Predictive Factors for New-Onset Left Bundle Branch Block in Patients with Left Ventricular Systolic Dysfunction and
Mu-Zhang Li1, Jia-Ying Chen1, Shu-Fang Chen1
1Central China Fuwai Hospital of Zhengzhou University, Fuwai Central China Cardiovascular Hospital.
In patients with left ventricular systolic dysfunction (LVSD), dilated cardiomyopathy (DCM), coronary artery disease (CAD), and paroxysmal atrial fibrillation (PAF) predict new-onset left bundle branch block (LBBB). New LBBB indicates a poorer prognosis.
Area of Science:
- Cardiology
- Electrophysiology
- Heart Failure Research
Background:
- Left ventricular systolic dysfunction (LVSD) is associated with structural heart changes.
- The relationship between ventricular remodeling and the development of left bundle branch block (LBBB) in LVSD requires further clarification.
Purpose of the Study:
- To investigate the predictors of new-onset LBBB in patients with LVSD.
- To evaluate the prognostic implications of new-onset LBBB in this patient cohort.
Main Methods:
- Prospective study enrolling 801 hospitalized patients with LVSD (ejection fraction < 50%).
- Assessed new-onset LBBB and a composite endpoint including heart failure hospitalization, mortality, ventricular tachycardia, or ICD/CRT implantation.
- Utilized multivariate Cox regression and Kaplan-Meier survival analysis.
Main Results:
- New-onset LBBB occurred in 10.1% of patients over a median follow-up of 56 months.
- Independent predictors of new LBBB included dilated cardiomyopathy (DCM), coronary artery disease (CAD), paroxysmal atrial fibrillation (PAF), increased QRS duration, and left ventricular end-diastolic dimension (LVEDD).
- New-onset LBBB was associated with significantly higher rates of adverse outcomes, including composite endpoints, heart failure hospitalizations, and ventricular arrhythmias requiring device implantation.
Conclusions:
- DCM, LVEDD, CAD, PAF, and QRS duration are significant predictors for developing LBBB in LVSD patients.
- New-onset LBBB serves as an independent marker for a poor prognosis in patients with LVSD.
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