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: An apparatus comprising a pump configured to deliver insulin, an input configured to receive blood glucose data, a user interface, and a controller communicatively coupled to the pump, the input, and the user interface. The controller includes a blood glucose data module to compare the blood glucose data to a target blood glucose level for an insulin pump user. The controller is configured to present a question related to the blood glucose level via the user interface when the blood glucose level is different than the target blood glucose level, receive a response to the question via the user interface, and present a recommended user action based at least in part on the response. Other devices, systems, and methods are disclosed.

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 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: The Problems To dissipate or remove droplets of sweat fluid discharged from sweat glands of the finger placed on the sensor surface, which is the cause of the residual fingerprint image, from the surface of the fingerprint image sensor. Means for Solving the Problem On the surface of a fingerprint image acquisition sensor consisting of the electrode 2 of the minimum functional element separated with the grid 1, a coating layer on which the groove 30 is etched on the surface of the coating layer 32, running along the center of each grid line for draining the sweat fluid discharged from the sweat glands on the finger placed on the fingerprint image acquisition sensor.

Abstract: A safety needle assembly has a collar or ring that is rotatably mounted to a needle hub. The needle assembly may be connected to a syringe by the user grasping the needle hub in first and second embodiments, or turning of the needle sheath in other embodiments. The collar of the needle assembly may be rotated by turning the needle sheath. The needle hub may also interact with the collar by rotating the needle sheath. Mechanisms are provided at both the collar and the housing so that once the contaminated needle is covered, the needle assembly may be removed from the syringe for disposal by rotating the needle housing.

Abstract: A method and system to update a syringe pump is provided. The pump supports a syringe having a plunger and includes a piston drive to couple to the plunger, a processor to control movement of the piston drive, and a memory to store syringe profiles for different syringes. Each syringe profile contains data for the processor to control the piston drive to expel fluid from a respective syringe at a rate. The method includes, with a computing system containing a database of data correlated to an array of syringes for which the pump could be used, culling from the database a syringe profiles for the syringes to be used by the pump within the facility or portion thereof, and updating the memory of the pump while in the facility with the culled syringe profiles whereby to update the pump for operation with syringes to be used with the syringe pump.

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 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: Temperature detection circuitry is selectively coupled to a thermistor and one of two sources representing the impedance at respective ends of the expected range of temperature to which the thermistor is to be exposed. The offset of an amplifier and a scale factor to account for gain set of the amplifier are determined in an automatic calibration process while coupled to the source(s), and thereafter temperature readings are taken from the thermistor. During the calibration process, if the gain or scale factor are outside of expected ranges, a failure is determined and an alarm given and/or a heater is disabled.

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 gas vent valve assembly may be attached or incorporated to a disposable fluid transfer set used with a fluid warmer to administer an infusate to a patient. The gas vent valve assembly has a housing having a fluid inlet, a gas outlet and a fluid outlet. The gas outlet is located at the top of the housing while the fluid outlet is located at the bottom of the housing. Inside the housing is an actuator float that has an upper seal and a lower seal. The dimension of the float relative to the chamber of the housing is such that the float is freely movable within the housing to an upper position whereby its upper seal closes the gas outlet while the fluid outlet is opened, and to a lower position whereby its lower seal closes the fluid outlet and the gas outlet is opened.

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 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 one piece molded vacuum tube holder is fitted with a one piece molded needle hub assembly. A needle protection device is further rotatably mounted to the neck of the one piece vacuum tube holder. 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, so that when the needle hub assembly is press fit to the vacuum tube holder, the two portions of the locking mechanism will coact to fixedly retain the needle hub assembly within 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.

Abstract: A system and method for optical spectroscopic measurements is described. One embodiment includes a measurement head for optical spectroscopic measurements, the measurement head comprising an illumination source configured to illuminate a sample, a collection optic configured to view the sample, and an internal reference, wherein the internal reference can be illuminated by the illumination source and viewed by the collection optic.

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 so as to allow the canting wall to be tilted over center in a ready state, 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.

Abstract: A safety needle assembly has a collar or ring that is rotatably mounted to a needle hub, which may be connected to a medical device such as a syringe. The needle assembly may be connected to the syringe by the user grasping the needle hub in first and second embodiments, or turning of the needle sheath in other embodiments. In all of the embodiments, the collar of the needle assembly may be rotated by turning the needle sheath, which is designed to interact with the collar. In some of the embodiments, the needle hub likewise interacts with the collar in such a way that by rotating the needle sheath, the needle hub is likewise rotated for connection to a syringe. When an exposed needle is to be covered, after the needle sheath has been removed, a housing connected to the collar is pivotally moved to cover the needle.

Abstract: Methods, a medical device, and a computing system configured to interassociate data of the medical device are provided. The medical device uses a processor to collect data and include a respective event set identifier with data developed in connection with activity starting with a respective identifiable event of the medical device. The data may thus be parsed based on the event set identifier to access data for an identifiable event.