Injectable Hydrogel Electrodes to Prevent Ventricular Arrhythmias
Injectable Hydrogel Electrodes to Prevent Ventricular Arrhythmias
批准号:
10583238
负责人:
Elizabeth Marie Cosgriff-Hernandez
金额:
$56.19万
依托单位国家:
美国
项目类别:
财政年份:
2023
资助国家:
美国
项目状态:
未结题
起止时间:
2023-01-05 至 2026-12-31
关键词:
Anti-Arrhythmia AgentsAreaBiocompatible MaterialsCardiacCardiac ablationCardiomyopathiesCathetersCessation of lifeChemistryCicatrixClinicalContrast MediaCoronary VesselsCustomDevelopmentDiseaseElectric CountershockElectric StimulationElectrodesElectrophysiology (science)EngineeringFrequenciesGenetic Complementation TestGrantHeartHeterogeneityHumanHydrogelsImplantable DefibrillatorsIn SituIn VitroInjectableLeadLengthLifeMethodsModelingMyocardial InfarctionMyocardial tissueMyocardiumPacemakersPainPain ThresholdPainlessPhysiologic pulsePositioning AttributeQuality of lifeResearchSafetyScienceShockSiteSourceStimulusStructure of left gastric veinSudden DeathSurfaceSystemTechnologyThickTissuesUnited StatesVenousVenous systemVentricularVentricular ArrhythmiaWorkcardiac resynchronization therapyclinical translationdesignefficacy validationflexibilityflexible electronicsgraspheart rhythmimprovedin vivoin vivo evaluationinnovationminimally invasivenovelporcine modelpreventpsychological traumasafety assessmentstandard of caresudden cardiac deathtool
中文摘要
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英文摘要
Injectable Hydrogel Electrodes to Prevent Ventricular Arrhythmias
In the United States, sudden cardiac death accounts for 350,000 deaths per year with the leading cause being
lethal ventricular arrhythmias. The underlying electrophysiologic derangement mechanistically responsible for
ventricular arrhythmias is delayed conduction velocity in scarred or otherwise diseased myocardium. Access to
the smaller vessels and tributaries that cross over scarred region of the heart could provide improved pacing;
however, there are no pacing leads small enough to navigate these smaller tributaries. In this research, we
propose a novel method to treat and manage ventriculararrhythmias – developmentof a newconductive material
that can fill both large and small coronary vessels and convert these tributaries into flexible electrodes to restore
capture across regions of scarring. Our collaborative team that combines clinical expertise (Razavi) and
biomaterial science (Cosgriff-Hernandez) has demonstrated early feasibility of pacing myocardium with an in situ
curing hydrogel in a pig model. We plan to build on this initial proof of concept to develop a combined material
and delivery system that can interface with existing pacemaker technology to greatly expand their capability to
treat ventricular arrhythmias. Upon successful completion of these aims, we will have utilized a battery of in vitro
and in vivo tests to establish the safety and efficacy of this new injectable hydrogel electrode. Confirmation of
increased activation area as compared to standard-of-care single point pacing will validate the efficacy of this
innovative approach to eliminate the conduction delay in scarred myocardium that results in lethal ventricular
arrhythmias. We will use a post-myocardial infarct model to demonstrate that hydrogel electrode pacing reduces
the frequency of ventricular arrhythmias and defibrillation shocks. Painless stimulation of wide areas of the heart
using planar wavefront propagation from these hydrogel electrodes provides a new cardiac resynchronization
therapy that will alter the landscape of cardiac rhythm management.
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