Key result
Computational models of cardiac electrophysiology, electromechanics, and hemodynamics provide insights into heart failure pathology and have the potential to optimize cardiac resynchronization therapy.
Computational modeling of the heart holds potential as a clinical tool to personalize and optimize cardiac resynchronization therapy, aiming to reduce the 40-50% non-responder rate.
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May support computational modeling for CRT personalization; leaves open prospective validation before clinical adoption.
Cardiac resynchronization therapy (CRT) is an effective treatment for heart failure (HF) patients with an electrical substrate pathology causing ventricular dyssynchrony. However 40-50% of patients do not respond to treatment. Cardiac modeling of the electrophysiology, electromechanics, and hemodynamics of the heart has been used to study mechanisms behind HF pathology and CRT response. Recently, multi-scale dyssynchronous HF models have been used to study optimal device settings and optimal lead locations, investigate the underlying cardiac pathophysiology, as well as investigate emerging technologies proposed to treat cardiac dyssynchrony. However the breadth of patient and experimental data required to create and parameterize these models and the computational resources required currently limits the use of these models to small patient numbers. In the future, once these technical challenges are overcome, biophysically based models of the heart have the potential to become a clinical tool to aid in the diagnosis and treatment of HF.
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Lee et al. (2018) conducted a review in Heart failure and left bundle branch block (LBBB). Computational Modeling for Cardiac Resynchronization Therapy was evaluated. Computational models of cardiac electrophysiology, electromechanics, and hemodynamics provide insights into heart failure pathology and have the potential to optimize cardiac resynchronization therapy.
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