Abstract: A liquid excipient is added to a lock solution formulation containing a lower alcohol and an anti-coagulant, antibiotic, and/or anti-microbial, such as the ethanol and tri-sodium citrate lock solution formulation, to prevent citrate from crystallizing in catheters made from silicone. The locking solution could include a liquid excipient, such as glycerol, polysorbate-20, or polyethylene glycol (PEG)-400, along with a lower alcohol, such as ethanol, and an anti-coagulant, such as tri-sodium citrate, antibiotic, and/or anti-microbial.

Abstract: A system for treating a patient suffering from obstructive sleep apnea or snoring is diclsoed. The system includes an air flow generator configured to deliver an air flow at a positive therapeutic pressure during the treatment, and an expiratory valve with an open pressure connected air flow generator. The open pressure is dependent on the therapeutic pressure from the air flow generator. The expiratory valve further exerts a back pressure upon each exhalation from the patient sufficient to create a pneumatic splint in the patient's respiratory tract. The exhalation from the patient has a first half followed by a second half and the back pressure is varied such that during the start of the first half the back pressure is between 0 and 50% of a peak back pressure and increases to a peak back pressure in the second half.

Abstract: An inspection device calibration method includes mounting a laser-operated calibration device to a calibration fixture including an adjustable target having alignment indicia; illuminating the adjustable target with laser lien from the calibration device; adjusting the adjustable target to operatively align the alignment indicia with the laser light; removing the calibration device from the calibration fixture; mounting to the calibration fixture, an inspection device including one or more adjustable features; and operating the optical inspection device, including adjusting the inspection device to operatively align the inspection device with the adjustable target.

Abstract: A syringe assembly including: (1) a syringe barrel defining a chamber; (2) a plunger mounted in the chamber and moveable with respect to the barrel; and (3) a cap holder assembly containing a cap and an absorbent material removably attached to the syringe.

Abstract: A social welfare services management method, apparatus, and computer readable medium is provided. The method includes inputting data about entities, linking the entities based on relationship between the entities; and performing a government defined unit of work based on said linking. The government defined unit of work relates to the social welfare services. As a result, a people centric approach to managing social welfare is provided.

Abstract: Methods and apparatus to use vibration data to determine a condition of a process control device are disclosed. An example apparatus includes a vibration monitoring circuit to: collect first vibration data associated with a process control device during calibration of the process control device; calculate an operating threshold of the process control device based on the first vibration data; collect usage information associated with the process control device, the usage information indicative of a remaining portion of useful life associated with the process control device; adjust the operating threshold based on the usage information, the adjusted operating threshold reflective of the remaining portion of useful life associated with the process control device; and determine a condition of the process control device if second vibration data associated with the process control device collected after the calibration exceeds the adjusted operating threshold.

Abstract: A device for treating a patient suffering from obstructive sleep apnea or snoring can include an expiratory valve connected to a manifold. The expiratory valve can include a body portion including a feedback port configured to be connected to an air flow generator. The expiratory valve can include a plunger at least partially disposed in the body portion. The expiratory valve can include a pressurizing chamber positioned between an end of the plunger and an end of the expiratory valve. The pressurizing chamber can be configured to receive air from the air flow generator through the feedback port.

Abstract: A liquid excipient is added to a lock solution formulation containing a lower alcohol and an anti-coagulant, antibiotic, and/or anti-microbial, such as the ethanol and tri-sodium citrate lock solution formulation, to prevent citrate from crystallizing in catheters made from silicone. The locking solution could include a liquid excipient, such as glycerol, polysorbate-20, or polyethylene glycol (PEG)-400, along with a lower alcohol, such as ethanol, and an anti-coagulant, such as tri-sodium citrate, antibiotic, and/or anti-microbial.

Abstract: A control circuit determines that a wireless portable electronic device currently being serviced via licensed wireless spectrum should also be served via unlicensed wireless spectrum and then transmits a Radio Resource Control (RRC) message to cause the wireless portable electronic device to connect to a network node operating in the unlicensed wireless spectrum. By one approach this control circuit comprises an Evolved Node-B base station in a Long Term Evolution (LTE) Radio Access Network (RAN) and the network node operating in the unlicensed wireless spectrum comprises an 802.11-compatible wireless local area network node.

Abstract: A device for treating a patient suffering from obstructive sleep apnea or snoring can include an expiratory valve connected to a manifold. The expiratory valve can include a body portion including a feedback port configured to be connected to an air flow generator. The expiratory valve can include a plunger at least partially disposed in the body portion. The expiratory valve can include a pressurizing chamber positioned between an end of the plunger and an end of the expiratory valve. The pressurizing chamber can be configured to receive air from the air flow generator through the feedback port.

Abstract: An antiseptic dead-end cap includes a base having first and second sides, a first annular wall extending from the first side of the base, a cylindrical center plug extending from the first side of the base, and a second annular wall extending from the second side of the base. The first annular wall has an outer and an inner surface. The cylindrical center plug has an outer and an inner surface, and is positioned within the first annular wall to form an annular chamber. The second annular wall has an outer and an inner surface, and defines a second chamber having an open end. The second chamber is further defined by the inner surface of the cylindrical center plug. An antiseptic material is on at least one of the first annular wall inner surface, second annular wall inner surface, second annular wall outer surface, and cylindrical center plug outer surface.

Abstract: A decoy tethering device for deploying and retrieving a decoy assembly includes a housing. A line is selectively extensible from and retractable into the housing. A fastener is selectively couplable to the line. A coupler that is coupled to the housing is configured to couple to a keel of a decoy. A connector that is coupled to a second end of the line is configured to couple to a weight. The fastener is positioned to decouple from the line to both extend and retract the line from the housing, and to couple to the line to retain the line in an extended configuration. The coupler is configured to couple the housing to the keel of the decoy. The connector is configured to couple to the weight to position the weight to retain the decoy in place on a surface of a body of water in which the weight is positioned.

Abstract: An interlock for an enclosure can include a primary door activator with an activator arm, a secondary door activator, and a rotatable arrangement that links the primary and secondary door activators. The activator arm can block a primary door of the enclosure from being closed when the activator arm is in an open configuration. The activator arm can be configured to rotate with the rotatable arrangement in a first direction towards the open configuration as the primary door is opened, and in a second direction away from the open configuration as the primary door is closed. The secondary door activator can be configured to engage the rotatable arrangement to prevent rotation of the rotatable arrangement when the secondary door is open, and to permit rotation of the rotatable arrangement when the secondary door is closed.

Abstract: The disclosure provides rotary machines that include, in one embodiment, a rotatable shaft defining a central axis A, the shaft having a first end and a second end. The shaft can have a first hub disposed thereon with a plurality of cavities. At least one contour is slidably received into an arcuate cavity in an exterior surface of the hub. The contour has a convex outer surface that cooperates with an inwardly facing curved surface of a housing to form a working volume.

Abstract: An antiseptic dead-end cap includes a base having first and second sides, a first annular wall extending from the first side of the base, a cylindrical center plug extending from the first side of the base, and a second annular wall extending from the second side of the base. The first annular wall has an outer and an inner surface. The cylindrical center plug has an outer and an inner surface, and is positioned within the first annular wall to form an annular chamber. The second annular wall has an outer and an inner surface, and defines a second chamber having an open end. The second chamber is further defined by the inner surface of the cylindrical center plug. An antiseptic material is on at least one of the first annular wall inner surface, second annular wall inner surface, second annular wall outer surface, and cylindrical center plug outer surface.

Abstract: An antiseptic cap and packaging for use with a connector are provided. The antiseptic cap includes a material containing an antiseptic solution. Upon application of the cap to the connector, the material compresses thereby releasing the antiseptic solution. Packaging of the antiseptic cap typically includes a cap holder and a lid. A user could remove the cap from the cap holder before applying it to a connector. Alternatively, the cap holder may be used to apply the cap to the connector.

Abstract: Methods and apparatus to test acoustic emission sensors are disclosed herein. An example apparatus includes a process control device, an acoustic emission sensor coupled to the process control device, where the acoustic emission sensor detects an operational condition of the process control device, and a piezoelectric tuning fork acoustically coupled to the acoustic emission sensor to test the operational condition of the acoustic emission sensor.

Abstract: A wireless communication may receive a composite signal that includes data symbols, a code division multiplexing (CDM) pilot sequence that is spread with a first channelization code, and a time division multiplexing (TDM) pilot sequence including a cyclic prefix where the TDM pilot sequence is spread with a second channelization code. The composite signal may be received within a designated time region such that the CDM pilot sequence has non-cyclic properties over the designated time region. The composite signal may be descrambled with a non-cyclic scrambling code.

Abstract: Methods, apparatus, systems, and articles of manufacture to monitor health information of a valve are disclosed. An example system includes a field device in a process control network to monitor a valve, and a valve health monitor to be communicatively coupled to the field device to obtain operational health information from the field device when the valve is commanded to move from a first position to a second position, the first position opposite the second position, identify a condition of the valve based on the operational health information, and send an alert via the process control network based on the condition of the valve.

Abstract: An antiseptic cap and packaging for use with a connector are provided. The antiseptic cap includes a material containing an antiseptic solution. Upon application of the cap to the connector, the material compresses thereby releasing the antiseptic solution. Packaging of the antiseptic cap typically includes a cap holder and a lid. A user could remove the cap from the cap holder before applying it to a connector. Alternatively, the cap holder may be used to apply the cap to the connector.