[LEFT HIS BUNDLE BRANCH BLOCK ASSOCIATED WITH LEFT VENTRICULAR TORSION AND REDUCED EJECTION FRACTION]
Insights
Left His bundle branch block (LBBB) significantly impairs left ventricular (LV) torsion and increases mechanical desynchronization in cardiomyopathy patients. This study reveals LBBB negatively affects LV electrical activation and contractility, leading to abnormal torsion.
Area of Science:
- Cardiology
- Electrophysiology
- Cardiac Mechanics
Context:
- Left His bundle branch block (LBBB) is common in cardiomyopathy patients.
- Its impact on left ventricular (LV) torsion and mechanics is not fully understood.
- Cardiomyopathy is defined as LV ejection fraction less than 40%.
Purpose:
- To evaluate the influence of LBBB on LV torsion.
- To assess the hemodynamic consequences of LBBB-induced changes in LV torsion.
- To investigate the relationship between LBBB, LV rotation, and mechanical desynchronization.
Summary:
- Sixty-four cardiomyopathy patients (ischemic and dilated) were studied, divided into groups with narrow and LBBB (middle QRS duration: 153 ms).
- Despite similar LV contractility, LBBB patients exhibited significantly reduced LV rotation and torsion (2.95 ± 3.34 vs. 5.87 ± 3.83, p < 0.01).
- LBBB was associated with more abnormal unidirectional rotation (50% vs. 21.9%, p < 0.001) and greater posterior wall contractility delay (63.3 ± 35.1 ms vs. 8.0 ± 17.9 ms, p < 0.001), indicating increased mechanical desynchronization.
Impact:
- LBBB negatively affects LV electrical activation and contractility.
- LBBB results in abnormal LV torsion and increased mechanical desynchronization.
- Findings highlight the detrimental role of LBBB in cardiac mechanics for cardiomyopathy patients.
Abstract:
The influence of left His bundle branch block (LBBB) on left ventricular (LV) torsion in patients with cardiomyopathy remains to be elucidated. The aim of this study was to evaluate LV torsion associated with LBBB and hemodynamic consequences of possible changes. We studied 64 patients with ischemic and dilatation cardiomyopathy (LV ejection fraction less than 40%) divided into 2 groups, with narrow and middle (153 ms) duration QRS complexes. Despite similar LV contractility, patients with LBBB had much less pronounced LV rotation and torsion. Torsion in patients with LBBB and narrow QRS complex was estimated at 2.95 ± 3.34 and 5.87 ± 3.83 respectively (p < 0.01). Moreover; the group of patients with LBBB contained much more subjects with abnormal unidirectional rotation of the basal and apical parts than the group with narrow QRS complex, namely 11 (50%) and 9 (21.9%) respectively (p < 0.001). Patients with LBBB and abnormal LV rotation sowed much longer delay of posterior wall contractility (63.3 ± 35.1 mc) compared with those having LBBB and multidirectional physiological LV rotation (8.0 ± 17/9 mc) (p < 0.001) which suggests a higher degree of mechanical desynchronization. T is concluded that LBBB has negative effect on LV electrical activation and contractility resulting in abnormal torsion and mechanical desynchronization.
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