The Multitude is a registry of patients who receive commercially available CIEDs that remotely communicate through the LATITUDE monitoring system and transfer data to a central database.

The registry is designed to constitute a shared environment for the collection, management, analysis and reporting of clinical and diagnostic data, adopted by a network of European scientifically-motivated physicians who use rhythm management diagnostic and therapeutic solutions from Boston Scientific in their clinical practice.

The Multitude study will facilitate the sharing of scientific proposals within a large network of researchers, and it will allow researchers to record the experience with medical devices throughout the device and patient lifecycle.

Inclusion Criteria:

• Subject is willing and capable of providing informed consent to collect/store/process personal health information by the sponsor or such consent is provided by a legally designated representative, if required by local law or regulation.

• Subject is:

  1. prospectively scheduled for receiving a device monitored through the LATITUDE monitoring system
  2. retrospectively enrolled after having received a device monitored through the LATITUDE monitoring system

Exclusion Criteria:

• Subject foreseen not to be followed at the enrolling center for at least 1 year after having received the device.
• Subject is receiving a device that is not approved for commercial use at the time of procedure.

The subjects will be recruited from the general patient population of the participating centers who are

• receiving diagnosis or treatment using a device monitored through the LATITUDE monitoring system and
• fulfilling all inclusion criteria and none of the exclusion criteria.