Cardiac Implantable Device Registry

The Cardiac Implantable Device Registry is designed to provide support to KP Physicians, Staff, and Systems via extensive tracking mechanisms and surveillance of pacemakers, implantable cardiac defibrillators (ICDs), and stents. Specifically, this product registry is responsible for: xray
  • The identification of all patients receiving these cardiac implants
  • Reporting KP utilization of all specified devices to support the selection, contraction, and implementation of implantable devices
  • The provision of a device surveillance system for the purpose of rapid and efficient identification in the event of a product advisory or recall
  • Assist in product analysis by tracking long term health outcomes on large patient populations

This Registry will provide a single source of data for all participating KP regions, and will significantly improve data reporting methods, analytic resources, and tracking between and across facilities via interface with KP HealthConnect. This registry has great potential to enhance quality of care, allow rapid response in a product recall situation and has potential to contribute important decision support information for contacting and management areas.