• Alan Cheng, Darshan Dalal, Barbara Butcher, Sanaz Norgard, Yiyi Zhang, Timm Dickfeld, Zayd A Eldadah, Kenneth A Ellenbogen, Eliseo Guallar, and Gordon F Tomaselli.
• Department of Medicine, Johns Hopkins University, Baltimore, MD.
• J Am Heart Assoc. 2013 Feb 1; 2 (1): e000083.

BackgroundPrimary-prevention implantable cardioverter-defibrillators (ICDs) reduce total mortality in patients with severe left ventricular systolic function. However, only a minority of patients benefit from these devices. We designed the Prospective Observational Study of Implantable Cardioverter-Defibrillators (PROSE-ICD) to identify risk factors and enhance our understanding of the biological mechanisms that predispose to arrhythmic death in patients undergoing ICD implantation for primary prevention of sudden death.Methods And ResultsThis is a multicenter prospective cohort study with a target enrollment of 1200 patients. The primary end point is ICD shocks for adjudicated ventricular tachyarrhythmias. The secondary end point is total mortality. All patients undergo a comprehensive evaluation including history and physical examination, signal-averaged electrocardiograms, and blood sampling for genomic, proteomic, and metabolomic analyses. Patients are evaluated every 6 months and after every known ICD shock for additional electrocardiographic and blood sampling. As of December 2011, a total of 1177 patients have been enrolled with more nonwhite and female patients compared to previous randomized trials. A total of 143 patients have reached the primary end point, whereas a total of 260 patients died over an average follow-up of 59 months. The PROSE-ICD study represents a real-world cohort of individuals with systolic heart failure receiving primary-prevention ICDs.ConclusionsExtensive electrophysiological and structural phenotyping as well as the availability of serial DNA and serum samples will be important resources for evaluating novel metrics for risk stratification and identifying patients at risk for arrhythmic sudden death.Clinical Trial RegistrationURL: http://clinicaltrials.gov/ Unique Identifier: NCT00733590.

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