Impact on Patient Outcome of Cardiac Implantable Electronic Device Complications

Azienda Ospedaliera Cardinale G. Panico2,811 enrolled

Overview

The purpose of this registry is to evaluate the impact on patient outcome and on healthcare utilization of cardiac implantation electronic device complications during a long-term follow-up.

Multicentric, observational, prospective registry enrolling consecutive patients underwent pacemaker or defibrillator implantation, aimed to evaluate the impact of cardiac implantable device complications requiring surgical revision on healthcare utilization (number and length of hospitalizations), and on patient outcome (all-cause mortality and cardiac mortality), during a long-term follow-up.

Study Type

OBSERVATIONAL

Enrollment

2,811

Conditions

Cardiac Implantable Electronic Device Complications

Interventions

Implantation of a cardiac implantable electronic deviceDEVICE

All patients enrolled in the registry underwent cardiac implantable electronic device implantation

Eligibility

Sex: ALL

Medical Language ↔ Plain English

Inclusion Criteria: * patients underwent cardiac implantable electronic device implantation according to current guidelines during the enrollment period. Exclusion Criteria: * patients already carriers of a cardiac implantable electronic device underwent replacement or upgrading of device.

Locations (6)

"Card. G. Panico" Hospital

Tricase, Lecce, Italy

Federico Guerra

Ancona, Italy

Policlinico S.Orsola-Malpighi

Bologna, Italy

Mattia Laffi

Genova, Italy

Monaldi Hospital

Outcomes

Primary Outcomes

All-cause Death (dead/alive status assessment during follow-up)

Evaluation of all-cause mortality during follow-up

Time frame: An average of 48 months

Secondary Outcomes

Occurrence of hospitalizations related to cardiac implantable electronic device complications

Evaluation of hospitalizations related to cardiac implantable electronic device complications

Time frame: An average of 48 months

Data from ClinicalTrials.gov

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