TY - JOUR
T1 - Differences in underlying cardiac substrate among S-ICD recipients and its impact on long-term device-related outcomes
T2 - Real-world insights from the iSUSI registry
AU - i-SUSI Investigators
AU - Gasperetti, A.
AU - Schiavone, Marco
AU - Milstein, Jenna
AU - Compagnucci, P.
AU - Vogler, J.
AU - Laredo, Mikael
AU - Breitenstein, Alexander
AU - Gulletta, S.
AU - Martinek, Martin
AU - Casella, M.
AU - Kaiser, Lukas
AU - Santini, L.
AU - Rovaris, G.
AU - Curnis, Antonio
AU - Biffi, M.
AU - Kuschyk, Jürgen
AU - Di Biase, Luigi
AU - Tilz, R.
AU - Tondo, C.
AU - Forleo, G. B.
AU - Gasperetti, A.
AU - Arosio, R.
AU - Viecca, M.
AU - Forleo, G. B.
AU - Schiavone, M.
AU - Tondo, C.
AU - Ziacchi, M.
AU - Diemberger, I.
AU - Angeletti, A.
AU - Biffi, M.
AU - Fierro, N.
AU - Gulletta, S.
AU - Della Bella, P.
AU - Curnis, G. Mitacchione A.
AU - Compagnucci, P.
AU - Casella, M.
AU - Russo, A. Dello
AU - Santini, L.
AU - Pignalberi, C.
AU - Magnocavallo, M.
AU - Piro, A.
AU - Lavalle, C.
AU - Picarelli, F.
AU - Ricciardi, D.
AU - Bressi, E.
AU - Calò, L.
AU - Montemerlo, E.
AU - Vogler, J.
AU - Fink, T.
AU - Tilz, R.
N1 - Publisher Copyright:
© 2023 Heart Rhythm Society
PY - 2024/4
Y1 - 2024/4
N2 - Background: Outcome comparisons among subcutaneous implantable cardioverter-defibrillator (S-ICD) recipients with nonischemic cardiomyopathies are scarce. Objective: The aim of this study was to evaluate differences in device-related outcomes among S-ICD recipients with different structural substrates. Methods: Patients enrolled in the i-SUSI (International SUbcutaneouS Implantable cardioverter defibrillator registry) project were grouped according to the underlying substrate (ischemic vs nonischemic) and subgrouped into dilated cardiomyopathy, hypertrophic cardiomyopathy, Brugada syndrome (BrS), arrhythmogenic right ventricular cardiomyopathy (ARVC). The main outcome of our study was to compare the rates of appropriate and inappropriate shocks and device-related complications. Results: Among 1698 patients, the most common underlying substrate was ischemic (31.7%), followed by dilated cardiomyopathy (20.5%), BrS (10.8%), hypertrophic cardiomyopathy (8.5%), and ARVC (4.4%). S-ICD for primary prevention was more common in the nonischemic cohort (70.9% vs 65.4%; P = .037). Over a median (interquartile range) follow-up of 26.5 (12.6–42.8) months, no differences were observed in appropriate shocks between ischemic and nonischemic patients (4.8%/y vs 3.9%/y; log-rank, P = .282). ARVC (9.0%/y; hazard ratio [HR] 2.492; P = .001) and BrS (1.8%/y; HR 0.396; P = .008) constituted the groups with the highest and lowest rates of appropriate shocks, respectively. Device-related complications did not differ between groups (ischemic: 6.4%/y vs nonischemic: 6.1%/y; log-rank, P = .666), nor among underlying substrates (log-rank, P = .089). Nonischemic patients experienced higher rates of inappropriate shocks than did ischemic S-ICD recipients (4.4%/y vs 3.0%/y; log-rank, P = .043), with patients with ARVC (9.9%/y; P = .001) having the highest risk, even after controlling for confounders (adjusted HR 2.243; confidence interval 1.338–4.267; P = .002). Conclusion: Most S-ICD recipients were primary prevention nonischemic cardiomyopathy patients. Among those, patients with ARVC tend to receive the most frequent appropriate and inappropriate shocks and patients with BrS the least frequent appropriate shocks.
AB - Background: Outcome comparisons among subcutaneous implantable cardioverter-defibrillator (S-ICD) recipients with nonischemic cardiomyopathies are scarce. Objective: The aim of this study was to evaluate differences in device-related outcomes among S-ICD recipients with different structural substrates. Methods: Patients enrolled in the i-SUSI (International SUbcutaneouS Implantable cardioverter defibrillator registry) project were grouped according to the underlying substrate (ischemic vs nonischemic) and subgrouped into dilated cardiomyopathy, hypertrophic cardiomyopathy, Brugada syndrome (BrS), arrhythmogenic right ventricular cardiomyopathy (ARVC). The main outcome of our study was to compare the rates of appropriate and inappropriate shocks and device-related complications. Results: Among 1698 patients, the most common underlying substrate was ischemic (31.7%), followed by dilated cardiomyopathy (20.5%), BrS (10.8%), hypertrophic cardiomyopathy (8.5%), and ARVC (4.4%). S-ICD for primary prevention was more common in the nonischemic cohort (70.9% vs 65.4%; P = .037). Over a median (interquartile range) follow-up of 26.5 (12.6–42.8) months, no differences were observed in appropriate shocks between ischemic and nonischemic patients (4.8%/y vs 3.9%/y; log-rank, P = .282). ARVC (9.0%/y; hazard ratio [HR] 2.492; P = .001) and BrS (1.8%/y; HR 0.396; P = .008) constituted the groups with the highest and lowest rates of appropriate shocks, respectively. Device-related complications did not differ between groups (ischemic: 6.4%/y vs nonischemic: 6.1%/y; log-rank, P = .666), nor among underlying substrates (log-rank, P = .089). Nonischemic patients experienced higher rates of inappropriate shocks than did ischemic S-ICD recipients (4.4%/y vs 3.0%/y; log-rank, P = .043), with patients with ARVC (9.9%/y; P = .001) having the highest risk, even after controlling for confounders (adjusted HR 2.243; confidence interval 1.338–4.267; P = .002). Conclusion: Most S-ICD recipients were primary prevention nonischemic cardiomyopathy patients. Among those, patients with ARVC tend to receive the most frequent appropriate and inappropriate shocks and patients with BrS the least frequent appropriate shocks.
UR - http://www.scopus.com/inward/record.url?scp=85184259192&partnerID=8YFLogxK
U2 - 10.1016/j.hrthm.2023.12.007
DO - 10.1016/j.hrthm.2023.12.007
M3 - Journal articles
C2 - 38246594
AN - SCOPUS:85184259192
SN - 1547-5271
VL - 21
SP - 410
EP - 418
JO - Heart Rhythm
JF - Heart Rhythm
IS - 4
ER -