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Published on: December 11, 2017
Usefulness of QRS axis change to predict mortality in patients with left bundle branch block
Parin J Patel1, Ralph J Verdino
1Hospital of the University of Pennsylvania, Philadelphia, PA, USA. parin.patel1@uphs.upenn.edu
Insights
Left bundle branch block (LBBB) with left-axis deviation (LAD) does not increase mortality risk. However, developing LAD after a normal axis in LBBB patients indicates significantly higher mortality, suggesting a potential prognostic indicator.
Area of Science:
- Cardiology
- Electrocardiography
- Prognostic Biomarkers
Background:
- Left bundle branch block (LBBB) is associated with poor prognosis, but the prognostic value of left-axis deviation (LAD) in LBBB patients remains unclear.
- Existing research highlights QRS duration's correlation with outcomes in LBBB, necessitating further investigation into other electrocardiographic markers like LAD.
Purpose of the Study:
- To investigate whether left-axis deviation (LAD) confers an independent mortality risk in patients diagnosed with left bundle branch block (LBBB).
- To identify significant risk factors for all-cause mortality in a cohort of patients with LBBB.
Main Methods:
- A retrospective, population-based cohort study including 2,794 patients with LBBB over a 17-year follow-up period.
- Analysis of all-cause mortality rates and time-to-event data, assessing the association of LAD with mortality.
- Bivariate analysis to identify factors associated with LAD, including atrial fibrillation, ventricular tachycardia, age, and congestive heart failure.
Main Results:
- Left-axis deviation (LAD) was present in 50% of patients with left bundle branch block (LBBB) and was not independently associated with increased all-cause mortality.
- Significant mortality risk factors identified included elevated creatinine, low hemoglobin, history of atrial fibrillation, prior myocardial infarction, and ventricular tachycardia.
- Patients with LBBB who developed LAD from a normal axis during follow-up exhibited significantly higher mortality (p = 0.02).
Conclusions:
- Left-axis deviation (LAD) does not appear to be an independent predictor of mortality in patients with left bundle branch block (LBBB).
- The development of LAD in patients with a pre-existing normal axis and LBBB may indicate a worse prognosis, warranting further investigation into the underlying mechanisms.
- While concurrent LBBB and LAD may not increase risk, a change to LAD may signal a poorer outcome in LBBB patients.
Abstract:
QRS duration correlates with poor prognosis in patients with left bundle branch block (LBBB), but the importance of left-axis deviation (LAD) is not well established. To determine if LAD confers a mortality risk in patients with LBBB, a single-center, retrospective, population-based cohort study was conducted. Included were all patients at 1 hospital with LBBB on electrocardiography from 1995 to 2005 over a 17-year follow-up period (n = 2,794, median follow-up duration 20 months, interquartile range 6 to 64). Half of all patients with LBBB had LAD. The all-cause mortality rate in the entire cohort was 15%. LAD was not associated with mortality, either as a single outcome (odds ratio [OR] 1.1, 95% confidence interval [CI] 0.88 to 1.3, p = 0.50) or in time-to-event analysis (p = 0.40). Significant risk factors for mortality included high creatinine (OR 1.2, 95% CI 1.1 to 1.3), low hemoglobin (OR 1.2, 95% CI 1.1 to 1.3), history of atrial fibrillation (OR 1.6, 95% CI 1.3 to 2.1), electrocardiographic evidence of previous infarct (OR 1.5, 95% CI 1.2 to 1.9), and history of ventricular tachycardia (OR 1.4, 95% CI 1.0 to 1.9). On bivariate analysis, LAD was associated with atrial fibrillation, ventricular tachycardia, age, and congestive heart failure. Patients with LBBB who converted from normal axis to LAD had significantly higher mortality in time-to-event analysis (p = 0.02). In conclusion, in patients with LBBB, LAD does not confer significant mortality risk. However, those with normal axis who developed LAD during the study period had significantly higher mortality. Perhaps when LBBB and LAD develop concurrently, there is no increased risk over baseline LBBB development, but it may herald a worse prognosis if LAD develops against the background of previous LBBB, from an unknown mechanism.
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