Abstract: An apparatus and method that is effective for the treatment of skin itch and skin rash is disclosed. The apparatus is contained within a body which can be easily manipulated with one hand, and which is powered by a self-contained battery. Also contained within the body is a heating means, controlled by a thermostat, a temperature selector if the heating means if intended to provide multiple temperatures, and means to warn the user when the desired temperature is reached. In addition the apparatus includes means to apply the heat in a cyclical manner, in which the heat is repeatedly applied and removed, with a cycle time and pulse width in which is controlled by user by means of a control located on the body heater and some other elements that can ensure only one substantially unique temperature is used.

Abstract: The present invention comprises a system that incorporates the natural relationships of patient parameters into a medical monitoring system in order to increase monitoring specificity by reducing false positive alarms resulting from spurious data and inconclusive data. The invention also comprises a system that incorporates the natural relationships of patient parameters in order to use the data obtained from those parameters to non-invasively monitor a patient parameter that typically precludes direct monitoring.

Abstract: A navigation-assisted fitness device broadly comprising a location determining component, a fitness monitoring component and a display. The location determining component determines location data for a user of the device as the user exercises. The fitness monitoring component is coupled with the location determining component and calculates fitness information for the user as the user exercises. The display displays the fitness information and other information and data. The fitness information may include an indication of the intensity level of the user's exercise, the total amount of calories burned by the user during the exercise, the amount of fat calories burned, and the amount of carbohydrate calories burned. The device calculates the ratio of fat calories burned versus carbohydrate calories burned based on the intensity level.

Abstract: A pulse oximeter which determines multiple heart rates, and selects between them based on the metrics of only one of the heart rate calculations. A primary heart rate calculation method is selected, and is used unless its metrics indicate questionable accuracy, in which case an alternative rate calculation is available and is used instead.

Abstract: A device and method can monitor or trend a patient's respiration rate measurements according to the time of day. The device, which may be implantable or external, collects and classifies respiration rate measurements over time. The trended information about particular classes of respiration rate measurements is then communicated to a remote external device, which in turn provides an indication of heart failure decompensation. Examples of classes of respiration rate measurements include a daily maximum respiration rate value, a daily minimum respiration rate value, a daily maximum respiration rate variability value, a daily minimum respiration rate variability value, and a daily central respiration rate value. These respiration rate measurements can be further classified into daytime or nighttime respiration rate measurements.

Abstract: A technique is disclosed for determining blood flow in a living body by changing the thermal energy level in the venous blood flow path and determining temperatures in both the venous and arterial blood flow paths. Blood flow is calculated as a function of the change in energy level and the temperature differences in the venous and arterial blood flow paths.

Abstract: A method of creating an analyte sensor. The method starts with the step of providing an electrochemically active surface. Then, at least one nub made of dielectric material and extending transversely outwardly from the electrochemically active surface is created. A curable liquid is applied to the electrochemically active surface and the nub and is then cured. In this process, the nub, which could be one of several nubs, serves to support the liquid before and during the curing.

Abstract: A cuff (1) for measuring arterial pressure including a tubular sleeve (2) with an integrated inflatable chamber (11), which is adapted to be wrapped around the arm of a patient; the cuff includes fastening means (10) adapted to fasten the cuff (1) around the arm of the patient and to detect the circumference of the arm, in order to use the circumference datum as a connection factor for measuring the arterial pressure detected by means of the cuff (1).

Abstract: Apparatus and methods that use the acoustic characteristics of vascular blood flow to assess vascular conditions are disclosed. An example method for detecting a change in a vascular condition receives sound information associated with blood flowing through a vascular structure and converts the sound information into data associated with a plurality of cardiac cycles. The example method processes the data associated with the plurality of cardiac cycles to determine an acoustic characteristic associated with a current state of the vascular condition and detects the change in the vascular condition based on a difference between the acoustic characteristic associated with the current state of the vascular condition and a baseline acoustic characteristic associated with an earlier state of the vascular condition.

Abstract: A cuff-block for a finger arterial blood pressure monitor is able to relieve a blood flow impediment and the hindrance of a finger motion at the measuring site during the finger arterial blood pressure monitoring. A disk-like cuff (12) for local pressurization is attached over a finger artery (6) on a proximal finger portion (4) of a measured finger (1), this cuff (12) is held by a cuff-holding portion (11a) of an annular cuff-fixing member (11) put from the tip end portion of the measured finger (1), and the cuff-fixing member (11) is supported on the measured finger (1) with local supportings by forked supporting points (11a, 11b) of the cuff-fixing member (11) placed on respectively portions of a proximal joint (1c) and a medial one (1b).

Abstract: A method and apparatus for the transcutaneous monitoring of blood gases generally comprises a blood gas data acquisition device, a vacuum source and a blood gas transducer unit. The blood gas transducer unit is adapted for application to a patient's skin and administration of a local vacuum at the area of patient application. It further comprises an electrochemical blood gas transducer, well known to those of ordinary skill in the art, which is disposed entirely within the local vacuum at the area of patient application. The vacuum source is placed in fluid communication with the blood gas transducer unit, through a hydrophobic membrane filter for safety purposes, in order to induce a condition of hyperperfusion in the locality of the electrochemical blood gas transducer. Under the control of a microcontroller, or equivalent means, the blood gas acquisition device is then utilized to capture a measure of skin surface oxygen or carbon dioxide pressure.

Abstract: A catheter terminates at a tip that includes an array of pressure sensors. The sensors are responsive to detect and alert the user to variations of pressure that indicate the tip is either encountering an obstruction or constriction of smaller diameter than the catheter, as well as to guide the catheter through the conduit into which it is being inserted.

Abstract: A lung sound diagnostic system for use in collecting, organizing and analyzing lung sounds associated with the inspiration(s) and expiration(s) of a patient. The system includes a plurality of transducers that may be placed at various sites around the patient's chest. The microphones are coupled to signal processing circuitry and A/D converters which digitize the data and preferably provides the digital data to a computer station. A data collection and organization program, executing on the computer station, organizes and formats the data into a combination display for display or printing. The combinational display includes at least two display elements. In a first display element, the data is shown for both inspiration and expiration combined in a first time scale. In a second display element, the data for inspiration and expiration are shown individually in a second time scale that is time-expanded relative to the first time scale.

Abstract: A blood pressure measuring apparatus to measure blood pressure based on a change in a pressure by a cuff mounted to a subject comprises: cuff pressure controlling means for deflating the cuff after avascularization by the cuff at a body part around which the cuff is placed; detecting means for detecting the change in a pressure by the cuff and outputting the detection as an electrical signal; extracting means for extracting a pulse wave signal from the electrical signal; and calculating means for calculating a systolic blood pressure value and a diastolic blood pressure value based on a relation between a change rate of an index value which is calculated by multiplying a maximum amplitude of each pulse of the pulse wave signal by the cuff pressure corresponding to the maximum amplitude and a predetermined value. The blood pressure measuring apparatus achieves a high-speed measurement while suppressing the reduction of accuracy.

Abstract: The invention relates to systems and methods for site selection and placement of extra-anatomic passages altering gaseous flow in a diseased lung.

Abstract: An implantable cell/tissue-based biosensor device detects and/or monitors the amount of one or more specific analytes within a patient. Stimulation circuitry stimulates the cells/tissue of the biosensor device causing the cells/tissue to evoke a response that is altered by the presence of a specific analyte. Sensing circuitry detects the evoked response and the amount of analyte is determined based on the detected response.

Abstract: A system is provided for monitoring glucose in a host, including a continuous glucose sensor that produces a data stream indicative of a host's glucose concentration and an integrated receiver that receives the data stream from the continuous glucose sensor and calibrates the data stream using a single point glucose monitor that is integral with the integrated receiver. The integrated receiver obtains a glucose value from the single point glucose monitor, calibrates the sensor data stream received from the continuous glucose sensor, and displays one or both of the single point glucose measurement values and the calibrated continuous glucose sensor values on the user interface.

Abstract: A system and computer implemented method for operating a respiratory ventilator ventilating a subject. One or more body signals obtained from the subject indicative of the subject's ventilation are analyzed so as to perform a spirometric assessment of the ventilation. It is then determined whether the spirometric assessment satisfactorily conforms to one or more predetermined spirometric standards. If the spirometric assessment does not satisfactorily conform to the spirometric standard, the operating parameters of the ventilator are adjusted. The invention also provides a system for carrying out the method.

Abstract: A noninvasive blood glucose level measurement system for determining the glucose level of blood, including a processor configured for determining a blood glucose level from a measurement of arterial pressure. Also included is a method of determining a blood glucose level from a measurement of arterial pressure.

Abstract: A sensor array designed to be continuously indexed through a compatible blood glucose test monitor for the purpose of conducting multiple consecutive blood glucose measurements. The sensor array can be configured to substantially conform to a non-planar surface. In one embodiment, the sensor array includes first and second test sensors which are hingedly coupled together through a pin and socket interconnection. In another embodiment, the sensor array includes a unitary, non-conductive substrate which is scored to define one or more fold lines, a first set electrodes deposited on the substrate to define a first test sensor, and a second set of electrodes deposited on the substrate to define a second test sensor.