Abstract: A needle protector that protects the tip or distal end of a cannula, a trocar, or a cannula/trocar combination, is provided by an extruded tubing that has at least a section thereof that includes one or a plurality of protrusions or protuberances that are configured in a given fashion so that there is a slight bend created at that section of the tube, when the tube is fitted onto a cannula or trocar with the protrusions coming into contact with the outer diameter surface of the cannula or trocar. This results in friction contact between the protrusions and the cannula or trocar to maintain the tube protector in place relative to the cannula or trocar. The protrusions may be punched or lanced in the tube to a given depth towards the interior of the tube to establish a given friction contact.

Abstract: A medication pump includes a housing including an external wall and a plurality of internal adjoining housings, including a first housing enclosing a cartridge. The pump includes a primary vent for venting the medication pump to atmosphere, the primary vent including a primary liquid barrier allowing passage of gas therethrough while preventing passage of liquid therethrough. The pump includes a secondary vent on the first housing, the secondary vent including a secondary liquid barrier allowing passage of gas therethrough to an interior of the housing while preventing passage of liquid therethrough.

Abstract: A pressurized respiratory gas humidifier adapter with a pressure relief valve having an audible signal generating device incorporated into a low-flow respiratory gas supply system at a position in the system wherein the pressure relief valve and an audible signal generating device are protected from inadvertent damage during use of the humidification system, especially during connection of the adapter into the respiratory gas supply system and when the adapter is connected to a humidifier container prior to coupling into the gas supply system.

Abstract: An allergy testing tray assembly has an outer tray and an inner tray fitted in the outer tray. Each one piece tray is molded to have three longitudinal areas separated by two rows of spaced posts. A plurality of allergy testing needles are removably held between the adjacent posts. These syringes each have needle protective housing and a sheath that covers the needle prior to use color coded to reflect the gauge of the needle of the syringe. The plunger end of each of the syringes is capped so that each syringe is isolated from the environment. The trays are sealed by a cover sheet that may also have markings in the same color as the color of the housing and the sheath, so that a clinician can readily tell the gauge of the needle of the syringes stored in the trays, without having to remove the cover sheet.

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 disposable warmer cartridge is used to heat fluids to be infused to the patient to prevent hypothermia in the patient. The cartridge has in its chamber a pair of spaced in parallel electrodes that have substantially the same dimension. When RF power is fed to the electrodes, an alternating electric field is generated between the electrodes to directly heat the fluid that is in the chamber. The heating of the fluid is achieved in a substantially instantaneous manner by controlling the energization of the electrodes through the distributed impedance of the electric field between the electrodes. Heat is readily controlled by modulating the RF power fed to the electrodes. Feedback to control the temperature of the fluid in the cartridge may be provided by non-contact and direct contact sensor(s).

Abstract: A pole clamp has two legs wherebetween poles of different diameters may be positioned. One of the legs is configured to grip one side surface of the pole. The other leg of the clamp member has a channel through which a threaded shaft is movable along a longitudinal axis toward the one leg. Also formed in the other leg is a bore orthogonally to the channel. A guide that may be in the form of a half nut is movable within the bore, with the threaded surface of the half nut being in a threaded relationship with the threads of the shaft, when the guide is in a first position, so that the shaft is movable along the axis when it is turned. The guide is movable to a second position to disengage its threaded surface from the shaft. When thus disengaged, the shaft is movable bidirectionally along the axis by simple push and pull movements. A second embodiment of the pole clamp utilizes a yoke slider guide having two arms with a narrow gap and a wider gap between the two arms.

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 site is coupled to the skin of a patient by an adhesive portion including a release feature that allows the patient to remove the adhesive portion from the skin. The set can be coupled to the site by, for example, placing the set over the site and moving the set from an unlocked to a locked position. The substance can then be delivered through the set to the site, and from the site into the patient through the cannula. 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.

Abstract: An apparatus comprising a controller. The controller includes an input/output (I/O) module and a rule module. The I/O module is configured to present a question for a patient when communicatively coupled to a user interface and receive patient information in response to the question via the user interface. The rule module is configured to apply a rule to the patient information and generate a suggested insulin pump setting from application of the rule. Other devices, systems, and methods are disclosed.

Abstract: A system and method for adjusting insulin infusion volume based on air in an infusion set tube includes inputting at least one location and length of an air bubble along the infusion set tube. An air bubble volume is determined in the infusion set tube. An insulin infusion volume is determined based on a desired insulin infusion. A determination is then made whether the desired insulin infusion would include the air bubble volume based on the inputted location and length of the air bubble. The air bubble volume is added to the insulin infusion volume to make an adjusted insulin infusion volume if the insulin infusion volume includes the air bubble.

Abstract: A connector assembly for a heat exchanger has a fitting and a mount to which the fitting couples. The fitting has an elongate body having a proximal portion and a distal portion. At the proximal portion there is a crossbar, and at the distal portion there are an inlet and an outlet that protrude away from the body. Two wings extend from the body in a direction opposite to that of the inlet and outlet. There is formed on each of the wings a locking protrusion. The mount has a top portion where there is a groove dimensioned to accept the crossbar of the fitting. A longitudinal channel is formed orthogonal to the groove in the mount. Two sidewalls extend from the mount each for accepting a corresponding one of the wings, when the fitting is coupled to the mount.

Abstract: An apparatus comprises receiving a user prompt in a blood glucose (BG) management device to start a determination of an effective correction factor, receiving sampled blood glucose data of a patient obtained during a specified time duration, including a time duration after delivery of an initial insulin correction bolus, determining the effective correction factor using the BG management device according to a determined decrease in the blood glucose level of the patient and an amount of insulin in the initial insulin correction bolus, and cancelling the determination of the effective correction factor if a blood glucose level of the patient is outside of a specified range of blood glucose levels.

Abstract: A needle tip spring protector for a needle having a proximal end, a distal end, and a shaft extending therebetween. The needle tip spring protector includes a spring that circumferentially surrounds a portion of the needle shaft and is restrained in a state wherein its inner diameter is large enough to allow the shaft to move freely within the spring. When the needle is moved to a position in which its distal end is at least partly within the spring, at least one of the ends of the spring releases from restraint such that the spring automatically returns to a state in which its inner diameter is sized so as to grippingly engage the shaft of the needle. Thus, after activation, the spring securely surrounds the distal end of the needle to protect healthcare workers and others from accidental contact with the needle's distal end. When used in conjunction with a catheter assembly, the needle tip spring protector may passively release from the catheter hub after the spring is automatically activated.

Abstract: A combination underbody and overbody blanket has first and second portions sandwiching a middle portion. The first portion may be shorter than the second portion. An opening is provided at the middle portion, or at a location that overlaps the middle and first portions. The opening has a dimension sufficiently large to enable the head of a patient to pass through. At least one air inlet is provided at the middle portion to allow air to be input into the blanket. The blanket is configured in the shape of a poncho, with the first portion covering the front torso of the patient and the second portion covering the back of the patient. A tearable seal is provided at the first portion that allows the first portion to be separated into two halves to expose the front upper torso of the patient and/or to facilitate the placement of the middle portion about the neck and onto the shoulders of the patient.

Abstract: A convective warming blanket has a head portion and a plurality of peripheral sections extending orthogonally from each side of a central section that extends uninterrupted from a proximal end below the head portion to a distal foot end of the blanket. Each peripheral section is separable from its adjacent peripheral section by a frangible or tearable common seal. At least one through passage connects each peripheral section to the central section, so that the peripheral sections are inflated when heated air is input to the blanket. The multiple peripheral sections each are movable relative to the central section, so that different body parts of the patient may be selectively accessed. The head portion of the blanket is formed by two tubular sections that extend from the proximal portion of the blanket to encircle the head of the patient, when the blanket is placed over the patient.

Abstract: A full body blanket has a central bonded strip that extends from a distal end of an upper portion of the blanket to the foot end of the blanket to divide the main body of the blanket into two longitudinal portions. A discontinuous slit or tearable line is provided along the length of the strip to enable the longitudinal portions to be separable from each other by a user applying a force along the tearable strip. The strip may be torn anywhere along its entire length so that the longitudinal portion to be removed from the patient may be folded back anywhere along the length of the strip to selectively expose particular body parts of the patient. The blanket is inflated by heated air, and the heated air is circulated by channels that extend longitudinally along each of the longitudinal portions. Rows of apertures provided along the channels at the layer of the blanket that makes contact with the patient output the heated air to warm the patient.

Abstract: A heater unit includes power failure management to detect disruptions in the electrical power supply, such as the AC supply, for the unit. The heater unit emits an audible alarm in response to detection of such a disruption, and may shut down the heater(s) and visuals display(s). The heater unit advantageously includes a power storage device, such as a super-capacitor, to temporarily power the electronic circuitry of the heater unit. Operating parameters, such as of a processor of the electronic circuitry, may be stored in a non-volatile memory response to the disruption, and recalled if the disruption terminates before the level of power has gotten too low to sustain reliable operation of the processor.

Abstract: A convective warming blanket is configured to have an upper body portion and two leg portions that extend from a distal end of the upper body portion. The leg portions are separated by a space sufficient to expose a lateral side of a patient covered by the blanket. A flap separable from the leg portion that extends from the mid-section of the upper body portion may be used to securely wrap around the extended arms of the patient, who is lying on his side. Adhesive tapes are provided on the outside edges of the leg portions to secure the blanket to the surface onto which the patient lies. Apertures are appropriately formed at the sheet that comes into contact with the patient at the upper body portion and along the respective inner side edges of the leg portions so that both the upper body and the exposed lower body of the patient are warmed by heated air. The blanket is designed to have mirror image versions usable for exposing the lateral left side or the lateral right side of the patient.

Abstract: A needle guard includes a clip with a canting wall to grip the needle shaft and a distal wall to block the tip thereof, wherein the canting and distal walls may be interconnected by an angled strut, a spring member, such as a leaf spring, may have a portion extending past an edge of the strut to bias the clip to grip the needle shaft, and the distal wall may be or include a stylus and have an L-shape to define a lip to help block the needle tip. The clip may have a depending heel to help pivot the clip about a ledge to grip the needle shaft. A needle support may be provided to limit flexure of the needle which might otherwise allow the needle to come loose from the clip. Arrangements for limiting rotation of the needle hub and needle guard housing are provided, as is a protective shroud to reduce the risk of inadvertent activation of the needle guard. Further, the needle guard may be used with a catheter assembly. Also provided is an improved duckbill release mechanism.