Abstract: An adapter assembly including a manifold and a valve assembly. The valve assembly includes a seat and a valve body having a circular base and a wall. The wall extends from a trailing side of the base to form a dome-like shape terminating at an end at which a slit is formed, with the wall defining opposing sealing edges at the slit. The seat has an upper circumferential surface and a lower circumferential surface. The upper surface engages a leading side of the base, whereas the lower surface engages a trailing side. At least one of the upper and lower surfaces forms a segment of increased height. Upon final assembly, the valve body is disposed across a passageway of the manifold, with the slit providing a selectively openable path. A force imparted by the segment of increased height flexes the base and biases the sealing edges into engagement.

Abstract: A patient interface assembly includes a housing that defines an inlet port and an outlet port. A jet pump receives pressurized gas flow from the inlet port and delivers the gas flow to the outlet port. A nebulizer is fluidly coupled to the outlet port and positioned to introduce medication into the gas flow and deliver medicated gas flow to a patient.

Abstract: A non-invasive ventilation patient interface comprises a fresh gas entry port, an exhaust gas entry port, and a facial skin interface. Fresh gas entry port is configured for coupling with a fresh gas supply. The exhaust gas vent port is configured for allowing expulsion of exhaust gas from the patient interface. The facial skin interface is configured for eliminating fluid from within the patient interface and for eliminating fluid from facial skin which is covered by the patient interface.

Abstract: A system and a method are configured to program, track and/or monitor infusion data (such as proper medication, dosage information, drug identification, patient identification, and/or other information believed to be relevant) for a drug infusion system. An electronic data tag, such as a radio frequency identification device (“RFID”) tag, may be coupled to one or more components of the infusion system, such as a medication container or infusion set.

Abstract: A fluid trap apparatus includes an inlet configured to receive a flow of composite fluid into the apparatus. The composite fluid contains at least a first fluid and a second fluid. An outer wall defines an interior chamber. A flow diffuser is interposed within the interior chamber. The flow diffuser directs the flow of the composite fluid to circulate through the interior chamber. The first fluid and the second fluid separate as the composite fluid circulates through the interior chamber. A method of separating a first fluid from a second fluid includes introducing a flow of composite fluid into a separate chamber. A pressure gradient is created within the separation chamber. A flow diffuser is interposed in a flow path between an inlet and an outlet. The flow diffuser directs the flow of the composite fluid within the separation chamber. The first fluid and the second fluid are separated.

Abstract: The present invention relates to a method for retrieving medication packages from a pharmacy order-picking device. In the method according to the invention, an operating device is displaced in a displacement position to a predetermined shelf position, at least one medication package on a shelf belonging to the shelf position is moved with a gripping device in the direction of a support and it is then checked whether the at least one medication package has moved fully onto the support. If the check has a negative outcome, an edge of the shelf on which the at least one medication package is stored is detected with a sensor of the operating device and said operating device is displaced to a corresponding shelf position, the gripping device having been brought into the displacement position before displacement.

Abstract: A system is disclosed for determining the location of fixed wireless assets (FWAs). The system includes at least one FWA having an asset tracking number, at least one mobile device wirelessly coupled to the FWA via a first communication link, and a database having information that associates people with locations. The mobile device is assigned to one of these people. The system also includes a computer that is coupled to the FWA via a second communication link and to the database. The FWA is configured to forward the data received from the mobile device to the computer along with the FWA's asset tracking number. The computer is configured to determine the location of the FWA based at least in part on the data received from the FWA and the information retrieved from the database.

Abstract: Described herein is a mask for delivery of gas, such as oxygen, to a patient and useable in a naso-gastric intubation procedure without disruption of the seal between the mask and the patient's face. The body of the mask includes a fenestration or opening through which the naso-gastric tube may be inserted. The fenestration is preferably shaped to support the tube in a manner that is comfortable for the patient and that eliminates or minimizes the amount of gas lost to the atmosphere outside the mask. In at least some embodiments, the fenestration is closed when a tube is not inserted therethrough so that the mask may be used normally without loss of the gas through the fenestration.

Abstract: A method, system and computer-readable medium are provided for determining compliance with one or more patient care rules and protocols, the method including the steps of sending infusion information from a pump to a processor pertaining to one or more drugs provided to a patient, sending ventilation information from a ventilator to the processor pertaining to ventilation provided to the patient and determining, with the processor, a variation between actual care of the patient and a set of rules and protocols associated with care of the patient at least in part based on the infusion information and the ventilation information.

Abstract: A method, system and computer-readable medium are provided for determining compliance with patient care protocols, comprising an infusion pump providing infusion information pertaining to one or more drugs administered to a patient, the one or more drugs including sedatives and analgesics, and a processor communicably coupled to the infusion pump and configured to determine information regarding the one or more drugs being administered to the patient based on the infusion information by determining a baseline threshold for the one or more drugs being administered to the patient according to the actual dosage of the one or more drugs administered to the patient prior to a current time, determining a dosage amount of the one or more drugs currently being administered to the patient and comparing the dosage amount of the one or more drugs currently being administered to the baseline threshold to determine a deviation from the baseline threshold.

Abstract: A mask for patient ventilation comprises a frame portion, a front portion, a retention strap, and a gas delivery orifice. The frame portion is for surrounding a respiratory opening of a patient. The front portion is coupled with the frame portion and covers the respiratory opening region. The retention strap is for maintaining positive pressure between the frame portion and the patient. The gas delivery orifice is coupled with the frame portion and configured such that the gas delivery orifice is lateral to the front portion.

Abstract: A carbon dioxide sensor for use in a respiratory therapy system. The carbon dioxide sensor determines whether a patient interface is fluidly coupled to a patient.

Abstract: A non-invasive ventilation patient interface comprises a fresh gas entry port, a frame, and a zygomatic facial interface. The fresh gas entry port is configured for coupling with a fresh gas supply. The frame is configured for coupling with a head strap system, wherein the head strap system is configured for supplying a securing force to secure the patient interface in a position over a respiratory opening of a patient. The zygomatic facial interface is coupled with the frame and configured for spreading the securing force away from a nasal bridge of the patient and onto left and right zygomatic arch regions of the patient.

Abstract: A control system for a high frequency oscillating ventilator (HFOV) includes an oscillator controller and a mean airway pressure (MAP) controller. The HFOV includes a reciprocating piston which is adapted to generate positive and negative pressure waves for delivery to a patient airway. The oscillator controller comprises a pair of closed loop control circuits including an oscillator pressure loop and a centering loop which are collectively adapted to regulate frequency and amplitude of piston reciprocations and centering of the piston. The MAP controller comprises a closed loop control circuit that is adapted for regulating MAP at the patient utilizing feedback in the form of patient circuit pressure. Likewise, the oscillator controller utilizes patient circuit pressure as well as piston displacement feedback in order to regulate movement of the piston.

Abstract: An applicator assembly includes a head portion having a proximal, a distal end, and an interior portion defining a fluid chamber, a container slidably coupled to the body, a sealing member sealing an end of the container, and a lifting member, wherein the lifting member is mounted in the interior portion of the head portion and an interior of the container is placed in fluid communication with the application member by way of a fluid conduit that is formed around the sealing member from the container to the fluid chamber when the container is axially translated toward the head portion and the lifting member lifts the sealing member.

Abstract: Methods for managing a return of a prepared medication are provided. In one aspect, a method includes receiving an identification of at least one returned medication delivered to a first location, and receiving an order for another medication. The method also includes determining whether the at least one returned medication is usable for completing the order of the other medication, and when the determination indicates that the at least one returned medication is usable for completing the order of the other medication, providing a notification indicating that the at least one returned medication is usable for completing the order of the other medication. Systems and machine-readable media are also provided.

Abstract: Methods for managing a delivery of prepared medications are provided. In one aspect, a method includes receiving first information includes a delivery deadline for a first medication, and receiving second information includes a preparation status of a second medication. The method also includes comparing the first information includes the delivery deadline for the first medication with the second information includes the preparation status of the second medication to determine whether the first medication should be indicated for delivery prior to completing preparation of the second medication, and providing a notification indicating when to deliver the first medication based on the determination. Systems and machine-readable media are also provided.

Abstract: Systems for managing a retrieval of a prepared medication are provided. In one aspect, a system includes a memory that includes instructions, and one or more processors. The one or more processors is configured to execute the instructions to receive an identification of a plurality of unused medications and a current location of each of the plurality of unused medications, and determine an order in which to retrieve at least two of the plurality of unused medications and return the at least two of the plurality of unused medications to a return location. The one or more processors is also configured to execute the instructions to provide, for display, a listing of the at least two of the plurality of unused medications based on the order for retrieving the at least two of the plurality of unused medications. Methods and machine-readable media are also provided.

Abstract: Methods for managing preparation of a medication for a patient are provided. In one aspect, a method includes receiving information indicative of an order for medication for a patient from an electronic data feed, and determining whether the order for medication for the patient can be filled with a returned medication. The method also includes providing a notification to fill the order with the returned medication when the determination indicates the order can be filled with a returned medication, and providing a notification to fill the order by preparing the medication when the determination indicates a returned medication is not available to fill the order. Systems and machine-readable media are also provided.

Abstract: An integrated package is disclosed that is configured for an adhesive dressing having at least one area coated with an adhesive. The integrated package includes first and second packaging elements that, when coupled together, form a sealed volume with the adhesive dressing disposed within the sealed volume. The integrated package has at least one release surface coupled to the first packaging element, wherein a first portion of the release surface is removably coupled to the adhesive of the dressing. When the adhesive dressing is removed from the integrated package, the adhesive of the dressing is exposed without requiring a second step of removing a protective sheet. The release surface may be provided as a coating on the first packaging element or as a surface of a release sheet having an edge captured between the first and second packaging elements.