A motion pillow according to an embodiment of the present disclosure includes a body, a motion system, a connector, and a valve. The body includes a plurality of airbags provided therein. The motion system includes a pump allowing air to enter and exit the airbags, a sensor measuring air pressures of the airbags, a sound receiver receiving sound from around the body, and a controller controlling operating mode in accordance with measurements of the sensor. The connector connects the airbags and the motion system. The valve opens and closes the connector. When at least one airbag among the plurality of airbags is pressed and air is introduced to the sensor through the connector, the controller is configured to switch the operating mode from standby mode to active mode. Significantly improved convenience and satisfaction of sleep are provided to users.

A peritoneal dialysis (“PD”) system includes a housing; a dialysis fluid pump housed by the housing; a dual lumen patient line extending from the housing; a filter set including a final stage filter located along a first line, and which includes a second line in parallel with the first line, the first line in fluid communication with a first lumen of the dual lumen patient line, and the second line in fluid communication with a second lumen of the dual lumen patient line; a pressure sensor located within the housing and positioned so as to sense a static or substantially static PD fluid pressure in the second lumen while fresh PD fluid is pumped through the first lumen and the final stage filter; and a control unit configured to use the sensed static or substantially static pressure in a pressure control routine for the dialysis fluid pump.

A device for placing a lung in a variety of different inflation states using positive air pressure. An exemplary device includes a housing and an air supply component. The housing includes a platform receives at least one of a synthetic lung or a real lung. The platform is at the same air pressure as a surrounding environment. The air supply component is located within the one or more internal cavities of the housing. The air supply component inflates the synthetic lung or the real lung with positive pressure.

Embodiments of the present disclosure relate to techniques, processes, devices or systems for pump devices for providing a fixed volume of fluid, which is delivered and refilled within one pumping cycle. In one approach, a wearable drug delivery device may include a reservoir configured to store a liquid drug, and a drive mechanism coupled to the reservoir for receiving the liquid drug. The drive mechanism may include a housing defining a chamber, the housing including an inlet valve operable to receive the liquid drug and an outlet valve operable to expel the liquid drug from the chamber, and a resilient sealing member within the chamber. The drive mechanism may further include a shape memory wire coupled to the resilient sealing member, wherein the shape memory wire is operable to bias the resilient sealing member within the chamber.

In one embodiment, system for real time monitoring of catheter aspiration includes a housing having a first port adapted for connection to a vacuum source and a second port adapted for connection with an aspiration catheter, a pressure sensor in fluid communication with an interior of the housing, a measurement device coupled to the pressure sensor and configured for measuring deviations in fluid pressure, and a communication device coupled to the measurement device and configured to generate an alert signal when a deviation in fluid pressure measured by the measurement device exceeds a pre-set threshold. In another embodiment, the system for real time monitoring of catheter aspiration further includes a vacuum source for connection to the first port and an aspiration catheter having an aspiration lumen for connection to the second port.

A method for inflating an inflatable balloon of a catheter for a bowel irrigation system is disclosed. The bowel irrigation system comprises a container for holding a liquid, a catheter, a tubing connecting the container and the catheter, a pump, a control unit, and a pressure sensor. The catheter is adapted for being inserted into a rectum of a user and comprises an inflatable balloon. The pump is adapted for pumping liquid from the container to the balloon through the tubing. The control unit comprises a processor. The pressure sensor is in fluid communication with an interior of the inflatable balloon. The method comprises the steps of providing a liquid in the container and initiating an inflation process comprising a feedback loop comprising the steps of (i) inflating the balloon by a predefined amount of liquid, (ii) assessing a static pressure inside the balloon, and (iii) selecting an output based on the static pressure as assessed according to step (ii), the output being selected from restarting the feedback loop according to step (i), skipping step (i) and proceeding to assessing the static pressure according to step (ii), and terminating the feedback loop. Thereby, a method for providing a stepwise inflation of an inflatable balloon for a bowel irrigation system is provided.

A bowel irrigation system comprising a container adapted for containing a liquid, a catheter comprising an inflated balloon, a tubing connecting the container and the catheter, a pump, a control unit for controlling a flow of fluid in the system, and a pressure sensor is disclosed. The system comprises means for deflating the balloon, as a response to an assessment of a first pressure inside the balloon being greater than a first threshold value, by reducing the amount of liquid inside the balloon by a first amount of liquid. In addition, a method for deflating an inflatable balloon, as a response to an assessment of a first pressure inside the balloon being greater than a first threshold value, by reducing the amount of liquid inside the balloon by a first amount of liquid is disclosed.

A dialysis machine (e.g., a peritoneal dialysis (PD) machine) can include a pressure sensor mounted at a proximal end of a patient line made of a distensible material that provides PD solution to a patient through a catheter. During treatment, an occlusion can occur at different locations in the patient line and/or the catheter. When an incremental volume of additional solution is provided to the patient line while the occlusion is present, a change in pressure results. The change in pressure depends on the dimensions and the distensibility of the non-occluded portion of the patient line. If the change in pressure, the incremental volume, the properties related to the distensibility of the patient line, and some of the dimensions of the patient line are known, the location of the occlusion can be inferred. The occlusion type can be inferred based on the determined location.

An irrigation system for anal or stomal irrigation includes a tubing system attachable between a reservoir and a catheter. The tubing system has a proximal portion attachable to the reservoir and a distal portion including a distal end that is attachable to the catheter, with the tubing system providing an irrigation flow path from the proximal portion attachable to the reservoir through the distal end attachable to the catheter. A pump is operable to move the liquid through the irrigation flow path to provide the anal or stomal irrigation out of the catheter. A pressure control device is attachable to the distal portion of the tubing system and communicates with the catheter. The pressure control device has a valve that is adapted to limit an irrigation pressure for the anal or stomal irrigation out of the catheter to a value less than a pre-determined pressure threshold.

In a method for intermittently occluding the coronary sinus, in which the coronary sinus is occluded using an occlusion device, the fluid pressure in the occluded coronary sinus is continuously measured and stored, the fluid pressure curve is determined as a function of time, and the occlusion of the coronary sinus is triggered and/or released as a function of at least one characteristic value derived from the measured pressure values. The pressure increase and/or pressure decrease per time unit each occurring at a heart beat are used as characteristic values.