A personalized acute care treatment kit is provided that includes components necessary for a lay caregiver to treat an acute cardiac event. The kit includes a medication box provided with medications selected according to the needs of the owner, a CPR device, a pacemaker, a defibrillator, monitoring and diagnostic devices and a computing device. The computing device is provided with a mobile application that captures patient data from the devices in the kit and automatically sends an alarm to a treatment professional when the patient data exceeds a predetermined threshold and establishes a communication link to with the treatment professional to allow the treatment professional to instruct the lay caregiver in using the contents of the kit to provide acute care.

A fluid dispenser assembly having a nasal fluid dispenser device (1000) with a reservoir (30) and, a dispenser head (1) assembled on the reservoir (30); a remote mobile device (2000); and an orientation sensor (113) to obtain optimal orientation of the dispenser device (1000) when actuated. The sensor determines the three-dimensional orientation of the device, including the angle (α) of the device relative to said remote mobile device. A second sensor (121) is provided for detecting when the device (1000) is actuated by the user. The remote mobile device includes an accelerometer to determine its position in three-dimensional space, in particular the angle (β) of the remote mobile device (2000) relative to the vertical.

A medical system, usable for example in connection with a dialysis apparatus, may utilize radar waves for monitoring a patient, a medical area, or an object. The medical system includes at least one sending device for sending radar waves, and at least one receiving device for receiving reflected radar waves. The medical system further includes an evaluation unit for evaluating the reflected radar waves which have been received by the at least one receiving device, resulting in obtaining a result, and an output device for outputting the result or a signal based on the result.

A controller for an implantable blood pump, includes an accelerometer configured to measure at least one from the group consisting of position and movement of the controller. Processing circuitry is configured to control operation of the implantable blood pump, the processing circuitry being in communication with the accelerometer, the processing circuitry being configured to adjust a speed of the implantable blood pump if the measured at least one from the group consisting of position and movement deviates from a respective predetermined threshold.

A sleep therapy system comprises a sensor arrangement for detecting physiological parameters of a subject, a detection system for detecting a sleeping position of the subject and an alert system for instructing a change in sleep position of the subject. From the monitored physiological parameters, fluid accumulation is identified in a region of the body of the subject. The alert system is controlled to instruct a change in sleep position thereby to reverse the fluid accumulation.

A sleep therapy system comprises a sensor arrangement for detecting physiological parameters of a subject, a detection system for detecting a sleeping position of the subject and an alert system for instructing a change in sleep position of the subject. From the monitored physiological parameters, fluid accumulation is identified in a region of the body of the subject. The alert system is controlled to instruct a change in sleep position thereby to reverse the fluid accumulation.

A respiratory pressure therapy (RPT) system may include a housing portion forming a plenum chamber pressurizable to a therapeutic pressure; a seal-forming structure constructed and arranged to with a region of the patients face; a positioning and stabilising structure constructed and arranged to provide an elastic force to hold the seal-forming structure in a therapeutically effective position on the patients head; a blower configured to pressurize the plenum chamber to the therapeutic pressure; a vent assembly configured to discharge gas from a plenum chamber to atmosphere; a sensor port positioned downstream of the vent assembly such that the sensor port is in pneumatic communication with the air within the plenum chamber in any position of the vent assembly; and a sensor in pneumatic communication with the air within the plenum chamber via the sensor port.

A respiratory pressure therapy (RPT) system may include a housing portion forming a plenum chamber pressurizable to a therapeutic pressure; a seal-forming structure constructed and arranged to with a region of the patients face; a positioning and stabilising structure constructed and arranged to provide an elastic force to hold the seal-forming structure in a therapeutically effective position on the patients head; a blower configured to pressurize the plenum chamber to the therapeutic pressure; a vent assembly configured to discharge gas from a plenum chamber to atmosphere; a sensor port positioned downstream of the vent assembly such that the sensor port is in pneumatic communication with the air within the plenum chamber in any position of the vent assembly; and a sensor in pneumatic communication with the air within the plenum chamber via the sensor port.

Described herein are methods, devices and systems for predicting ventilator associated events (VAEs). In an example, data of a patient including one or more features useful in predicting VAEs is accessed and the features are extracted. The extracted features are evaluated automatically to determine a probability that a VAE will occur. If it is determined, based on the evaluating, that a VAE has a probability of occurring that exceeds a threshold, an indication that the VAE is predicted to occur is provided. Other examples are disclosed and claimed.

A bed includes components to control pressure of a sleep surface, for example based on sleep position and sleep stages of a user. In some embodiments target pressures for the sleep surface are iteratively adjusted over multiple sleep sessions so to achieve improvements in sleep states and/or sleep quality for the user.