Safety and Efficacy of a Totally Subcutaneous Implantable-Cardioverter Defibrillator

Author:

Weiss Raul1,Knight Bradley P.1,Gold Michael R.1,Leon Angel R.1,Herre John M.1,Hood Margaret1,Rashtian Mayer1,Kremers Mark1,Crozier Ian1,Lee Kerry L.1,Smith Warren1,Burke Martin C.1

Affiliation:

1. From The Ohio State University, Columbus (R.W.); Northwestern University, Chicago, IL (B.P.K.); Medical University of South Carolina, Charleston (M.R.G.); Emory University, Atlanta, GA (A.R.L.); Sentara Cardiology Specialists, Norfolk, VA (J.M.H.); Auckland City Hospital, Auckland, New Zealand (M.H., W.S.); Foothill Cardiology, Pasadena, CA (M.R.); Novant Heart and Vascular Institute, Charlotte, NC (M.K.); Christchurch Hospital, Christchurch, New Zealand (I.C.); Duke University, Durham, NC (K.L.L.);...

Abstract

Background— The most frequent complications associated with implantable cardioverter-defibrillators (ICDs) involve the transvenous leads. A subcutaneous implantable cardioverter-defibrillator (S-ICD) has been developed as an alternative system. This study evaluated the safety and effectiveness of the S-ICD System (Cameron Health/Boston Scientific) for the treatment of life-threatening ventricular arrhythmias (ventricular tachycardia/ventricular fibrillation). Methods and Results— This prospective, nonrandomized, multicenter trial included adult patients with a standard indication for an ICD, who neither required pacing nor had documented pace-terminable ventricular tachycardia. The primary safety end point was the 180-day S-ICD System complication-free rate compared with a prespecified performance goal of 79%. The primary effectiveness end point was the induced ventricular fibrillation conversion rate compared with a prespecified performance goal of 88%, with success defined as 2 consecutive ventricular fibrillation conversions of 4 attempts. Detection and conversion of spontaneous episodes were also evaluated. Device implantation was attempted in 321 of 330 enrolled patients, and 314 patients underwent successful implantation. The cohort was followed for a mean duration of 11 months. The study population was 74% male with a mean age of 52±16 years and mean left ventricular ejection fraction of 36±16%. A previous transvenous ICD had been implanted in 13%. Both primary end points were met: The 180-day system complication-free rate was 99%, and sensitivity analysis of the acute ventricular fibrillation conversion rate was >90% in the entire cohort. There were 38 discrete spontaneous episodes of ventricular tachycardia/ventricular fibrillation recorded in 21 patients (6.7%), all of which successfully converted. Forty-one patients (13.1%) received an inappropriate shock. Conclusions— The findings support the efficacy and safety of the S-ICD System for the treatment of life-threatening ventricular arrhythmias. Clinical Trial Registration— URL: http://www.clinicaltrials.gov . Unique identifier: NCT01064076.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine

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