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Updated: Aug 11, 2026

Robotic Ablation of Atrial Fibrillation
Published on: May 29, 2015
Insights
Idiopathic bilateral bundle branch fibrosis is the most frequent cause of permanent atrioventricular block, accounting for 33% of cases. Other causes include ischemic damage, calcific atrioventricular block, and cardiomyopathies.
Area of Science:
- Cardiology
- Pathology
Background:
- Permanent atrioventricular (A-V) block is a significant clinical condition with diverse underlying causes.
- Understanding the etiology of A-V block is crucial for diagnosis and management.
Purpose of the Study:
- To identify and quantify the common causes of permanent A-V block in a cohort of 177 patients.
- To delineate the spectrum of idiopathic bundle branch fibrosis, including Lev's and Lenègre's diseases.
Main Methods:
- Retrospective analysis of 177 cases of permanent A-V block.
- Categorization of causes based on pathological findings and clinical data.
Main Results:
- Idiopathic bilateral bundle branch fibrosis was the most common cause (33%), encompassing Lev's and Lenègre's diseases.
- Ischemic damage accounted for 17% of cases, often following septal infarction.
- Calcific A-V block (10%) and cardiomyopathies (14%) were other significant etiological categories.
- Numerous other rare causes were identified, including tumors, congenital defects, and iatrogenic damage.
Conclusions:
- Idiopathic bilateral bundle branch fibrosis is the predominant cause of permanent A-V block.
- A comprehensive etiological workup is necessary for chronic A-V block, considering both common and rare causes.
Abstract:
Study of 177 cases of permanent A-V block shows idiopathic bilateral bundle branch fibrosis to be the commonest single cause (33%). This entity covers a spectrum of localised loss of conduction fibres in the proximal left bundle branch and bifurcating main bundle (Lev's disease) to moore periphery loss of conduction fibres in the bundle branches alone (Lenègre's disease). The aetiological factors in idiopathic bundle branch fibrosis are still obscure. Ischaemic damage is responsible for 17% of cases and are usually patients who have survived destruction of the bundle branches in septal infarction. Calcific A-V block is the term applied to destruction of the main bundle by large masses of calcification in the mitral or aortic valve rings and is responsible for 10% of cases of chronic A-V block. The mass of calcium is visible to the naked eye at autopsy or by X ray in life. Cardiomyopathies of all types (except hypertrophic obstructive cardiomyopathy) involve the conduction system and produce 14% of cases of A-V block. The remaining numerous causes of chronic A-V block are individually very rare ranging through tumour involvement, congenital defects, collagen diseases and surgical or traumatic damage.
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