Abstract: The current subject matter describes a delivery of medication to a patient based on a scan of a medication container by a scanner implemented on an infusion system. The medication can include oral medications, injection medications, patches, and/or medication drops. The scanner can scan a machine-readable representation (for example, a barcode) on the medication container to obtain recommended delivery data. A user interface device of the infusion system can display the recommended delivery data on a graphical user interface. Based on the recommended delivery data and based on a patient diagnosis by a clinician, the clinician can determine actual delivery data. Based on the determined actual delivery data, the medication can be delivered to the patient via a non-infusion channel. Related apparatus, systems, techniques and articles are also described.

Abstract: A pump is disclosed that comprises a primary control unit comprising a first processor and one or more modular pumping units removably docked to the primary control unit. Each modular pumping unit comprises a pumping mechanism and a second processor configured to control the pumping mechanism and communicate with the first processor. 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.

Abstract: An infusion pump system includes an infusion channel, and a display associated with the infusion channel. The display is for rendering a scannable barcode.

Abstract: A method for health care facility ventilation management is described. The method includes accessing ventilator data generated by a ventilator for a patient and providing patient information of the patient for the ventilator. The patient information is configured for contextualizing the ventilator data. The method also includes providing protocols and rules for the ventilator.

Abstract: 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.

Abstract: A stylet-guided balloon vertebroplasty system, as well as methods for bone augmentation using same are provided. In certain embodiments, a pre-curved stylet with an overlying delivery tube may be used to target an approximately centered target site within a bone structure, facilitating direction thereto of an expandable member useful for creating a cavity that may receive curable material to restore bone height and/or to reinforce the bone structure.

Abstract: A nasal continuous positive airway pressure (nCPAP) device having a hollow body with a proximal wall, a distal wall, and an exhaust port extending through the distal wall. A proximal tubular member extends through the proximal wall of the body and is arranged such that a stream of gas entering the body through the proximal tubular member will exit the proximal tubular member in a first direction and then enter the exhaust port. A nozzle extends through the body and is arranged such that a stream of gas entering the body through the nozzle will exit the nozzle and then enter the proximal tubular member in a second direction that is opposite the first direction.

Abstract: A valve for a needleless valve system. The valve includes a body configured to be disposed in the needleless valve system and controlling fluid flow through the needleless valve system and wherein the body is tail-less. The body includes a continuous top surface, and a compression feature configured to control how the body is compressed to allow fluid flow through the needleless valve system.

Abstract: A method of infusing a fluid includes receiving values of one or more infusion parameters for an infusion of a fluid. Based on the received infusion parameter values, an occlusion pressure threshold for the infusion of the fluid is automatically calculated. During the infusion, a fluid pressure value is sensed. An indication is provided responsive to whether a value of the sensed fluid pressure is greater than the occlusion pressure threshold.

Abstract: A pumping mechanism is disclosed that includes a plurality of peristaltic pumping actuators configured to selectively and sequentially compress adjacent portions of a first portion of an at least partially compressible pumping element having an inlet that is upstream of an outlet. The plurality of pumping actuators are further configured to reciprocate at a common drive frequency with a first phase offset between each adjacent pair of pumping actuators. The pumping mechanism also includes at least one compensation actuator arranged to selectively compress a second portion of the at least partially compressible pumping element that is disposed between the first portion and the outlet. The at least one compensation actuator is configured to reciprocate at an optimal displacement and at a modulation frequency that is an integer multiple of the fundamental drive frequency and with a second phase offset between the at least one compensation actuator and the adjacent pumping actuator.

Abstract: A lung ventilation apparatus and system are described. The lung ventilation apparatus may include a control panel; and a graphical user interface associated with the control panel, the graphical user interface comprising a central strip content item covering at least 50% of a total area of the graphical user interface, the central strip content item representing at least one of a patient monitoring screen or surveillance screen, the central strip content item comprising a first portion and a second portion, wherein the first portion comprises numerical elements indicating ventilation parameters of a patient, and the second portion comprises a graphical element indicating pressure at a patient airway.

Abstract: A method for controlling mechanical lung ventilation is described. The method may include supplying a breathing gas to an airway of a patient in an intermittent way such that a plurality of respiratory cycles are formed; measuring a volume received by the patient in one or more respiratory cycles of the plurality of respiratory cycles; comparing the measured volume of each of the one or more respiratory cycles with a user defined target volume; attributing a classifying score to each of the one or more respiratory cycles based at least partially on a deviation between the measured volume and the user defined target volume; summing the classifying scores and dividing the result by a sample size of the one or more respiratory cycles; attributing a pressure step value based at least partially on the division result; and adding the pressure step value to a present pressure.

Abstract: A method for controlling mechanical lung ventilation is described. The method may include intermittently switching the airway pressure of the patient from a substantially constant high baseline pressure level to a substantially constant low baseline pressure and vice-versa such that the patient is able to breathe spontaneously in both high and low baseline pressure levels; detecting an inspiration effort by the patient inside a trigger time window that immediately precedes a switching event of the intermittently switching the airway pressure; maintaining a baseline pressure at the level in which the inspiration effort was detected so that the patient can complete the inspiration-exhalation cycle; and switching the baseline pressure level after a delay time.

Abstract: A latch assembly is disclosed that has a latch, a locking lever having locked and unlocked positions, and a detent lever having engaged and disengaged positions. The locking lever is configured to secure the latch in the closed position when the locking lever is in the locked position and the detent lever is configured to provide a detent function when the detent lever is in the engaged position. In certain aspects, the latch assembly includes a single motor and cam assembly having three configurations, wherein the locking lever and detent lever are respectively in the unlocked and disengaged positions while in the first configuration, in the unlocked and engaged positions while in the second configuration, and in the locked and engaged positions while in the third configuration.

Abstract: A method and system for controlling fluid flow settings by receiving a precondition pressure wave function, representative of a precondition frequency, a precondition amplitude and a precondition pressure of the fluid flow in the system, establishing an operating pressure wave function, representative of an operating frequency, an operating amplitude and an operating pressure of the fluid flow desired in the system, determining cycle error between the precondition pressure wave function and the operating pressure wave function, converting the cycle error to flow adjustment, and updating an operating flow with the flow adjustment.

Abstract: A system and method for disinfecting an exposed portion of a female luer connector is disclosed. A male luer connector coupled to a male luer connector cap is provided where the male luer connector cap has a chamber containing a disinfectant and a sealing member for sealing the disinfectant in the chamber. The chamber is at least partly opened and the disinfectant exposed by movement of the sealing member. An exposed surface of a female luer connector is caused to come in contact with the disinfecting fluid in the chamber prior to the female luer connector mating with the male luer connector.

Abstract: A pressure relief device comprising a valve configured to resiliently deform in response to a predetermined pressure; and a sound dampener configured to dampen a sound generated by the valve when the valve resiliently deforms in response to said predetermined pressure.

Abstract: Needleless connectors are described. An example needleless connector includes a housing and a compressible valve. The housing may define an internal cavity and may include a body section having a first port and one or more internal contact tabs and a base section having a valve mount and a second port. The compressible valve may be disposed within at least a portion of the internal cavity and be movably retained within the housing. The compressible valve may include a flange portion for securing the compressible valve within the housing. A central longitudinal axis of the housing may be defined by a coaxial arrangement of the first and second port. The one or more internal contact tabs may be arranged to contact an outer side surface of the flange portion such that a radial force substantially orthogonal to the central longitudinal axis is provided for securement.

Abstract: A vertebral augmentation system and methods for vertebral augmentation and/or fusion using same are provided. In certain embodiments, a pre-curved stylet or needle with an overlying delivery tube may be used to target a site within a bone structure, facilitating direction thereto of an expandable member useful for creating a cavity that may receive curable material to restore bone height, to reinforce the bone structure, and/or to fuse two, three, or more adjacent vertebrae. An expandable member such as, for example, a balloon can be used to create a plurality of voids by displacing bone material, where the voids can be filled with curable material to augment the vertebrae and intervening space can be filled to fuse those adjacent vertebrae.

Abstract: Storage systems for inventory control are disclosed. The storage systems include a vertical storage structure having a plurality of vertically-stacked pockets. Each vertically-stacked pocket can be configured to be separately openable for providing user access to contents of the vertically-stacked pocket. The vertical storage structure can be a vertical sliding-type door, a hinged-type door, or a wall-mounted cabinet.