A blood filtration system may to couple to an infusion pump that is external to the blood filtration system. The blood filtration system may include a blood circuit, for instance a variable-volume blood circuit. An infusion port may be in communication with the blood circuit and may receive an infusion fluid pumped by the infusion pump. A filtration pump may extract a filtrate fluid from a filter. The filtrate fluid may include filtered plasma constituents. A fluid characteristic sensor may measure one or more of pressure or flow rate of the infusion fluid pumped by the infusion pump. A controller may monitor the fluid characteristic sensor to determine a change in the pressure or flow rate of the infusion fluid. The controller may modulate a speed of the variable-speed filtration pump based on the change in the pressure or flow rate of the infusion fluid.

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.

Systems, methods, and apparatuses for regulating the delivery of negative-pressure therapy are described. The system includes a negative-pressure source, an energy source, and a switch. The switch can include a first conductor electrically coupled to the negative-pressure source, a second conductor electrically coupled to the energy source, and a diaphragm having a first position electrically coupling the first conductor to the second conductor and a second position separated from the first conductor and the second conductor. The diaphragm is configured to move between the first position and the second position in response to a differential between a control pressure and a therapy pressure.

The present disclosure pertains to a system configured to amplify the pressure and/or flow rate of a pressurized flow of breathable gas by entraining oxygen gas and/or ambient air with an air amplifier and a venturi valve at or near a blending gas source, distally (e.g., remotely) from an interface appliance of a subject interface (e.g., away from the face of the subject) to reduce noise from the system heard by the subject. The system is configured to provide this pressure support and/or ventilation with oxygen therapy. The system is configured to deliver ventilatory and/or pressure support with oxygen therapy while decreasing output requirements of the blending gas source and/or pressure generator.

The present invention relates to a method for filling a membrane filter of a blood treatment system, the blood treatment system comprising at least one blood treatment machine, a membrane filter, in particular a hollow fiber membrane filter, having a first and a second chamber which are semi-permeably separated by a membrane, and at least one first partial circuit and at least one second partial circuit. The first chamber of the membrane filter is arranged in the first partial circuit and the second chamber of the membrane filter is arranged in the second partial circuit. The first chamber of the membrane filter is filled with liquid via the first partial circuit, whilst the second chamber is still filled with air, and a pump is arranged in the first partial circuit upstream of the membrane filter. According to the invention,

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 medical fluid-line arrangement and a medical elastomeric pump having such a fluid-line arrangement. The fluid-line arrangement transfers a medical fluid between a medical elastomeric pump and a patient port. The fluid-line arrangement has a fluid-line channel with an inlet and an outlet. The inlet connects to an outlet of the elastomeric pump, and the outlet connects to the patient port. A throttle element is connected in a fluid-conducting manner to the inlet and outlet of the fluid-line channel. A portion of the fluid-line channel extends through the throttle element. The throttle element causes a narrowing of an active-flow cross section of the fluid-line channel. The throttle element is encapsulated at least partially in a thermally conductive body having a heat-absorption surface that is larger than an outer surface of the throttle element and that is intended to be applied flat to a skin surface of a patient.

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.