Abstract: An underbody convective warming blanket that may be used by a pediatric or neonate patient includes a head portion configured with multiple substantially U-shaped channels each having a plurality of adjacent rows of apertures that circumscribe the head of the patient positioned on the blanket. The adjacent rows of apertures are configured on the upper layer of the blanket so as to be positioned at an orientation or angle relative to the base plane of the blanket or the head of the patient such that those apertures would substantially face the head of the patient when the blanket is inflated, so that the heated air output from the apertures is directed substantially towards the head of the patient to thereby effect an invisible dome of heated air that envelopes the head of the patient.

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 safety catheter includes a catheter hub, a needle cannula having a tip, and a tip protector. The tip protector includes an outer member and an inner member therein. The outer member has a projection releasably engaging the catheter hub. The inner member has a pair of arms extending to free ends from a base. The inner member is axially shiftable relative to the outer member between a first position wherein the needle tip is distal of the tip protector and the free ends of the arms are spread apart such that the distal tip is not shielded, and a second position wherein the tip is within the inner and outer members and the free ends of the arms are brought into close proximity such that the distal tip is shielded. The inner member is entirely received within the outer member in both the fort and the second positions thereof.

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 temperature probe, such as for a respiratory system in which breathable gases are supplied to a patient, includes a housing having an external wall and an internal cavity defining an end and an internal cavity and further includes a temperature-responsive device in an area of the cavity near the end, such as in thermal communication with the external wall. A first potting compound that is deformable and/or has a relatively high thermal conductivity holds the temperature-responsive device in the cavity and a second potting compound having a relatively low thermal conductivity may be in the cavity behind the first potting compound. The housing may be made thin to enhance thermal conductivity, at least in the area containing the temperature-responsive device.

Abstract: A safety catheter device includes a catheter hub, a housing removably coupled to the catheter hub; a needle, and a member, the housing including a radially outwardly directed projection operable to engage the interior aspect of the catheter hub and radially moveable inwardly sufficiently to disengage therefrom, the projection being held against moving radially inwardly sufficiently to disengage when the needle is in a first position with the needle distal tip exposed and being free to move radially inwardly sufficiently to disengage coincident with the needle being moved into a second position with the needle distal tip disposed in the housing.

Abstract: A heater unit is adapted to determine if a humidification chamber thermally coupled to a hot plate of the heater unit is effectively dry based on determining a thermal response of a hot plate of the heater unit. Also, the activation period during which the hot plate is being heated is adjusted toward an optimum period by adjusting the energization or power level to the heater element thereof in relation to the duration of a prior activation period. Further, the air flow rate of gas through the humidification chamber may be estimated based on a temperature of the hot plate determined in predetermined relationship to the beginning of an activation period.

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. 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 low flow heated/humidified respiratory gas delivery system, especially useful for low flow rates as preferred in the treatment of neonate and other such patients, wherein the respiratory gas is heated and humidified as desired for delivery to the patient and the temperature is monitored at the point of delivery to the patient.

Abstract: A system and method for determining bias in a spectrometer is described. One embodiment includes a method for determining bias in a spectrometer system, the method comprising over-scanning a grating in a near-zero-response wavelength range; and determining a bias based on the over-scanning. This methodology allows for over-scanning a grating in a near-zero-response wavelength range as a substitute for using shutters or other mechanisms to block light from entering a detector in the system.

Abstract: An apparatus and method for detecting an occlusion in a downstream fluid line of a medical pump in relation to increased pressure in the downstream fluid line between the beginning and the end of each interval of a series of intervals of operation of the pump even if one or more intervals between the first and last intervals does not reflect such an increase in pressure in the downstream fluid line.

Abstract: A flow-through fluid reservoir includes a body with a first fluid port, a member movable within the body by an actuator to increase or decrease a volume of a chamber defined by a sidewall of the body. The actuator has a second fluid port. Movable member has a fluid path therethrough such that fluid ports are in fluid communication irrespective of the position of the movable member or the volume of chamber. A shaped slot on the shell of the actuator and a projection on the body cooperate to constrain relative movement of the body and actuator along a path corresponding to the shaped slot. The slot advantageously may include a stop intermediate therealong. A canted aspect of the slot may be used to initiate relative movement of the member within body. The body includes an end wall through which the first fluid port communicates. A shroud is defined by a coaxial extension of the sidewall beyond the end wall to surround the first fluid port, and gripping elements may be provided on the shroud.

Abstract: A safety catheter includes a catheter hub, a catheter tube, a needle hub, a needle cannula having a tip, and a tip protector. The tip protector includes an outer member having a flexible tab configured to releasably engage with the catheter hub and release therefrom upon inward flexing of the tab. An inner member is positioned entirely within the outer member and has a portion that impedes inward flexing of the tab when disposed adjacent the tab. The inner member is axially shiftable relative to the outer member between a first position wherein the needle tip is distal of the tip protector and the inner member portion is disposed adjacent the tab to impede release from the catheter hub, and a second position wherein the tip is within the outer member and the inner member portion is no longer adjacent the tab and no longer impedes release from the catheter hub.

Abstract: A low flow heated/humidified respiratory gas delivery system, especially useful for low flow rates as preferred in the treatment of neonate and other such patients, wherein the respiratory gas is heated and humidified as desired for delivery to the patient and the temperature is monitored at the point of delivery to 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.

Abstract: A heater unit for a respiratory system is designed for natural convection cooling air to pass first through a transformer in the heater unit and then through a heat sink in the heater unit to which is mounted a power switch to conduct heat from the power switch to the cooling air passing through the heat sink. A thermal break may be provided between the heat sink and the transformer. The transformer may be a toroidal transformer with the air passing through an aperture thereof such as from a hollow projection of the heater unit extending into the aperture. One side of the transformer may be situated along a surface of the heater unit and the heat sink secured to the heater unit against the opposite side of the transformer to hold the transformer in place. A venting chamber may be associated with an air exhaust of the heater unit to provide a circuitous exit path for air exiting the heater unit. The venting chamber may extend in generally surrounding relationship with the heater of the heater unit.

Abstract: A safety needle assembly has a needle hub and a collar. Integrally formed from the proximal portion of the needle hub is a ring that surrounds its luer base. At the distal portion of the needle hub there are coaxially formed circumferential flanges which act to allow the collar to be rotatable about the needle hub. A needle protection housing is connected to the collar and is pivotable to cover the needle that extends from the distal end of the needle hub. Before use, the needle extending from the needle hub is covered by a needle sheath that has a groove formed circumferentially at its proximal end that snap-fits to a circumferential rib formed at the distal end of the collar.

Abstract: A method of configuring a programmable pump for delivering an agent to a patient. The method comprises generating a user interface having a plurality of pages, at least one of the pages being a home page; retrieving at least one banner from memory; and displaying the retrieved at least one banner in the home page.

Abstract: An apparatus, method and program product detects an occlusion in a fluid line by determining if a relationship between force measurements departs from an expected relationship.

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.