J Innov Card Rhythm Manag. 2025 Jul 15;16(7):6385-6390. doi: 10.19102/icrm.2025.16074. eCollection 2025 Jul.
ABSTRACT
Hypertrophic cardiomyopathy (HCM) is an inherited disease present in 1 in 500 individuals and is the most common cause of sudden cardiac death in children. We present the case of a 17-year-old boy with HCM and a primary prevention subcutaneous implantable cardioverter-defibrillator (S-ICD) who developed left ventricular outflow tract obstruction and a myocardial bridge of the left anterior descending coronary artery. The patient underwent a septal myectomy/myotomy and muscular bridge unroofing. The S-ICD system was undisturbed during the surgery, with no loss of function. Septal myectomy may be accomplished in pediatric HCM patients following optimal S-ICD placement with maintained S-ICD function.
PMID:40766958 | PMC:PMC12320910 | DOI:10.19102/icrm.2025.16074