Abstract

Implantable cardioverter defibrillators (ICDs) have been shown to reduce the risk of sudden cardiac death in primary or secondary prevention with thousands of ICDs implanted every year worldwide. Whilst ICD are more commonly implanted transvenously (TV), this approach carries high risk of peri- and post-procedural complications. Subcutaneous ICD (S-ICD) have been introduced to overcome the intravascular complications of TV system by placing all metalware outside the chest cavity for those with an indication for a defibrillator and no pacing requirements. In conclusion, a review of the current guidelines recommendations regarding S-ICD may be needed considering the emerging evidence which shows high efficacy and safety with contemporary devices and programming algorithms. A stronger recommendation may be developed for selective patients who have an indication for single-chamber ICD in the absence of negative screening, recurrent monomorphic ventricular tachycardia, cardiac resynchronization therapy, or pacemaker indication. These criteria encapsulate a large proportion (around 70%!) of all ICD eligible patients.

Highlights

  • Despite the advances in diagnostics and therapies of cardiovascular disease, sudden cardiac death (SCD) remains a major challenge accounting for approximately 0.1–0.2% deaths per year [1]

  • TV-Implantable cardioverter defibrillators (ICDs) is prone to systemic infections which may result in the need for device extraction and the subsequent morbidity and mortality [8]

  • The overall lead failure rate is still lower than what has been reported with TV-ICD leads [5, 11, 12]

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Summary

Introduction

Despite the advances in diagnostics and therapies of cardiovascular disease, sudden cardiac death (SCD) remains a major challenge accounting for approximately 0.1–0.2% deaths per year [1]. Implantable cardioverter defibrillators (ICDs) have been shown to reduce the risk of SCD in primary or secondary prevention [1, 2] with thousands of ICDs implanted every year worldwide [3, 4]. Pooled data from long-term registries showed the devicerelated complications after S-ICD implantation occurred in 11.1% of patients at 3 years [9].

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