Restoration of Cardiac Function in Left Bundle Branch Block-Induced Cardiomyopathy via Conduction System Pacing: A
Jing Wang1, Bing Han2, Xiaojuan Wang2
1Department of Geriatrics, The First Hospital of Lanzhou University, Lanzhou, Gansu, China.
Insights
Left bundle branch block-induced cardiomyopathy (LIC) can cause heart dysfunction. Conduction system pacing (CSP) effectively restored cardiac function in a patient with LIC, highlighting the importance of early diagnosis and intervention.
Area of Science:
- Cardiology
- Electrophysiology
Background:
- Left bundle branch block (LBBB) can lead to left ventricular dysfunction, termed left bundle branch block-induced cardiomyopathy (LIC), in the absence of other causes.
- LIC presents with progressive dyspnea and reduced exercise tolerance, accompanied by a decline in left ventricular ejection fraction (LVEF).
Purpose of the Study:
- To present a case of LIC diagnosed within one year of LBBB onset.
- To evaluate the efficacy of conduction system pacing (CSP) in restoring cardiac function in a patient with LIC.
Main Methods:
- A 57-year-old woman with new-onset LBBB developed symptoms of heart failure and reduced LVEF.
- Diagnostic workup excluded other etiologies and revealed interventricular mechanical dyssynchrony consistent with LIC.
- The patient underwent conduction system pacing (CSP) for cardiac resynchronization therapy after medical therapy failed.
Main Results:
- The patient's LVEF declined from 55% to 31% within a year of LBBB onset.
- Following CSP, LVEF improved to 54% at 6 months and 56% at 30 months, indicating near-normalization.
- Symptoms of dyspnea and reduced exercise tolerance resolved post-pacing.
Conclusions:
- LIC is a distinct clinical entity characterized by LBBB-associated ventricular dysfunction and dyssynchrony.
- CSP demonstrates significant potential in correcting electrical dyssynchrony and improving cardiac function in LIC patients.
- Early diagnosis and prompt intervention with CSP are crucial for favorable outcomes in LIC.
Abstract:
BACKGROUND Left bundle branch block (LBBB) is not uncommon. In certain cases, patients with LBBB exhibit a deterioration of cardiac function, ultimately progressing to a clinical phenotype resembling cardiomyopathy in the absence of an alternative etiology, a condition referred to as left bundle branch block-induced cardiomyopathy (LIC). We present a case of a 57-year-old woman who developed LIC 1 year after the onset of new LBBB. Following conduction system pacing (CSP), her cardiac function was completely restored. CASE REPORT A 57-year-old woman presented with normal electrocardiograms (ECGs) and heart function 1 year prior. After developing LBBB, she experienced progressive dyspnea and reduced exercise tolerance over the subsequent year, during which her left ventricular ejection fraction (LVEF) declined from 55% to 31%. A comprehensive diagnostic workup revealed interventricular mechanical dyssynchrony and excluded ischemic or structural etiologies, which is consistent with LIC. Guideline-directed medical therapy was initiated; however, her symptoms persisted after 6 months of therapy. Following CSP for cardiac resynchronization therapy, the patient's LVEF improved to 54% at 6 months and further increased to 56% at 30 months, approaching normalization. CONCLUSIONS LIC is a recently identified condition wherein patients with LBBB experience left ventricular dysfunction and mechanical dyssynchrony without an alternative etiology. Emerging evidence indicates that CSP may effectively correct the electrical dyssynchrony associated with LBBB. We present a case of a patient diagnosed with LIC within 1 year of symptom onset, who exhibited significant improvement following CSP treatment. This case highlights the critical importance of early diagnosis and timely intervention.
Related Concept Videos
Cardiomyopathy II: Dilated Cardiomyopathy
Cardiomyopathy V: Interprofessional Care
Cardiomyopathy III: Hypertrophic Cardiomyopathy
Conduction System of the Heart
This system relies on the unique properties of nodal and Purkinje cells:...


