© 2004 by European Society of Cardiology
Copyright © 2004, European Society of Cardiology
The fine-scale architecture of defibrillation
Computational Biology Laboratory, School of Biomedical Sciences, University of Leeds, Leeds LS2 9JT, United Kingdom
* Tel.: +44 113 343 4251; fax: +44 113 343 4230. Email address: arun@cbiol.leeds.ac.uk
Received 12 September 2004; accepted 20 September 2004
| The first 10% of the full text of this article appears below. |
See article by Sharifov et al. (pages 448–456) in this issue
| 1. Introduction |
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Ventricular fibrillation is fatal, unless it self-terminates or is terminated by an intervention. It probably is partially responsible for most non-violent deaths and is the immediate cause of death in most sudden cardiac deaths, which form up to a fifth of adult premature deaths in the developed world [1]. The only effective treatment is prompt defibrillation by a brief, large-amplitude electrical shock that produces a field of more than 5 V/cm in the myocardium. Since DC cardiac defibrillation/cardioversion was pioneered by Lown [2] in the 1960s, there have been substantial improvements in the engineering of defibrillators, leading to implantable devices for high-risk patients and public access automatic defibrillators in public areas [1,3]. However, the cellular and tissue electrophysiological
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