Right, but not left, bundle branch block is associated with large anteroseptal scar

David G Strauss1, Zak Loring, Ronald H Selvester

  • 1Office of Science and Engineering, Center for Devices and Radiological Health, U.S. Food and Drug Administration, Silver Spring, Maryland, USA. david.strauss@fda.hhs.gov

Insights

Right bundle branch block (RBBB) is linked to larger heart scar size compared to left bundle branch block (LBBB) in patients with reduced ejection fraction. This suggests RBBB may result from more extensive damage, often from coronary artery issues.

Area of Science:

  • Cardiology
  • Electrophysiology
  • Cardiac Imaging

Background:

  • The right bundle branch (RBB) and left anterior fascicle are typically supplied by the left anterior descending (LAD) coronary artery.
  • Occlusion of the LAD coronary artery is thus expected to cause RBBB rather than LBBB.

Purpose of the Study:

  • To investigate the hypothesis that patients with RBBB have a larger cardiac scar size than those with LBBB.
  • To compare scar size and location in patients with RBBB, LBBB, and other conduction delays.

Main Methods:

  • Electrocardiograms and cardiac magnetic resonance imaging were used for scar quantification in 233 patients with left ventricular ejection fraction ≤35%.
  • A secondary cohort of 20 hypertrophic cardiomyopathy patients undergoing alcohol septal ablation was studied to induce controlled myocardial infarction.

Main Results:

  • RBBB patients exhibited significantly larger scar size (24.0%) compared to LBBB patients (6.5%) in the primary cohort.
  • Patients with RBBB were more likely to have ischemic heart disease (79% vs. 29%).
  • In the ablation cohort, 75% developed RBBB, while none developed LBBB.

Conclusions:

  • RBBB in patients with reduced ejection fraction is associated with significantly larger scar burden than LBBB.
  • Occlusion of a proximal LAD septal perforator is a cause of RBBB, often linked to ischemic heart disease.
  • LBBB is more frequently associated with non-ischemic etiologies.
Abstract

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