Abstract:
A rotatable electrical connector can include a base housing having a bottom surface, a top housing that is rotatably engaged with the base housing, and a plurality of contact pads that are arranged radially within the base housing. The contact pads each have a top surface and a bottom surface. A plurality of signal pins are individually associated with the plurality of contact pads; and each of the signal pins correspondingly project outwardly from the bottom surface of an associated contact pad and outwardly from the bottom surface of the base housing. A center ground pad, having a top surface and a bottom surface, is provided within the base housing. A ground pin projects outwardly from the bottom surface of the center ground pad and outwardly from the bottom surface of the base housing. A plurality of conductors is arranged radially within the top housing. The conductors individually correspond to the plurality of contact pads within the base housing. Each of the conductors has (i) a bottom surface that is capable of being in rotatable contact with the top surface of each of the contact pads and (ii) a top surface that projects outwardly from the top housing. A ground conductor is centrally located within the top housing and is surrounded by the plurality of conductors. The ground conductor has a bottom surface that is in rotatable contact with the top surface of the center ground pad in the base housing, and a top surface that projects outwardly from the top housing.
Abstract:
A medication safety device and method can include an infusion pump and a drug library in communication with the infusion pump. The drug library can have upper hard and soft limits and lower hard and soft limits associated with at least one drug. A graphical user interface can display a bar chart showing upper and lower soft limit bars for the at least one drug. The upper and lower soft limit bars can be grabbed and dragged on the graphical user interface in touch-screen fashion to new positions associated with new upper and lower soft limits. The graphical user interface and associated hardware and software can be configurable to responsively re-analyze data and compare a particular infusion to the new upper and lower soft limits.
Abstract:
An aural volume feedback system is implemented in a center having a plurality of agents working thereat. Each agent is situated at a work station for being in calling contact with a client. At the work station, a microphone transforms aural speech of the agent into an electrical format, and a volume detector samples the electrical format and generates based on the sampling an instantaneous volume level. The volume detector compares the generated volume level to a predetermined threshold to determine that the agent is speaking excessively loudly, and thereafter outputs a trigger signal. A feedback generator receives the trigger signal, and based thereon generates a feedback to be perceived by the offending agent at the work station, where the perceived feedback hopefully causes the offending agent to reduce the aural volume thereof.
Abstract:
An embodiment is directed to pressure plate for attachment to an infusion pump, where the pressure plate includes a tubing support surface at least partially surrounded by a raised perimeter support. The pressure plate includes a plurality of guide structures extending from the raised perimeter support that define a passageway for an infusion pump tube. Additionally an attachable flow stop assembly is included that includes an attachable occlusion arch and an attachable flow stop arm. The attachable occlusion arch includes a plurality of tab structures that couple to the raised perimeter support. The occlusion arch further includes an aperture configured to surround an infusion pump tube threaded therethrough. The attachable flow stop arm is operatively coupled to the raised perimeter support adjacent the attachable occlusion arch in a spring-biased fashion such that the aperture in the occlusion arch may be selectively occluded by the flow stop arm.
Abstract:
A connector has a first member with a distal portion non-removably coupled to a proximal portion of a second member. Respective through passages at the first and second members are in alignment to establish a through channel longitudinally along the connector. A seal in the connector prevents fluid leakage from the connector. A conventional fitting may be provided at one of the ends and a non-conventional fitting may be provided at the other end of the connector so that the connector may connect a device with a conventional fitting to a device with a non-conventional fitting. Once connected to the connector, the device with the conventional fitting is not removable from the connector. The first and second members are rotatable relative to each other about the longitudinal axis of the connector to enable rotational alignment of devices connected to the connector.
Abstract:
An apparatus for maintaining a library of program data for medical pumps, the apparatus comprising: memory loaded with a database, the database including a plurality of program data records and a plurality of data key records, each program data record containing a set of program data items, at least some of the program data items included in the database for controlling operation of a medical pump, each data key record containing a data key and each data key identifying one of the data program records; a database management system programmed to link a data key to a set of program data; and a scanner in data communication with the database management system, the database management system being further programmed to receive a code scanned by the scanner, save the code in a data key record, and link the code to a set of program data, the code being a data key.
Abstract:
A regional anesthesia catheter used with a guide, for example a cannula, has a distal portion integrally connected to its main portion by a junction portion that has a cross-sectional profile different from the distal and main portions, so as to predispose the distal portion of the catheter to move in a given direction when it is not constrained by the guide. The cross-sectional profile of the junction portion may be configured in a particular shape, or be constructed to have a flexibility that predisposes the distal portion to bend, curve or move toward a given direction. A number of portions of a catheter may be configured to bend at a predefined direction. Further, a catheter may be configured to have a cross sectional profile or a predefined flexibility along its entire length to cause the catheter to move in a predefined direction.
Abstract:
A fitting has a first end conventional connector and a second end non-conventional connector of a given configuration that is matable only to a counterpart non-conventional connector having a configuration complementary to the given configuration. The body of the fitting has two extending wings that merge with a partition that separates the conventional connector from the body. A label may be mounted about the neck extension of the male connector to convey information to the user. The portion along the fitting between the label and the partition provides a location whereat the user can position his fingers to grasp the fitting. The partition prevents the fingers of the user from coming into contact with and contaminating the conventional connector, while the label, in addition to conveying information to the user, also acts a barrier to prevent contamination of the non-conventional connector by the fingers of the user.
Abstract:
A free-flowing anti-coagulant powder composition, the anti-coagulant composition containing heparin and a bulking agent that is lyophilized or spray dried and ground into a powder. The powdered anti-coagulant composition can be dry filled into syringes and other blood collections systems for rapid dissolution and mixing with collected blood sample without agitation of the container. The formulation may also retain a portion of the initial moisture, which may improve the shelf life and stability of the composition.
Abstract:
A safety catheter insertion assembly including a catheter hub coupling assembly. The safety catheter insertion assembly having a needle hub slideably coupled to a needle housing such that the needle hub is moveable between a first position wherein an insertion needle extends from the needle housing, and a second position wherein the sharp distal tip is housed within the needle housing, the catheter hub coupling assembly coupling the catheter hub to the needle housing in the first position and releasing the catheter hub from the needle housing in the second position.