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 generally rigid molded plastic catheter hub attachment (16, 52, 74) includes one or more co-molded elastomeric gaskets (22, 58).

Abstract: An enclosed needle catheter insertion device includes a catheter assembly and a need insertion device having a needle guard housing to enclose a needle in a shielded position and a needle support supporting the needle for movement between a ready position, with the tip of the needle exposed, to a shielded position with the needle within the needle guard housing. Movement of the needle support and the needle relative to the needle guard housing is accomplished by manual manipulation of a gripping component external of the needle guard housing. A separate, proximal end cap external of the needle guard housing encloses a proximal portion of the needle guard housing, and is affixed to the needle support.

Abstract: An apparatus comprising a user interface configured to generate an electrical signal to begin determination of an effective correction factor when prompted by a user, an input configured to receive sampled blood glucose data of a patient that is obtained during a specified time duration, including a time duration after delivery of an initial insulin correction bolus, and a controller in electrical communication with the input and the user interface. The controller includes a correction factor module configured for determining an effective correction factor according to an amount of insulin in the initial insulin correction bolus and a decrease in the blood glucose level determined using the sampled blood glucose data. Other devices and methods are disclosed.

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: An inflatable convective thermal blanket is designed to have at least one section on its top surface that has securely mounted thereon at least one fluid absorbent mechanism for absorbing fluids from a subject that is placed onto the blanket, or from fluids fallen onto the blanket from other sources. The one section is configured onto the blanket in such a way that it forms a well for collecting the fluids. The fluid absorbent mechanism, which may be in the form of a pad, would absorb the collected fluid to thereby minimize evaporative and cooling effects on the subject. Instead of mounting it on top of the blanket, the fluid absorbent pad may be mounted to the underside of the blanket, with appropriate holes and/or openings provided at the fluid collecting section, so that the collected fluids are drained onto the fluid absorbent pad.

Abstract: A multi-use, hand held, single patient oscillatory positive expiratory pressure respiratory therapy device which is easily assembled and disassembled for cleaning, and which is not position dependent during therapy, but operable through a wide range of device orientation.

Abstract: A device for inserting a cannula of a subcutaneous infusion device into a subcutaneous layer of skin of a patient. For example, some devices automatically retract a needle used to introduce the cannula of a subcutaneous infusion device into the subcutaneous layer of skin of a patient. The device can include a housing with an internal cavity, as well as a needle coupled to the housing. The needle can be coupled to a cannula of a subcutaneous infusion device. A member can move the needle. Upon full introduction of the needle and associated cannula of the subcutaneous infusion device into a subcutaneous layer of skin of a patient, the member is automatically actuated to move the needle into the internal cavity of the housing into the retracted state while leaving the cannula of the subcutaneous infusion device in the subcutaneous layer of skin of the patient.

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, 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: The inventive blanket is an inflatable underbody convective thermal blanket whereon the head and the upper body of a patient may lie. The blanket is in the shape of a cross with a truncated lower vertical portion and an upper head portion onto which the head of the patient lies. The blanket has two horizontal arm portions that extend from the main body portion of the blanket and onto which the arms of the patient may be positioned. At each of the arm portions there is a flap that may be used to cover the arm of the patient. An inlet port is provided in an upper corner at the head portion of the blanket. The heated air input to the blanket is directed by a plurality of sealed strips to flow in respective desired directions around the arm portions and the lower truncated body portion of the blanket. Sets of apertures are provided along an inner sealed periphery that defines a T-shaped uninflated area onto which the torso of the patient lies.

Abstract: A safety device to be used with a vial, or capsule, has a collar dimensioned to slidably fit about the body of the vial. Extending from the collar is a neck member that has connected to its other end a housing pivotable to a position along the longitudinal axis of the vial. A latch member having a lip is integrated to the neck member and extends out from the neck member in a direction towards the center of the collar. Neck member is fabricated to have an elastic characteristic so that if it is not biased by any external force, it will return to its original position. As the collar of the safety device is moved along the body of the vial, neck member is biased away from the vial as the latch member maintains contact along the outer surface of the vial, and then the outer surface of the hub formed at the top end of the vial.

Abstract: A prepackaged safety needle device has fitted to a holder a double-ended needle assembly and a needle protection housing pivotally connected to the neck of the housing. The hub of the double-ended needle is mated to the neck of the holder. A circumferential sleeve extending from the neck of the holder envelops the hub so that when the needle that extends away from the holder is capped by a sheath, the lower portions of the sheath would coact with the sleeve to form a relatively tight fit. The configurations of the sleeve and the sheath with respect to the needle hub, at their respective interacting portions are such that a tortuous path is established which allows sterilizing gas to pass into the space capped by the sheath, but yet prevents bacteria or other contaminants from intruding into the space.

Abstract: A needle protective housing used to cover a contaminated needle after use is configured to have at least one cam positioned below the lip of the sheath attached to the base of the needle device for covering the needle prior to use. When the sheath is attached to the base of the needle device, the needle protective housing is positioned in proximity to the sheath. To remove the sheath, a user would pivotally move the needle protective housing in a direction away from the sheath so that the cam coacts against the lip of the sheath in an upward direction as the needle protective housing is pivoted downwards relative to the needle device. Consequently, the sheath that covers the needle prior to use is forced upwards until it is disengaged from the needle base. The cam may be an integral extension of the needle protective housing, or it may be a clip retrofittable to the needle protective housing.

Abstract: An inflatable convective thermal blanket is designed to have at least one section on its top surface that has securely mounted thereon at least one fluid absorbent mechanism for absorbing fluids from a subject that is placed onto the blanket, or from fluids fallen onto the blanket from other sources. The one section is configured onto the blanket in such a way that it forms a well for collecting the fluids. The fluid absorbent mechanism, which may be in the form of a pad, would absorb the collected fluid to thereby minimize evaporative and cooling effects on the subject. Instead of mounting it on top of the blanket, the fluid absorbent pad may be mounted to the underside of the blanket, with appropriate holes and/or openings provided at the fluid collecting section, so that the collected fluids are drained onto the fluid absorbent pad.

Abstract: An inflatable convective thermal blanket is designed to have at least one section on its top surface that has securely mounted thereon at least one fluid absorbent mechanism for absorbing fluids from a subject that is placed onto the blanket, or from fluids fallen onto the blanket from other sources. The one section is configured onto the blanket in such a way that it forms a well for collecting the fluids. The fluid absorbent mechanism, which may be in the form of a pad, would absorb the collected fluid to thereby minimize evaporative and cooling effects on the subject. Instead of mounting it on top of the blanket, the fluid absorbent pad may be mounted to the underside of the blanket, with appropriate holes and/or openings provided at the fluid collecting section, so that the collected fluids are drained onto the fluid absorbent pad.

Abstract: An enclosed needle catheter insertion device (10) includes a catheter (12) and a needle insertion device (14) which are held together by cooperating arms (52, 53) with one or more detents (56) cooperating with a radially projecting surface (26) of the catheter hub (16). Insertion device (14) includes a guard housing (30) to enclose a needle (34) in a shielded position and a support housing (32) supporting the needle (34) for movement between a ready position, with the tip (36) of the needle (34) exposed, to the shielded position. Cooperating lock elements (47, 78) are provided for the housings (30, 32) which are positioned to define a lock actuation stage between the ready and shielded positions, whereat the needle is still within a passageway (54) defined by the cooperating arms (52, 53).

Abstract: A menu driven reprogrammable drug pump is provided with a memory, such as flash memory, a display, a keyboard, and a communications port to allow a generic pump to be programmed with a desired pump application (therapy) program and patient specific settings. Programming and data transfer with another pump or a computer to and from the patient pump is by the communications port that allows local and/or remote communications with the pump. Flash memory stores the pump application program during use. Patient safety is provided by a cassette identification system, an occlusion detection system, and a latch/lock detection system. Automated testing of the pump is by a closed loop testing system.

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: 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.