2021
DOI: 10.1111/jce.15255
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Etiology and device therapy in complete atrioventricular block in pediatric and young adult population: Contemporary review and new perspectives

Abstract: Complete atrioventricular block (CAVB) is a total dissociation between the atrial and ventricular activity, in the absence of atrioventricular conduction. Several diseases may result in CAVB in the pediatric and young-adult population. Permanent right ventricular (RV) pacing is required in permanent CAVB, when the cause is neither transient nor reversible. Continuous RV apical pacing has been associated with unfavorable outcomes in several studies due to the associated ventricular dyssynchrony. This study aims… Show more

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Cited by 7 publications
(5 citation statements)
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“…Among arrhythmic disorders, we identified nine cases of thirddegree AV block, with an estimated incidence of 1 per 5,000 live births, which was higher than in a previous study (20). The risk of third-degree AV block was 10-fold higher in the SLE mother group.…”
Section: Discussionmentioning
confidence: 55%
“…Among arrhythmic disorders, we identified nine cases of thirddegree AV block, with an estimated incidence of 1 per 5,000 live births, which was higher than in a previous study (20). The risk of third-degree AV block was 10-fold higher in the SLE mother group.…”
Section: Discussionmentioning
confidence: 55%
“…Complete atrioventricular block (CAVB) is a life-threatening condition that requires prompt diagnosis and treatment. The most common causes of CAVB are degenerative changes of the conduction system, myocardial infarction, cardiac surgery, and drugs [ 1 ]. Coronary spasm is a rare cause of CAVB that can be triggered by various factors such as emotional stress, hyperventilation, cold exposure, smoking, and cocaine use.…”
Section: Introductionmentioning
confidence: 99%
“…In these, progressive cardiac conduction disease has sometimes been seen and associated mutations have been identified in genes including SCN1B, SCN5A, SCN10A, TRPM4, and KCNK17. Additionally, abnormalities in NKX2.5 and Tbx5 have been associated with conduction abnormalities at times with congenital heart disease 1,2 …”
Section: Introductionmentioning
confidence: 99%
“…Additionally, abnormalities in NKX2.5 and Tbx5 have been associated with conduction abnormalities at times with congenital heart disease. 1,2 Mutations in the Titin (TTN) gene is one of the leading causes of dilated cardiomyopathy (DCM) in adults and has also been associated with atrial fibrillation (AF). 3,4 There has not been a prior association with complete heart block or other primary conduction disease.…”
mentioning
confidence: 99%