摘要:
A wearable infusion pump assembly. The wearable infusion pump assembly includes a reservoir for receiving an infusible fluid and a fluid delivery system configured to deliver the infusible fluid from the reservoir to an external infusion set. The fluid delivery system includes a controller, a pump assembly for extracting a quantity of infusible fluid from the reservoir and providing the quantity of infusible fluid to the external infusion set, the pump assembly comprising a pump plunger, the pump plunger having distance of travel, the distance of travel having a starting position and an ending position, at least one optical sensor assembly for sensing the starting position and ending position of the pump plunger distance of travel and sending sensor output to the controller, and a first valve assembly configured to selectively isolate the pump assembly from the reservoir, wherein the controller receives the sensor output and determines the total displacement of the pump plunger.
摘要:
An apparatus and system is disclosed for applying a compressive force to the axilla of an individual to reduce or inter the flow of blood to the individual's upper extremity. An inflatable bladder may be mounted on a flexible plate and directed toward the apex of the axilla. The flexible plate may be attached to a flexible retention strap that can be wrapped around the individual's torso or over the individual's shoulder. The retention strap may be secured in a number of ways, and the flexible plate and attached strap provide enough stiffness to direct the expanding bladder toward the axilla. The expanded shape of the bladder may conform to the shape of the axillary recess, or an attached adjacent compression mass may be sufficiently flexible upon expansion of the bladder to conform to the shape of the axillary recess.
摘要:
A fluid pumping system. The system includes a fluid pump device including a pump housing; an adhesive located on the outside of the pump housing; and an adhesive cover attached to the adhesive; and a vial transfer station, wherein the adhesive cover is attached to the vial transfer station; wherein when the fluid pump device is removed from the vial transfer station, the adhesive cover is removed from the adhesive and the adhesive cover remains attached to the vial transfer station.
摘要:
The present invention comprises a method for identifying the presence or absence of a pulmonary embolism using a combination of tests and brightline thresholds. The first test is a blood based test measuring D-Dimer concentration and the second test is a respiratory analysis that determines a carboximetry ratio. If the measured D-Dimer value is at or above a threshold indicative of concern and the carboximetry value is equal to or less than a carboximetry ratio threshold, pulmonary embolism is present. If the measured D-Dimer value is at or above a threshold indicative of concern and the respiratory analysis yields a carboximetry ratio greater than the carboximetry ratio threshold, test results are inconclusive and additional testing is required to determine whether a pulmonary embolism is present.