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Benefits of Cardiac Resynchronization Therapy in an Asynchronous Heart Failure Model Induced by Left Bundle Branch Ablation and Rapid Pacing
Published on: December 11, 2017
Hemodynamic implications of left bundle branch block
1Department of Internal Medicine and the Sanger Clinic, P.A., Carolinas Medical Center, Charlotte, NC 28232, USA. LLittmann@carolinas.org
Insights
Left bundle branch block (LBBB) significantly impacts heart function, causing hemodynamic changes and ventricular remodeling. Research explores LBBB
Area of Science:
- Cardiology
- Electrophysiology
- Cardiovascular Medicine
Background:
- Left bundle branch block (LBBB) is traditionally an electrophysiologic finding.
- LBBB is increasingly recognized for its significant hemodynamic effects and role in ventricular remodeling.
- LBBB is associated with impaired systolic and diastolic function, particularly in dilated cardiomyopathy (DCM).
Purpose of the Study:
- To explore the hemodynamic effects of LBBB.
- To investigate the relationship between LBBB and ventricular remodeling, myocardial ischemia, and asynergy.
- To examine the impact of LBBB on patients with dilated cardiomyopathy (DCM) and potential benefits of interventions.
Main Methods:
- Review of existing literature on LBBB and its hemodynamic consequences.
- Analysis of exercise nuclear studies showing perfusion defects in LBBB patients.
- Observational comparison of DCM patients with and without LBBB.
Main Results:
- LBBB causes asynchronous myocardial activation, potentially leading to ventricular remodeling.
- Reversible perfusion defects and angina can occur in LBBB patients, possibly due to asynergy.
- DCM patients with LBBB exhibit progressive LV dilatation, mitral regurgitation, and poorer outcomes.
Conclusions:
- LBBB has profound hemodynamic effects beyond its electrophysiologic definition.
- The interplay between LBBB, ischemia, and ventricular dysfunction requires further elucidation.
- Interventions aimed at normalizing ventricular activation sequences, such as pacing, show promise for DCM patients with LBBB.
Abstract:
Left bundle branch block (LBBB), traditionally viewed as an electrophysiologic abnormality, is increasingly recognized for its profound hemodynamic effects. LBBB causes asynchronous myocardial activation, which, in turn, may trigger ventricular remodeling. Exercise nuclear studies frequently show reversible perfusion defects in the absence of obstructive coronary artery disease and some patients with intermittent LBBB develop angina coincident with the onset of LBBB. It is uncertain, however, if these phenomena are because of myocardial ischemia or ventricular asynergy. LBBB is associated with impaired systolic and diastolic function. In patients with dilated cardiomyopathy (DCM), LBBB is accompanied by progressive left ventricular (LV) dilatation and mitral regurgitation. It is not known whether LBBB is the cause or the consequence of LV dilatation. DCM patients with LBBB, as compared to those with normal intraventricular conduction, are more likely to have a nonischemic etiology, profound LV dilatation, lower ejection fraction, increased symptomatology, and shorter survival. Patients with DCM and acceleration-dependent LBBB may benefit from restoration of a narrow QRS complex by suppressing the heart rate with beta-blocker. There is extensive research underway in patients with DCM and LBBB to evaluate the short and long-term effects of normalization of ventricular activation sequence with high septal, LV, or biventricular pacing.
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