Electrical and Computer Engineering
Committee name fr
Génie électrique et informatique
Area of application code
1102
Area of application group en
Health, education and social services
Area of application group fr
Santé publique, éducation et services sociaux
Area of application en
Biomedical engineering
Area of application fr
Génie biomédical
Research subject code
1900
Research subject group en
Biomedical engineering
Research subject group fr
Génie biomédical
Research subject en
Biomedical engineering
Research subject fr
Génie biomédical
Installment
inst:3
Partie
1
Nb partie
5
Application title
Adaptive Data Processing, Modeling, and Quantification Methods for Analyzing Cardiac Fibrillation
Application summary
Heart is a vital organ that beats (i.e. expands and contracts) nonstop to maintain blood circulation to keep us alive. The rhythmic contractions and expansion of the heart transports nutrients and oxygen via blood to all parts of the body to sustain life. When this rhythmic functioning of the heart gets disturbed because of various pathophysiological reasons, arrhythmic contractions result in compromising the normal functioning of the heart. Depending on the origin of these arrhythmic contractions, it may lead to lethal conditions. The most lethal of the arrhythmias is Ventricular Fibrillation (VF) which originates from the lower chambers of the heart (i.e. ventricles). VF can lead to sudden cardiac death (SCD) if no medical attention is provided within minutes of onset. About 300,000 SCDs are reported every year in North America (45,000 in Canada) most of which are VF related. Atrial fibrillation (AF) originating from atria, although not as lethal as VF, can seriously impact quality of life and increases the risk of stroke. Despite research efforts over many decades, there is still a significant knowledge gap in understanding the mechanistic basis of cardiac fibrillation which is preventing effective means to reduce the mortality rates associated with cardiac fibrillation (especially for VF). This strongly motivates the need for developing new engineering methods in understanding mechanisms behind these arrhythmias and translating them to realizable practical solutions to reduce the mortality associated with the arrhythmias. Major bottle necks in decoding the mechanisms behind lethal VF is that SCD occurs within minutes and that in most cases [especially in out-of-the-hospital cardiac arrests (OHCA)] the only immediately available information on the electrical state of the heart is through surface electrocardiograms. In addressing the above knowledge gap, the proposed research program will develop new ways of analyzing and extracting information from multi-channel electrograms and electrocardiograms during arrhythmia and build computer simulation models to decipher the mechanistic insights of cardiac fibrillation. Specifically, the research, in collaboration with Toronto General and St. Michael's Hospitals, will develop advanced data processing and modeling techniques to characterize and regionally locate the sources that initiate and sustain cardiac arrhythmias. The informative clues on these fibrillatory sources will be appropriately translated into electrograms and multi-channel electrocardiogram signal morphologies. These discriminative signal morphologies along with the evolution of the arrhythmia over time will then be used to develop intelligent ablation and defibrillation strategies. The mechanistic knowledge gained through the proposed research program and the developed analysis strategies will significantly augment long-term focused (in-hospital) medical strategies for arrhythmias as well as improve survival rates in OHCA.