Combined leadless pacing and subcutaneous defibrillation strategy in a high-risk patient: first case report from Peru

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We present the case of a 51-year-old male with non-ischemic dilated cardiomyopathy and complete atrioventricular block, who was previously implanted with a cardiac resynchronization therapy defibrillator. The patient developed signs of pocket infection with a high risk of extrusion. Partial system e...

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Detalles Bibliográficos
Autores: Vallejos-Barrientos, Alexis, Davila-Flores, Diego, Soto-Becerra, Richard, Cabrera-Saldaña, Mario, Guevara-Caicedo, Carolina, Gonzales-Luna , Ana Cecilia, Cueva-Parra, Ángel, Payano-Rojas, Marisel, Zelaya-Castro, Pío
Formato: artículo
Fecha de Publicación:2025
Institución:Instituto Nacional Cardiovascular
Repositorio:Archivos peruanos de cardiología y cirugía cardiovascular
Lenguaje:inglés
OAI Identifier:oai:apcyccv.org.pe:article/513
Enlace del recurso:https://apcyccv.org.pe/index.php/apccc/article/view/513
Nivel de acceso:acceso abierto
Materia:Pacemaker, Artificial
Defibrillators
Heart Failure
Infection
Descripción
Sumario:We present the case of a 51-year-old male with non-ischemic dilated cardiomyopathy and complete atrioventricular block, who was previously implanted with a cardiac resynchronization therapy defibrillator. The patient developed signs of pocket infection with a high risk of extrusion. Partial system extraction was performed, followed by 14 days of intravenous antibiotic therapy. Due to a history of ventricular fibrillation and permanent pacing dependency, and in the absence of viable transvenous access, a sequential implantation strategy was adopted using a leadless pacemaker (Micra AV, Medtronic) and a subcutaneous implantable cardioverter-defibrillator (EMBLEM, Boston Scientific). Both procedures were completed without complications, and the patient showed favorable recovery, with effective pacing, no arrhythmic recurrences, and no signs of infection at the six-month follow-up. This case illustrates the feasibility of a fully leadless approach in high-risk patients with contraindications to conventional transvenous systems.
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