Modern Subcutaneous Implantable Defibrillator Therapy in Patients with Cardiomyopathies and Channelopathies: Data from a Large Multicentre Registry
Overview
Physiology
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Aims: Patients with cardiomyopathies and channelopathies are usually younger and have a predominantly arrhythmia-related prognosis; they have nearly normal life expectancy thanks to the protection against sudden cardiac death provided by the implantable cardioverter defibrillator (ICD). The subcutaneous ICD (S-ICD) is an effective alternative to the transvenous ICD and has evolved over the years. This study aimed to evaluate the rate of inappropriate shocks (IS), appropriate therapies, and device-related complications in patients with cardiomyopathies and channelopathies who underwent modern S-ICD implantation.
Methods And Results: We enrolled consecutive patients with cardiomyopathies and channelopathies who had undergone implantation of a modern S-ICD from January 2016 to December 2020 and who were followed up until December 2022. A total of 1338 S-ICD implantations were performed within the observation period. Of these patients, 628 had cardiomyopathies or channelopathies. The rate of IS at 12 months was 4.6% [95% confidence interval (CI): 2.8-6.9] in patients with cardiomyopathies and 1.1% (95% CI: 0.1-3.8) in patients with channelopathies (P = 0.032). No significant differences were noted over a median follow-up of 43 months [hazard ratio (HR): 0.76; 95% CI: 0.45-1.31; P = 0.351]. The rate of appropriate shocks at 12 months was 2.3% (95% CI: 1.1-4.1) in patients with cardiomyopathies and 2.1% (95% CI: 0.6-5.3) in patients with channelopathies (P = 1.0). The rate of device-related complications was 0.9% (95% CI: 0.3-2.3) and 3.2% (95% CI: 1.2-6.8), respectively (P = 0.074). No significant differences were noted over the entire follow-up. The need for pacing was low, occurring in 0.8% of patients.
Conclusion: Modern S-ICDs may be a valuable alternative to transvenous ICDs in patients with cardiomyopathies and channelopathies. Our findings suggest that modern S-ICD therapy carries a low rate of IS.
Clinical Trial Registration: URL: http://clinicaltrials.gov/Identifier: NCT02275637.
Russo V, Caturano A, Bianchi V, Rago A, Ammendola E, Papa A Front Cardiovasc Med. 2025; 12:1539125.
PMID: 40046959 PMC: 11880277. DOI: 10.3389/fcvm.2025.1539125.
Substrates of Sudden Cardiac Death in Hypertrophic Cardiomyopathy.
Sclafani M, Falasconi G, Tini G, Musumeci B, Penela D, Saglietto A J Clin Med. 2025; 14(4).
PMID: 40004861 PMC: 11857077. DOI: 10.3390/jcm14041331.
Ziacchi M, Ottaviano L, Checchi L, Viani S, Nigro G, Bianchi V Europace. 2025; 27(2).
PMID: 39834232 PMC: 11822678. DOI: 10.1093/europace/euaf011.
Zhang Z, Wu K, Wu Z, Xiao Y, Wang Y, Lin Q BMC Pediatr. 2024; 24(1):729.
PMID: 39533234 PMC: 11558885. DOI: 10.1186/s12887-024-05216-w.
Thuraiaiyah J, Philbert B, Jensen A, Xing L, Joergensen T, Lim C Europace. 2024; 26(9).
PMID: 39345160 PMC: 11440178. DOI: 10.1093/europace/euae245.