Because the implantable cardioverter defibrillator (ICD) was introduced into clinical practice, insertion of these devices has typically involved defibrillation testing (DT). However, DT has never been shown to independently improve patient outcomes. The rationale for DT has always been that the induction of ventricular fibrillation (VF) immediately after ICD insertion allows the implanting team to verify that the ICD can appropriately sense VF and deliver a high-energy shock that can effectively terminate this arrhythmia.1 The first ICD systems were complex, using epicardial patches and monophasic shock waveforms, thus accurate sensing and termination of VF were frequently in question. However, the ICD evolved over time, with the introduction of transvenous systems, biphasic waveforms, and active cans, which made failure to sense and treat VF much less common.2,3 Modern ICDs are also capable of delivering energies >40 J, thus many have started to question the rationale for DT in the modern era.
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Response by Russo et al on p 351During the past 10 years, there has been a dramatic shift in practice, such that DT is performed in <50% of ICD implants in some jurisdictions. This change was not driven by the results of randomized trials, but by changing opinions of clinicians, 4 based on the following insights from observational studies: (1) intraoperative DT is usually successful and clinicians do not always act on unfavorable results; (2) intraoperative DT is an unproven surrogate for clinical shock efficacy; (3) the likelihood of a failed appropriate clinical shock is low and does not appear lower among patients who have DT; and (4) DT is associated with uncommon, but serious complications and adds cost and complexity to the ICD implant procedure. A large randomized evaluation of DT will soon be completed 8 ; however, the observational data seem to suggest that it may not demonstrate a benefit of DT.7 Pending on the results of this trial, DT should not be routinely performed at the time of ICD implantation, as the benefits of DT are unproven, whereas its hazards are real.
Intraoperative DT Is Usually Successful and Clinicians Do Not Always Act on Unfavorable ResultsThe main rationale of conducting DT at the time of ICD implantation is that if the ICD fails to terminate an episode of induced VF, then the ICD system can be modified to make it more effective. 3 Thus, any potential benefit of DT would only be realized by those patients whose ICD fails to terminate VF at the time of intraoperative testing. However, recent registries and clinical trials show that in 90% to 95% of cases, the initial ICD configuration successfully terminates VF 9-13 and when measured, the defibrillation threshold is far below the maximum output of modern devices (Table 1). Even among patients with advanced heart failure, in whom observational (Circ Arrhythm Electrophysiol. 2014;7:347-351.)