This document discusses, among other things, systems and methods to determine an alert state for each of a plurality of patients using received physiologic information, determine an event rate for the plurality of patients for a specific alert state, and adjust a composite HF risk determination for the plurality of patients using the determined event rate.

This document discusses, among other things, systems and methods to determine an indication of discharge readiness for a patient using received physiologic information of the patient corresponding to hospitalization of the patient and received physiologic information of the patient corresponding to a time after hospitalization.

A lead body is operable to be implanted proximate a target nerve tissue of a patient. A sensing electrode is configured to sense biopotentials over a first partial circumference of the lead body. A stimulation electrode is configured to deliver stimulation energy over a second partial circumference of the lead body. A signal generator is electrically coupled to the stimulation electrode and a sensing circuit is coupled to the sensing electrode. A processor is operable to apply a stimulation signal to the stimulation electrode via the signal generator and, via the sensing circuit, sense an evoked response to the stimulation signal that propagates along a neural pathway.

A system for detecting an anastomotic leak includes a sensor assembly implanted at an anastomosis site. The system also includes a reader configured to receive sensor signals from the sensor assembly and a computing device configured to communicate with the reader. The computing device may be configured to analyze the sensor signals to determine a status of the anastomosis site.

The invention relates to an active implantable medical device comprising a processing unit able to be alternately operated during a predetermined period of activity and on standby during a standby period in a cyclical manner, and means for acquiring data relating to physiological and/or physical activity. The device also comprises means for calculating a frequency analysis of the data acquired, said calculating means being capable of successively perform part of the frequency analysis during periods of activity of the processing unit.

Example implementations relate to an implantable device that can accommodate a vessel of a living body and can detect light transmitted across the vessel. The implantable device transmits a wireless transmitter signal corresponding to the intensity of the detected light. The intensity of the detected light correlates to patency of the vessel.

A system for reducing and/or eliminating noise in chronic neural recording of low amplitude neural signals from conscious, freely-moving subjects. Triboelectric noise effects are reduced or eliminated using in implant lead with insulating materials with charge affinities separated by 10 nC/J or less. The recording device can include a preamplifier device that uses capacitors with a low-distortion dielectric material.

Methods and systems for programming stimulation parameters for an implantable medical device for neuromodulation, such as spinal cord stimulation (SCS) are disclosed. The stimulation parameters define user-configured waveforms having at least a first phase having a first polarity and a second phase having a second polarity, wherein the first and second phases are separated by an interphase interval (IPI). By delivering user-configured waveforms with different IPIs, stimulation geometry, and other waveform settings, therapeutic asynchronous activation of dorsal column fibers can be obtained.

Disclosed is a reader device, system, and method for communicating with a wireless sensor. The reader device may be configured to communicate wirelessly with an implant device associated with a proprietary system provided by a first entity. An external device, that may not be associated with said first entity, is provided and is configured to be calibrated to communicate with the implant device that is located within a patient. The external device may be used in place of an existing reader device that was initially calibrated to communicate with the implant device prior to the implant device being placed within the patient. The external device may be particularly useful for implant devices that communicate wirelessly with external devices where said implant devices are intended to be located within the human body on a permanent or indefinite duration of time.

The control module of a first pacemaker included in an implantable medical device system including the first pacemaker and a second pacemaker is configured to set a pacing escape interval in response to a far field pacing pulse sensed by the first pacemaker. The far field pacing pulse is a pacing pulse delivered by the second pacemaker. The pacing escape interval is allowed to continue without restarting the in response to a far field intrinsic event sensed by the first pacemaker during the pacing escape interval. The first pacemaker delivers a cardiac pacing pulse to the heart upon expiration of the pacing escape interval.