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The number of cardiac implantable electronic device (CIED) recalls and advisories has increased over the past 3 decades, yet no consensus exists on how to best manage patients with these CIEDs, partially because rates of complications from prophylactic replacement are unknown.The purpose of this study was to establish rates of complications when recalled CIED generators are replaced prophylactically...
Whether there is an optimal time to place an implantable cardioverter-defibrillator (ICD) more than 40 days after myocardial infarction (MI) in guideline-eligible patients is unknown.To evaluate the effect of time from MI to randomization on mortality, rehospitalizations, and complications.Individual data on patients enrolled in 9 primary prevention ICD trials were provided. Clinical trials were eligible...
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