Ventricular fibrillation (VF) is a leading cause of death in the industrialized world. The only effective treatment for VF is electrical defibrillation. In te US alone, approximately 150,000 patients at high risk of VF receive implantable cardioverter defibrillators (ICDs) each year. The large shocks delivered by ICDs may lead to cardiac damage and anxiety in patients. Significant reductions in defibrillation shock energy may lead to reduced mortality and improved quality of life for ICD patients. The overall goal of this proposal is to develop a clinically relevant defibrillation strategy that significantly lowers the shock energy below the pain and damage thresholds of conventional defibrillation shocks. The main hypothesis of this proposal is that critically timed pacing-level pulses delivered directly to the Purkinje system will capture a critical mass of cardiac tissue and terminate VF. This work builds on recent understanding that the Purkinje system plays and active role in the maintenance of VF, a recent resurgence of work in low-energy defibrillation techniques, and the emergence of clinically available lead systems that directly interface the His-Purkinje system.
The specific aims of this proposal are to: 1) demonstrate that there is an excitable gap in the His-Purkinje system in VF during which pacing pulses capture large regions of fibrillating tissue, 2) determine which low-energy defibrillation algorithm terminates VF with the least amount of energy, and 3) demonstrate the implementation of these techniques in a clinically relevant model that may be integrated into current ICD technology. Completion of these aims will lead to further understanding of the role and importance of the Purkinje system in cardiac arrhythmias. It will demonstrate that low energy defibrillation techniques which have only been demonstrated to be effective in small animal hearts and simulations are effective in larger hearts if the specialized conduction system is used to distribute pacing pulses throughout the working myocardium. The techniques will be developed and tested in normal and heart failure animal models. The end result of this project will be a clinically translatable technique and algorithm for terminating VF with pulse so small that damage and pain from defibrillation therapy with ICDs will be eliminated entirely.

Public Health Relevance

In patients with implantable cardioverter defibrillators (ICDs), tissue damage and patient anxiety may accompany defibrillation shocks. This proposal seeks to develop techniques that make use of the specialized conduction system of the heart to defibrillate with much less energy than current ICD techniques. The techniques and algorithms developed in this proposal will improve mortality, morbidity, and quality of life for patients with ICDs.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
5R01HL128752-04
Application #
9475289
Study Section
Bioengineering, Technology and Surgical Sciences Study Section (BTSS)
Program Officer
Tinsley, Emily
Project Start
2015-07-01
Project End
2020-04-30
Budget Start
2018-05-01
Budget End
2019-04-30
Support Year
4
Fiscal Year
2018
Total Cost
Indirect Cost
Name
University of Utah
Department
Biomedical Engineering
Type
Biomed Engr/Col Engr/Engr Sta
DUNS #
009095365
City
Salt Lake City
State
UT
Country
United States
Zip Code
84112
Yamashita, Kennosuke; Hu, Nan; Ranjan, Ravi et al. (2018) Clinical Risk Factors for Postoperative Atrial Fibrillation among Patients after Cardiac Surgery. Thorac Cardiovasc Surg :
Thomas, Samuel; Silvernagel, Josh; Angel, Nathan et al. (2018) Higher contact force during radiofrequency ablation leads to a much larger increase in edema as compared to chronic lesion size. J Cardiovasc Electrophysiol 29:1143-1149
Ghafoori, Elyar; Kholmovski, Eugene G; Thomas, Sam et al. (2017) Characterization of Gadolinium Contrast Enhancement of Radiofrequency Ablation Lesions in Predicting Edema and Chronic Lesion Size. Circ Arrhythm Electrophysiol 10:
Panitchob, Nuttanont; Li, Li; Huang, Jian et al. (2017) Endocardial Activation Drives Activation Patterns During Long-Duration Ventricular Fibrillation and Defibrillation. Circ Arrhythm Electrophysiol 10:
Huang, Shangwei; Wu, Liqun; Huang, Jian et al. (2017) Restitution characteristics of His bundle and working myocardium in isolated rabbit hearts. PLoS One 12:e0186880
Warren, Mark; Zaitsev, Alexey V (2017) CaMKII blockade, cardiac conduction, and arrhythmia. Cardiovasc Res 113:1798-1799
Polejaeva, Irina A; Ranjan, Ravi; Davies, Christopher J et al. (2016) Increased Susceptibility to Atrial Fibrillation Secondary to Atrial Fibrosis in Transgenic Goats Expressing Transforming Growth Factor-?1. J Cardiovasc Electrophysiol 27:1220-1229
Angel, Nathan; Li, L I; Macleod, Rob S et al. (2015) Diverse Fibrosis Architecture and Premature Stimulation Facilitate Initiation of Reentrant Activity Following Chronic Atrial Fibrillation. J Cardiovasc Electrophysiol 26:1352-60