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: An infusion planning system that improves timeliness and efficiency of patient care and includes methods, systems, and apparatuses for planning, visualizing, and coordinating medication delivery. These methods, systems and apparatuses can include improved scheduling capabilities for infusion pumps and other medical devices in hospitals or health care facilities. Some embodiments relate to improved recording and reporting of medical care information as well.

Abstract: A combined detectional and positional sensor for a syringe pump. The sensor can comprise a syringe thumbpress clamp that is pivotable so that an engagement pin deflects a linear membrane potentiometer first circuit thus providing a closed switch for detection of a syringe in the pump and a variable signal return for indication of plunger head position. Embodiments of the sensor can be used in relatively large syringe pumps and in relatively small syringe pumps, for example.

Abstract: A needle guard clip assembly has a clip and a spring, the clip having a first wall with a needle passage therethrough, a generally parallel second wall, a strut connecting the two walls, and a heel extending from the first wall. The walls, strut, and heel are an integral piece. The spring is associated with and extends from the first wall.

Abstract: A pole clamp for mounting a medical device to a pole. The pole clamp includes a main body, including a first portion including a threaded hole therethrough, a second portion that is disposed at an angle relative to the first portion, and a pivot post disposed in the second portion. A threaded adjustment rod is rotatably disposed in and through the threaded hole of the first portion. The threaded adjustment rod has a knob at a first end thereof and a push plate at a second end thereof. A rotatable stop block has a plurality of faces and is rotatably coupled to the pivot post. The rotatable stop block is rotatable to a plurality of positions to align a selected one of the plurality of faces opposite the push plate.

Abstract: An implantable portal includes a septum that has embedded therein a plurality of formations that together form an indicia adapted to identify at least one characteristic of the portal. The formations are configured from impressions formed on different layers of the septum spatially separated along the vertical axis of the septum. The impressions are filled with a radiopaque material. The superposed formations do not overlap when viewed from atop the septum. When viewed under radiographic imaging from the top of the septum, a 3-D identification indicia is presented to the viewer. The 3-D indicia may be used as a 3-D marker to focus the location of the septum where a needle to access the fluid reservoir of the portal may be inserted.

Abstract: An illuminated medical tubing set that provides visual indications of characteristics relating to the type and operating status of the tubing. An illuminated tubing set system generally comprises an optical element, a fluid conduit, and a power source. In general, the fluid conduit is used to transmit fluid in a critical care environment. The power source interfaces with the optical element. The optical element is configured to illuminate the tubing set after being powered by the power source. Optionally, the illuminated tubing set can further comprise a pressure sensor and a microcontroller. Additional sensors, such as to monitor other characteristics of the tubing, fluid, or surrounding environment, can also be included. For example, an occlusion sensor, temperature sensor, or flow sensor, or any combination thereof, can be included.

Abstract: A system for medical tubing detection and management could include an infusion manifold housing having at least one fluid channel therethrough. At least one fluid input port could be provided in the infusion manifold housing and could be configured to connect fluidically to illuminated medical tubing and communicate with the at least one fluid channel through the infusion manifold housing. A fluid output port could be provided in the infusion manifold housing and be configured to be in fluidic communication with the at least one fluid channel through the infusion manifold housing. At least one photosensor could be provided in the infusion manifold housing and be configured to receive light from the illuminated medical tubing; and the fluid output port could be configured to connect fluidically to fluid output tubing.

Abstract: To determine the heat output efficacy of a heating device such as a convective warming blanket, a conduit structure is constructed to have coiled metal tubings that form the head, torso and other non-moving parts of a person analog. Flexible tubings interconnect the metal tubings to establish a continuous conduit between an inlet and an outlet of the structure, so that a fluid having a particular heat capacity may flow uninterrupted through the conduit structure. Respective temperature sensors at the inlet and outlet measure the input and output temperatures of the fluid. Using the flow rate, the heat capacity and the respective temperatures of the fluid measured at the inlet and outlet, the heat output efficiency of the blanket may be calculated. A FLIR camera may be used to obtain an IR image to confirm the heat output efficiency of the blanket.

Abstract: An aural volume feedback system is implemented in a center having agents each situated at a work station in calling contact with a client. At the work station, a first microphone closer to the agent transforms aural speech thereof into an electrical format forwarded toward the client. A second microphone farther from the agent transforms aural speech thereof into an electrical format forwarded toward a volume detector which samples same and generates based thereon 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 outputs a trigger signal. A feedback generator receives the trigger signal, and 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: A luer adapter fitting has a luer at one end and an elongate cylindrical insert at another end. The insert has a plurality of longitudinal ribs spatially formed about the insert. Each of the ribs has a sharp longitudinal edge. A needle extends from the end of the insert away from the luer. The luer adapter fitting is press-fitted to an internally threaded through bore at the neck of a tube holder. The circumferential dimension formed by the plurality of ribs is larger than the opening of the threaded through bore, so that when the insert is press-fitted to the through bore, the longitudinal sharp edges of the ribs would score the threads at the through bore to prevent relative rotation between the fitting and the holder. A flange at the insert snap catches onto the interior shoulder of the holder to fixedly couple the insert to the holder.

Abstract: A device for inserting a needle used to introduce a cannula can include a housing including a closed end, an open end, and an arm including a tab extending from the open end, and a sleeve configured to be placed against the patient's skin, the sleeve defining a slot extending along a length of the sleeve, and a barb positioned adjacent to an end of the slot. The slot is sized to receive at least a portion of the arm and the tab of the housing so that the arm and the tab of the housing slides within the slot as the housing is moved relative to the sleeve, and the barb is positioned to engage the tab of the housing to limit movement of the housing relative to the sleeve. The device can also include a threaded portion of the housing extending towards the closed end of the housing.

Abstract: A drug delivery system has a fluid store that has a first tubing having an outlet fitted with a connector of a given configuration that prevents the connector from being coupled to a conventional counterpart connector. The system further has a tube retaining device that has a catheter extending out of one of its ends and an inlet connector at its other end that has a configuration complementary to the configuration of the outlet connector of the first tubing, so that the first tubing may be matingly connected to the tube retaining device to establish a through fluid path from the first tubing to the catheter. A one-way valve may be provided to the tubing to prevent fluid from flowing backwards into the tubing. The tubing can be selectively occluded and opened to regulate the flow of fluid from the tubing to the catheter.

Abstract: A positive oscillatory expiratory air pressure respiratory therapy device which is adapted to receive a nebulizer for administering aerosolized medicant for selective administration during oscillatory positive expiratory pressure (PEP) therapy.

Abstract: To enable a user to readily determine the gauge of the needle of a needle assembly that has a base and a needle protective housing pivotably attached thereto, the needle assembly is injection molded from a color coded molding material which color was preassigned to correspond to the gauge of the needle. As a result, both the base and the protective housing of the needle assembly have—the same specific color, and reflect or provide an indication of the given gauge of the needle. The needle sheath that covers the needle prior to use may be made of a plastics material that may be clear, or have the same or a different color than that of the needle assembly. The gauge of the needle of a fixed needle syringe could also be ascertained by its color coded needle protective housing. Color coded markings that correspond to the gauge of the needle may also be printed onto the syringe barrel of the fixed needle syringe.

Abstract: A convective blanket has multiple sets of discontinuous bonding strips that bond or attach its upper layer to its lower layer to form a number of air flow guides within the blanket. There is at least one set of substantially parallel discontinuous strips proximate to the air input port of the blanket and another set of substantially parallel discontinuous strips remote from the air input port. For each set of in parallel discontinuous bond strips, the respective distal and proximal ends of each successive strips are aligned with the distal and proximal ends of a corresponding substantially in parallel strip to effect a cross channel so that air flowing along the air flow guide may escape to different sections of the blanket. To output the heated air from the blanket, respective single rows of successively spaced air holes are formed adjacent to and substantially along the length of the discontinuous bond strips that are located proximate to the air input port.

Abstract: Various security features for a medical infusion pump are disclosed. The security features include providing dual verification for standing orders, allowing multiple levels of access rights to features of the medical infusion pump, and incorporating a security touch screen in the medical infusion pump. Methods of use and operation of these features are disclosed as well.

Abstract: An infusion device including a site and a set for delivery of a substance to a patient. The site can include a cannula that is introduced into a subcutaneous layer of skin of the patient. The set can be coupled to the site by placing the set over the site and moving the set from an unlocked to a locked position. The set can be oriented at multiple rotational orientations with respect to the site, and can be coupled and uncoupled with the site multiple times. Also included is a device for inserting a subcutaneous infusion device into a subcutaneous layer of skin of a patient. Some devices automatically retract a needle used to introduce the cannula. Upon full introduction of the needle and associated cannula of the subcutaneous infusion device into a subcutaneous layer of skin of a patient, the device can move the needle into a retracted state.

Abstract: A tip protector for a safety catheter includes an outer member releasably engaged with the interior cavity of the catheter hub. The outer member includes a generally fixed radially outwardly projecting portion to provide a holding force, and an inner member axially shiftably received within the outer member. A needle cannula received in the inner and outer members is operable to axially shift the inner member between a distal position wherein the distal tip extends distally of the tip protector, and a proximal position wherein the distal tip is within the outer member. The holding force of the outer member to the interior wall of the catheter hub remains substantially constant irrespective of the position of the inner member between the distal and proximal positions.

Abstract: A blunt cannula includes a distal portion and a proximal portion. The distal portion has a non-uniform taper defined by a plurality, such as four, differently tapered segments. The proximal portion may additionally or alternatively have a non-circular, such as oval, cross-section. At least the major diameter (D.sub.MAJ) of the proximal portion my taper toward the distal portion.