Abstract: A context-aware healthcare notification system determines, in response to a user device has moved within a proximity of an infusion device and within a proximity of a patient identification device associated with a patient, that the infusion pump is currently experiencing an error condition regarding an administration of medication by the infusion pump to the patient. A corrective action is determined for the error condition and a notification is provided to the user device indicating that the user device is within the proximity of the infusion device and that the infusion device is experiencing the error condition, and information regarding the corrective action. The infusion device may then be caused to adjust the administration of medication by the infusion pump to the patient.

Abstract: A peer network may include nodes corresponding to different clinicians. An edge may interconnect the two nodes based on the corresponding clinicians sharing at least one common attribute such as for example, treating the same patients and/or interacting with the same medical devices. A machine-learning model may be applied to identify, in the peer network, one or more peer communities of clinicians. The activity pattern of a clinician may be compared to the activity patterns of other clinicians in the same peer community to determine whether that clinician exhibits anomalous behavior. An investigative workflow may be triggered when the clinician is determined to exhibit anomalous behavior. The investigative workflow may include generating an alert, activating surveillance devices, and/or isolating medication accessed by the clinician.

Abstract: A flow controller having an internal tubing is provided. The flow controller may include an upper housing having a plurality of graduations, a lower housing engaged with and slidably coupled to the lower housing, and a cavity defined between the upper and lower housings for accommodating at least a portion of internal tubing. The flow controller may further include a flexible clamp having an upper section mounted in the upper housing and a lower section slidably disposed in the lower housing. The upper and lower housings may be slidably coupled relative to each other to transition the internal tubing from (i) an open position where a lumen of the internal tubing is uncompressed by the flexible clamp to (ii) a closed position where the lumen of the tubing is at least partially constricted by the flexible clamp.

Abstract: A container is disclosed that has a housing and a lid. The lid has a planar portion and a latch that is freely movable parallel to the planar portion of the lid. The latch has a retention feature and a first reference surface that is perpendicular to the planar portion of the lid. There is a latch mechanism coupled to the housing that has an engagement element configured to engage the retention feature of the latch and a first alignment feature having a first alignment surface. The first alignment feature is configured to laterally displace the latch in a first direction such that the first reference surface aligns with the first alignment surface when the lid is brought together with the housing with the fastener laterally displaced away from the engagement element in a second direction that is opposite to the first direction.

Abstract: Peristaltic pumps are described herein. In certain embodiments, a peristaltic pump includes a plunger and a feeler pin. The plunger is movable to selectively engage a pumping volume of a tubing segment to expand the pumping volume to draw fluid flow into the pumping volume and to contract the pumping volume to conduct fluid flow from the pumping volume. The feeler pin extends through the plunger and movable to maintain contact with the tubing segment, wherein the feeler pin is movable in response to a height of the pumping volume.

Abstract: A manifold for control of fluid and/or vapor flow between a container and a pump cartridge for a compounder system is provided. One or more manifolds may be disposed in a magazine configured to secure and align the manifolds with a plurality of ports in the cartridge. Each manifold may include a needle having forward and rear openings to a central bore. A needle housing may include a slot configured to receive a push rod for actuating the needle forward and backward. In a forward, engaged position, the openings in the needle may be disposed on opposite sides of a sealing member of the manifold to form a fluid pathway through the manifold. In a rearward, disengaged position, both the forward and rear openings in the needle may be disposed on the same side of the sealing member to prevent fluid and vapor from flowing through the manifold.

Abstract: A cap for coupling to a medical adapter may include a housing with a closed top end and an open bottom end with legs that extend from the housing away from the bottom end. Members may extend from an inner surface of the legs to engage and secure the cap to a medical adapter or an insert configured to mate with a medical adapter. A cap may include angular ridges between a cap housing and an insert to permit rotation of the cap in single direction and prevent removal of the cap from a medical adapter. A cap may include hinged legs to permit the cap to be secured to a medical adapter by rotating the legs toward each other until a portion of a collar on each leg may be matingly joined around the medical adapter.

Abstract: A check valve includes an upper housing defining an inlet of the check valve, a lower housing defining an outlet of the check valve, and a cavity interposed between and defined by the upper and lower housings for fluidly connecting the inlet and the outlet. The check valve further includes a valve member mounted in the cavity to selectively permit fluid flow in a first direction, and prevent fluid backflow in a second direction opposite to the first direction. The valve member includes a valve body and a valve stem portion extending axially through a central axis of the valve body. The valve member may further include a plurality of feet disposed about and extending longitudinally from an outer circumferential perimeter of the valve body.

Abstract: A medication delivery module is mounted to a patient care device, and a first graphic representative of the first medication delivery module is displayed on a display screen of the device, wherein the first graphic includes an information display area for display of infusion information associated with the first medication delivery module, and a status indicator for display of status information associated with the medication delivery module. Responsive to the indication, the status indicator is dynamically orienting such that the status indicator is displayed on a side of the first graphic nearest the coupling of the first medication delivery module. Infusion information from the first medication delivery module is displayed within the display area of the first graphic.

Abstract: A mobile smart container system comprises a housing, an access component configured to secure access to a compartment within the housing when in a closed position, a communication interface configured to wirelessly receive a request to access the compartment, a perceivable output device, an electromechanical latch configured to engage with the access component to releasably lock the access component in the closed position, and a processor. The processor receives and authenticates the request to access the compartment and, in response to receiving and authenticating the request, activates the electromechanical latch to unlock the access component to make the compartment accessible, and outputs, upon actuation of the electromechanical latch, an alert via the perceivable output device to identify the smart container system.

Abstract: Spigot tube couplers for fluid flow sets and devices are provided. The spigot tube coupler includes a stop surface and a spigot extending from the stop surface and configured to be inserted into a tube. The spigot includes an insertion end, a fluid port, an outer surface, a collar and a plurality of grooves disposed around the outer surface. The plurality of grooves are configured to receive a bonding agent to provide a plurality of bonding areas between the spigot and the tube. Methods for assembling a spigot tube coupler and a tube are also provided.

Abstract: A method may include identifying a shift associated with a clinician by applying a machine learning model trained to identify, based on a series of transaction records associated with the clinician, one or more shifts associated with the clinician. The clinician may be identified as likely to engage in a hazardous behavior based at least on the shift associated with the clinician. In response to determining that the clinician as likely to engage in the hazardous behavior, activating a protective workflow. The protective workflow may be configured to prevent the clinician from engaging in the hazardous behavior as well as to collect evidence associated with the hazardous behavior. Related methods and articles of manufacture are also disclosed.

Abstract: Systems and methods for enforcing a cleaning of a medical device are disclosed. A method includes receiving an indication that a medical device has been exposed to a contaminate, providing, responsive to receiving the indication, an instruction to disable the medical device, receiving, after transmitting the instruction, cleaning information indicating that a cleaning of the medical device was attempted, identifying a predetermined cleaning procedure corresponding to the medical device and the contaminate, determining, based on the cleaning information, that the medical device was cleaned according to the predetermined cleaning procedure corresponding to the medical device and the contaminate, and enabling the medical device responsive to determining that the medical device was cleaned according to the predetermined cleaning procedure.

Abstract: A flow control device includes an upper housing, a lower housing, a chamber interposed between and defined by the upper and lower housings, and a valve member. The upper housing includes a primary inlet having an internal surface defining a cavity and a secondary inlet. The lower housing defines an outlet of the flow control device. The chamber fluidly connects the primary and secondary inlets with the outlet. A valve member is reciprocally disposed at least partially in the cavity and partially in the chamber to (i) selectively permit fluid flow in the primary inlet in a first direction when a fluid level in the chamber is below a predetermined level, and (ii) prevent fluid backflow in a second direction opposite to the first direction when the fluid level in the chamber is above the predetermined level.

Abstract: A system is disclosed for determining the location of hospital assets. The system includes one or more communication devices each associated with a respective asset identification and a computing device configured to communicate with the communication devices via a network. The computing device receives, from a respective communication device, data comprising the respective asset identification of the respective communication device an identifier associated with a patient or a patient care device, obtains, from a database based on the identifier, additional information pertaining to the patient or the patient care device, and determines a location of the respective communication device based on the data received from the respective communication device and the obtained additional information.

Abstract: A self-flushing connector includes a housing having a cavity, a first inlet port, a second inlet port, and an outlet port. A collapsible valve is disposed within the cavity. A first flow path extends from the first inlet port to the outlet port. The first inlet port and the second inlet port are fluidly connected through a gap defined between the body of the collapsible valve and an inner wall of the housing defining the cavity. A second flow path extends from the second inlet port to the first flow path. When the collapsible valve is in a closed state, the collapsible valve fluidly disconnects the second flow path from the first flow path while allowing fluid to flow through the first flow path. When the collapsible valve is in an open state, the second flow path is fluidly connected to the first flow path.

Abstract: A method, system and computer-readable medium are provided for weaning patients from ventilation, the method including the steps of receiving infusion and ventilation information, and determining whether to initiate termination of the ventilation. The method further including determining whether a timing of an extubation was performed according to the rules and protocols, and providing a notification to a client device regarding the timing of the extubation.

Abstract: Disclosed are systems and methods for managing secure refrigerated bin systems. A system receives a request to access a respective compartment of a plurality of compartments in a dispensing device. Responsive to receiving the access request-and identifying one or more medications in the respective compartment, a safe temperature range specific to the identified one or more medications is determined, and a temperature of the respective compartment is determined using a respective temperature sensor of the respective compartment. The system determines whether the determined temperature of the respective compartment is within the safe temperature range of the identified one or more medications causes an alert to be displayed when the determined temperature of the respective compartment is outside of the safe temperature range of the identified one or more medications.

Abstract: A method may include presenting, on a display of an infusion device, a first patient parameter and a second patient parameter. The infusion device may receive a first entry, which may include a first value of the first patient parameter. The infusion device may determine a default value of the second patient parameter based on the entered first value of the first patient parameter. The infusion device may present the determined default value of the second patient parameter. The infusion device may receive a second entry, which includes a second value of the second patient parameter. The second value may be an adjustment of the default value of the second patient parameter that is an accurate representation of the second patient parameter. Related methods and articles of manufacture, including apparatuses and computer program products, are also disclosed.