Abstract: A respiratory therapy device including a housing, a flow diverter structure, a high frequency pressure port (HF port), and an entrainment port. The housing defines a primary passageway having a patient interface side. The flow diverter structure is in fluid communication with the primary passageway and is characterized by the absence of a venturi tube. The HF port is configured for fluid connection to a source of oscillatory gas flow, and is fluidly associated with the flow diverter structure. The entrainment port is openable to ambient air, and is fluidly associated with the flow diverter structure. With this construction, the device is configured such that flow characteristics of gas flow from an external source are altered upon interacting with the flow diverter structure to create a pressure drop for drawing in ambient air through the entrainment port in delivering a percussive pressure therapy to the patient side.

Abstract: A curable material delivery cannula device and method are disclosed. The device includes a cannula and a hub. The cannula includes an open proximal end, a deflectable segment forming a pre-set curve, a lumen, and side orifice(s) adjacent, and proximally spaced from, the distal end and fluidly connected to the lumen. When inserted within a guide cannula, the deflectable segment straightens. When distally extended from the guide cannula, the deflectable segment reverts to the curved shape, which may be used to create a void in the bone for receiving curable material. The distal end has a blunt tip for non-traumatic interface with bodily material. During use, curable material, such as bone cement, is delivered from the side orifice(s) in a radial direction relative to the lumen.

Abstract: An intravenous fluid pump (IV) contains a disposable part including a fluid chamber having a resilient top membrane and a non-disposable part including a piston abutting a resilient membrane and a vacuum chamber fitted on top of the resilient top membrane. An external pump is used to create vacuum in the vacuum chamber, resulting in the resilient top membrane being held taut. The flow rate through the pump is relatively independent of changes in the pressure of IV fluid on the upstream and the downstream due to changes in the relative elevation of the fluid reservoir and the patient with respect to the fluid pump.

Abstract: A portable ventilator uses a ROOTS-type blower as a compressor to reduce both the size and power consumption of the ventilator. Various functional aspects of the ventilator are delegated to multiple subassemblies having dedicated controllers and software that interact with a ventilator processor to provide user interface functions, exhalation control and flow control servos, and monitoring of patient status. The ventilator overcomes noise problems through the use of noise reducing pressure compensating orifices on the ROOTS-type blower housing and multiple baffling chambers. The ventilator is configured with a highly portable form factor, and may be used as a stand-alone device or as a docked device having a docking cradle with enhanced interface and monitoring capabilities.

Abstract: An intravenous (IV) pump is disclosed. The IV pump includes a housing, a permanent magnet, an electromagnet, and a switch configured to selectably energize or de-energize the electromagnet. The permanent magnet generates a magnetic field and the electromagnet, when energized, generates a magnetic field that approximately cancels the magnetic field of the permanent magnet.

Abstract: A connector is disclosed that has a housing having a fluid path from a first port through an internal cavity to a second port. The connector also includes a plug that has first and second positions within the internal cavity, where the plug blocks the fluid path between the first port and the internal cavity when in the first position. The plug has a diaphragm that separates the internal cavity into a first volume that is vented and a second volume that includes the fluid path. The plug also includes a biasing element that is disposed within the first volume and that urges the plug toward the first position. Displacement of the plug from the first position toward the second position opens the fluid path and increases the second volume.

Abstract: An in-line laparoscopic surgical instrument is provided, including a ratchet mechanism. The ratchet mechanism includes a single actuating means that may be used to engage, release, or defeat a ratchet engagement between portions of the handle.

Abstract: An electrically activated access valve arrangement having a male connector, a female connector, and a valve. In certain embodiments, the male connector includes a conductive element, and the female connector includes contacts. Insertion of the male into the female connector completes a circuit and sends an electrical signal to the valve. This transitions the valve from the normally closed position to the opened position. In certain embodiments, the male connector has a connection port that connects to a connection port of the female connector. A pump, such as an infusion pump, sends an electrical signal through the connection ports, which causes the valve to transition from the normally closed position to the opened position. The electrically activatable valve of the connectors is prevented from opening if mated with conventional male and female luers.

Abstract: The present invention is directed to a system and method for percutaneous delivery of bone cement during a surgical procedure. The system of the present invention has a plunger assembly 100, comprising: a shaft having a first end, a middle section, and a second end, wherein the middle section is threaded; and a handle attached to the first end of the shaft. The system further comprises a dispenser hub assembly 200 around the shaft having a collar and a hand-grip attached to the collar, and a threaded portion formed on an interior surface of the collar. The system may further comprise a hollow tube 300 for containing the bone cement during the surgical procedure having a first end and a second end, the first end of the hollow tube adapted to be removably engaged with the threaded portion of the dispenser hub assembly. The shaft is axially displaceable through the hollow tube for controlled displacement of the bone cement through the second end of the hollow tube.

Abstract: Systems and methods of extending battery life in inventory control devices are disclosed. A passive receiver configured to wirelessly receive an initiation signal having an associated energy field from a remote control system and to output a mode change signal is provided. The passive receiver is configured to be powered by an energy field associated with the initiation signal. A functional module coupled to the passive receiver and configured to be powered by a self-contained power source when the functional module is in an active mode is provided. The functional module is further configured to receive the mode change signal from the passive receiver and to change from an inactive mode to the active mode. The functional module draws more power from the power source in the active mode than in the inactive mode.

Abstract: An automatic pump relay system includes controllers coupled to drivers for sequentially discharging fluid from a plurality of medication containers into a coupler having a reflux barrier from which fluid is administered to a patient. The internal fluid pressure of the coupler is determined by a pressure sensing device or devices that provide signals to the controllers that, based at least on the sensor signals, cause the drivers to operate in reverse and forward directions so as to rapidly decrease and raise the fluid pressure within the coupler during a relay from an empty syringe to a filled syringe, thereby avoiding bolus formation and an interruption in infusion therapy. Independently operable syringes pumps are contemplated to be connected in relay fashion to form a modular system. An associated method is also disclosed wherein a fluid administration pressure is stored for use as a reference during a syringe changeover.

Abstract: A modular electronics enclosure for reducing electromagnetic interference (EMI) is disclosed. The electronics assembly includes a first electronic component having an output, a second electronic component having an input with an input impedance, and a circuit matching element having an input coupled to the output of the first electronic component and an output coupled to the input of the second electronic component. The output of the circuit matching element is configured to provide an output impedance that matches the input impedance of the second electronic component. The electronics assembly also includes a conductive surface that forms a volume that encloses the first electronic component and the circuit matching element. All non-conductive passages from the volume to the external environment have at least one cross-sectional opening having a continuous conductive perimeter with a maximum linear length within the opening of less than one quarter wavelength of a maximum shielding frequency.

Abstract: Systems for use with a medical device for reducing medication errors are provided. In one aspect, a system includes a medical device that is configurable with operating limit parameters for providing medication to a patient, and a limiting system. The limiting system includes a memory that includes patient-specific information for the patient and a database includes acceptable operating parameters for providing the medication to the patient using the medical device, and a processor. The processor is configured to compare the acceptable operating parameters with the patient-specific information, and provide a modification of the operating limit parameters for providing the medication to the patient based on the comparison of the acceptable operating parameters with the patient-specific information. Methods and machine-readable media are also provided.

Abstract: A pharmacy workflow management system may include a processor and a memory. The memory may include instructions that, when executed by the processor, cause the processor to receive, from at least one healthcare device, at least one information item pertaining to progress of delivery of a first medication of a first order, where additional medication is required for the first order when the delivery is complete, receive a second order for a second medication from a healthcare system, the second medication being different than the first medication, and schedule a first preparation of the additional medication for the first order and a second preparation of the second medication of the second order such that the additional medication is prepared and available upon completion of the delivery of the first medication, where the scheduling is based at least in part on the at least one information item.

Abstract: A healthcare validation system may include a processor and a memory. The memory may include instructions that, when executed by the processor, cause the processor to receive an order for a medication from a healthcare system, receive, from at least one healthcare device, at least one information item pertaining to progress of delivery of the medication to a patient, wherein the at least one healthcare device facilitates the delivery of the medication to the patient, validate the medication being delivered to the patient based at least in part on the received order and the received at least one information item, and store an indication of whether the medication being delivered to the patient was validated. In one or more embodiments, the processor may provide an alert to a user device of a healthcare professional when the medication being delivered to the patient is not validated.

Abstract: A healthcare communication system may include a communication network along with healthcare systems and healthcare devices that are communicatively coupled to the communication network. At least one of the healthcare systems may transmit first messages that include orders for patients over the communication network to the healthcare devices. The healthcare devices facilitate providing healthcare to the patients, and transmit, to the healthcare system over the communication network and in response to receiving the first messages, second messages that indicate that the first messages comprising the orders have been received, The healthcare devices may transmit, to the healthcare system over the communication network and while the orders are being administered, third messages that each include information relating to a progress of one of the orders.

Abstract: A context-aware healthcare notification system may include a processor and a memory. The memory may include instructions that, when executed by the processor, cause the processor to determine when a user device is within a proximity of a healthcare device or a patient, receive information related to the healthcare device or patient from multiple healthcare systems, when the user device is determined to be within the proximity of the healthcare device or the patient, and transmit, to the user device over the communication network, at least a portion of the information. In one or more embodiments, the instructions, when executed by the processor, may further cause the processor to receive information from the healthcare device, when the user device is determined to be within the proximity of the healthcare device or the patient, and transmit, to the user device over the communication network, at least a portion of the information.

Abstract: Methods for monitoring delivery of a medication are provided. In one aspect, a method includes receiving first information indicating an order for a fluid medication in a container for a patient, and second information indicating a current status of delivery of fluid medication to the patient. The method also includes determining whether the order for the fluid medication for the patient is consistent with the current status of delivery of fluid medication to the patient, and providing an alert indicating an inconsistency between the order for the fluid medication and the current status of delivery of fluid medication when the order for the fluid medication for the patient is inconsistent with the delivery of fluid medication to the patient. Systems and machine-readable media are also provided.

Abstract: Methods for facilitating safe use of a medical item are provided. In one aspect, a method includes receiving a first identifier for a medical entity located in an institution. The medical entity includes at least one of a patient, medical device, medical location, or medical item. The method also includes receiving a second identifier for a first course of action associated with the medical entity. The method further includes generating, based on a history of the medical entity and the first course of action associated with the medical entity, a second course of action for the medical entity, and providing a notification to a device indicating the second course of action. Systems and machine-readable media are also provided.

Abstract: A respiratory apparatus including an adapter assembly and a catheter assembly. The adapter assembly includes ventilator, respiratory, access, and flush ports. The access port includes a conduit defining a passageway. The flush port projects from the conduit and is fluidly open to the passageway at an outlet. The catheter assembly includes a catheter assembled to a fitting. The fitting includes a hub and a tube, with the tube defining an exterior surface, an interior surface forming a lumen, a circumferential groove in the exterior surface, and a plurality of apertures fluidly open to the lumen and the circumferential groove. The tube is sized to be slidably received within the passageway such that upon final assembly, a fluid pathway is formed between the flush port and a distal end of the catheter via the flush port outlet, the circumferential groove, the plurality of apertures, and the lumen.