Abstract: A phase-controlled power supply is disclosed. The power supply includes a power conditioner with an input configured to connect to an external source of electrical power, the power conditioner being configured to provide conditioned power on its output. The power supply also includes a transformer having a primary winding and a secondary winding, and a switching module coupled between the output of the power conditioner and to the primary winding of the transformer. The switching module has two modes of operation and a control signal input configured to accept a first control signal. The switching module includes a switching element configured to connect the power conditioner output to the primary winding of the transformer. The switching module operates in the first mode when the first control signal is in a first state, switching the first switching element at a first frequency and first duty cycle.

Abstract: A cable for enhancing biopotential measurements, including a core, the core including a first conductive line, a first shield that surrounds the first conductive line, and a first insulator that surrounds the first shield. The cable further includes a control section located outside the core, which includes a second conductive line, a second shield that surrounds the conductive line, and a second insulator that surrounds the second shield.

Abstract: An infusion data communication system provides a communication link among a fluid container, an infusion pump, and a patient through which identification data may be communicated. Data devices are located at the fluid container and the patient and conduct low frequency RF energy at a low power level containing the data into the medical fluid. The data-laden RF energy propagates through the medication fluid to data readers at the infusion pump which receives the RF energy and reads the data. A comparison is made to verify that the right medication is mounted to the infusion pump for administration to the right patient. RFID devices may be used for the data devices and readers. Pump programming data may also be propagated to the infusion pump from the container RFID tag. The RFID device at the patient may be writable and may be used to store a patient MAR.

Abstract: A connector is described which includes a valve housing comprising a valve housing base and a valve cap, the valve housing defining an inlet port, and an outlet port, the valve housing further including a fluid path from the inlet port to the outlet port, the fluid path including a channel formed in an inner wall of the valve housing. A valve insert in the valve housing defines a bowl sealed by a diaphragm, such that the sealed bowl forms an inner volume in the valve housing. A valve plug operable seals the inlet port when the connector is in an unactuated state thereby closing the fluid path through the connector. Upon actuation of the connector the valve plug deforms the diaphragm into the inner volume thereby unsealing the inlet port and opening the fluid path through the connector. Because of the arrangement of the valve plug, valve insert and diaphragm, the connector has a low priming volume and has positive fluid displacement characteristics upon actuation.

Abstract: A connection device has a male connector and a female connector. The female connector will only accommodate the dedicated male connector, thereby prohibiting a misconnection with the wrong male connector. In certain embodiments, a member prohibits male connectors, other than a dedicated male connector, from being inserted into the female connector. In certain other embodiments, a post prohibits male connectors, other than a dedicated male connector including a slot, from being inserted into the female connector. In still certain other embodiments, a series of prongs in the male connector and corresponding grooves in the female connector ensure the proper connection. Once the male connector is inserted and secured within the female connector, a fluid-tight seal is formed between the male connector and the female connector.

Abstract: A circulation system for use in a rebreathe system includes a base and a fan assembly coupled to the base. The base includes a motor and a rotatable drive shaft coupled to the motor. The fan assembly includes a housing with an inlet and outlet. The fan assembly further includes a fan coupled to the drive shaft to rotate therewith and is fluidly isolated from the drive shaft.

Abstract: A sensor assembly includes a sensing element and an actuator. The sensing element measures a parameter associated with gas in an airway. The actuator actuates the sensing element to prevent contamination build up on the sensing element.

Abstract: Described herein are embodiments of systems and methods for providing an automated medication handling system that can, among other things, single-dose package medications, store and dispense medications in a pharmacy, transport medications to a nursing unit or other remote location, store them at that remote location, and load them into a portable unit carried by a nurse, who may dispense the medication at a bedside.

Abstract: A method comprises loading a tooling module onto a module carrier unit, inserting the module carrier unit into a molding press so that the carrier unit rests on a supporting member of an injection molding press, and closing the molding press until the tooling module is mated to an ejection side of a mold base.

Abstract: A valve for controlling delivery of fluid includes a valve seat comprising a fluid inlet, a fluid outlet and a conical well having an opening, a beveled surface and a bottom, and a valve membrane comprising a conical portion having a base and a tip. The conical portion is configured to fit within the conical well of the valve seat. The valve membrane is configured to fluidly connect the fluid inlet to the fluid outlet when the valve membrane is in an undeformed position and fluidly disconnect the fluid inlet from the fluid outlet when the valve membrane is in a radially deformed position.

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 system and method for communicating and validating patient information including medication delivery information in a care-giving facility is provided. A medical transaction carrier is used to communicate information regarding medication delivery and other patient information between a control system in communication with the care-giving facility's other information systems and a patient specific asset such as an infusion pump. All information carried by the medical transaction carrier is validated both at the patient specific asset and at the control system. This validation allows for positive control of all transactions even if a medical transaction carrier is lost. The medical transaction carrier may be a smartcard, a FDA such as a Palm™ Pilot, laptop computer, pager, mobile phone, or other device capable of storing and communicating information. The system may use either wired or wireless connections to communicate information between the components of the system.

Abstract: Disclosed is a method and system for analyzing patient hospitalization data to determine a Nosocomial Infection Marker (NIM), the method comprising receiving from a database hospitalization data associated with at least one patient, calculating from the hospitalization data the number of specimens with non-duplicate hospital isolates (SNDHI) markers, calculating from the hospitalization data antibiotic utilization criteria (AUC) markers, and determining the nosocomial infection marker (NIM) for each patient, based upon the calculated SNDHI and AUC markers.

Abstract: Disclosed is a method and system for analyzing patient hospitalization data to determine a Nosocomial Infection Marker (NIM), the method comprising receiving from a database hospitalization data associated with at least one patient, calculating from the hospitalization data the number of specimens with non-duplicate hospital isolates (SNDHI) markers, calculating from the hospitalization data antibiotic utilization criteria (AUC) markers, and determining the nosocomial infection marker (NIM) for each patient, based upon the calculated SNDHI and AUC markers.

Abstract: The present invention provides for a system an method of monitoring the status of a plurality of medical devices connected to a central computer or server using a wired or wireless network, and displaying information representative of the status of the medical devices to a user on a display screen using both graphics and text. The system is also capable of determining when a condition or alarm warranting notification of the care giver to correct the condition exists, and displaying information about the condition or alarm on the display, including associating a warning graphic or icon representative of the condition or alarm with an icon representing a specific medical device or portion of a medical device. The system includes a rules data base and decision engine that may be used to determine the existence of conditions that require notification to the care giver.

Abstract: An optical flow sensor is provided, including a heater configured to heat an aliquot of fluid in an adjacent fluid-delivery channel and a sensor disposed adjacent to the fluid-delivery channel downstream from the heater. The sensor is configured to illuminate fluid in the fluid-delivery channel, to collect reflected light from the illuminated fluid, and to determine when the heated aliquot passes the sensor based upon an amount of the reflected light. A method for determining a flow rate of a fluid is also provided.

Abstract: A system and method in accordance with the invention allow a user to select when messages relating to medication events are sent and to select the content parameters of those messages. In one aspect, a user selects certain event types, the occurrence of which will cause a message to be sent to the user. For example, the user may select a message type that pertains to the availability of a medication in an automated dispensing machine for that user's patient. In another aspect, the user may customize the contents of the message to include or exclude certain information. For example, the user may desire the message to indicate only the patient's name and not the patient's gender or age. In yet another aspect, the user may filter messages so that only certain messages are sent. For example, the user may select a filter that permits only messages pertaining to his or her patients to be sent.

Abstract: A heated humidifier including an autofeed mechanism disposed within a humidifier chamber. The autofeed mechanism includes a housing, a float, a stem, and a sealing body. The housing defines an inlet, an outlet, a first chamber connected to the inlet, and a second chamber connected to the outlet and the first chamber by a channel. The float moves within the second chamber with the stem projecting therefrom and through the channel. The sealing body is within the first chamber and cooperates with the stem. In an open state, the sealing body is displaced from the channel to permit filling of the humidifier chamber. In a closed state, the sealing body seals the channel to prevent liquid flow to the outlet. A location of the sealing body relative to the channel is controlled by the float as a function of a humidifier chamber liquid level.

Abstract: A catheter integral with a valved needle-free connector provides a safety catheter device configured to receive a blunt cannula and sharp needle forming an insertion mechanism. The sharp needle is mounted within a needle tube and a control handle is used to slide the sharp needle out of and into the protective needle tube. When the insertion mechanism is mounted to the connector and the control handle is used to slide the sharp needle out of the tube, a blunt cannula first moves into contact with and enters the bore of the valve mechanism of the connector opening it and protecting it from damage that may be caused by the sharp needle. The sharp needle is then extended through the connector and extends out the distal end of the catheter so that a venipuncture procedure may be performed to properly locate the catheter in the patient's circulatory system. Once located, the needle may be retracted into the insertion mechanism, the insertion mechanism disconnected from the connector, and discarded.

Abstract: Systems and methods of measuring pressure of fluid in a disposable IV set connected to a fluid supply pump is disclosed. At least one sensing arrangement coupled to the fluid supply pump is provided. A chamber having a movable element is provided, the movable element configured to move in response to changes in fluid pressure within the disposable IV set and thereby cause a change in a sensed measurement variable associated with the sensing arrangement without contacting the sensing arrangement. A measuring signal indicative of the sensed measurement variable is generated. The fluid pressure within the disposable IV set is determined based on the measuring signal.