Abstract: A medical pumping system is provided. The medical pumping system includes a fluid pump having a fluid inlet connection, a fluid outlet connection, an actuator and a backing surface. A tube of an intravenous set is disposed between the fluid inlet connection and the fluid outlet connection of the fluid pump, and disposed between the actuator and the backing surface, and a binding contact interface. The tube and the actuator are coupled together by the binding contact interface. The actuator is configured to actively pull a portion of the tube into an open position during a pump cycle. A medical pump and an infusion set are also provided.

Abstract: Fluid connector systems including first and second connector portions couplable together to form a fluid pathway therethrough, and can resist fluid flow through the connector when the connector portions are separated from each other. A connector portion can include a connector housing, a luer portion, and a deformable valve member. The deformable valve member is disposed within the connector housing and includes a spherical portion extending partially through a valve opening of the connector housing. The spherical portion defines a slit, and the deformable valve member is configured to selectively prevent fluid flow from the housing volume through the valve opening and to deform to expand the slit and permit fluid flow from the housing volume through the valve opening.

Abstract: A medical device controller operating in conjunction with a medical device determines one or more current versions of executable code associated with one or more processors in a medical device. Medical devices may include infusion pumps, other patient treatment devices as well as vital signs monitors. The medical device controller determines one or more current versions of executable code and configuration information associated with the one or more processors in the medical device. The medical device controller further determines which of the processors in the medical device require updated executable code, and which of the processors in the medical device require updated configuration information. The medical device controller distributes to the medical device as required at least one of the updated executable code and the updated configuration information. The medical device deploys the distributed updates, and activates the updates at a clinically appropriate time.

Abstract: Described herein are methods and systems for automated dispensing of individual medicament portions. The systems can include a housing that encloses a receiving space having a bottom surface. A separation device may be provided and arranged on the bottom surface with at least one channel to receive at least one medicament portion. At least one channel may have an opening facing the receiving space and an opening facing the bottom surface. The opening facing the bottom surface may be associated with a contact area on the bottom surface, over which contact area the medicament portions may be guided upon a movement of separation device. At least one recess may be arranged in the bottom surface outside of the contact area to receive contamination particles present in the container.

Abstract: A device for coupling to a fluid connector of an IV administration set to resist contamination of the fluid connector and IV administration set and permit priming of the IV administration set. The device including a cover body having a cavity for receiving the fluid connector, a priming passage for priming fluid from the IV administration set through the fluid connector, and a coupling tab extending from the cover body, the coupling tab permitting the cover body to be coupled to a length of an IV line or other portion of the IV administration set to resist contamination and permit priming of the IV administration set.

Abstract: A system and method are disclosed that allow a user to select when messages related to medication events are sent and to select the content parameters of those messages. In one aspect, a medication dispenser is configured to notify a messaging processor when an identified medication that was not previously loaded in the medication dispenser is newly loaded into the medication dispenser, and the messaging processor is configured to send a message to a user through a communication link upon receipt of this notification. In another aspect, the medication is identified during a review of a new medication order issued by a doctor.

Abstract: A catheter for use in treating pleural diseases, such as pleural effusions and pneumothorax, includes a tip portion that is configured to irritate the pleura when the catheter is inserted in the pleural cavity, thereby initiating mechanical pleurodesis. The tip portion has a substantially rough configuration and may include one or more protrusions that contact the pleura when the catheter is in use, thereby irritating the layers. This irritation causes the creation of fibrous adhesions between the parietal and visceral layers that close off the pleural cavity and prevent further fluid and/or air accumulations that occur as a result of pleural diseases.

Abstract: Systems and methods for updating firmware of medical devices while minimizing clinical impact are described. A method includes receiving, by a control module of a patient care device, a new configuration package, including firmware for the control module and/or a first functional module of the patient care device, storing the new configuration package in a first memory bank of the control module, wherein a second configuration package comprising a current version of firmware for at least one of the control module and the first functional module is currently stored in a second memory bank of the control module, determining whether the new configuration package includes a new version of the firmware, and when a new version is included, transmitting the new version to the first functional module, for storage in a different memory bank than a memory bank currently storing a firmware currently used by the first functional module.

Abstract: Systems and methods are provided for identifying and tracking diverters of controlled medications. A system may receive signals indicative of medication dispensing activities by one or more health care providers such as nurses, physicians, or pharmacists. Based on the received signals, the system may determine suspected diverters and provide a graphical interface identifying corresponding factors related to usage, waste, dosage, or other factors associated with the suspected diverters. The graphical interface may provide a list of top diverters and display dispensing transactions performed at a dispensing device.

Abstract: A system and method for facilitating safe use of a medical device is provided. In one aspect, a method includes receiving an indication that a user has entered a set of parameters into a medical device to provide a medical treatment to a patient, receiving a history of previous medical treatment provided to the patient using the medical device, generating one or more alternative parameters for providing the medical treatment to the patient based on the set of parameters and the received history of previous medical treatment, causing, based on the generating of the one or more alternative parameters, a locking of the medical device to restrict operation of the medical device until an override of the lock is received, providing a notification for display to the user regarding the alternative parameters.

Abstract: An exemplary syringe adapter for coupling with a syringe may include a housing. A needle-free connector may be disposed in the housing. A communication member may be in slidable engagement with the housing. The communication member may be slidable, with respect to the housing, between an unactuated state and an actuated state of the syringe adapter. A cannula may extend from the communication. In the unactuated state, the cannula may be retracted within the needle-free connector. In the actuated state, the cannula may protrude through and axially beyond the needle-free connector.

Abstract: A camera assembly may include a camera and one or more heat sinks configured to dissipate heat generated by the camera. The heat sinks being in thermal contact with a printed circuit board including the camera. A housing of the camera assembly may be configured to maintain the camera in a fixed position while the camera assembly is mounted on a medical device such as a dispensing cabinet. The camera in the fixed position may have a deterministic field of view that includes a first area in which interactions with the medical device and adjacent medical devices occurs or is expected to occur. The deterministic field of view of the camera may further exclude a second area where surveillance is unsuitable, prohibited, and/or unnecessary. Images captured by the camera may be analyzed to detect anomalous behavior such as diversion, medical error, hazardous behavior, and protocol noncompliance.

Abstract: A fluid-fitting tool is disclosed that can align with and rotationally couple with a fluid fitting where the fluid-fitting tool can include a passage and an engagement feature for engaging against the fluid fitting such that when the fluid-fitting tool is spaced apart from the fluid fitting, the fluid-fitting tool can move in a longitudinal direction toward and away from the fluid fitting, and can rotate relative to the fluid fitting around a longitudinal axis of the passage, and when a portion of the fluid-fitting tool and the fluid fitting are rotationally aligned and longitudinally overlap, the fluid-fitting tool can move longitudinally relative to the fluid fitting, and the fluid fitting is rotated when the fluid-fitting tool is rotated around a longitudinal axis of the passage.

Abstract: A system and method for operating an analgesia administration system is disclosed. A control device is associated with a drug delivery device and configured to receive a first user input including at least a portion of a fingerprint of a patient, together with a second user input corresponding to a request to administer medication. The portion of the fingerprint is compared with previously-stored fingerprints to determine an identity of the patient and, in response to receiving the second user input and determining that the patient is an authorized user, one or more sensors are used to obtain one or more signals indicative of a state of the patient. If the state of the patient satisfies a set of medication delivery criteria, the drug delivery device is caused to administer a predefined amount of medication to the patient.

Abstract: A valve member for a connector includes a head portion, a body portion, and a circumferential lip seal extending radially outward from an outer surface of the head portion. The head portion includes a top section defining a first seal portion. The body portion extends longitudinally from the head portion and defines a second seal portion at a proximal end thereof. The second seal portion is disposed distally to the first seal portion. The circumferential lip seal is disposed between the first and second seal portions.

Abstract: Tubing, such as medical tubing for administration of intravenous fluid, can include an inner layer, an outer layer concentrically disposed about and surrounding the inner layer, and an intermediate layer interposed between the inner and outer layers. The intermediate layer may include a light protection additive therein.

Abstract: A method for tracking dose pattern and patient response may include determining, based at least on one or more dose events at a pump configured to deliver a medication to a patient, a dose pattern for delivering the medication to the patient. One or more vital signs associated with the patient may be received from a patient monitor. A presence of one or more anomalies may be determined based at least on the dose pattern at the pump and the one or more vital signs of the patient. An electronic alert may be sent to a mobile device in response to determining the presence of the one or more anomalies. Related methods and articles of manufacture, including apparatuses and computer program products, are also disclosed.

Abstract: Methods and systems for infusing a user. An infusion pump includes a housing with an elastic component configured to expand and store potential energy. The infusion pump includes a first tube fluidically coupled to an outlet of the housing. The first tube is configured to conduct the fluid from the housing at a first flow rate. The infusion pump includes an air filter fluidically coupled to a distal end of the first tube via an air filter inlet. The infusion pump includes a second tube fluidically coupled to the air filter via an air filter outlet. The second tube is configured to adjust the first flow rate of the fluid conducted from the housing to a second flow rate. The infusion pump further includes one or more components for distributing the fluid to a user, the one or more components fluidically coupled to an outlet of the second tube.

Abstract: An apparatus for coupling to a fluid delivery system and for receiving a fluid into the apparatus; a portion of the apparatus permitting a change in shape or size to accommodate the fluid volume or pressure received therein. The apparatus including a housing with a cavity, an expandable reservoir with an opening and a passage, and a cap; the expandable reservoir positioned within the cavity and coupled to a fluid source. The expandable reservoir includes an unrestrained orientation when a fluid volume or pressure therein is below a threshold, and an expanded orientation, when the fluid volume or pressure therein is above the threshold; the expandable reservoir moving toward the expanded orientation to accommodate a fluid volume or pressure received through an opening, and the expandable reservoir moving toward the unrestrained orientation to direct a fluid volume or pressure through an opening.

Abstract: Check valve are disclosed having a primary seal and a secondary seal, where the primary and secondary seals resist movement of a fluid through the check valve, and the secondary seal can provide a backup seal in an instance where the check valve does not function as intended. The primary and secondary seals can be formed by first and second sealing ridges, respectively, and a valve body can be positioned within the check valve, between a valve support, the first sealing ridge, and a second sealing ridge. The valve body is configured to move relative to the first and second sealing ridges, and can have a position wherein a portion of the valve body is engaged against any of the first and second sealing ridges.