Management of information from active implantable medical device

A system for managing information relating to at least one patient with an active implantable medical device (AIMD) comprising at least one sensor, said system comprising:

• a server comprising at least one processor configured to:
• access, from a device manufacturer's platform, at least one manufacturer information representative of an output of the respective AIMD over time;
• analyze the received at least one manufacturer information based on at least one first type rule, each first type rule being associated to a predefined first sensor event and to at least one patient's clinical information relating to a patient medical status, said analysis comprising applying each first type rule to the received at least one manufacturer information in order to determine, depending on each corresponding patient's clinical information, whether the corresponding predefined first sensor event has occurred and is relevant for diagnosis;
• provide at least one label associated to the at least one manufacturer information based on a result of said analysis;
• wherein the received at least one manufacturer information comprises information associated to the predefined first sensor event;
• at least one output adapted to provide data representative of at least one labeled manufacturer information for diagnosis taking account of the predefined first sensor event occurrence and relevancy.

A computer-implemented method for managing information relating to at least one patient with an active implantable medical device (AIMD), said method comprising, for each patient:

• accessing at least one manufacturer information representative of an output of the respective AIMD over time from a device manufacturer's platform;
• analyzing the received manufacturer information based on at least one first type rule, each first type rule being associated to a predefined first sensor event and to at least one patient's clinical information relating to a patient medical status, the analyzing comprising applying each first type rule to the received manufacturer information in order to determine, depending on each corresponding patient's clinical information of the patient, whether the corresponding predefined first sensor event has occurred and is relevant for diagnosis;
• wherein the received at least one manufacturer information comprises information associated to the predefined first sensor event being generated by the device manufacturer's platform;
• labeling the manufacturer information based on a result of the analyzing;
• outputting data representative of the labeled manufacturer information for diagnosis taking account of the predefined first sensor event occurrence and relevancy.