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Grant: Collaborative Health Research Projects

Simon Fraser University

$117,250.00

Optical mapping of the neonate heart to determine the etiology of Junctional Ectopic Tachycardia

EF 2012-13

Résumé
Junctional Ectopic Tachycardia (JET) is a supraventricular tachycardia that occurs post-operatively after open heart surgery in young children. JET can occur in >20% of patients undergoing correction for specific congenital heart defects and is associated with significant morbidity and mortality. Since the etiology of JET is not understood, clinical treatment often lacks efficacy and often results in poor patient outcomes. Cardiac synchrony is maintained by a complex arrangement of primary and secondary pacemaking foci. These foci communicate with the rest of the myocardium through electrical conduction pathways and it is this co-ordinated communication that ensures cardiac synchrony and adequate blood flow to the brain and to the rest of the body. Electrical propagation in the heart is directional: electrical wave fronts do not spread evenly in all directions but rather follow electrical pathways formed by various heart tissues. Electrical conduction follows the myofibril alignment of the heart muscle and surgery may disrupt these conduction pathways. In the absence of primary pacemaker activity, secondary and or ectopic pacemaking sites may further disrupt cardiac synchrony. However, neither electrical conduction nor myofibril alignment is easily detected. An instrument that can visualize both electrical conduction pathways as well as the cardiac tissue that delineates these conduction pathways is required to minimize dyssynchrony. Two separate technologies exist that can visualize these respective attributes. Fluorescent optical action potential mapping (APM) can resolve electrical conduction pathways and optical coherence tomography (OCT) can resolve myofibril alignments. Optical mapping is a fluorescent imaging technique that replaces the traditional microelectrode with a voltage-sensitive dye and a high performance digital camera. The fluorescent dye encodes changes in cellular membrane potential into changes in cellular fluorescence and provides non-contact action potential recordings. Optical coherence tomography utilizes back-scattered light, similar to the acoustical reflections used in ultrasound imaging devices, and creates a depth-resolved image indicating tissue type and myofibril direction as a function
Programme
Collaborative Health Research Projects
Emplacement
British Columbia, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
NSERC's Awards Data

Tel que publié

Application id
399237-2011
Name nom
Tibbits, Glen
Department département
Biomedical Physiology and Kinesiology
Organization id
5
Institution établissement
Simon Fraser University
Province en
British Columbia
Province fr
Colombie-Britannique
Country en
CANADA
Country fr
CANADA
Fiscal year exercice financier
2012
Competition year année de concours
2011
Award amount
117250
Program id
CHRPJ
Program name en
Collaborative Health Research Projects
Program name fr
Projets de recherche concertée sur la santé
Group en
Discovery grants programs
Group fr
Programmes de subventions à la découverte
Committee code
360
Committee name en
Collaborative Health Research Projects Selection Panel
Committee name fr
Comité de sélection de projets de recherche concertée sur la santé
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
5506
Research subject group en
Animal biology
Research subject group fr
Biologie animale
Research subject en
Animal circulation
Research subject fr
Circulation animale
Partie
2
Nb partie
3
Application title
Optical mapping of the neonate heart to determine the etiology of Junctional Ectopic Tachycardia
Keyword
NSERC
Application summary
Junctional Ectopic Tachycardia (JET) is a supraventricular tachycardia that occurs post-operatively after open heart surgery in young children. JET can occur in >20% of patients undergoing correction for specific congenital heart defects and is associated with significant morbidity and mortality. Since the etiology of JET is not understood, clinical treatment often lacks efficacy and often results in poor patient outcomes. Cardiac synchrony is maintained by a complex arrangement of primary and secondary pacemaking foci. These foci communicate with the rest of the myocardium through electrical conduction pathways and it is this co-ordinated communication that ensures cardiac synchrony and adequate blood flow to the brain and to the rest of the body. Electrical propagation in the heart is directional: electrical wave fronts do not spread evenly in all directions but rather follow electrical pathways formed by various heart tissues. Electrical conduction follows the myofibril alignment of the heart muscle and surgery may disrupt these conduction pathways. In the absence of primary pacemaker activity, secondary and or ectopic pacemaking sites may further disrupt cardiac synchrony. However, neither electrical conduction nor myofibril alignment is easily detected. An instrument that can visualize both electrical conduction pathways as well as the cardiac tissue that delineates these conduction pathways is required to minimize dyssynchrony. Two separate technologies exist that can visualize these respective attributes. Fluorescent optical action potential mapping (APM) can resolve electrical conduction pathways and optical coherence tomography (OCT) can resolve myofibril alignments. Optical mapping is a fluorescent imaging technique that replaces the traditional microelectrode with a voltage-sensitive dye and a high performance digital camera. The fluorescent dye encodes changes in cellular membrane potential into changes in cellular fluorescence and provides non-contact action potential recordings. Optical coherence tomography utilizes back-scattered light, similar to the acoustical reflections used in ultrasound imaging devices, and creates a depth-resolved image indicating tissue type and myofibril direction as a function