Fluid supply systems and methods for therapeutic fluid delivery systems, including those used for negative pressure wound therapy (NPWT) systems and methods.

Data is received that characterizes infusions administered to a patient among each of a plurality of infusion channels. Thereafter, a plurality of infusion events and respective event times are identified based on the received data. A temporal view of the infusion events can then be displayed in a graphical user interface and/or the temporal view of the infusion events can form part of a report. The temporal view segregates each channel into a separate swim lane with each swim lane visualizing infusion events for the corresponding channel at the respective event times. Related apparatus, systems, techniques and articles are also described.

An LVP that provides peristaltic pumping to removably couplable administration set tubing assemblies supplying medical infusate. The LVP includes a housing, a drive-train assembly, and a controller. The housing includes an assembly receptacle configured to receive an administration set tubing assembly. The drive-train assembly provides mechanical peristaltic movement within the assembly receptacle. The drive-train assembly includes a stepper motor located within the housing and a camshaft assembly, driven by the stepper motor and at least partially extending into the assembly receptacle. The camshaft assembly includes a unitary camshaft and a plurality of tube engaging members that cooperatively move according to rotation of the unitary camshaft. Further, the controller is located within the housing that controls operation of the stepper motor and the camshaft assembly.

In some embodiments, apparatuses and methods are provided herein useful to provide fluid nutrition and hydration. In one illustrative example, a feeding set for use with a peristaltic enteral feeding pump has sections of flexible tubing or conduit, a dispensing control valve that is in fluid communication with the tubing, and a retention disk. In some configurations, the feeding set has as attachment mechanism, which may be formed by one clips or hooks extending from the dispensing control valve and coupling geometry of the retention disk. By some approaches, the clips or hooks and the coupling geometry are configured to attach the feeding set with the pump, such as by attaching the feeding set to an internal panel of the feeding pump. In operation, the feeding set and pump are used to move fluid nutrition and hydration from a container or bag to the patient in a controlled manner.

Force sensing assemblies for an infusion pump are provided. A force sensing assembly includes a processor and an occlusion sensor coupled to the processor. The occlusion sensor is positioned opposed to an occluder valve when the platen is closed. The force sensing assembly measures one or more forces exerted on a fluid tube during a pump cycle. Infusion pump assemblies, methods of operating an infusion pump with a force sensing assembly, systems for controlling an infusion pump and an infusion device are also provided.

A peristaltic pump is disclosed that includes a plunger, a spring, an actuator, a position sensor, and a processor. The plunger actuates toward and away from a tube. The spring biases the plunger toward the tube. The actuator actuates the plunger away from the tube and mechanically engages and disengages from the plunger. The position sensor senses a position of the plunger. The processor receives the sensed position of the plunger and estimates fluid flow within the tube using a first position of the plunger when the actuator is engaged with the plunger and a second position of the plunger when the actuator is disengaged from the plunger.

A system for monitoring upstream flow characteristics for a pump is provided. The system may receive one or more outputs from a fluid level sensor coupled with a pump. The system may detect based on at least the one or more outputs, an abnormal upstream flow condition in the pump, such as a full upstream occlusion in the tube, a partial upstream occlusion in the tube, an empty reservoir, and/or a backflow of the fluid into the drip chamber. The system may adjust, based on the detection of an abnormal upstream flow condition in the pump, operation of the pump.

An infusion pump for delivering an intravenous (“IV”) fluid includes a housing comprising an actuation area that engages a portion of an IV tube. The actuation area includes a first end that receives the IV tube from a fluid container and a second end that provides the IV tube to a patient. The housing also includes a seal section located along a perimeter of at least a portion of the actuation area. The seal section includes a gasket rib positioned along the seal section and a tube channel configured to cradle the IV tube. The example infusion pump also includes a door connected to the housing and configured to engage the gasket rib to enclose the actuation area of the housing.

A method includes measuring a fluid pressure of fluid in a fluid supply line of an infusion pump. The fluid pressure includes a motor pressure and a patient pressure. The method also includes determining the patient pressure. The determining includes removing, by an adaptive filter, to remove the motor pressure from the measured fluid pressure. The removing includes generating a predicted motor pressure based on the current of the motor, generating an error signal based on a comparison between the predicted motor pressure and the measured fluid pressure, and removing the motor pressure from the measured fluid pressure when an error value indicative of the error signal is less than an error threshold. The method also includes adjusting, based on the patient pressure, a setting of the infusion pump. Related methods and articles of manufacture, including apparatuses and computer program products, are also disclosed.

A waste-reducing pumping system and method for delivering a liquid to a patient according to a predetermined therapy protocol is characterized by a stored flush mode routine executable by a processor after an end-of-therapy stoppage of a pumping mechanism, whereby the pumping mechanism is operated to deliver residual liquid remaining in downstream tubing of an administration set to the patient to prevent the residual liquid from being wasted or manually administered at an unsafe rate.