Clinical course of hypertrophic cardiomyopathy patients implanted with a transvenous or subcutaneous defibrillator

Author:

Francia Pietro1ORCID,Ziacchi Matteo2ORCID,Adduci Carmen1ORCID,Ammendola Ernesto3,Pieragnoli Paolo4ORCID,De Filippo Paolo5ORCID,Rapacciuolo Antonio6ORCID,Rella Valeria7ORCID,Migliore Federico8ORCID,Viani Stefano9ORCID,Musumeci Maria Beatrice1,Biagini Elena2ORCID,Lovecchio Mariolina10,Baldini Rossella1ORCID,Falasconi Giulio1112ORCID,Autore Camillo1,Biffi Mauro2ORCID,Cecchi Franco47ORCID

Affiliation:

1. Cardiology, Department of Clinical and Molecular Medicine, Sant’Andrea Hospital , University Sapienza, Rome , Italy

2. Institute of Cardiology, Department of Experimental, Diagnostic and Specialty Medicine, University of Bologna, Policlinico S.Orsola-Malpighi , Bologna , Italy

3. Department of Translational Medical Sciences, University of Campania ‘Luigi Vanvitelli’, Monaldi Hospital , Naples , Italy

4. Careggi University Hospital, University of Florence , Florence , Italy

5. Papa Giovanni XXIII Hospital , Bergamo , Italy

6. Department of Advanced Biomedical Sciences, Federico II University, Naples, Italy

7. Department of Cardiovascular, Neural and Metabolic Sciences, IRCCS, Istituto Auxologico Italiano, San Luca Hospital , Milan , Italy

8. Department of Cardiac, Thoracic Vascular Sciences and Public Health University of Padova , Padova , Italy

9. Second Cardiology Division, Cardio-Thoracic and Vascular Department, University Hospital of Pisa , Pisa , Italy

10. Boston Scientific , Milan , Italy

11. Campus Clínic, University of Barcelona , Barcelona , Spain

12. IRCCS Humanitas Research Hospital , Milan , Italy

Abstract

Abstract Aims The implantable cardioverter-defibrillator (ICD) is a life-saving therapy in patients with hypertrophic cardiomyopathy (HCM) at risk of sudden cardiac death. Implantable cardioverter-defibrillator complications are of concern. The subcutaneous ICD (S-ICD) does not use transvenous leads and is expected to reduce complications. However, it does not provide bradycardia and anti-tachycardia pacing (ATP). The aim of this study was to compare appropriate and inappropriate ICD interventions, complications, disease-related adverse events and mortality between HCM patients implanted with a S- or transvenous (TV)-ICD. Methods and results Consecutive HCM patients implanted with a S- (n = 216) or TV-ICD (n = 211) were enrolled. Propensity-adjusted cumulative Kaplan–Meier curves and multivariate Cox proportional hazard ratios were used to compare 5-year event-free survival and the risk of events. The S-ICD patients had lower 5-year risk of appropriate (HR: 0.32; 95%CI: 0.15–0.65; P = 0.002) and inappropriate (HR: 0.44; 95%CI: 0.20–0.95; P = 0.038) ICD interventions, driven by a high incidence of ATP therapy in the TV-ICD group. The S- and TV-ICD patients experienced similar 5-year rate of device-related complications, albeit the risk of major lead-related complications was lower in S-ICD patients (HR: 0.17; 95%CI: 0.038–0.79; P = 0.023). The TV- and S-ICD patients displayed similar risk of disease-related complications (HR: 0.64; 95%CI: 0.27–1.52; P = 0.309) and mortality (HR: 0.74; 95%CI: 0.29–1.87; P = 0.521). Conclusion Hypertrophic cardiomyopathy patients implanted with a S-ICD had lower 5-year risk of appropriate and inappropriate ICD therapies as well as of major lead-related complications as compared to those implanted with a TV-ICD. Long-term comparative follow-up studies will clarify whether the lower incidence of major lead-related complications will translate into a morbidity or survival benefit.

Publisher

Oxford University Press (OUP)

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine

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