The study is a prospective registry. Consecutive patients with indications of implant / replacement or upgrade of pacemaker (PM), implantable cardioverter defibrillator (ICD), Implanted loop recorder (ILR) will be enrolled. The primary objective of the study is to describe the clinical events during a long-term follow-up of non-selected population of patients implanted with an PM, ICD or ILR.
Study Type
OBSERVATIONAL
Enrollment
5,000
Implantation of single chamber, dual chambers or triple chambers PM/ICD
Vincenzo Russo
Naples, Napoli, Italy
RECRUITINGCIEDs Infection
The number of patecipants with infections following implantation of cardiac implantable electronic devices
Time frame: through study completion, an average of 1 year
Appropriate ICD Therapies Antitachycardia pacing therapy or shock delivered by ICD for device detected ventricular arrhythmia
The number of partecipants with a least one episode of antitachycardia pacing therapy or shock delivered by ICD for device detected ventricular arrhythmias.
Time frame: through study completion, an average of 1 year
Inappropriate ICD Therapies
The number of partecipants with at least one episode of antitachycardia pacing therapy or shock delivered by ICD for device detected sopraventricular arrhythmias.
Time frame: through study completion, an average of 1 year
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