Lead Extraction of Cardiac Rhythm Devices: A Report of a Single-Center Experience

• Published in: Frontiers in cardiovascular medicine 2017-04, Vol.4, p.18-18
• Main Authors: Azevedo, Ana Isabel, Primo, João, Gonçalves, Helena, Oliveira, Marco, Adão, Luís, Santos, Elisabeth, Ribeiro, José, Fonseca, Marlene, Dias, Adelaide V, Vouga, Luís, Ribeiro, Vasco Gama
• Format: Article
• Language: English
• Subjects: Cardiovascular Medicine
• ISSN: 2297-055X; 2297-055X
• DOI: 10.3389/fcvm.2017.00018

The rate of implanted cardiac electronic devices is increasing as is the need to manage long-term complications. Lead removal is becoming an effective approach to treat such complications. We present our experience in lead removal using different approaches, analyzing the predictors of the use of mechanical extractors/surgical removal. Retrospective analysis of lead extractions in a series of 76 consecutive patients (mean age 70.4 ± 13.8 years, 73.7% men) between January 2009 and November 2015. One hundred thirty-five leads from permanent pacemakers (single chamber 19.7%; dual-chamber 61.8%), implantable cardioverter defibrillators (5.3%), and cardiac resynchronization devices (CRT-P 2.6%; CRT-D 7.9%) were removed, 72.5 ± 73.2 months after implantation. A total of 45.9% were ventricular leads, 40.0% atrial leads, 8.9% defibrillator leads, and 5.2% leads in the coronary sinus; 64.4% had passive fixation. The most common indications for removal were pocket infection (77.8%), infective endocarditis (9.6%), and lead dislodgement (3.7%). A total of 76.3% of the leads were explanted, 20.0% were extracted, and 3.7% were surgically removed. Extraction of the entire lead was achieved in 96.3% of the procedures. After logistic regression (age adjusted), time since implantation was the sole predictor of the need of mechanical extractors/surgical removal. All patients were discharged without major complications. There were no deaths at 30 days. Our experience in lead removal was effective and safe. Performing these procedures by experienced electrophysiologists with an adequate cardiothoracic surgery team on standby to cope with any complications is required. Referral of high-risk patients to a high-volume center is recommended to optimize clinical success and minimize procedural complications.