Natural history and clinical significance of isolated complete left bundle branch block without associated structural
Hasan Ashraf1, Pradyumna Agasthi1, Robert J Siegel2
1Department of Cardiovascular Medicine, Mayo Clinic; Phoenix, Arizona-United States.
Insights
Isolated Left Bundle Branch Block (LBBB) without heart disease has a low risk of mortality and cardiomyopathy. This study clarifies the clinical significance of LBBB in patients without underlying cardiac conditions.
Area of Science:
- Cardiology
- Electrophysiology
- Heart Failure Research
Background:
- Left bundle branch block (LBBB) is linked to cardiac disease and may contribute to cardiomyopathy via conduction delays and dyssynchrony.
- The independent role of LBBB in mortality and heart failure development remains unclear.
- Previous studies have not definitively established the clinical significance of isolated LBBB.
Purpose of the Study:
- To investigate the natural history of isolated LBBB in patients without structural heart disease.
- To determine the clinical significance and long-term outcomes of isolated LBBB.
- To assess the association of isolated LBBB with mortality and cardiomyopathy development.
Main Methods:
- Retrospective chart review of patients with complete LBBB and normal echocardiograms.
- Exclusion of patients with coronary artery disease, structural heart disease, or cardiac devices.
- Evaluation of mortality, cardiomyopathy incidence, and heart failure hospitalizations over 1 and 10 years.
Main Results:
- 2522 eligible patients were identified with a mean follow-up of 8.4 years.
- 10-year mortality rate was 22.0% and cardiomyopathy incidence was 9.1%.
- No significant difference in QRS duration was observed between deceased and alive patients, or between those with and without cardiomyopathy.
Conclusions:
- Isolated LBBB in the absence of structural heart disease, ventricular dysfunction, or CAD is associated with a low mortality rate.
- The incidence of cardiomyopathy is also low in patients with isolated LBBB.
- This finding suggests that isolated LBBB may not be an independent predictor of adverse cardiac events when other cardiac pathologies are absent.
Objective:
Left bundle branch block (LBBB), which is associated with underlying cardiac disease, is believed to play a role in the pathogenesis of cardiomyopathy through delays in interventricular conduction, leading to dyssynchrony. However, this has not been established in previous studies. It is unclear whether LBBB indicates clinically advanced cardiac disease or is an independent factor responsible for increased mortality and the development of heart failure. We investigated the natural history of isolated LBBB without any associated structural heart disease in order to determine its clinical significance.
Methods:
We performed a retrospective chart review on consecutive patients who fulfilled the 12-lead electrocardiographic (ECG) criteria for complete LBBB and had a normal echocardiogram with no evidence of structural heart disease and left or right ventricular systolic dysfunction within three months of the initial ECG between January 1, 2000 and December 31, 2009. We excluded patients with documented coronary artery disease (CAD) at any time, any structural heart disease, or cardiac devices. We evaluated the primary endpoints of mortality and incidence of cardiomyopathy, as well as any heart failure hospitalizations over a 1- and 10-year period.
Results:
We identified 2522 eligible patients. The mean follow-up duration was 8.4±3.2 years. The one-year mortality rate was 7.8%, with a 10-year mortality rate of 22.0%. The incidence of cardiomyopathy over one year was 3.2% and over 10 years was 9.1%. There was no significant difference in QRS duration between patients who were alive and those that were deceased at 10 years (141+/-18 vs. 141+/-17 ms; p=0.951) and patients with and without cardiomyopathy at 10 years (142±17 vs. 141±17 ms; p=0.532).
Conclusion:
Isolated LBBB occurring without structural heart disease, ventricular dysfunction, or CAD is associated with a low mortality rate and incidence of cardiomyopathy.
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