Idiopathic/Iatrogenic Left Bundle Branch Block-Induced Reversible Left Ventricle Dysfunction: JACC State-of-the-Art
Vincent Auffret1, Raphaël P Martins1, Claude Daubert2
1Université de Rennes1-Faculté de Médecine, Rennes, France; Service de Cardiologie, Centre Hospitalier Universitaire, Rennes, France; LTSI-INSERM U1099, Rennes, France.
Idiopathic or iatrogenic left bundle branch block (LBBB) causes ventricular dyssynchrony and dysfunction. Cardiac resynchronization therapy (CRT) may reverse these effects and prevent heart failure progression in at-risk patients.
Area of Science:
- Cardiology
- Electrophysiology
- Heart Failure Research
Background:
- Left bundle branch block (LBBB) creates electro-mechanical ventricular dyssynchrony.
- Chronic LBBB in animal models leads to progressive left ventricular (LV) dysfunction and structural remodeling.
- Human LBBB presents as chronic isolated LBBB or acute iatrogenic LBBB post-aortic valve interventions.
Purpose of the Study:
- To explore the impact of LBBB on ventricular function and remodeling.
- To evaluate the potential of cardiac resynchronization therapy (CRT) in managing LBBB-induced cardiac issues.
- To identify the need for further research and clinical trials in specific patient populations.
Main Methods:
- Review of chronic animal models of LBBB.
- Analysis of human LBBB dyssynchronopathy models.
- Discussion of existing evidence and proposed future studies.
Main Results:
- Isolated LBBB induces reversible structural remodeling and LV dysfunction in animal models.
- LBBB-induced cardiomyopathy is presumed in humans, potentially benefiting from CRT.
- Current epidemiological and clinical data require strengthening.
Conclusions:
- LBBB-induced cardiomyopathy is a potential concern in humans, warranting further investigation.
- CRT may be beneficial for patients with LBBB, particularly after aortic valve interventions.
- Large cohort studies and randomized CRT trials are needed to confirm incidence, evolution, and efficacy.
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