Systems and methods are provided herein for estimating a position of a heart pump system in a patient. The system receives first data indicative of a time-varying motor current during a first time period. The motor current corresponds to an amount of current delivered to a motor, while the heart pump system is operating in the patient. The system receives second data indicative of a time-varying differential pressure during the first time period. The differential pressure is indicative of a position of the heart pump system relative to patient's heart. The system receives third data indicative of time-varying motor current during a second time period, and determines an estimate of differential pressure during the second period of time from the third data and a relationship between the first data and the second data. The estimate is usable to predict the position of the heart pump system in the patient.

The disclosure relates to a control method of a syringe pump, a syringe pump and a computer-readable storage medium. In the control method of the syringe pump, by determining whether a pressure of the first pressure sensor is less than a first pressure threshold and actively stopping an injection process when the pressure of the first pressure sensor is greater than or equal to the pressure threshold, it can be achieved to accurately determine whether a subject can bear an injection pressure, and to actively stop the injection and sound an alarm when a pressure in the infusion tube exceeds a bearing limit of the subject, thus ensuring personal safety of the subject. When the pressure of the first pressure sensor is less than the first pressure threshold, it is further determined whether a pressure of the second pressure sensor with higher sensitivity is less than a second pressure threshold, and when the pressure of the second pressure sensor is greater than or equal to the pressure threshold, the injection process can be actively stopped and an alarm can be sounded, thus realizing dual monitoring of the pressure in the infusion tube.

The disclosure relates to a control method of a syringe pump, a syringe pump and a computer-readable storage medium. In the control method of the syringe pump, by determining whether a pressure of the first pressure sensor is less than a first pressure threshold and actively stopping an injection process when the pressure of the first pressure sensor is greater than or equal to the pressure threshold, it can be achieved to accurately determine whether a subject can bear an injection pressure, and to actively stop the injection and sound an alarm when a pressure in the infusion tube exceeds a bearing limit of the subject, thus ensuring personal safety of the subject. When the pressure of the first pressure sensor is less than the first pressure threshold, it is further determined whether a pressure of the second pressure sensor with higher sensitivity is less than a second pressure threshold, and when the pressure of the second pressure sensor is greater than or equal to the pressure threshold, the injection process can be actively stopped and an alarm can be sounded, thus realizing dual monitoring of the pressure in the infusion tube.

A pump system is disclosed that comprises a control unit and one or more modular pumping units removably docked to the primary control unit. Each modular pumping unit comprises a pumping mechanism and a processor configured to control the pumping mechanism and communicate with the control unit. The modular pumping unit is configured to manipulate a portion of a fluid delivery set to pump a fluid. The first processor and the second processor are configured to exchange one or more operating parameters when the modular pumping unit is docked to the primary control unit. The modular pumping unit is configured to pump the fluid after being undocked.

An automated peritoneal dialysis system provides both cycler-assisted peritoneal dialysis treatment and also continuous ambulatory peritoneal dialysis (CAPD). The system includes a fluid preparation and treatment device with a concentrate dilution components connected to a source of purified water and medicament concentrate. The treatment device has at least one mixing container connected via a pump and valves to the sources, the valves and the pump mixing and diluting the concentrate to form a medicament. An auxiliary port is provided for attaching a CAPD container and for receiving medicament. A controller is programmed to control the fluid preparation and treatment device to implement one or more cycler-assisted peritoneal dialysis treatment cycles using medicament from the mixing container and also to control the preparation of additional dialysate at the end of the cycler-assisted peritoneal dialysis treatment cycles to dispense additional dialysate through the auxiliary port for use in CAPD.

A treatment device system includes a treatment machine for performing a therapy on a patient, the treatment machine including at least one fluid conveyor and a controller, the controller having a first memory, to cause the at least one fluid conveyor to produce a therapeutic fluid by mixing purified water and at least one concentrate. The system also includes and a water purifier in fluid communication with and providing the purified water to the treatment machine. A wired or wireless control line provides two way communication between the controller of the treatment machine and the internal central controller of the water purifier, wherein the controller of the treatment machine transmits data via the control line to the internal central controller of the water purifier for control of the water purifier, the data provided based on at least one of the operator inputs received via the user interface.

A treatment device system includes a treatment machine for performing a therapy on a patient, the treatment machine including at least one fluid conveyor and a controller, the controller having a first memory, to cause the at least one fluid conveyor to produce a therapeutic fluid by mixing purified water and at least one concentrate. The system also includes and a water purifier in fluid communication with and providing the purified water to the treatment machine. A wired or wireless control line provides two way communication between the controller of the treatment machine and the internal central controller of the water purifier, wherein the controller of the treatment machine transmits data via the control line to the internal central controller of the water purifier for control of the water purifier, the data provided based on at least one of the operator inputs received via the user interface.

Methods and systems for increasing oxygen concentration. An example system includes an oxygen valve configured to be coupled to an oxygen source, an oxygen plenum coupled to the valve, and a mixing valve. The mixing valve includes an oxygen inlet coupled to the oxygen plenum, an ambient-air inlet, and an outlet configured to be attached to an inlet of a blower of a ventilator. The system also includes a pressure sensor, coupled to the oxygen plenum, and a control device communicatively coupled to the pressure sensor and the oxygen valve. The control device receives a differential pressure, measured by the pressure sensor, and based on the measured differential pressure, generates a control signal to control the oxygen valve to maintain a target pressure of gas within the oxygen plenum.

An infusion system for being operatively connected to a fluid delivery line and to an infusion container includes a pump, a plurality of different types of sensors connected to the pump or the fluid delivery line, at least one processor, and a memory. The plurality of different types of sensors are configured to indicate whether air is in the fluid delivery line. The memory includes programming code for execution by the at least one processor. The programming code is configured to, based on measurements taken by the plurality of different types of sensors, determine: whether there is air in the fluid delivery line; whether there is a partial occlusion or a total occlusion in the fluid delivery line; or a percentage of the air present in the fluid delivery line or the probability of the air being in the fluid delivery line.

A renal failure therapy system (10) includes a dialyzer (102); a blood circuit (100) in fluid communication with the dialyzer (102); a dialysis fluid circuit (30) in fluid communication with the dialyzer (102); and an electrically floating fluid pathway (140) comprising at least a portion of the blood circuit (100) and at least a portion of the dialysis fluid circuit (30), wherein the only electrical path to ground is via used dialysis fluid traveling through machine (12) to earth ground (28), and wherein at least one electrical component (46, 90, 82, 66, 102, 116) in the at least a portion of the dialysis fluid circuit (30) of the electrically floating fluid pathway (140) is electrically bypassed.