Methods, systems, and devices for an adaptable blood pump are disclosed herein. The blood pump can be part of a mechanical circulatory support system that can include a system controller and the blood pump. The blood pump can include a rotary motor and a control unit that can communicate with the system controller. The blood pump can determine when communication with the system controller is established or has been lost. The blood pump can retrieve one or several back-up parameters when communication with the system controller has been lost, and can operate according to these back-up parameters.

An infusion pump assembly includes a locking tab and a pump barrel inside a pump barrel housing, where the pump barrel accommodates a reservoir assembly. The reservoir assembly includes a reservoir and a plunger rod. The infusion pump assembly also includes a locking disc at a terminus of the pump barrel. The locking disc includes a clearance hole for the plunger rod. The locking disc also includes at least one locking tab notch in close proximity with the locking tab. The locking tab is in moveable engagement with the locking tab notch, and the reservoir moves the locking tab from a locked position to an unlocked position when the plunger rod is inserted through clearance hole. The locking disc rotates upon torque being applied to the reservoir assembly, the locking disc rotating from a non-loaded position to a loaded position with respect to the plunger rod and a drive screw.

An example breast pump system can include: a control unit including a processor and memory, the control unit including an interface to control the breast pump system; a vacuum unit controlled by the control unit, the vacuum unit including pump motors to create suction for pumping milk; a support mechanism located remotely from the control unit; and a member extending between the control unit and the support mechanism, the member being movable to allow the control unit to be repositioned relative to the support mechanism. The memory encodes instructions which, when executed by the processor, cause the breast pump system to: select at least a first pump motor from the plurality of pump motors for a first pumping timeframe; and select at least a second pump motor from the plurality of pump motors for a second pumping timeframe.

ModuleVide™ takes a unique approach to sustaining vacuum service in Critical Zones within a hospital or other medical facility. This solution relates to a medical facility with a main vacuum plant connected via a main piping with branches that deliver vacuum to different areas within the facility. Critical Zone branches off the central vacuum piping system are augmented with integrated branch backup vacuum generating devices (ModuleVide™). Upon failure of vacuum in the branch piping, the ModuleVide™ activates to reestablish vacuum service in that branch piping segment. The branch of piping may for example correspond to the surgical theater suit of a hospital. The vacuum capacity of the ModuleVide™ is sized to match the specific Critical Zone branch's expected demand.

A system and method for monitoring and delivering medication to a patient. The system includes a controller that has a control algorithm and a closed loop control that monitors the control algorithm. A sensor is in communication with the controller and monitors a medical condition. A rule based application in the controller receives data from the sensor and the closed loop control and compares the data to predetermined medical information to determine the risk of automation of therapy to the patient. A system monitor is also in communication with the controller to monitor system, remote system, and network activity and conditions. The controller then provides a predetermined risk threshold where below the predetermined risk threshold automated closed loop medication therapy is provided. If the predetermined risk threshold is met or exceeded, automated therapy adjustments may not occur and user/clinician intervention is requested.

Systems, circuits, and methods to mitigate effects of short-term power losses in medical systems are provided. An exemplary surgical system includes a fluidics subsystem, a surgical instrument subsystem that couples to a surgical instrument and a power supply subsystem coupled to the surgical instrument subsystem. The power supply subsystem includes a main power supply connectable to AC mains to generate a voltage, a power bus connected to the main power supply, an alternate power supply, and a circuit that monitors the voltage on the power bus for powering the surgical instrument subsystem. The circuit automatically connects the power bus to the alternate power supply when the voltage drops below a reference voltage due to a power loss from the main power supply.

The bifurcated peritoneal catheter serves as a peritoneal dialysis device for patients with kidney failure. The catheter includes a primary tube with two porous internal tubes extending therefrom at a small acute angle to one another. The two internal tubes provide a solution to the potential problem of blockage in a single catheter tube, greatly reducing the potential need for surgery to remove and replace such a single catheter tube. The bifurcated peritoneal catheter includes a subcutaneous cuff, and can include a second deep cuff in the abdominal wall. Either or both of the internal tubes can be straight, curved or coiled, with the curvatures and coils oriented in the same direction, toward one another, or away from one another.

The present disclosure provides in part improved apparatuses, systems, and methods for providing therapy to a wound. A system can include a first power source configured to power an electronic component and a second power source configured to power the electronic component in place of the first power source. Responsive to a first condition, the second power source can power the electronic component in place of the first power source. In some cases, the system can include a pressure source that is configured to provide negative pressure to a wound dressing positioned over a wound. The wound dressing can support the first power source or the second power source.

A blood glucose control system is configured to modify therapy provide to a subject and determine whether the modified therapy results in a statistically significant improvement in glycemic control. The system obtains glycemic control information resulting from delivery of first therapy using a first value of a control parameter and determines a first effect corresponding to the first therapy. The control parameter is set to a second value that differs from the first value. The system obtains glycemic control information resulting from the delivery of the second therapy using the second value of the control parameter and determines a second effect corresponding to the second therapy. The system can perform a comparative assessment and determine whether the second value for the control parameter results in a statistically significant improvement in glycemic control for the subject.

A repeater system may control a pump by using a repeater and a user interface. An adhesive patch system may be used for affixing a pump or other object to a human body. Such an adhesive patch system may include two sets of adhesive members, each member including an adhesive material on at least one side so as to attach to the body. The members of the first set are spaced to allow the members of the second set to attach to the body in spaces provided between the members of the first set, and the members of the second set are spaced to allow members of the first set to detach from the body without detaching the members of the second set. Also, fill stations and base stations are provided for personal pump systems.