A61M2205/331

AIR DETECTION SYSTEM AND METHOD FOR DETECTING AIR IN A PUMP OF AN INFUSION SYSTEM

Various systems and methods for detecting air in a chamber of an infusion system are disclosed. In one embodiment, a determination is made that air is contained in the chamber on the basis of a change in the average force exerted against the plunger utilizing a derivative spike for event detection and a systematic reduction in the average force to confirm the nature of the change. In another embodiment, a determination is made that the chamber contains air when a difference between the current force profile and a baseline force profile crosses a threshold. In an additional embodiment, a force profile is classified as being an air force profile or a liquid force profile based on extracted features of the force profile.

SMART VALVED HOLDING CHAMBER

A medication delivery system including a holding chamber having an input and an output end, a backpiece coupled to the input end of the holding chamber and having an electrical circuit and an opening. An MDI includes an insert portion moveable between an engaged position wherein the insert portion is received in the opening and a disengaged position wherein the insert portion is removed from the opening, and at least one contact that completes the electrical circuit when the insert portion is in the engaged position.

AN APPARATUS FOR EXTRACORPOREAL BLOOD TREATMENT
20240238492 · 2024-07-18 ·

A control unit of an apparatus for extracorporeal blood treatment is configured to perform a control procedure. The control procedure includes calculating parameter control values to be set during a time interval after the instant in which the control is made, on the basis of actual values and of prescription values of variation in blood volume, ultrafiltration flow rate, and concentration of sodium. The control procedure further includes imposing the parameter control values during the time interval consecutive to the instant in which the control is made such that the actual values of the variation in blood volume track the prescription values of the variation in blood volume over a predetermined treatment time. The control unit is further configured to perform a procedure for automatically estimating/calculating a target plasma conductivity and/or a target concentration of sodium in plasma to be reached at the end of the extracorporeal blood treatment.

APPARATUS AND SYSTEM FOR MEASURING VOLUME OF BLOOD LOSS

A system for measuring the blood loss comprises a measuring device that determines a hemoglobin concentration of fluid within a container utilizing a light source and a light detector. The container receives blood and other fluids from a patient during a medical procedure. Light from the light source is passed through the blood and other fluids in the container and is detected by the light detector. Based upon a magnitude of light detected, a hemoglobin concentration of the fluid in the container can be determined. A volume-measuring device determines the volume of blood and fluid in the container. Knowing the hemoglobin concentration and volume of fluid in the container, the volume of patient blood loss in the container can be determined. The blood loss measuring device in combination with infusion systems maintains a real-blood volume status so that proper infusion of blood, crystalloid and/or colloid solutions occurs.

BODILY FLUID MANAGEMENT SYSTEM

In some embodiments, an external bladder management system that is configured to reside within a urine collection receptacle (e.g., a toilet) includes a body that houses a fluid testing chamber. The fluid testing chamber is fluidically coupled to a fluid inlet and a fluid outlet. The system further includes a fluid capturing funnel fluidically coupled to and extending from the body and configured to couple the body to the urine collection receptacle. The system further includes an optical sensor disposed within the body and including (1) an emitter configured to convey light across the fluid testing chamber, and (2) an optical detector capable of measuring an intensity of the light as the light exits the fluid testing chamber. The fluid inlet, fluid testing chamber, and fluid outlet are collectively configured to encourage a laminar flow profile of the fluid as it flows through the fluid testing chamber.

AIR DETECTION SYSTEM AND METHOD FOR DETECTING AIR IN A PUMP OF AN INFUSION SYSTEM

Various systems and methods for detecting air in a chamber of an infusion system are disclosed. In one embodiment, a determination is made that air is contained in the chamber on the basis of a change in the average force exerted against the plunger utilizing a derivative spike for event detection and a systematic reduction in the average force to confirm the nature of the change. In another embodiment, a determination is made that the chamber contains air when a difference between the current force profile and a baseline force profile crosses a threshold. In an additional embodiment, a force profile is classified as being an air force profile or a liquid force profile based on extracted features of the force profile.

PERISTALTIC PUMPING DEVICE AND MEDICAL APPARATUS, IN PARTICULAR FOR DIALYSIS, INCORPORATING IT
20240261481 · 2024-08-08 · ·

A peristaltic pumping device of linear type, includes a section of deformable tube crossed by a fluid whereon at least a peristaltic compression is implemented; and an actuator, including a rotating element provided with one or more helical ribs arranged projecting from its surface to interfere, along the rotation of the rotating element, with said deformable tube and, so as to determine thereon at least a localized, movable and continuous squeezing, moving along a predetermined direction, which implements peristaltic compression, the helical ribs are arranged along a helical axis with respect thereto they are fixed, the position thereof being tied with respect to the rotating element, wherein at least a portion of helical rib, which interferes with said deformable tube, is rotatable around the respective helical axis, thereby minimizing the friction thereof on the surface of the deformable tube, thereby allowing to reduce effectively the stress on the deformable tube.

Tele-care management systems and methods for peritoneal dialysis

A tele-care management system for peritoneal dialysis (PD) includes at least a container, a holder, a removable detection device and a mobile device. The container is for placing effluent fluid of peritoneal dialysis. The holder is for placing the container. The removable detection device includes a detection unit, a processor and a communication interface, wherein the processor detects the turbidity and the chrominance of the effluent fluid and performs a quantitative analysis on the effluent fluid, and generates a turbidity prediction value based on the detection result of the detection unit. The processor respectively calculates first and second turbidity values, which correspond to first and second turbidity respectively, for the effluent fluid according to first and second algorithms and selects one from the first and second turbidity values to generate the turbidity prediction value based on a predetermined threshold value sent to a mobile device for further processing.

AN INJECTION DEVICE
20180333540 · 2018-11-22 ·

An injection device comprising: a housing arranged to contain a liquid medicament or a medicament cartridge; an electrical coil arranged around an inner surface or an outer surface of the housing; an electricity storage apparatus electrically connected to the electrical coil; and a magnet arranged to be movable axially within a defined space with respect to the electrical coil, such that electrical voltage is induced in the electrical coil and a current is generated to charge the electricity storage apparatus.

Blood component separation device
10112003 · 2018-10-30 · ·

A blood component separation device includes a centrifuge bowl for separating a blood component from blood, a plasma bag for storing a plasma component, a platelet intermediate bag for storing high-concentration platelet liquid having high-concentration of platelets, and a temporary storage bag (also used as a buffy coat bag) for storing low-concentration platelet liquid having low-concentration of platelets. The blood component separation device performs control, from the second cycle onward, to mix the low-concentration platelet liquid stored in the temporary storage bag in the immediately preceding cycle with whole blood to supply the mixed liquid to the centrifuge bowl. An amount of high-concentration platelet liquid to be collected in the platelet intermediate bag in the first cycle is set to be smallest among all cycles, and an amount of high-concentration platelet liquid to be collected in a last cycle is set to be greatest among all the cycles.