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Refractory adenosine-sensitive congenital His bundle tachycardia: response to calcium-channel blockers
K Sharada1, C Narasimhan, K Nageshwar Rao
1Care Hospital, The Institute of Medical Sciences, Nampally, Hyderabad.
Insights
Congenital His bundle tachycardia is a rare pediatric arrhythmia. Calcium-channel blockers are effective when other drugs fail, offering a new treatment avenue for this condition.
Area of Science:
- Pediatric Cardiology
- Electrophysiology
- Arrhythmology
Background:
- Congenital His bundle tachycardia is a rare pediatric arrhythmia.
- Tachycardiomyopathy can result from incessant arrhythmias in children.
Observation:
- A 7-year-old child presented with tachycardiomyopathy due to incessant His bundle tachycardia detected in infancy.
- The arrhythmia was resistant to amiodarone and beta-blockers.
Findings:
- Electrophysiologic study showed conversion to sinus rhythm with intravenous adenosine and diltiazem.
- The child maintained sinus rhythm on oral verapamil.
Implications:
- Calcium-channel blockers represent a viable treatment option for congenital His bundle tachycardia.
- This finding is significant as the arrhythmia often proves resistant to multiple antiarrhythmic drugs.
Abstract:
The congenital form of His bundle tachycardia is an uncommon pediatric arrhythmia. We report the case of a 7-year-old child with tachycardiomyopathy. The incessant arrhythmia, detected in infancy, was resistant to amiodarone and beta-blockers. During electrophysiologic study, the tachycardia converted to sinus rhythm with intravenous adenosine and diltiazem. Subsequently, the child is maintaining sinus rhythm on oral verapamil. Calcium-channel blockers should be considered for the treatment of this arrhythmia, which is often resistant to multiple antiarrhythmic drugs.
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