(Circulation. 2008;118:2015-2018.)
© 2008 American Heart Association, Inc.
Editorial |
From the Heart and Vascular Center, MetroHealth Campus, Case Western Reserve University, Cleveland, Ohio.
Correspondence to David S. Rosenbaum, MD, Professor of Medicine, Biomedical Engineering, Physiology, and Biophysics, Director, Heart and Vascular Center, Metro Health Campus, Case Western Reserve University, 2500 MetroHealth Dr, Hamman 330, Cleveland, OH 44109-1998. E-mail drosenbaum@metrohealth.org
Key Words: Editorials death, sudden heart failure cardioversion prevention
An extract of the first 250 words of the full text is provided, because this article has no abstract. |
| Introduction |
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Article p 2022
Two major randomized clinical trials demonstrated that implantable cardioverter defibrillators (ICDs) reduce mortality in patients selected for primary prevention of SCD on the basis of reduced left ventricular ejection fraction (LVEF) alone.1,2 However, recent studies have questioned whether LVEF used in isolation from other disease markers is sufficient to guide SCD prevention.3 Although ICDs are highly effective in aborting SCD from ventricular fibrillation, only
1 of 15 patients satisfying current guidelines for prophylactic ICDs on the basis of an LVEF <0.35 benefit from ICDs. Moreover, current guidelines fail to address the largest source of SCD victims (ie, patients with LVEF >0.35). Also, we have yet to ascertain how to incorporate estimates of competitive risk from nonarrhythmic and noncardiac mortality into the decision to implant ICDs. Finally, current paradigms that focus on assessing risk at 1 time point do not account for dynamic time-varying modulation of SCD substrates that occur in response to
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