Abstract: A single use, self-contained, self-powered disposable oximeter, in the form of a patch or a bandage strip, has mounted thereto a light emitter and a light sensor that together measure at least the SpO2 of the patient. Mounted to an electronics layer of the patch is an application specific integrated circuit (ASIC) that has electronics integrated thereto that controls the operation of the light emitter and light sensor, and the algorithm for calculating from the data collected by the sensor at least the SpO2 of the patient. Optionally, a display and an alarm may also be mounted or embedded onto the patch for respectively displaying at least the SpO2, and for informing the caregiver/patient that at least the SpO2 is not within an acceptable range, if such is the case. Also provided in the patch is a battery that powers the operation of the ASIC circuit and the emitter, as well as the display and alarm if such optional components are provided on the patch. An attachment mechanism is also provided on the patch.

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: An adapter is placed between the needle and a conventional fluid store, or medical line. The end of the adapter that connects to the needle assembly is formed to have a configuration that is complementary to that of the hub of the needle assembly, so that the adapter and the needle hub may be readily mated to each other. The other end of the adapter is formed to have another configuration, for example a conventional luer, that is readily connectable to a conventional fluid store, such as a syringe that has a conventional luer. The adapter is formed by inter-fitting two elements to effect an integral locking mechanism to prevent the uncoupling of the fluid store and the adapter, once they are securely coupled.

Abstract: Methods and apparatus for programming a medical infusion pump are disclosed. One method includes displaying a meter having two or more locations, each of the two or more locations representing a corresponding parameter value programmable into the medical infusion pump. The method further includes displaying an indicator having a selectable positional relationship to the meter, the selected position corresponding to a parameter value.

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 needle assembly has a needle hub that has a body to which are formed two plates at opposite sides thereof in a parallel relationship. The plates have respective upper edges and lower edges that lie substantially along respective planes, so that the needle hub may be stably placed onto a surface by means of the respective edges. The plates also prevent the rolling of the needle between the fingers of the clinician when the clinician holds the needle assembly by means of the plates. A partition is formed orthogonally proximate to the front ends of the parallel plates. The connector at the proximal portion of the needle hub is configured to have a non-conventional configuration that allows it to mate only with a counterpart connector that has a complementary non-conventional configuration.

Abstract: The inventive flexible structure has at least two heat transfer portions. One of heat transfer portions is positioned in contact with the body of the patient. The structure is hermetically sealed and a fluidized medium responsive to temperature change is provided in the structure between the heat transfer portions. The fluid is changeable between a liquid state and a gaseous state, when it is exposed to heat and cold. The heat absorbed by the heat transfer portion in contact with the patient is carried by the fluidized medium, as latent heat in the gas that results when the liquid is vaporized to its gaseous state, to the heat transfer portion layer not in contact with the patient, so that the latent heat in the gaseous vapor is dissipated. Upon dissipation, the gaseous vapor is condensed and the fluidized medium returns to its liquid state.

Abstract: A one piece molded vacuum tube holder is fitted with a one piece molded needle hub assembly. One portion of a locking mechanism is provided at the neck of the one piece vacuum tube holder and a second portion of the locking mechanism is provided at the needle hub of the needle hub assembly. The needle hub assembly is press fit to the vacuum tube holder. The one piece vacuum tube holder is configured to have an elongate needle cover integrally extending from its neck. A tamper evident notched joint is provided at the junction where the needle cover is connected to the neck. The opening of the vacuum tube holder through which a conventional vacuum tube is inserted may be sealed for sterilization and transport of the device. A wingnut finger grasp mechanism may be coupled to the needle cover.

Abstract: A single use, self-contained, self-powered disposable oximeter, in the form of a patch or a bandage strip, has mounted thereto a light emitter and a light sensor to measure the SpO2 of the patient. Mounted to an electronics layer of the patch is an application specific integrated circuit (ASIC) that has electronics integrated thereto that controls the operation of the light emitter and light sensor, and the algorithm for calculating from the data collected by the sensor at least the SpO2 of the patient. The patch oximeter may also be equipped with a transceiver, and the appropriate electronics, for wirelessly transceiving information to/from a remote device or another wireless patch oximeter.

Abstract: An adapter is placed between the needle and a conventional fluid store, or medical line. The end of the adapter that connects to the needle assembly is formed to have a configuration that is complementary to that of the hub of the needle assembly, so that the adapter and the needle hub may be readily mated to each other. The other end of the adapter is formed to have another configuration, for example a conventional luer, that is readily connectable to a conventional fluid store, such as a syringe that has a conventional luer. The adapter is formed by inter-fitting two elements to effect an integral locking mechanism to prevent the uncoupling of the fluid store and the adapter, once they are securely coupled.

Abstract: A convective underbody blanket has a head portion and a body portion. Provided at the head portion is a non-inflatable head area surrounded by a channel that has arranged thereat at least one row of air apertures that are oriented toward the non-inflatable head area when the channel is inflated. At the body portion there is provided a non-inflatable body area. Along each longitudinal side of the body area there is at least one longitudinal channel. Each of the longitudinal channels is in fluid communication with the channel that surrounds the non-inflatable head area. The longitudinal channels that sandwich the non-inflatable body area extend substantially along the length of the non-inflatable body area and are in fluid communication with each other by way of a cross channel formed at the foot end of the blanket.

Abstract: An adapter bridging a medication providing device and a fluid connector includes a housing shroud that is fitted at one end with a core and at its other end with an inner shroud. Once fitted to the housing shroud, the core and the inner shroud each are not removable from the housing shroud. A catch hub is provided within the housing shroud for non-removably maintaining the core to the housing shroud. The core is rotatable relative to the housing shroud. Once the medication providing device is coupled to the core, additional rotational movement, in either direction, of the medication providing device would only cause the core to rotate freely relative to the housing shroud, thereby preventing the medication providing device from being removed from the adapter. The inner shroud has a catch mechanism that enables it to mate readily with a connector when rotated in one direction.

Abstract: A wireless network having an architecture that resembles a peer-to-peer network has two types of nodes, a first sender type node and a second receiver/relay type node. The network may be used in a medical instrumentation environment whereby the first type node may be wireless devices that could monitor physical parameters of a patient such as for example wireless oximeters. The second type node are mobile wireless communicators that are adapted to receive the data from the wireless devices if they are within the transmission range of the wireless devices. After an aggregation process involving the received data, each of the node communicators broadcasts or disseminates its most up to date data onto the network. Any other relay communicator node in the network that is within the broadcast range of a broadcasting communicator node would receive the up to date data.

Abstract: An oximeter has a housing configured to have a cavity defining portion that is adapted to be fitted with covers of various dimensions to effect receptacles of different dimensions for accommodating differently sized sensor of sensor assemblies that are matable to the oximeter for sensing physical attributes of a patient. Each of the covers, once fully fitted to the housing, is fixedly latched thereto unless a force that overcomes the latching is applied to remove the cover. The effected receptacle is adapted to biasedly retain a corresponding sensor placed therein. The holstered sensor therefore would not accidentally fall out or be removed from the receptacle, until the user deliberately applies a force to remove the sensor from the receptacle.

Abstract: A regional anesthesia catheter used with a guide such as for example a needle cannula has a distal portion integrally connected to a main portion of the catheter 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 the distal portion is not guided by or constrained by the needle cannula. 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.

Abstract: A connector and method of connecting are described for connecting a first and second catheter at an overlap area where the first catheter fits within the second catheter. The connector includes a collar that surrounds a portion of the overlap area and a clamp that applies a radially inward force to the collar and encircles a portion of the overlap area.

Abstract: A female connector for medical infusion systems has a main body that has two curved wings that extend from the outer circumferential surface of the body. The respective front ends of the wings are joined integrally to a substantially circumferential partition that also extends circumferentially from the outer circumferential surface of the fitting. The connector of the fitting has a non-conventional configuration with at least two protuberances offset at an angle. The non-conventional configuration of the connector allows the fitting to only mate with a counterpart connector that has a complementary non-conventional configuration.

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: An answering service answers calls on behalf of called parties when callers place incoming calls to the called parties and the called parties are unable or unwilling to answer the incoming calls directly. A dynamic shield is employed to detect and respond to unwanted (“junk”) calls from nuisance callers. The dynamic shield includes: a detection module that detects patterns from calls received at the answering service and, for each of one or more nuisance callers, identifies the nuisance caller from the detected patterns; a database module within which the detection module creates and stores a caller record corresponding to the identified nuisance caller; and a shield module operating with reference to the caller record in the database module to screen out further junk calls from the identified nuisance caller.