Transvenous pacing in pediatric patients with bipolar lumenless lead: Ten-year clinical experience. (15th March 2018)

• Record Type: Journal Article
• Authors: De Filippo, Paolo; Giofrè, Fabrizio; Leidi, Cristina; Senni, Michele; Ferrari, Paola
• Is Part Of: International journal of cardiology. Volume 255(2018)
• Page Start: 45
• Page End: 49
• Publication Date: 2018-03-15
• Subjects: Cardiology -- Periodicals; Electronic journals; 616.12
• DOI: 10.1016/j.ijcard.2018.01.007
• Languages: English
• ISSNs: 0167-5273

Abstract

Abstract: Introduction: A number of challenges can affect long-term performance of endocardial implanted systems in pediatric patients. Select Secure™ lead offers potential advantages for this population. This analysis aims to evaluate long-term performance of this lead in children, with and without congenital heart disease. Methods: A retrospective analysis of all patients younger than 16 years, implanted with at least one Select Secure™ lead at our institution, was performed. Clinical patient characteristics, electrical lead parameters, implant related complications, occurrence of surgical revisions and other complications were analyzed. Results: From 2006 to 2016, 40 pediatric patients (26 males; age: 10.3 ± 4.6 years) underwent a cardiac device implantation with at least one Select Secure™ lead. Axillary vein access was chosen in 77.5% of the procedures. The intra-atrial loop of the leads was successfully created and the generator was placed in a sub-pectoral pocket in all patients. A total of 57 Select Secure™ leads were implanted: 23 in the right atrium and 34 in the right ventricle. PM/ICDs implantation was uneventful in all 40 patients. One lead, dislodged the day after implantation, was successfully extracted and replaced in the same day. Adequate pacing parameters were achieved during a follow-up of 6 ± 2.9 years (range 0.9–10.8 years). Conclusions: In a pediatric population, the Select Secure™ lead used in the axillary vein, the creation of an intra-atrial loop and the placement of the generator in a sub-pectoral pocket ensured a safe implantation of pacemaker or ICD and an effective stimulation at medium-term follow-up. Highlights: We describe medium-term safety and efficacy of the cardiac device implantation technique in pediatric patients. Utilization of axillary access, intra-cardiac loop, sub-pectoral pocket and bipolar lumenless lead ensure safe implantation and an effective stimulation at medium-term follow-up. In pediatric patients bipolar lumenless lead has shown good electrical performance both acutely and during a follow-up of 6 ± 2.9 years (range 0.9-10.8 years).